New Treatments for Asthma

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    DOI: 10.1542/pir.24-7-2222003;24;222Pediatr. Rev.Mary V. Lasley

    New Treatments for Asthma

    http://pedsinreview.aappublications.org/cgi/content/full/24/7/222located on the World Wide Web at:

    The online version of this article, along with updated information and services, is

    Pediatrics. All rights reserved. Print ISSN: 0191-9601. Online ISSN: 1526-3347.Boulevard, Elk Grove Village, Illinois, 60007. Copyright 2003 by the American Academy of published, and trademarked by the American Academy of Pediatrics, 141 Northwest Pointpublication, it has been published continuously since 1979. Pediatrics in Review is owned,Pediatrics in Review is the official journal of the American Academy of Pediatrics. A monthly

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    New Treatments for AsthmaMary V. Lasley, MD*

    Objectives After completing this article, readers should be able to:1. Dene asthma.2. List conditions that mimic asthma.3. Delineate the factors that predict the persistence of asthma.4. Describe the objective measurements of pulmonary function required for evaluation

    and treatment of asthma.5. Explain the role of anti-inammatory medications in the management of persistent

    asthma.6. Determine when a child should be referred to an asthma specialist.

    EpidemiologyOver the past 15 years, the number of people affected by asthma has more than doubled. Asthma is the most common pediatric chronic disease, aficting nearly 5 million children younger than age 18 years in the United States. Asthma affects 1 of every 13 schoolchil-dren. Every year, asthma accounts for more than 3 million physician visits and 200,000pediatric hospitalizations, with rates highest among African-American children. Asthmamortality nearly doubled between 1980 and 1993 (17 and 32 asthma deaths per 1 millionpopulation, respectively). More than 5,500 people die from asthma every year. Asthma isa major cause of school absenteeism, with an estimated 10 million missed schooldays each year. The economic impact of asthma is enormous, approaching $3 billion annually. Thisencompasses direct costs such as medical expenses and indirect costs of parents andcaregivers taking time away from work to care for their ill children, which has beenestimated at $1 billion anually.

    Asthma severity is greater in urban minority populations, both African-American andHispanic. Children living in inner cities often do not receive appropriate treatment toreduce their asthma severity and live in situations where it is difcult to control environ-mental exposures.

    PathogenesisInammation is present even in the airways of young patients who have mild asthma. A complex orchestration of inammatory cells (eg, mast cells, eosinophils, T lymphocytes,and neutrophils), chemical mediators (eg, histamine, leukotrienes, platelet-activatingfactor, bradykinin), and chemotactic factors (eg, cytokines, eotaxin) results in the under-lying inammation found in asthmatic airways (Fig. 1). Inammation of the airwayscontributes to airway hyperresponsiveness, which is characterized as the tendency for theairways to constrict in response to allergens, irritants, viral infections, and exercise. It alsoresults in edema, increased mucus production in the lungs, an inux of inammatory cellsinto the airway, and epithelial cell denudation. Chronic inammation can lead to airway remodeling, which results from a proliferation of extracellular matrix proteins and vascularhyperplasia (Fig. 1). Chronic remodeling may lead to irreversible structural changes and aprogressive loss of pulmonary function. Exactly when the child is most susceptible toremodeling and whether therapeutic intervention can prevent this is still unknown.

    Airow limitation due to the effects of airway inammation leads to the respiratory

    *Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine, Northwest Asthma & Allergy Center,

    Seattle, WA.

    Article respiratory disorders

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    Figure 1. Airway inammation in asthma. A. Cellular mechanisms involved in airway inammation. B. Airway remodeling due tochronic airway inammation. Ig immunoglobulin, IL interleukin.

    respiratory disorders asthma

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    symptoms of coughing, wheezing, shortness of breath,and chest tightness that are observed in children whosuffer from asthma.

