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香港儿童闭塞性细支气管炎 20 年病例系列研究。

Childhood bronchiolitis obliterans in Hong Kong-case series over a 20-year period.

机构信息

Department of Paediatrics, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong.

Department of Paediatrics and Adolescent Medicine, Tuen Mun Hospital, Tuen Mun, Hong Kong.

出版信息

Pediatr Pulmonol. 2021 Jan;56(1):153-161. doi: 10.1002/ppul.25166. Epub 2020 Nov 24.

Abstract

BACKGROUND AND OBJECTIVE

Bronchiolitis obliterans (BO) is a rare but serious condition. The natural history and outcomes remain poorly understood. In this clinical review, we aimed to describe the clinical characteristics and outcomes of children diagnosed with BO in Hong Kong (HK).

METHODS

This was a retrospective study of pediatric patients with BO under the care of six respiratory units in HK from January 1996 to December 2015. Information was retrieved from medical records.

RESULTS

Fifty-six patients were included with a male predominance (67.9%). The median age at diagnosis was 1.98 years (interquartile range [IQR]: 0.84-4.99 years). Postinfectious BO (PIBO) was the commonest cause (64.3%) followed by posthematopoietic stem-cell transplant (21.4%). Adenovirus (63.2%) was the commonest causative pathogen among PIBO. The median follow-up duration was 9.7 years (IQR: 2.9-14.3 years). Twenty-five patients (44.6%) could achieve symptom-free recovery at the time of follow-up. Five (8.9%) and three (5.4%) were oxygen or ventilator dependent, respectively. There were two deaths, both had posttransplant BO. Patients who developed BO after transplant had significantly worse lung function than those with PIBO. There were no risk factors significantly associated with worse clinical outcomes (oxygen/ventilator dependence or death) by logistic regression. Among patients with PIBO, coinfection at presentation was significantly associated with persistent symptoms at follow-up (p = .028).

CONCLUSIONS

The most common cause of childhood BO in HK is postinfectious and coinfection at presentation was associated with persistent symptoms at follow-up. Further studies are needed to better elucidate disease progression, treatment options and long term outcomes.

摘要

背景与目的

闭塞性细支气管炎(BO)是一种罕见但严重的疾病,其自然史和结局仍知之甚少。在本次临床综述中,我们旨在描述在香港(HK)确诊为 BO 的儿童的临床特征和结局。

方法

这是一项对 1996 年 1 月至 2015 年 12 月在 HK 六家呼吸科接受治疗的 BO 儿科患者进行的回顾性研究。信息从病历中提取。

结果

共纳入 56 例患者,其中男性居多(67.9%)。中位诊断年龄为 1.98 岁(四分位距 [IQR]:0.84-4.99 岁)。感染后 BO(PIBO)是最常见的病因(64.3%),其次是造血干细胞移植后(21.4%)。腺病毒(63.2%)是 PIBO 中最常见的病原体。中位随访时间为 9.7 年(IQR:2.9-14.3 年)。25 例(44.6%)在随访时可无症状恢复。5 例(8.9%)和 3 例(5.4%)分别需要吸氧和呼吸机支持。有 2 例死亡,均为移植后 BO。移植后发生 BO 的患者肺功能明显较 PIBO 患者差。Logistic 回归未发现与临床结局(需氧/呼吸机依赖或死亡)相关的显著危险因素。在 PIBO 患者中,就诊时合并感染与随访时持续存在症状显著相关(p=0.028)。

结论

HK 儿童 BO 的最常见病因是感染后,就诊时合并感染与随访时持续存在症状显著相关。需要进一步研究以更好地阐明疾病进展、治疗选择和长期结局。

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