Audio-Digest Foundation: family-practice

Main Written Summaries Listing | Family-practice: 2007 Listings
Audio-Digest FoundationFamily Practice


Volume 55, Issue 04
January 28, 2007

The following is an abstracted summary, not a verbatim transcript, of the lectures/discussions on this audio program. If, after reviewing this written summary, you would like to hear the contents and/or earn CME/CE credit:

View Main Program Listing

Visit Audio-Digest Home Page

Family Practice Program InfoAccreditation InfoCultural & Linguistic Competency Resources





WHEEZING, SNEEZING, AND DIFFICULT BREATHING

From the American Academy of Family Physicians’ 2006 Scientific Assembly, Washington, DC

ASTHMA IN CHILDREN AND ADOLESCENTS— Thomas G. Irons, MD, Professor of Pediatrics, Brody School of Medicine, East Carolina University, Greenville, NC
Assessment and monitoring: look for pattern of symptoms, history of recurrent episodes, and reversible airway obstruction; rule out other conditions; easy breathing screening test—assess following occurrences within last 12 mo; wheezing or whistling in chest; awakening at night with cough; wheezing, coughing, or shortness of breath with exercise (and need to stop exercise); and whether cough persists when child has a cold; diagnosis of asthma—>3 episodes of wheezing lasting >1 day and interfering with sleep, and parental asthma or documented atopic dermatitis, or 2 signs (eg, physician-diagnosed allergic rhinitis apart from colds, wheezing apart from colds, peripheral blood eosinophilia with other diagnoses ruled out)
Severity of asthma: determine how often patient had problems with coughing, wheezing, shortness of breath, and tightness in chest during day and night in past 2 wk; how often patient had to use rescue inhaler; ask about awakening in morning or missing school due to symptoms; symptoms with exercise or play; ask about highest and lowest peak flow; determine whether peak flow dropped below 80% of personal best; persistent—symptoms present >2 times per week or patient awakens at night >2 times per month; intermittent—daytime symptoms present 2 times per week; mild— daytime symptoms present >2 times per week but <1 time daily; moderate—daytime symptoms present daily; severe— day- and night-time symptoms continual; patient categorized based on most severe feature
Routine follow-up: required every 1 to 6 mo, depending on severity; spirometry every 1 to 2 yr (at minimum); peak flow may not be true indicator of severity because patient can transiently produce substantial pressure with short tidal volume (forced expiratory volume in 1 sec [FEV1 ] more accurate); ask about severity, self-management skills, medication use, and care plan; when to refer—severe asthma; allergic rhinitis not controlled with medication; control cannot be achieved with good case management and compliance; comorbidities
Triggers: discuss exposure to tobacco smoke; assess and counsel patients about exercise-induced bronchospasm; common triggers include infection, animal dander, dust mites, molds, pollen, cockroaches, weather change, strong odors, fumes, chemicals, and smoke; trigger controls—discontinue smoking (tobacco) in house or car; bathe cat or keep outdoors; wash stuffed animals (every few months) and place in dark plastic bag for 24 hr once weekly; cover pillows; comorbid conditions—rhinitis; sinusitis; gastroesophageal reflux disease (GERD; no evidence that treatment of GERD improves asthma); viral illness; provide influenza vaccine
Treatment: inhaled antiinflammatory agents for persistent asthma (montelukast [Singulair] acceptable alternative); increase when needed, decrease when possible; provide delivery devices; most patients benefit from use of spacer; recommend use of peak-flow meters; severe asthma—high-dose inhaled steroids with long-acting β-agonist (possible increase in exacerbation of severe disease and death rate in adults); oral steroids when needed; moderate persistent asthma—low- to medium- dose inhaled steroid with long-acting β-agonist, or medium-dose inhaled steroid (preferred for children <5 yr of age); low- to medium-dose inhaled steroid and leukotriene modifier or theophylline; rescue albuterol; mild persistent asthma—low- dose inhaled steroid; leukotriene modifier or cromolyn; theophylline (fewer side effects at 5 µg/mL)
Inhaled antiinflammatory agents: many studies show little or no effect of long-term use on growth or complications (eg, cataracts); oral steroids should be used in exacerbations triggered by respiratory infection, regardless of severity; acceptable to use high-dose inhaled steroids, but oral steroids superior for relapse at 48 hr and symptom scores 12 hr after treatment; use of oral dexamethasone for exacerbations in office and in emergency department (ED) may be superior to prednisone because only 2 doses needed, taste better, and compliance better
Spacers: in young patient with properly fitted mask, spacer can be as effective as nebulizer; mometasone powder inhaler avoids use of spacer (used once daily); salmeterol and fluticasone effective (maintenance medication [not to be used for rescue]); monitor β-agonist use (re-evaluate patients who use >1 canister per month)
