≥ 92% of participants will know the current evidence-based practice for safe, effective, and patient-centered care to individuals living with asthma.

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≥ 92% of participants will know the current evidence-based practice for safe, effective, and patient-centered care to individuals living with asthma.
Upon completion of this course, the learner will be able to:
The purpose of this course is to provide nurses and healthcare professionals with a comprehensive understanding of asthma’s pathophysiology, presentation, diagnostic criteria, and management, addressing a common gap in practice where asthma is frequently underdiagnosed, misclassified, or inadequately controlled. This course equips learners to differentiate asthma from similar conditions, tailor care across age groups, and respond effectively in both outpatient and acute settings.
Asthma is a highly prevalent, chronic inflammatory disease of the airways characterized by variable and reversible airflow obstruction. Asthma presents with symptoms such as wheezing, cough, chest tightness, and shortness of breath that can range from mild to life-threatening. Despite advances in treatment, asthma continues to be underdiagnosed, often poorly controlled, and a significant cause of emergency visits and hospitalizations.
Understanding asthma requires not only recognition of its hallmark symptoms but also a deeper grasp of its complex pathophysiology, diagnostic challenges, and the interplay of pharmacologic and nonpharmacologic management strategies. This course explores evidence-based practices that enable clinicians to provide safe, effective, and patient-centered care to individuals living with asthma.
Asthma affects millions of people worldwide and represents a major public health concern. Globally, it is estimated that more than 260 million people live with asthma, and the disease contributes significantly to disability-adjusted life years (DALYs) (World Health Organization [WHO], 2024).
In the United States, asthma remains a significant public health concern, with 24.9 million people affected in 2021, about 7.7% of the population (Centers for Disease Control and Prevention [CDC], 2023). Trends over the past two decades show that overall prevalence has increased slightly, rising from 7.4% in 2001 to 7.7% in 2021 (CDC, 2023). Notably, asthma prevalence among adults increased during this period, while the prevalence among children (ages 0 - 17) declined, particularly after 2010. These contrasting trends suggest that while asthma remains common in youth, public health and clinical interventions may be contributing to improved diagnosis and control in pediatric populations, even as adult asthma continues to pose challenges (CDC, 2023).
Risk factors for asthma are multifactorial, including both genetic and environmental factors. A family history of asthma or allergies is a strong predictor, pointing to a hereditary component.
Asthma Triggers
(*Please click on the image above to enlarge.)
Additionally, access to healthcare, health literacy, housing quality, and environmental changes play critical roles in asthma prevalence and outcomes. Children in households with limited access to consistent medical care are less likely to receive preventive treatments, leading to higher emergency department visits and hospitalizations. Inadequate insurance coverage can also delay diagnosis or limit access to inhaled corticosteroids. Ultimately, while genetics and biology lay the foundation for asthma risk, social and environmental factors shape its epidemiology and outcomes on a population level (NHLBI, 2024).
The pathophysiology of asthma can be described as a two-step process involving both immediate and delayed immune responses following exposure of the airway epithelium to allergens or irritants. When the airway epithelium is exposed to an antigen, the immune system initiates a cascade of events designed to protect the individual, but in asthma, these mechanisms become exaggerated and cause more harm than good. This dysregulated immune response results in airway inflammation, hyperresponsiveness, and remodeling over time.
Clinically, this manifests as acute-onset wheezing, chest tightness, and shortness of breath. While this acute onset can resolve spontaneously or with treatment, it leaves the airway primed for further inflammation (Brashers et al., 2025).
The delayed response, also called the late-phase reaction, develops hours after initial exposure. It is driven by IL-5 and other cytokines that recruit eosinophils, neutrophils, and lymphocytes into the airway tissues. Eosinophils play a particularly destructive role by releasing toxic proteins that damage epithelial cells, leading to tissue injury.
Progression of Airway Inflammation in Asthma
(*Please click on the image above to enlarge.)
Together, these immediate and delayed responses create the progression of asthma. The immediate response is dominated by mast cell degranulation and acute bronchoconstriction, while the delayed response reflects persistent inflammation, immune cell recruitment, and structural airway changes. The interplay between these two phases results in airway hyperresponsiveness, recurring symptoms, and, if uncontrolled, long-term remodeling that makes the disease more difficult to treat (Brashers et al., 2025).
