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DOI 10.1097/ccm.0000000000007134

Медицинская библиотека · Critical care medicine · 2026

Ivermectin for Critically and Noncritically Ill Hospitalized Patients With COVID-19: Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community-Acquired Pneumonia (REMAP-CAP).

Hashmi Madiha, Haniffa Rashan, Jayakumar Deva, Beane Abigail, Lorenzi Elizabeth, Berry Lindsay R, Nasir Khoso Muhammad, Ain Khan Quratul, Kumar Ashok, Altaf Kidwai Aneela, Hills Thomas E, Annane Djillali, Aryal Diptesh, Au Carly, Baillie Kenneth, Beasley Richard, Best-Lane Janis, Bonten Marc, Bradbury Charlotte A, Brunkhorst Frank M, Burrell Aidan, Buxton Meredith, Cecconi Maurizio, Cheng Allen C, Cove Matthew E, de Jong Menno, Detry Michelle A, Duffy Eamon, Estcourt Lise J, Fitzgerald Mark, Fowler Rob, Goossens Herman, Green Cameron, Hays Leanne M C, Higgins Alisa M, Huang David T, Ichihara Nao, Koirala Sabin, Lamontagne François, Lawler Patrick R, Lewis Roger J, Litton Edward, Mahon Niamh, Marshall John C, McAuley Daniel F, McGlothlin Anna, McGuinness Shay, McQuilten Zoe K, McVerry Bryan J, Mouncey Paul R, Morpeth Susan, Netea Mihai, Orr Katrina, Parke Rachael L, Parker Jane C, Patanwala Asad, Peters Svenja, Reyes Luis Felipe, Rowan Kathryn M, Saito Hiroki, Saunders Christina T, Santos Marlene, Seymour Christopher W, Shankar-Hari Manu, Singh Vanessa, Slater Matthew, Tambyah Paul A, Tong Steven Y C, Turgeon Alexis F, Turner Anne M, van de Veerdonk Frank, Weis Sebastian, Zarychanski Ryan, McArthur Colin J, Angus Derek C, Berry Scott M, Gordon Anthony C, Derde Lennie P G, Webb Steve A, Murthy Srinivas, Arabi Yaseen, Nichol Alistair D, and the Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community-Acquired Pneumonia (REMAP-CAP) Investigators

СтатьяРандомизированное исследованиеAdaptive Clinical TrialПеревод в очереди

Аннотация

OBJECTIVE

To determine whether ivermectin improves outcomes for critically and noncritically ill hospitalized patients with COVID-19.

DESIGN

An ongoing international, multifactorial, adaptive platform, randomized, controlled trial.

SETTING

Hospitals in Pakistan, India, and Ireland between June 11, 2021, and September 9, 2022.

PATIENTS: Critically and noncritically ill patients.

INTERVENTIONS: Randomized to ivermectin or no ivermectin (control).

MEASUREMENTS AND MAIN

RESULTS

The primary outcome was respiratory and cardiovascular organ support-free days, assessed on an ordinal scale combining in-hospital death (assigned a value of -1) and days free of organ support through day 21 in survivors. Analyses used a Bayesian cumulative logistic model. Enrollment was closed for operational futility, following external evidence suggesting no benefit with ivermectin in nonhospitalized patients with COVID-19. Among 61 critically ill patients, the median number of organ support-free days was -1, indicating death was the most common vital outcome (interquartile range [IQR], -1 to 17), for the ivermectin group and -1 (IQR, -1 to 17.25) for the control group (adjusted proportional odds ratio [OR], 0.94; 95% credible interval [CrI], 0.40-2.07) and the posterior probability of superiority to control was 44.2%. Among 89 noncritically ill patients, the median number of organ support-free days was 22 (IQR, 18.5-22) for ivermectin and 22 (IQR, 16-22) for control (adjusted proportional OR, 1.04; 95% CrI, 0.48-2.34) and the posterior probability of superiority was 53.7%. Among critically ill patients, hospital survival was 35.1% (13/37) for ivermectin and 37.5% (9/24) for control (adjusted OR, 1.00; 95% CrI, 0.39-2.32), posterior probability of superiority was 50.0%. Among noncritically ill patients, hospital survival was 84.1% (37/44) for ivermectin and 77.8% (35/45) for control (adjusted OR, 1.16; 95% CrI, 0.5-3.07), posterior probability of superiority was 63.3%.

CONCLUSIONS

For critically and noncritically ill hospitalized patients with COVID-19, ivermectin was unlikely to improve the primary composite outcome of organ support-free days and hospital survival.

Для цитирования: Hashmi Madiha, Haniffa Rashan, Jayakumar Deva, Beane Abigail, Lorenzi Elizabeth, Berry Lindsay R, Nasir Khoso Muhammad, Ain Khan Quratul, Kumar Ashok, Altaf Kidwai Aneela, Hills Thomas E, Annane Djillali, Aryal Diptesh, Au Carly, Baillie Kenneth, Beasley Richard, Best-Lane Janis, Bonten Marc, Bradbury Charlotte A, Brunkhorst Frank M, Burrell Aidan, Buxton Meredith, Cecconi Maurizio, Cheng Allen C, Cove Matthew E, de Jong Menno, Detry Michelle A, Duffy Eamon, Estcourt Lise J, Fitzgerald Mark, Fowler Rob, Goossens Herman, Green Cameron, Hays Leanne M C, Higgins Alisa M, Huang David T, Ichihara Nao, Koirala Sabin, Lamontagne François, Lawler Patrick R, Lewis Roger J, Litton Edward, Mahon Niamh, Marshall John C, McAuley Daniel F, McGlothlin Anna, McGuinness Shay, McQuilten Zoe K, McVerry Bryan J, Mouncey Paul R, Morpeth Susan, Netea Mihai, Orr Katrina, Parke Rachael L, Parker Jane C, Patanwala Asad, Peters Svenja, Reyes Luis Felipe, Rowan Kathryn M, Saito Hiroki, Saunders Christina T, Santos Marlene, Seymour Christopher W, Shankar-Hari Manu, Singh Vanessa, Slater Matthew, Tambyah Paul A, Tong Steven Y C, Turgeon Alexis F, Turner Anne M, van de Veerdonk Frank, Weis Sebastian, Zarychanski Ryan, McArthur Colin J, Angus Derek C, Berry Scott M, Gordon Anthony C, Derde Lennie P G, Webb Steve A, Murthy Srinivas, Arabi Yaseen, Nichol Alistair D, and the Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community-Acquired Pneumonia (REMAP-CAP) Investigators. Ivermectin for Critically and Noncritically Ill Hospitalized Patients With COVID-19: Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community-Acquired Pneumonia (REMAP-CAP).. Critical care medicine. 2026. DOI: 10.1097/ccm.0000000000007134.

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