Ambulatory management of primary spontaneous pneumothorax: an open-label, randomised controlled trial

Primary spontaneous pneumothorax occurs in otherwise healthy young patients. Optimal management is not defined and often results in prolonged hospitalisation. Data on efficacy of ambulatory options are poor. We aimed to describe the duration of hospitalisation and safety of ambulatory management com...

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Veröffentlicht in:The Lancet (British edition) 2020-07, Vol.396 (10243), p.39-49
Hauptverfasser: Hallifax, Rob J, McKeown, Edward, Sivakumar, Parthipan, Fairbairn, Ian, Peter, Christy, Leitch, Andrew, Knight, Matthew, Stanton, Andrew, Ijaz, Asim, Marciniak, Stefan, Cameron, James, Bhatta, Amrithraj, Blyth, Kevin G, Reddy, Raja, Harris, Marie-Clare, Maddekar, Nadeem, Walker, Steven, West, Alex, Laskawiec-Szkonter, Magda, Corcoran, John P, Gerry, Stephen, Roberts, Corran, Harvey, John E, Maskell, Nick, Miller, Robert F, Rahman, Najib M
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container_issue 10243
container_start_page 39
container_title The Lancet (British edition)
container_volume 396
creator Hallifax, Rob J
McKeown, Edward
Sivakumar, Parthipan
Fairbairn, Ian
Peter, Christy
Leitch, Andrew
Knight, Matthew
Stanton, Andrew
Ijaz, Asim
Marciniak, Stefan
Cameron, James
Bhatta, Amrithraj
Blyth, Kevin G
Reddy, Raja
Harris, Marie-Clare
Maddekar, Nadeem
Walker, Steven
West, Alex
Laskawiec-Szkonter, Magda
Corcoran, John P
Gerry, Stephen
Roberts, Corran
Harvey, John E
Maskell, Nick
Miller, Robert F
Rahman, Najib M
description Primary spontaneous pneumothorax occurs in otherwise healthy young patients. Optimal management is not defined and often results in prolonged hospitalisation. Data on efficacy of ambulatory options are poor. We aimed to describe the duration of hospitalisation and safety of ambulatory management compared with standard care. In this open-label, randomised controlled trial, adults (aged 16–55 years) with symptomatic primary spontaneous pneumothorax were recruited from 24 UK hospitals during a period of 3 years. Patients were randomly assigned (1:1) to treatment with either an ambulatory device or standard guideline-based management (aspiration, standard chest tube insertion, or both). The primary outcome was total length of hospital stay including re-admission up to 30 days after randomisation. Patients with available data were included in the primary analysis and all assigned patients were included in the safety analysis. The trial was prospectively registered with the International Standard Randomised Clinical Trials Number, ISRCTN79151659. Of 776 patients screened between July, 2015, and March, 2019, 236 (30%) were randomly assigned to ambulatory care (n=117) and standard care (n=119). At day 30, the median hospitalisation was significantly shorter in the 114 patients with available data who received ambulatory treatment (0 days [IQR 0–3]) than in the 113 with available data who received standard care (4 days [IQR 0–8]; p
doi_str_mv 10.1016/S0140-6736(20)31043-6
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Optimal management is not defined and often results in prolonged hospitalisation. Data on efficacy of ambulatory options are poor. We aimed to describe the duration of hospitalisation and safety of ambulatory management compared with standard care. In this open-label, randomised controlled trial, adults (aged 16–55 years) with symptomatic primary spontaneous pneumothorax were recruited from 24 UK hospitals during a period of 3 years. Patients were randomly assigned (1:1) to treatment with either an ambulatory device or standard guideline-based management (aspiration, standard chest tube insertion, or both). The primary outcome was total length of hospital stay including re-admission up to 30 days after randomisation. Patients with available data were included in the primary analysis and all assigned patients were included in the safety analysis. The trial was prospectively registered with the International Standard Randomised Clinical Trials Number, ISRCTN79151659. Of 776 patients screened between July, 2015, and March, 2019, 236 (30%) were randomly assigned to ambulatory care (n=117) and standard care (n=119). At day 30, the median hospitalisation was significantly shorter in the 114 patients with available data who received ambulatory treatment (0 days [IQR 0–3]) than in the 113 with available data who received standard care (4 days [IQR 0–8]; p&lt;0·0001; median difference 2 days [95% CI 1–3]). 110 (47%) of 236 patients had adverse events, including 64 (55%) of 117 patients in the ambulatory care arm and 46 (39%) of 119 in the standard care arm. All 14 serious adverse events occurred in patients who received ambulatory care, eight (57%) of which were related to the intervention, including an enlarging pneumothorax, asymptomatic pulmonary oedema, and the device malfunctioning, leaking, or dislodging. Ambulatory management of primary spontaneous pneumothorax significantly reduced the duration of hospitalisation including re-admissions in the first 30 days, but at the expense of increased adverse events. This data suggests that primary spontaneous pneumothorax can be managed for outpatients, using ambulatory devices in those who require intervention. 