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Pain Assessment and Management: Massachusetts

2 Contact Hours including 2 Advanced Pharmacology Hours
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This peer reviewed course is applicable for the following professions:
Advanced Practice Registered Nurse (APRN), Certified Nurse Midwife, Certified Nurse Practitioner, Certified Registered Nurse Anesthetist (CRNA), Certified Registered Nurse Practitioner, Clinical Nurse Specialist (CNS), Licensed Practical Nurse (LPN), Licensed Vocational Nurses (LVN), Midwife (MW), Nursing Student, Occupational Therapist (OT), Occupational Therapist Assistant (OTA), Physical Therapist (PT), Physical Therapist Assistant (PTA), Registered Nurse (RN), Registered Nurse Practitioner, Respiratory Therapist (RT)
This course will be updated or discontinued on or before Thursday, April 22, 2027

Nationally Accredited

CEUFast, Inc. is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center's Commission on Accreditation. ANCC Provider number #P0274.


Outcomes

≥ 92% of participants will know how to assess and manage pain.

Objectives

By the end of the activity, the learner will be able to:

  1. Outline the multidimensional nature of pain.
  2. Summarize the assessment and measurement of pain.
  3. Describe the risks of abuse and addiction associated with opioid medications.
  4. Differentiate pharmacological and non-pharmacological techniques to manage pain.
  5. Compare and contrast the assessment and management of pain in infants, children, adults, and geriatric patients.
  6. Explain the use of opioid antagonists and partial agonists in the management of opioid addiction.
  7. Evaluate clinical conditions and treatment options in conditions with pain as a major component.
CEUFast Inc. and the course planners for this educational activity do not have any relevant financial relationship(s) to disclose with ineligible companies whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.

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Pain Assessment and Management: Massachusetts
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To earn a certificate of completion you have one of two options:
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Author:    Raymond Lengel (MSN, FNP-BC, RN)

Introduction

Pain is a universal experience. It can be the result of a single trauma or the symptom of many diseases. Although pain is seen as an adverse occurrence, in many instances, it is beneficial, a warning signal that the body needs care and protection.

Pain is a subjective experience, and the context in which it happens influences both how the pain is experienced and its meaning to the individual. Defining and quantifying pain has never been easy. As part of the human experience, pain has been described from the earliest times. The prehistoric person related pain and pain relief to the acceptance or anger of the gods. The French physician Dr. Albert Schweitzer proclaimed in 1931, "Pain is a more terrible lord of mankind than even death itself" (AZ Quotes, n.d.).

Multidimensional Nature of Pain

Pain is a significant problem in today's society. Pain carries consequences across various categories, including ethical, social, economic, and legal arenas. The International Association for the Study of Pain defines pain as "An unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage" (International Association for the Study of Pain [IASP], 2020). Margo McCaffery's landmark definition describes pain as: "whatever the experiencing person says it is, existing whenever and wherever the person says it does" (Pirschel, 2018). Chronic pain is not acute pain that refuses to go away, and it can be seen as a disease in its own right.

It is estimated that 20.4 percent of adults in the United States suffer from chronic pain, and eight percent of adults have high-impact pain (Dahlhamer et al., 2018). These numbers make it easy to understand why pain is one of the most popular reasons people pursue medical attention.

Persistent pain is often associated with anxiety, depression, functional impairment, sleep disturbances, disability, and impairment in activities of daily living. Low back pain is a common cause of chronic pain. Low back pain costs Brazil 2.2 billion dollars annually, with total health care costs of about 460 million dollars. Low back pain results in millions of missed work days yearly (Carregaro et al., 2020). Persistent pain is a significant cause of morbidity and is associated with significant costs.

Chronic non-malignant pain is defined as pain lasting more than three months and may affect any part of the body (Dydyk & Conermann, 2024). Chronic pain is multifaceted and presents in many ways. Incorrectly treated, acute pain can convert to chronic pain, and in many instances of chronic pain, the cause is unknown (National Institute of Neurological Disorders and Stroke, 2025). Chronic pain can also have a psychological impact that results in anxiety, depression, or the manifestation of somatization disorders. Treatment of chronic pain requires a patient-centered approach to enhance patients' well-being and improve their overall quality of life.

A consistent finding is that chronic pain occurs more frequently in women than in men. Complex Regional Pain Syndrome (CRPS) presents in three times as many women as men (van Velzen et al., 2019). It is estimated that global migraine prevalence is 14–15 percent, and it explains five percent of the time of those who live with a disability (Steiner & Stovner, 2023). Despite their higher prevalence of chronic pain, women’s pain complaints are sometimes dismissed or underestimated, leading to delayed diagnoses and treatment (Samulowitz et al., 2018).

Acute pain typically has an abrupt onset and is often described as sharp. It is often caused by events such as a broken bone, surgery, childbirth, dental pain, or burns. Acute pain may last a short period or a few months. The pain dissipates when the underlying cause has healed. When acute pain lasts longer than 3-6 months, it is termed chronic (Dydyk & Conermann, 2024). Acute pain that is not appropriately treated may lead to chronic pain.

Multiple barriers to effective pain management exist. These include many individual, family, healthcare provider, societal, and political barriers. The good news is that we have the knowledge and skills to manage most pain effectively. So, what is the problem? Why is unrelieved pain still so prevalent?

Knowledge is important. Clinicians and patients need to be knowledgeable about assessing and managing pain. Knowledge alone rarely changes practice. Efforts must go beyond education alone if pain treatment is to improve. Pain needs to be made visible so it will not go unnoticed by clinicians.

Pain Theories

Nerve fibers transmit pain impulses to the brain, where the brain can personalize the pain experience. Pain theories help clinicians understand the pain and help guide the treatment of pain. One of the first theories of pain was formulated by the French philosopher Rene Descartes in the 17th Century and was titled the 'Specificity Theory' (Moayedi & Davis, 2013).

Descartes believed that the human soul resided in the pineal gland, the source of sensations the individual experienced, including pain. The Specificity Theory of Pain suggests that specific pain receptors send signals to the brain that create pain awareness. According to the theory, pain is an independent sensation with particular peripheral sensory receptors, which drive signals through the nervous system to centers in the brain (Moayedi & Davis, 2013).

Other theories that came to light in the 1900s include the Pattern Theory, Central Summation Theory, the Fourth Theory of Pain, and the Sensory Interaction Theory.

Another theory is the Gate Control Theory (Moayedi & Davis, 2013). Pain stimulation is transmitted by small, slow fibers that go into the spinal cord's dorsal horn. The theory states that a gate in the spinal cord controls sensory information through the cord. When there is more pain stimulation, the gate blocking is less effective, and the gates remain open. When stimulation of the A-beta fibers occurs, such as lightly touching the skin, the gates may be closed, thus inhibiting pain perception. Also, messages that descend from the brain – such as those in anxiety states or extreme excitement – can affect the gates' opening or closing.

The Neuromatrix Theory of Pain (Melzack, 1999) offers a comprehensive framework for understanding pain as a multifaceted and individualized experience. Unlike earlier models, such as the Gate Control Theory, which emphasizes the role of sensory input in pain, the Neuromatrix Theory highlights the central nervous system's active role in generating pain.

According to this theory, pain arises from a "neuromatrix," a widespread network of neurons in the brain that integrates sensory, cognitive, and emotional information. The neuromatrix processes inputs from multiple sources, including sensory signals from the body, psychological states (e.g., stress, anxiety), memories of past experiences, and genetic predispositions. This integrated activity produces the "pain neurosignature," a unique pattern of neural activity that underpins the subjective experience of pain.

Types of Pain

  • Acute pain – Pain that has an abrupt onset and warns of a disease process or a threat to the body (National Institute of Neurological Disorders and Stroke, 2025).
  • Chronic pain – Pain that lasts beyond the usual duration that an insult or injury to the body needs to heal. Pain without apparent biological value that lasted beyond the usual tissue healing time (typically at least three months) (Dydyk & Conermann, 2024).
  • Maladaptive pain – Pain that is not useful and is out of proportion to tissue damage. This type of pain lasts long after tissue healing and is often due to changes in the central nervous system (Walters, 2019).
  • Allodynia — Pain from a stimulus that typically does not cause pain (National Institute of Neurological Disorders and Stroke, 2025).
  • Hyperesthesia – Increased sensitivity to stimulation (National Institute of Neurological Disorders and Stroke, 2025).
  • Paresthesia — An unusual sensation often described as burning or prickling and commonly affects the extremities (Hammi & Yeung, 2022).
  • Visceral pain – Pain from the viscera mediated by stretch receptors. This pain is commonly described as deep, dull, poorly localized, and cramping (Grundy et al., 2019).
  • Nociceptive pain – Pain from threatened or real tissue damage to non-neural tissue caused by nociceptor activation (National Institute of Neurological Disorders and Stroke, 2025).
  • Neuropathic pain – Pain from an abnormal neural activity from an injury, disease process, or nervous system dysfunction (National Institute of Neurological Disorders and Stroke, 2025).
  • Mononeuropathy - Neuropathy that affects one nerve (Hammi & Yeung, 2022).
  • Polyneuropathy – Neuropathy that affects several nerves (Hammi & Yeung, 2022).

Pain Anatomy and Physiology

Anatomy and physiology are key factors in understanding pain. The central nervous system's primary function is to deliver information about actual or potential threats or injuries. Stimulation of pain receptors (nociceptors) results in physiological pain (Armstrong & Herr, 2023).

Two major types of physiological pain are somatic pain and visceral pain. Somatic pain originates from the skin, muscles, bones, joints, or connective tissues (Armstrong & Herr, 2023). Depending on the structures involved, it is categorized as superficial or deep. Superficial somatic pain arises from the skin or mucous membranes and is often sharp or burning, such as a cut or a minor burn. Deep somatic pain originates from muscles, bones, tendons, or ligaments and is typically described as aching, throbbing, or dull, such as pain from a sprain or a bone fracture (Armstrong & Herr, 2023).

Somatic pain is transmitted by nociceptors, which detect injury or inflammation and send signals to the brain through the peripheral and central nervous systems. This type of pain is usually well-localized, allowing individuals to pinpoint the affected area.

Somatic pain serves a protective function, alerting the body to injury and promoting behaviors that facilitate healing, such as resting the affected area. It is distinct from visceral or neuropathic pain.

Visceral pain arises from stimulating pain receptors in the internal organs such as the heart, intestines, lungs, liver, and pancreas. It is less specific than somatic pain. The number of cells in the spinal cord receiving signals from the internal organs is less than those that get responses for the superficial body locations (Robinson & Gebhart, 2008). It is often difficult for the patient to pinpoint the exact location of the pain; consequently, it is often experienced as referred pain coming from the body surface. Visceral pain receptors include chemoreceptors, but they are not limited to them. Instead, visceral pain is detected by various specialized nociceptors in the walls of internal organs, which respond to different stimuli. The viscera's pain chemoreceptors respond to different chemicals, including those from activating the inflammatory process. Pain receptors in the viscera can also respond to stretching of the organs, temperature, and organ ischemia.

Pathological pain is caused not by stimulation of pain receptors but by damage to the central nervous system itself, including changes in the spinal cord's neural pathways, the trigeminal nucleus, and other brain areas. It is highly complex and difficult to treat. Pathological pain includes central neuropathic pain and pain in diseases including CRPS, fibromyalgia syndrome (FMS), and irritable bowel syndrome (Dydyk & Givler, 2023)

Primary afferent fibers transmit noxious stimuli from the body's periphery to the spinal cord's dorsal horn. The A-delta fibers have a small diameter, are lightly myelinated, and conduct pain signals relatively quickly. They transmit rapid, sharp pain and give precise information regarding the anatomical location of the pain. C fibers are small and unmyelinated fibers that conduct slowly, respond to multiple stimuli, and lead to dull, achy pain (Anwar, 2016).

The Periaqueductal Gray (PAG) is an area of the midbrain, and it plays a major role in processing pain, particularly in the modulation of pain signals transmitted back to the dorsal horn of the spinal cord and the trigeminal nucleus (Mokhtar & Singh, 2023). Modulation describes how numerous systems affect pain intensity, and several spinal cord and brain systems modulate pain. Endogenous opiates are one way to affect the intensity of pain. When the pain is identified in the cerebral cortex, it descends back to the periphery. Descending pathways for pain begin in many brain areas and travel to cells in the spinal cord's dorsal horn and the trigeminal nucleus cells and are usually parallel to the ascending pathways. The vagus nerve provides an additional route for sensory and pain information to the brain, especially from the viscera (Kenny & Bordoni, 2022).

The neurons transmit pain by releasing substances and neurotransmitters (Teleanu et al., 2022). The excitatory substances contributing to pain include substance P, glutamate, prostaglandins, and nitrous oxide. Inhibitory neurotransmitters inhibit, or partially inhibit, the transmission of pain. Common inhibitory neurotransmitters include glycine, serotonin, norepinephrine, acetylcholine, and gamma-aminobutyric acid (GABA) (Teleanu et al., 2022). Certain medications are involved in modulating these neurotransmitters to help reduce pain.

The Impact of Pain

Pain affects multiple aspects of life. Pain can lead to physiological changes and potentially to physical illness. It may lead to cognitive changes, as many patients with chronic pain suffer from depression and anxiety. In primary care clinics, up to 46 percent of people with chronic pain also suffer from depression (Meda et al., 2022). Pain can change how one thinks and acts, leading to behavioral changes.

Pain has the potential to affect an individual's social life. Chronic pain may limit the patient's desire to interact in social settings. Social consequences of unrelieved pain may include isolation, inability or reduced desire to go to work, and overall reduced quality of life (Ashton-James et al., 2022). Expression and reporting of pain can vary by culture. Some cultures have a more stoic attitude to pain, while others may express more emotion.

The biopsychosocial model of pain care leads to a significant step in how people with pain are perceived and handled. This holistic approach to pain acknowledges the importance of the psychological and social factors that play a role in the patient's subjective pain experience and considers cognitive, emotional, spiritual, and cultural issues unique to the individual and their pain journey (Borrell-Carrió et al., 2004). Suffering related to pain is an individual experience. One of the biopsychosocial model's core principles is permitting patients to take part in and direct their care (Borrell-Carrió et al., 2004).

The political arena can greatly affect pain in society. Previously, pain management has focused on eliminating and reducing pain at all costs. This attitude has contributed to the opioid epidemic and many problems for society. In recent years, politicians have been implementing laws to ensure that pain is sufficiently assessed and treated with extra caution in stopping medication abuse and addiction.

Substance Abuse

Substance abuse issues are a real concern in the management of pain. Inappropriate prescriptions of pain medications have the potential to increase patient's chances of medication abuse. Below are some statistics regarding the current state of substance abuse.

  • In 2020, 40.3 million Americans had a substance use disorder, and only 6.5 percent received treatment (National Institute of Drug Abuse, 2023).
  • Black, American Indians, and Native Alaskans had the largest number of fatal overdoses (National Institute of Drug Abuse, 2023).
  • The number of annual opioid overdose deaths is more than six times higher than it was in 1999 (Federal Communications Commission, n.d.).
  • In 2022, nearly 108,000 drug overdose deaths occurred in the United States, with approximately 82,000 (about 76%) involving opioids (Centers for Disease Control and Prevention [CDC], 2024).

The CDC 2022 Guideline for Prescribing Opioids for Chronic Pain (Dowell et al., 2022) reiterates the need for adequate pain control and the challenges involved, particularly in chronic pain control. It recommends that providers utilize the "full range of therapeutic options" to treat chronic pain (Dowell et al., 2022). The report states that it is hard to quantify the number of individuals who could benefit from long-term use of opioid medications.

The report states that between 1999 and 2014, more than 165,000 people died from opioid overdoses (Dowell et al., 2022). Research has found practices that have contributed to the opioid overdose epidemic, the most important of which are prescribing high doses of opioids, overlapping opioid and benzodiazepine prescriptions, and the use of extended-release opioids for acute pain (Dowell et al., 2022).

The CDC guidelines make recommendations in three areas of opioid use:

  • Determining when to start or continue opioid medications in the treatment of chronic pain
  • Selection, dosage, duration of therapy, follow-up, and medication discontinuation
  • Assessment of risk factors and tackling the harmful consequences that can occur with opioid use

The guideline recommends that non-pharmacologic therapies and non-opioid medications are the first-line treatment when treating chronic pain (Dowell et al., 2022). The CDC recommends using immediate-release opioids at the lowest effective dose, rather than the extended-release form, to treat acute pain (Dowell et al., 2022).

Before starting opioid therapy to treat chronic pain, clinicians must establish goals with the patient that involve realistic outcomes for pain relief and improved activity (Dowell et al., 2022). Continue opioids only if there is sufficient improvement in the patient's pain levels and a positive impact on their quality of life that outweighs the possible adverse side effects of opioid use. After one to four weeks of opioid therapy, the provider needs to reassess the patient. Continued opioid therapy evaluations for the benefits and risks of opioid therapy need to be done at least every three months. When discontinuing opioids, a reduction of 10% of the medication dose per week should alleviate the symptoms of opioid withdrawal.

Extra caution should be implemented in some groups of patients. Areas of risk for opioid use include patients with sleep apnea, pregnancy, patients with renal or hepatic insufficiency, those older than 65, people with mental health disorders, patients with substance abuse disorders, and individuals with a previous non-fatal overdose (Dowell et al., 2022).

The CDC guidelines also note the clinician's importance of using state Prescription Drug Monitoring Program (PDMP) data to verify whether or not the patient is getting opioid medications or dangerous medication combinations that place them at high risk for overdose (Dowell et al., 2022).

Prescription drug misuse is the use of prescription medication in a method or intent inconsistent with how it was prescribed. Misuse includes using medication to get high, selling or sharing it with others (diversion), overuse, having multiple prescribers, and concurrent use of alcohol or other illicit substances. Misuse is a necessary criterion, but solely sufficient, for a substance use disorder (American Psychiatric Association, 2022).