Self-management plan: develop written plan; discuss with teachers; educate patients about how and why to take long- term and quick-relief medication, correct technique for using devices (eg, inhaler, peak flow meter), peak flow monitoring, and effort dependence; nurse-led community teamwork effective; comprehensive education and review of printed or electronic materials; home visits for selected high-risk patients; home monitoring; explain difference between control and rescue medications
Literature topics: prolonged breast-feeding (>6 mo) may protect against development of asthma; asthma flares usually related to infection; consider Chlamydia pneumoniae in patient with multiple flares during respiratory infection season; sputum eosinophilia persists in patients with controlled asthma; 33% of hockey players have bronchial hyperresponsiveness (associated with chronic exposure to cold air); study found health care providers overestimated degree of control of asthma in children 33% of time; high-efficiency particulate air (HEPA) filters shown ineffective against cat allergy; conflicting evidence about dust mite control (effective interventions include removing carpet and using pillow covers); monitoring exhaled nitric oxide may become useful; planned-care intervention (nurse-mediated training of office staff and physicians) more effective than peer leader education (eg, lecture given by pediatrician) or conventional management alone; inhaled steroids given at school (vs home) improve outcomes only if child not exposed to secondhand smoke at home; some evidence that levalbuterol (Xopenex) superior to albuterol in ED because of reduced side effects with repeated dosing; ipratropium (Atrovent) rarely used in children; Atrovent inhaler contraindicated in presence of peanut or soy allergy; symptoms of depression and anxiety in teenagers closely related to asthma (screen teenagers with asthma for depression); peak flow not as effective as spirometry in classifying severity of asthma; high-dose inhaled fluticasone inferior to oral prednisolone in acute exacerbations of mild or moderate asthma, with significant difference in 48-hr relapse rate (0% in oral prednisolone group, 13% in inhaled fluticasone group) and symptoms at discharge; lung function inversely related to carbon content of airway macrophages
ALLERGIC RHINITIS Harold H. Hedges III, MD, Associate Clinical Professor, Department of Family Medicine, University of Arkansas School of Medicine, Little Rock
Introduction: allergic rhinitis affects 20% to 40% of pediatric population; mean onset of allergies in children 8 to 10 yr of age (70% develop at <20 yr of age); symptoms—rhinorrhea; rhinitis; disruption of sleep; fatigue; negative effects— school or work absenteeism; cognitive impairment; fearfulness; poor social interaction; poor performance in school or work; decreased self-esteem; depression; anxiety; shyness
Distinguishing allergic from nonallergic rhinitis: based on patient history and physical examination; no objective diagnostic test; helps determine specific cause of rhinitis; demonstrates allergy triggers (so can be avoided); aids in selection of appropriate medication (eg, azelastine [antihistamine nasal spray] or nasal steroids for nonallergic rhinitis); reduces cost of inappropriate medication; helps explain inefficacy of antihistamines or immunotherapy; 52% of patients present with nonallergic rhinitis, 48% with allergic rhinitis; few studies done on mixed rhinitis; study of 16,000 patients found 7% had pure allergic rhinitis, 10% had pure nonallergic rhinitis, and 82% had mixed rhinitis (diagnoses not based on objective test); symptoms and signs of allergic rhinitis—rhinorrhea; nasal congestion; sneezing; watery itchy eyes; itchy nose; postnasal drip; symptoms present before age 20 yr; positive family history; symptoms or exacerbations seasonal; symptoms improve in air conditioning or filtered air; fatigue, sinusitis, otitis media, and asthma concomitant conditions; antihistamines reduce symptoms; symptoms may be caused by exposure to animal; symptoms and signs of non-allergic rhinitis—congestion; rhinorrhea; symptoms perennial; negative family history; symptoms present after age 20 yr; caused by perfumes, potpourri, burning candles, tobacco smoke, chemical exposures, office machines, weather changes, automobile exhaust, gasoline, paints, fumes; no significant response to exposure to animal; symptoms respond to decongestants but not to antihistamines; mixed rhinitis—combination of symptoms of allergic and nonallergic rhinitis; diagnosis based on objective evidence of allergy by skin testing or in vitro testing and positive history for nonallergic triggers; negative allergy test best test for nonallergic rhinitis; objective evidence of allergic rhinitis—decrease in allergic symptoms with oral antihistamines, intranasal antihistamines, or steroids; nasal cytology positive for eosinophils, positive allergy skin test, or positive in vitro test results
