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Michael G. Miller, EdD, ATC, CSCS; John M. Weiler, MD; Robert Baker, MD, PhD, ATC; James Collins, ATC; and Gilbert D'Alonzo, DO, contributed to conception and design; acquisition and analysis and interpretation of the data; and drafting, critical revision, and final approval of the article.
Objective: To present guidelines for the recognition, prophylaxis, and management of asthma that lead to improvement in the quality of care certified athletic trainers and other heath care providers can offer to athletes with asthma, especially exercise-induced asthma.
Background: Many athletes have difficulty breathing during or after athletic events and practices. Although a wide variety of conditions can predispose an athlete to breathing difficulties, the most common cause is undiagnosed or uncontrolled asthma. At least 15% to 25% of athletes may have signs and symptoms suggestive of asthma, including exercise-induced asthma. Athletic trainers are in a unique position to recognize breathing difficulties caused by undiagnosed or uncontrolled asthma, particularly when asthma follows exercise. Once the diagnosis of asthma is made, the athletic trainer should play a pivotal role in supervising therapies to prevent and control asthma symptoms. It is also important for the athletic trainer to recognize when asthma is not the underlying cause for respiratory difficulties, so that the athlete can be evaluated and treated properly.
Recommendations: The recommendations contained in this position statement describe a structured approach for the diagnosis and management of asthma in an exercising population. Athletic trainers should be educated to recognize asthma symptoms in order to identify patients who might benefit from better management and should understand the management of asthma, especially exercise-induced asthma, to participate as active members of the asthma care team.
Asthma is defined as a chronic inflammatory disorder of the airways characterized by variable airway obstruction and bronchial hyperresponsiveness.1 Airway obstruction can lead to recurrent episodes of wheezing, breathlessness, chest tightness, and coughing, particularly at night or in the early morning.1 Asthma can be triggered by many stimuli, including allergens (eg, pollen, dust mites, animal dander), pollutants (eg, carbon dioxide, smoke, ozone), respiratory infections, aspirin, nonsteroidal anti-inflammatory drugs (NSAIDs), inhaled irritants (eg, cigarette smoke, household cleaning fumes, chlorine in a swimming pool), particulate exposure (eg, ambient air pollutants, ice rink pollution), and exposure to cold and exercise.1–5 Airflow limitation is often reversible, but as asthma symptoms continue, patients may develop “airway remodeling” that leads to chronic irreversible airway obstruction.6,7 Severe attacks of asthma can also cause irreversible airflow obstruction that can lead to death.4,8
The National Heart, Lung, and Blood Institute of the National Institutes of Health launched the National Asthma Education and Prevention Program (NAEPP) in March 1989 to address the increasing prevalence of asthma in the United States and its economic costs to the society; the program was updated in 1997 (as NAEPPII).1 An updated expert panel report from the NAEPP is expected to be released in 2006. The Global Initiative for Asthma (GINA) was also developed to provide worldwide guidelines for asthma awareness and management.2 These guidelines are extremely comprehensive and have been regularly updated to reflect advances in the diagnosis and management of asthma. Nevertheless, the guidelines do not describe the role of certified athletic trainers or other allied health care professionals in recognizing and managing asthma in an athletic population.
The purpose of this position statement is to provide athletic trainers and other allied health care professionals who care for athletes with information to:
Based on current research and literature, the National Athletic Trainers' Association provides the following guidelines for the identification, examination, management, and prophylaxis of asthma, including EIA, and the education of athletes, parents, coaches, and health care personnel about asthma. Not all individuals who suffer from asthma present in the same manner, nor do they all respond to the same management or treatment plan. Therefore, these recommendations are intended to provide the certified athletic trainer and other health care professionals with an overall guide for a better understanding of the asthmatic condition.
Asthma is a common condition that has been recognized for more than 2000 years.56 Asthma is usually defined operationally as a chronic inflammatory disorder of the airways.1,2,4,56 In many patients, this chronic inflammation causes an increase in airway hyperresponsiveness, leading to recurrent episodes of wheezing, breathlessness, chest tightness (or chest pain in children), and coughing, particularly at night or in the early morning and after exercise, especially in cold, dry environments. These episodes are associated with widespread but variable airflow obstruction that is often reversible, either spontaneously or with treatment.1,2,4 This definition implies that asthma has multiple causes, and indeed, it is a complex disorder.