Susceptible individuals are at risk of misusing medications that stimulate the brain's reward center, including opioid analgesics, stimulants, benzodiazepines, or tranquilizers. Drug abuse is when drugs are not used medically or socially appropriately. Controlled substances may lead to dependence, either physical or psychological, or both. Physical dependence transpires when there are withdrawal symptoms such as anxiety, elevated heart rate, hypertension, sweating, an unstable mood, or dysphoria after the substance is stopped (Szalavitz et al., 2021).

Psychological dependence is the perceived need for the substance. It makes the person feel as though they cannot function if they do not have the substance. Psychological dependence often kicks in after physical dependence wears off. It typically lasts much longer than physical dependence and often is a substantial contributing factor to relapse (Wyoming Legislature, n.d; Szalavitz et al., 2021).

The National Institute on Drug Abuse provides multiple definitions for substance use/abuse-related terms (Wyoming Legislature, n.d.). Addiction is psychological dependence and extreme behavior patterns associated with the drug. At this point, there is typically a loss of control regarding drug use. The drug is continued despite severe medical and social consequences. Tolerance, increasing doses of the medication needed to produce an equivalent effect, is typically seen by the time addiction is present. Physical dependence can occur without addiction. Individuals who take chronic pain medication may be dependent on the medication but not addicted.

Addiction is a major concern for those taking opioids. When prescribing opioids, it is important to determine who is likely to participate in aberrant drug-related behaviors. Inappropriate use may occur in those with major depression, psychotropic medication use, younger age, or those with a family or personal history of drug or alcohol misuse (Dowell et al., 2022; Webster, 2017).

Aberrant behaviors may include abuse, misuse, or addiction. Examples of aberrant drug-related behaviors include (Dowell et al., 2022; Maumus et al., 2020):

  • Requests for early refills
  • Not taking medications as prescribed
  • Failure to keep appointments
  • Visits in distress
  • Frequent reports of lost medication
  • Using multiple prescribers
  • Positive urine drug test for illicit substances
  • Altering prescriptions
  • Resistance to referrals
  • Resistance to providing prior medical records
  • Resistance to change in therapy
  • Increasing the dose without telling the prescriber
  • Requests for specific drugs

Why Patients Do Not Report Pain

The reality is that many patients do not report pain or minimize the severity of the pain they are experiencing. There are several reasons, including poor communication between patients and healthcare providers. There are increased anxiety levels for those admitted to an acute care facility, seeing several different providers, not being entirely sure whom to report their pain to, and the sense of helplessness in finding themselves in a hospital gown and a strange environment. Nurses are vital as the patient's advocate and navigator through the system's complexity to ensure that pain is appropriately addressed.

Ethics and Pain

Multiple ethical issues surround pain and its management. Healthcare providers should attempt to minimize pain and suffering while maintaining a balance between adequate pain management and minimizing harm from pain treatment.

Ethical issues surround end-of-life care. Pain management at the end of life is a moral duty for the healthcare professional caring for a terminal patient. While opioid use may suppress respiration and may even accelerate death, pain treatment is a necessary part of care for intractable pain as death approaches. The goal of pain management is to ease suffering, not accelerate death. Palliative sedation is used to manage refractory pain at the end of life.

Pain Assessment and Measurement

The Joint Commission (2022) emphasizes the value of efficient pain assessment and management across healthcare settings. Organizations are responsible for guaranteeing that suitable screening and assessment tools are accessible and used appropriately. These tools must be evidence-based and designed for the patient's age, condition, and understanding capacity.

A 'screening' evaluates the potential presence of a problem. An 'assessment' gathers more specified information through data collection, observation, and physical exam. Pain assessment tools should be evidence-based and include an evaluation of pain intensity, location, quality, and associated symptoms (The Joint Commission, 2022).

Regardless of the patient setting, the intensity of pain should be assessed and documented at these times:

  1. During the first evaluation of the patient.
  2. After any pain-producing procedure.
  3. With each new report of pain.
  4. At suitable intervals after pharmacologic (45-60 minutes after an oral intervention; 15-30 minutes after parenteral intervention) or non-pharmacologic intervention to assess the existing pain treatment plan.

Pain threshold refers to the minimal level at which an individual senses pain as a harmful stimulus (Lalouni et al., 2021). It is the level at which the patient first states that what they are feeling is painful, which varies significantly from patient to patient. Pain tolerance refers to the degree of pain a person can tolerate before it becomes unbearable. Pain tolerance differs from patient to patient and varies for the same individual depending on numerous factors, including time, setting, and stimulus (Fillingim, 2017). Healthcare providers must resist the temptation to compare patients' pain threshold and tolerance, especially those with similar procedures.

Measuring the severity of pain is often done on scales. Pain scales compare the intensity of the patient's pain at different time points, not to compare one person's pain to another. The use of pain scales assists the healthcare provider in determining the effectiveness of pain treatment.

The most effective pain assessment scales are concise, valid, require minimal training, and incorporate both behavioral and descriptive pain measures (Herr et al., 2011). When selecting a scale, it is essential to consider the individual needs of the patient to ensure accurate pain assessment (Pasero & McCaffery, 2011). Additionally, patient education regarding pain assessment plays a critical role in effective pain management.

A "0 to 10" numerical scale is a widely used measure to assess pain intensity (Nugent et al., 2021). When using the Numerical Rating Scale (NRS), patients rate their pain from 0 to 10, with "0" equaling no pain and "10" equaling the worst possible pain they can imagine. This numeric pain scale has become widely used. Still, an unexpected result of its use is the practice of prescribing specific doses of opioid pain medication centered exclusively on pain intensity. Prescribing pain medication in this way is a practice that is commonly referred to as "Dosing to Numbers" and has become an issue for several reasons: pain ratings are a completely subjective finding, pain cannot be measured objectively, and pain ratings are frequently not a repeatable finding even for the same patient (Quinlan-Colwell et al., 2022).

No research indicates that a given dose of opioids will produce pain relief for a specific pain intensity level in all patients. In a position paper released by the American Society of Pain Management Nursing (ASPMN), the organization states that "prescribing doses of opioids based solely on a patient's pain intensity should be prohibited" (Quinlan-Colwell et al., 2022). The ASPMN believes that this practice does not consider other facets of pain management assessment, and basing opioid administration entirely on a numeric value on a pain intensity scale results in poor pain control. The ASPMN advocates that "safe and effective opioid dosing is dependent on the careful assessment of multiple objective measures," and they include in these findings the following (Quinlan-Colwell et al., 2022):

  • Age of the patient
  • Other existing healthcare conditions
  • Level of sedation
  • Patient's respiratory status
  • Other sedating medications being used
  • Patient's previous response to opioid medication
  • A subjective measure of pain intensity

Another scale allows the patient to rate their pain as "no pain, mild pain, moderate pain, severe pain, or unbearable pain" (Haefeli & Elfering, 2006). Pain maps can be used for those who have a difficult time speaking. In a pain map, there is a front and rear view of the body on a piece of paper, and the patient draws on the location of the pain and may rate the severity of the pain.

Since we have no instrument to measure pain intensity, like a sphygmomanometer measures blood pressure objectively, self-report is used as a valid measure of pain. Sometimes, healthcare providers think they are the best judges of a person's pain; however, they often either over or underestimate a patient's pain.photo of pain scale

Pain Scale

For patients who are NOT cognitively impaired but cannot respond verbally to rate their pain numerically, face scales with happy faces representing no pain (0) and progressively sadder faces representing increasing pain intensity may be used. The patient chooses the face that best depicts how they are feeling. Being unable to report pain reliably makes a patient vulnerable to under-appreciation of their pain and the possibility of under- or over-treatment. Nurses must ensure that pain is accurately assessed and treated in these vulnerable populations (Table 1).

Table 1: Pain Assessment Overview
This table outlines a pain assessment to ensure a comprehensive understanding of a patient’s pain. Key elements include:
  1. Location – Identifies where the pain originates and if it radiates.
  2. Pain Intensity – Evaluates the worst, best, and acceptable pain levels.
  3. Character/Quality – Helps establish the type of pain (somatic, visceral, or neuropathic).
  4. Onset & Pattern – Assesses when the pain starts, its duration, and any variations.
  5. Alleviating Factors – Identifies what relieves the pain.
  6. Aggravating Factors – Determines what worsens the pain.
  7. Impact on Life – Examines how pain affects daily activities, emotions, and relationships.
Types of Pain & Treatments
  • Neuropathic Pain (burning, shooting, tingling) – Treated with antidepressants, anticonvulsants, and local anesthetics.
  • Visceral Pain (squeezing, cramping, deep) – Managed with non-opioids like acetaminophen.
  • Somatic Pain (dull, achy, throbbing) – Treated with non-steroidal anti-inflammatory drugs (NSAIDs), opioids, corticosteroids, and local anesthetics.
(Fink, 2000; Haefeli & Elfering, 2006)

Pain assessment should include documentation of its impact on a patient’s quality of life. Key questions to consider include (Australian Pain Society, n.d., Haefeli & Elfering, 2006; Wahezi et al., 2022):

  • Does pain restrict physical activity or exercise?
  • Does pain impact sleep?
  • Do you need assistance or mobility aids because of your pain?
  • Has your pain limited your ability to work or perform household tasks?
  • Are there any hobbies or activities you have stopped because of pain?
  • Can you perform essential daily living activities such as bathing, dressing, feeding, toileting, or brushing your teeth?
  • Does your pain affect your mood or cause feelings of anxiety, stress, or depression?
  • Does pain lower energy levels?
  • Does pain limit participation in activities and social interactions?
  • Does pain impact personal relationships?
  • Does pain interfere with instrumental activities of daily living (IADLs), such as using the telephone, doing laundry, managing medications, or handling finances?

Understanding how pain was treated in the past for the patient will help the clinician treat the current pain. Reviewing past medical records will help the pain management team evaluate the condition. Reviewing all previous history, diagnostic testing, treatment options, and the efficacy of those treatment options will help the team make an accurate diagnosis and manage pain appropriately. Certain treatment modalities, including specific medications, are often more effective in one individual when compared to another based on individual differences.

Understanding all medical and surgical conditions can help ensure proper pain management. A chronic disease may have a substantial impact on the management of pain. Chronic kidney disease, for example, reduces medication excretion. The use of NSAIDs can lead to kidney failure in those with chronic kidney disease (Baker & Perazella, 2020).

Many factors contribute to chronic pain. A mental health evaluation can help the clinician understand the best way to manage pain. Mood or cognitive disorders can impact the way the pain is treated. Chronic pain cannot be adequately managed in those with unidentified and untreated mental illness. A history of drug abuse is an essential factor to ascertain, which could profoundly affect chronic pain treatment. Personal characteristics may have a substantial effect on pain management. Factors influencing pain include race, age, culture, religion, sex, or language.

A review of the patient's perception of the pain is essential. Why does the patient believe they have persistent pain? Does the patient feel there was adequate workup done on their condition? What does the patient expect from treatment, and what are the patient's goals? Psychological factors contributing to the pain should be assessed to help assess the patient's expectations. Patients need to have realistic expectations about pain management.

A complete physical exam is an essential part of the management of pain. It is vital to have a baseline examination so that subsequent evaluations will allow the healthcare team to determine pain management and functional capacity progress. The physical exam should include a detailed neurological exam, including the patient's ambulation ability. Observing hygiene, posture, dress, and appearance is essential. Those with severe pain will often have poor hygiene, unkempt dress, and appear to be in pain. Observe for any splinting, which may suggest a painful part of the body. Assessing skin and joints for redness, swelling, or deformities helps determine the location and etiology of the pain. Perform an abdominal exam for any tenderness or distention. Also, checking joints for a full range of motion is essential to the physical exam in chronic pain. The exam should evaluate functional capacity, strength, endurance, and pain-related limitations (Haefeli & Elfering, 2006; Wahezi et al., 2022).

Ongoing monitoring for the efficacy and effectiveness of the implemented plan is essential. Utilizing similar assessment tools, the healthcare provider can document the effectiveness of the pain management plan on the patient, including improvements in the quality of life.

Diagnostic Tests

Diagnostic testing can help evaluate painful conditions. It is essential to realize that an abnormal diagnostic test does not confirm the source of the pain. Blood tests can be helpful in some conditions to determine or monitor specific causes of pain. For example, an elevated C-reactive protein or an erythrocyte sedimentation rate may be seen in those with polymyalgia rheumatica, infection, or rheumatoid arthritis (RA) (all conditions that may cause pain) (Bitik et al., 2015).

Imaging may be necessary for some situations of chronic pain. X-rays, computed tomography, and magnetic resonance imaging can help define the etiology of the pain. Use caution with imaging, as many abnormalities that are not the source of pain may be detected on imaging tests.

Electromyography (EMG) and nerve conduction studies (NCS) are diagnostic tests used to evaluate the health and function of muscles and peripheral nerves. EMG measures the electrical activity of muscles at rest and during contraction using a fine needle electrode inserted into the muscle. This test helps detect abnormalities in muscle function, such as those caused by nerve disorders, muscle diseases, or neuromuscular junction issues. On the other hand, nerve conduction studies assess how well electrical signals travel along a nerve. During NCS, small electrical pulses are applied to a nerve, and the responses are recorded to determine conduction speed and strength. Together, these tests provide valuable information for diagnosing conditions like carpal tunnel syndrome, peripheral neuropathy, radiculopathy, and other neuromuscular disorders (National Library of Medicine, 2024).

Management of Pain

The goals of pain management are not necessarily complete pain relief. They may include a reduction in pain, improved quality of life, improved physical and psychological functioning, improved ability to work, improved ability to function in society, and reduced healthcare utilization.

A pain management plan is more than just a prescription for pain medication. In addition to pharmacotherapy, it should include psychological and physical modalities to manage pain. It should be modified when interventions are not sufficient. Successful treatment of chronic pain requires an interdisciplinary healthcare team's input and a holistic approach to care to improve the patient's overall quality of life. One of our most essential roles is listening to our patients, which is especially important for pain patients, particularly those with chronic pain. These patients frequently suffer from intense fear, anxiety, insecurity about the future, social isolation, and loneliness. The opportunity to tell one's story to someone consciously listening is therapeutic.

Educate the patient regarding the plan. Education should include information about prescribed medications, other treatment options, and methods to contact the pain management team.

When developing a treatment plan, there are many considerations. Consider the type of pain and its effect on lifestyle, including psychological, social, and biological components. Many factors affect the success of the treatment plan. Issues related to the patient, such as their ability to understand and apply the management plan, will help determine its success. The patient's willingness to implement the whole plan can profoundly affect the success of the plan. If a patient is willing to take a pill but is unwilling to work on non-pharmacologic interventions (such as physical therapy or weight loss), the plan will lose its effectiveness.

Caregiver or healthcare provider issues often affect the pain management plan. Many caregivers and healthcare providers do not accurately comprehend the patient's pain and may hold false beliefs regarding pain management. Caregivers and healthcare providers may be inhibited by fear of side effects from medications or concerns of drug addiction; therefore, they may withhold medication to those in pain. Also, caregivers/healthcare providers and patients may have conflicting goals.

Controlled substances should be prescribed for a legitimate medical purpose with careful consideration of the patient's safety, therapy goals, and efficacy. Not only should the treatment of pain include pharmacotherapy, but physical and psychological therapies should also be used. Many caregivers lack knowledge and understanding of non-pharmacological pain treatments and cannot provide patients with the full scope of available pain therapies. Referral to a pain management specialist may be indicated for those who have debilitating symptoms, those who need increased doses of pain medications, those who are non-responsive to treatments, or those with symptoms at multiple sites.

Non-pharmacological Therapy

Numerous non-pharmacologic therapies manage pain. These may include a combination of physical and psychological techniques. Some methods used other than medications include physical therapy, exercise, massage, ultrasound therapy, heat/cold application, joint manipulation, psychotherapy, biofeedback, relaxation therapy, acupuncture, transcutaneous electrical nerve stimulation (TENS), music therapy, injections, neuromodulation, spinal cord stimulation, deep brain stimulation, and radiofrequency ablation of nerve tissue.

For those with pain, a physical or occupational therapy trial can be helpful. With the help of a physical therapist, exercises targeting a specific type of pathology can help manage pain. Occupational therapists can help recommend devices that can enhance daily living activities. With chronic pain, there is a tendency not to move, which leads to deconditioning and further incapacity—deconditioning results in more significant pain with any form of movement.

Maintaining muscle mass prevents this downward spiral. It has also been shown that the more an individual participates in exercise, the less probability they develop back pain. Physical activity has significantly improved the overall health of those with lower back pain. Exercise, especially those performed in water, benefits patients with arthritis pain, and aerobic exercise has effectively decreased pain connected with FMS (Couto et al., 2022).

Yoga and Pilates have also become popular alternative treatments, especially for back pain. However, some yoga poses can be a potential cause of injury, especially those that involve overstretching of the neck. Tai Chi, another practice involving slow, gentle movements, deep breathing, and relaxation, has positive effects on pain relief for several conditions, including FMS, arthritis, and low back pain.

Massage is soothing and relaxing, both physically and mentally. Massage may decrease pain by relaxing muscle tension and increasing blood flow, thereby improving general circulation (Weerapong et al., 2005).

Heat and cold therapies can assist in the management of pain. Heat lowers inflammation and helps relaxation, and it may occur in the form of hot tub baths, heating pads, or heat packs. Cold is often more helpful in reducing pain than heat. The application of cold reduces muscle spasms secondary to underlying skeletal muscle spasms, joint pathology, or nerve root irritation. Cold application methods include ice massage, ice bags, and gel packs. Alternating heat and cold is more effective than using either alone (Malanga et al., 2015).

