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The editor gratefully acknowledges contributions by Drs. Robert W. Wilmott, Bradley A. Becker, Ellen R. Kaplan, Carlos R. Perez, William D. Hardie, Barbara A. Chini, and Cori L. Daines that were retained from previous editions of Pediatric Secrets .
Very common . Ten percent to 30% of children and adults in the developed world experience allergic rhinitis, which is the most common manifestation of allergic disease and one of the most common chronic diseases of childhood.
“Allergic facies”: Open mouth, midface hypoplasia
“Allergic nasal crease”: Nasal crease on bridge of the nose as a result of chronic upward rubbing with the palm of the hand (the “allergic salute”)
Diminished sense of taste and smell
Dental malocclusion
Allergic “shiners” (dark circles under the eyes)
Multiple infraorbital folds
Cobblestoning of the posterior oropharynx ( Fig. 16.1 )
Pale, boggy appearance of the nasal mucosa
Tharpe CA, Kemp SF. Pediatric allergic rhinitis. Immunol Allergy Clin North Am. 2015;35(1):185–198.
Male gender (females have a higher incidence of rhinitis in adulthood)
Not having early contact with siblings at home or children in day care
Not having early contact with pets or not living on a farm
Matheson MC, Dharmage SC, Abramson MJ, et al. Early-life risk factors and incidence of rhinitis: results from the European Community Respiratory Health Study—An international population-based cohort study. J Allergy Clin Immunol. 2011;128(4):816–823.
Tree pollen is usually associated with the onset of the growing season. After local tree pollination, grass pollens appear; this may occur earlier in locales where there are short winters. Weed pollen other than ragweed is associated with the late-summer pollen peak. In the autumn, ragweed is the major pollen allergen. It pollinates from mid-August until the first freeze in most of the United States. Counts are especially high in eastern and central North America. Fungal aeroallergens span the growing season. Relative concentrations of household animal allergens, dust mites, and indoor fungi generally increase when doors and windows are closed. However, dust mites and molds proliferate in areas of high humidity and may cause perennial symptoms.
Naclerio R, Solomon W. Rhinitis and inhalant allergens. JAMA. 1997;278(22):1842–1848.
A patient is taking a medication that blocks allergy skin testing, such as an antihistamine that cannot be stopped for at least 3 days.
A patient has a skin condition such as eczema or psoriasis without sufficient unaffected areas to do skin testing.
Blood testing would be better tolerated, such as in an infant or young child.
American College of Allergy, Asthma and Immunology. www.acaai.org . Accessed March 11, 2020.
In vitro tests
No risk for anaphylaxis
Results not influenced by medications (e.g., antihistamines), dermatographism, or extensive dermatologic disease
More costly
Better predictive value for some common food allergens
Skin testing
Less costly
More sensitive than in vitro tests
Results immediately available
Environmental control measures for allergen avoidance are the mainstay of treatment. Relevant allergens are recommended for exposure reduction on positive skin or serum-specific IgE testing correlated with the presence of symptoms on allergen exposure.
Pharmacotherapy , including nasal corticosteroid sprays, antihistamines (given orally or by nasal spray), oral antileukotrienes, or combinations of these medications are effective treatments.
Immunotherapy is reserved for those with persistent symptoms despite the previous treatment and for those who want control of symptoms with fewer medications.
American Academy of Allergy, Asthma and Immunology. www.aaaai.org . Accessed March 11, 2020.
History (symptoms, family history, and worsening with environmental exposure) is the key to diagnosis.
With two atopic parents, the risk to the child is 50% to 70%.
Sensitivity of testing ranks as follows: intradermal (may yield false-positive results) > skin prick > in vitro allergen-specific IgE quantification.
IgE ImmunoCAP testing is indicated in patients with severe skin disorders or those unable to temporarily discontinue H 1 -blocking antihistamines.
Allergic features include shiners (dark circles under eyes), increased infraorbital folds, transverse nasal bridge crease, boggy pale-blue nasal mucosa, and cobblestoning of conjunctiva and posterior oropharynx.
Immunotherapy should be considered when allergen avoidance and pharmacotherapy have produced suboptimal results.