The chronic inflammatory process causes excess mucus production and bronchial smooth muscle constriction,57–61 which result from a release of inflammatory mediators that include histamine, tryptase, prostaglandin, and leukotrienes from mast cells.62–66 Airways may also accumulate thick, viscous secretions produced by goblet cells and submucosal glands; moreover, there is leakage of plasma proteins and accumulated cellular debris.57–61,67 Although airway narrowing affects the tracheobronchial tree, small bronchi (2–5 mm in diameter) are most affected.68–70 Maximal expiratory flow rate is reduced and residual lung volumes are increased as air is trapped behind the blocked airways.71 As a result, during an asthma attack, the respiratory rate increases to compensate for the increased obstruction of the airways and the inability of the usually elastic lung to recoil (dynamic hyperinflation). The patient must work harder to breathe as the thorax becomes overinflated. With progression of the attack, the diaphragm and intercostal muscles must compensate and contribute more energy during respiration.72 In a severe attack, muscle efficiency is eventually lost, and the increased breathing rate leads to respiratory muscle fatigue and physical distress that may result in death. Indeed, as many as 4200 to 5000 people die from asthma each year in the United States.73
Environmental factors, such as allergens, air pollution, occupational sensitizers, and tobacco smoke, may cause or exacerbate asthma.74–79 These factors are important triggers that should be considered when evaluating a patient with asthma.79–83
Recently, concern about indoor air pollution has been heightened.79,80,82–84 Indoor ambient air can contain allergens and pollution that can cause or exacerbate asthma and other respiratory ailments when susceptible individuals are exposed to these environments.85 Many factors should be considered indoors, such as adequacy of ventilation, humidity level, presence of allergens, presence of wall-to-wall carpeting and upholstered furniture, and types of building materials.85–87 Indoor animal allergens (such as from cats, dogs, and other pets) are an important trigger of symptoms in many people.88 Cockroach allergens are commonly seen indoors (such as in swimming pool locker rooms), and the cockroach allergenic materials can remain for a long period of time, even after extermination.89–92 Indoor mold and fungal spores, house dust mites, and particulate matter, such as aerosols or smoke from cigarettes, wood, or fossil fuels, also can trigger asthma symptoms.93–107 Tobacco smoke is a risk factor for the development of asthma, and smoking tobacco appears to increase asthma severity.108–110
Other indoor air irritants, such as chlorine, can exacerbate asthma and cause eye and lung irritation.111,112 School-age children who frequently visit chlorinated pools may have an increased risk of developing asthma, especially if they have other risk factors for asthma.113 Even individuals who do not usually enter the water but who are exposed to indoor chlorinated pools (eg, lifeguards, coaches) may have respiratory irritation on exposure to chlorine.114,115
Many actions can be taken to limit indoor allergen exposure, including prohibiting smoking indoors, using air cleaners equipped with a high-efficiency particulate air cleaner (HEPA) filter, washing walls, vacuuming carpets, and cleaning mattress covers weekly.116–119 Additional measures include removing carpets and installing linoleum or wood flooring, washing pets (dogs and cats) and their bedding twice a week, keeping pets out of the bedroom or living room at all times to reduce exposure, covering mattresses and pillows, and controlling humidity to help manage dust mites and mold.81,82,120 Some of these measures, such as the removal of a family pet from the home, can be very difficult, so it is necessary to discuss the effect of these exposures with the asthma patient. Although air filters might help, the house should be cleaned thoroughly before their use and regularly thereafter.33
When inhaled, outdoor air pollution, caused by sulfur dioxide, carbon monoxide, nitrogen dioxide, ozone, and particulate matter, can cause pulmonary function decrements, increased reliance on medications, bronchial hyperresponsiveness, and increased asthma symptoms.121–125 Many pollens (trees, grasses, and weeds) are inhaled into the bronchi and cause allergen-induced asthma.126,127 Tree pollens predominate in the spring, grass pollens in the late spring or early summer (and fall), and weed pollens in the late summer and fall in the United States, depending on geographic location, but may be present at other times of the year in locations outside of the United States.128,129 Information about the pollen seasons in the United States can be accessed from the National Allergy Bureau Web site.
Although it is virtually impossible to avoid all outdoor pollution and allergens, some practical precautions can be implemented: move indoors and close all windows, close car windows when traveling, limit exposure when pollen is at its highest levels, monitor local weather stations for allergy reports, and practice indoors if possible when pollen counts are high.
