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Ambulatory management of secondary spontaneous pneumothorax: A randomised controlled trial

Walker, Steven P.; Keenan, Emma; Bintcliffe, Oliver; Stanton, Andrew E.; Roberts, Mark; Pepperell, Justin; Fairbairn, Ian; McKeown, Edward; Goldring, James; Maddekar, Nadeem; Walters, James; West, Alex; Bhatta, Amrithraj; Knight, Matthew; Mercer, Rachel; Hallifax, Rob; White, Paul; Miller, Robert F.; Rahman, Najib M.; Maskell, Nick A.

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Authors

Steven P. Walker

Emma Keenan

Oliver Bintcliffe

Andrew E. Stanton

Mark Roberts

Justin Pepperell

Ian Fairbairn

Edward McKeown

James Goldring

Nadeem Maddekar

James Walters

Alex West

Amrithraj Bhatta

Matthew Knight

Rachel Mercer

Rob Hallifax

Paul White Paul.White@uwe.ac.uk
Professor in Applied Statistics

Robert F. Miller

Najib M. Rahman

Nick A. Maskell



Abstract

Secondary spontaneous pneumothorax (SSP) is traditionally managed with an intercostal chest tube attached to an underwater seal. We investigated whether use of a one-way flutter valve shortened patients' length of stay (LoS). This open-label randomised controlled trial enrolled patients presenting with SSP and randomised to either a chest tube and underwater seal (standard care: SC) or ambulatory care (AC) with a flutter valve. The type of flutter valve used depended on whether at randomisation the patient already had a chest tube in place: in those without a chest tube a pleural vent (PV) was used; in those with a chest tube in situ, an Atrium Pneumostat (AP) valve was attached. The primary end-point was LoS. Between March 2017 and March 2020, 41 patients underwent randomisation: 20 to SC and 21 to AC (13=PV, 8=AP). There was no difference in LoS in the first 30 days following treatment intervention: AC (median=6 days, IQR 14.5) and SC (median=6 days, IQR 13.3). In patients treated with PV there was a high rate of early treatment failure (6/13; 46%), compared to patients receiving SC (3/20; 15%) (p=0.11) Patients treated with AP had no (0/8 0%) early treatment failures and a median LoS of 1.5 days (IQR 23.8). There was no difference in LoS between ambulatory and standard care. Pleural Vents had high rates of treatment failure and should not be used in SSP. Atrium Pneumostats are a safer alternative, with a trend towards lower LoS.

Citation

Walker, S. P., Keenan, E., Bintcliffe, O., Stanton, A. E., Roberts, M., Pepperell, J., …Maskell, N. A. (2021). Ambulatory management of secondary spontaneous pneumothorax: A randomised controlled trial. European Respiratory Journal, 57(6), Article 2003375. https://doi.org/10.1183/13993003.03375-2020

Journal Article Type Article
Acceptance Date Nov 30, 2020
Online Publication Date Jun 24, 2021
Publication Date Jun 1, 2021
Deposit Date Dec 7, 2020
Publicly Available Date Jun 2, 2022
Journal European Respiratory Journal
Print ISSN 0903-1936
Electronic ISSN 1399-3003
Publisher European Respiratory Society
Peer Reviewed Peer Reviewed
Volume 57
Issue 6
Article Number 2003375
DOI https://doi.org/10.1183/13993003.03375-2020
Public URL https://uwe-repository.worktribe.com/output/6912932

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This is an author-submitted, peer-reviewed version of an article that has been accepted for publication in the European Respiratory Journal, prior to copy-editing, formatting and typesetting. This version of the article may not be duplicated or reproduced without prior permission from the copyright owner, the European Respiratory Society. The publisher is not responsible or liable for any errors or omissions in this version of the article or in any version derived from it by any other parties. The final, copy-edited, published article, which is the version of record, is available online from the European Respiratory Journal without a subscription 12 months after the date of issue publication


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http://www.rioxx.net/licenses/all-rights-reserved

Publisher Licence URL
http://www.rioxx.net/licenses/all-rights-reserved

Copyright Statement
This is an author-submitted, peer-reviewed version of an article that has been accepted for publication in the European Respiratory Journal, prior to copy-editing, formatting and typesetting. This version of the article may not be duplicated or reproduced without prior permission from the copyright owner, the European Respiratory Society. The publisher is not responsible or liable for any errors or omissions in this version of the article or in any version derived from it by any other parties. The final, copy-edited, published article, which is the version of record, is available online from the European Respiratory Journal without a subscription 12 months after the date of issue publication






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