    DiagnosisIt can be dif cult to diagnose asthma in children; asthmaoften is underdiagnosed among infants and young chil-dren who wheeze during respiratory infections. It also isimportant to recognize that cough and wheeze do notalways reect asthma. Care is needed to avoid prescribinginappropriate prolonged asthma medications. Otherconditions that mimic asthma are shown in Table 1. Forsome children, symptoms of wheezing accompanyingrespiratory infections subside in the preschool years;other children develop persistent symptoms. However,the strongest predictor for wheezing developing into

    asthma is atopy. Approximately 70% to 90% of children who have asthma and are older than 5 years of age havepositive allergy skin tests. Other predictive factors in-clude parental history of asthma, peripheral blood eosin-ophilia, wheezing episodes apart from upper respiratory tract infections, and presence of atopic dermatitis orallergic rhinitis.

    Three steps for diagnosing asthma are to obtain acareful history, perform a thorough physical examina-tion, and objectively measure pulmonary function. Thehistory should elicit the child s symptoms of coughing, wheezing, shortness of breath or rapid breathing, or

    chest tightness and the frequency and severity of such

    symptoms. Symptoms tend to occur or worsen at night, waking the child or parent. Asthma symptoms frequently are exacerbated by viral infections, exposure to allergensand irritants (smoke, strong odors and fumes), exercise,emotions, and changes in weather/humidity. A family history of allergy and asthma is a useful nding; allergicdiseases tend to occur in families. On examination, phys-ical ndings may be subtle. Wheezing may not bepresent. Evidence of other atopic diseases such as eczemaor allergic rhinitis can help guide the clinician to thecorrect diagnosis.

    If possible to obtain, objective measurements of pul-monary function (spirometry) are essential to establishthe diagnosis and treatment of asthma. Spirometry should be undertaken at the initial visit as well as at return visits to document attainment of normal pulmonary

    functions. Spirometry testing can help monitor the pa-tient s response to the treatment plan, assess the degreeof reversibility with optimal asthma management, andmeasure the severity of an asthma exacerbation. Spirom-etry should be obtained at least annually to ensure pres-ervation of airway function, at visits where there arereports of pulmonary instability, and if there have beenchanges in the medication regimen. Children older than5 years usually can perform spirometry maneuvers. Sev-eral practice sessions may be necessary for the youngerchild to master spirometry techniques.

    Because atopy plays an important role in asthma per-

    sistence, allergy skin testing should be considered.

    Table 1. Differential Diagnosis of Cough and Wheeze in Infants andChildrenUpper Respiratory Tract Middle Respiratory Tract Lower Respiratory Tract

    Allergic rhinitisAdenoid/tonsillar hypertrophyForeign bodyInfectious rhinitisSinusitis

    Bronchial stenosisEnlarged lymph nodesEpiglottitisForeign bodyLaryngeal websLaryngomalaciaLaryngotracheobronchitisPertussisToxic inhalationTracheoesophageal stulaTracheal stenosisTracheomalaciaTumor Vascular rings Vocal cord dysfunction

    AsthmaBronchiectasisBronchopulmonary dysplasiaChlamydia trachomatis Chronic aspirationCystic brosisForeign bodyGastroesophageal re uxHyperventilation syndromeObliterative bronchiolitisPulmonary hemosiderosisToxic inhalationTumor Viral bronchiolitis

    Adapted from Lemanske RF Jr,Green CG. Asthmain infancy and childhood. In: Middleton E Jr,Reed CE,Ellis EF, et al, eds. Allergy: Principles & Practice.5th ed. St. Louis, Mo: Mosby-Year Book, Inc; 1998:878.

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    A board-certi ed allergistoffers the special skill of admin-istering and interpreting skin tests to determine immedi-ate hypersensitivity to aeroallergens. Studies have dem-onstrated that positive skin test results correlate strongly with bronchial allergen provocative challenges. In vitrotests, such as radioallergosorbent test and enzyme-linked

    immunosorbent assay, are other options to measure lev-els of antigen-speci c immunoglobulin E. However,compared with skin testing, in vitro testing generally isnot as sensitive in de ning clinicallypertinent allergens, ismore expensive, and requires several days for results(compared with several minutes for skin tests).

