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一名感染新型冠状病毒肺炎的胰岛移植受者中抗病毒药物与他克莫司之间的延迟药物相互作用

Delayed Drug-Drug Interaction Between Antiviral Drugs and Tacrolimus in a Pancreatic Islet Transplant Recipient With SARS-CoV-2 Pneumonia.

作者信息

Sabo Amelia-Naomi, Cunat Sibylle, Kemmel Véronique

机构信息

Laboratoire de Biochimie et Biologie Moléculaire, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Laboratoire de Pharmacologie et Toxicologie Neurocardiovasculaire, Unité de recherche 7296, Faculté de Médecine de Maïeutique et des Sciences de la Santé, Centre de Recherche en Biomédecine de Strasbourg (CRBS), Strasbourg, France ; and.

出版信息

Ther Drug Monit. 2025 Jun 1;47(3):326-329. doi: 10.1097/FTD.0000000000001306. Epub 2025 Feb 3.

Abstract

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.

摘要

背景

PAXLOVID(奈玛特韦和利托那韦)和VEKLURY(瑞德西韦)分别是用于有严重形式的严重急性呼吸综合征冠状病毒2感染(COVID-19)风险的成年患者(如移植受者)的一线和二线抗病毒药物。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会使患者面临较高的药物相互作用(DDI)风险。

病例报告

一名接受胰岛移植的72岁男性患者在治疗严重急性呼吸综合征冠状病毒2肺炎期间,抗病毒治疗与他克莫司之间发生了药物相互作用。患者接受了单剂量的奈玛特韦/利托那韦,随后接受了单剂量的瑞德西韦。在抗病毒治疗期间,他克莫司治疗中断,他克莫司浓度处于该患者的目标范围内。一旦停止抗病毒治疗,他克莫司以初始剂量重新开始使用。在第6天,患者出现了与他克莫司过量一致的临床和生物学参数。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开始使用,随后根据治疗药物监测逐渐增加至初始剂量。临床和生物学参数逐渐恢复到基线水平。

结论

他克莫司与抗严重急性呼吸综合征冠状病毒2药物之间的药物相互作用管理需要大量的治疗干预,并在抗病毒治疗期间及之后数天进行密切的治疗药物监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1744/12061378/d02c2b80fe79/tdm-47-326-g001.jpg

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