A meta-analysis of controlled trials of recombinant human activated protein C therapy in patients with sepsis

<p>Abstract</p> <p>Background</p> <p>Meta-analysis of two randomised controlled trials in severe sepsis performed with recombinant human activated protein C may provide further insight as to the therapeutic utility of targeting the clotting cascade in this syndrome.<...

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Main Authors: Wiedermann Christian J, Kaneider Nicole C
Format: Article
Language:English
Published: BMC 2005-10-01
Series:BMC Emergency Medicine
Online Access:http://www.biomedcentral.com/1471-227X/5/7
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spelling doaj-46de639be70a4225bc7faf56029bf8102020-11-25T02:28:29ZengBMCBMC Emergency Medicine1471-227X2005-10-0151710.1186/1471-227X-5-7A meta-analysis of controlled trials of recombinant human activated protein C therapy in patients with sepsisWiedermann Christian JKaneider Nicole C<p>Abstract</p> <p>Background</p> <p>Meta-analysis of two randomised controlled trials in severe sepsis performed with recombinant human activated protein C may provide further insight as to the therapeutic utility of targeting the clotting cascade in this syndrome.</p> <p>Methods</p> <p>In search for relevant studies published, two randomized clinical trials were found eligible.</p> <p>Results</p> <p>The studies, PROWESS and ADDRESS, enrolled a total of 4329 patients with risk ratio (RR) and 95% confidence interval (CI) data for effect on 28-day mortality relative to control treatment of 0.92 (0.83–1.02) suggesting that recombinant human activated protein C is not beneficial in severe sepsis. In PROWESS, 873 of 1690 patients presented with low risk, and 2315 of 2639 patients in ADDRESS as defined by APACHE II score < 25. In this low-risk stratum, no effect of recombinant human activated protein C administration on 28-day mortality was observed. This observation appears to be consistent and homogenous. Heterogeneity between the two studies, however, was seen in patients with APACHE II score ≥ 25 in whom recombinant activated protein C was effective in PROWESS (n = 817; RR 0.71, CI 0.59–0.85) whereas a tendency toward harm was present in ADDRESS (n = 324; RR 1.21, CI 0.85–1.74). Even though the overall treatment effect in this high-risk population was still in favour of treatment with recombinant activated protein C (n = 1141; RR 0.80, CI 0.68–0.94), the observed heterogeneity suggests that the efficacy of recombinant human activated protein C is not robust. Not unlikely, the adverse tendency observed could have become significant with higher statistical power would ADDRESS not have been terminated prematurely.</p> <p>Conclusion</p> <p>This meta-analysis, therefore, raises doubts about the clinical usefulness of recombinant activated protein C in patients with severe sepsis and an APACHE II score ≥ 25 which can only be resolved by another properly designed clinical trial.</p> http://www.biomedcentral.com/1471-227X/5/7
collection DOAJ
language English
format Article
sources DOAJ
author Wiedermann Christian J
Kaneider Nicole C
spellingShingle Wiedermann Christian J
Kaneider Nicole C
A meta-analysis of controlled trials of recombinant human activated protein C therapy in patients with sepsis
BMC Emergency Medicine
author_facet Wiedermann Christian J
Kaneider Nicole C
author_sort Wiedermann Christian J
title A meta-analysis of controlled trials of recombinant human activated protein C therapy in patients with sepsis
title_short A meta-analysis of controlled trials of recombinant human activated protein C therapy in patients with sepsis
title_full A meta-analysis of controlled trials of recombinant human activated protein C therapy in patients with sepsis
title_fullStr A meta-analysis of controlled trials of recombinant human activated protein C therapy in patients with sepsis
title_full_unstemmed A meta-analysis of controlled trials of recombinant human activated protein C therapy in patients with sepsis
title_sort meta-analysis of controlled trials of recombinant human activated protein c therapy in patients with sepsis
publisher BMC
series BMC Emergency Medicine
issn 1471-227X
publishDate 2005-10-01
description <p>Abstract</p> <p>Background</p> <p>Meta-analysis of two randomised controlled trials in severe sepsis performed with recombinant human activated protein C may provide further insight as to the therapeutic utility of targeting the clotting cascade in this syndrome.</p> <p>Methods</p> <p>In search for relevant studies published, two randomized clinical trials were found eligible.</p> <p>Results</p> <p>The studies, PROWESS and ADDRESS, enrolled a total of 4329 patients with risk ratio (RR) and 95% confidence interval (CI) data for effect on 28-day mortality relative to control treatment of 0.92 (0.83–1.02) suggesting that recombinant human activated protein C is not beneficial in severe sepsis. In PROWESS, 873 of 1690 patients presented with low risk, and 2315 of 2639 patients in ADDRESS as defined by APACHE II score < 25. In this low-risk stratum, no effect of recombinant human activated protein C administration on 28-day mortality was observed. This observation appears to be consistent and homogenous. Heterogeneity between the two studies, however, was seen in patients with APACHE II score ≥ 25 in whom recombinant activated protein C was effective in PROWESS (n = 817; RR 0.71, CI 0.59–0.85) whereas a tendency toward harm was present in ADDRESS (n = 324; RR 1.21, CI 0.85–1.74). Even though the overall treatment effect in this high-risk population was still in favour of treatment with recombinant activated protein C (n = 1141; RR 0.80, CI 0.68–0.94), the observed heterogeneity suggests that the efficacy of recombinant human activated protein C is not robust. Not unlikely, the adverse tendency observed could have become significant with higher statistical power would ADDRESS not have been terminated prematurely.</p> <p>Conclusion</p> <p>This meta-analysis, therefore, raises doubts about the clinical usefulness of recombinant activated protein C in patients with severe sepsis and an APACHE II score ≥ 25 which can only be resolved by another properly designed clinical trial.</p>
url http://www.biomedcentral.com/1471-227X/5/7
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