Multiple psychological techniques can aid in reducing pain. The basis for using these methods is that thought influences feelings, and if thought (and behaviors) can be modified, so can feelings and even sensations, such as pain. Cognitive-behavioral methods command the patient's active participation. Cognitive-behavioral therapy (CBT) has proven to be an effective coping skill for those with chronic pain. CBT emphasizes the present moment, where individuals become aware of their thoughts, feelings, and behaviors and journal these perceptions. CBT helps decrease the emotional distress associated with chronic pain by focusing on how one perceives pain and adjusts to it. A recent study showed that CBT was superior to other therapies in improving disability, pain, fear avoidance, and self-efficacy (Yang et al., 2022).

Relaxation is a state of relative freedom from anxiety and skeletal muscle tension, a quieting or calming of the mind and muscles. Although relaxation is a learned technique, it can be attained quickly in a motivated patient.

Imagery/visualization involves mentally constructing a picture by utilizing one's imagination. This mental picture may focus on a close person, a place of enjoyment, a past event, or anything that brings pleasure. An occupied mind does not focus on the pain.

Distraction from pain is concentrating on stimuli other than the pain sensation. The stimuli focused upon can be auditory, visual, or tactile-kinesthetic. Focusing on stimuli other than pain directs the pain to the periphery of awareness. Distraction does not make the pain go away, nor does the effectiveness of distraction indicate the absence of pain. Music and humor are acceptable instruments of distraction.

TENS supplies low-voltage electricity to the body via electrodes placed on the skin. TENS may ease acute or chronic pain (Johnson et al., 2022). Electrical stimulation of sensory nerves helps block pain signals going to the brain. TENS is contraindicated in patients with pacemakers, electrical implants, cardiac arrhythmias, circulation problems, and pregnancy (NHS, 2022b).

Biofeedback is a technique to harness the mind's power to allow the patient to be more aware of the body's sensations. The exact mechanism is unclear, but it promotes relaxation and helps reduce pain (National Library of Medicine, 2018).

Acupuncture is a neurostimulation technique that manages pain by inserting small, solid needles into the skin at varying depths. Various theories explain how acupuncture works. The Chinese acupuncture theory allows the release of blocked energy in the body. In Chinese medicine, this energy source is known as Qi, and its ability to flow freely through the body is related to overall well-being (National Library of Medicine, 2018).

Different surgical interventions or procedures can be used in the pain management plan. Procedures may include injections, spinal cord stimulation, deep brain stimulation, neural ablative techniques, and surgical interventions. These are potential options for those in whom other methods have not controlled the pain.

Teaching Coping Skills

Pain has two parts; first of all, there is the perception of pain, which is related to the strength and characteristics of the pain, and secondly, there is the effect the pain has on the individual. What is its emotional impact, and how is it impacting their quality of life? When healthcare providers perform a pain assessment, the strength or intensity of the measured pain may not reflect how the pain affects their lives. How pain affects an individual is intimately associated with their ability to cope.

Coping can be defined as what an individual thinks and does in a situation that causes them stress. It is greatly affected by the resources available to the person to manage the event. Coping is a crucial part of pain management, especially for those with chronic pain (American Psychological Association, 2011). Nurses need to be aware of the need to assess patients' coping patterns as they relate to pain and to be able to discuss necessary coping skills with them.

Catastrophizing is the opposite of coping and is the idea that a situation will continue to worsen. It is an essential predictor of pain and pain adjustment, especially in chronic pain. The individual experiences heightened worry and fear that have intensified the pain the person feels. Instead of problem-solving, the individual tends to turn away and feel hopeless about their situation. Nurses must watch for catastrophizing when assessing a patient's pain by listening carefully to how the patient illustrates their pain and how they identify its effect on their life now and in the future.

Pharmacologic Interventions

Pharmacological pain management involves the use of medications to alleviate pain, categorized into non-opioid, opioid, and adjuvant analgesics. Non-opioids, such as acetaminophen and NSAIDs, are effective for mild to moderate pain and have anti-inflammatory properties. Opioids are used for moderate to severe pain but require careful monitoring due to the risk of dependence and side effects. Adjuvant analgesics, like antidepressants and anticonvulsants, enhance pain relief, particularly in neuropathic pain. A multimodal approach, combining different drug classes, is often recommended for optimal pain control while minimizing side effects and the risk of tolerance.

Prescribing oral analgesic agents is convenient and allows a relatively steady blood concentration of the drug. Pain medication may be administered on an as-needed basis for episodic pain or given routinely for chronic persistent pain. Routine, around-the-clock medication sustains a steady state in the blood and offers better pain relief for those with persistent pain (Von Korff et al., 2011). Consider side effects when deciding which medication to use.

Considering all co-morbidities is an essential step in the management of pain. For example, when a patient suffers from chronic pain and depression, some medications may help effectively manage both conditions (for example, duloxetine is approved to treat chronic musculoskeletal pain, including discomfort from osteoarthritis (OA) and chronic lower back pain in addition to depression). It is also essential to establish the pain syndrome's pathophysiology, evaluate the medication list, and consider side effects.

The clinician should distinguish between neuropathic pain and nociceptive pain. Establish the etiology of neuropathic pain and, if the etiology is reversible, manage the underlying problem. For example, if a medication (e.g., metronidazole, nitrofurantoin, isoniazid, or many cancer agents) is the cause of the neuropathy, consider altering that medication.

Medications used in treating neuropathic pain include calcium channel alpha 2-delta ligands (gabapentin and pregabalin), tricyclic antidepressants (TCAs), serotonin-norepinephrine uptake inhibitors (SNRIs), the lidocaine patch, and narcotic analgesics (Finnerup et al., 2021).

Treat nociceptive pain with non-narcotic and opioid analgesia. Common causes of nociceptive pain include arthritis and chronic low back pain. Acetaminophen is often used as a first-line agent in the management of nociceptive pain (Fitzcharles et al., 2021). However, acetaminophen has become a chief cause of acute liver failure. According to government statistics, there are close to 2600 hospital admissions and 500 deaths annually associated with acetaminophen overdose (Agrawal & Khazaeni, 2023). Patients must be warned that alcohol and acetaminophen are a hazardous combination, and alcohol consumption should not occur when taking this medication. In January 2011, the Federal Drug Administration (FDA) requested drug manufacturers to limit acetaminophen in combined products to 325 milligrams per dose (National Institute of Diabetes and Digestive and Kidney Diseases [NIDDK], 2023). The FDA also required that labels carry a 'black-box' warning, highlighting that acetaminophen can result in severe liver damage.

Acetaminophen is not an anti-inflammatory agent but is a very common over-the-counter medication used to manage pain. Acetaminophen is commonly administered with opioid medications to reduce the amount of opioid medication needed to manage the pain.

Acetaminophen is dosed with 325 to 650 milligrams (mg) every four hours or 500 to 1000 mg every six hours, not exceeding 3000 to 4000 mg daily (Gerriets et al., 2024). In the pediatric population, acetaminophen is dosed at 10-15 mg/kilogram (kg)/dose every 4-6 hours, with a maximum of 75 mg/kg/day, but no more than 4000 mg daily (Gerriets et al., 2024). Reduce the dose in those with hepatic insufficiency or alcohol abuse. Absolute contraindication to acetaminophen is liver failure, while relative contraindications include chronic alcohol abuse or hepatic insufficiency. Those on a statin cholesterol medication may need a lower dose of acetaminophen.

NSAIDs are used as alternative options to acetaminophen and are indicated for mild to moderate pain, and some manage severe pain. Like acetaminophen, they act synergistically with opioids.

Because they act as an anti-inflammatory agent, they are often used for arthritis, strains, sprains, bursitis, and tendonitis (Ghlichloo & Gerriets, 2023). Frequently used NSAIDs are acetylsalicylic acid (Aspirin, which is the oldest known NSAID), ibuprofen (Advil®, Motrin®), naproxen (Aleve®), and diclofenac (Voltaren®). NSAIDs inhibit the production of the cyclooxygenase (COX) 2 (COX-2) and (COX-1) involved in synthesizing prostaglandins that mediate inflammatory responses and cause pain. COX-1 is involved in protecting the stomach lining from the damaging effects of acid, and one of the most frequently cited side effects of NSAIDs is stomach bleeding (Ghlichloo & Gerriets, 2023).

When compared to acetaminophen, NSAIDs are associated with more side effects and are potentially more problematic, especially in older adults. In older adults, the American Geriatric Society guidelines recommend that persistent pain due to OA not be primarily managed with NSAIDs (Ali et al., 2018). The use of topical NSAIDs is a good option for those with localized pain (Ghlichloo & Gerriets, 2023).

NSAIDs are not recommended for those with an active peptic ulcer, chronic kidney disease, or heart failure. Caution should be used in those with a history of peptic ulcer disease, Helicobacter pylori infection, hypertension, or concomitant use of selective serotonin receptor inhibitors (SSRIs) or corticosteroids (Ghlichloo & Gerriets, 2023).

NSAIDs' side effects include renal insults, adverse cardiovascular effects, headaches, constipation, and mental status changes. Gastrointestinal effects may include gastric ulceration and dyspepsia. Taking the medication with food or antacids may reduce the risk of dyspepsia. Those at high risk of gastric ulceration – older age, those on corticosteroids, bleeding problems, or a history of gastric ulceration – should not use NSAIDs. For those with compromised gastrointestinal tracts, the use of a proton pump inhibitor reduces the risk of gastric ulceration when NSAIDs are necessary (Moore et al., 2015). NSAIDs interact with many antihypertensive medications, aspirin, SSRIs, corticosteroids, and warfarin (Moore et al., 2015).

NSAIDs have the potential to cause nephrotoxicity. They inhibit prostaglandin synthesis, which leads to vasoconstriction of the afferent arteriole in the kidney, thus reducing the glomerular filtration rate. They should be used cautiously in renal impairment patients (Ali et al., 2018).

NSAIDs lead to cardiovascular complications and increase the risk of myocardial infarctions, especially in patients who take high doses over a prolonged period (Ghlichloo & Gerriets, 2023; Moore et al., 2015). For those with increased cardiovascular risk, their use should be limited.

Do not use NSAIDs in those with thrombocytopenia (low platelet count). Patients receiving warfarin or heparin should not receive NSAIDs. NSAIDs impede thrombocyte aggregation, increasing the risk of bleeding (Ghlichloo & Gerriets, 2023; Moore et al., 2015).

Antidepressant Use in Pain Management

Antidepressant medications are effective for multiple chronic pain types, including neuropathic pain, FMS, and pain associated with depression (Finnerup et al., 2021). This next section will look at some of the antidepressants used in the management of pain.

TCAs modify pain by inhibiting the uptake of norepinephrine and serotonin and blocking multiple channels, including the sodium, adrenergic, cholinergic, and histaminergic channels (Schneider et al., 2019). Medications in this class include nortriptyline, desipramine, amitriptyline, and imipramine. These agents are often used in managing neuropathic pain or in chronic pain management as adjuvant agents.

TCAs need to be used cautiously, especially in older adults. They have many side effects, including constipation, dry mouth, mental status changes, blurred vision, urinary retention, blood pressure changes, tachycardia, and heart block (Reinert et al., 2023). They should be used cautiously or not at all in those with cardiac or electrocardiographic abnormalities. The analgesic effect is typically noticed in a shorter time and at a lower dose than when treating depression (Schneider et al., 2019).

SNRIs are used for neuropathic pain but also treat other types of pain. Duloxetine (Cymbalta®) is indicated for diabetic neuropathy and painful chronic musculoskeletal conditions such as OA, chronic low back pain, and FMS (Birkinshaw et al., 2023). Common side effects include insomnia, drowsiness, dry mouth, fatigue, nausea, and dizziness. Avoid use in those with severe renal insufficiency or hepatic insufficiency (National Health Service [NHS], 2022a). When stopped, it should be tapered slowly due to withdrawal symptoms.

Antiepileptic Agents

Gabapentin is approved in adults for post-herpetic neuralgia up to 3600 mg per day in divided doses. Adjust the dose in those with renal disease. It comes in an extended-release form called Gralise®. Gabapentin is often used off-label for other neuropathic conditions, including diabetic neuropathy, generalized neuropathic pain, anxiety, and postoperative pain (Yasaei et al., 2024).

Pregabalin (Lyrica®) is approved in adults for FMS, neuropathic pain (diabetes-related), neuropathic pain in those with spinal cord injury, and post-herpetic neuralgias. Both pregabalin and duloxetine have been given regulatory approval for pain management in neuropathic diabetic pain in the United States, Canada, and Europe (Dowell et al., 2022).

Other Agents

Topical lidocaine is a first-line therapy for post-herpetic neuralgia. It is applied to intact skin, and up to three patches are applied for no more than 12 hours in 24 hours (Queremel Milani & Davis, 2023).

Muscle relaxers are commonly used to manage chronic pain when muscle spasms, tension, or spasticity contribute to discomfort (Chang, 2020). These medications fall into two main categories: antispasmodics, which target acute musculoskeletal conditions, and antispastics, used for neurological disorders like multiple sclerosis or spinal cord injuries. Muscle relaxers can effectively reduce muscle spasms, alleviate pain, and improve sleep, particularly for conditions such as FMS or tension-related pain. Their sedative properties can also help with sleep disturbances, which are often exacerbated by chronic pain. However, muscle relaxers are generally recommended for short-term use, as their long-term efficacy and safety are less well-studied. Potential side effects include drowsiness, dizziness, dry mouth, and, in some cases, dependency, particularly with medications like carisoprodol.

Opioids

In recent times, opioid therapy has become more commonly used. In the past, it was only used for severe acute pain and cancer pain. A position paper from the American Academy of Neurology suggested evidence for adequate short-term pain relief with opioids (Franklin & American Academy of Neurology, 2014). However, no good evidence exists for the continuation of pain relief or enhanced function for long periods without experiencing serious risk of dependence, overdose, or addiction (Dowell et al., 2022).

Opioids function by activating opioid receptors that are located in the spinal cord and the brain. The majority of the pain relief related to opioids is due to their actions on the periaqueductal gray (PAG) cells and the descending pain pathways (Lueptow et al., 2018). Opioid receptors are molecules located on the surface of cells; opioid substances attach themselves to them and release their effects.

There are three different types of opioid receptors found in the brain: mu, kappa, and delta receptors (Herman et al., 2024). Mu and kappa receptors are also found in the spinal cord and mediate pain transmission from the brain's peripheral nervous system. The most important pain receptor in opioid abuse and treatment is the mu receptor. When opioids activate mu receptors, the most significant potential for pain relief and addiction is initiated (Herman et al., 2024). However, kappa and delta receptors also play a role in opioid addiction.

Opioid agonists, partial agonists, and antagonists are drugs that interact with opioid receptors in the brain. Agonists, like heroin or morphine, fully activate these receptors, producing pain relief and euphoria. Partial agonists, such as buprenorphine, also bind to these receptors but activate them to a lesser extent, providing pain relief without the same level of euphoria or risk of overdose. Antagonists, like naloxone, block opioid receptors, reversing the effects of opioids and potentially causing withdrawal symptoms. Understanding these distinctions is crucial for managing pain, treating opioid addiction, and preventing overdose.

Side Effects of Opioids

Opioid medications are associated with multiple side effects, including constipation, nausea, vomiting, pruritus, abdominal cramping, sedation, and mental status changes (National Institute of Drug Abuse, 2024). Multiple interventions are available to reduce side effects.

  • Constipation is a frequent issue in those who use opioids. Risk factors for constipation include older age, intra-abdominal pathology, and those who eat a low-fiber diet. Those on opiates should be encouraged to increase fiber intake, drink plenty of fluids, and be encouraged to exercise. Stool softeners (e.g., docusate sodium) and stimulants (e.g., bisacodyl) may be needed to manage constipation. An osmotic laxative such as polyethylene glycol or lactulose may also be considered, which may be added to stool softeners/stimulants for resistant constipation.
  • Antiemetic medication can help treat nausea.
  • Antihistamines can treat pruritus.
  • Opioids are associated with somnolence and other mental status changes. Patients do develop tolerance to these symptoms over weeks. Reducing the dose may lessen the mental status changes. An adjunctive medication may be added to the lower dose of opioids to help manage the pain. Rarely, the use of a stimulant can be used to manage sedation due to opioid use.
  • Respiratory depression may occur, but it is uncommon when the medication is used carefully. Starting low and slowly titrating the dose will reduce the risk of respiratory depression. Problems arise with rapid titration, the addition of another drug that may suppress the respiratory drive (benzodiazepine, alcohol, or a barbiturate), or the patient overdoses. Sedation precedes respiratory depression, so when starting a patient on opioid therapy, encourage them to take the first dose in the office to be monitored or in the presence of a responsible adult who can help monitor the patient. The level of consciousness should be assessed 30-60 minutes after the opioid is given. Contact the prescriber immediately if there is a reduced level of consciousness, the patient has hypoxia, or has a respiratory rate of less than 10 per minute.
  • The most serious risk linked with opioid use is an overdose. From 2009 to 2019, the age-adjusted death rate for drug overdose increased from 11.9 per 100,000 to 21.6 (CDC, 2023).

The June 2024 report by the Massachusetts Department of Public Health examines opioid-related overdose deaths in the state (Massachusetts Department of Public Health, 2024). In 2023, there were 2,125 estimated deaths, marking a decline from 2022. Fentanyl remains a key driver, found in 90% of cases with toxicology data. Other substances, like cocaine (54%) and xylazine (9%), are increasingly present, reflecting shifts in drug supply dynamics. While rural communities experience higher adjusted death rates, urban areas also report significant impacts. Trends show a decrease in heroin-related deaths, replaced by the rise of synthetic opioids and stimulants, underscoring the volatile and dangerous nature of illicit drug markets.

Massachusetts Medical Society Guidelines

The Massachusetts Medical Society (Massachusetts Medical Society, n.d.) issued guidelines to support the idea that physicians use "best clinical judgment in patients' treatment." They also supported the adoption of separate guidelines for treating acute and chronic pain and chronic pain guidelines are used with patients who are on opioid therapy for more than 90 days. The guidelines would not apply to cancer patients, those in hospice and palliative care, and inpatients in hospitals and nursing homes.

