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Pleural disease · Primary spontaneous pneumothorax

RAMPP

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.
Secondary endpoints Adverse events, serious adverse events, re-intervention

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.

  • Median hospital stay fell from 4 days to 0
  • Adverse events rose from 39% to 55%