Afyonkarahisar Health Sciences University, Department of Cardiology, Afyonkarahisar, Turkey.
Provincial Directorate of Health, Department of Public Health, Afyonkarahisar, Turkey; Public Health Specialist, Afyonkarahisar, Turkey.
Med Clin (Barc). 2023 Jan 20;160(2):71-77. doi: 10.1016/j.medcli.2022.05.009. Epub 2022 Jul 15.
To evaluate the effect of drug interactions with chronic direct oral anticoagulants (DOAC) on mortality in older atrial fibrillation (AF) patients during the Coronavirus disease 2019(COVID-19) pandemic.
We followed a total of 601 elderly patients (65 years of age) from the NOEL-Drug Registry cohort who were referred to a tertiary outpatient clinic between 9 March 2020 and 1 March 2021. We recorded clinical characteristics and medications for the last 3 months. In addition, all drug interactions were identified using Lexicomp®. Finally, we recorded retrospectively all death events, COVID-19 diagnosis, and relevant deaths from the database at the end of the study. According to logistic regression, we performed propensity score (PS) matching to reduce potential bias. Factors associated with total mortality in the 12 months were analyzed using multivariable Cox proportion hazard analysis.
The mean age [standard deviation (SD)] was 74.5 (±6.9), and the male/female ratio was 337/264. The prevalence of total mortality was 16.9% (n=102). A total of 4472 drugs were analyzed for DOAC interaction. 81.8% of older AF patients were not at risk in terms of potential interaction. In the Cox proportional hazard model after PS-matching, previous DOAC use with class X interaction was associated with significantly higher mortality risk (adjusted hazard ratio: 2.745, 95% confidence interval: 1.465-5.172, p=0.004).
Our study showed that while most co-medications do not have significant interactions with DOACs, few serious drug interactions contribute to mortality in elderly patients with AF during the pandemic.
评估新冠肺炎(COVID-19)大流行期间慢性直接口服抗凝药物(DOAC)与药物相互作用对老年心房颤动(AF)患者死亡率的影响。
我们随访了总共 601 名来自 NOEL-Drug 登记处队列的老年患者(年龄≥65 岁),他们于 2020 年 3 月 9 日至 2021 年 3 月 1 日期间被转诊至三级门诊诊所。我们记录了他们的临床特征和过去 3 个月的用药情况。此外,我们还使用 Lexicomp® 来识别所有的药物相互作用。最后,我们从数据库中回顾性地记录了研究结束时所有的死亡事件、COVID-19 诊断和相关死亡。根据逻辑回归,我们进行倾向评分(PS)匹配以减少潜在的偏倚。使用多变量 Cox 比例风险分析来分析 12 个月内与总死亡率相关的因素。
患者的平均年龄(标准差)为 74.5(±6.9)岁,男女比例为 337/264。总死亡率为 16.9%(n=102)。共分析了 4472 种 DOAC 相互作用药物。81.8%的老年 AF 患者没有潜在相互作用的风险。在 PS 匹配后的 Cox 比例风险模型中,先前使用与 X 类相互作用的 DOAC 与死亡率显著增加相关(调整后的危险比:2.745,95%置信区间:1.465-5.172,p=0.004)。
我们的研究表明,虽然大多数合并用药与 DOAC 无明显相互作用,但少数严重的药物相互作用会导致 COVID-19 大流行期间老年 AF 患者的死亡率增加。