| Asthma is closely linked to atopy, a genetic tendency to develop allergic diseases such as eczema, allergic rhinitis, and food allergies. This relationship is part of what is often referred to as the “atopic march”. This is where children with early allergic conditions like eczema or food allergy are more likely to develop allergic rhinitis and asthma as they grow older. The shared underlying mechanism is an exaggerated Type 2 helper T cell-mediated immune response, leading to increased production of IgE antibodies and heightened airway inflammation when exposed to allergens. Children with comorbid atopic conditions not only face a higher risk of developing asthma but also tend to have a more severe disease and exacerbations triggered by environmental exposures. The presence of eczema and allergies serves as an important clinical clue for asthma risk. Infants and young children with moderate to severe eczema are significantly more likely to develop asthma later in childhood, especially if they also have sensitization to airborne allergens. Similarly, children with allergic rhinitis often experience overlapping symptoms such as nasal congestion and cough, which can worsen asthma control and increase the frequency of exacerbation. Recognizing this connection is critical for clinicians, as early identification of at-risk children provides opportunities for closer monitoring, early initiation of controller therapy, and aggressive management of comorbid atopic diseases (Asthma and Allergy Foundation of America [AAFA], 2022). |
Presentation of asthma can vary depending on age, severity, and the setting in which symptoms arise, but it typically involves a combination of chronic and acute manifestations.
Acute presentation is characterized by sudden exacerbations or “asthma attacks,” during which symptoms become more severe and may include pronounced wheezing, tachypnea, use of accessory muscles for breathing, or difficulty speaking in full sentences. In severe cases, cyanosis, confusion, or “silent chest” are ominous findings that require immediate intervention (Brashers et al., 2025).
In children, asthma may present subtly, especially in its chronic form. Parents often report a recurring cough, particularly at night, after play, or following respiratory infections. Wheezing may be heard intermittently, but in some children, cough is the predominant or only symptom, leading to a diagnosis of “cough variant asthma.” Reports of recurrent episodes of “bronchitis” or “pneumonia” may also suggest undiagnosed asthma. During acute exacerbations, children may present with rapid breathing, retractions, nasal flaring, and difficulty speaking or feeding. Because children may struggle to describe their symptoms, clinicians rely heavily on parental reports of coughing patterns, nighttime awakenings, and response to bronchodilators (Martin et al., 2022).
One useful tool for evaluating asthma in pediatric patients is the Childhood Asthma Control Test (C-ACT), an evidence-based questionnaire designed for children ages 4 to 11. The C-ACT combines the child's self-reported responses (with pictorial response options to aid understanding) and input from the parent or caregiver. Questions focus on the frequency of symptoms such as coughing, wheezing, nighttime awakenings, activity limitations, and the need for rescue inhaler use over the previous four weeks. Each response is scored, and the total score helps determine whether the child’s asthma is well controlled, not well controlled, or poorly controlled. A score of 19 or less generally indicates that asthma is not adequately controlled and may warrant a step-up in therapy, re-evaluation of environmental triggers, or evaluation of treatment adherence. The simplicity and reliability of the C-ACT make it a valuable tool for clinicians, as it provides structured insight into the child’s daily symptom burden and quality of life, supporting both diagnosis and ongoing management (Martin et al., 2022; van Dijk et al., 2020).
In adults, asthma is often easier to recognize by the pattern of wheezing, chest tightness, and variable breathlessness. Adults may describe episodic symptoms that interfere with sleep, physical activity, or work performance. A thorough history should include questions about occupational exposures (e.g., dust, fumes, or chemicals), smoking status, and environmental triggers at home. Adults with asthma often have comorbidities such as allergic rhinitis, gastroesophageal reflux disease (GERD), or obesity, which can complicate presentation and control. Clinicians assessing adults should document the frequency of daytime and nighttime symptoms, the use of rescue inhalers, and any limitations in daily activities, as this information is key to classifying asthma severity and guiding treatment decisions.
Across all age groups, critical assessment data for clinicians include vital signs (respiratory rate, oxygen saturation, heart rate), auscultation findings (wheezing, decreased air entry), and the presence of accessory muscle use, tripod position, or retractions. History-taking should emphasize symptom variability, triggers, family history of asthma or allergies, and response to previous treatments. Identifying patterns such as worsening symptoms at night, improvement after bronchodilator use, or exacerbations linked to allergens provides strong clues toward the diagnosis. Collectively, these clinical observations form the foundation for confirming asthma with objective testing (Brashers et al., 2025).
Asthma is diagnosed primarily through a combination of clinical evaluation and objective testing, as there is no single definitive test. The diagnostic criteria typically include a history of recurrent, reversible respiratory symptoms such as wheezing, coughing (especially at night or early morning), shortness of breath, and chest tightness that vary over time and intensity. One hallmark of asthma is the presence of variable and reversible airflow limitation. This means that lung function can fluctuate and improve with bronchodilator therapy. Clinicians also look for a pattern of symptom triggers that strongly suggest asthma rather than another respiratory disorder, such as allergens, exercise, cold air, or respiratory infections.