House dust mites (HDMs), animal dander , cockroach , and molds .
Allergens from HDMs are among the most common triggers for allergic rhinitis and asthma. They are found throughout homes, but accumulate in bedding, soft furnishings, and carpet. HDM allergen reduction methods include the following:
Encasing pillows, mattresses, and box springs in allergen-proof, zippered covers (plastic or fine woven fabric). Although not effective as a single measure, there is evidence these covers may be of benefit when used as part of an extensive bedroom-based dust mite allergen reduction program.
Bedding may be washed in hot (131°F [55°C]) water. Drying the bedding in high heat in a dryer is an alternative that may prevent scalding injuries in children from having the water heater temperature raised above 120°F (50°C).
Humidity should be reduced indoors to ≤ 45% using a dehumidifier and/or air conditioning with the windows closed.
Wall-to-wall carpeting should be removed as much as possible and replaced with throw rugs. These should be regularly washed or dry-cleaned.
Wilson JM, Platts-Mills TAE. Home environmental interventions for house dust mite. J Allergy Clin Immunol Pract. 2018;6(1):1–7.
Sheikh A, Hurwitz B, Nurmatov U, et al. House dust mite avoidance measures for perennial allergic rhinitis. Cochrane Database Syst Rev. 2010;(7):CD001563.
Remove upholstered furniture, carpet, and other sources harboring the allergen.
Use high-efficiency particulate air (HEPA) filters and vacuum cleaners.
Wash the cat regularly if feasible.
Consider a “felinectomy.”
Alas, the hypoallergenic dog appears to be a myth . Although certain dogs (e.g., poodles, Spanish waterdogs, Airedale terriers, and a hybrid, the Labradoodle) are commonly marketed as “hypoallergenic,” comparison of the quantity of the dog allergen (Can f 1, an allergen specific to dogs) in hair and coat samples and in the surrounding surface environment found no differences compared with control breeds. In the United States, about 78 million dogs occupy homes, so this is not good news to the 20% of the general population who may be allergic to dogs.
Vredegoor DW, Willemse T, Chapman MD, et al. Can f 1 levels in hair and homes of different dog breeds: lack of evidence to describe any dog breed as hypoallergenic. J Allergy Clin Immunol. 2012;130(4):904-909.e7.
Allergen immunotherapy is an effective treatment for allergic rhinitis, asthma, and the prevention of venom anaphylaxis. It also may be of benefit in atopic dermatitis. For allergic rhinitis and allergic asthma, immunotherapy should be considered in patients who (1) are not well controlled despite attempts at allergen exposure reduction and pharmacotherapy or (2) in patients who wish to take less medication. Subcutaneous or sublingual routes (for certain inhalant allergens) are approved in the United States. In children, immunotherapy has been shown to prevent the progression of allergic rhinitis to asthma and may prevent sensitization to new allergens in monosensitized individuals.
Berings M, Karaaslan C, Altunbulakli C, et al. Advances and highlights in allergen immunotherapy: on the way to sustained clinical and immunological tolerance. J Allergy Clin Immunol. 2017;150(5):1250–1267.
Exercise is a trigger of bronchoconstriction in 40% to 50% of children with allergic rhinitis compared with 90% of those diagnosed with asthma and 10% of those not known to have asthma or respiratory allergies. EIB (also known as exercise-induced bronchospasm ) is defined as a 10% drop in FEV 1 from the value before exercise.
Randolph C. Exercise-induced bronchospasm in children. Clinic Rev Allerg Immunol. 2008;34(2):205–216.
Innate immunity : intrinsic tendency of individual immune system to respond in a certain pattern; specifically to produce Th2 cytokines rather than Th1 in response to a given stimulus
Genetics : asthma has a heritable component, but the genetics are complex; although several loci have been implicated, none account for a substantial proportion of disease
Environmental : two major factors have been identified in the development and persistence of asthma: aeroallergens (particularly sensitization and exposure to dust mites and Alternaria mold) and viral infections (e.g., respiratory syncytial virus [RSV], rhinovirus). Other, less well-established environmental influences in the development of asthma include tobacco smoke, air pollution, and obesity.