    Environmental ControlOptimal medical treatment of asthma is based on threekey components: environmental control, pharmacologictherapy, and patient education, including acquisition of self-management skills.

    Because children have a high incidence of allergy

    related to asthma, steps should be taken to minimizeallergen exposure (Table 2). For all children who haveasthma, common sense dictates that exposures to to-bacco and wood smoke as well as viral infections beminimized.

    Pharmacologic TherapyCurrent therapy is based on the concept that chronicinammation is a fundamental feature of the disease. TheNational Asthma Education and Prevention Programrecently published an update on classi cation and treat-ment based on asthma severity. The stepwise approachfor management of infants and young children is shownin Figure 2 and for children 5 years of age and older isshown in Figure 3. A short-acting bronchodilator shouldbe available for all children who have asthma. Intermit-tent asthma is de ned as the presence of asthma symp-toms less frequently than twice weekly. To determine if a

    child is having more persistent asthma, the rule of twos

    Table 2. Controlling Factors Contributing to Asthma SeverityMajor Indoor Triggers for Asthma Suggestions for Reducing Exposure

    Viral upper respiratory tract infections Limit exposure to viral infections (ie, smaller size child care)Inuenza Administer annual inuenza shots to children who have persistent asthma

    (who are not allergic to eggs)Tobacco smoke, wood smoke Do not smoke around the child or in childs home

    Help parents and caregivers quit smoking Eliminate use of wood stoves and replaces

    Dust mites Essential actions: Encase pillow, mattress, and box spring in allergen-impermeable

    encasement Wash bedding in hot water weeklyDesirable actions: Avoid sleeping or lying on upholstered furniture

    Minimize number of stuffed toys in child s bedroom Reduce indoor humidity to < 50% If possible, remove carpets from bedroom and play areas; if not possible,

    vacuum frequentlyAnimal dander Remove the pet from the home or keep outdoors

    If removal is not acceptable:Keep pet out of bedroomUse lters on air ducts in child s roomWash pet weekly (although evidence to support the bene t of this action

    has not been rmly established)Cockroach allergens Do not leave food or garbage exposed

    Use boric acid traps Reduce indoor humidity to < 50% Fix leaky faucets, pipes

    Indoor mold Fix leaky faucets, pipes Avoid vaporizers Reduce indoor humidity to < 50%

    Adapted from American Academy of Allergy, Asthma & Immunology, Inc. Pediatric Asthma: Promoting Best Practice. Milwaukee, Wisc: American Academy of Allergy, Asthma, and Immunology, Inc; 1999:50.

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    Figure 2. Stepwise approach for managing infants and young children < 5 y who have acute or chronic asthma. From NHLBI,National Asthma Education and Prevention Program. Expert Panel Report: Guidelines for the Diagnosis and Management of

    Asthma

    Update on Selected Topics . 2002.

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    Figure 3. Stepwise approach for managing asthma in adults and children > 5 y. From NHLBI, National Asthma Education andPrevention Program. Expert Panel Report: Guidelines for the Diagnosis and Management of Asthma Update on Selected Topics .

    2002.

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    can be helpful. The presence of daytime symptoms twoor more times per week or night-time awakening two ormore times per month may indicate a need for daily controller medication that has anti-in ammatory activ-ity. For infants and young children who have had threeepisodes of wheezing in the previous year as well as risk factors for the development of asthma (ie, parentalasthma, peripheral blood eosinophilia, wheezing be-tween upper respiratory tract infections, personal atopy)or who have severe exacerbations fewer than 6 weeksapart, long-term controller medications may be desir-able.