Diagnostic testing is essential for confirming asthma, particularly because symptoms alone can overlap with many other respiratory and cardiac conditions.
Spirometry
Spirometry remains the gold standard for diagnosis and is recommended for all patients aged 5 years and older who are suspected of having asthma. During the test, the patient takes a deep breath and then exhales forcefully into a mouthpiece connected to the spirometer, which records airflow and lung volumes. This is done both before and after administration of a bronchodilator to compare function.
Two key measurements are obtained:
The ratio of FEV1 to FVC (FEV1/FVC) helps determine the presence of airway obstruction.
In asthma, a reduced FEV1 and FEV1/FVC ratio indicates airway obstruction, and
Peak Expiratory Flow (PEF)
For patients with intermittent symptoms, spirometry may appear normal between episodes, making asthma difficult to confirm. In these cases, Peak Expiratory Flow (PEF) monitoring is particularly useful for diagnosis. A peak flow meter is a handheld device that measures the maximum speed of expiration, providing an objective way to detect variability in airflow limitation. By recording PEF values several times daily over 1 - 2 weeks, clinicians can assess fluctuations that are consistent with asthma, especially if values improve with bronchodilator use. Establishing a patient’s “personal best” baseline is essential, since PEF varies by age, sex, and height. Significant variability, typically more than 20% between readings or compared with baseline, supports the diagnosis of asthma and helps differentiate it from other chronic respiratory conditions (American Lung Association [ALA], 2024).
Bronchoprovocation
Fractional Exhaled Nitric Oxide
Imaging
Imaging studies, such as chest X-rays or CT scans, are typically normal in patients with asthma. Yet imaging can be useful for ruling out structural lung disease, pneumonia, a foreign body, or other pulmonary pathology.
Because asthma is a clinical syndrome rather than a single disease, clinicians must carefully consider differential diagnoses to avoid misdiagnosis and inappropriate treatment.
For adults, the following conditions must be considered and ruled out:
For children, alternative diagnoses often reflect developmental and infectious causes.
Asthma is classified based on several key dimensions: severity, control, and phenotype. These categories help guide treatment decisions, predict prognosis, and tailor therapy to the individual patient. Severity reflects the intrinsic intensity of the disease before treatment, while control reflects how well symptoms are managed with current therapy. Phenotyping, a more recent development, categorizes asthma into biologically or clinically distinct subtypes that may respond differently to targeted therapies.
Asthma severity is traditionally classified into four categories and is based on symptom frequency, nighttime awakenings, use of rescue inhalers, limitations of activity, and spirometry results (FEV1 and FEV1/FVC ratio) (Merck Manual Professional Version, 2025).
Emphasized in more recent guidelines, asthma control classification assesses the effectiveness of ongoing treatment. Control is generally categorized as (GINA, 2020):
Criteria include daytime symptom frequency, nighttime awakenings, need for rescue medication, limitations in daily activities, and objective measures such as lung function or peak flow. A patient whose asthma was initially moderate persistent may become well controlled with appropriate therapy. This approach also allows clinicians to systematically step up or step down therapy, aligning with guideline-directed management.
| In the past 4 weeks, has the patient had: y/n | Well Controlled | Partly Controlled | Uncontrolled |
|---|---|---|---|
| None of these | 1-2 of these | 3-4 of these |
Beyond severity and control, asthma is increasingly understood in terms of phenotypes and endotypes. Phenotypes include allergic asthma (often beginning in childhood with atopy and elevated IgE), nonallergic asthma, late-onset asthma, obesity related asthma, and asthma with persistent airflow limitation.
Endotyping goes further by identifying distinct molecular pathways, such as type 2 inflammation mediated by IL-4, IL-5, and IL-13, versus non-type 2 asthma. These classifications are typically made using a combination of clinical history, pulmonary function testing, and laboratory markers such as serum IgE levels, blood eosinophil counts, and exhaled nitric oxide FeNO. Because this level of evaluation goes beyond standard primary care, phenotyping and endotyping are most often performed by pulmonologists, allergists, or immunologists, who can integrate advanced diagnostic tools and determine eligibility for targeted biologic therapies. A phenotype and endotype classification can be useful in guiding biologic therapies, such as omalizumab for IgE mediated disease or mepolizumab for eosinophilic asthma (Kuruvilla et al., 2019).
Once asthma has been classified, a multimodal treatment approach is essential to achieve optimal control and prevent long-term complications. This approach integrates pharmacologic therapy with nonpharmacologic interventions and should be individualized for each unique patient. Further discussion of management strategies is below.