Asthma can be difficult to diagnose and classify (see Table 1). Some individuals, especially elite athletes, do not display consistent signs or symptoms of asthma.9,10,130 Asthma symptoms may be present only during certain times (seasons) of the year or only after exercise and may be highly variable, depending upon the athlete, the environment, and the activity.13
The first step in determining whether asthma is present is to obtain a detailed medical history. Questions regarding past experiences, symptoms, smoking history, and family history can help to rule out other respiratory disorders such as chronic bronchitis, emphysema, bronchiectasis, allergic rhinitis, upper respiratory infection, congestive heart failure, disorders of the upper airway (eg, vocal cord dysfunction), and nonrespiratory conditions such as anxiety. Most importantly, the athletic trainer should ask general questions as listed in Recommendation 3 to assist in making a proper diagnosis.13 If a patient appears to have one or more symptoms suggestive of asthma, then lung function testing should be performed (see Table 1).9 However, it is important to recognize that the history and baseline physical examination will fail to identify many patients with EIA.9,10,12
Lung function tests are essential to assess asthma severity and airflow limitation and to determine whether the obstruction is fully reversible with treatment.16–18,131–133 The most common measures of airway function are the forced expiratory volume in 1 second (FEV1), the forced vital capacity (FVC), and the peak expiratory flow rate (PEFR). These tests can be performed while the patient is at rest or after a challenge. The FEV1 measures the volume of air in liters forcefully exhaled out of the airway in 1 second after a full inspiration. The FVC measures the total volume of air in liters forcefully exhaled out of the airway when the breath continues (usually for a period of 6 or more seconds). The FVC procedure is effort dependent and requires the patient to fully understand that he or she needs to inhale a deep breath and then “blast” the air out of the lungs into the measurement device. The FVC testing also requires considerable expertise by the technician and the ability to communicate with the patient. The PEFR measures the maximal flow rate of air (in L/s or L/min) out of the airways and is easier to perform than an FEV1 or FVC maneuver, although PEFR testing is also effort dependent. A flow volume curve (flow loop) provides a graphic depiction of the breathing effort in which flow rate is plotted against volume (in L/s) of air exhaled and inhaled (in L), as shown in Figure 3. A volume-time curve (called a spirogram) is another way to plot the breath, in which the volume of air exhaled (in L) is plotted against time (in seconds). The FEV1/FVC ratio is also examined, along with a variety of measures of flow, such as the flow between 25% and 75% of the FVC (called the FEF25–75).
Asthma is an example of an obstructive lung disease in which the airways obstruct the outflow of air. In contrast, pulmonary fibrosis is an example of a restrictive lung disease in which the functional size of the lungs decreases. In obstructive lung diseases, the FEV1 decreases, whereas the FVC remains relatively normal, so the FEV1/FVC ratio decreases (until late in the disease or with severe exacerbations, when the FVC may also decrease).131 In restrictive lung disease, both the FEV1 and the FVC decrease proportionally (so that the FEV1/ FVC ratio is normal). Nomograms exist to provide guidance as to normal ranges for FEV1 and FVC based on age, size and race.134,135 It is important to recognize racial differences in the normal values for these tests. Generally, levels should be at least 80% of the predicted values to be considered “normal.” The FEV1/FVC ratio should also be above 80%. An increase of 12% or more in FEV1 after an inhaled bronchodilator (eg, a β2-agonist such as albuterol) suggests reversible airway disease and may be used as a diagnostic criterion of asthma.131 A decrease in FEV1 after a challenge (such as after inhalation of methacholine or running on a treadmill) suggests that the airways are reactive to the stimulus.19 It is important to determine a patient's personal best FEV1, FVC, and PEFR, which are identified by plotting these values over time. These values can also demonstrate variability between morning and evening and over time, which may reflect airway hyperreactivity.
Spirometers are used in the clinic or training room to determine these pulmonary function values.136 Patients may also be given a PFM to measure PEFR away from the clinic or athletic training room (Tables 2 and and3).3). The PFM is a small, handheld device that measures maximal flow rate during forced exhalation.137–140 Maximal flow rate usually occurs within the first 120 to 150 milliseconds of a forced exhalation.140 When used properly, a PFM can be somewhat helpful in following the course of asthma and might even be useful in suggesting the presence of asthma. The PFM can also be used to identify asthma triggers and to monitor medication changes, and it may help to reduce asthma morbidity.141–147 The device allows the asthmatic patient to measure lung variability over time to assist in determining when to seek medical attention. The PFM should be used at least daily (in the morning after awakening) and preferably also in the late afternoon or evening.1,2,148 At least 2 or 3 trials should be performed at each specified time and the highest value recorded. The device should be used before taking any medications and at least 4, but preferably 8, hours after inhalation of a bronchodilator, if possible. The device should be used for at least a 2- to 3-week monitoring period. Some devices record the PEFR electronically, which can assist the patient in keeping the data secure and available. Over time, the patient's personal best value will be determined. Subsequently, if the PEFR value is less than 80% of the personal best or if daily variability is greater than 20% of the morning value, then the patient should be reevaluated in an attempt to find better control measures. If the PEFR value is less than 50% of the personal best, the individual should seek immediate attention (see Table 2).1 Spirometry, including the use of PFMs, may be especially useful in patients who do not perceive the severity of their symptoms.149,150
The PFM should be used regularly, even if asthma symptoms appear to be well controlled.132,151–153 Patients who have good PFM technique (see Table 3) adhere to their treatment plan and control their symptoms better than those who have poor technique. The PFM should be available in all athletic training facilities and on the field in medical kits.
