中重度新冠肺炎心肌损伤患者服用与不服用azvudine的全因死亡率:倾向评分匹配分析。

Q4 Medicine Cardiology Plus Pub Date : 2023-04-01 Epub Date: 2023-05-31 DOI:10.1097/CP9.0000000000000049
Ru Chen, Yi Guo, Shan Deng, Jian Wang, Meng Gao, Hongli Han, Lin Wang, Hongwei Jiang, Kai Huang
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引用次数: 0

摘要

奥密克戎目前是严重急性呼吸综合征冠状病毒2型的主要毒株,但对奥密克龙相关心肌损伤的特征和管理,特别是抗病毒药物阿兹夫定的潜在益处知之甚少。方法:纳入2022年12月7日至12月30日武汉协和医院收治的2019年确诊和疑似冠状病毒病(新冠肺炎)患者。Cox回归分析用于确定全因死亡率的危险因素。以1:1的比例进行倾向评分匹配分析,相关混杂因素的标准差为0.1。结果:最终分析共包括332名患者(167例确诊病例和165例疑似病例),42.77%(142/332)的患者年龄在80岁或以上,68.67%(228/332)为男性,158名患者接受了阿兹夫定治疗。在匹配队列中,总死亡率为30.30%(60/198),40名(20.20%,40/198)患者接受了无创通气,22名(11.11%,22/198)患者进行了有创通气,34名(17.17%,34/198)患者入住重症监护室(ICU)。休克、多器官损伤和心律失常的发生率分别为11.62%(23/198)、20.20%(40/198)和12.12%(24/198)。在接受或不接受azvudine治疗的患者中,这些临床结果没有显著差异。即使在调整了包括糖皮质激素、免疫球蛋白和抗凝治疗在内的其他治疗后,阿兹夫定也降低了早期死亡率(入院后14天内)(风险比:0.37,95%置信区间:0.18-0.77),但没有降低患者的最终住院死亡率。结论:COVID-198相关心肌损伤患者的死亡率约为30.30%(60/198)。阿兹夫定提高了患者的早期生存率,但没有提高最终死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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All-cause mortality in moderate and severe COVID-19 patients with myocardial injury receiving versus not receiving azvudine: a propensity score-matched analysis.

Omicron is currently the dominant strain of severe acute respiratory syndrome coronavirus 2, but little is known about the characteristics and management of omicron related myocardial injury, particularly the potential benefit of the antiviral agent azvudine.

Methods: Patients with confirmed and suspected coronavirus disease 2019 (COVID-19) admitted to Wuhan Union Hospital from December 7, 2022, to December 30, 2022, were included in this study. Cox regression was conducted to identify risk factors for all-cause mortality. A propensity score-matched analysis was performed at a 1:1 ratio with a caliper of 0.1 pooled standard deviations of relevant confounders.

Results: The final analysis included a total of 332 patients (167 confirmed cases and 165 suspected cases), 42.77% (142/332) of the patients were 80 years of age or older and 68.67% (228/332) of them were men, 158 patients were treated with azvudine. In the matched cohort, the total mortality was 30.30% (60/198), 40 (20.20%, 40/198) patients received noninvasive ventilation and 22 (11.11%, 22/198) received invasive ventilation, 34 (17.17%, 34/198) patients were admitted to intensive care unit (ICU). The rate of shock, multiple organ damages and arrhythmia were 11.62% (23/198), 20.20% (40/198), and 12.12% (24/198), respectively. There was no significant difference on these clinical outcomes in patients treated with azvudine or not. Azvudine reduced early mortality (within 14 days from admission) (hazard ratio: 0.37, 95% confidence interval: 0.18-0.77) even after adjusting for other treatments including glucocorticoids, immunoglobin and anticoagulant therapy, but not the final in-hospital mortality of patients.

Conclusions: Patients with COVID-19-related myocardial injury had a high mortality of about 30.30% (60/198). Azvudine improved the early survival of the patients but not final mortality.

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32 weeks
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