Management of asthma often starts with nonpharmacological methods to reduce exposure to triggers, monitoring disease activity, and promoting long-term control. Appropriate nonpharmacological management can improve the efficacy or even reduce the intensity of pharmacological management needed.
Of highest priority is identifying and avoiding asthma triggers, which vary from person to person but often include allergens such as dust mites, mold, pollen, animal dander, and cockroach debris, as well as irritants like tobacco smoke, air pollution, strong odors, and cold air. Respiratory infections and exercise can also precipitate exacerbations. Careful history-taking and, when indicated, allergy testing can help patients identify their specific triggers and develop individualized strategies to reduce exposure.
Nurses, physical therapists (PTs) (especially those specializing in pulmonary rehabilitation), and athletic trainers (ATs) all play key roles in educating patients about non-pharmacologic asthma management.
The stepwise approach to asthma management is a guideline-based framework that tailors medication therapy to a patient’s symptom severity and control. The goal is to achieve the lowest effective medication dose that maintains control, while adjusting treatment upward (“step up”) during times of poor control and downward (“step down”) when stable. This approach is grounded in the two-step pathophysiology of asthma: the immediate phase, driven by acute bronchoconstriction and mediator release, and the delayed phase, characterized by chronic inflammation, eosinophil recruitment, and airway remodeling. Understanding this dual process is crucial, as it explains why treatment must address both rapid symptom relief and long-term control of airway inflammation.
Step-up Treatment of Asthma

The stepwise approach differs slightly between children and adults in terms of medication preference and safety considerations. Children are more likely to begin treatment with ICS earlier, as LTRAs are sometimes preferred over LABAs for safety reasons. Monitoring growth is important in children on long-term ICS therapy, though the benefits in controlling inflammation generally outweigh the risks. Adults, on the other hand, often require earlier introduction of combination ICS/LABA therapy if symptoms are persistent, and comorbidities such as COPD or cardiovascular disease may influence drug choice (Burchum & Rosenthal, 2025).
For mild to moderate asthma exacerbations, outpatient management can be highly effective when combined with close follow-up. In these cases, patients may be treated with a short “burst” of oral corticosteroids, such as prednisone or prednisolone (Orapred), typically prescribed for 5 to 10 days. This approach rapidly reduces airway inflammation, restores responsiveness to bronchodilators, and helps prevent relapse of symptoms.
Tapering of corticosteroids is generally not required if the course is 10 days or less, as adrenal suppression is unlikely with short-term use. However, if therapy is extended beyond 10 days, tapering should be considered to allow the hypothalamic pituitary adrenal (HPA) axis to recover and to avoid withdrawal symptoms. Outpatient care should also emphasize frequent use of inhaled SABAs as needed, monitoring of peak expiratory flow, and reinforcement of the patient’s asthma action plan to ensure early recognition of worsening symptoms (Burchum & Rosenthal, 2025).
Understanding the mechanisms of action of asthma medications is essential for clinicians. While this is not a pharmacology course, a brief description of each class’s mechanism of action will improve clinician understanding and guide safe prescribing, patient education, and recognition of potential side effects.
SABAs act on beta2 adrenergic receptors in the airway smooth muscle. These receptors are typically stimulated by catecholamines like epinephrine and norepinephrine. In a fight or flight response, the airways dilate to improve respiration and meet increased oxygen demand. By binding to those same receptors, SABAs mimic that sympathetic nervous system response and lead to rapid relaxation of bronchial smooth muscle. This results in quick bronchodilation and relief of acute symptoms like wheezing, chest tightness, and shortness of breath.
LABAs act on the same receptors as SABAs but have a longer duration of action (12 hours or more). By providing sustained bronchodilation, they reduce nighttime symptoms and improve lung function.
Systemic corticosteroids share the same mechanism as ICSs but act throughout the body. They are powerful suppressors of inflammation and immune activity, used for acute exacerbations or severe refractory asthma. Because of significant side effects, they are reserved for short-term use or as a last-line option.
LTRAs block leukotriene D4 receptors in the airway. Leukotrienes are potent inflammatory mediators involved in the asthma response. LTRAs prevent leukotriene activity. By blocking leukotrienes, LTRAs reduce both bronchospasm and inflammation. This mechanism makes them particularly useful in patients with asthma triggered by allergies or exercise.
In addition to beta₂ adrenergic receptors, the smooth muscle of the airways also has muscarinic receptors (M3) that can be stimulated by the parasympathetic nervous system. Typically, acetylcholine binding to these receptors results in bronchoconstriction and increased mucus secretion; however,
As with all medication therapies, asthma controller drugs are not without risks and educational requirements for proper use and outcome maximization.
