Hydroxychloroquine: Pharmacokinetics and Toxicity

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Journal of Clinical Pharmacy and Therapeutics Pub Date : 2024-01-24 DOI:10.1155/2024/6500340
Philippe Brouqui, Eric Chabrière, Didier Raoult
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引用次数: 0

Abstract

Background/Purpose(s). We have extensively used HCQ at 200 mg three times a day (tid) to treat various infections such as Q fever and Whipple’s disease. Serum levels of between 1 μg/ml and 2 μg/ml serum level are recommended to achieve the safety and efficacy of these treatments. Our aim in this paper is to describe our experience regarding the pharmacokinetics and toxicity of HCQ in another infection caused by SARS-CoV-2. Methods. As recommended, we performed electrocardiograms before administering HCQ off-label. The HCQ concentration in the serum was monitored to ensure the effectiveness and safety of the treatment. We retrospectively analysed HCQ serum concentrations measured over time and toxicity data in patients with COVID-19 who were treated with HCQ at the IHU Marseille Infection. We did not treat patients with HCQ contraindications with this medication. Results. We measured HCQ concentrations in 1310 serum samples from 989 patients with COVID-19. The mean ± SD HCQ concentration increased in patients’ sera during treatment from day 1 (0.10 μg/ml ± 0.08) to day 11 (0.85 μg/ml ± 0.44), confirming that HCQ accumulates in the body during short-term therapy. However, the observed concentrations did not exceed the therapeutic range for other indications (0.80–1.20 μg/mL in Q fever patients treated for between 18 and 24 months). In patients treated with HCQ, major side effects included intestinal disorders (nausea, vomiting, and gastric pain) and QT prolongation. No conduction disorders (including torsades de pointes and ventricular arrhythmia), cardiomyopathy, retinopathy, or HCQ-related deaths were observed. Conclusions. In patients treated over a short time period with 200 mg tid of HCQ, therapeutic concentrations in serum were obtained in most patients without significant side effects or complications. Although patients must be carefully evaluated for HCQ contraindications, HCQ 200 mg tid for ten days can be considered an appropriate and safe dosage in patients with COVID-19.

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羟氯喹药代动力学和毒性
背景/目的。我们已广泛使用 HCQ 治疗 Q 热和惠普尔病等各种感染,剂量为 200 毫克,每天三次(tid)。建议血清中的 HCQ 水平在 1 μg/ml 至 2 μg/ml 之间,以实现这些治疗的安全性和有效性。本文旨在介绍在另一种由 SARS-CoV-2 引起的感染中使用 HCQ 的药代动力学和毒性方面的经验。研究方法根据建议,我们在标示外使用 HCQ 前进行了心电图检查。监测血清中的 HCQ 浓度,以确保治疗的有效性和安全性。我们回顾性分析了在马赛感染研究所接受 HCQ 治疗的 COVID-19 患者血清中 HCQ 的浓度和毒性数据。我们没有对有 HCQ 禁忌症的患者使用该药物进行治疗。结果。我们测量了 989 名 COVID-19 患者 1310 份血清样本中的 HCQ 浓度。在治疗过程中,患者血清中 HCQ 浓度的平均值(± SD)从第 1 天(0.10 μg/ml ± 0.08)增加到第 11 天(0.85 μg/ml ± 0.44),证实在短期治疗过程中 HCQ 会在体内蓄积。不过,观察到的浓度并未超过其他适应症的治疗范围(Q 热患者治疗 18 至 24 个月的浓度为 0.80-1.20 μg/ml)。在接受 HCQ 治疗的患者中,主要副作用包括肠道功能紊乱(恶心、呕吐和胃痛)和 QT 延长。未发现传导障碍(包括室性心动过速和室性心律失常)、心肌病、视网膜病变或与 HCQ 相关的死亡病例。结论在短时间内使用 200 毫克滴注 HCQ 治疗的患者中,大多数患者的血清中都能达到治疗浓度,且无明显副作用或并发症。虽然必须仔细评估患者是否有 HCQ 禁忌症,但对于 COVID-19 患者来说,HCQ 200 毫克/次、10 天的剂量是适当而安全的。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
226
审稿时长
6 months
期刊介绍: The Journal of Clinical Pharmacy and Therapeutics provides a forum for clinicians, pharmacists and pharmacologists to explore and report on issues of common interest. Reports and commentaries on current issues in medical and pharmaceutical practice are encouraged. Papers on evidence-based clinical practice and multidisciplinary collaborative work are particularly welcome. Regular sections in the journal include: editorials, commentaries, reviews (including systematic overviews and meta-analyses), original research and reports, and book reviews. Its scope embraces all aspects of clinical drug development and therapeutics, including: Rational therapeutics Evidence-based practice Safety, cost-effectiveness and clinical efficacy of drugs Drug interactions Clinical impact of drug formulations Pharmacogenetics Personalised, stratified and translational medicine Clinical pharmacokinetics.
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