Triggers of allergic rhinitis and anaphylaxis: pollen from trees, grasses, and weeds; molds; animal dander; foods (eg, peanuts, shellfish); hymenoptera; consider chronic rhinosinusitis in patient with asthma who does not improve with usual treatment; if patient doing well on asthma treatment, allergy testing or immunotherapy not required; obstruction of osteomeatal complex (from, eg, broken nose, Down syndrome) can cause rhinitis
Signs of allergic rhinitis in children: nasal symptoms; chronic fatigue; Morgan’s line (Dennie’s sign); nasal crease; nasal voice; irritability; poor appetite
Physical changes: allergic rhinitis—pale blue edematous turbinates; clear watery nasal discharge; crease from “nasal salute”; adenoid facies; lymphoid hyperplasia; nonallergic rhinitis—less mucosal edema; nonspecific nasal discharge (usually not “crystal clear”); crease from nasal salute; biopsies show normal mucosal pattern and cell structure; not typical inflammatory phenomenon
Treatment: immunotherapy helps allergic rhinitis, but not nonallergic rhinitis; nasal irrigation—removes triggers and prevents changes that cause symptoms; Waterpik with nasal irrigator; ceramic Neti pots for saline; “hose in the nose” (disposable enema bucket filled with 2 tsp of salt, 1 tsp of baking soda, and 1 qt of warm water; washes triggers off nasal mucosa); nasal steroids—indicated in all types of rhinitis; better than antihistamines for true allergic rhinitis, but patients often reluctant to use; no good supporting evidence for homeopathic therapy (eg, acupuncture, herbal remedies; patients who appear to improve should not be discouraged); intranasal steroids, astelazine, and decongestants for nonallergic rhinitis
Treatment of rhinitis medicamentosa: eg, oxymetazoline (Afrin); topical steroids can be initiated bilaterally while discontinuing decongestant in one nostril (after 7-10 days, stop and treat other nostril); 1-wk tapered steroid dose; evaluate underlying cause of rhinitis
Diseases associated with rhinitis: asthma (treating sinusitis helps control asthma); otitis media with effusion; upper respiratory infections; polyposis
Reasons to consider immunotherapy: drugs highly effective, but provide only symptomatic treatment; immunotherapy alters natural course of disease; allergy treatment (including sublingual immunotherapy) in monosensitized children prevents development of new sensitizations; allergy vaccination or sublingual immunotherapy may prevent onset of asthma in patients with rhinoconjunctivitis
Indications for allergy testing and immunotherapy: inadequate control of symptoms with avoidance and pharmacotherapy; prolonged or recurrent symptoms; intolerable side effects from medication; desire for long-lasting control without medication; to decrease possibility of developing other new sensitizations or asthma; contraindications—short season (ie, patient can be treated with antihistamines for 4-8 wk or steroid injections that cover through spring or fall); well controlled asthma; patients with cardiovascular disease; patients on β-blocking drugs or levobunolol (Betagan Liquifilm); patients with severe uncontrolled asthma (FEV1 should be 70% of best effort [not predicted]); patients with severe immunodeficiency disease; pregnancy—do not start immunotherapy in newly pregnant patients; if patient becomes pregnant while on immunotherapy (at baseline or on maintenance dose), continue immunotherapy through pregnancy
Allergy screening: use 6 to 10 allergens to determine presence of allergy; same allergens common in patients in same geographic area; testing for allergies to most common tree, grass, and weed pollens, mold, house dust mites, and cats identifies 90% of allergic patients; interpreting results—if all tests negative except for positive control (histamine), patient has hypoactive skin (most likely due to antihistamine); discontinue antihistamine for 7 to 10 days and retest, or perform in vitro testing (eg, radioallergosorbent testing [RAST]); if tests for grass, tree, or weed pollens or mold allergens positive, test for all local allergens (36-46 additional allergens); if tests for house dust mite or cat only positive results, no further testing required (counsel patient about avoidance; consider immunotherapy); advantages— differentiates allergic patient from nonallergic patient; eliminates need for unnecessary testing; helps determine pharmacotherapy; identifies allergens to avoid; cost-effective; reliable
Objective allergy testing: nasal cytology—identifies patients with nonallergic rhinitis-eosinophilia syndrome (NARES); useful for patients who present with allergy symptoms and negative allergy test results; individual skin prick testing—Duotip-Test; Morrow Brown needle; GreerPick; multiple antigen applicators; Multi-Test; QUINTEST; before testing, educate patients about type of testing and time involved in testing and immunotherapy programs; discuss potential for local and systemic side effects, rare possibility of anaphylaxis, and risk for death from allergy vaccinations; document and obtain consent