Healthcare considerations for ICSs include monitoring adherence, assessing inhaler technique, and ensuring patients rinse their mouths after each use to reduce the risk of oropharyngeal side effects such as thrush and dysphonia (hoarseness). Though rare, higher doses or long-term use can lead to systemic absorption, contributing to slowed growth velocity in children, bone demineralization, or adrenal suppression. Careful monitoring of growth patterns in pediatric patients, bone health in adults, and signs of adrenal insufficiency in all patients is essential to ensure safety. Patient and caregiver education should also highlight the preventive nature of ICSs, as many families mistakenly discontinue them when symptoms improve.
Combination inhalers (ICS + LABA), such as budesonide-formoterol (Symbicort) or fluticasone-salmeterol (Advair), improve adherence by consolidating controller therapy. As mentioned above, a critical prescribing consideration is that LABAs should never be used as monotherapy in asthma due to increased risk of severe exacerbations and death. They must always be paired with an ICS. Healthcare providers should monitor for side effects similar to SABAs (tremor, palpitations), ensure patients understand the difference between daily and as-needed dosing, and reinforce that symptom improvement does not mean discontinuing ICS.
LTRAs are generally well tolerated, but clinicians should be aware of a black box warning for rare neuropsychiatric side effects, including mood changes, depression, and suicidal ideation, especially in children and adolescents. Families should be counseled to monitor behavior and report any concerning changes promptly.
Biologic therapy infusions or injections are reserved for severe asthma and require careful phenotyping to ensure appropriate selection. They are administered via subcutaneous injection (except reslizumab, which is IV) and often require coordination with specialty clinics. Nursing responsibilities include monitoring for injection site reactions, hypersensitivity, and, in rare cases, anaphylaxis. Patients receiving omalizumab should be observed after injections for potential reactions. These agents reduce exacerbations and oral steroid dependence, but their high cost and need for regular administration require careful patient education and follow-up.
Systemic corticosteroids remain essential in acute exacerbations but carry significant risks when used long-term. Side effects include weight gain, mood changes, hyperglycemia, hypertension, osteoporosis, and adrenal suppression. Nurses should monitor blood pressure, blood glucose, and signs of infection, and educate patients about the importance of tapering if prescribed for more than 10 days to avoid an adrenal crisis. Prescribers should balance the need for short-term control with the risks of chronic exposure, reserving systemic steroids for acute management or refractory disease (Burcham & Rosenthal, 2025; Buttaro et al., 2025).
Image: Inhaler Use with a Spacer

Image of Nebulizer

Exercise-induced bronchoconstriction (EIB) is a common issue among athletes, affecting 20-70% of athletes across specific sports, and is often referred to as exercise-induced asthma; however, it is distinct from chronic asthma (Ora et al., 2024; UPMC, 2021). As described earlier, chronic asthma can be triggered by a variety of factors, including allergies that trigger the airways in the lungs to become inflamed and narrowed.
Management of EIB encompasses both pharmacological and non-pharmacological approaches. Short-acting beta-2 agonists (SABAs), such as albuterol, administered 15–20 minutes before exercise, remain the first-line preventive therapy (Global Initiative for Asthma [GINA], 2024). Long-term control may involve inhaled corticosteroids or leukotriene receptor antagonists for individuals with persistent symptoms (Weiler et al., 2016). Non-pharmacologic strategies include adequate warm-up, nasal breathing when possible, and environmental modifications to reduce exposure to cold or irritants (Anderson & Kippelen, 2019).
Athletic trainers (ATs) must be prepared to care for patients experiencing respiratory emergencies, such as asthma and EIB. Administering a short-acting bronchodilator via a metered-dose inhaler and using a nebulizer are longstanding skills of ATs; in fact, the 2020 Commission on Accreditation of Athletic Training Education (CAATE) curricular standards require AT students to be trained to administer lifesaving medications, including bronchodilators (CAATE, 2020; Hoffman et al, 2021). ATs play a crucial role in identifying, managing, and preventing EIB among athletes. They are often the first to recognize symptoms during activity and should ensure that athletes with known EIB have a current asthma action plan and access to inhalers (National Athletic Trainers’ Association [NATA], 2015). While clear protocols exist for administering nebulized albuterol in emergency situations, the optimal dosages for metered-dose inhalers are less clear. The AT should follow the patient’s asthma action plan provided by the prescribing physician (Hoffman et al, 2021)
ATs are not authorized to legally dispense prescription medication, but may be authorized to administer emergency medication, such as albuterol, under specific conditions as directed by the team physician. Standing orders should be established regarding AT use of bronchodilators such as inhalers and nebulizers, and these standing orders should be clearly documented and reviewed annually. It is important to recognize that laws change frequently, and all members of the sports medicine team must be aware of federal, state, and institutional regulations related to standing orders and the dispensing of both over-the-counter and prescription medications (Chang et al., 2018; Hoffman et al., 2021). The sports medicine team may include ATs, team physicians, physical therapists, and school nurses, so it is essential that each member remain in compliance with all current federal, state, and institutional regulations concerning medication management in a sports medicine setting (Chang et al., 2018; Hoffman et al., 2021).
