Department of Anesthesiology and Intensive Care Medicine, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Campus Benjamin Franklin, Berlin, Germany.
Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
Sci Rep. 2024 May 27;14(1):12138. doi: 10.1038/s41598-024-62302-w.
The COVID-19 pandemic has posed a major challenge to healthcare systems globally. Millions of people have been infected, and millions of deaths have been reported worldwide. Glucocorticoids have attracted worldwide attention for their potential efficacy in the treatment of COVID-19. Various glucocorticoids with different dosages and treatment durations have been studied in patients with different severities, with a suitable dosage and treatment duration not yet defined. This study aimed to investigate whether in-hospital survival differs between critically ill patients treated with low-dose glucocorticoids, high-dose glucocorticoids or no glucocorticoids. All critically ill patients admitted to the intensive care unit of the Charité Hospital-Universitätsmedizin Berlin between February 2020 and December 2021 with COVID-19 pneumonia receiving supplemental oxygen were eligible to participate in this multicenter real-world data study. Patients were retrospectively assigned to one of three groups: the high corticosteroid dose (HighC) group (receiving 6 mg parenteral dexamethasone or an equivalent corticosteroid dosage for ten days), the low corticosteroid dose (LowC) group (receiving less than 6 mg parenteral dexamethasone or an equivalent corticosteroid dosage for ten days), or the no corticosteroid (NoC) group. Overall survival and risk effects were compared among groups within the total observation period, as well as at 35 days after the onset of COVID-19 symptoms. Adjusted multivariable Cox proportional hazard regression analysis was performed to compare the risk of death between the treatment groups. Out of 1561 critically ill COVID-19 patients, 1014 were included in the baseline analysis. In the survival study, 1009 patients were assigned to the NoC (n = 346), HighC (n = 552), or LowC group (n = 111). The baseline characteristics were balanced between groups, except for age, BMI, APACHE II score, SOFA and SAPS II. While the 35-day survival did not show any differences, a landmark analysis of the patients surviving beyond 35 days revealed differences between groups. The restricted mean survival time was 112 days in the LowC group [95% CI: 97 - 128], 133 days in the HighC group [95% CI: 124 - 141] and 144 days in the NoC group [95% CI: 121 - 167]. The multivariable-adjusted Cox proportional hazard analysis indicated that, regardless of age, sex, health status or invasive oxygenation, a low-dose treatment increased the hazard of death of critically ill COVID-19 patients by a factor of 2.09 ([95% CI: 0.99, 4.4], p = 0.05) and a high-dose corticosteroid treatment increased the risk by a factor of 1.07 ([95% CI: 0.53, 2.15], p = 0.85) compared to no treatment with glucocorticoids. The analysis reveals that corticosteroid treatment does not influence the survival of critically ill COVID-19 patients in the intensive care unit within 35 days. Our evaluations further suggest that regardless of ventilation status, the decision-making process for administering corticosteroid therapy should account for the individual severity of the illness.
COVID-19 大流行对全球医疗系统构成了重大挑战。数以百万计的人受到感染,全球报告了数以百万计的死亡。糖皮质激素因其在 COVID-19 治疗中的潜在疗效而引起了全球关注。不同剂量和治疗持续时间的各种糖皮质激素已在不同严重程度的患者中进行了研究,但尚未确定合适的剂量和治疗持续时间。本研究旨在探讨在接受低剂量糖皮质激素、高剂量糖皮质激素或不接受糖皮质激素治疗的危重症患者中,住院病死率是否存在差异。所有在 2020 年 2 月至 2021 年 12 月期间因 COVID-19 肺炎接受补充氧气而入住柏林夏洛蒂大学医院重症监护病房的危重症患者均有资格参加这项多中心真实世界数据研究。患者回顾性地被分配到以下三组之一:高皮质激素剂量(HighC)组(接受 6 毫克静脉注射地塞米松或等效皮质激素剂量 10 天)、低皮质激素剂量(LowC)组(接受少于 6 毫克静脉注射地塞米松或等效皮质激素剂量 10 天)或无皮质激素(NoC)组。在总观察期内以及 COVID-19 症状发作后 35 天比较各组的总生存率和风险效应。使用多变量 Cox 比例风险回归分析比较治疗组之间的死亡风险。在 1561 名危重症 COVID-19 患者中,有 1014 名患者纳入基线分析。在生存研究中,1009 名患者被分配到 NoC(n=346)、HighC(n=552)或 LowC 组(n=111)。各组之间的基线特征平衡,除年龄、BMI、APACHE II 评分、SOFA 和 SAPS II 外。虽然 35 天生存率没有差异,但对超过 35 天存活的患者进行的里程碑分析显示出组间差异。低剂量组的限制性平均生存时间为 112 天[95%CI:97-128],高剂量组为 133 天[95%CI:124-141],无皮质激素组为 144 天[95%CI:121-167]。多变量调整后的 Cox 比例风险分析表明,无论年龄、性别、健康状况或有创性氧合如何,低剂量治疗都会使危重症 COVID-19 患者的死亡风险增加 2.09 倍[95%CI:0.99,4.4],高剂量皮质激素治疗使死亡风险增加 1.07 倍[95%CI:0.53,2.15],与不使用糖皮质激素治疗相比(p=0.05)。分析表明,皮质激素治疗在 35 天内不会影响重症监护病房内危重症 COVID-19 患者的生存率。我们的评估进一步表明,无论通气状态如何,皮质激素治疗决策过程都应考虑到疾病的个体严重程度。