Kojima Yusuke, Katada Yoshiki, Nakagawa Shunsaku, Umemura Keisuke, Katsube Yurie, Hira Daiki, Tsuda Masahiro, Ishimura Hiroki, Matsumura Katsuyuki, Hirai Machiko, Nagao Miki, Tanaka Satona, Nakajima Daisuke, Date Hiroshi, Terada Tomohiro
Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital, Sakyo-ku, Kyoto, Japan; Department of Infection Control and Prevention, Kyoto University Hospital, Sakyo-ku, Kyoto, Japan.
Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital, Sakyo-ku, Kyoto, Japan; Department of Infection Control and Prevention, Kyoto University Hospital, Sakyo-ku, Kyoto, Japan.
J Infect Chemother. 2025 Aug;31(8):102745. doi: 10.1016/j.jiac.2025.102745. Epub 2025 Jun 2.
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(GCV)在预防肺移植后巨细胞病毒(CMV)感染中发挥着重要作用。由于GCV药代动力学存在较大的个体间和个体内变异性,有人提出需要根据血药浓度制定个体化剂量。然而,静脉-动脉体外膜肺氧合(VA-ECMO)期间GCV的药代动力学尚不清楚。在此,我们描述了一例肺移植后在ECMO期间测量GCV血药浓度的病例。此外,我们将该病例中GCV的血药浓度与11例未接受ECMO的肺移植受者的血药浓度进行了比较。一名40多岁接受脑死亡供体双侧肺移植的女性术后接受了长时间的VA-ECMO治疗。术后第7天开始预防性给予GCV(2.5mg/kg/12小时)。ECMO期间(术后第8 - 28天)GCV谷浓度为940±854ng/mL。术后第23天观察到血小板减少和肾功能不全。相反,同年接受肺移植但未使用ECMO的11例成年患者在术后第8 - 28天的GCV谷浓度为445±263ng/mL。这是首例关于肺移植后接受VA-ECMO患者GCV谷浓度的报告。与未接受ECMO的肺移植患者相比,该接受ECMO的患者GCV血药谷浓度升高,同时伴有急性肾损伤和血小板减少。在VA-ECMO期间给予GCV时,可能需要进行治疗药物监测以预防不良反应并考虑个体内变异性。