关键词: COVID-19 geriatrics nirmatrelvir remdesivir ritonavir

Mesh : Humans Antiviral Agents / therapeutic use adverse effects Female Male Aged, 80 and over Retrospective Studies COVID-19 Drug Treatment Alanine / analogs & derivatives therapeutic use adverse effects Adenosine Monophosphate / analogs & derivatives therapeutic use adverse effects SARS-CoV-2 / drug effects Aged Ritonavir / therapeutic use adverse effects Drug Interactions COVID-19 / virology Adenosine / analogs & derivatives

来  源:   DOI:10.3390/v16060864   PDF(Pubmed)

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:老年患者患冠状病毒病-2019(COVID-19)并发症的风险很高,是抗病毒药物的良好候选药物。(2)方法:对电子健康记录(EHRs)进行回顾性研究,旨在描述抗病毒药物(尼马特雷韦和利托那韦(尼马特雷韦/r)或雷德西韦)的使用,老年患者(75岁及以上)的药物-药物相互作用(DDI)和药物不良反应(ADR),2022年7月至2023年6月期间因轻度至中度COVID-19住院。(3)结果:491例患者(平均年龄:86.9岁),180人(36.7%)接受了尼玛特雷韦/r,78人(15.9%)接受了雷姆德西韦,233(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学数据之间没有发现关联。没有观察到严重的ADR。65%的肾功能损害患者的Nirmatrelvir/r剂量调整不足。总的来说,128名患者(71%)在尼马特雷韦/r有潜在的药代动力学DDIs,43导致可能相关的ADR。在Remdesivir组,药效学DDI更频繁,56例患者有QTc延长风险(72%)。只有20例患者接受了心电图随访,4.显示QTc延长。(4)结论:尽管有合理的适应症,但抗病毒药物的利用不足。Nirmatrelvir/r剂量很少根据肾功能进行调整。由于药物相互作用的高风险,需要剂量调整和更密切的监测。
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