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在奥密克戎浪潮中老年患者的轻度至中度 SARS-CoV-2 感染中的抗病毒治疗应用。

Antiviral Use in Mild-to-Moderate SARS-CoV-2 Infections during the Omicron Wave in Geriatric Patients.

机构信息

Division of Clinical Pharmacology and Toxicology, Department of Anesthesiology, Pharmacology, Intensive Care, and Emergency Medicine, Geneva University Hospitals, 1205 Geneva, Switzerland.

Faculty of Medicine, University of Geneva, 1206 Geneva, Switzerland.

出版信息

Viruses. 2024 May 28;16(6):864. doi: 10.3390/v16060864.

Abstract

(1) Background: Geriatric patients are at high risk of complications of Coronavirus disease-2019 (COVID-19) and are good candidates for antiviral drugs. (2) Methods: A retrospective study of electronic health records (EHRs) aiming to describe antiviral (nirmatrelvir and ritonavir (nirmatrelvir/r) or remdesivir) use, drug-drug interactions (DDIs) and adverse drug reactions (ADRs) in elderly patients (75 and over), hospitalized with mild-to-moderate COVID-19 between July 2022 and June 2023. (3) Results: Out of 491 patients (mean age: 86.9 years), 180 (36.7%) received nirmatrelvir/r, 78 (15.9%) received remdesivir, and 233 (47.4%) received no antiviral therapy. No association was found between the choice of antiviral and the demographic or medical data. No serious ADR was observed. Nirmatrelvir/r dosage adjustment was inadequate in 65% of patients with renal impairment. In total, 128 patients (71%) on nirmatrelvir/r had potential pharmacokinetic DDIs, with 43 resulting in a possibly related ADR. In the remdesivir group, pharmacodynamic DDIs were more frequent, with QTc prolongation risk in 56 patients (72%). Only 20 patients underwent follow-up ECG, revealing QTc prolongation in 4. (4) Conclusions: There is an underutilization of antivirals despite their justified indications. Nirmatrelvir/r dosage was rarely adjusted to renal function. Dose adjustments and closer monitoring are needed due to the high risk of drug interactions.

摘要

(1) 背景:老年患者感染 2019 年冠状病毒病(COVID-19)并发症的风险较高,是抗病毒药物的良好候选者。(2) 方法:对电子健康记录(EHR)进行回顾性研究,旨在描述 2022 年 7 月至 2023 年 6 月期间,因轻度至中度 COVID-19 住院的老年(75 岁及以上)患者使用抗病毒药物(奈玛特韦和利托那韦(奈玛特韦/利托那韦)或瑞德西韦)、药物-药物相互作用(DDI)和药物不良反应(ADR)的情况。(3) 结果:在 491 名患者中(平均年龄:86.9 岁),180 名(36.7%)接受了奈玛特韦/利托那韦,78 名(15.9%)接受了瑞德西韦,233 名(47.4%)未接受抗病毒治疗。抗病毒药物的选择与人口统计学或医疗数据之间没有关联。未观察到严重的 ADR。在肾功能受损的患者中,奈玛特韦/利托那韦的剂量调整不足的占 65%。共有 128 名(71%)接受奈玛特韦/利托那韦的患者存在潜在的药代动力学 DDI,其中 43 例导致可能相关的 ADR。在瑞德西韦组中,药效动力学 DDI 更为常见,56 例(72%)患者出现 QTc 延长风险。仅有 20 名患者接受了后续心电图检查,发现 4 例 QTc 延长。(4) 结论:尽管有合理的适应症,但抗病毒药物的使用率较低。奈玛特韦/利托那韦的剂量很少根据肾功能进行调整。由于药物相互作用的风险较高,需要调整剂量并进行更密切的监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf27/11209592/d8e6281b29c0/viruses-16-00864-g001.jpg

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