Educational Objectives

The goal of this program is to educate the listener about asthma in children and adolescents and about allergic rhinitis. After hearing and assimilating this program, the participant will be better able to:
1. Classify severity of asthma in children.
2. Select appropriate treatment for asthma, based on severity and clinical findings.
3. Distinguish allergic rhinitis from nonallergic rhinitis.
4. Select patients with allergies who may benefit from immunotherapy.
5. Administer appropriate tests to identify and manage allergies.

Discussed on This Program

Albuterol (salbutamol sulphate in United Kingdom) [several trade names]
Azelastine HCl [Astelin, Optivar]
Cromolyn sodium [several trade names]
Dexamethasone [several trade names]
Fluticasone propionate [several trade names]
Fluticasone propionate/salmeterol [Advair Diskus]
Influenza virus vaccine [Fluarix, FluMist, Fluvirin, Fluzone]
Ipratropium bromide [Atrovent]
Levalbuterol HCl [Xopenex, Xopenex HFA]
Levobunolol hydrochloride [AKBeta, Betagan Liquifilm]
Mometasone furoate [Elocon, Asmanex Twisthaler]
Montelukast sodium [Singulair]
Oxymetazoline HCl [several trade names]
Prednisolone [several trade names]
Prednisone [several trade names]
Theophylline [several trade names]

Suggested Reading

Amirav I et al: Aerosol therapy with valved holding chambers in young children: importance of the facemask seal. Pediatrics 108:389, 2001; Dell S et al: Breastfeeding and asthma in young children: findings from a population-based study. Arch Pediatr Adolesc Med 155:1261, 2001; Dykewicz MS et al: Diagnosis and management of rhinitis: complete guidelines of the Joint Task Force on Practice Parameters in Allergy, Asthma and Immunology. American Academy of Allergy, Asthma, and Immunology. Ann Allergy Asthma Immunol 81:478, 1998; Halterman JS et al: Benefits of a school-based asthma treatment program in the absence of secondhand smoke exposure: results of a randomized clinical trial. Arch Pediatr Adolesc Med 158:460, 2004; Johnstone DE: Immunotherapy in children: past, present, and future. (Part I). Ann Allergy 46:1, 1981; Lozano P et al: A multisite randomized trial of the effects of physician education and organizational change in chronic-asthma care: health outcomes of the Pediatric Asthma Care Patient Outcomes Research Team II Study. Arch Pediatr Adolesc Med 158:875, 2004; Moller C et al: Pollen immunotherapy reduces the development of asthma in children with seasonal rhinoconjunctivitis (the PAT-study). J Allergy Clin Immunol 109:251, 2002; Passalacqua G et al: Long-lasting clinical efficacy of allergen specific immunotherapy. Allergy 57:275, 2002; Qureshi F et al: Comparative efficacy of oral dexamethasone versus oral prednisone in acute pediatric asthma. J Pediatr 139:20, 2001; Smith AD et al: Use of exhaled nitric oxide measurements to guide treatment in chronic asthma. N Engl J Med 352:2163, 2005.

Faculty Disclosure

In adherence to ACCME guidelines, the Audio-Digest Foundation requests all lecturers to disclose any significant financial relationship with the manufacturer or provider of any commercial product or service discussed. The following has been disclosed: Dr. Hedges is on the Speakers’ Bureau and has received honoraria from Antigen Laboratory. Dr. Hedges also provides testing materials to Lincoln Diagnostics for hands-on testing courses.


Drs. Irons and Hedges spoke in Washington, DC, at the 2006 Scientific Assembly, presented September 27 to October 1, 2006, by the American Academy of Family Physicians (AAFP). The Audio-Digest Foundation thanks the speakers and the AAFP for their cooperation in the production of this program.


Reproduction of this summary in whole or in part in any form or medium without express written permission is prohibited.

If, after reviewing this written summary, you would like to hear the contents and/or earn CME/CE credit:

View Main Program Listing

Visit Audio-Digest Home Page