Unfortunately, some reports suggest that PFM recordings are not always reliable indicators of airflow obstruction.154–159 In certain cases, elite or well-trained athletes may possess large lung capacities, which may exceed the measuring capacity of the PFM. In addition, it appears that PFM values are not consistent from one to another PFM from the same manufacturer, across different PFM devices, when men and women use PFMs, with different techniques while using a single PFM, and at high altitudes.159–164 The most accurate spirometry testing is performed with office-based spirometry testing equipment.140 However, as noted above, spirometry testing requires training22,165 and may be impractical for everyday asthma management, especially in primary care settings in which most patients are not being seen for asthma.140
If baseline lung function tests are within normal values and the reversibility test with a β2-agonist is equivocal, then a challenge test (eg, with methacholine) may be performed to test for bronchial hyperresponsiveness.19 During these tests, progressively increasing concentrations of the aerosolized drug are administered during a multistage procedure.19 After each stage, spirometry testing is performed to determine whether a 20% reduction in FEV1 from baseline is obtained. If the reduction is less than 20% after all stages have been performed, then the test is considered negative, and the patient is determined not to have bronchial hyperresponsiveness. It is important to note, however, that these tests alone are not diagnostic of asthma. A positive test must be interpreted in the context of other information to make the definitive diagnosis of asthma.
It is important to ascertain the correct diagnosis before medications are prescribed and for the health care professional to know the types of medications that are prescribed.1,2,24–30,166,167 Only a small percentage of asthmatic patients take their medications precisely as prescribed by their physician; the most common cause of treatment failure is failure to use the prescribed treatment.167 Regardless, asthma can be managed through various medications to prevent or control symptoms; for an updated medication list, refer to the NAEPPII and GINA guidelines.1,2 The medications used to treat asthma are classified as either controller or rescue (reliever) medications.
Controller medications are daily, long-term interventions used prophylactically to manage the symptoms of mild, moderate, and severe asthma and generally should not be used to manage acute asthmatic symptoms.1,2,25–28 Examples include inhaled corticosteroids, systemic corticosteroids, cromones (sodium cromolyn and nedocromil sodium), long-acting inhaled β2-agonists, theophylline, and leukotriene modifiers (Table 4 provides sample agents).
Inhaled corticosteroids are effective controller medications for treating persistent mild, moderate, and severe asthma.1,2 They act by decreasing airway inflammation, mucus production, and bronchial hyperresponsiveness.168–173 Proper use of inhaled corticosteroids can lead to a decrease in the number and severity of asthma exacerbations, improve lung function, lessen bronchial hyperresponsiveness, and reduce the need for symptom relief with short-acting β2-agonists.174–180 Inhaled corticosteroids should not be used to treat acute asthmatic attacks.25 Their adverse effects include hoarseness, coughing, and occasionally thrush or oral candidiasis.177,181 However, rinsing the mouth after inhalation and using a spacer generally help to prevent oral candidiasis.
Systemic corticosteroids are administered orally or parenterally for individuals who have severe persistent asthma that remains poorly responsive to inhaler therapy.182 Systemic therapy has the same mechanisms of action as inhaled corticosteroids. However, long-term use of systemic agents can cause more significant systemic adverse events than inhaled corticosteroids, including osteoporosis, glucose intolerance, glaucoma, weight gain, skin thinning, bruising, fluid and electrolyte abnormalities, growth suppression, and muscle weakness.1,2,183 To minimize these adverse events, oral corticosteroids are often taken daily in the morning or every other day, and patients should be monitored closely by a physician.183 Oral corticosteroids are used much less frequently today than in the past since the advent of high-potency inhaled corticosteroids such as fluticasone and budesonide.1,2
The cromones, cromolyn sodium and nedocromil sodium, are inhaled asthma medications used to control mild persistent asthma and are considered less effective anti-inflammatory agents than inhaled corticosteroids.25,26,184 Although the exact mechanisms of action are poorly understood, they are thought to inhibit IgE-mediated mediator release from mast cells and, thus, to inhibit acute airflow limitations induced by exercise, cold air, and allergens. The cromones are generally used to treat mild persistent asthma and to prevent EIA.1,2 Cromones should be used as second-line drug therapy alternatives for treating mild persistent asthma, perhaps combined with an inhaled β2-agonist; however, several doses each day are usually needed to control asthma.1,2 Only minimal adverse events are seen with these agents, including occasional coughing and an unpleasant taste, particularly with nedocromil sodium.