National Asthma Education and Prevention Program: Expert Panel Report III. Guidelines for the diagnosis and management of asthma. www.nhlbi.nih.gov . Accessed June 20, 2019.
About 50% of childhood asthma develops before the age of 3 years, and nearly all has developed by the age of 7 years. The signs and symptoms of asthma, including chronic cough, may be evident much earlier than the actual diagnosis, but may be erroneously attributed to recurrent pneumonia.
American Lung Association. www.lungusa.org . Accessed May 19, 2019.
Although about one-third of children will have an episode of wheezing before they are 1 year of age, most (80%) do not develop persistent wheezing after age 3 years. Risks factors for persistence include the following:
Positive family history of asthma (especially maternal)
Increased IgE levels
Atopic dermatitis
Rhinitis not associated with colds
Secondhand smoke exposure
Taussig LM, Wright AL, Holberg CJ, et al. Tucson Children’s Respiratory Study: 1980 to present. J Allergy Clin Immunol. 2003;111(4):661–675.
Seasonal nature with concurrent rhinitis (suggesting pollen)
Symptoms worsen when visiting a family with pets (suggesting animal dander)
Wheezing occurs when carpets are vacuumed or bed is made (suggesting mites)
Symptoms develop in damp basements or barns (suggesting molds)
Upper airway infections (rhinitis, sinusitis)
Cold air
Weather changes
Exercise
Environmental (pollutants, cigarette smoke)
Irritants (strong odors, paint fumes, chlorine)
Emotional extremes (stress, fear, crying, laughing)
Medications (nonsteroidal anti-inflammatory drugs, aspirin, beta blockers)
Foods, food additives
Gastroesophageal reflux disease
Hormonal (menstrual, premenstrual)
American Academy of Allergy, Asthma and Immunology. www.aaaai.org . Accessed March 11, 2020.
EIB is condition in which there is an acute onset of bronchoconstriction that typically occurs after (sometimes during) exercise. Five percent to 20% of the general population may have EIB compared with up to 90% of those diagnosed with symptomatic persistent asthma. Symptoms are most commonly cough (although these can include wheezing, chest tightness, and unusual shortness of breath or excess mucus) with a peak 5 to 10 minutes after the conclusion of exercise and with resolution within 30 to 60 minutes.
Weiler JM, Brannan JD, Randolph CC, et al. Exercise-induced bronchoconstriction update—2016. J Allergy Clin Immunol. 2016;138(5):1292–1295.e36.
Exercise challenge is the preferred method. EIB is likely if the peak flow rate or FEV 1 drops by 10% after 6 minutes of vigorous exercise, either in a laboratory or field setting. This exercise can include jogging on a motor-driven treadmill (15% grade at 3 to 4 mph), riding a stationary bicycle, or running up and down a hallway or around a track in field testing. The greatest reduction in FEV 1 is usually seen 5 to 10 minutes after exercise. As further verification of the diagnosis, if the patient has developed a decreased peak flow (and possibly wheezing), two puffs of a beta-2 agonist should be administered to attempt to reverse the bronchospasm.
Aggarwal B, Mulgirigama A, Berend N. Exercise-induced bronchoconstriction: prevalence, pathophysiology, patient impact, diagnosis and management. NPJ Prim Care Respir Med. 2018;28(1):31.
The leading theory is an osmotic one. Increased ventilation during the hyperventilation of exercise (especially in dry air) causes water loss from airway surfaces through evaporation. This reduction in epithelial liquid volume causes osmotic changes, which in turn lead to mast cell degranulation. Mast cells release prostaglandins (especially prostaglandin D2), leukotrienes, histamine, and tryptase. Many of these are signaling molecules, which mediate airway smooth muscle contraction and increase mucus production, microvascular permeability, and sensory nerve activation. The release of these mast cell components, initially generated by osmotic changes, are thought to be the main stimulus for bronchoconstriction and airway edema.
Aggarwal B, Mulgirigama A, Berend N. Exercise-induced bronchoconstriction: prevalence, pathophysiology, patient impact, diagnosis and management. NPJ Prim Care Respir Med. 2018;28(1):31.