Additionally, ATs should monitor environmental conditions, promote compliance with medication regimens, and educate athletes on self-management techniques and emergency response procedures. Collaboration with physicians and respiratory specialists is essential to optimize performance and safety.
Beyond performance limitations of athletes with exercise-induced asthma or exercise-induced bronchospasm, the implications of pharmacological management must be at the forefront of consideration for elite, semi-professional, and professional athletes. The World Anti-Doping Agency (WADA) is an independent, international organization that establishes anti-doping rules across countries and sports. WADA creates a comprehensive list and document that serves as the international standard for identifying substances and methods prohibited in sport. The list is updated and published annually, and the new list goes into effect January 1 of each year. It is important for athletes and members of sports medicine teams to be aware of annual changes and to review the list regularly regarding medications and supplements that athletes may be prescribed, to ensure compliance with WADA regulations, especially if there is a chance the athlete might undergo random drug testing. An athlete could face sanctions, even for an unintentional violation.
WADA maintains strict regulations on the use of glucocorticoids and inhaled Beta2 agonists for asthma, requiring athletes to use specific, permitted, therapeutic doses.
Key points include (USADA):
| Beta2 Agonists with Permitted Inhaled Dosage Thresholds | ||
|---|---|---|
| Beta2 Agonist | Permitted Dosage- Metered dose inhaler only (nebulization prohibited) | Warnings/Conditions |
| Albuterol (salbutamol) (ProAir, Proventil, Ventolin) (NOT levalbuterol- which is prohibited at all times) | 600 micrograms/8 hours (maximum 1600 micrograms/24 hours) | No permitted dosage if you are on medication in class S5. Diuretics or Masing Agents. Use of inhaler must be according to therapeutic guidelines in divided doses- can't use all at once! |
| Formoterol (NOT arformoterol- which is prohibited at all times) | 36 micrograms/12 hours (maximum 54 micrograms/24 hours) | |
| Salmeterol (Serevent) | 200 micrograms/24 hours | Use of the inhaler must be according to therapeutic guidelines |
| Vilanterol (Anoro, Breo) | 25 micrograms/24 hours | |
**Please note that common names are for example only, and the complete list should be consulted regarding a product or prohibited status
Knowing how many micrometers are dispensed per actuation (puff) will help you calculate how many puffs fall within the permitted range and which would exceed the permitted threshold (resulting in an anti-doping violation). Exceeding specific limits requires a Therapeutic Use Exemption (TUE). If emergency treatment is necessary, the athlete's health is paramount, and treatment should not be withheld. An emergency retroactive TUE can be submitted after the treatment. TUE’s require specific documentation. A medical file to support an application for a TUE in the case of an athlete with asthma should include (WADA, 2026):
Management of acute asthma exacerbations focuses on rapid reversal of airway obstruction, reduction of inflammation, and prevention of re-obstruction. Often, this can be caught early and managed in an outpatient setting with close follow-up. However, if the patient presents with a more severe exacerbation or fails to improve with current treatment interventions, emergency or critical care approaches must be used.
Management approaches for severe exacerbations include frequent or continuous administration of SABAs such as albuterol, often delivered via nebulizer. In moderate to severe cases, ipratropium bromide, a short-acting muscarinic antagonist, may be added to enhance bronchodilation. Systemic corticosteroids can be given orally or IV, ideally within the first hour of presentation to the emergency department, to address the underlying inflammation and prevent symptom progression. If needed, supplemental oxygen should be provided to maintain oxygen saturation above 90-92%. Close monitoring of respiratory rate, oxygenation, and peak expiratory flow is critical, as deterioration can occur rapidly.
Further escalation of therapy may include magnesium sulfate IV for patients who do not respond to initial bronchodilator therapy, as it relaxes smooth muscle and provides additional bronchodilation. In cases of impending respiratory failure, evidenced by worsening hypoxemia, rising carbon dioxide, exhaustion, or altered mental status, advanced airway support may be necessary. Intubation is considered a last resort because mechanical ventilation in asthmatics can be technically challenging due to dynamic hyperinflation and risk of barotrauma. Non-invasive ventilation may be attempted in carefully selected patients but requires close monitoring.
