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Summary
The child who has recurrent infections poses one of the most difficult diagnostic challenges in pediatrics. The outcome may be anything from reassurance that the child is normal to the diagnosis of a life-threatening condition. A huge range of tests is available (Box 9). Box 9. Summary of potential investigations in the child who has recurrent infections Suspected CF Sweat test CF genotype Electrical potentials (nasal, bronchial, rectal biopsy) Supportive tests (eg, human fecal elastase-1) Suspected PCD Screening: saccharine test, nasal nitric oxide Ciliary structure and function: high-speed videomicroscopy, electron microscopy Culture of ciliary biopsy Genetic studies Immunostaining of specific dynein proteins Screening for suspected immune deficiency (referral to a pediatric immunologist mandatory for most specific immunodeficiencies) Full blood cell count (neutropenia, lymphopenia) T-cell subsets Immunoglobulins Immunoglobulin subclasses Vaccine antibody responses Complement studies HIV test Suspected gastroesophageal reflux pH-metry Impedance probe Isotope milk scan Barium swallow (exclude anatomic causes such as hiatus hernia) Esophageal manometry Suspected incoordinated swallowing Videofluoroscopy Rigid endoscopy to exclude laryngeal cleft Suspected aspiration HRCT scan: dependant bronchocentric consolidation (not specific) Lipid-laden macrophages (absence probably excludes significant aspiration) BAL pepsin (gastric contents) Suspected structural esophageal disease Tube esophagram Bronchoscopy (H-type fistula) Barium swallow Suspected structural airway disease Bronchoscopy Endobronchial ultrasound CT reconstruction Suspected bronchiectasis HRCT scanning Exclude CF, PCD, immunodeficiency, tuberculosis (see other sections) Consider excluding esophageal disease, incoordinated swallowing, reflux, and aspiration Echocardiogram, overnight saturation studies Suspected tuberculosis See Box 8 Suspected cardiovascular disease Echocardiogram (enlarged cardiac chambers caused by left-to-right shunt, vascular ring) Barium swallow (vascular ring) CT or MRI with vascular reconstruction (vascular ring) Suggested vasculitis or connective tissue disease (referral to pediatric rheumatologist probably is advisable) Erythrocyte sedimentation rate, C-reactive protein Double-stranded DNA Rheumatoid factor Antineutrophil cytoplasmic antibody studies Circulating immune complexes Anti-glomerular basement membrane antibodies The clinician faces a twofold challenge in determining: 1. Is this child normal? (This question may be the most difficult in all clinical practice.) 2. If this child seems to have a serious disease, how can the diagnosis be confirmed or excluded with the minimum number of the least-invasive tests? It is hoped that, in the absence of good-quality evidence for most clinical scenarios, the experience-based approach described in this article may prove a useful guide to the clinician. |