Weiler JM, Brannan JD, Randolph CC, et al. Exercise-induced bronchoconstriction update—2016. J Allergy Clin Immunol. 2016;138(5):1292–1295.e36.
Eucapnic voluntary hyperventilation (EVH) involves breathing a dry gas at an increased respiratory rate in an effort to induce bronchospasm and a decrease of FEV 1 of > 10%.
Pharmacologic challenge by inhalation of agents that act on smooth muscle (e.g., methacholine or histamine) or osmotic provocation (mannitol). The threshold concentration required to induce bronchospasm (decline in FEV 1 by 20%) is determined and compared with that required in healthy controls.
Antigen challenge can be used for specific identification of a suspected allergen or occupational trigger. This is done only at specialized centers and may require prolonged observation (> 24 hr) to identify and potentially treat a late-phase response.
Aspirin challenge is performed in patients with suspected aspirin-exacerbated respiratory disease (AERD) who have a medical indication for treatment with aspirin or nonsteroidal anti-inflammatory drugs (NSAIDs).
Leuppi JD. Bronchoprovocation tests in asthma: direct versus indirect challenges. Curr Opin Pulm Med. 2014;20(1):31–36.
Boulet LP, Gauvreau G, Boulay ME, et al. The allergen bronchoprovocation model: an important tool for the investigation of new asthma anti-inflammatory therapies. Allergy. 2007;62(10):1101–1110.
Exercise-induced laryngeal obstruction (EILO). This group of diagnoses includes vocal cord dysfunction and exercise-induced laryngomalacia . In the former, during exercise, the vocal cords adduct during inspiration to cause shortness of breath, chest tightness, cough, or stridor. In the latter, there is inspiratory prolapse of supraglottic structures, which causes dyspnea and/or stridor. In both cases, there is paradoxical laryngeal motion—narrowing occurs when a bigger breath is taken. The precise reasons are unclear but may be related to smaller airway dimensions, inhibition of laryngeal reflexes, or impaired innervation and/or power of the laryngeal muscles. The gold-standard test for diagnosis is flexible nasoendoscopy with continuous video recording of the larynx throughout exercise.
Nordang L, Norlander K, Walsted ES. Exercise-induced laryngeal obstruction—an overview. Immunol Allergy Clin North Am. 2018;38(2):271-280.
The main causes of airflow obstruction in acute asthma are airway inflammation , including edema , bronchospasm , and increased mucus production . Chronic inflammation may eventually result in airway remodeling, which may not be clinically apparent without pulmonary function testing.
Papi A, Brightling C, Pedersen SE, Reddel HK. Asthma. Lancet. 2018;391(10122):783–800.
Aspiration pneumonitis: especially in a neurologically impaired infant or an infant with gastroesophageal reflux, and especially if there is coughing, choking, or gagging with feedings. If there is a clear association with feedings, consider the possibility of a tracheoesophageal fistula.
Bronchiolitis obliterans: chronic wheezing often after infection (e.g., Mycoplasma or viral illnesses, especially adenovirus)
Bronchopulmonary dysplasia: especially if there has been prolonged oxygen therapy or a ventilatory requirement during the neonatal period
Ciliary dyskinesia: especially if recurrent otitis media, sinusitis, or situs inversus is present
Congenital malformations: including tracheobronchial anomalies, tracheomalacia, lung cysts, and mediastinal lesions
Cystic fibrosis (CF): if wheezing is recurrent and associated with failure to thrive, chronic diarrhea, or recurrent respiratory infections
Congenital cardiac anomalies: especially lesions with large left-to-right shunts
Foreign-body aspiration: if associated with an acute choking episode in an infant > 6 months
Vascular rings, slings, or airway compression
See Table 16.1 .
