The Clinical Respiratory Journal (Sep 2023)

Etiology and clinical features of children with bronchiectasis in China: A 10‐year multicenter retrospective study

  • Hao Wang,
  • Bao‐ping Xu,
  • Yan‐min Bao,
  • Yungang Yang,
  • Li‐ling Qian,
  • Hai‐lin Zhang,
  • Chun‐mei Zhu,
  • Yong Yin,
  • Min Jiang,
  • Ji‐hong Dai,
  • Yong‐sheng Xu,
  • Xiao‐hua Zhu,
  • Xiao‐ping Zhu,
  • Kun‐ling Shen

DOI
https://doi.org/10.1111/crj.13630
Journal volume & issue
Vol. 17, no. 9
pp. 841 – 850

Abstract

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Abstract Introduction The current study aims to investigate the etiology spectrum and the clinical characteristics of bronchiectasis in Chinese children. Methods The study is designed as a multicenter retrospective study. 193 cases were enrolled in 13 centers in China between 2008 and 2017. The inclusive cases must meet the clinical as well as the HRCT criteria. Only if both two radiologists confirmed the diagnosis, the case could be enrolled. The cases that could not provide clinical and imageology data were excluded. The data were entered into the specialized system and then analyzed. Results One hundred sixty‐nine cases (87%) were found to have the underlying etiology. Post‐infective (46%), primary immunodeficiency (14%), and PCD (13%) were the common causes. All cases came from 28 provinces in Mainland China. The median age of symptom onset was 5.8 (2.0, 8.9) years. The median age of diagnosis was 8.4 (4.5, 11.6) years. The main symptoms were cough, sputum expectoration, and fever during the exacerbation. Nineteen percent of patients suffered from limited exercise tolerance. Clubbing was found in 17% of cases. Nearly 30% of patients presented growth limitations. On the HRCT findings, 126 cases had diffused bronchiectasis, and bilateral involvement was found in 94 cases. The lower lobes and right middle lobes were most commonly involved. Approximately 30% of cultures of sputum and bronchoalveolar lavage were positive. Conclusion A majority of cases could be found the underlying etiology. Post‐infective, primary immunodeficiency, and PCD were the most common causes. Some clinical figures might indicate a specific etiology.

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