Association of mortality and aspirin use for COVID-19 residents at VA Community Living Center Nursing Homes

Y. Abul, F. Devone, Thomas A Bayer, C. Halladay, K. McConeghy, Nadia Mujahid, Mriganka Singh, C. Leeder, S. Gravenstein, James L. Rudolph
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Abstract

Background/Objectives: Coronavirus disease 2019 (COVID-19) is associated with a hypercoagulable state and increased thrombotic risk in infected individuals. Several complex and varied coagulation abnormalities were proposed for this association1 .Acetylsalicylic acid(ASA, aspirin) is known to have inflammatory, antithrombotic properties and its use was reported as having potency to reduce RNA synthesis and replication of some types of coronaviruses including human coronavirus-299E (CoV-229E) and Middle East Respiratory Syndrome (MERS)-CoV 2,3. We hypothesized that chronic low dose aspirin use may decrease COVID-19 mortality relative to ASA non-users. Methods: This is a retrospective, observational cohort analysis of residents residing at Veterans Affairs Community Living Centers from December 13, 2020, to September 18, 2021, with a positive SARS-CoV-2 PCR test. Low dose aspirin users had low dose (81mg) therapy (10 of 14 days) prior to the positive COVID date and were compared to aspirin non-users (no ASA in prior 14 days). The primary outcome was mortality at 30 and 56 days post positive test and hospitalization within 14 days of positive test result. Results: We identified 1.823 residents who had SARS-CoV-2 infection and 1,687 residents were eligible as a final analytic sample after excluding high dose and intermittent/partial dose aspirin users. Overall mean age was 72.28+/-11.66 years and 3.3% (n=67) female in the final analytic sample. Among the 511 (30.3%) residents taking chronic low dose aspirin, 30-day mortality after an initial SARS-CoV-2 test establishing infection was 6.46% (n=33) compared to 10.29% (n=121) of non-users (SMD >0.1). 56-day mortality after initial SARS-CoV-2 test establishing infection was 9.0% (n=46) compared to 13.18% (n=155) not taking low dose aspirin (SMD >0.1). Cox proportional hazards model showed that aspirin use was independently associated with a reduced risk of 30 days of mortality (adjusted HR, 0.60, 95% CI, 0.40-0.90) and 56 days of mortality (adjusted HR, 0.67, 95% CI, 0.47-0.95) Conclusion: In this retrospective observational study of VA Community Living Center residents infected with SARS-CoV-2, low dose aspirin use for primary or secondary prevention of cardiovascular events is associated with lower COVID-19 mortality and fewer breakthrough cases. Although additional randomized controlled trials are required to understand these associations and the potential implications more fully for improving care, aspirin remains a medication with known side effects and clinical practice should not change based on these findings.
弗吉尼亚州社区生活中心养老院COVID-19居民死亡率与阿司匹林使用的关系
背景/目的:冠状病毒病2019 (COVID-19)与感染者的高凝状态和血栓形成风险增加有关。一些复杂而多样的凝血异常被认为与此相关1 .乙酰水杨酸(ASA,阿司匹林)已知具有炎症和抗血栓特性,据报道,它的使用具有减少某些类型冠状病毒的RNA合成和复制的能力,包括人类冠状病毒- 299e (CoV-229E)和中东呼吸综合征(MERS)-CoV 2,3。我们假设,相对于非ASA使用者,慢性低剂量阿司匹林使用可能会降低COVID-19死亡率。方法:对2020年12月13日至2021年9月18日在退伍军人事务社区生活中心居住的SARS-CoV-2 PCR检测阳性的居民进行回顾性、观察性队列分析。低剂量阿司匹林使用者在COVID阳性日期之前接受了低剂量(81mg)治疗(14天中的10天),并与非阿司匹林使用者(前14天没有ASA)进行了比较。主要转归是阳性检测后30天和56天的死亡率以及阳性检测结果后14天内的住院率。结果:我们确定了1.823名感染SARS-CoV-2的居民,在排除高剂量和间歇性/部分剂量阿司匹林使用者后,有1687名居民符合最终分析样本的条件。最终分析样本的总体平均年龄为72.28±11.66岁,女性占3.3% (n=67)。在511名(30.3%)服用慢性低剂量阿司匹林的居民中,首次进行SARS-CoV-2检测确定感染后的30天死亡率为6.46% (n=33),而非服药者(SMD >0.1)的死亡率为10.29% (n=121)。初始SARS-CoV-2检测确定感染后56天死亡率为9.0% (n=46),而未服用低剂量阿司匹林(SMD >0.1)的患者为13.18% (n=155)。Cox比例风险模型显示,阿司匹林的使用与降低30天死亡率(校正HR, 0.60, 95% CI, 0.40-0.90)和56天死亡率(校正HR, 0.67, 95% CI, 0.47-0.95)的风险独立相关。在这项对VA社区生活中心感染SARS-CoV-2的居民的回顾性观察研究中,低剂量阿司匹林用于心血管事件的一级或二级预防与较低的COVID-19死亡率和较少的突破性病例相关。尽管需要额外的随机对照试验来了解这些关联以及更充分地改善护理的潜在影响,但阿司匹林仍然是一种已知副作用的药物,临床实践不应根据这些发现而改变。
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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