Table 1.
Trial | Actual/Planned recruitment | % of planned recruitment | % Assigned DAA who Died | % Assigned Placebo who Died | RR DAA vs. Placebo | 95% CI for RR |
---|---|---|---|---|---|---|
PROWESS All patients | 1,690/2,280 | 74.1% | 24.7% | 30.8% | 0.80 | 0.69–0.94 |
PROWESS APACHE II < 25 | 873 | NA | 18.8 | 19.0 | 0.99 | 0.75–1.30 |
PROWESS APACHE II > 24 | 817 | NA | 30.9% | 43.7% | 0.71 | 0.59–0.85 |
PROWESS single organ failure | 418 | NA | 19.5% | 21.2% | 0.92 | 0.63–1.35 |
PROWESS > 1 organ failure | 1,271 | NA | 26.5% | 33.9% | 0.78 | 0.66–0.93 |
ADDRESS: All patients | 2,640/11,444 | 23.1% | 18.5% | 17.0% | 1.09 | 0.92–1.28 |
ADDRESS APACHE II > 24 | 321 | NA | 29.5% | 24.7% | 1.22 | 0.85–1.74 |
ADDRESS > 1 Organ failure | 862 | NA | 20.7% | 21.9% | 0.94 | 0.73–1.22 |
RESOLVE | 477/6,000 | 8.0% | 17.2% | 17.5% | 0.98 | 0.66–1.46 |
DAA Drotrecogin alfa (activated), RR relative risk, 95% CI = 95% confidence interval, NA not applicable