• Jean-Louis Vincent, Bruno Francois, Igor Zabolotskikh, Mradul Kumar Daga, Lascarrou Jean-Baptiste JB Centre Hospitalier Universitaire de Nantes, Nantes, France., Mikhail Y Kirov, Ville Pettilä, Xavier Wittebole, Ferhat Meziani, Emmanuelle Mercier, Suzana M Lobo, Philip S Barie, Mark Crowther, Charles T Esmon, Jawed Fareed, Satoshi Gando, Kenneth J Gorelick, Marcel Levi, Jean-Paul Mira, Steven M Opal, Joseph Parrillo, James A Russell, Hidehiko Saito, Kazuhisa Tsuruta, Takumi Sakai, David Fineberg, and SCARLET Trial Group.
• Department of Intensive Care, Erasme Hospital, Université libre de Bruxelles, Brussels, Belgium.
• JAMA. 2019 May 28; 321 (20): 1993-2002.

ImportancePrevious research suggested that soluble human recombinant thrombomodulin may reduce mortality among patients with sepsis-associated coagulopathy.ObjectiveTo determine the effect of human recombinant thrombomodulin vs placebo on 28-day all-cause mortality among patients with sepsis-associated coagulopathy.Design, Setting, And ParticipantsThe SCARLET trial was a randomized, double-blind, placebo-controlled, multinational, multicenter phase 3 study conducted in intensive care units at 159 sites in 26 countries. All adult patients admitted to one of the participating intensive care units between October 2012 and March 2018 with sepsis-associated coagulopathy and concomitant cardiovascular and/or respiratory failure, defined as an international normalized ratio greater than 1.40 without other known etiology and a platelet count in the range of 30 to 150 × 109/L or a greater than 30% decrease in platelet count within 24 hours, were considered for inclusion. The final date of follow-up was February 28, 2019.InterventionsPatients with sepsis-associated coagulopathy were randomized and treated with an intravenous bolus or a 15-minute infusion of thrombomodulin (0.06 mg/kg/d [maximum, 6 mg/d]; n = 395) or matching placebo (n = 405) once daily for 6 days.Main Outcome And MeasuresThe primary end point was 28-day all-cause mortality.ResultsAmong 816 randomized patients, 800 (mean age, 60.7 years; 437 [54.6%] men) completed the study and were included in the full analysis set. In these patients, the 28-day all-cause mortality rate was not statistically significantly different between the thrombomodulin group and the placebo group (106 of 395 patients [26.8%] vs 119 of 405 patients [29.4%], respectively; P = .32). The absolute risk difference was 2.55% (95% CI, -3.68% to 8.77%). The incidence of serious major bleeding adverse events (defined as any intracranial hemorrhage; life-threatening bleeding; or bleeding event classified as serious by the investigator, with administration of at least 1440 mL [typically 6 units] of packed red blood cells over 2 consecutive days) was 23 of 396 patients (5.8%) in the thrombomodulin group and 16 of 404 (4.0%) in the placebo group.Conclusions And RelevanceAmong patients with sepsis-associated coagulopathy, administration of a human recombinant thrombomodulin, compared with placebo, did not significantly reduce 28-day all-cause mortality.Trial RegistrationClinicalTrials.gov Identifier: NCT01598831.

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