Symptoms and Signs | Initial PEF (or FEV 1 ) | Clinical Course | |
---|---|---|---|
Mild | Dyspnea only with activity (assess tachypnea in young children) | PEF ≥ 70% predicted or personal best |
|
Moderate | Dyspnea interferes with or limits usual activity | PEF 40%-69% predicted or personal best |
|
Severe | Dyspnea at rest; interferes with conversation | PEF < 40% predicted or personal best |
|
Subset: Life threatening | Too dyspneic to speak; perspiring | PEF < 25% predicted or personal best |
|
A chest radiograph should be considered for a first-time wheezing patient in the following situations:
Findings on physical examination that may suggest other diagnoses
Marked asymmetry of breath sounds (suggesting a foreign-body aspiration)
Suspected pneumonia
History suggestive of foreign-body aspiration
Hypoxemia or marked respiratory distress
Older child with no family history of asthma or atopy
Suspected congestive heart failure (CHF)
History of trauma that may have caused injury to the airway (e.g., burns, scalds, blunt or penetrating injury)
The most common finding is hypocapnia (i.e., low Pa co 2 ) because hypoxemia intensifies respiratory drive, resulting in hyperventilation (unless the child is being treated with oxygen). Hypercapnia is a serious sign that suggests the child is nearing respiratory failure. This finding should prompt consideration of ventilatory support by noninvasive means (bilevel positive airway pressure [BiPAP]) or endotracheal intubation and mechanical ventilation.
After therapy in the emergency department, admission is advisable if a child has any of the following:
Depressed level of consciousness
Incomplete response with moderate retractions and/or wheezing, peak flow of < 50% predicted, pulsus paradoxus of > 15 mm Hg, Sa o 2 of ≤ 90%, Pa co 2 ≥ 42 mm Hg
Breath sounds diminished significantly
Evidence of dehydration
Pneumothorax
Residual symptoms and history of severe attacks involving prolonged hospitalization (especially if intubation was required)
Parental unreliability
An equally difficult (and very unpredictable) challenge relates to predicting which patients will relapse after responding to therapy and subsequently require hospitalization. This is a major problem because rates of relapse in asthma can approach 20% to 30%.
General: hypoxemia, tachyphylaxis
Renal: hypokalemia
Cardiovascular: tachycardia, palpitations, premature ventricular contractions, atrial fibrillation
Neurologic: headache, irritability, insomnia, tremor, weakness
Gastrointestinal: nausea, heartburn, vomiting
Magnesium sulfate is a known smooth muscle relaxant most commonly used in the treatment of preeclampsia. In asthmatic patients, when used in conjunction with standard bronchodilators and corticosteroids, intravenous magnesium sulfate can provide additional bronchodilation, with a reduced likelihood of hospital admission. It is most commonly used when severely ill patients have failed to respond to conventional therapy. Inhaled magnesium sulfate as an adjuvant therapy in children is currently under study. Adult studies have demonstrated significant improvements in respiratory function and lower hospital admission rates.
Su Z, Li R, Gai Z. Intravenous and nebulized magnesium sulfate for treating acute asthma in children: a systematic review and meta-analysis. Ped Emerg Care. 2018;34(6):390–395.
Knightly R, Milan SJ, Hughes R, et al. Inhaled magnesium sulfate in the treatment of acute asthma. Cochrane Database Syst Rev. 2017;11:CD003898.
The National Heart, Lung, and Blood Institute and National Asthma Education and Prevention Program (NAEPP) define severity in terms of impairment and risk. Four categories are listed: intermittent , mild persistent , moderate persistent , and severe persistent . Categorization, which is also separately done for 0 to 4 years and ≥ 12 years, helps guide therapy ( Table 16.2 ).
National Asthma Education and Prevention Program Expert Panel Report 3. Guidelines for the Diagnosis and Management of Asthma. Full Report 2007 . Bethesda, MD: National Heart, Lung, and Blood Institute; 2007: NHLBI publication 08–4051.
