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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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 |
format | Article |
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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<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.</description><identifier>ISSN: 0140-6736</identifier><identifier>EISSN: 1474-547X</identifier><identifier>DOI: 10.1016/S0140-6736(20)31043-6</identifier><identifier>PMID: 32622394</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>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</subject><ispartof>The Lancet (British edition), 2020-07, Vol.396 (10243), p.39-49</ispartof><rights>2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license</rights><rights>Copyright © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.</rights><rights>2020. The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. This work is published under https://creativecommons.org/licenses/by/3.0/ (theLicense”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c495t-5327e17ceaa5477ff74e4dda45d4e4860bf53f5b9de8d8009cd73282c3cc4abf3</citedby><cites>FETCH-LOGICAL-c495t-5327e17ceaa5477ff74e4dda45d4e4860bf53f5b9de8d8009cd73282c3cc4abf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0140673620310436$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32622394$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hallifax, Rob J</creatorcontrib><creatorcontrib>McKeown, Edward</creatorcontrib><creatorcontrib>Sivakumar, Parthipan</creatorcontrib><creatorcontrib>Fairbairn, Ian</creatorcontrib><creatorcontrib>Peter, Christy</creatorcontrib><creatorcontrib>Leitch, Andrew</creatorcontrib><creatorcontrib>Knight, Matthew</creatorcontrib><creatorcontrib>Stanton, Andrew</creatorcontrib><creatorcontrib>Ijaz, Asim</creatorcontrib><creatorcontrib>Marciniak, Stefan</creatorcontrib><creatorcontrib>Cameron, James</creatorcontrib><creatorcontrib>Bhatta, Amrithraj</creatorcontrib><creatorcontrib>Blyth, Kevin G</creatorcontrib><creatorcontrib>Reddy, Raja</creatorcontrib><creatorcontrib>Harris, Marie-Clare</creatorcontrib><creatorcontrib>Maddekar, Nadeem</creatorcontrib><creatorcontrib>Walker, Steven</creatorcontrib><creatorcontrib>West, Alex</creatorcontrib><creatorcontrib>Laskawiec-Szkonter, Magda</creatorcontrib><creatorcontrib>Corcoran, John P</creatorcontrib><creatorcontrib>Gerry, Stephen</creatorcontrib><creatorcontrib>Roberts, Corran</creatorcontrib><creatorcontrib>Harvey, John E</creatorcontrib><creatorcontrib>Maskell, Nick</creatorcontrib><creatorcontrib>Miller, Robert F</creatorcontrib><creatorcontrib>Rahman, Najib M</creatorcontrib><title>Ambulatory management of primary spontaneous pneumothorax: an open-label, randomised controlled trial</title><title>The Lancet (British edition)</title><addtitle>Lancet</addtitle><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<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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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<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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