Some key points in the Acute Care Guidelines for Opioid Prescription include the following (Massachusetts Medical Society, n.d.):

  • Thorough screening of the patient before initiating therapy will include:
    • Screening for pregnancy.
    • Obtaining and reviewing personal or family histories of a substance abuse disorder.
    • Evaluating the patient's mental status or pertinent behavioral issues.
  • Patients with complex pain issues, mental health conditions, or other serious illnesses should be considered for referral to a specialized pain clinic.
  • The patient's medication profile must be carefully reviewed. Is the patient on benzodiazepines and other medications that can potentiate the danger of opioid use?
  • Patients should be started on a trial of short-acting opioid medication. During this trial period, the patient should be closely monitored for both the positive and negative effects of the medication – is it relieving the pain, and how is it affecting the patient's level of functioning and quality of life? Are there any cognitive side effects or safety issues?
  • Educate patients to keep opioid medication safely, preferably in a locked cabinet. Under no circumstances should opioid medications be shared with others. Properly dispose of unused or expired medications. Most communities have secure drop-off locations for unwanted medications, many at the local police stations.

Some key points in the Chronic Pain Guidelines for Opioid Use include (Massachusetts Medical Society, n.d.):

  • Once a 90-day threshold has been reached, a complete re-evaluation of the patient should be done.
  • The patient is asked to complete an objective pain assessment tool, and the provider assesses the risk of substance abuse. Baseline urine drug testing may be done.
  • If continued opioid therapy is deemed appropriate, a treatment plan for treatment goals should be put in place and re-evaluated every 60 to 90 days.
  • Female patients should be educated on the risks of opioid use during pregnancy.
  • In consultation with the patient, a treatment agreement should be drawn up and preferably signed by the patient; it then becomes part of the medical record. Treatment agreements include the following:
    • Measurable goals for the reduction of pain.
    • A plan for a reduction in opioid medication that will mirror the decrease in pain and improved function.
    • Quality of life measurements should also be included in the plan.
    • Circumstances where a patient could get prescriptions from other providers should be discussed.
  • All clinicians who work with pain patients must prescribe naloxone and educate patients on how it works in reversing opioid overdose.

Morphine

While there are many opioids, morphine is considered by many as a standard comparator for other drugs. It is used for moderate to severe acute pain and severe chronic pain.  Morphine can be given orally, rectally, intravenously, subcutaneously, or intramuscularly (Murphy et al., 2023).

Side effects of morphine are similar to other opioid analgesics and include dry mouth, constipation, bradycardia, hypotension, nausea, drowsiness, dizziness, mental status changes, fever, itching, weakness, hypoxia, and urinary retention (Murphy et al., 2023).

Morphine should not be used in those with a hypersensitivity to morphine, those with toxin-mediated diarrheal disease, severe/acute asthma, paralytic ileus, or severe respiratory depression. The extended-release form should not be used in those with gastrointestinal obstruction. The extended-release forms of morphine are not interchangeable. Changing from one medication to another should be done only by those experienced in how to do this. Extreme caution should be used when using highly concentrated solutions so overdoses do not occur.

Drug interactions commonly seen with morphine include (Medscape, 2024c; Murphy et al., 2023):

  • Amphetamines may increase the effect of morphine.
  • Anticholinergic agents may increase the side effects of morphine (constipation and urinary retention).
  • Antipsychotic agents with morphine may reduce blood pressure.
  • Nasal azelastine with morphine enhances the central nervous system (CNS) depression effect.
  • Clopidogrel's therapeutic efficacy may be reduced with morphine.
  • Diuretic side effects may be increased with morphine.
  • Hydrocodone enhances CNS depression.
  • Hydroxyzine enhances CNS depression.
  • Monoamine oxidase inhibitors (MAOIs) enhance the side effects of morphine.
  • SSRIs with morphine enhance the serotonergic effect and CNS depression.
  • Zolpidem enhances CNS depression.

Fentanyl

Fentanyl, a potent synthetic opioid, is available in various formulations tailored to specific medical needs. It is commonly used in healthcare settings for pain management, particularly in severe or chronic cases. Formulations include multiple oral formulations, intravenous injections for rapid pain relief during surgery or emergencies, and transdermal patches for continuous pain control in chronic conditions. The transdermal patch is used in opioid-tolerant patients with moderate to severe pain and is often started at 25 micrograms (mcg) per hour and changed every 72 hours (Ramos-Matos et al., 2023).

Fentanyl can be used for multiple reasons, including premedication for surgery, general anesthesia, as an adjunct to general and regional anesthesia, and chronic pain management. The transdermal patch is indicated for around-the-clock pain management in those with chronic severe pain (Ramos-Matos et al., 2023).

Common side effects of fentanyl include dry mouth, edema, bradycardia, dehydration, respiratory depression, shortness of breath, diaphoresis, nausea/vomiting, constipation, application site erythema (patch), weakness, muscle rigidity, mental status changes, headache, sedation, and CNS depression (Medscape, 2024b; Ramos-Matos et al., 2023). As with most opioids, contraindications include hypersensitivity, toxin-mediated diarrheal disease, and paralytic ileus.

The patch should not be exposed to external heat, which increases absorption. Exercising with the patch and suffering from a fever increases the absorption of fentanyl. The patch should only be applied to intact skin and removed before a magnetic resonance imaging (MRI) as it could overheat, leading to burns.

Like many opioids, multiple potential interactions exist (Medscape, 2024b; Ramos-Matos et al., 2023). Some more common interactions include:

  • Alcohol may enhance CNS depression.
  • Beta-agonists may decrease the serum concentration of fentanyl.
  • Amphetamines may enhance the effects of fentanyl.
  • Anticholinergic medications, along with fentanyl, increase the risk of urinary retention and constipation.
  • Antipsychotic agents may increase the risk of low blood pressure.
  • Azelastine nasal spray may enhance CNS depression.
  • Beta-blockers with fentanyl enhance bradycardia.
  • Calcium channel blockers may enhance hypotension or bradycardia.
  • Hydrocodone may enhance CNS depression.
  • SSRIs with fentanyl may enhance serotonergic properties.
  • Zolpidem effects may be enhanced.

Oxycodone

Oxycodone is a Schedule II controlled substance and is available in multiple forms (Sadiq et al., 2024).

  • The immediate-release oral formulation is dosed with 5-30 mg every 4-6 hours (lower range for opioid-naive patients).
  • There are abuse-deterrent formulations and extended-release formulations.
  • It also comes as an oral concentrate and oral solution.
  • Oxycodone is often combined with other analgesic agents such as acetaminophen, aspirin, and ibuprofen.

Those with a creatinine clearance of less than 60 milliliters (mL)/min should have the dose reduced as the serum concentration of oxycodone will increase in renal insufficiency. Oxycodone is contraindicated in paralytic ileus, significant respiratory depression, hypercarbia, acute or severe bronchial asthma, and gastrointestinal obstruction (Sadiq et al., 2024).

Side effects include drowsiness, dizziness, itching, constipation, nausea, and vomiting. Less common side effects include dry mouth, headache, abnormal dreaming, blood pressure changes, diaphoresis, weakness, and fever.

Caution should be used in those with biliary tract impairment, as it may constrict the sphincter of Oddi. It may lead to an elevation of intracranial pressure (ICP) and should be used carefully for those with intracranial lesions, elevated ICP, or a head injury.

Common drug interactions with oxycodone include (Sadiq et al., 2024):

  • Alcohol may enhance CNS depression.
  • Amphetamines may increase the effect of oxycodone.
  • Anticholinergic agents may increase the side effects of oxycodone (constipation and urinary retention).
  • Antipsychotic agents with oxycodone may reduce blood pressure.
  • Diuretic side effects may be increased with oxycodone.
  • Hydroxyzine enhances CNS depression.
  • MAOIs enhance the side effects of oxycodone.
  • Mirtazapine may enhance CNS depression.
  • Rifampin may decrease the serum concentration of oxycodone.
  • SSRIs with oxycodone enhance the serotonergic effect and CNS depression.

Hydrocodone

Hydrocodone, classified as a Schedule II controlled substance in October of 2014, is available as a combination pill with non-narcotic analgesic and by itself in an extended-release form. The combination pill has a short-acting version of hydrocodone and is dosed with 2.5 to 10 mg of hydrocodone every 4-6 hours as needed for moderate to severe pain (Cofano et al., 2024).

Those with hepatic impairment should start at the lowest dose and titrate up very slowly while monitoring side effects. Caution should be used with renal impairment as plasma concentration may rise.

Side effects include constipation, nausea, vomiting, dry mouth, drowsiness, headache, dizziness, pruritus, and nausea (Cofano et al., 2024). Contraindications to hydrocodone include paralytic ileus, severe asthma, severe respiratory depression, and hypercarbia.

Drug interactions may include (Medscape, 2024a):

  • Alcohol may enhance CNS depression.
  • Amphetamines may increase the effect of hydrocodone.
  • Anticholinergic agents may increase the side effects of hydrocodone (constipation and urinary retention).
  • Nasal azelastine (Astelin®) enhances CNS depression.
  • Diuretic side effects may be increased with hydrocodone.
  • MAOIs enhance the side effects of hydrocodone.
  • SSRIs with hydrocodone enhance the serotonergic effect and CNS depression.
  • Zolpidem enhances CNS depression.

Tramadol

Tramadol is a Schedule IV controlled substance and is indicated for moderate to severe pain (Dhesi et al., 2024). The immediate release form is dosed at 25-100 mg every 4-6 hours for a maximum of 400 mg a day. Tramadol extended-release form is dosed with 100 mg once daily and may be titrated by 100 mg every five days to a maximum dose of 300 mg daily (Dhesi et al., 2024).

Tramadol is also indicated for chronic moderate to severe pain. Those who do not need a rapid onset of pain relief and are affected by side effects may be dosed at 25 mg/day and titrated every three days to 50-100 mg every 4-6 hours to a maximum of 400 mg a day (Dhesi et al., 2024; Medscape, n.d.).

When prescribing tramadol to older adults, use the lower end of the dosage range and titrate slowly. In those over 75 years old, 300 mg a day should not be exceeded, and utilize extreme caution with the extended-release form (Dhesi et al., 2024; Medscape, n.d.).

In those with a creatinine clearance of less than 30 mL/min, only the immediate-release formulation should be used with 25-100 mg split every 12 hours (maximum 200 mg a day). In those with severe liver impairment, the immediate release form should be given at a maximum of 50 mg every 12 hours (Dhesi et al., 2024; Medscape, n.d.).

Side effects include flushing, dizziness, constipation, nausea, vomiting, dyspepsia, itching, headache, somnolence, and weakness. Less common side effects include orthostatic hypotension, mental status changes, euphoria, rash, hot flashes, diarrhea, dry mouth, anorexia, joint pain, blurred vision, and sweating.

Patients may experience withdrawal symptoms from tramadol, including nausea, diarrhea, anxiety, pain, sweating, tremors, and rigors (Dhesi et al., 2024; Medscape, n.d.). Extended tramadol use may lead to dependence, and these medications should be tapered slowly to reduce the risk of withdrawal symptoms.

Tramadol has been shown to increase the risk of seizures (Dhesi et al., 2024; Medscape, n.d.). This risk is increased in those who take SSRIs, TCAs, neuroleptics, other opioids, or other drugs that lower the seizure threshold. The risk may also be increased in those who have seizures or are at risk for seizures, such as those who have a CNS infection, cancer, a history of head trauma, or while patients are going through drug or alcohol withdrawal.

Caution should be used in those with respiratory disease as those with significant disease may be at increased risk for respiratory depression.

Drug interactions may include (Dhesi et al., 2024; Medscape, n.d.):

  • Alcohol may enhance CNS depression.
  • Amphetamines may increase the effect of tramadol.
  • Anticholinergic agents may increase the side effects of tramadol (constipation and urinary retention).
  • Antiemetics may reduce the effects of tramadol.
  • Antipsychotics and tramadol may result in reduced blood pressure, increased risk of neuroleptic malignant syndrome, and increased risk of serotonin syndrome.
  • Nasal azelastine enhances CNS depression.
  • Carbamazepine with tramadol may enhance CNS depression; tramadol may reduce the therapeutic effect of carbamazepine.
  • Cyclobenzaprine and tramadol may increase the risk of seizures or increase the risk of serotonin syndrome.
  • Diuretic side effects may be enhanced with tramadol.
  • Hydrocodone may enhance CNS depression.
  • Hydroxyzine may enhance CNS depression.
  • MAOIs with tramadol may increase the risk of seizures or increase the risk of serotonin syndrome.
  • Metoclopramide with tramadol may increase the side effects of metoclopramide or increase the risk of serotonin syndrome or neuroleptic malignant syndrome.
  • SSRIs with tramadol may increase the risk of seizures or increase the risk of serotonin syndrome.
  • TCAs with tramadol may increase the risk of seizures or increase the risk of serotonin syndrome.
  • Warfarin with tramadol may affect the anticoagulant effect.
  • Zolpidem enhances CNS depression.

Other Medication

Oxymorphone, a schedule II medication, can be given orally. The immediate-release tablet is used for acute pain, and initial dosing is at 5-10 mg every 4-6 hours as needed for opioid-naïve patients. For those with chronic severe pain, the extended-release tablet is used and is started at 5 mg every 12 hours and may be titrated up at 5-10 mg increments every 12 hours every three to seven days (Medscape, 2024d). Caution should be used in those with a creatinine clearance of less than 50 mL/minute, and the medication should not be used in moderate to severe hepatic impairment.

Hydromorphone is available in various forms, including immediate-release tablets, oral solutions, extended-release formulations, suppositories, and injectable preparations, allowing flexibility in administration (Abi-Aad & Derian, 2023). For opioid-naïve patients, the initial dose typically starts at 1-2 mg orally every 4-6 hours as needed for pain, with lower doses recommended for older adults or those with renal or hepatic impairment. Intravenous or subcutaneous dosing generally begins at 0.2-0.5 mg every 2-3 hours, adjusted based on efficacy and tolerability (Abi-Aad & Derian, 2023). Extended-release hydromorphone is reserved for opioid-tolerant patients and is administered once daily to provide continuous pain control, with doses individualized based on prior opioid use.

Methadone, which is often used as medication-assisted treatment, is a long-acting opioid analgesic used for the management of chronic pain, particularly in patients who have not responded to other opioids or who require long-term pain control. Dosing methadone for pain requires significant caution due to its variable absorption, metabolism, and prolonged half-life, which can lead to drug accumulation and increase the risk of respiratory depression (Durrani & Bansal, 2024).

For opioid-naïve patients, initial dosing typically starts at 2.5-5 mg every 8-12 hours, with careful titration over one week to allow steady-state levels to stabilize (Durrani & Bansal, 2024). For opioid-tolerant patients transitioning to methadone, conversion must be individualized and guided by equianalgesic opioid conversion ratios, recognizing that methadone’s potency increases at higher doses of the previous opioid. Due to its complex pharmacology, methadone dosing should be adjusted conservatively, with close monitoring for efficacy and side effects such as sedation, respiratory depression, QT prolongation, and constipation (Durrani & Bansal, 2024).

Prevention of Misuse

To prevent prescription drug abuse, the clinician needs to ensure:

  • Patients are assessed and reassessed
  • Treatment agreements are used
  • Prescription monitoring occurs
  • Safe prescription methods are practiced

Patients' risks should be assessed, and contraindications should be immediately identified. Contraindications to opioid treatment include those who have erratic follow-up, suffer from current untreated addiction, or have poorly controlled mental illness.

When taking a patient history, document the opioid currently prescribed, its dose, frequency, and duration. It is important to query the state monitoring program to confirm the patient’s medication use and, if appropriate, contact past providers to obtain medical records (Dowell et al., 2022).

History of illegal substance use, alcohol use, tobacco use, prescription drug use, family history of substance abuse and psychiatric disorders, history of sexual abuse, legal history, behavioral problems, employment history, marital history, social network, and cultural background should be assessed before controlled substances are prescribed. A history of substance abuse does not prohibit treatment with opioids but may necessitate more intensive monitoring or referral to an addiction specialist.

Multiple tools are available to evaluate opioid risk. The Opioid Risk Tool (Brott et al., 2022) is a tool used in primary care to screen adults for the risk of aberrant behaviors when prescribed opioids for chronic pain. It is a copyrighted tool, encompasses five questions, and takes about one minute to use. It classifies a patient as low, moderate, or high risk to abuse opioids. Those who are high risk have a high likelihood of aberrant drug-related behavior. It is not validated in individuals without pain. The five questions include asking about family and personal history of substance abuse (alcohol, prescription drugs, or illegal drugs), age (risk is 16-45 years old), psychological disease, and preadolescence sexual abuse history. The questions are scored with different points assigned for each question, which is variable between men and women, and the total score is tallied. The patient is placed into low, moderate, or high risk.

Regular follow-up is essential and should occur at least every three months. When assessing the pain patient, the five A's should be assessed: analgesia, addiction, activities of daily living, adherence, and adverse effects (Maumus et al., 2020). Part of the follow-up should be urine drug testing, which can detect medication adherence and illicit and non-prescription drug use. It is critical that the clinician adequately document any interactions with patients, assessments, and results of testing and treatment plans.

Written treatment agreements, which should be used between prescribers and patients when controlled substances are used, help guide the conversation. It discusses expectations, the risks, and the monitoring of controlled substances (Table 2).

Table 2: Points Commonly Seen in Opioid Agreements
  • Early refills will generally not be given
  • The patient will not seek controlled substances from another provider
  • The patient will use only one pharmacy
  • Permission for the prescriber to speak freely with other healthcare providers, pharmacists, and family members regarding opioid use
  • The patient will submit to a urine drug test
  • The patient will safeguard the medications
  • Common side effects of the medication will be discussed
(Food and Drug Administration, n.d.)