Long-acting inhaled β2-agonists (eg, salmeterol and formoterol) have the same mechanisms of action as short-acting β2-agonists but a 12-hour duration of action, compared with 4 to 6 hours for the short-acting agents.185–190 A single dose of formoterol or salmeterol before exercise can protect the athlete from asthma symptoms associated with exercise for up to 12 hours.191–193 Formoterol has a shorter onset of action than salmeterol, approximately 5 minutes as compared with 15 to 30 minutes.192,194 All β2-agonists, including formoterol and salmeterol, are restricted asthma medications according to the International Olympic Committee, World Anti-Doping Agency, and United States Anti-Doping Agency; elite athletes taking these medications, their physicians, and their athletic trainers should review the guidelines posted by these agencies.
Patients using long-acting β2-agonists regularly may display a decrease in the duration of action.195–197 In one study, formoterol had a shortened duration of action by day 14 of regular daily use.198 Thus, patients should not expect these drugs to remain effective over the 12-hour dosing interval after regular, daily, extended use. Studies also show that the use of long-acting β2-agonists does not affect persistent airway inflammation.199 These agents should only be used in combination with inhaled corticosteroids, which may be more beneficial than ingesting each drug separately.200–202 Combination therapy (an inhaled, long-acting β2-agonist and an inhaled corticosteroid) has been shown to decrease the need for short-acting β2-agonists, decrease nocturnal asthma, improve lung function, decrease asthma exacerbations, and prevent EIA.200,202–205
Leukotriene modifiers, taken orally, block leukotriene synthesis or block leukotriene receptors.206–208 Leukotriene modifiers can be used to control allergen-, aspirin-, and exercise- induced bronchoconstriction; improve lung function; and decrease asthma exacerbations.209–215 Used primarily as second-line therapy, leukotriene modifiers can reduce the dose of an inhaled corticosteroid required to treat mild persistent asthma and may improve asthma control.214–217 Adverse events are usually minimal, with reports of headaches and gastrointestinal discomfort. However, zileuton (Zyflo, Abbott Laboratories, Abbott Park, IL) may be associated with liver toxicity; therefore, liver function should be monitored regularly when using this medication.218 Unlike β2-agonists, the duration of action of the leukotriene modifiers does not diminish over time.215 In the past, theophylline has been used alone as a controller agent, but now it is usually used in combination with another agent, such as an inhaled corticosteroid.219
Finally, some patients who have allergic asthma may benefit over the long term from the administration of various forms of allergy immunotherapy.220–222 The decision to initiate such therapy must be made by the patient and physician after a careful evaluation. Even in the most successful cases, additional medical therapy is often required in conjunction with immunotherapy.
Rescue medications act rapidly to treat acute bronchoconstriction and associated symptoms of coughing, wheezing, shortness of breath (dyspnea), and chest tightness.1,2,25–28 Several classes of drugs act in this manner, including rapid-acting inhaled β2-agonists, inhaled anticholinergics, and short-acting theophylline.
Rapid-acting inhaled β2-agonists are the most commonly used reliever therapy for chronic asthma. These β2-agonists act quickly to cause bronchodilation by relaxing airway smooth muscle, decreasing vascular permeability, and modifying mediator release from mast cells.185 Rapid-acting inhaled β2-agonists are also the most frequently used agents to prevent EIA and to treat its symptoms.223 These medications can be used as “rescue therapy” at times of an acute attack. However, because of their relatively short duration of action (2–4 hours), repeat treatments may be necessary for EIA. Some authors224,225 suggest that repeated use of short-acting β2-agonists can lead to tolerance and less effectiveness over time. Furthermore, the chronic use of long-acting inhaled β2-agonists can decrease the effectiveness of the short-acting inhaled β2-agonists.189,225
Inhaled anticholinergic agents (eg, ipratropium) may be used as bronchodilators.226 These agents block acetylcholine release from cholinergic innervation in airway smooth muscle but have no anti-inflammatory action.
Short-acting theophylline is a bronchodilator that has been used for many years to relieve asthma exacerbations.29,227 Theophylline's onset of action is delayed when compared with that of β2-agonists, and so it is not currently used as first-line rescue therapy.1,2 Theophylline is a controversial drug because its benefits might be outweighed by potential adverse events such as seizures.228 Adverse events can be serious and severe if dosing is not closely monitored. Short-acting theophylline should not be administered to patients who are already receiving chronic therapy with sustained-release theophylline therapy.