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Optimal management is not defined and often results in prolonged hospitalisation. Data on efficacy of ambulatory options are poor. We aimed to describe the duration of hospitalisation and safety of ambulatory management compared with standard care. In this open-label, randomised controlled trial, adults (aged 16–55 years) with symptomatic primary spontaneous pneumothorax were recruited from 24 UK hospitals during a period of 3 years. Patients were randomly assigned (1:1) to treatment with either an ambulatory device or standard guideline-based management (aspiration, standard chest tube insertion, or both). The primary outcome was total length of hospital stay including re-admission up to 30 days after randomisation. Patients with available data were included in the primary analysis and all assigned patients were included in the safety analysis. The trial was prospectively registered with the International Standard Randomised Clinical Trials Number, ISRCTN79151659. 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Ambulatory management of primary spontaneous pneumothorax significantly reduced the duration of hospitalisation including re-admissions in the first 30 days, but at the expense of increased adverse events. This data suggests that primary spontaneous pneumothorax can be managed for outpatients, using ambulatory devices in those who require intervention. 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Newsstand Professional</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Lancet (British edition)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hallifax, Rob J</au><au>McKeown, Edward</au><au>Sivakumar, Parthipan</au><au>Fairbairn, Ian</au><au>Peter, Christy</au><au>Leitch, Andrew</au><au>Knight, Matthew</au><au>Stanton, Andrew</au><au>Ijaz, Asim</au><au>Marciniak, Stefan</au><au>Cameron, James</au><au>Bhatta, Amrithraj</au><au>Blyth, Kevin G</au><au>Reddy, Raja</au><au>Harris, Marie-Clare</au><au>Maddekar, Nadeem</au><au>Walker, Steven</au><au>West, Alex</au><au>Laskawiec-Szkonter, Magda</au><au>Corcoran, John P</au><au>Gerry, Stephen</au><au>Roberts, Corran</au><au>Harvey, John E</au><au>Maskell, Nick</au><au>Miller, Robert F</au><au>Rahman, Najib M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ambulatory management of primary spontaneous pneumothorax: an open-label, randomised controlled trial</atitle><jtitle>The Lancet (British edition)</jtitle><addtitle>Lancet</addtitle><date>2020-07-04</date><risdate>2020</risdate><volume>396</volume><issue>10243</issue><spage>39</spage><epage>49</epage><pages>39-49</pages><issn>0140-6736</issn><eissn>1474-547X</eissn><abstract>Primary spontaneous pneumothorax occurs in otherwise healthy young patients. Optimal management is not defined and often results in prolonged hospitalisation. Data on efficacy of ambulatory options are poor. We aimed to describe the duration of hospitalisation and safety of ambulatory management compared with standard care. In this open-label, randomised controlled trial, adults (aged 16–55 years) with symptomatic primary spontaneous pneumothorax were recruited from 24 UK hospitals during a period of 3 years. Patients were randomly assigned (1:1) to treatment with either an ambulatory device or standard guideline-based management (aspiration, standard chest tube insertion, or both). The primary outcome was total length of hospital stay including re-admission up to 30 days after randomisation. Patients with available data were included in the primary analysis and all assigned patients were included in the safety analysis. The trial was prospectively registered with the International Standard Randomised Clinical Trials Number, ISRCTN79151659. Of 776 patients screened between July, 2015, and March, 2019, 236 (30%) were randomly assigned to ambulatory care (n=117) and standard care (n=119). At day 30, the median hospitalisation was significantly shorter in the 114 patients with available data who received ambulatory treatment (0 days [IQR 0–3]) than in the 113 with available data who received standard care (4 days [IQR 0–8]; p&lt;0·0001; median difference 2 days [95% CI 1–3]). 110 (47%) of 236 patients had adverse events, including 64 (55%) of 117 patients in the ambulatory care arm and 46 (39%) of 119 in the standard care arm. All 14 serious adverse events occurred in patients who received ambulatory care, eight (57%) of which were related to the intervention, including an enlarging pneumothorax, asymptomatic pulmonary oedema, and the device malfunctioning, leaking, or dislodging. Ambulatory management of primary spontaneous pneumothorax significantly reduced the duration of hospitalisation including re-admissions in the first 30 days, but at the expense of increased adverse events. This data suggests that primary spontaneous pneumothorax can be managed for outpatients, using ambulatory devices in those who require intervention. UK National Institute for Health Research.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>32622394</pmid><doi>10.1016/S0140-6736(20)31043-6</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0140-6736
ispartof The Lancet (British edition), 2020-07, Vol.396 (10243), p.39-49
issn 0140-6736
1474-547X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7607300
source MEDLINE; Elsevier ScienceDirect Journals
subjects Adult
Ambulatory Care - statistics & numerical data
Chest tubes
Clinical trials
Edema
Emergency medical services
Female
Health services
Hospitalization
Humans
International standards
Intervention
Length of Stay - statistics & numerical data
Male
Patient Readmission - statistics & numerical data
Patients
Pneumothorax
Pneumothorax - therapy
Randomization
Safety management
Standard of Care
Thoracic surgery
United Kingdom
title Ambulatory management of primary spontaneous pneumothorax: an open-label, randomised controlled trial
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