Components of Severity | Classifying Asthma Severity and Initiating Therapy in Children | ||||||||
---|---|---|---|---|---|---|---|---|---|
Persistent | |||||||||
Intermittent | Mild | Moderate | Severe | ||||||
Ages 0-4 | Ages 5-11 | Ages 0-4 | Ages 5-11 | Ages 0-4 | Ages 5-11 | Ages 0-4 | Ages 5-11 | ||
Impairment | Symptoms | ≤ 2 days/week | > 2 days/week but not daily | Daily | Throughout the day | ||||
Nighttime awakenings | 0 | ≤ 2 ×/month | 1-2 ×/month | 3-4 ×/month | 3-4 ×/month | > 1 ×/week but not nightly | > 1 ×/week | Often 7 ×/week |
|
Short-acting beta-2 agonist use for symptom control | ≤ 2 days/week | > 2 days/week but not daily | Daily | Several times per day | |||||
Interference with normal activity | None | Minor limitation | Some limitation | Extremely limited | |||||
Lung function | N/A | Normal FEV 1 between exacerbations | N/A | > 80% >80% |
N/A | 60%-80% 75%-80% |
N/A | < 60% <75% |
|
|
> 80%
>85% |
||||||||
Risk | Exacerbations requiring oral systemic corticosteroids (consider severity and interval since last exacerbation) | 0-1/year | ≥ 2 exacerbations in 6 months requiring oral synthetic corticosteroids or ≥ 4 wheezing episodes/1 year lasting > 1 day and risk factors for persistent asthma. | ≥ 2 ×/year (see notes) Relative annual risk risk may be related to Fev 1 |
Inhaled corticosteroids. Daily administration significantly improves symptoms, reduces exacerbations, and allows healing of the chronic inflammatory changes that have taken place in the airways over time. Dosing and the use of adjunctive medications (e.g., long-acting inhaled beta-2 agonists, leukotriene-receptor antagonists) depend on frequency and severity of symptoms and exacerbations.
Ramadan AA, Gaffin JM, Israel E, Phipatanakul W. Asthma and corticosteroid responses in childhood and adult asthma. Clin Chest Med. 2019;40(1):163–177.
According to the NAEPP, optimal asthma care should cover all of the following domains:
Assessment and monitoring of symptoms
Education
Control of environmental factors and comorbidities
Review and adjustment of medications
National Asthma Education and Prevention Program. Expert Panel Report III: guidelines for the diagnosis and management of asthma. www.nhlbi.nih.gov . Accessed June 19, 2019.
Results are conflicting but tend to indicate that mild growth suppression occurs among children receiving moderate to high doses, particularly in children with more severe asthma and primarily during the first year of therapy (about 1 cm). The reduction in growth is generally not progressive. It is important that children who require the extended use of inhaled steroids are monitored for height and height velocity and for cataracts.
Wolfgram PM, Allen DB. Effects of inhaled corticosteroids on growth, bone metabolism, and adrenal function. Adv Pediatr. 2017;64(1):331–345.
Zhang L, Prietsch SO, Ducharme FM. Inhaled corticosteroids in children with persistent asthma: effects on growth. Cochrane Database Sys Rev. 2014;7:CD009471.
Kelly HW, Sternberg AL, Lescher R, et al. Effect of inhaled glucocorticoids in childhood on adult height. N Engl J Med. 2012;367(10):904–912.
Omalizumab is a humanized monoclonal anti-IgE antibody approved for adjunctive therapy of severe persistent asthma in patients aged 6 years and older with an elevated total IgE and sensitivity to perennial allergens. It prevents free serum IgE from binding to its high-affinity receptors on mast cells and basophils. Omalizumab has been shown to reduce asthma exacerbations. It should be considered as an add-on for children > 6 years of age who have inadequately controlled, severe, persistent allergic IgE-mediated asthma who require continuous or frequent oral corticosteroids. Rarely, symptoms of anaphylaxis may develop up to 24 hours after administration, so the clinician administering the drug should be prepared to treat anaphylaxis, and the patient should carry self-injectable epinephrine for 1 day after administration.
Corren J, Kavati A, Ortiz B, et al. Efficacy and safety of omalizumab in children and adolescents with moderate-to-severe asthma: a systematic literature review. Allergy Asthma Proc. 2017;38(4):250-263.
Normansell R, Walker S, Milan SJ, et al. Omalizumab for asthma in adults and children. Cochrane Database Syst Rev. 2014;1:CD003559.
There are no clear directions or guidelines for the use of complementary and alternative medicines for children with asthma, although these therapies are often independently used by families. Hypnosis, yoga, relaxation techniques, acupuncture, and massage have shown benefit in some studies, but a review of studies involving mind–body techniques, relaxation, manual therapies, and diet has found a tendency to little or no significant difference between sham (placebo) and active therapy.