Short-acting oral β2-agonists, although rarely used, function primarily by relaxing airway smooth muscle within a few minutes after administration and for a period of up to 4 hours; however, they have no anti-inflammatory actions.24,29 Adverse events include tachycardia, hypertension, and decreased appetite. If used chronically, increasing doses of short-acting oral β2-agonists might indicate loss of control of asthma.1,2 All athletes using short-acting oral β2-agonists should be advised that many sporting organizations restrict or prohibit the use of these agents.
Finally, systemic glucocorticosteriods are administered orally or parenterally for individuals who have acute asthma exacerbations. The mechanisms of action are similar to those for corticosteroids used to treat chronic severe asthma.1,2
Many of the newer asthma medications are delivered to the lungs by inhalation devices.23 The most common types of inhalers are MDIs and dry powder inhaler devices. The MDIs release a specific amount of a drug from a pressurized canister to propel medication into the lungs when the patient takes a breath. When using MDIs, patients must exhale first, then place the inhaler at or slightly in front of the lips, and slowly inhale at the same time that they are activating the inhaler to release the drug. Patients hold their breath for a few seconds (approximately 10) before exhaling. Patients who have difficulty coordinating MDI activation with breathing generally benefit from the use of a spacer.229–231 A spacer is attached to the MDI device to reduce side effects of inhaled corticosteroids in the mouth and for patients who have difficulty coordinating the activation of an MDI and breathing. Dry powder inhalers are often easier to use than MDIs, and they do not permit use of a spacer.
Aspirin-sensitive athletes may manifest nasal congestion; itchy, watery, or swollen eyes; coughing; difficulty breathing; wheezing; urticaria; and possible shock when they ingest aspirin or other NSAIDs.232–236 This is not a true allergy because it is not caused by IgE, but it is treated in the same manner as an allergic reaction. Athletic trainers should also be aware of triad syndrome: athletes with asthma, nasal polyps, and aspirin sensitivity may have a severe asthma attack when they take an NSAID.237
Although only a small percentage of the population has aspirin-sensitive asthma,238–240 this condition is particularly concerning in an athletic population because many athletes who have asthma use anti-inflammatory drugs to treat injuries. Therefore, athletic trainers must understand that some patients who have asthma could suffer fatal consequences if they take aspirin or NSAIDs.
Aspirin-sensitive athletes should also avoid COX-2 inhibitors, but acetaminophen in moderate doses can usually be taken without difficulty.241 Salsalate, choline magnesium trisalicylate, and dextropropoxyphene may be used as substitute medication in patients with aspirin sensitivity if tolerated.240,242 Athletic trainers should be familiar with the many prescription and over-the-counter products that contain aspirin and other NSAIDs, including ibuprofen (eg, Motrin, McNeil-PPC, Fort Washington, PA; Advil, Wyeth, Madison, NJ) and naproxen (eg, Aleve, Bayer, Morristown, NJ). Health care professionals should supply as much information to the patient as possible, including a list of products to avoid (Table 5).
Athletes with asthma need to keep their asthma under optimal control to prevent exercise-induced breathing symptoms.31,32,243,244 Masks and nose breathing help to warm and moisturize inhaled air before it reaches the smaller airways. This may decrease the inflammatory reaction in the airways and thus decrease the frequency and intensity of EIA. These maneuvers are effective for some but not all athletes.224 Nose breathing is not effective at high ventilation rates. Limiting environmental exposures (eg, to cold air and pollen) may decrease symptoms in susceptible athletes; however, this may not be practical in some sports.
Theoretically, exercise training might decrease symptoms by conditioning the body to exercise, but research has not supported this theory.245,246 Nevertheless, an asthmatic individual should participate in exercise programs tailored to his or her capacity to perform.55
A refractory period can occur after exercise, when the airway response to exercise is inhibited for up to 2 to 3 hours. Some athletes have taken advantage of this phenomenon to help control EIA.31,32,34,247–251 However, there are no specific guidelines to follow, and each athlete must experiment to determine the best individual protocol.
Because hyperosmolarity plays a role in mediating EIA, limiting sodium in the diet has received some attention. Restricting dietary salt may cause a relative decrease in airway obstruction.252,253 Both sodium and chloride appear to play roles, but this remains an area of active investigation, and no specific guidelines are available.254 A diet supplemented with n-3 polyunsaturated fatty acid in fish oil has shown favorable results in elite athletes with EIA.255
Most asthmatic individuals have a flare of their asthma after exercise.256,257 Some individuals only have asthma signs and symptoms associated with exercise.13 By definition, a temporary narrowing of the airways (bronchospasm) induced by strenuous exercise in which the patient has no symptoms is known as EIB.13 When symptoms are present, EIB is described as EIA.13 This section reviews the incidence of EIA and EIB in the athletic population and considers special diagnostic or therapeutic measures that should be taken in an athletic population.