The Global Initiative for Asthma (GINA) is an international collaborative program launched in 1993 under the World Health Organization and the National Heart, Lung, and Blood Institute (Global Initiative for Asthma [GINA], 2024). Its purpose is to provide evidence-based, annually updated recommendations for the diagnosis, management, and prevention of asthma worldwide. Because asthma prevalence and healthcare resources vary significantly across regions, GINA’s guidance is designed to be adaptable to diverse clinical settings, from high-resource health systems to low- and middle-income countries. GINA’s strength lies in its frequent updates, global scope, and emphasis on both clinical and public health approaches to asthma management (GINA, 2024).
In the United States, asthma care has traditionally been guided by the National Asthma Education and Prevention Program (NAEPP) under the National Heart, Lung, and Blood Institute (NHLBI), with the most recent focused updates published in 2020 (NHLBI, 2021). While both GINA and NAEPP share the overarching goal of improving asthma outcomes, they differ in key areas. GINA has eliminated short-acting beta₂ agonist (SABA) monotherapy, recommending that all patients (even those with mild asthma) receive inhaled low-dose formoterol as needed. In contrast, NAEPP still permits SABA-only treatment for intermittent asthma, especially in children and adults with infrequent symptoms, and introduces ICS therapy only when asthma becomes persistent (GINA, 2024; NHLBI, 2021).
Additionally, GINA emphasizes a two-track approach: track 1 with formoterol preferred, track 2 with SABA + ICS as an alternative, while NAEPP maintains a more traditional stepwise ladder of increasing therapy. GINA also more explicitly integrates biomarkers (eosinophils, IgE) and biologics into its recommendations for severe asthma, while NAEPP references these therapies but with less prescriptive guidance.
These differences have important clinical implications. By discouraging SABA-only treatment, GINA directly addresses evidence that SABA monotherapy is linked to a higher risk of severe exacerbations and even asthma-related death. Following GINA’s approach may therefore reduce hospitalizations and improve long-term control, but it can also increase medication costs and raise issues of accessibility in resource-limited systems. In contrast, the NAEPP’s more conservative stance reflects a balance between efficacy, safety, and practical considerations within the U.S. healthcare system, where insurance coverage and prescribing patterns play major roles (GINA, 2024; NHLBI, 2021).
For clinicians, being aware of both sets of guidelines is important. GINA offers a more preventive and globally harmonized strategy, while NAEPP remains the standard reference for U.S.-based practice.
Scenario
Maria, a 22-year-old college student, presents to her primary care clinic with complaints of recurrent wheezing, chest tightness, and coughing that have worsened over the past two weeks. She reports waking up at night three times per week due to coughing and needing to use her albuterol inhaler almost daily. Maria has a history of asthma diagnosed in childhood, but has not been on a daily controller medication since high school. She lives in a dormitory where dust and mold are common, and she admits to skipping cleaning because of her busy schedule. Her physical exam reveals expiratory wheezes, oxygen saturation (SpO₂) of 94% on room air, and a peak flow measurement at 65% of her predicted personal best, which improves following bronchodilator administration.
Interventions
The provider initiates Step 3 therapy using a low-dose inhaled corticosteroid (ICS) and long-acting beta2 agonist (LABA) combination inhaler (budesonide formoterol [Symbicort]), with instructions for both daily maintenance and as-needed use. Maria is educated on proper inhaler technique and provided a spacer to improve medication delivery. She is also instructed on the use of a peak flow meter to track her lung function at home, establishing her “personal best” baseline for comparison. Environmental control strategies are discussed, including frequent cleaning, use of dust-mite covers, and reducing mold exposure. Additionally, she is referred to the university’s asthma education program for ongoing support and provided with an individualized asthma action plan to guide her in adjusting therapy based on symptoms and peak flow readings.
Discussion
This case highlights the importance of reassessing asthma severity when symptoms worsen. Based on her frequency of nighttime awakenings, daily SABA use, and spirometry results, Maria’s asthma is best classified as moderate persistent, warranting escalation to Step 3 therapy. The combination of an ICS with a LABA not only targets acute bronchoconstriction but also addresses underlying airway inflammation, which is crucial for long-term control. Education was a key component of her care; without correct inhaler technique and trigger avoidance, medication alone may not achieve adequate control. The use of a peak flow meter adds an objective measure that empowers the patient to recognize early declines in lung function.