Prescription monitoring programs are available in all states, including Massachusetts. They provide an online database that lists all prescriptions of controlled substances dispensed for each patient by pharmacies. Ideally, the prescriber should check the database before prescribing controlled substances. If a patient has an undisclosed prescription for controlled substances, it is prescription drug misuse.

When abuse/misuse is detected, how should the clinician respond? If it is a single, minor deviation, then counseling and more intensive monitoring may be needed. Tapering controlled substances to reduce the risk of withdrawal is appropriate in more severe or persistent misuse cases. When diversion is the cause of misuse, immediate prescription removal is likely the most appropriate course. If a substance abuse disorder is suspected, a referral to an addiction specialist is recommended.

Case Study One

Ms. L is a 52-year-old female with a history of bilateral knee OA; she currently rates the pain as a 7/10 in her right knee and a 6/10 in her left knee. She takes celecoxib 200 mg twice a day and uses 1000 mg of acetaminophen for breakthrough pain three times a day. She has taken the same medications over the last six months, but over the last month, she has not been getting adequate relief from her pain, has been progressively disabled, and has stopped exercising because of pain in her knees.

In addition to OA, she has a past medical history of hypertension, dyslipidemia, depression, and obesity. She has a past surgical history of an inguinal hernia repair as a child and is currently on simvastatin, lisinopril, celecoxib, and acetaminophen. She has no known allergies.

She has no history of alcohol, drug, or substance abuse. She has a strong family network, including a supportive husband of 25 years and two sons who live within twenty miles of her home. She has a history of depression but is currently not depressed.

The physical exam exhibits bilateral knee crepitus and obesity (body mass index [BMI] 35). She is unable to extend the right knee due to pain.

An X-ray demonstrates moderate arthritic changes in both knees. The patient is unwilling to consider surgery on her knees.

The prescriber offers tramadol immediate-release 25 mg in the morning, titrated every three days in 25 mg increments to 25 mg three times a day. Pain control was still not adequate, and the dose was then increased by 25 mg every three days to 50 mg every 8 hours.

Pain control was significantly improved, and then the patient was given extended-release tramadol 200 mg once a day. The patient was able to function and exercise. Her quality of life was much improved.

Pain in Special Populations

Pediatrics

Pain in neonates is a critical but often underrecognized aspect of neonatal care. Historically, it was believed that neonates experience less pain due to immature nervous systems. However, extensive research has demonstrated that neonates perceive pain and may experience it more intensely due to heightened peripheral sensitivity and immature inhibitory pain pathways in the CNS (García-Valdivieso et al., 2023; Perry et al., 2018).

It is important to have a standard method to assess pain in neonates. It is difficult to assess pain in neonates and infants because they have limited capability to communicate. In this population, assessment is based on physiological and behavioral factors. Factors that suggest pain in neonates and infants include vital signs, oxygen saturation, skin color, crying pattern, facial expressions, muscle tone, and consolability.

Pain assessment in neonates poses unique challenges due to their inability to verbalize discomfort, necessitating the use of observational and behavioral pain scales. Commonly employed tools include the Neonatal Infant Pain Scale (NIPS), the Premature Infant Pain Profile (PIPP), and the Crying, Requires Oxygen, Increased Vital Signs, Expression, and Sleeplessness (CRIES) scale. These scales evaluate a combination of physiological and behavioral indicators such as facial expressions, crying, changes in heart rate, oxygen saturation, and sleep patterns. For example, the NIPS assesses facial expression, cry, breathing patterns, arm and leg movements, and arousal state, assigning scores to each parameter to quantify pain levels (Sarkaria & Gruszfeld, 2022). Conversely, the PIPP incorporates gestational age and physiological changes like heart rate, oxygen saturation, and behavioral cues (Núñez-López et al., 2022). The CRIES scale is particularly useful for postoperative neonates (Glenzel et al., 2023). These tools are essential in guiding pain management strategies, ensuring timely and appropriate interventions to alleviate neonatal discomfort while minimizing potential long-term impacts of unaddressed pain.

Due to the difficulty in finding and quantifying pain in the neonate and young child, pain management should include an attempt to reduce or prevent pain in the face of potentially painful situations. Limiting the number of painful procedures performed on young children is vital.

Pain assessment in children is similar to adults. The source of the pain, along with its location and severity, should be ascertained. In older children, self-reporting is a useful technique to assess pain. For those too young to understand self-reporting, scales such as the facial expression scale can be used. With the help of a caregiver, observing the child for verbal responses, motor responses, or facial expressions will help the clinician determine the degree of pain in a non-verbal child.

Pain management in children should work to control, lower, or prevent the pain. Pain management techniques are based on the severity, type, duration, and source of pain. Non-pharmacological measures to control pain include physical/occupational therapy and cognitive/behavioral therapy.

Pharmacological agents may also be considered (Banerjee & Butcher, 2020). Mild pain can be managed with NSAIDs or acetaminophen; when pain is not responsive to these medications, stronger medications, including opioids, are considered. Regular assessment of pain control during treatment will help ensure proper pain management. When pain is moderate to severe, providing pain medication around the clock is a reasonable option.

Adjunctive therapy can be used in children, including medications to manage comorbid depression and anxiety. The use of anticonvulsants for neuropathic pain may also be considered (Banerjee & Butcher, 2020).

Older Adults

Pain is a universal human experience, but its prevalence and complexity often increase with age. Pain can significantly impact older adults' quality of life, physical functioning, and mental health. Despite its commonality, pain in older adults is frequently underdiagnosed and undertreated, largely due to misconceptions, communication barriers, and age-related factors. Addressing pain in this population requires a holistic approach that accounts for its multifaceted nature, the challenges of aging, and the need for individualized care.

Chronic pain is particularly common among older adults, with studies suggesting that up to 68 percent of older adults have experienced low back pain over the last year (Wong et al., 2022). Conditions such as arthritis, osteoporosis, neuropathy, and post-surgical complications are among the primary contributors. Acute pain, though less frequent, also poses challenges due to slower recovery rates and increased vulnerability to complications.

Several barriers hinder the effective management of pain in older adults. One significant challenge is underreporting, as many seniors normalize pain as an inevitable part of aging. Others may fear being perceived as complainers or worry about the side effects of treatment, such as dependency on pain medications. Cognitive impairments like dementia further complicate communication, making it harder for individuals to express their discomfort.

From a clinical perspective, healthcare providers may underestimate pain in older adults or prioritize other medical issues, inadvertently sidelining pain management. Age-related physiological changes also affect the metabolism and excretion of medications, increasing the risk of adverse effects. As a result, prescribers may hesitate to provide adequate pain relief, leaving patients to endure unnecessary suffering.

Unmanaged pain in older adults can lead to a cascade of negative outcomes. Physically, it limits mobility, increasing the risk of falls, frailty, and loss of independence. Persistent pain is also closely linked to psychological distress, contributing to depression, anxiety, and social isolation. Additionally, chronic pain can interfere with sleep, exacerbate cognitive decline, and diminish overall well-being.

The economic burden of pain is another concern. Frequent medical visits, hospitalizations, and long-term care costs strain healthcare systems and families. These consequences underscore the urgent need for comprehensive pain management strategies tailored to older adults.

Effective pain management in older adults necessitates a multidisciplinary methodology. Non-pharmacological interventions, including physical therapy, acupuncture, and CBT, can be useful alternatives or complement medication. Pharmacological options should be chosen carefully, balancing efficacy with safety. Low-dose regimens and regular monitoring are essential to minimize risks.

Educating patients and caregivers about pain management is equally important. Empowering older adults to advocate for themselves fosters better communication and enhances their involvement in care decisions.

Nonverbal Patients

Since pain is a subjective experience, it is measured by the patient’s self-report. Unfortunately, adult patients who have cognitive/expressive deficits or who are intubated, sedated, and unconscious are unable to offer a self-report. Individuals who cannot communicate their pain are difficult to manage and at increased risk for inadequate pain control.

When patients are unable to self-report, alternative methods must be employed to assess their pain. Despite their inability to communicate verbally, these individuals still have the right to proper pain evaluation and management. Reliable and valid assessment tools for nonverbal patients are essential. The American Society for Pain Management advocates for a multifaceted approach to detect pain in the non-verbal population effectively (Herr et al., 2006).

  • Use the hierarchy of importance of measures of pain intensity for nonverbal patients.Self-reporting of pain is the most dependable method for assessing pain.
    • While individuals with mild to moderate cognitive impairment may still be able to self-report pain, the ability declines as dementia progresses and eventually becomes impossible. However, the inability to communicate pain does not eliminate the experience of pain itself.
      • Critically ill patients may face challenges in reporting pain due to factors such as delirium, decreased consciousness, endotracheal intubation, sedatives, or neuromuscular blocking agents. In these cases, the capacity for self-reporting may fluctuate, making it essential to conduct serial assessments to evaluate their ability to communicate pain.
    • Search for potential causes of pain.
      • Intervene when common issues frequently associated with pain are present or during procedures known to cause pain, even without behavioral indicators of pain.
      • Manage problems that may cause discomfort (e.g., infection, constipation, urinary retention).
      • Consider chronic pain causes that may have been present before (e.g., history of arthritis or low back pain).
    • Observe patient behaviors –  The American Geriatrics Society recognizes six main types of pain behaviors: (1) facial expressions (for example, scowling), (2) verbalizations or vocalizations (such as moaning), (3) body movements such as rigid posture, (4) changes in interpersonal interactions (such as acting aggressively), (5) changes in activity patterns (for example not eating or increased wandering), and (6) mental status changes like emotional changes or increased confusion (Herr et al., 2006).
    • Encourage family members or caregivers familiar with the patient to provide proxy pain ratings when self-reporting is impossible. Ask about behaviors that may signal pain and consider any preexisting conditions, such as arthritis, that could contribute to discomfort.
    • Conduct an analgesic trial for procedures or conditions likely to cause pain or when pain-related behaviors persist despite addressing basic needs and comfort. Adjust treatment as needed, including dosage increases or the addition of other analgesics, if pain-related behaviors continue or new potentially painful procedures arise.
  • Use behavioral pain assessment tools as appropriate (Herr et al., 2006).
    • Behavioral pain assessment tools are indispensable for identifying and managing pain in non-verbal adults. While these tools have limitations, their thoughtful application, combined with clinical judgment and input from caregivers, enables healthcare providers to address pain effectively. As the population of older adults and patients with complex health conditions grows, ongoing research and refinement of these tools will be crucial for improving care outcomes and ensuring that pain does not go unnoticed or untreated.
    • Pain behavior scales assess the degree of observed pain-related behaviors rather than pain intensity. One example is the Pain Assessment in Advanced Dementia Scale (PAINAD) (Dunford et al., 2022), which evaluates five behavioral categories: breathing, negative vocalization, facial expression, body language, and consolability. Each category is scored from 0 to 2, with any positive score suggesting the presence of pain. While these scores help assess the effectiveness of interventions, they do not measure pain intensity. For accurate use, the patient must exhibit behaviors in all categories; for instance, PAINAD is unsuitable for patients with quadriplegia since body language cannot be assessed.
    • Behavior checklists differ from pain behavior scales in that they assess the presence or absence of behaviors rather than the degree to which they occur. Unlike pain behavior scales, checklists do not require patients to exhibit all specified behaviors. An example is the Pain Assessment Checklist for Seniors with Limited Ability to Communicate (PACSLAC) (Fuchs-Lacelle & Hadjistavropoulos, 2004), which evaluates 60 behaviors, including restlessness, agitation, decreased activity, and appetite changes. The total number of behaviors observed does not correlate with pain intensity; however, changes in an individual’s score over time may indicate increasing or decreasing pain and help assess response to interventions.
      • Research does not support the use of vital sign changes to identify pain (Dayoub & Jena, 2015). The absence of increased blood pressure, respiratory rate, or heart rate does not denote an absence of pain.
      • Nurses should reassess and document. As with patients who self-report pain, reassessment of pain in non-verbal patients should occur after the intervention and regularly over time. The reassessment should use the same initial behavioral pain assessment tool to observe any changes in those behaviors following effective treatment.

Pain in the Psychiatric Patient

Psychiatric disorders are three times higher in those with chronic pain than in the general population, with depression, anxiety, and post-traumatic stress disorder being the most common disorders (Johnston & Huckins, 2022). The patient with pain and psychiatric disease typically reports more intense pain than the patient without comorbid mental illness.

Chronic pain management has multiple challenges in psychiatric patients. Optimizing treatment of the underlying psychiatric illness is an important step to achieve an optimal reduction in pain. It is also important to screen and treat for any substance abuse or substance-induced disorder. This screening will help ensure appropriate and adequate treatment of pain. Medications with abuse potential should be used cautiously, as there is a high prevalence of drug use disorders in psychiatric patients. Exercise and CBT are important steps in managing pain in the psychiatric patient. Also, monitoring for compliance is an integral part of managing the psychiatric patient who suffers from chronic pain.

Specific Pain Syndromes

Visceral Pain

Many conditions lead to visceral pain. Visceral pain occurs when there is a stimulation of the nociceptors of the organs in the abdomen, pelvis, or chest (Collett, 2013). Visceral pain is diffuse, hard to localize, and frequently referred from a remote structure. Visceral structures are aggravated by ischemia, inflammation, and stretch.

Chest pain can occur from many different etiologies. A few life-threatening situations must be considered, including myocardial infarction, pulmonary embolism, aortic dissection, tension pneumothorax, and esophageal rupture. The majority of chest pain is not life-threatening, and selected causes include chest wall pain (costochondritis, muscle strain), panic attacks, pneumonia, pleurisy, myocarditis, and gastroesophageal reflux disease.

Abdominal pain is a common problem, and most cases are not life-threatening. Like chest pain, it is essential to rule out serious causes of abdominal pain immediately. Severe causes of abdominal pain are suggested by unstable vital signs, high fever, an inability to pass gas or have a bowel movement, vomiting blood, or dark/tarry stools. Common diagnoses that can potentially be life-threatening include acute bowel obstruction, acute mesenteric ischemia, bowel perforation, ulcer, acute myocardial infarction, and ectopic pregnancy. Other causes of abdominal pain include appendicitis, gallbladder disease, diverticulitis, constipation, kidney stones, lactose intolerance, and inflammatory bowel disease.

Many people suffer from chronic abdominal pain, with numerous of these cases being benign, such as functional dyspepsia or irritable bowel syndrome. If no organic disease is found, that patient should be treated symptomatically. Those individuals over the age of 50 are more likely to have a more serious cause of chronic abdominal pain, and functional abdominal pain should be made only after more serious causes have been ruled out.

Pelvic pain is a common problem in women and may represent a urologic, gynecologic, gastrointestinal, musculoskeletal, metabolic, or vascular issue. Acute pelvic pain may be of visceral or somatic origin. In all women who have the possibility of being pregnant, a pregnancy test should be done. Other testing to rule out other pelvic pain causes includes a complete blood count, sedimentation rate, chlamydia/gonorrhea testing, a serum human chorionic gonadotropin (HCG) level, and a urinalysis.

Diagnostic testing may include a pelvic ultrasound to rule out a mass or ectopic pregnancy, or laparoscopy can help determine if endometriosis is present. Features that suggest a severe pelvic pain cause include peritoneal signs, brisk vaginal bleeding, high fever, or unstable vital signs.

There are many potential causes of chronic pelvic pain. Diagnosing and treating chronic pelvic pain can be difficult. Determining the exact cause of the abdominal pain may include extensive laboratory evaluation, imaging modalities, and exploratory surgery. For those with chronic pelvic pain, the examination may use a pain map and identify tender areas to see if physical exam tender areas match the pain map. Ideally, the clinician should attempt to treat the underlying cause of the pelvic pain. Still, a non-specific treatment may be considered without a specific diagnosis.

Sickle Cell Disease

The hallmark of sickle cell disease is the polymerization of hemoglobin S, which leads to red blood cell distortion into a sickle shape under deoxygenated conditions. Sickle cell crisis is a vaso-occlusive phenomenon leading to pain associated with blood cell destruction and subsequent anemia. While not the only feature of sickle cell disease, pain is a significant component of the condition. Acute sickle cell disease pain is secondary to vaso-occlusion and the consequent tissue ischemia and inflammation. Over time, chronic pain may result.

An acute painful episode can be precipitated by multiple events such as stress, infection, weather conditions, dehydration, or alcohol consumption. Pain can affect many body parts, such as the chest, back, extremities, or abdomen, and may be associated with fever, elevated breathing rate, hypertension, nausea, and vomiting.

Treatment of pain in chronic disease can be challenging to manage. If mild pain is present and the patient is not on chronic opioid therapy, pain management should be started with non-opioid therapy and move to opioids when the pain becomes more severe. Individuals who are on chronic opioids will require additional opioids for breakthrough pain. When treated in the emergency room, intravenous medication can be used. If pain cannot be relieved with two doses, then admitting the patient to the hospital for pain management may be necessary. Many patients with sickle cell disease have chronic pain managed with long-acting opioids (Dowell et al., 2022).

Headaches

Headaches are a frequent cause of recurrent pain and one of the most common diagnoses seen in healthcare. There are multiple types of headaches, including migraine, tension, and cluster headaches. Tension headaches are the most common. The healthcare provider needs to understand red flags that indicate an ominous cause of a headache. When a severe cause of a headache is suspected, urgent evaluation is necessary and may include brain imaging to rule out an underlying secondary cause of a headache. Signs/symptoms that suggest a more severe cause of headache include:

  • New-onset headache, especially in those over the age of 40
  • Worst headache ever experienced
  • A headache with an accompanied neurologic sign or symptom – e.g., confusion, stiff neck, seizure, focal neurologic sign (e.g., one-sided weakness), or impaired alertness
  • Headaches that awaken the patient from sleep
  • Fever and stiff neck
  • Pregnancy – may suggest pre-eclampsia
  • History of cancer
  • History of human immunodeficiency virus (HIV) or immune compromise
  • Headache made worse by cough, exertion, or the Valsalva maneuver
  • Recent head trauma
  • Illicit drug use
  • Progressive headache

Tension headaches may occur every day and have a variable presentation. Typically, they are described as pressure, tightness, or aching. They may feel like a band around the head and be bifrontal, bitemporal, or generalized. Tension headaches can be intermittent with a variable duration.