Exercise-induced asthma is commonly seen in athletes in all levels of athletic competition.5,9,10,31,243,244,258–269 In most patients who have chronic asthma (at least 80%), exercise is a trigger for bronchoconstriction.13,243 Exercise-induced asthma can also occur in patients who do not otherwise have asthma, such as in about 40% of patients who suffer from allergic rhinitis in season.243,270,271 The incidence of EIA in the general population has been estimated to be between 12% and 15%.13,271 Rates as high as 23% have been reported in school-age children, and the incidence in athletes may also be this high.258,262,263,265 Exercise-induced asthma may be more common in urban environments than in rural areas.261 Other factors, such as high ozone levels, might also account for increased EIA rates.272
Exercise-induced asthma can be a significant disability for the athlete, especially in endurance sports.262,263,273 For example, EIA is relatively common in cross-country skiers, and some studies suggest that the cold air athletes breathe while cross-country skiing may provoke inflammation.274,275 Similarly, athletes who participate in swimming and long-distance running have a high incidence of asthma.262 Among Olympic athletes, asthma appears to be more common in those who participate in winter sports than in those who participate in summer sports.262,263 At least 1 in 5 United States athletes who participated in the 1998 Winter Olympics had the condition, compared with 1 in 6 at the 1996 Summer Olympic Games.262,263 Wilber et al265 found a 23% overall incidence of EIA among athletes in the 7 winter sports tested. In addition, more females than males participating in the Winter Games reported an asthma condition or medication use.262,263,265 Of the winter sports athletes tested, females had an incidence of 26%, compared with 18% in males.265
Although EIA impairs performance, it can be overcome. Amy Van Dyken, an athlete who suffered from relatively severe asthma, won 4 gold medals in swimming in the 1996 Olympic Games.273 Other well-known elite athletes have also been able to excel when their asthma was under good control.273
Two major theories exist to explain EIA: the cooling/warming hypothesis and the drying hypothesis.31,256,257,260,276–287 As ventilation increases, airways progressively cool, which results in bronchoconstriction. This theory is supported by the higher incidence of EIA in athletes participating in cold environments.263 In addition to cooling, the increased ventilation can lead to airway dehydration as inhaled air is humidified. The main effect of inhaling cold air is actually attributable to the fact that cold air carries less moisture. As with chronic asthma, inflammatory cells and mediators may increase in the lung in response to exercise in patients with EIA.248,279,288–290 Environmental allergens may enhance the likelihood of bronchoconstriction, and irritants such as sulfur dioxide, nitrogen dioxide, ozone, and chlorine have been implicated as causing patients to have exercise-induced symptoms.31,243,291
First, the patient has any of a constellation of symptoms associated with exercise, including shortness of breath (dyspnea), coughing, chest tightness (or chest pain in children), wheezing, and decreased exercise tolerance.13,262,263 Symptoms generally occur 5 to 8 minutes after sufficiently intense exercise starts. The EIA may be associated with specific sports as well as specific environments.262–267 Where allergens are present, outdoor activities and cold air exposure may be more likely to foster the appearance of EIA, which would not occur in other environments.
Second, the patient should have objective evidence of airway obstruction associated with exercise.224 Generally, a drop from baseline of at least 10% to 15% in FEV1 after a challenge test supports the diagnosis of EIA.19,292 Pulmonary function should be monitored 5, 10, 15, and 30 minutes after the challenge.19 The exercise needs to last for 6 to 8 minutes at an intensity level high enough to raise the athlete's heart rate to at least 80% of maximum19 and ventilation to approximately 40% to 60% of maximum.19 Exercise challenges can be performed in a laboratory (using a treadmill, a cycle ergometer, a rowing machine, or a free running asthma screening test [FRAST]).293 Alternatively, an exercise challenge test in the laboratory can attempt to mimic the conditions and intensity of the sport.20,21 Indeed, 78% of cross-country skiers reported a false-negative test during standard laboratory exercise challenges, suggesting that the standard tests are not as sensitive as sport-specific exercise challenge tests for endurance athletes.20,21 Cold, dry air and near-maximal exercise intensity (greater than 90% peak heart rate) are required to provoke a positive result, especially in the cold-weather athlete. Time of day can be important: in a group of asthmatics, a greater drop in pulmonary function (FEV1) to exercise challenge was measured in the evening than in the morning.294
Additional challenge tests include eucapnic voluntary hyperventilation or inhalation of hypertonic saline.21,269,295 The former test requires the athlete to hyperventilate dry air containing 5% carbon dioxide, 21% oxygen, and the balance of nitrogen at 30 times FEV1 for 6 minutes.21
It is important to evaluate athletes with atypical EIA symptoms because upper airway conditions such as vocal cord dysfunction or abnormal movement of the arytenoids region may be the cause.15,53 The signs and symptoms of vocal cord dysfunction can be similar to asthma and can be confused with EIA.54,296,297 This laryngeal disorder involves the unintentional paradoxic adduction of the vocal cords with breathing and can be triggered by exercise.296,297 The patient is often female and may also have gastroesophageal reflux disease or a psychiatric illness. Vocal cord dysfunction often occurs with asthma, making control of EIA difficult. Diagnosis of vocal cord dysfunction involves the direct visualization of the paradoxic vocal cord motion, but the condition is often suspected when voice changes and inspiratory stridor occur during an attack, as well as when the inspiratory (bottom) portion of the flow volume loop is truncated.
