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UNIVERSITY OF PRINCE EDWARD N232 INTRODUCTORY PHARMACOLOGY ASTHMA Asthma is a common, chronic disorder that occurs in children and adults. Characteristic signs and symptoms are a sense of breathlessness and tightness in the chest, wheezing, dyspnea, and cough. The underlying cause is immune-mediated airway inflammation. This chapter discusses basic considerations in asthma, anti-inflammatory drugs, bronchodilators, glucocorticoid/longacting beta2 agonist (LABA) combinations and the management of chronic asthma. Words/Concepts to Know: asthma dry-powder inhalers (DPIs) exercise-induced bronchospasm (EIB) forced expiratory volume in 1 second (FEV1) forced vital capacity (FVC) leukotriene modifiers mast cell stabilizers metered-dose inhaler (MDI) methylxanthines peak expiratory flow (PEF) Learning Objectives: After reading and studying this chapter, the student should be able to do the following: A. State a reasonably accurate definition of asthma that includes an understanding of the roles and involvement of airway smooth muscle hyperresponsiveness and inflammation in the disease. Describe the typical signs and symptoms that would lead to the diagnosis of a respiratory disorder as asthma. B. State the criteria used to classify severity of asthma based on impairment and risk. C. Summarize the mechanisms of action, roles, and limitations of the following drugs in the therapy of asthma: 1. 2. 3. 4. 5. 6. 7. Beta-adrenergic agonists Glucocorticoids Methylxanthines Mast cell stabilizers Leukotriene modifiers Anticholinergic drugs Glucocorticoid/LABA combinations D. Describe the two basic goals in the treatment of chronic asthma. E. Compile a list of drugs or drug groups that are relatively or absolutely contraindicated for patients with asthma, and state their main problems. F. Discuss some nondrug interventions that might be used to decrease the frequency and severity of asthma attacks. KEY POINTS: Asthma is a chronic inflammatory disease characterized by inflammation of the airways, bronchial hyperreactivity, and bronchospasm. Allergy is often the underlying cause. Asthma is treated with anti-inflammatory drugs and bronchodilators. KEY POINTS: Most drugs for asthma are administered by inhalation, a route that increases therapeutic effects (by delivering drugs directly to their site of action), reduces systemic effects (by minimizing drug levels in blood), and facilitates rapid relief of acute attacks. Three devices are used for inhalation: MDIs, DPIs, and nebulizers. Patients will need instruction on their use. KEY POINTS: Beta2 agonists promote bronchodilation by activating beta2 receptors in bronchial smooth muscle. Inhaled short-acting inhaled beta2 agonists (SABAs) are the most effective drugs for relieving acute bronchospasm and preventing exercise-induced bronchospasm. Three inhaled beta2 agonists—arformoterol, formoterol, and salmeterol—have a long duration of action, and hence are indicated for long-term control. Inhaled SABAs rarely cause systemic side effects. Excessive dosing with oral beta2 agonists can cause tachycardia and angina by activating beta1 receptors on the heart. (Selectivity is lost at high doses.) Inhaled LABAs can increase the risk of asthma-related death, but only when used incorrectly. Accordingly, LABAs should be used only by patients taking an inhaled glucocorticoid for long-term control, and only if the glucocorticoid has been inadequate by itself. KEY POINTS: Glucocorticoids are the most effective antiasthma drugs available. Glucocorticoids reduce symptoms of asthma by suppressing inflammation. As an added bonus, glucocorticoids promote synthesis of bronchial beta2 receptors, and increase their responsiveness to beta2 agonists. Inhaled and systemic glucocorticoids are used for long-term prophylaxis of asthma—not for aborting an ongoing attack. Accordingly, they are administered on a fixed schedule— not PRN. Unless asthma is severe, glucocorticoids should be administered by inhalation. Inhaled glucocorticoids are generally very safe. Their principal side effects are oropharyngeal candidiasis and dysphonia, which can be minimized by employing a spacer device during administration and by gargling after. Inhaled glucocorticoids can promote bone loss. To minimize loss, dosage should be as low as possible, and patients should perform regular weight-bearing exercise and should ensure adequate intake of calcium and vitamin D. Inhaled glucocorticoids can slow the growth rate of children, but they do not reduce adult height. Prolonged therapy with oral glucocorticoids can cause serious adverse effects, including adrenal suppression, osteoporosis, hyperglycemia, peptic ulcer disease, and growth suppression. Because of adrenal suppression, patients taking oral glucocorticoids (and patients who have switched from oral glucocorticoids to inhaled glucocorticoids) must be given supplemental doses of oral or IV glucocorticoids at times of stress. KEY POINTS: Cromolyn is an inhaled anti-inflammatory drug used for prophylaxis of asthma. Cromolyn reduces inflammation primarily by preventing release of mediators from mast cells. For long-term prophylaxis, cromolyn is taken daily on a fixed schedule. For prophylaxis of exercise-induced bronchospasm, cromolyn is taken 15 minutes before anticipated exertion. Cromolyn is the safest drug for asthma. Serious adverse effects are extremely rare. KEY POINTS: There are four classes of chronic asthma: intermittent, mild persistent, moderate persistent, and severe persistent. Diagnosis is based on current impairment and future risk. For therapeutic purposes, asthma drugs can be classified as long-term control medications (eg, inhaled glucocorticoids) and quick-relief medications (eg, inhaled SABAs). In the stepwise approach to asthma therapy, treatment becomes more aggressive as impairment and/or risk becomes more severe. The goals of stepwise therapy are to prevent symptoms, maintain near-normal pulmonary function, maintain normal activity, prevent recurrent exacerbations, minimize the need for SABAs, minimize drug side effects, minimize emergency department visits, prevent progressive loss of lung function, and meet patient and family expectations about treatment. The step chosen for initial therapy is based on the pretreatment classification of asthma severity, whereas moving up or down a step is based on ongoing assessment of asthma control. Intermittent asthma is treated PRN, using an inhaled SABA to abort the few acute episodes that occur. For persistent asthma (mild, moderate, or severe), the foundation of therapy is daily inhalation of a glucocorticoid. An inhaled LABA is added to the regimen when asthma is more severe. A short-acting beta2 agonist is inhaled PRN to suppress breakthrough attacks. For acute severe exacerbations of asthma, patients should receive oxygen to reduce hypoxemia, a systemic glucocorticoid (to reduce airway inflammation), and a nebulized SABA plus nebulized ipratropium (to relieve airflow obstruction) To prevent exercise-induced bronchospasm, patients can inhale a SABA just prior to strenuous activity. Patients should avoid allergens that can cause airway inflammation and triggers that can provoke exacerbations. Important sources of allergens are the house dust mite, warmblooded pets, cockroaches, and molds. Important triggers are tobacco smoke, wood smoke, and household sprays. Asthma Severity Intermittent Mild Persistent Moderate Persistent Severe Persistent Symptoms 2 or less days per week More than 2 days per week Daily Throughout the day Nighttime Awakenings 2 X's per month or less 3-4 X's per month More than once per week but not nightly Nightly Rescue Inhaler Use 2 or less days per week More than 2 days per week, but not daily Daily Several times per day Interference With Normal Activity None Minor limitation Some limitation Extremely limited Lung Function FEV1 >80% predicted and normal between exacerbations FEV1 >80% predicted FEV1 60-80% predicted FEV1 less than 60% predicted