Migraine headaches are classically one-sided (but may be generalized) and are described as pounding or throbbing. Patients with migraines often have co-existent nausea/vomiting and photophobia.

An acute migraine can be managed with multiple agents. The use of acetaminophen or NSAIDs may be considered. When simple analgesics are not effective in controlling pain, the use of migraine-specific agents (triptans or dihydroergotamine) may be considered. These agents are available in oral, rectal, and injectable formulations. Many patients prefer oral agents, but for those with severe nausea that accompanies a migraine, a non-oral route is the best option.

Selected first-line prophylactic agents for migraines include propranolol, amitriptyline, topiramate, and valproic acid.

Neuropathic Pain Conditions

Many conditions lead to neuropathic pain, including multiple sclerosis, post-stroke pain, spinal cord injury, traumatic brain injury, trigeminal neuralgia, peripheral neuropathy, and post-herpetic neuralgia.

Multiple sclerosis is commonly associated with pain. It is estimated that chronic pain affects 50–75% of patients with multiple sclerosis at some point (Racke et al., 2022). Common painful symptoms include dysesthesia pain, back pain, spasms, Lhermitte sign, visceral pain, and trigeminal neuralgia.

Central post-stroke pain is experienced as unilateral head/facial pain that starts within six months of a stroke. It affects up to 25 percent of stroke victims (Anosike & Rajaram Manoharan, 2024). The pain is typically persistent but may come and go. The severity of the pain may be variable, and stress often exacerbates the pain.

Treatment of central post-stroke pain includes benzodiazepines; anticonvulsants such as gabapentin, pregabalin, lamotrigine, or carbamazepine; baclofen; antidepressants such as amitriptyline or an SSRI; and clonidine. When pain is resistant to pharmacotherapy, neuromodulation (deep brain stimulation) and surgery may be considered.

Spinal cord injury patients often develop chronic pain that affects their quality of life. Pain is often poorly localized and neuropathic (e.g., burning, stabbing). The pain can be evoked or spontaneous. There may be pain caused by injury to the nerve roots and dorsal gray matter causing pain at the injury level. Pain can also be below the spinal cord injury level, which is thought to be caused by injury to the spinothalamic tracts and thalamic deafferentation.

Pain may be managed with antidepressants (e.g., TCAs), antiepileptics (e.g., gabapentin, lamotrigine, or valproate), and standard analgesic medications. When medications are not effective, the use of invasive treatments is considered. These may include deep brain stimulation, cordotomy, or motor cortex stimulation.

Trigeminal neuralgia results in head/facial pain from one or more of the trigeminal nerve branches. Classically, the pain is unilateral, brief, stabbing, and lancinating that is sudden in onset. Imaging, typically with an MRI, is sometimes done to distinguish primary from secondary trigeminal neuralgia. The primary disease has no identifiable lesion causing the symptoms. Secondary causes of trigeminal neuralgia include acoustic neuromas, multiple sclerosis, cerebral aneurysms, and trigeminal neuromas. The secondary disease is more common if there is bilateral involvement, occurs at a younger age, or there is associated sensory loss. Conditions that may mimic trigeminal neuralgia include dental pain, multiple sclerosis, herpes zoster, or atypical headaches.

Treatment for the pain of trigeminal neuralgia includes carbamazepine and oxcarbazepine. For those who are intolerant or non-responsive to these agents, baclofen or lamotrigine can be used. Surgical options are sometimes tried for refractory cases.

Peripheral neuropathy can come from many etiologies, including diabetes, cancer, alcohol, and HIV, and typically presents with distal sensory loss, weakness, numbness, and burning. The presentation may be variable.

Neuropathy due to diabetes is one of the more common types of neuropathies. It typically results in symptoms that begin in the lower extremities. Sensory symptoms are seen first, followed by motor symptoms. Patients complain of gradual sensory loss, numbness, a burning sensation and pain in the feet, and mild gait abnormalities. Over time, weakness may develop, and a "stocking and glove" distribution of sensory loss may occur. Physical exam findings depend on which nerve fibers are involved.

Treatment of neuropathies includes managing the underlying disease (e.g., controlling blood sugar in diabetes) and medications to treat the symptoms. Medications used to manage neuropathy pain include TCAs, duloxetine, gabapentin, pregabalin, carbamazepine, topiramate, tramadol, and NSAIDs.

Post-herpetic neuralgia is pain that presents after a Herpes zoster infection caused by the Varicella-zoster virus. Certain groups are at higher risk of getting pain after a Herpes zoster infection. These include older individuals, those with higher acute pain levels during the acute infection, and those with a more severe rash (Cunningham & Dworkin, 2000).

Herpes zoster is an infection that starts with a sharp, burning, stabbing pain that follows a dermatome. A rash will be seen a few days later along the same dermatome. Commonly affected dermatomes include the thoracic, cervical, and trigeminal nerves. After the rash abates, some individuals develop pain along the same dermatome that persists longer than four months. Pain may persist for years or even throughout life. Allodynia is often seen in those with post-herpetic neuralgia.

Post-herpetic neuralgia is commonly treated with TCAs, pregabalin, and gabapentin. Topical capsaicin or lidocaine can be used. Opioids are sometimes used but should be used cautiously. They are considered second or third-line options and are sometimes used while the TCAs, pregabalin, and gabapentin take effect, then tapered. If all other options are not sufficient, the use of intrathecal glucocorticoids may be considered.

Back Pain

Back pain is typically non-specific and will recover after a few weeks with conservative treatment, but some go on to having chronic pain. Those more likely to develop chronic back pain include those with functional impairment, poor health, comorbid psychiatric conditions, maladaptive pain-coping behaviors, and non-organic signs – such as pain in the lower back when pressing directly on top of the head. A small percentage of people with back pain have a serious source of back pain, and less than ten percent have specific etiologies (Casiano et al., 2023). When back pain is present, it is essential to rule out any severe pathologies. Certain red flags suggest serious pathologies (See Table 3).

A complete history and physical exam are essential to rule out serious causes of back pain and help identify the cause of the back pain. Certain more urgent conditions require immediate imaging with an MRI and referral, including those with red flags. Imaging may be considered if no improvement is seen within six weeks of conservative therapy (Casiano et al., 2023). Patients who have conditions that may benefit from surgery or epidural injections should have imaging.

Back pain should not be treated with bed rest, but modifying activity slightly to account for the pain is appropriate. Oral analgesics should be used short-term to provide pain control. Re-evaluation should occur at four weeks to ensure improvement, evaluate for any needed testing, and reevaluate the need for pain medications.

Initial oral agents should include NSAIDs for 2-4 weeks. Those with an allergy or contraindication to NSAIDs may consider acetaminophen. When pain is not controlled with NSAIDs, the use of a muscle relaxant may be considered. For those who cannot take a muscle relaxant, the combination of an NSAID and acetaminophen is an option.

The use of opioids should be used very judiciously in acute lower back pain and only in those who are not getting pain control from other agents or in those with contraindications to those other agents.

Physical therapy can be used for acute low back pain but is more often used for chronic low back pain. Education is one of the most critical aspects of managing back pain. Patients should be educated on the causes of back pain, the expected course, an encouraging prognosis, the value of diagnostic testing, treatment options, and when to contact their healthcare provider.

Table 3: Back Pain Red Flags
  • New bowel or bladder incontinence
  • Saddle anesthesia – loss of sensation in the perineum, buttocks, and inner thighs
  • Severe neurological deficits
  • Weight loss
  • New-onset pain in those over age 50 years old or under 18 years old
  • Progressive motor deficit
  • Night pain or rest pain
  • Fever – concern for infection – recent urinary tract infection or history of intravenous drug use
  • Current or recent cancer diagnosis or significant risk factor for cancer
  • Pain persists beyond six weeks
  • Suspected vertebral fracture
(Casiano et al., 2023)

Neck Pain

Neck pain is a common condition caused by various factors, ranging from lifestyle habits to medical conditions. One primary cause is poor posture, often due to prolonged sitting, using mobile devices, or working at a computer. These activities strain neck muscles and lead to imbalances. Another common cause is muscle strain, often resulting from sudden movements or overuse. Degenerative conditions, such as cervical spondylosis or herniated discs, can also contribute to neck pain, particularly in older adults. Injuries, like whiplash from accidents, and medical issues, such as infections or RA, are other potential causes.

Treatment for neck pain depends on its severity and underlying cause. For mild cases, self-care measures are often effective. These include resting, applying heat or ice, and practicing gentle stretching or exercises to improve posture and mobility. Over-the-counter pain relievers like ibuprofen can reduce inflammation and discomfort.

For more persistent or severe pain, physical therapy is often recommended. Therapists teach strengthening and flexibility exercises tailored to the individual’s condition. Chiropractic adjustments or acupuncture can provide relief for some patients. If these measures fail, medical interventions such as corticosteroid injections, muscle relaxants, or, in rare cases, surgery may be necessary.

Preventing neck pain involves maintaining good posture, taking routine breaks from sustained activities, and strengthening neck and shoulder muscles. Ergonomic adjustments to workspaces and proper techniques for physical activities can also reduce the risk of developing neck pain.

Complex Regional Pain Syndrome

CRPS is broken down into types I and II. It is a disorder of the extremities illustrated by regional pain that is inconsistent in degree or time with the expected pain. The pain is localized around a specific territory.

The primary clinical manifestation is pain typically described as stinging, burning, or tearing and is exacerbated by movement, temperature variation, stress, or any contact. Also, some individuals have allodynia or hyperalgesia. The patient may also notice differences in skin color or temperature. The affected side may be more edematous or sweat more when compared to the other side. Limb movement is typically impaired by pain, edema, or contractures. The patient with CRPS may also have unilateral variations in hair or nail growth and skin atrophy.

The progression of the condition is variable over time. The underlying pathology is poorly understood but may include inflammation and pain perception changes in the CNS (Harden et al., 2022).

CRPS I is the more common type diagnosed when the typical symptoms are present, and there is no evidence of a peripheral nerve injury. CRPS II is less common and is present when there is evidence of a peripheral nerve injury (Harden et al., 2022).

CRPS is more commonly seen in women. It is often associated with some acute event that starts the syndrome. Examples of trauma may include a broken bone or a crush injury. The diagnosis is made on clinical exam after other conditions are ruled out.

Treatment of CRPS should involve a multidisciplinary approach, including physical and occupational therapy, physiological interventions, and pharmacotherapy. Pharmacologic options include NSAIDs, TCAs, gabapentin, or topical treatments (lidocaine or capsaicin). Other less common options include bisphosphonates, glucocorticoids, alpha-adrenergic agonists/antagonists (e.g., clonidine), ketamine, and opioids. Multiple interventional approaches may be considered, including regional sympathetic nerve blocks, trigger/tender point injections, and spinal cord stimulation.

Phantom Limb Pain

Phantom limb pain is aching, burning, or shock-like pain where an amputated limb used to be and is related to the perception of self. Sensory input from various parts of the body forms a ‘body map’ in the brain, and when a limb is amputated, that map still exists in the brain. Because the body map still exists, this can lead to pain and other sensations in the amputated body part.

Before diagnosing phantom limb pain, it is essential to rule out other causes of the symptoms, such as infection or a wound on the stump, ischemia, or neuroma. The incidence of this condition is variable, and it is hypothesized that not controlling pain before and after the surgery increases the risk of phantom limb pain. It has been shown that stopping pain transmission in the spinal cord for 48 hours before the amputation surgery using lumbar epidural blockage (LEB) has a positive long-term effect in preventing amputation pain. Also, aggressively managing pain immediately after surgery reduces the risk of developing phantom limb pain (Ahuja et al., 2018).

Multiple agents help manage phantom limb pain, including acetaminophen, NSAIDs, TCAs, and anti-epileptic agents. In addition to medication, non-pharmacologic methods to manage pain include TENS units, mirror therapy (which helps resolve the visual-proprioceptive disconnect), biofeedback, and occasionally surgical interventions.

Cancer Pain

Pain is very prevalent in cancer. According to some estimates, it is present in up to one-half of patients when first diagnosed with cancer and, according to some estimates, up to 80 percent of people with advanced cancer (National Cancer Institute, 2024). Nurses play an essential role in improving outcomes for cancer patients. To ensure appropriate pain treatment, nurses working with cancer patients must recognize and routinely assess the patient’s pain and communicate their findings to other care team members.

Pain in cancer can be acute or chronic. Acute pain is seen during interventions such as surgery, tissue injury, or radiation therapy. Acute pain can also be felt secondary to cancer itself, such as an obstructed bowel, a perforated bile duct, bleeding from liver cancer, or a pathological fracture. Chronic pain during cancer is typically related to the tumor itself or as a complication of treatment.

Neuropathic pain is also seen in cancer patients. Neuropathic pain in cancer can arise from the tumor pressing on a nerve or nerve plexus. Also, neuropathic pain can result from the treatment, as many chemotherapeutic agents or radiation therapy can cause nerve injury. Many conditions that result in neuropathic pain - such as Herpes zoster and post-herpetic neuralgia - are relatively common in cancer patients.

Management of cancer pain is typically aggressive. The use of opioids is common in chronic cancer pain, and doses should be titrated to find effective pain control. Dosing is commonly started with short-acting agents, but those with chronic pain switching over to a long-acting formulation are preferred with the continued use of short-acting agents for breakthrough pain.

While evaluating cancer pain, it is also important to consider pain related to cancer treatment, including chemotherapy pain. Several chemotherapy agents can cause neuropathic pain. Chemotherapy can also result in the development of mouth sores, stomatitis, or mucositis. These sores cause pain in the patient’s mouth and throat, making eating, drinking, and even talking painful.

Radiation therapy for cancer patients can cause skin burns and injury to the patient’s throat, intestines, and bladder. The patient may complain of pain if these body parts are involved in radiation treatment (National Cancer Institute, 2024).

Palliative and End-of-Life Care

Palliative and end-of-life care have become two distinct terms. The population of palliative care patients has expanded to include those who are not necessarily close to death but are suffering from chronic conditions that require symptom control and pain management.

End-of-life care necessitates skilled pain management to allow for a serene death with dignity. Morphine is the gold standard for end-of-life pain relief and is the most effective medication for dyspnea treatment. Morphine changes the patient’s awareness of their breathing experience by decreasing the respiratory drive and oxygen intake.

Fibromyalgia

FMS is a condition characterized by chronic, widespread musculoskeletal pain. Patients also complain of fatigue, sleep disturbances, psychiatric symptoms, cognitive disturbances, and multiple other somatic complaints. The etiology and pathophysiology are unclear.

In FMS, pain is typically diffuse and persistent. It is characterized as stiffness, deep aching, soreness, burning, or throbbing. Patients usually report that pain is persistently present, but the intensity may vary. Poor sleep, excessive stress, and exposure to cold may exacerbate the pain. Generally, pain is worse in the morning and improves throughout the day. Pain commonly affects the neck, shoulders, back, arms, legs, and chest wall.

FMS is six times more common in women when compared to men. Some research shows that the prevalence is about 6.4 percent in the United States. It is the most common cause of generalized musculoskeletal pain in females aged 20 to 55 (Bhargava & Hurley, 2023).

Patients with FMS often complain of hurting all over or feeling as though they have the flu. It is diagnosed in those with chronic pain and no markers of muscle inflammation. Differential diagnoses of FMS include OA, autoimmune disease, RA, systemic lupus erythematosus, hypothyroidism, inflammatory myopathy, systemic inflammatory arthropathies, spondyloarthritis, ankylosing spondylitis, myositis, and polymyalgia rheumatica.

Education is a critical step in the treatment of FMS. The condition must be explained to the patient, including treatment approaches. Key aspects of patient education include:

  • Sleep hygiene.
  • Symptoms will vary over time – fatigue and pain typically persist.
  • The patient must understand that the disease will not lead to deformity, a cosmetic issue, or become life-threatening.
  • Emotional or physical stress may increase symptoms. The patient should be taught stress-reduction and relaxation techniques to help manage the condition.
  • While infection may be a precipitating factor, it is not a persistent infection that causes the symptoms.
  • Neurohormonal abnormalities may account for fatigue, pain, mood disturbance, and sleep disturbance.
  • Exercise is recommended, although it may increase pain – particularly early in an exercise program.
  • Other non-pharmacological methods to manage FMS include supervised physical therapy, CBT, biofeedback, Tai Chi, or yoga.

Medications are often used in the management of FMS. Typically, non-pharmacological methods are used first, and when they are not sufficient, the addition of medication is considered. Commonly used medications include low-dose TCAs, SSRIs, pregabalin, duloxetine, cyclobenzaprine, and milnacipran (Bhargava & Hurley, 2023). When utilizing medications, the dose should be started low and built up gradually.

Pregabalin, milnacipran, and duloxetine are FDA-approved agents for FMS. A Cochrane review on SNRIs for FMS suggested that SNRIs (milnacipran and duloxetine) may modestly reduce pain, improve quality of life, and alleviate fatigue for some patients, though side effects are common (Welsch et al., 2018).

At times, the addition of analgesics or anti-inflammatory medication can be tried. The use of acetaminophen or NSAIDs may be considered to target pain when more traditional FMS agents do not work. Generally, opioids should be avoided in FMS.

Rheumatoid Arthritis

RA, a chronic, destructive, sometimes deforming disease, attacks the body's collagen, especially in the joints. RA is associated with widespread symptoms such as fatigue, fever, poor appetite, nerve damage, and increased size of the spleen and lymph nodes. RA can irreversibly damage joints; therefore, early diagnosis and treatment to control inflammation can improve the disease's outcomes.

Treatment options include psychosocial care, patient education, therapy, and pharmacologic treatment. A rheumatologist should be involved in the care of patients with RA as disease-modifying antirheumatic drugs (DMARD) are complex to use. If therapy is started soon, the patient will experience better outcomes. DMARD therapy is complex, requires much monitoring, and is beyond the scope of this article.

