High-Dose Steroids for Nonresolving Acute Respiratory Distress Syndrome in Critically Ill COVID-19 Patients Treated With Dexamethasone: A Multicenter Cohort Study

医学 急性呼吸窘迫综合征 危险系数 比例危险模型 内科学 前瞻性队列研究 倾向得分匹配 队列研究 呼吸窘迫 地塞米松 肺炎 外科 置信区间
作者
Julien Lopinto,Romain Arrestier,Bastien Peiffer,Antoine Gaillet,Guillaume Voiriot,Tomas Urbina,Charles‐Édouard Luyt,Raphaël Bellaïche,Tài Pham,Zakaria Ait-Hamou,Damien Roux,Raphaël Clère-Jehl,Élie Azoulay,Stéphane Gaudry,Julien Mayaux,Armand Mekontso Dessap,Florence Canouï‐Poitrine,Nicolas de Prost
出处
期刊:Critical Care Medicine [Lippincott Williams & Wilkins]
卷期号:51 (10): 1306-1317 被引量:8
标识
DOI:10.1097/ccm.0000000000005930
摘要

To determine the impact of high doses of corticosteroids (HDCT) in critically ill COVID-19 patients with nonresolving acute respiratory distress syndrome (ARDS) who had been previously treated with dexamethasone as a standard of care.Prospective observational cohort study. Eligible patients presented nonresolving ARDS related to severe acute respiratory syndrome coronavirus 2 infection and had received initial treatment with dexamethasone. We compared patients who had received or not HDCT during ICU stay, consisting of greater than or equal to 1 mg/kg of methylprednisolone or equivalent for treatment of nonresolving ARDS. The primary outcome was 90-day mortality. We assessed the impact of HDCT on 90-day mortality using univariable and multivariable Cox regression analysis. Further adjustment for confounding variables was performed using overlap weighting propensity score. The association between HDCT and the risk of ventilator-associated pneumonia was estimated using multivariable cause-specific Cox proportional hazard model adjusting for pre-specified confounders.We included consecutive patients admitted in 11 ICUs of Great Paris area from September 2020 to February 2021.Three hundred eighty-three patients were included (59 in the HDCT group, 324 in the no HDCT group).None.At day 90, 30 of 59 patients (51%) in the HDCT group and 116 of 324 patients (35.8%) in the no HDCT group had died. HDCT was significantly associated with 90-day mortality in unadjusted (hazard ratio [HR], 1.60; 95% CI, 1.04-2.47; p = 0.033) and adjusted analysis with overlap weighting (adjusted HR, 1.65; 95% CI, 1.03-2.63; p = 0.036). HDCT was not associated with an increased risk of ventilator-associated pneumonia (adjusted cause-specific HR, 0.42; 95% CI, 0.15-1.16; p = 0.09).In critically ill COVID-19 patients with nonresolving ARDS, HDCT result in a higher 90-day mortality.
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