    The preferred rst-line controller medication for chil-dren of all ages who have persistent asthma is inhaledcorticosteroids. In clinical trials comparing inhaled cor-ticosteroids with cromolyn, nedocromil, leukotrienemodi ers, or theophylline, inhaled corticosteroids werethe most effective medications in improving long-termasthma control. Low-dose inhaled corticosteroids arerecommended for children who have mild persistentasthma. For children older than 5 years of age who havemoderate persistent asthma, combining long-actingbronchodilators with low to medium doses of inhaledcorticosteroids improves lung function and reduces res-cue medication usage. The evidence for adding a leuko-triene modi er or theophylline or for doubling the doseof corticosteroid is not as well supported by clinicalstudies. For children younger than 5 years of age whohave moderate persistent asthma, medication combina-tions have not been as well studied. The preferred ther-apy is either a combination of low-dose inhaled cortico-steroids and long-acting bronchodilators or mediumdoses of inhaled corticosteroids. High-dose inhaled cor-ticosteroids and long-acting bronchodilators are the pre-ferred therapies for children who have severe persistentasthma. The guidelines also recommend that patients beassessed every 1 to 6 months to determine whethermedications should be reduced (step-down) or increased

    (step-up), depending on disease control.Long-term controller medications are taken daily to

    achieve and maintain control of persistent asthma. Somecontroller medications, such as cromolyn, nedocromil,and theophylline, have been available for many years and will not be reviewed in this article. Discussion of thenewer medications, including inhaled corticosteroids,leukotriene modi ers, and long-acting bronchodilators,follows.

    Inhaled CorticosteroidsInhaled corticosteroids are the most effective anti-

    inammatory medications for the treatment of chronic

    persistent asthma. Inhaled corticosteroids are available asmetered-dose inhalers (MDI), dry powder inhalers(DPI), and nebulizer solutions. The inhaled corticoste-roids available in the United States include beclometha-sone, budesonide, unisolide, uticasone, and triamcin-olone, with mometasone forthcoming. Clinical trials with the next generation of inhaled corticosteroids areproceeding.

    The greatest concern of parents and physicians aboutthese medications is the risk of systemic corticosteroidactivity. In general, if the medications are used in doses of less than 400 mcg/day (beclomethasone equivalent),there is little risk of systemic effects.

    Information about the effects of corticosteroids onlinear growth is con icting in the literature. Short-termstudies suggest growth delay of about 1 cm/y. Thereliability of this growth delay is tempered by the appar-ent similarity of heights compared with normal peersdemonstrated in long-term studies. The Childhood Asthma Management Program (CAMP) trial providesthe largest and longest double-blind, randomized trial of inhaled corticosteroid treatment compared with placeboin children as well as a cohort of children treated withnonsteroidal anti-in ammatory therapy (nedocromil).There was a 1.1-cm difference in growth between thechildren assigned to budesonide and those assigned toplacebo that occurred as a result of a decrease in growth velocity. This reduction in growth velocity took place within the rst year of steroid therapy and was notprogressive thereafter. TheCAMP Continuation Study isongoing, and more information will be forthcomingabout the growth of these children as they reach theiradult heights. The practitioner must monitor for poten-tial growth suppression in individualpatients by regularly scheduled height measurements, preferably with a stadi-ometer. Rinsing the mouth after inhalation of corticoste-roidsand using spacers help to lessen local adverse effectsof dysphonia and candidiasis as well as to decrease sys-

    temic absorption from the gastrointestinal tract. To min-imize adverse effects, the goal is to use the lowest effec-tive dose that controls the child s asthma.

