Respiratory Trials·org

ARDS · Corticosteroids in ARDS

LaSRS randomised trial

Efficacy and safety of corticosteroids for persistent acute respiratory distress syndrome

LaSRS trial design and results
Design Multicentre randomised, double-blind, placebo-controlled trial
Treatment Methylprednisolone started 7 to 28 days after ARDS onset
Control Placebo
Population 180 patients with persistent ARDS
Follow-up 180 days
Primary endpoint 60-day mortality
Result Hospital mortality at 60 days was 28.6% with placebo (95% CI 20.3 to 38.6) and 29.2% with methylprednisolone (20.8 to 39.4), p=1.0. At 180 days the rates were similar. Cardiopulmonary physiology improved with steroids. Patients enrolled 14 or more days after ARDS onset had increased 60-day mortality on methylprednisolone.
Secondary endpoints 180-day mortality, ventilator-free days, physiological measures, neuromuscular weakness

These results do not support the routine use of methylprednisolone for persistent ARDS despite the improvement in cardiopulmonary physiology. In addition, starting methylprednisolone therapy more than two weeks after the onset of ARDS may increase the risk of death.

The trial authors, in the published abstract

How it has aged

A textbook dissociation between physiology and outcome, and the origin of the rule that steroids started beyond two weeks may kill. It sits uneasily beside DEXA-ARDS, which gave steroids early and found benefit — timing appears to be the whole story.

Publications

Efficacy and safety of corticosteroids for persistent acute respiratory distress syndrome

Steinberg KP, Hudson LD, Goodman RB, et al. Efficacy and safety of corticosteroids for persistent acute respiratory distress syndrome. N Engl J Med 2006 Apr 20;354(16):1671-84.

  • No difference in 60-day or 180-day mortality
  • Cardiopulmonary physiology improved on steroids
  • Increased mortality when started more than 14 days after ARDS onset