NSAIDs and glucocorticoids are also used in the management of RA. They can be used as bridging therapy to control inflammation until the DMARDs take effect quickly, and they can also be used for pain control.

Osteoarthritis

OA is the most common joint condition globally and is one of the leading sources of pain and disability in older adults (Hunter & Bierma-Zeinstra, 2019).

Arthritis affects twenty percent of adults and costs more than $136 billion annually in the United States (Osteoarthritis Action Alliance, n.d.). As the population ages, the burden of OA will increase. Managing OA improves mobility, decreases falls, decreases death rates, and improves the quality of life.

OA is a joint disease that results in deterioration of the joint and abnormal bone formation. OA is present when the bones' endings - called cartilage, which generally cushion the bones - no longer do their job. The ends of the bones rub together, and the cartilage wears away (Sen & Hurley, 2023).

Treatment of OA focuses on pain control and maintaining function. In the future, treatments may be available to reverse or even cure the disease process, but symptom control is currently the only option. Treatment focuses on medications and non-medication means to control the pain and minimize disability.

Non-drug treatment is first-line management as it bypasses the adverse effects drugs have on the body. Non-drug treatments include exercise, nutrition, physical and occupational therapy, heat and cold therapies, weight loss, and patient education.

When non-drug methods do not provide adequate relief, medications are used to treat OA. Acetaminophen is no longer recommended as a first-line agent because of safety concerns and lack of efficacy. Non-steroidal anti-inflammatory agents are now recommended ahead of acetaminophen (Hunter & Bierma-Zeinstra, 2019).

Topical NSAIDs may be used, especially if the disease is localized to one area. Topical agents are associated with a significantly less adverse event profile than systemic agents. In the United States, diclofenac sodium topical gel is available to manage OA (Sen & Hurley, 2023).

Other topical agents can provide significant relief for patients with OA. Capsaicin (Zostrix) decreases the neurotransmitter called substance P, which transmits pain. Capsaicin is applied three to four times a day and takes a few weeks before it provides significant pain relief. Hands should be washed after contact with the substance.

Another topical agent sometimes used for the treatment of localized pain is the lidocaine patch. The FDA does not approve the lidocaine patch for OA, but it is used. It is a small patch applied to the skin around the painful joint and worn for no more than 12 hours a day.

Occasionally, opioids are used in the management of OA.

Intra-articular steroid injections can be used for painful joints, which involves placing a needle directly into the arthritic joint and injecting a steroid along with a numbing agent. 

When medical treatment fails, surgery is the next option. Surgical options include arthroscopy, osteotomy, total joint arthroplasty, or joint fusion.

Case Study Two

Chris is a 44-year-old secretary who presents to her primary care provider with back pain for the last three weeks. The pain started after she lifted a heavy box at work. Her self-management regime included bed rest and taking acetaminophen alternating with ibuprofen for the last three weeks. She reports that the pain is not getting any better. The pain is described as aching and diffuse along her lower back. She says the pain worsens with walking and prolonged standing or sitting and is relieved when lying down. She reports that the pain radiates into her right buttock but not down the leg.

Chris is generally healthy. The only medication that she takes regularly is sertraline for depression. She has never had any surgeries and has no allergies to medications.

On physical exam, her vitals are stable, and she appears comfortable. She walks with a slight limp. The exam shows diffuse tenderness across her lumbar spine. There is no deformity, the straight leg raise is negative, the sensation is intact to the lower extremities, and her exam's remaining aspects show no focal neurological finding. Recent labs demonstrated a normal blood count and normal liver and renal function.

Her primary care physician recommends that she go to physical therapy, prescribes diclofenac 50 mg three times a day for three weeks, and encourages her to use acetaminophen for breakthrough pain.

At the three-week follow-up, Chris is doing better. Her primary care physician recommends continued home exercises as recommended by the physical therapist and, as needed, acetaminophen for pain; the NSAID is stopped at this time as there is likely limited inflammation contributing to the pain.

This case is typical of back pain; it resolved within six weeks. The pain was caused by an acute injury with muscle spasms causing referral of pain into the buttock. Radicular pain was not present. Radicular pain would be present if there were inflammation, compression, or injury to a spinal nerve root.

Imaging is not indicated in this case because there were no red flags. Typically, this type of back pain responds to simple analgesics; the use of opioids is not necessary. Acetaminophen is preferred for analgesia because of its relatively safe profile. The use of an NSAID may be needed because of its anti-inflammatory effect. Sometimes, short-term use of a muscle relaxer may help muscle spasms, which often contributes to this type of acute pain. 

The goal is to minimize disability and return Chris to her baseline function as soon as possible. Relative rest may be appropriate, but prolonged bed rest will contribute to deconditioning and stiffness and prolong recovery. The patient with acute lower back pain should have exercises to strengthen the lower back, stomach, and other core muscles and stretch the lower back and legs. Appropriate healthcare for back pain will get patients back to normal functioning quickly while minimizing the risk of dangerous treatment options.

Opioid Antagonists

Opioid antagonists and overdose prevention treatments are critical tools in combating opioid overdoses, which have become a major public health crisis. Opioid antagonists are medications that bind to opioid receptors in the brain but do not activate them, thus blocking the effects of opioids like heroin, morphine, and prescription painkillers. The primary opioid antagonist used in overdose prevention is naloxone (brand names include Narcan® and Evzio®).

  • Naloxone: Quickly reverses opioid overdoses by displacing opioids from their receptors in the brain. It can be administered through an injection or nasal spray.
  • Naltrexone: Another opioid antagonist, but it is used for longer-term treatment of opioid addiction rather than for immediate overdose reversal.

In addition to naloxone, overdose prevention efforts focus on harm reduction strategies and long-term treatment for opioid use disorder (OUD).

Prevention methods include:

  • Naloxone distribution: Ensuring that naloxone is widely available, particularly to individuals at risk of opioid overdose, their families, and first responders.
  • Medication-assisted treatment (MAT): Use of medications such as buprenorphine and methadone, combined with counseling and behavioral therapies, to help patients reduce or quit opioid use.
  • Education on safe opioid use: Educating patients about the risks of opioids, safe storage, and proper disposal of unused medications.

Patients might be counseled on opioid antagonists and overdose prevention treatments in several key scenarios. Individuals with high-risk opioid use are the first groups of patients who may benefit. Patients prescribed opioids for chronic pain management may be advised on naloxone use if they have a history of substance use disorder or if they are prescribed high doses. People who use opioids recreationally, particularly those using street drugs (e.g., heroin or fentanyl), should be educated on naloxone and overdose risks.

Other groups that should be considered include family and caregivers of opioid users, patients in recovery, and those being discharged from medical care. Family members or caregivers of individuals at risk for opioid overdose are often provided with naloxone and trained on how to administer it in case of an emergency. Individuals undergoing treatment for OUD or who have a history of opioid addiction might be encouraged to have naloxone available to prevent accidental overdose relapses.

They may also be advised on long-term treatments like MAT, including access to buprenorphine, methadone, or naltrexone. Patients leaving the hospital after being treated for an opioid overdose are typically given naloxone and information on how to access further care, including overdose prevention services. Discharged patients may also be directed to local harm reduction programs, needle exchange programs, and outpatient treatment for addiction management.

Buprenorphine is a medication commonly used as part of MAT for OUD. It helps individuals reduce or quit the use of opioids such as heroin, prescription painkillers, and other opioid substances. Buprenorphine is effective because it addresses both the physical and psychological components of opioid addiction.

Buprenorphine is a partial opioid agonist. It activates opioid receptors in the brain, but not to the same degree as full agonists like heroin or prescription opioids. Buprenorphine reduces cravings and withdrawal symptoms without producing the intense "high" associated with opioid abuse (Kumar et al., 2024). The "ceiling effect" of buprenorphine limits its potential for misuse, as higher doses do not produce greater effects beyond a certain point.

Formulations of buprenorphine include oral and injectable formulations. Suboxone® is a combination of buprenorphine and naloxone (the latter helps deter misuse by causing withdrawal symptoms if the medication is injected). Subutex® contains only buprenorphine and is often used in specific cases such as pregnancy or individuals with naloxone sensitivities. Buprenorphine extended-release injections provide long-acting options that help reduce the burden of daily dosing.

The benefits of buprenorphine in MAT include reducing opioid cravings, minimizing withdrawal symptoms, improving retention in treatment, and lowering the risk of overdose. It reduces opioid cravings by stimulating opioid receptors, making it easier for patients to avoid relapse. It minimizes withdrawal symptoms by alleviating the uncomfortable and often painful withdrawal symptoms, which are a significant barrier to recovery. Buprenorphine improves retention by improving engagement in treatment, which increases the chances of long-term recovery. Lastly, the partial agonist property of buprenorphine lowers the risk of overdose compared to full opioid agonists.

Buprenorphine has nuances in administration and supervision. The induction phase is typically introduced when the patient is in mild-to-moderate withdrawal from opioids to avoid triggering more severe withdrawal symptoms. In the stabilization phase, the patient’s dose is adjusted to reduce withdrawal and cravings without causing sedation or intoxication. In the maintenance phase, the optimal dose is established, and patients can remain on buprenorphine for months or even years, depending on individual needs and recovery progress. Buprenorphine can be prescribed by trained healthcare providers in an office-based setting, offering more flexibility than other treatments like methadone, which must be administered in specialized clinics.

Buprenorphine is most effective when combined with behavioral therapy and counseling. A complete methodology addresses the psychological, social, and environmental factors contributing to opioid addiction. CBT, contingency management, and motivational interviewing are some therapeutic methods used alongside MAT to improve outcomes.

Buprenorphine is associated with risks, including diversion/misuse, side effects, and risk in pregnancy. While buprenorphine has a lower potential for abuse, there is still some risk, particularly if not taken as prescribed. This is why formulations like Suboxone® (with naloxone) are preferred for outpatient treatment. Common side effects include constipation, headache, nausea, and insomnia (Kumar et al., 2024). Rarely, patients may experience respiratory depression if combined with other CNS depressants.

Conclusion

Pain is a disagreeable sensory and emotional experience connected with actual or potential tissue damage or explained in terms of such damage. Many conditions have the potential to cause pain. Understanding, assessing, and treating these conditions is vital in appropriately managing the pain. In the current healthcare system, many aspects of pain are not even addressed. Many regulatory agencies have implemented guidelines within the healthcare system to help address the pain epidemic.

The healthcare team's role is to perform a good initial and ongoing pain assessment. Proper pain management requires a team approach to evaluate and treat pain. Many options are available to manage pain, including non-pharmacological options, non-opioid medications, opioid medications, and adjunctive medications. Opioid analgesics, while very good at managing pain, have led to many social and legal problems, including overuse and diversion.

The healthcare team is also responsible for partnering with the patient to manage the pain adequately. Each healthcare team member has a role in the management of pain. Pain management is a significant focus for nurses. If healthcare team members perform their function and the patient takes an active role in their care, adequately treating pain is a very attainable goal.

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Implicit Bias Statement

CEUFast, Inc. is committed to furthering diversity, equity, and inclusion (DEI). While reflecting on this course content, CEUFast, Inc. would like you to consider your individual perspective and question your own biases. Remember, implicit bias is a form of bias that impacts our practice as healthcare professionals. Implicit bias occurs when we have automatic prejudices, judgments, and/or a general attitude towards a person or a group of people based on associated stereotypes we have formed over time. These automatic thoughts occur without our conscious knowledge and without our intentional desire to discriminate. The concern with implicit bias is that this can impact our actions and decisions with our workplace leadership, colleagues, and even our patients. While it is our universal goal to treat everyone equally, our implicit biases can influence our interactions, assessments, communication, prioritization, and decision-making concerning patients, which can ultimately adversely impact health outcomes. It is important to keep this in mind in order to intentionally work to self-identify our own risk areas where our implicit biases might influence our behaviors. Together, we can cease perpetuating stereotypes and remind each other to remain mindful to help avoid reacting according to biases that are contrary to our conscious beliefs and values.