    Leukotriene ModiersLeukotriene modi ers are a new class of oral daily-useasthma medication. Leukotrienes, synthesized via thearachidonic acid metabolism cascade, are potent media-tors of in ammation and smooth muscle bronchocon-striction. Leukotriene modi ers have been designed toinhibit edema, mucus secretion, smooth muscle contrac-tion, and eosinophil migration into the airways. There

    are two classes of leukotriene modi ers based on their

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    site of action: leukotriene synthesis inhibitors (eg, zileu-ton) and cysteinyl leukotriene receptor antagonists (eg,zarlukast and montelukast). Zileuton is approved foruse in children older than 12 years of age. It is used lesscommonly than other leukotriene modi ers because of aneed to monitor liver enzymes regularly, the possibility of drug interactions, and an initial dosing regimen of fourtimes per day. The leukotriene receptor antagonists havemuch wider appeal. Za rlukast has been approved forchildren older than 7 years of age and is administeredtwice daily. Montelukast is dosed once daily at night as4-mg or 5-mg chewable tablets for ages 2 to 5 years and6 to 14 years, respectively. A 10-mg tablet is available foradolescents older than 15 years. Pediatric studies dem-onstrate the usefulness of leukotriene modi ers in mildasthma and the attenuation of exercise-induced bron-choconstriction. These agents also are useful as steroid-sparing agents for patients whose asthma is more dif cultto control.

    Although leukotriene modi ers are considered alter-native therapy for long-term control in children whohave mild persistent asthma, they are appealing becauseof their easy administration and excellent safety pro le.In addition, these medications do not provoke steroidphobia in families or physicians, which can be a reasonfor the undertreatment of asthma with inhaled cortico-steroids.

    Long-acting Beta-2 AgonistsNewly available long-acting beta-2 agonists include for-moterol and salmeterol. These medications are adminis-tered twice daily and exhibit bronchodilatory effects forup to 12 hours. It is important to recognize that theseagents do not have any signi cant anti-in ammatory effects. Studies have demonstrated that adding a long-acting bronchodilator to inhaled corticosteroid therapy is more bene cial than doubling the dose of inhaledcorticosteroids. Formoterol, available in the DPI form, is

    approved for use in children older than 5 years formaintenance asthma therapy and for prevention of exercise-induced asthma among children older than 12 years. Formoterol has a rapid onset of action that issimilar to albuterol (15 min) compared with a 30-minuteonset of action for salmeterol. Salmeterol is available inthe MDI form for children 12 years of age and older; theDPI form is approved for children 4 years of age andolder.

    In spring 2001, a uticasone/salmeterol combinationproduct, Advair (GlaxoSmithKline), received UnitedStates Food and Drug Administration approval for chil-

    dren older than 12 years for maintenance treatment of

    asthma. It is available as a DPI in three doses, based onthe amount of corticosteroid available (100 mcg,250 mcg, or 500 mcg). Each of the strengths contains50 mcg of salmeterol. Its advantages include possibleimproved compliance because it is administered as onepuff twice daily and the combination of two potentasthmamedications. Study trials forcombination therapy for younger children are ongoing.

    Novel Therapies With an improved understanding of the basic mecha-nisms of airway inammation, future asthma treatment will target the components of the in ammatory cascade.Possibilities include anti-immunoglobulin E and anticy-tokine therapies. Research is preliminary, and time willtell whether these therapies will be a helpful addition tothe physician s armamentarium.

    Other TherapiesThe management of children in respiratory failure fromstatus asthmaticus is beyond the scope of this article.Generally, medical therapy involves the use of frequentor continuous beta-2 agonist nebulization therapy andoral or intravenous corticosteroids. Chest physiotherapy can help move secretions to central airways, where coughcan expel the secretions, and can be helpful in asthmaticpatients who have coexisting chronic obstructive pul-monary disease or emphysema. Typically, these are notpediatric patients. Mucolytic agents, such asN-acetylcysteine, may induce bronchoconstriction andshould be used with caution. Only when adequate me-chanical ventilation is in progress should sedative, nar-cotic, or anxiolytic drugs be administered to the patientin status asthmaticus.

