Evidence map›Paper›PMID 39887574›Full record

ArticleJournal of paediatrics and child health2025

Surgery for Bronchiectasis: Experience and Outcomes at Starship Children's Hospital, Auckland, New Zealand.

Clara Watson, Dug Yeo Han, Catherine A Byrnes, James Hamill, Philip Morreau, Elizabeth Edwards

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Article in Journal of paediatrics and child health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Clara WatsonPaediatric Registrar, Starship Children's Hospital, Auckland, New Zealand.
Dug Yeo HanDepartment of Clinical Research, Starship Children's Hospital, Auckland, New Zealand.
Catherine A ByrnesDepartment of Respiratory Medicine, Starship Children's Hospital, Auckland, New Zealand.ORCID https://orcid.org/0000-0002-3032-3172
James HamillDepartment of Paediatric Surgery, Starship Children's Hospital, Auckland, New Zealand.
Philip MorreauDepartment of Paediatric Surgery, Starship Children's Hospital, Auckland, New Zealand.
Elizabeth EdwardsDepartment of Respiratory Medicine, Starship Children's Hospital, Auckland, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSurgical 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.

methodsRetrospective 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.

resultsNineteen 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).

conclusionLobectomy 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.

Indexed as

BronchiectasisAdolescentChildChild, PreschoolFemaleHospitals, PediatricHumansMaleNew ZealandRetrospective StudiesTreatment Outcomebronchiectasischildsurgeryyoung adult

Identifiers

PMID39887574
PMCPMC11883041

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.