Phocean Nephrology Institute, Clinique Bouchard, Marseille, France.
Association pour le Traitement des Urémiques en Provence, Marseille, France.
Nephrol Dial Transplant. 2020 Aug 1;35(8):1346-1353. doi: 10.1093/ndt/gfaa191.
Haemodialysis patients are at risk of developing severe forms of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection: coronavirus disease 2019 (COVID-19). In March 2020, hydroxychloroquine (HCQ) and azithromycin (AZI) were proposed as potential treatments of COVID-19, but with warnings concerning their possible toxicity. No data are available regarding the toxicity of this treatment in haemodialysis patients.
We report the use of HCQ and AZI in a cohort of COVID-19 haemodialysis patients with focus on safety concerns.
Twenty-one patients received 200 mg HCQ thrice daily during 10 days, and AZI 500 mg on Day 1, and 250 mg on the four following days. HCQ plasma concentrations were within the recommended range (0.1-1.0 µg/mL) in all patients except one, in which maximum concentration was 1.1 µg/mL. HCQ concentration raised until the third day and remained stable thereafter. No cardiac event occurred in spite of progressive lengthening of corrected QT interval (QTc) during the treatment. One patient experienced a long QTc syndrome (QTc >500 ms) without any arrhythmia episode, although HCQ concentration was in the target range. Five (23.8%) patients experienced hypoglycaemia, a well-known HCQ side-effect. SARS-CoV-2 RNA remained detectable in nasopharyngeal swabs for a long time in haemodialysis patients (mean time 21 days).
HCQ and AZI are safe in haemodialysis patients at these doses but can lead to long QTc syndrome and hypoglycaemia. HCQ concentrations were not correlated with side effects. We recommend monitoring of the QTc length throughout treatment, as well as glycaemia. SARS-CoV-2 could persist for longer in haemodialysis patients than in the general population.
血液透析患者有发生严重严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)感染的风险,即 2019 年冠状病毒病(COVID-19)。2020 年 3 月,羟氯喹(HCQ)和阿奇霉素(AZI)被提议作为 COVID-19 的潜在治疗方法,但有关于其潜在毒性的警告。目前尚无关于血液透析患者这种治疗方法毒性的数据。
我们报告了在 COVID-19 血液透析患者中使用 HCQ 和 AZI 的情况,重点关注安全性问题。
21 例患者接受了 200mg HCQ,每日三次,持续 10 天,AZI 在第 1 天 500mg,随后 4 天每天 250mg。除 1 名患者外,所有患者的 HCQ 血浆浓度均在推荐范围内(0.1-1.0μg/ml),该患者的最大浓度为 1.1μg/ml。HCQ 浓度在治疗期间直到第 3 天升高,此后保持稳定。尽管在治疗过程中校正 QT 间期(QTc)逐渐延长,但未发生心脏事件。尽管 HCQ 浓度在靶范围内,1 例患者仍出现长 QTc 综合征(QTc>500ms)而无心律失常发作。5 例(23.8%)患者发生低血糖,这是 HCQ 的已知副作用。SARS-CoV-2 RNA 在血液透析患者的鼻咽拭子中可长时间检测到(平均时间 21 天)。
在这些剂量下,HCQ 和 AZI 对血液透析患者是安全的,但可导致长 QTc 综合征和低血糖。HCQ 浓度与副作用无关。我们建议在整个治疗过程中监测 QTc 长度以及血糖水平。SARS-CoV-2 在血液透析患者中的持续时间可能比在普通人群中更长。