    Patient EducationEducation plays an important role in helping asthmaticpatients and their families adhere to the prescribed ther-

    apy and needs to begin at the time of diagnosis. Key educational messages include basic asthma facts, the roleof medications, environmental control measures, moni-toring skills to recognize the symptoms of asthma thatindicate adequate or inadequate asthma control, and anasthma management plan for exacerbations as well asdaily control. Absorbing such information can be over- whelming in a 15-minute appointment, but other healthcare team members and of ce staff can help reinforce theeducational messages. Education is an ongoing process,and information needs to be adjusted appropriately forthe child as he or she ages and for the family as they

    become more educated. Many outside resources can

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    provide additional educational services to families. The Asthma and Allergy Foundation of America (www.aafa.org), the American Lung Association(www2.lungusa.org), the Allergy and Asthma Network Mothers of Asthmatics (www.aanma.org), American Acadmey of Allergy, Asthma, and Immunology (www.aaaai.org), and American College of Allergy, Asthma, and Immunology (www.acaii.org) are excel-lent sources of information.

    A key message for families is that children who haveasthma should be seen not only when they are ill, but also

    when they are healthy. Regular of ce visits allow the

    health care team to review adherence to medication andcontrol measures and to determine if medication dosesneed adjustment.

    Families need to have an asthma management plan(Fig. 4) for daily care and for exacerbations. Peak ow monitoring is a self-assessment tool that encouragesasthma management. Reliable measurements often canbe obtained in children older than 5 years. Use of thepeak ow meter is advisable for children who are poorperceivers of airway obstruction, who have moderate-to-severe asthma, or who have a history of severe exacer-

    bations. Peak ow monitoring also can be useful for

    Figure 4. Sample asthma management plan for long-term control and for treating asthma exacerbations. Reprinted with permissionfrom American Academy of Allergy, Asthma & Immunology, Inc.Pediatric Asthma: Promoting Best Practice, Milwaukee, Wisc:American Academy of Allergy, Asthma & Immunology, Inc; 1999.

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    children recently diagnosed with asthma who are stilllearning to recognize asthma symptoms.

    To use a peak ow meter, a child should be standing with the indicator placed at the bottom of the scale. Thechild must inhale deeply, place the device in the mouth,bite down on the mouthpiece, seal his or her lips aroundthe mouthpiece, and blow out forcefully and rapidly. Theindicator moves up the numeric scale. The peak expira-tory ow rate (PEFR) is the highest number achieved.The test is repeated three times to obtain the best possi-

    ble effort. Peak ow meters are available as low-range(measurement up to 300 L/s) and high-range (measure-ment up to 700 L/s). It is important to provide theappropriate range meter to obtain accurate measure-ments and to avoid discouraging the child whose blowsbarely move the indicator.

    A childs personal best is the highest PEFR achievedover a 2-week period when stable. A written plan is based

    on the child s personal best. There are three PEFR zones,similar to a stoplight (Fig. 4). The green zone indicates aPEFR of 80% to 100% of the child s personal best value.In this zone, the child is likely asymptomatic and shouldcontinue with medications as usual. The yellow zoneindicates a PEFR of 50% to 80% of the child s personalbest value and generally coincides with the child havingmore asthma symptoms. Rescue medications such asalbuterol are added to the therapy, and a phone call tothe physician may be warranted if the peak ows do notreturn to the green zone within the next 24 to 48 hoursor if asthma symptoms are increasing. The red zoneindicates a PEFR below 50% and is a medical emergency.The rescue medication should be taken immediately. If the PEFR remains in the red zone or the child is experi-encingsigni cant airway compromise, a phone call to thephysician or emergency care is needed.

    When to ReferGuidelines for when a child should be referred to anasthma specialist are shown in Table 3. To optimize careof the child who has asthma, the specialist must work closely with the primary care physician.

