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血液透析和腹膜透析患者中伐昔洛韦相关神经毒性:一项基于全国人群的研究。

Valacyclovir-associated neurotoxicity among patients on hemodialysis and peritoneal dialysis: A nationwide population-based study.

作者信息

Wang Yi-Chun, Juan Shu-Hui, Li Ching-Hao, Chou Chu-Lin, Chen Li-Ying, Chien Li-Nien, Fang Te-Chao

机构信息

Division of Nephrology, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City, Taiwan.

School of Medicine, Tzu Chi University, Hualien, Taiwan.

出版信息

Front Med (Lausanne). 2022 Sep 20;9:997379. doi: 10.3389/fmed.2022.997379. eCollection 2022.

Abstract

Whether valacyclovir-associated neurotoxicity (VAN) occurs more frequently in patients with end-stage renal disease (ESRD) on dialysis is unknown. This is the first population-based study to examine the risk of VAN associated with ESRD patients on dialysis. Among 2,284,800 patients diagnosed as having herpes zoster from 2002 to 2016, patients with ESRD on dialysis and individuals with normal renal function were enrolled in this study. Following propensity score matching, we compared the risk of altered mental status between valacyclovir users and non-users in the ESRD and normal renal function cohorts over a 30-day follow-up period. In the ESRD cohort, the incidence of altered mental status was 1.68 and 0.52 per 1,000 person-day in valacyclovir users and non-users, respectively, with an adjusted hazard ratio (HR) of 3.22 (95% confidence interval [CI]: 2.04-4.99, < 0.001). The incidence of altered mental status of valacyclovir users on hemodialysis (HD) and peritoneal dialysis (PD) was higher than that of non-users. The adjusted HR was 3.20 (95% CI: 1.98-5.15, < 0.001) for those on HD and 3.44 (95% CI: 1.13-10.49, = 0.030) for those with PD. However, altered mental status was not observed in patients on HD receiving ≤500 mg of valacyclovir three times per week or in those on PD receiving ≤500 mg of valacyclovir per day. The findings demonstrate that adjusting the valacyclovir dosage and monitoring VAN in patients with HD and PD who have herpes zoster is crucial.

摘要

伐昔洛韦相关神经毒性(VAN)在接受透析的终末期肾病(ESRD)患者中是否更频繁发生尚不清楚。这是第一项基于人群的研究,旨在探讨与接受透析的ESRD患者相关的VAN风险。在2002年至2016年诊断为带状疱疹的2284800例患者中,本研究纳入了接受透析的ESRD患者和肾功能正常的个体。在倾向得分匹配后,我们比较了伐昔洛韦使用者和非使用者在ESRD和肾功能正常队列中30天随访期内精神状态改变的风险。在ESRD队列中,伐昔洛韦使用者和非使用者精神状态改变的发生率分别为每1000人日1.68和0.52,调整后的风险比(HR)为3.22(95%置信区间[CI]:2.04-4.99,<0.001)。接受血液透析(HD)和腹膜透析(PD)的伐昔洛韦使用者精神状态改变的发生率高于非使用者。HD患者的调整后HR为3.20(95%CI:1.98-5.15,<0.001),PD患者为3.44(95%CI:1.13-10.49,=0.030)。然而,每周接受≤500mg伐昔洛韦三次的HD患者或每天接受≤500mg伐昔洛韦的PD患者未观察到精神状态改变。研究结果表明,调整带状疱疹患者HD和PD患者的伐昔洛韦剂量并监测VAN至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ff1/9530346/627d5790a86f/fmed-09-997379-g001.jpg

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