The case also demonstrates the real-world impact of social determinants of health. Maria’s dorm environment exposed her to common triggers like dust and mold, illustrating how living conditions can undermine asthma management. Her busy academic schedule contributed to neglecting cleaning and self-care, emphasizing the need for practical, patient-centered strategies. Addressing these contextual factors is as critical as prescribing medications.
Strengths
This case emphasizes a holistic approach to asthma management: pharmacological escalation consistent with guideline-based care, reinforcement of inhaler technique, nonpharmacological trigger reduction, and patient education. By including a peak flow meter and an asthma action plan, the intervention promotes self-management, which is strongly linked to reduced emergency visits and improved outcomes. The referral to an asthma education program also demonstrates strong interprofessional collaboration.
Weaknesses
One limitation in Maria’s management is the potential for adherence challenges. Young adults often struggle with consistent use of daily controller therapy, particularly when they feel better after initial improvement. Her living environment poses ongoing challenges that may be difficult to fully resolve without structural changes, such as moving to different housing. Additionally, while pharmacologic therapy was escalated appropriately, the provider may need to monitor closely for side effects or overreliance on as-needed LABA use. Finally, psychosocial factors such as stress and academic pressures were not directly addressed, though these may influence symptom control.
Scenario
Ethan, a 6-year-old boy, is brought to the pediatric clinic by his parents with a history of recurrent coughing and wheezing episodes over the past six months. The parents report that his cough is worse at night and is often triggered by playing outside or during viral URIs. They note two urgent care visits in the past year for “bronchitis,” where he was treated with antibiotics and short courses of oral steroids, with temporary improvement. His medical history is significant for eczema, and his mother has asthma. On today’s visit, Ethan is afebrile, with a respiratory rate of 24 breaths per minute, heart rate of 105, and oxygen saturation (SpO₂) of 95% on room air. On auscultation, bilateral expiratory wheezes are noted. A peak flow measurement is 70% of predicted for his age and height, and symptoms improve after albuterol via nebulizer.
Interventions
The pediatrician discusses the likelihood of asthma based on the pattern of recurrent, variable respiratory symptoms, family history of atopy, and Ethan’s positive response to bronchodilator therapy. A diagnosis of mild persistent asthma is made. Ethan is prescribed a low-dose inhaled corticosteroid (fluticasone [Flovent]) with a spacer to be used daily, along with an as-needed short-acting beta₂-agonist (albuterol [Ventolin]) for acute symptoms. His parents are educated on proper inhaler and spacer technique, and an asthma action plan is developed, including guidance for managing exacerbations and when to seek urgent care. Environmental control strategies are reviewed, including minimizing dust exposure, controlling pollen entry by keeping windows closed during allergy season, and avoiding exposure to secondhand smoke. Ethan’s parents are also instructed to monitor daily peak flow to track lung function variability.
Discussion
This case illustrates the process of diagnosing asthma in a young child, which is often challenging because symptoms can overlap with recurrent viral infections or bronchitis. Key features supporting the diagnosis include nighttime cough, symptom triggers (exercise, viral illness, allergens), recurrent episodes requiring systemic steroids, family history of asthma, and reversibility of airway obstruction with bronchodilators. Initiating a controller medication (ICS) is appropriate for mild persistent asthma, as daily anti-inflammatory therapy reduces symptom frequency, prevents exacerbations, and improves quality of life. Teaching parents correct inhaler technique and trigger management is equally important, as poor technique or ongoing environmental exposures can undermine treatment effectiveness.
Strengths
This case highlights early recognition of asthma and the importance of establishing control before the disease progresses to more severe forms. Strengths of the management include the use of guideline-based therapy with low-dose ICS, the provision of a personalized asthma action plan, and the education of parents to become active participants in care. Including peak flow monitoring empowers the family to detect early warning signs and reinforces self-management.
Weaknesses
Challenges in this case include the potential difficulty young children have in consistently using inhalers correctly, even with a spacer. Parental adherence to daily controller therapy may also be variable, especially if symptoms improve quickly, leading to underuse of ICS. Additionally, exposure to triggers in the home or school environment may not be fully controllable, limiting the impact of environmental interventions. Finally, objective testing such as spirometry is less reliable in young children, so diagnosis often relies on clinical patterns and treatment response, which can lead to uncertainty in early management.
Asthma remains a complex, multifactorial disease that requires careful assessment and a comprehensive management approach. By ensuring a deep understanding of the disease, clinicians can better tailor care to individual patients across the lifespan. Emphasis on stepwise management ensures care that reduces exacerbations and improves quality of life. Ultimately, integrating evidence-based recommendations with patient-centered care empowers healthcare professionals to address disparities, optimize outcomes, and meet the ongoing public health challenge posed by asthma.
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.