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羟氯喹和达芦那韦或洛匹那韦治疗 COVID-19 感染的安全性。

Safety of hydroxychloroquine and darunavir or lopinavir in COVID-19 infection.

机构信息

CHU de Bordeaux, Service de médecine interne et maladies infectieuses, Hôpital Saint-André, F-33000 Bordeaux, France.

Univ. Bordeaux, F-33000 Bordeaux, France.

出版信息

J Antimicrob Chemother. 2021 Jan 19;76(2):482-486. doi: 10.1093/jac/dkaa441.

Abstract

BACKGROUND

Combination therapy with hydroxychloroquine and darunavir/ritonavir or lopinavir/ritonavir has been suggested as an approach to improve the outcome of patients with moderate/severe COVID-19 infection.

OBJECTIVES

To examine the safety of combination therapy with hydroxychloroquine and darunavir/ritonavir or lopinavir/ritonavir.

METHODS

This was an observational cohort study of patients hospitalized for COVID-19 pneumonia treated with hydroxychloroquine and darunavir/ritonavir or lopinavir/ritonavir. Clinical evaluations, electrocardiograms and the pharmacokinetics of hydroxychloroquine, darunavir and lopinavir were examined according to clinical practice and guidelines.

RESULTS

Twenty-one patients received hydroxychloroquine with lopinavir/ritonavir (median age 68 years; 10 males) and 25 received hydroxychloroquine with darunavir/ritonavir (median age 71 years; 15 males). During treatment, eight patients (17.4%) developed ECG abnormalities. Ten patients discontinued treatment, including seven for ECG abnormalities a median of 5 (range 2-6) days after starting treatment. All ECG abnormalities reversed 1-2 days after interrupting treatment. Four patients died within 14 days. ECG abnormalities were significantly associated with age over 70 years, coexisting conditions (such as hypertension, chronic cardiovascular disease and kidney failure) and initial potential drug interactions, but not with the hydroxychloroquine concentration.

CONCLUSIONS

Of the patients with COVID-19 who received hydroxychloroquine with lopinavir or darunavir, 17% had ECG abnormalities, mainly related to age or in those with a history of cardiovascular disease.

摘要

背景

联合应用羟氯喹和达芦那韦/利托那韦或洛匹那韦/利托那韦治疗中重度 COVID-19 感染患者,被认为可以改善患者的预后。

目的

评估羟氯喹联合达芦那韦/利托那韦或洛匹那韦/利托那韦治疗的安全性。

方法

这是一项观察性队列研究,纳入了因 COVID-19 肺炎住院接受羟氯喹联合达芦那韦/利托那韦或洛匹那韦/利托那韦治疗的患者。根据临床实践和指南,对患者的临床评估、心电图和羟氯喹、达芦那韦和洛匹那韦的药代动力学进行了检查。

结果

21 例患者接受了羟氯喹联合洛匹那韦/利托那韦治疗(中位年龄 68 岁,男性 10 例),25 例患者接受了羟氯喹联合达芦那韦/利托那韦治疗(中位年龄 71 岁,男性 15 例)。在治疗过程中,8 例(17.4%)患者出现心电图异常。10 例患者停止了治疗,其中 7 例在开始治疗后 5 天内(中位数,2-6 天)因心电图异常而停药。所有心电图异常在停药后 1-2 天内逆转。4 例患者在 14 天内死亡。心电图异常与年龄超过 70 岁、并存疾病(如高血压、慢性心血管疾病和肾衰竭)以及初始潜在药物相互作用显著相关,但与羟氯喹浓度无关。

结论

在接受羟氯喹联合洛匹那韦或达芦那韦治疗的 COVID-19 患者中,17%出现心电图异常,主要与年龄或心血管疾病史相关。

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