Watson Clara, Han Dug Yeo, Byrnes Catherine A, Hamill James, Morreau Philip, Edwards Elizabeth
Paediatric Registrar, Starship Children's Hospital, Auckland, New Zealand.
Department of Clinical Research, Starship Children's Hospital, Auckland, New Zealand.
J Paediatr Child Health. 2025 Mar;61(3):491-498. doi: 10.1111/jpc.16775. Epub 2025 Jan 30.
Surgical management for bronchiectasis is uncommon. This study reviewed the experience of bronchiectasis surgery and subsequent outcomes at a tertiary paediatric centre over a 20 year period.
Retrospective audit of children aged < 18 years who underwent bronchiectasis surgery at Starship Children's Hospital between 2001 and 2021. Cases were identified from clinical coding, with demographics, pre-operative investigations and outcomes obtained from clinical records.
Nineteen children (11 females, 42% Pasifika, 26% Māori and 26% New Zealand European) were included. Mean age of bronchiectasis diagnosis was 6.3 years (range 2.1-13.9 years) and mean age of surgery was 8.5 years (range 2.6-15.9 years). Indications for surgery included localised bronchiectasis (n = 7), main burden of multilobar disease in one lobe (n = 5) and persistent lobar collapse (n = 3). Pre-operative investigations included chest computerised tomography scan (68%), bronchoscopy (37%) and overnight oximetry (42%). One child underwent documented pre-operative clinical optimisation. For children with bronchiectasis < 5 years (n = 11), 81% demonstrated improved symptoms, 9% were unchanged and 9% deteriorated. All children with bronchiectasis > 5 years had symptomatic improvement. The mean number of daily symptoms decreased by 2.4 (p < 0.0001).
Lobectomy resulted in significant symptomatic improvement in 89% of children. However, pre-operative work-up was variable. The study highlights the importance of establishing a protocol for identification of children with bronchiectasis who would benefit from surgery and developing a consistent preparatory approach to ensure optimal and equitable outcomes.
支气管扩张症的外科治疗并不常见。本研究回顾了一家三级儿科中心在20年期间进行支气管扩张症手术的经验及后续结果。
对2001年至2021年期间在星际儿童医院接受支气管扩张症手术的18岁以下儿童进行回顾性审计。通过临床编码识别病例,并从临床记录中获取人口统计学信息、术前检查和结果。
纳入了19名儿童(11名女性,42%为太平洋岛民,26%为毛利人,26%为新西兰欧洲人)。支气管扩张症诊断的平均年龄为6.3岁(范围2.1 - 13.9岁),手术的平均年龄为8.5岁(范围2.6 - 15.9岁)。手术指征包括局限性支气管扩张(n = 7)、一个肺叶多叶病变的主要负担(n = 5)和持续性肺叶塌陷(n = 3)。术前检查包括胸部计算机断层扫描(68%)、支气管镜检查(37%)和夜间血氧饱和度测定(42%)。一名儿童接受了记录在案的术前临床优化。对于支气管扩张症<5岁的儿童(n = 11),81%症状改善,9%无变化,9%恶化。所有支气管扩张症>5岁的儿童症状均有改善。每日症状的平均数量减少了2.4(p < 0.0001)。
肺叶切除术使89%的儿童症状得到显著改善。然而,术前检查存在差异。该研究强调了制定一个方案以识别能从手术中获益的支气管扩张症儿童,并制定一致的准备方法以确保获得最佳和公平结果的重要性。