Ricklefs I, Hohmann-Ebbers M, Herz A, Kopp MV. Use of complementary and alternative medicine in children with asthma. Pediatr Allergy Immunol. 2018;29(3):326–328.
Snyder J, Brown P. Complementary and alternative medicine in children: an analysis of the recent literature. Curr Opin Pediatr. 2012;24:539–546.
For the treatment of exacerbations of asthma, nebulizers are primarily used in children < 2 years of age because of the ease of administration. Although an MDI with a spacer is used more commonly among older children, several studies in emergency rooms indicate that they are equally or more effective than nebulizers among young children, even those with moderate or severe acute asthma. Furthermore, the MDI with a spacer requires less treatment time, has fewer side effects, and often preferred by patients and parents. Children < 5 years typically require a facemask attached to the MDI/spacer device.
Smith C, Goldman RD. Nebulizers versus pressurized metered-dose inhalers in preschool children with wheezing. Can Fam Physician. 2012;58(5):528–530.
Castro-Rodriguez JA, Rodrigo GJ. Beta-agonists through metered-dose inhaler with valved holding chamber versus nebulizer for acute exacerbation of wheezing or asthma in children under 5 years of age: a systematic review with meta-analysis. J Pediatr. 2004;145(2):776–779.
Spirometry is used for both the diagnosis and monitoring of asthma in children ≥ 5 years of age. The diagnosis of asthma requires airflow obstruction with at least a 12% improvement, or reversibility, in FEV 1 from baseline with the inhalation of a short-acting beta agonist. Patient history and physical examination do not adequately predict the degree of a patient’s airflow obstruction. Spirometry is also used to monitor asthma after diagnosis and treatment. The goals of asthma therapy include normal or near-normal lung function with treatment. Spirometry should be performed on the patient after treatment has been initiated or changed, based on abnormal lung function, to assess improvement. It should also be performed during periods of prolonged loss of asthma control. Otherwise, in symptomatically controlled patients, it should be repeated at least yearly to monitor the patient long term. Handheld peak flow measurements are useful for monitoring patients, but not for initial diagnosis.
National Asthma Education and Prevention Program. Expert Panel Report III: guidelines for the diagnosis and management of asthma. www.nhlbi.nih.gov . Accessed June 19, 2019.
Popular pediatric teaching has been that most children with asthma outgrow their symptoms. However, studies suggest that this is erroneous, and that only 30% to 50% become free of symptoms, primarily those with milder disease. Many children who appear to outgrow symptoms have recurrences during adulthood. Studies also indicate that many infants who wheeze with viral infections and are asymptomatic between illnesses tend to outgrow their asthma. Children with (1) early-onset asthma (age < 3 years) with a positive parental history for asthma, (2) atopic dermatitis, or (3) sensitization to aeroallergens are more likely to have persistent or recurrent bronchospasm. Although the overall trend is for asthma to become milder, a large percentage of adults have persistent obstructive disease, both recognized and unrecognized.
Link HW. Pediatric asthma in a nutshell. Pediatr Rev. 2014;35(7):287–297.
Sears MR, Greene JM, Willan AR, et al. A longitudinal, population-based, cohort study of childhood asthma followed to adulthood. N Engl J Med. 2003;349(15):1414–1422.
Allergic bronchopulmonary aspergillosis . This is a T-cell–mediated hypersensitivity response to Aspergillus fumigatus (a ubiquitous fungus) that can cause migrating pulmonary infiltrates and central bronchiectasis. The condition occurs as a complication primarily in patients with asthma and CF. Diagnosis relies on an abnormal chest radiograph and CT scan, skin prick reactivity to A. fumigatus , elevated total serum IgE > 417 IU/L, and positive serum antibodies to A. fumigatus (IgE and/or IgG).
Agarwal R, Sehgal IS, Dhooria S, Aggarwal AN. Developments in the diagnosis and treatment of allergic bronchopulmonary aspergillosis. Expert Rev Respir Med. 2016;10(12):1317–1334.
