Elsevier

The Journal of Pediatrics

Volume 132, Issue 2, February 1998, Pages 312-318
The Journal of Pediatrics

Clinical utility of flexible bronchoscopy and bronchoalveolar lavage in young children with recurrent wheezing,☆☆,

Presented in part at the Annual Meeting of the Southern Society for Pediatric Research, Jan. 31-Feb. 2, 1996, and at the Annual Meeting of the American Thoracic Society, May 11-15, 1996.
https://doi.org/10.1016/S0022-3476(98)70451-2Get rights and content

Abstract

Objective: The objective of this study was to determine in young children with recurrent wheezing poorly responsive to bronchodilator therapy whether flexible bronchoscopy (FB) and bronchoalveolar lavage (BAL) provide clinically useful information, whether age-specific differences are present in bronchoscopic and BAL fluid (BALF) findings, and whether differential cellular analysis of BALF is useful in suggesting an infectious or inflammatory process. Study design: This was a retrospective case series with descriptive and analytical components. The study population included children referred to a large tertiary care children's hospital subspecialty service for further evaluation of recurrent wheezing. Clinical and demographic data and findings of FB and BALF studies were collected from chart review. For purposes of data analysis patients were divided into 0- to 6-, 7- to 12-, and 13- to 18-month age groups. Results: Thirty otherwise healthy children, 0 to 18 months of age with recurrent wheezing, who had undergone FB were identified; and 28 were found to have positive diagnostic findings. Airway abnormalities were found in 17 (57%) and tended to be more common in the 0- to 6-month age group. In the 27 who also had BAL performed, 3 (11%) had a positive bacterial culture, 9 (33%) a positive viral culture, and 5 (19%) an elevated lipid-laden macrophage index suggesting aspiration. Differential cellular analysis was abnormal in 11 (41%), a finding that was significantly associated with a positive bacterial culture, a positive viral culture, or an elevated lipid-laden macrophage index. Conclusions: In this population of young children with recurrent wheezing poorly responsive to bronchodilator therapy, FB and BAL yielded useful diagnostic findings in most children studied. In addition, in the presence of an infectious or inflammatory process, differential cellular analysis of BALF revealed an increased percentage of neutrophils. (J Pediatr 1998;132:312-8)

Section snippets

Study Population

All children who underwent FB with or without BAL between July 1993 and August 1995 for the primary indication of recurrent wheezing were identified from local flexible airway endoscopy and bronchoalveolar lavage databases. Demo- graphic and clinical data were obtained from retrospective chart review. Patients were included for further analysis if they were 0 to 18 months of age and had recurrent episodes of wheezing that were clinically refractory or poorly responsive to inhaled albuterol.

Patient Demographic and Clinical Characteristics

A total of 48 children were identified who had undergone FB for the primary indication of recurrent wheezing between July 1993 and August 1995, and 30 of the 48 children met the inclusion criteria. All 30 patients had received inhaled albuterol, and all had a history of recurrent wheezing for greater than 1 month. Secondary indications for FB included poor response to inhaled cromolyn or nedocromil (n = 16), poor response to inhaled corticosteroids (n = 3), poor response to one or more courses

Discussion

Our results indicate that in a selected group of otherwise healthy children 0 to 18 months of age with recurrent wheezing that was poorly responsive to bronchodilator therapy, FB and BAL yielded clinically useful information that led to therapeutic changes in most of the patients. In agreement with previous reports, we found airway abnormalities in most of our patients.6, 7, 8 However, the inverse relationship of age to the occurrence of airway abnormalities in young children with recurrent

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    From the Departments of Pediatrics and Pathology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.

    ☆☆

    Reprint requests: Dennis E. Schellhase, MD, Arkansas Children's Hospital, Department of Pediatrics, Pulmonary Medicine Section, 800 Marshall St., Little Rock, AR 72202-3591.

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