Most of the drugs described for the treatment of chronic asthma are used to prevent EIA attacks.1,2,269,298–300 Table 6 contains recommendations from the NAEPPII for the treatment of EIA.1 The key feature is that a β2-agonist can be used both to prevent attacks and to treat them when they occur. Once an asthmatic individual meets the requirements for stage 1 through 4 asthma, the NAEPPII treatment guidelines should be followed.
Throughout this position statement, information has been presented to inform and educate the athletic trainer and allied health personnel about asthma and asthma management. Of particular importance is a properly prepared asthma management plan. Educating athletes about asthma and having a written management plan will help control their disease.1,2,304 Several groups35–44,48–51 have shown that an effectively written management plan can reduce medication errors, asthma exacerbations, and hospital visits. Without a written asthma action plan, many patients have a difficult time controlling their asthma symptoms.45–47,305 It is also imperative that an accessible line of communication between the patient and health care professional be identified.
An effective management plan should include a written document that addresses the following: (1) goals of the patient, (2) proper use and frequency of PEFR monitoring, (3) guidelines for altering medications based upon readings from PFMs or asthma symptoms, (4) contact numbers for all health care professionals, including emergency numbers, and (5) environmental factors to avoid or monitor. The health care professionals developing the asthma management plan should discuss all goals or expectations with the athlete. This education empowers the athlete and promotes better compliance.
Athletic trainers working with elite or Olympic athletes must be familiar with International Olympic Committee, World Anti-Doping Agency, and United States Anti-Doping Agency medication guidelines (Table 7). Certain asthma medications may be banned, restricted, or permitted, depending on the organization and the medication. A banned medication is one the athlete cannot take. In some cases, a prohibited substance is prohibited at all times or only prohibited in competition, meaning the athlete must allow sufficient time for the substance to clear the system before competition. Restricted medications must have prior physician approval and completion of forms (such as the Therapeutic Use Exemption, or TUE) before the athlete can compete. For example, the United States Anti-Doping Agency lists salbutamol/albuterol, salmeterol, terbutaline, and formoterol as restricted β2-agonists that require a TUE before competition.
Additional information about the diagnosis and management of asthma can be obtained at the National Asthma Education and Prevention Program Web site (http://www.nhlbi.nih.gov/ health/prof/lung/index.htm or http://www.nhlbi.nih.gov/about/ naepp/) and the GINA Web site (www.ginasthma.com).
Asthma can affect individuals regardless of age, sex, or socioeconomic status. This National Athletic Trainers' Association asthma position statement is designed to present guidelines for the recognition, prophylaxis, and management of asthma. The information should lead to improvements in the quality of care certified athletic trainers and other heath care providers can offer to patients with asthma, particularly athletes and especially those with EIA. In the end, these guidelines should reduce the incidence of asthma complications and improve the quality of life for patients with asthma, especially those in whom exercise is an important trigger.
The NATA publishes its position statements as a service to promote the awareness of certain issues to its members. The information contained in the position statement is neither exhaustive not exclusive to all circumstances or individuals. Variables such as institutional human resource guidelines, state or federal statutes, rules, or regulations, as well as regional environmental conditions, may impact the relevance and implementation of these recommendations. The NATA advises its members and others to carefully and independently consider each of the recommendations (including the applicability of same to any particular circumstance or individual). The position statement should not be relied upon as an independent basis for care but rather as a resource available to NATA members or others. Moreover, no opinion is expressed herein regarding the quality of care that adheres to or differs from NATA's position statements. The NATA reserves the right to rescind or modify its position statements at any time.
We gratefully acknowledge the efforts of Michael C. Koester, MD, ATC; James L. Moeller, MD, FACSM; Kenneth W. Rundell, PhD; Chad Starkey, PhD, ATC; Randall L. Wilber, PhD; and the Pronouncements Committee in the preparation of this document.