References

  • Abi-Aad, K. R., & Derian, A. (2023). Hydromorphone. In StatPearls. StatPearls Publishing. Visit Source.
  • Agrawal, S., & Khazaeni, B. (2023). Acetaminophen Toxicity. In StatPearls. StatPearls Publishing. Visit Source.
  • Ahuja, V., Thapa, D., & Ghai, B. (2018). Strategies for prevention of lower limb post-amputation pain: A clinical narrative review. Journal of Anaesthesiology, Clinical Pharmacology, 34(4), 439–449. Visit Source.
  • Ali, A., Arif, A. W., Bhan, C., Kumar, D., Malik, M. B., Sayyed, Z., Akhtar, K. H., & Ahmad, M. Q. (2018). Managing chronic pain in the elderly: An overview of the recent therapeutic advancements. Cureus, 10(9), e3293. Visit Source.
  • American Psychiatric Association (APA). (2022). Diagnostic and statistical manual of mental disorders (5th ed., Text Revision). American Psychiatric Association. Visit Source.
  • American Psychological Association (APA). (2011). Coping with chronic pain. American Psychological Association. Visit Source.
  • Anosike, K. C., & Rajaram Manoharan, S. V. R. (2024). Central Post-Stroke Pain Syndrome. In StatPearls. StatPearls Publishing. Visit Source.
  • Anwar, K. (2016). Pathophysiology of pain. Disease-a-month: DM, 62(9), 324–329. Visit Source.
  • Armstrong, S. A., & Herr, M. J. (2023). Physiology, nociception. In StatPearls. StatPearls Publishing. Visit Source.
  • Ashton-James, C. E., Anderson, S. R., Mackey, S. C., & Darnall, B. D. (2022). Beyond pain, distress, and disability: The importance of social outcomes in pain management research and practice. Pain, 163(3), e426–e431. Visit Source.
  • Australian Pain Society. (n.d.). Example questions to ask during a comprehensive pain assessment interview. Australian Pain Society. Visit Source.
  • AZ Quotes. (n.d.). Albert Schweitzer quotes about pain. AZ Quotes. Visit Source.
  • Baker, M., & Perazella, M. A. (2020). NSAIDs in CKD: Are they safe? American Journal of Kidney Diseases: The Official Journal of the National Kidney Foundation, 76(4), 546–557. Visit Source.
  • Banerjee, S., & Butcher, R. (2020). Pharmacological interventions for chronic pain in pediatric patients: A review of guidelines. Canadian Agency for Drugs and Technologies in Health. Visit Source.
  • Bhargava, J., & Hurley, J. A. (2023). Fibromyalgia. In StatPearls. StatPearls Publishing. Visit Source.
  • Birkinshaw, H., Friedrich, C. M., Cole, P., Eccleston, C., Serfaty, M., Stewart, G., White, S., Moore, R. A., Phillippo, D., & Pincus, T. (2023). Antidepressants for pain management in adults with chronic pain: A network meta-analysis. The Cochrane Database of Systematic Reviews, 5(5), CD014682. Visit Source.
  • Bitik, B., Mercan, R., Tufan, A., Tezcan, E., Küçük, H., İlhan, M., Öztürk, M. A., Haznedaroğlu, S., & Göker, B. (2015). Differential diagnosis of elevated erythrocyte sedimentation rate and C-reactive protein levels: A rheumatology perspective. European Journal of Rheumatology, 2(4), 131–134. Visit Source.
  • Borrell-Carrió, F., Suchman, A. L., & Epstein, R. M. (2004). The biopsychosocial model 25 years later: Principles, practice, and scientific inquiry. Annals of Family Medicine, 2(6), 576–582. Visit Source.
  • Brott, N. R., Peterson, E., & Cascella, M. (2022). Opioid, risk tool. In StatPearls. StatPearls Publishing. Visit Source.
  • Carregaro, R. L., Tottoli, C. R., Rodrigues, D. D. S., Bosmans, J. E., da Silva, E. N., & van Tulder, M. (2020). Low back pain should be considered a health and research priority in Brazil: Lost productivity and healthcare costs between 2012 to 2016. PloS One, 15(4), e0230902. Visit Source.
  • Casiano, V. E., Sarwan, G., Dydyk, A. M., & Varacallo, M. A. (2023). Back pain. In StatPearls. StatPearls Publishing. Visit Source.
  • Centers for Disease Control and Prevention (CDC). (2023). Drug overdose deaths. Centers for Disease Control and Prevention. Visit Source.
  • Centers for Disease Control and Prevention (CDC). (2024). Understanding the opioid overdose epidemic. Centers for Disease Control and Prevention. Visit Source.
  • Chang, W. J. (2020). Muscle relaxants for acute and chronic pain. Physical Medicine and Rehabilitation Clinics of North America, 31(2), 245–254. Visit Source.
  • Cofano, S., Patel, P., & Yellon, R. (2024). Hydrocodone. In StatPearls. StatPearls Publishing. Visit Source.
  • Collett, B. (2013). Visceral pain: the importance of pain management services. British Journal of Pain, 7(1), 6–7. Visit Source.
  • Couto, N., Monteiro, D., Cid, L., & Bento, T. (2022). Effect of different types of exercise in adult subjects with fibromyalgia: A systematic review and meta-analysis of randomised clinical trials. Scientific Reports, 12(1), 10391. Visit Source.
  • Cunningham, A. L., & Dworkin, R. H. (2000). The management of post-herpetic neuralgia. BMJ (Clinical research ed.), 321(7264), 778–779. Visit Source.
  • Dahlhamer, J., Lucas, J., Zelaya, C., Nahin, R., Mackey, S., DeBar, L., Kerns, R., Von Korff, M., Porter, L., & Helmick, C. (2018). Prevalence of chronic pain and high-impact chronic pain among adults - United States, 2016. Morbidity and Mortality Weekly Report, 67(36), 1001–1006. Visit Source.
  • Dayoub, E. J., & Jena, A. B. (2015). Does pain lead to tachycardia? Revisiting the association between self-reported pain and heart rate in a national sample of urgent emergency department visits. Mayo Clinic Proceedings, 90(8), 1165–1166. Visit Source.
  • Dhesi, M., Maldonado, K. A., Patel, P., & Maani, C. V. (2024). Tramadol. In StatPearls. StatPearls Publishing. Visit Source.
  • Dowell, D., Ragan, K. R., Jones, C. M., Baldwin, G. T., & Chou, R. (2022). CDC clinical practice guideline for prescribing opioids for pain - United States, 2022. Morbidity and Mortality Weekly Report, 71(3), 1–95. Visit Source.
  • Dunford, E., West, E., & Sampson, E. L. (2022). Psychometric evaluation of the Pain Assessment in Advanced Dementia scale in an acute general hospital setting. International Journal of Geriatric Psychiatry, 37(12), 10.1002/gps.5830. Visit Source.
  • Durrani, M., & Bansal, K. (2024). Methadone. In StatPearls. StatPearls Publishing. Visit Source.
  • Dydyk, A. M., & Givler, A. (2023). Central pain syndrome. In StatPearls. StatPearls Publishing. Visit Source.
  • Dydyk, A. M., & Conermann, T. (2024). Chronic pain. In StatPearls. StatPearls Publishing. Visit Source.
  • Federal Communications Commission (FCC). (n.d.). Focus on broadband and opioids. Federal Communications Commission. Visit Source.
  • Fillingim, R. B. (2017). Individual differences in pain: Understanding the mosaic that makes pain personal. Pain, 158 Suppl 1(Suppl 1), S11–S18. Visit Source.
  • Fink, R. (2000). Pain assessment: The cornerstone to optimal pain management. Proceedings (Baylor University. Medical Center), 13(3), 236–239. Visit Source.
  • Finnerup, N. B., Kuner, R., & Jensen, T. S. (2021). Neuropathic pain: From mechanisms to treatment. Physiological Reviews, 101(1), 259–301. Visit Source.
  • Fitzcharles, M. A., Cohen, S. P., Clauw, D. J., Littlejohn, G., Usui, C., & Häuser, W. (2021). Nociplastic pain: Towards an understanding of prevalent pain conditions. Lancet (London, England), 397(10289), 2098–2110. Visit Source.
  • Food and Drug Administration (FDA). (n.d.) Opioid patient prescriber agreement (PPA). Food and Drug Administration. Visit Source.
  • Franklin, G. M., & American Academy of Neurology (2014). Opioids for chronic noncancer pain: A position paper of the American Academy of Neurology. Neurology, 83(14), 1277–1284. Visit Source.
  • Fuchs-Lacelle, S., & Hadjistavropoulos, T. (2004). Development and preliminary validation of the pain assessment checklist for seniors with limited ability to communicate (PACSLAC). Pain Management Nursing: Official Journal of the American Society of Pain Management Nurses, 5(1), 37–49. Visit Source.
  • García-Valdivieso, I., Yáñez-Araque, B., Moncunill-Martínez, E., Bocos-Reglero, M. J., & Gómez-Cantarino, S. (2023). Effect of non-pharmacological methods in the reduction of neonatal pain: Systematic review and meta-analysis. International Journal of Environmental Research and Public Health, 20(4), 3226. Visit Source.
  • Gerriets, V., Anderson, J., Patel, P., & Nappe, T. M. (2024). Acetaminophen. In StatPearls. StatPearls Publishing. Visit Source.
  • Ghlichloo, I., & Gerriets, V. (2023). Nonsteroidal Anti-Inflammatory Drugs (NSAIDs). In StatPearls. StatPearls Publishing. Visit Source.
  • Glenzel, L., do Nascimento Oliveira, P., Marchi, B. S., Ceccon, R. F., & Moran, C. A. (2023). Validity and reliability of pain and behavioral scales for preterm infants: A systematic review. Pain Management Nursing: Official Journal of the American Society of Pain Management Nurses, 24(5), e84–e96. Visit Source.
  • Grundy, L., Erickson, A., & Brierley, S. M. (2019). Visceral pain. Annual Review of Physiology, 81, 261–284. Visit Source.
  • Haefeli, M., & Elfering, A. (2006). Pain assessment. European Spine Journal: Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society, 15 Suppl 1(Suppl 1), S17–S24. Visit Source.
  • Hammi, C., & Yeung, B. (2022). Neuropathy. In StatPearls. StatPearls Publishing. Visit Source.
  • Harden, R. N., McCabe, C. S., Goebel, A., Massey, M., Suvar, T., Grieve, S., & Bruehl, S. (2022). Complex regional pain syndrome: Practical diagnostic and treatment guidelines, 5th Edition. Pain Medicine (Malden, Mass.), 23(Suppl 1), S1–S53. Visit Source.
  • Herman, T. F., Cascella, M., & Muzio, M. R. (2024). Mu Receptors. In StatPearls. StatPearls Publishing. Visit Source.
  • Herr, K., Coyne, P. J., Key, T., Manworren, R., McCaffery, M., Merkel, S., Pelosi-Kelly, J., Wild, L., & American Society for Pain Management Nursing. (2006). Pain assessment in the nonverbal patient: position statement with clinical practice recommendations. Pain Management Nursing: Official Journal of the American Society of Pain Management Nurses, 7(2), 44–52. Visit Source.
  • Herr, K., Coyne, P. J., McCaffery, M., Manworren, R., & Merkel, S. (2011). Pain assessment in the patient unable to self-report: Position statement with clinical practice recommendations. Pain Management Nursing, 12(4), 230-250. Visit Source.
  • Hunter, D. J., & Bierma-Zeinstra, S. (2019). Osteoarthritis. Lancet (London, England), 393(10182), 1745–1759. Visit Source.
  • International Association for the Study of Pain (IASP). (2020). IASP announces revised definition of pain. International Association for the Study of Pain. Visit Source.
  • Johnson, M. I., Paley, C. A., Jones, G., Mulvey, M. R., & Wittkopf, P. G. (2022). Efficacy and safety of transcutaneous electrical nerve stimulation (TENS) for acute and chronic pain in adults: a systematic review and meta-analysis of 381 studies (the meta-TENS study). BMJ open, 12(2), e051073. Visit Source.
  • Johnston, K. J. A., & Huckins, L. M. (2022). Chronic Pain and Psychiatric Conditions. Complex Psychiatry, 9(1-4), 24–43. Visit Source.
  • The Joint Commission (TJC). (2022). Pain assessment and management – Understanding the requirements. The Joint Commission. Visit Source.
  • Kenny, B. J., & Bordoni, B. (2022). Neuroanatomy, cranial nerve 10 (Vagus Nerve). In StatPearls. StatPearls Publishing. Visit Source.
  • Kumar, R., Viswanath, O., & Saadabadi, A. (2024). Buprenorphine. In StatPearls. StatPearls Publishing. Visit Source.
  • Lalouni, M., Fust, J., Vadenmark-Lundqvist, V., Ehrsson, H. H., Kilteni, K., & Birgitta Jensen, K. (2021). Predicting pain: differential pain thresholds during self-induced, externally induced, and imagined self-induced pressure pain. Pain, 162(5), 1539–1544. Visit Source.
  • Lueptow, L. M., Fakira, A. K., & Bobeck, E. N. (2018). The contribution of the descending pain modulatory pathway in opioid tolerance. Frontiers in Neuroscience, 12, 886. Visit Source.
  • Malanga, G. A., Yan, N., & Stark, J. (2015). Mechanisms and efficacy of heat and cold therapies for musculoskeletal injury. Postgraduate Medicine, 127(1), 57–65. Visit Source.
  • Massachusetts Department of Public Health (2024). Data brief: Opioid-related overdose deaths among Massachusetts residents. Massachusetts Department of Public Health. Visit Source.
  • Massachusetts Medical Society. (n.d.). Massachusetts Medical Society opioid therapy and physician communication guidelines. Massachusetts Medical Society. Visit Source.
  • Maumus, M., Mancini, R., Zumsteg, D. M., & Mandali, D. K. (2020). Aberrant drug-related behavior monitoring. Ochsner Journal, 20(4), 358–361. Visit Source.
  • Meda, R. T., Nuguru, S. P., Rachakonda, S., Sripathi, S., Khan, M. I., & Patel, N. (2022). Chronic pain-induced depression: A review of prevalence and management. Cureus, 14(8), e28416. Visit Source.
  • Medscape. (n.d.). Tramadol (Rx). Medscape. Visit Source.
  • Medscape. (2024a). Hydrocodone (Rx). Medscape. Visit Source.
  • Medscape. (2024b). Fentanyl (Rx). Medscape. Visit Source.
  • Medscape. (2024c). Morphine (Rx). Medscape. Visit Source.
  • Medscape. (2024d). Oxymorphone (Rx). Medscape. Visit Source.
  • Melzack, R. (1999). From the gate to the neuromatrix. Pain, Suppl 6, S121–S126. Visit Source.
  • Moayedi, M., & Davis, K. D. (2013). Theories of pain: From specificity to gate control. Journal of Neurophysiology, 109(1), 5–12. Visit Source.
  • Mokhtar, M., & Singh, P. (2023). Neuroanatomy, Periaqueductal Gray. In StatPearls. StatPearls Publishing. Visit Source.
  • Moore, N., Pollack, C., & Butkerait, P. (2015). Adverse drug reactions and drug-drug interactions with over-the-counter NSAIDs. Therapeutics and Clinical Risk Management, 11, 1061–1075. Visit Source.
  • Murphy, P. B., Bechmann, S., & Barrett, M. J. (2023). Morphine. In StatPearls. StatPearls Publishing. Visit Source.
  • National Cancer Institute (NCI). (2024). Cancer pain (PDQ®)–Health professional version. National Cancer Institute at the National Institutes of Health. Visit Source.
  • National Health Service (NHS). (2022a). Side effects of duloxetine. NHS. Visit Source.
  • National Health Service (NHS). (2022b). TENS. NHS. Visit Source.
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). (2023). Limits on acetaminophen in Aaetaminophen-opioid combination medications affected causes of acute liver failure. U.S. Department of Health and Human Services. Visit Source.
  • National Institution of Drug Abuse (NIDA). (2023). NIDA IC fact sheet 2024. U.S. Department of Health and Human Services. Visit Source.
  • National Institute of Drug Abuse (NIDA). (2024). Opioids. U.S. Department of Health and Human Services. Visit Source.
  • National Institute of Neurological Disorders and Stroke. (2025). Pain. National Institutes of Health. Visit Source.
  • National Library of Medicine. (2018). Non-drug pain management. MedlinePlus. Visit Source.
  • National Library of Medicine. (2024). Electromyography (EMG) and nerve conduction studies. MedlinePlus. Visit Source.
  • Nugent, S. M., Lovejoy, T. I., Shull, S., Dobscha, S. K., & Morasco, B. J. (2021). Associations of pain numeric rating scale scores collected during usual care with research administered patient reported pain outcomes. Pain Medicine (Malden, Mass.), 22(10), 2235–2241. Visit Source.
  • Núñez-López, I., Collados-Gómez, L., Abalo, R., Martínez-Pérez, P., Moreno-Vicente, Á., & Cid-Expósito, M. G. (2022). Cultural adaptation and validation of the premature infant pain profile-revised (PIPP-R) pain measurement scale: Research protocol. International Journal of Environmental Research and Public Health, 19(19), 12338. Visit Source.
  • Osteoarthritis Action Alliance. (n.d.). OA prevalence and burden. University of North Carolina at Chapel Hill. Visit Source.
  • Pasero, C., & McCaffery, M. (2011). Pain assessment and pharmacologic management. Elsevier/Mosby.
  • Perry, M., Tan, Z., Chen, J., Weidig, T., Xu, W., & Cong, X. S. (2018). Neonatal pain: Perceptions and current practice. Critical Care Nursing Clinics of North America, 30(4), 549–561. Visit Source.
  • Pirschel, C. (2018). Remembering Margo McCaffery’s contributions to pain management. ONS Voice. Visit Source.
  • Queremel Milani, D. A., & Davis, D. D. (2023). Pain management medications. In StatPearls. StatPearls Publishing. Visit Source.
  • Quinlan-Colwell, A., Rae, D., & Drew, D. (2022). Prescribing and administering opioid doses based solely on pain intensity: Update of a position statement by the American Society for Pain Management NursingⓇ. Pain Management Nursing: Official Journal of the American Society of Pain Management Nurses, 23(3), 265–266. Visit Source.
  • Racke, M. K., Frohman, E. M., & Frohman, T. (2022). Pain in multiple sclerosis: Understanding pathophysiology, diagnosis, and management through clinical vignettes. Frontiers in Neurology, 12, 799698. Visit Source.
  • Ramos-Matos, C. F., Bistas, K. G., & Lopez-Ojeda, W. (2023). Fentanyl. In StatPearls. StatPearls Publishing. Visit Source.
  • Reinert, J. P., Veronin, M. A., & Medina, C. (2023). Tricyclic antidepressants in nociceptive and neuropathic pain: A review of their analgesic properties in combination with opioids. The Journal of Pharmacy Technology: jPT: Official Publication of the Association of Pharmacy Technicians, 39(1), 35–40. Visit Source.
  • Robinson, D. R., & Gebhart, G. F. (2008). Inside information: The unique features of visceral sensation. Molecular Interventions, 8(5), 242–253. Visit Source.
  • Sadiq, N. M., Dice, T. J., & Mead, T. (2024). Oxycodone. In StatPearls. StatPearls Publishing. Visit Source.
  • Samulowitz, A., Gremyr, I., Eriksson, E., & Hensing, G. (2018). "Brave men" and "emotional women": A theory-guided literature review on gender bias in health care and pain management. Journal of Pain Research, 11, 1065–1075.
  • Sarkaria, E., & Gruszfeld, D. (2022). Assessing neonatal pain with NIPS and COMFORT-B: evaluation of NICU's staff competences. Pain Research & Management, 2022, 8545372. Visit Source.
  • Schneider, J., Patterson, M., & Jimenez, X. F. (2019). Beyond depression: Other uses for tricyclic antidepressants. Cleveland Clinic Journal of Medicine, 86(12), 807–814. Visit Source.
  • Sen, R., & Hurley, J. A. (2023). Osteoarthritis. In StatPearls. StatPearls Publishing. Visit Source.
  • Steiner, T. J., & Stovner, L. J. (2023). Global epidemiology of migraine and its implications for public health and health policy. Nature Reviews. Neurology, 19(2), 109–117. Visit Source.
  • Szalavitz, M., Rigg, K. K., & Wakeman, S. E. (2021). Drug dependence is not addiction-and it matters. Annals of Medicine, 53(1), 1989–1992. Visit Source.
  • Teleanu, R. I., Niculescu, A. G., Roza, E., Vladâcenco, O., Grumezescu, A. M., & Teleanu, D. M. (2022). Neurotransmitters-key factors in neurological and neurodegenerative disorders of the central nervous system. International Journal of Molecular Sciences, 23(11), 5954. Visit Source.
  • Von Korff, M., Merrill, J. O., Rutter, C. M., Sullivan, M., Campbell, C. I., & Weisner, C. (2011). Time-scheduled vs. pain-contingent opioid dosing in chronic opioid therapy. Pain, 152(6), 1256–1262. Visit Source.
  • van Velzen, G. A. J., Huygen, F. J. P. M., van Kleef, M., van Eijs, F. V., Marinus, J., & van Hilten, J. J. (2019). Sex matters in complex regional pain syndrome. European Journal of Pain, 23(6), 1108–1116. Visit Source.
  • Wahezi, S. E., Duarte, R., Kim, C., Sehgal, N., Argoff, C., Michaud, K., Luu, M., Gonnella, J., & Kohan, L. (2022). An algorithmic approach to the physical exam for the pain medicine practitioner: A review of the literature with multidisciplinary consensus. Pain Medicine (Malden, Mass.), 23(9), 1489–1528. Visit Source.
  • Walters, E. T. (2019). Adaptive mechanisms driving maladaptive pain: How chronic ongoing activity in primary nociceptors can enhance evolutionary fitness after severe injury. Philosophical Transactions of the Royal Society of London. Series B, Biological sciences, 374(1785), 20190277. Visit Source.
  • Webster, L. R. (2017). Risk factors for opioid-use disorder and overdose. Anesthesia and Analgesia, 125(5), 1741–1748. Visit Source.
  • Weerapong, P., Hume, P. A., & Kolt, G. S. (2005). The mechanisms of massage and effects on performance, muscle recovery and injury prevention. Sports Medicine (Auckland, N.Z.), 35(3), 235–256. Visit Source.
  • Welsch, P., Üçeyler, N., Klose, P., Walitt, B., & Häuser, W. (2018). Serotonin and noradrenaline reuptake inhibitors (SNRIs) for fibromyalgia. The Cochrane Database of Systematic Reviews, 2(2), CD010292. Visit Source.
  • Wong, C. K., Mak, R. Y., Kwok, T. S., Tsang, J. S., Leung, M. Y., Funabashi, M., Macedo, L. G., Dennett, L., & Wong, A. Y. (2022). Prevalence, incidence, and factors associated with non-specific chronic low back pain in community-dwelling older adults aged 60 years and older: A systematic review and meta-analysis. The Journal of Pain, 23(4), 509–534. Visit Source.
  • Wyoming Legislature. (n.d.). Substance use disorder defined by NIDA and SAMHSA. Wyoming Legislature. Visit Source.
  • Yang, J., Lo, W. L. A., Zheng, F., Cheng, X., Yu, Q., & Wang, C. (2022). Evaluation of cognitive behavioral therapy on improving pain, fear avoidance, and self-efficacy in patients with chronic low back pain: A systematic review and meta-analysis. Pain Research & Management, 2022, 4276175. Visit Source.
  • Yasaei, R., Katta, S., Patel, P., & Saadabadi, A. (2024). Gabapentin. In StatPearls. StatPearls Publishing. Visit Source.