抗病毒药物和他克莫司在胰岛移植患者SARS-CoV-2肺炎中的延迟药物-药物相互作用

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Therapeutic Drug Monitoring Pub Date : 2025-06-01 Epub Date: 2025-02-03 DOI:10.1097/FTD.0000000000001306
Amelia-Naomi Sabo, Sibylle Cunat, Véronique Kemmel
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引用次数: 0

摘要

背景:PAXLOVID (nirmatrelvir和ritonavir)和VEKLURY (remdesivir)是一线和二线抗病毒药物,用于有严重SARS-CoV-2感染(COVID-19)风险的成年患者,如移植受体。由于这一特定人群需要终身免疫抑制治疗,使用具有细胞色素p450调节特性的抗病毒药物使患者面临药物-药物相互作用(DDI)的高风险。病例介绍:一名接受胰岛移植的72岁男性患者在治疗SARS-CoV-2肺炎期间,在抗病毒治疗和他克莫司之间经历了DDI。患者接受了单剂量的尼马特韦/利托那韦,随后接受了单剂量的瑞德西韦。抗病毒治疗期间中断他克莫司治疗,他克莫司浓度在该患者的靶范围内。一旦停止抗病毒治疗,他克莫司重新以初始剂量使用。第6天,患者的临床和生物学参数与他克莫司过量相符。发现谷浓度比治疗目标高18倍,促使他克莫司停药9天,然后以较低剂量重新使用,随后根据治疗药物监测逐渐增加到初始剂量。临床和生物学参数逐渐恢复到基线水平。结论:处理他克莫司与抗sars - cov -2药物之间的DDI需要大量的治疗干预,并在抗病毒治疗期间和治疗后数天内密切监测治疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Delayed Drug-Drug Interaction Between Antiviral Drugs and Tacrolimus in a Pancreatic Islet Transplant Recipient With SARS-CoV-2 Pneumonia.

Background: PAXLOVID (nirmatrelvir and ritonavir) and VEKLURY (remdesivir) are the first- and second-line antivirals administered to adult patients at risk of severe forms of SARS-CoV-2 infection (COVID-19), such as transplant recipients. As this specific population requires lifelong immunosuppressive treatments, the administration of antivirals with cytochrome P450-modulating properties exposes patients to a high risk of drug-drug interactions (DDI).

Case presentation: A 72-year-old male patient who underwent a pancreatic islet transplant experienced DDI between antiviral treatment and tacrolimus during the management of SARS-CoV-2 pneumonia. The patient received a single dose of nirmatelvir/ritonavir followed by a single dose of remdesivir. Tacrolimus treatment was interrupted for the duration of the antiviral treatment, and the concentration of tacrolimus was within the target range for this patient. Once antiviral treatment was stopped, tacrolimus was reintroduced at the initial dose. On day 6, the patient presented with clinical and biological parameters consistent with a tacrolimus overdose. A trough concentration 18 times higher than the therapeutic target was found, prompting tacrolimus to be discontinued for 9 days and reintroduced at a lower dose, followed by a gradual increase based on therapeutic drug monitoring to the initial dose. Clinical and biological parameters gradually returned to baseline levels.

Conclusions: Management of DDI between tacrolimus and anti-SARS-CoV-2 drugs requires a substantial therapeutic intervention and close therapeutic drug monitoring during and for several days after antiviral treatment.

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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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