    Suggested Reading Agertoft L, Pedersen S. Effect of long-term treatment with inhaledbudesonide on adult height in children with asthma. N Engl

    J Med. 2000;343:1064 1069 American Academy of Allergy, Asthma & Immunology, Inc. Pedi-

    atric Asthma: Promoting Best Practice . Milwaukee, Wisc: Amer-ican Academy of Allergy, Asthma, and Immunology, Inc; 1999

    Lemanske RF Jr, Green CG. Asthma in infancy and childhood. In:Middleton E Jr, Reed CE, Ellis EF, et al, eds. Allergy: Principles & Practice . 5th ed. St. Louis, Mo: Mosby-Year Book, Inc;1998:877 900

    NHLBI, National Asthma Education and Prevention Program.Expert Panel Report: Guidelines for the Diagnosis and Manage- ment of Asthma Update on Selected Topics . NIH PublicationNo. 02 5075. Bethesda, Md: US Department of Health andHuman Services; 2002. Downloadable version of the executivesummary available at: http://www.nhlbi.nih.gov/guidelines/asthma/index.htm

    NHLBI, National Asthma Education and Prevention Program.Expert Panel Report II: Guidelines for the Diagnosis and Man- agement of Asthma . NIH Publication No. 97 4051. Bethesda,Md: US Department of Health and Human Services; 1997

    The Childhood Asthma Management Program Research Group.Long-term effects of budesonide or nedocromil in children withasthma. N Engl J Med. 2000;343:1054 1063

    Table 3. Referral To An AsthmaSpecialist Child has had a life-threatening asthma

    exacerbation. Goals of asthma therapy are not being met after

    3 to 6 months of treatment; earlier if child appearsunresponsive to treatment.

    Signs and symptoms are atypical. Consider otherdiagnoses.

    Other conditions complicate asthma or its diagnosis(eg, rhinitis, sinusitis, gastroesophageal re ux).

    Additional diagnostic testing is indicated (eg,pulmonary function testing, allergy skin testing).

    Child or family needs additional education andguidance on complications of therapy, problems withadherence, or avoidance of triggers.

    Child is being considered for immunotherapy. Child has severe persistent asthma. Child is younger than 3 years and has moderate or

    severe persistent asthma. Child has used prolonged courses of oral

    corticosteroids, high doses of inhaled corticosteroids,or more than two bursts of oral corticosteroids in 12months.

    Adapted from American Academy of Allergy, Asthma & Immunology,Inc. Pediatric Asthma: Promoting Best Practice. Milwaukee, Wisc: American Academy of Allergy, Asthma, and Immunology, Inc;1999:80.

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    PIR QuizQuiz also available online at www.pedsinreview.org.

    1. The pathophysiologic change seen only as a result of chronic inammation is:

    A. Airway constriction.B. Airway destruction.C. Airway edema.D. Airway hyperresponsiveness.E. Airway remodeling.

    2. The strongest predictor for chronic wheezing progressing to asthma is:

    A. Allergic rhinitis.B. Atopy.C. Cough.D. Family history.E. Upper respiratory tract infection associated with wheezing.

    3. The preferred rst-line controller medication for children of all ages who have persistent asthma is:

    A. Cromolyn.B. Inhaled corticosteroids.C. Leukotriene modiers.D. Short-acting bronchodilators.E. Theophylline.

    4. An asthma management treatment plan is best managed using the patient s:

    A. Frequency of asthma exacerbations.B. Level of physical activity.C. Number of medications used.D. Peak expiratory ow rate.E. Perception of airway obstruction.

    respiratory disorders asthma

    232 Pediatrics in Review Vol.24 No.7 July 2003. Provided by Health Internetwork on June 24, 2010http://pedsinreview.aappublications.orgDownloaded from

    http://http//pedsinreview.aappublications.orghttp://http//pedsinreview.aappublications.orghttp://http//pedsinreview.aappublications.orghttp://http//pedsinreview.aappublications.orghttp://http//pedsinreview.aappublications.org
  • 8/9/2019 New Treatments for Asthma

    13/13

    DOI: 10.1542/pir.24-7-2222003;24;222Pediatr. Rev.

    Mary V. LasleyNew Treatments for Asthma

    & ServicesUpdated Information

    http://pedsinreview.aappublications.org/cgi/content/full/24/7/222including high-resolution figures, can be found at:

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