Abstract

SummaryBackgroundPrimary 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.MethodsIn 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.FindingsOf 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.InterpretationAmbulatory 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.FundingUK National Institute for Health Research.

Highlights

  • Study design The Randomised Ambulatory Management of Primary Pneumothorax (RAMPP) trial was a multicentre, open-label, random­ ised controlled trial comparing ambulatory management of primary spontaneous pneumothorax with standard care based on national guidelines

  • The difference in overall hospital stay during 30 days was signif­ icant when calculated in hours; p

  • In the ambulatory care group, 73 (64%) of 114 patients with available data were discharged on the same day as admission, compared with 39 (34%) of 115 patients with available data in the standard care group (p

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Summary

Introduction

Current British Thoracic Society (BTS) guidelines suggest that aspiration of trapped air using a cannula and syringe should be considered, but more than 50% of patients subsequently require the inser­ tion of a chest tube, which is attached to an underwater seal drainage system.. Ambulatory management of patients with primary spon­ taneous pneumothorax potentially removes the need for long hospital admission by facilitating outpatient treatment. Reducing the need for chest tubes with bulky underwater systems might allow patients to remain mobile and facilitate early discharge with the device in situ. A systematic review of the literature found that 18 studies describing ambulatory management of both spontaneous and iat­ rogenic pneumothorax reported an overall success rate of 86% and successful outpatient management in 78% of cases, with few complications. The available evidence was described as poor quality with a high risk of bias, including two inadequately powered random­ ised trials and several retrospective case series.

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