Dapagliflozin for Critically Ill Patients With Acute Organ Dysfunction

医学 病危 达帕格列嗪 器官功能障碍 心力衰竭 肾脏疾病 重症监护医学 急性肾损伤 危重病 2型糖尿病 内科学 糖尿病 败血症 内分泌学
作者
Caio A.M. Tavares,Luciano César Pontes Azevedo,Álvaro Réa-Neto,Niklas Söderberg Campos,Cristina Prata Amêndola,Amanda Christina Kozesinski-Nakatani,Paula Geraldes David-João,Suzana Margareth Lobo,Thiago Corsi Filiponi,Guacyra Margarita Batista de Almeida,Ricardo Reinaldo Bergo,Mário R. R. Guimarães-Júnior,Rodrigo C. Figueiredo,Joan R. Castro,Clewer J. Schuler,Glauco Adrieno Westphal,Ana Carla Carioca,Frederico Monfradini,Josué Nieri,Flavia M. O. Neves
出处
期刊:JAMA [American Medical Association]
卷期号:332 (5): 401-401 被引量:42
标识
DOI:10.1001/jama.2024.10510
摘要

Importance Sodium-glucose cotransporter 2 (SGLT-2) inhibitors improve outcomes in patients with type 2 diabetes, heart failure, and chronic kidney disease, but their effect on outcomes of critically ill patients with organ failure is unknown. Objective To determine whether the addition of dapagliflozin, an SGLT-2 inhibitor, to standard intensive care unit (ICU) care improves outcomes in a critically ill population with acute organ dysfunction. Design, Setting, and Participants Multicenter, randomized, open-label, clinical trial conducted at 22 ICUs in Brazil. Participants with unplanned ICU admission and presenting with at least 1 organ dysfunction (respiratory, cardiovascular, or kidney) were enrolled between November 22, 2022, and August 30, 2023, with follow-up through September 27, 2023. Intervention Participants were randomized to 10 mg of dapagliflozin (intervention, n = 248) plus standard care or to standard care alone (control, n = 259) for up to 14 days or until ICU discharge, whichever occurred first. Main Outcomes and Measures The primary outcome was a hierarchical composite of hospital mortality, initiation of kidney replacement therapy, and ICU length of stay through 28 days, analyzed using the win ratio method. Secondary outcomes included the individual components of the hierarchical outcome, duration of organ support–free days, ICU, and hospital stay, assessed using bayesian regression models. Results Among 507 randomized participants (mean age, 63.9 [SD, 15] years; 46.9%, women), 39.6% had an ICU admission due to suspected infection. The median time from ICU admission to randomization was 1 day (IQR, 0-1). The win ratio for dapagliflozin for the primary outcome was 1.01 (95% CI, 0.90 to 1.13; P = .89). Among all secondary outcomes, the highest probability of benefit found was 0.90 for dapagliflozin regarding use of kidney replacement therapy among 27 patients (10.9%) in the dapagliflozin group vs 39 (15.1%) in the control group. Conclusion and Relevance The addition of dapagliflozin to standard care for critically ill patients and acute organ dysfunction did not improve clinical outcomes; however, confidence intervals were wide and could not exclude relevant benefits or harms for dapagliflozin. Trial Registration ClinicalTrials.gov Identifier: NCT05558098
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