Greenberger PA, Bush RK, Demain JG, et al. Allergic bronchopulmonary aspergillosis. J Allergy Clin Immunol Pract. 2014;2(6):703–708.
Asthma is characterized by recurrent reversible airway obstruction and inflammation, often with identifiable triggers.
Typical abnormalities on spirometry include the following: decreased FEV 1 and FEV 1 /FVC ratio; increase in FEV 1 (> 12%) with bronchodilator.
Classification is based on frequency of symptoms and exacerbations; nighttime awakenings; limitation of normal activities; use of oral steroids; and lung function—intermittent, mild persistent, moderate persistent, and severe persistent.
Pa co 2 measurements that are normal (40 mm Hg) or rising in an asthmatic patient with tachypnea, or significant respiratory distress, are worrisome for evolving respiratory failure.
Signs of impending respiratory failure include severe retractions, accessory muscle use (especially sternocleidomastoids), decreased muscle tone, and altered mental status.
Bronchiolitis is a clinical diagnosis, identifying a syndrome that occurs in children under 2 years of age, characterized by upper respiratory symptoms (rhinorrhea), usually with fever, followed by lower respiratory tract signs (tachypnea, wheezing, crackles). This is typically caused by infection with a viral pathogen. In young children, the presentation may overlap with recurrent virus-induced wheezing and asthma.
Respiratory syncytial virus (RSV ) is estimated to cause 50% to 80% of cases of bronchiolitis in children. Up to 100,000 children are hospitalized annually in the United States as a result of this pneumovirus, which is different from—but closely related to—the paramyxoviruses. Disease most commonly occurs during outbreaks in winter or spring in the United States and during the winter months of July and August in the Southern Hemisphere. In the first 2 years of life, 90% of children will become infected with RSV and up to 40% will develop some lower respiratory disease. Other agents responsible for bronchiolitis include human metapneumovirus (second most common cause), parainfluenza virus, influenza virus types A and B, adenovirus, rhinovirus, and coronavirus.
Teshome G, Gattu R, Brown R. Acute bronchiolitis. Pediatr Clin North Am. 2013;60(5):1019–1034.
Hall CB, Weinberg GA, Iwane MK, et al. The burden of respiratory syncytial virus infection in young children. N Engl J Med. 2009;360(6):588–598.
The single best predictor at an initial assessment appears to be oxygen saturation , which can be determined by pulse oximetry. An Sa o 2 of < 95% correlates with more severe disease; a low Sa o 2 is often not clinically apparent, and objective measurements are necessary. An arterial blood gas with a Pa o 2 ≤ 65 mm Hg or a Pa co 2 of > 40 mm Hg is particularly worrisome. Other predictors of increased severity include the following:
An ill or “toxic” appearance
History of prematurity (gestational age < 34 weeks)
Atelectasis on chest radiograph
Respiratory rate of > 60 breaths per minute
Infant < 3 months old
Presentation with apnea
The picture is varied . Most commonly, there is hyperinflation of the lungs. About 25% of hospitalized infants have atelectasis or infiltrates. Bilateral interstitial abnormalities with peribronchial thickening are common, or patients may have lobar, segmental, or subsegmental consolidation that can mimic bacterial pneumonia. Bacteremia or secondary bacterial pneumonia, however, is unusual in patients with bronchiolitis. With the possible exception of atelectasis, the chest radiograph findings do not correlate well with the severity of the disease. American Academy of Pediatrics (AAP) clinical practice guidelines recommend against routine chest x-rays for evaluation of infants presenting with classic features of bronchiolitis, as unnecessary chest x-rays contribute to health care costs, radiation exposure, and antibiotic overuse and provide no clinical benefit. However, radiography in the evaluation of bronchiolitis continues to be overused.
Burstein B, Plint AC, Papenburg J. Use of radiography in patients diagnosed as having acute bronchiolitis in US emergency departments, 2007-2015. JAMA. 2018;320(15):1598–1600.
Ralston SL, Lieberthal AS, Meissner HC, et al. AAP clinical practice guideline: the diagnosis, management and prevention of bronchiolitis. Pediatrics. 2014;134(5):e1474–e1502.
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