• REMAP-CAP Writing Committee for the REMAP-CAP Investigators, Charlotte A Bradbury, Patrick R Lawler, Simon J Stanworth, Bryan J McVerry, Zoe McQuilten, Alisa M Higgins, Paul R Mouncey, Farah Al-Beidh, Kathryn M Rowan, Lindsay R Berry, Elizabeth Lorenzi, Ryan Zarychanski, Yaseen M Arabi, Djillali Annane, Abi Beane, Wilma van Bentum-Puijk, Zahra Bhimani, Shailesh Bihari, BontenMarc J MMJMUniversity Medical Center Utrecht, Utrecht, the Netherlands., Frank M Brunkhorst, Adrian Buzgau, Meredith Buxton, Marc Carrier, Allen C Cheng, Matthew Cove, Michelle A Detry, Lise J Estcourt, Mark Fitzgerald, Timothy D Girard, Ewan C Goligher, Herman Goossens, Rashan Haniffa, Thomas Hills, David T Huang, Christopher M Horvat, Beverley J Hunt, Nao Ichihara, Francois Lamontagne, Helen L Leavis, Kelsey M Linstrum, Edward Litton, John C Marshall, Daniel F McAuley, Anna McGlothlin, Shay P McGuinness, Saskia Middeldorp, Stephanie K Montgomery, Susan C Morpeth, Srinivas Murthy, Matthew D Neal, Alistair D Nichol, Rachael L Parke, Jane C Parker, Luis F Reyes, Hiroki Saito, Marlene S Santos, Christina T Saunders, Ary Serpa-Neto, Christopher W Seymour, Manu Shankar-Hari, Vanessa Singh, Timo Tolppa, Alexis F Turgeon, Anne M Turner, Frank L van de Veerdonk, Cameron Green, Roger J Lewis, Derek C Angus, Colin J McArthur, Scott Berry, DerdeLennie P GLPGUniversity Medical Center Utrecht, Utrecht, the Netherlands., Steve A Webb, and Anthony C Gordon.
• University of Bristol, Bristol, England.
• JAMA. 2022 Apr 5; 327 (13): 124712591247-1259.

ImportanceThe efficacy of antiplatelet therapy in critically ill patients with COVID-19 is uncertain.ObjectiveTo determine whether antiplatelet therapy improves outcomes for critically ill adults with COVID-19.Design, Setting, And ParticipantsIn an ongoing adaptive platform trial (REMAP-CAP) testing multiple interventions within multiple therapeutic domains, 1557 critically ill adult patients with COVID-19 were enrolled between October 30, 2020, and June 23, 2021, from 105 sites in 8 countries and followed up for 90 days (final follow-up date: July 26, 2021).InterventionsPatients were randomized to receive either open-label aspirin (n = 565), a P2Y12 inhibitor (n = 455), or no antiplatelet therapy (control; n = 529). Interventions were continued in the hospital for a maximum of 14 days and were in addition to anticoagulation thromboprophylaxis.Main Outcomes And MeasuresThe primary end point was organ support-free days (days alive and free of intensive care unit-based respiratory or cardiovascular organ support) within 21 days, ranging from -1 for any death in hospital (censored at 90 days) to 22 for survivors with no organ support. There were 13 secondary outcomes, including survival to discharge and major bleeding to 14 days. The primary analysis was a bayesian cumulative logistic model. An odds ratio (OR) greater than 1 represented improved survival, more organ support-free days, or both. Efficacy was defined as greater than 99% posterior probability of an OR greater than 1. Futility was defined as greater than 95% posterior probability of an OR less than 1.2 vs control. Intervention equivalence was defined as greater than 90% probability that the OR (compared with each other) was between 1/1.2 and 1.2 for 2 noncontrol interventions.ResultsThe aspirin and P2Y12 inhibitor groups met the predefined criteria for equivalence at an adaptive analysis and were statistically pooled for further analysis. Enrollment was discontinued after the prespecified criterion for futility was met for the pooled antiplatelet group compared with control. Among the 1557 critically ill patients randomized, 8 patients withdrew consent and 1549 completed the trial (median age, 57 years; 521 [33.6%] female). The median for organ support-free days was 7 (IQR, -1 to 16) in both the antiplatelet and control groups (median-adjusted OR, 1.02 [95% credible interval {CrI}, 0.86-1.23]; 95.7% posterior probability of futility). The proportions of patients surviving to hospital discharge were 71.5% (723/1011) and 67.9% (354/521) in the antiplatelet and control groups, respectively (median-adjusted OR, 1.27 [95% CrI, 0.99-1.62]; adjusted absolute difference, 5% [95% CrI, -0.2% to 9.5%]; 97% posterior probability of efficacy). Among survivors, the median for organ support-free days was 14 in both groups. Major bleeding occurred in 2.1% and 0.4% of patients in the antiplatelet and control groups (adjusted OR, 2.97 [95% CrI, 1.23-8.28]; adjusted absolute risk increase, 0.8% [95% CrI, 0.1%-2.7%]; 99.4% probability of harm).Conclusions And RelevanceAmong critically ill patients with COVID-19, treatment with an antiplatelet agent, compared with no antiplatelet agent, had a low likelihood of providing improvement in the number of organ support-free days within 21 days.Trial RegistrationClinicalTrials.gov Identifier: NCT02735707.

41 keywords...

hide…