Pharmacokinetics of ganciclovir for prevention of cytomegalovirus infection in a lung transplant recipient on veno-arterial extracorporeal membrane oxygenation: A case report and literature review

IF 1.5 4区 医学 Q3 INFECTIOUS DISEASES
Yusuke Kojima , Yoshiki Katada , Shunsaku Nakagawa , Keisuke Umemura , Yurie Katsube , Daiki Hira , Masahiro Tsuda , Hiroki Ishimura , Katsuyuki Matsumura , Machiko Hirai , Miki Nagao , Satona Tanaka , Daisuke Nakajima , Hiroshi Date , Tomohiro Terada
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Abstract

Ganciclovir (GCV) plays an important role in preventing cytomegalovirus (CMV) infection after lung transplantation. Because of the large inter-individual and intra-individual variabilities in GCV pharmacokinetics, it has been suggested that individualized dosages based on blood levels are required. However, GCV pharmacokinetics during veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is unknown. Here, we describe a case in which blood levels of GCV were measured during ECMO after lung transplantation. Additionally, we compared the blood levels of GCV in this case with those of 11 lung transplant recipients who were not on ECMO. A woman in her 40s who underwent deceased-donor bilateral lung transplantation was treated with prolonged VA-ECMO postoperatively. Prophylactic administration of GCV (2.5 mg/kg/12 h) was initiated on postoperative day (POD) 7. The GCV trough concentration during ECMO (PODs 8–28) was 940 ± 854 ng/mL. Thrombocytopenia and renal dysfunction were observed on POD 23. Conversely, 11 adult patients who underwent lung transplantation in the same year as the present patient, but without ECMO, had a GCV trough concentration of 445 ± 263 ng/mL on PODs 8–28. This is the first report of GCV trough concentrations in a patient receiving VA-ECMO after lung transplantation. Compared with lung transplant patients not receiving ECMO, this patient undergoing ECMO exhibited elevated GCV blood trough concentrations, along with acute kidney injury and thrombocytopenia. When GCV is administered during VA-ECMO, therapeutic drug monitoring may be necessary to prevent adverse reactions and account for intra-individual variability.
更昔洛韦在静脉-动脉体外膜氧合下预防肺移植受体巨细胞病毒感染的药代动力学:1例报告并文献复习。
更昔洛韦(GCV)在肺移植术后预防巨细胞病毒(CMV)感染中起重要作用。由于GCV药代动力学存在很大的个体间和个体内差异,因此有人建议需要根据血液水平进行个体化剂量。然而,静脉-动脉体外膜氧合(VA-ECMO)期间的GCV药代动力学尚不清楚。在这里,我们描述了一例在肺移植后ECMO期间测量血液GCV水平的病例。此外,我们将该病例的GCV与11名未进行ECMO的肺移植受者的血液GCV水平进行了比较。一位40多岁的女性接受了死亡供体双侧肺移植手术,术后进行了长时间的VA-ECMO治疗。术后第1天(POD)开始预防性给予GCV (2.5 mg/kg/12 h) 7。ECMO期间GCV谷浓度(PODs 8-28)为940±854 ng/mL。POD 23观察血小板减少和肾功能不全。相反,与本例患者同一年接受肺移植但未进行ECMO的11例成人患者在PODs 8-28上的GCV谷浓度为445±263 ng/mL。这是首次报道肺移植后接受VA-ECMO的患者GCV谷浓度。与未接受ECMO的肺移植患者相比,接受ECMO的患者表现出GCV血槽浓度升高,并伴有急性肾损伤和血小板减少症。当在VA-ECMO期间给药GCV时,治疗药物监测可能是必要的,以防止不良反应并考虑到个体内的变异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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