Randomised Ambulatory Management of Primary Pneumothorax
RAMPP trial design and results
Design
Open-label randomised controlled trial
Treatment
Ambulatory management with a one-way valve device
Control
Standard care per guidelines
Population
236 patients with primary spontaneous pneumothorax, from 776 screened
Follow-up
30 days
Primary endpoint
Total length of hospital stay including re-admission in the first 30 days
Result
Median hospitalisation 0 days (IQR 0-3) with ambulatory care versus 4 days (IQR 0-8) with standard care (p<0.0001, median difference 2 days, 95% CI 1 to 3). Adverse events occurred in 64 of 117 (55%) ambulatory patients versus 46 of 119 (39%) standard care patients.
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.
The trial authors, in the published abstract
How it has aged
A genuine trade-off rather than a win: four hospital days saved against a 16 percentage point excess of adverse events. Read alongside PSP — between them, the modern algorithm is observe first, and use an ambulatory device for those who need drainage.
Publications
Ambulatory management of primary spontaneous pneumothorax: an open-label, randomised controlled trial
Hallifax RJ, McKeown E, Sivakumar P, et al. Ambulatory management of primary spontaneous pneumothorax: an open-label, randomised controlled trial. Lancet 2020 Jul 4;396(10243):39-49.