Aigner Clemens, Jaksch Peter, Winkler Guenther, Czebe Kriztina, Taghavi Shahrokh, Marta Gabriel, Klepetko Walter
Department of Cardiothoracic Surgery, Vienna General Hospital, Vienna Medical University, Vienna, Austria.
Wien Klin Wochenschr. 2005 Jul;117(13-14):480-4. doi: 10.1007/s00508-005-0413-0.
The most common opportunistic viral pathogen after lung transplantation is cytomegalovirus (CMV). Oral valganciclovir, a prodrug of ganciclovir, has been introduced as a potential drug for prophylaxis and treatment of CMV infection and disease in lung transplantation. The goal of this study was to describe our initial experience with oral valganciclovir for pre-emptive treatment of CMV infections after lung transplantation.
We summarize our experience with 19 patients who underwent lung transplantation and received pre-emptive oral valganciclovir therapy in the situation of positive CMV polymerase chain reaction (PCR) in either plasma or bronchoalveolar lavage. None of the patients presented with manifest CMV disease. Treatment dosage of valganciclovir was 450 mg to 1800 mg daily, depending on renal function and white blood count. Treatment was continued until the CMV PCR became negative, in any case for a period of at least 14 days.
Three patients received two courses of pre-emptive oral valganciclovir; 16 patients were treated once. Eleven patients (57.9%) were treated because of a positive plasma CMV PCR; in eight patients (42.1%) the PCR was positive only in bronchoalveolar lavage. Therapy was initiated 896 +/- 1186 days (range, 108-3911) after transplantation with a mean CMV PCR of 45,536 +/- 149,294 copies (range, 426-706,000). In all cases the PCR fell below detectability (<400 copies) after a period of 22 +/- 10 days of treatment (range, 7-50 days). Mild to moderate leucopenia was observed in seven patients (36.8%) during treatment. None of the patients developed new onset of other potentially drug-related disorders such as neutropenia, anemia, deterioration of renal function or gastrointestinal disorder.
Pre-emptive therapy with oral valganciclovir for CMV infections detected by PCR in either plasma or bronchoalveolar lavage after lung transplantation seems to be efficacious and safe. However, regular blood counts should be performed to detect developing leucopenia.
肺移植后最常见的机会性病毒病原体是巨细胞病毒(CMV)。口服缬更昔洛韦是更昔洛韦的前体药物,已被用作预防和治疗肺移植中CMV感染及疾病的潜在药物。本研究的目的是描述我们使用口服缬更昔洛韦对肺移植后CMV感染进行抢先治疗的初步经验。
我们总结了19例接受肺移植并在血浆或支气管肺泡灌洗中CMV聚合酶链反应(PCR)呈阳性情况下接受抢先口服缬更昔洛韦治疗的患者的经验。所有患者均未出现明显的CMV疾病。缬更昔洛韦的治疗剂量为每日450毫克至1800毫克,具体取决于肾功能和白细胞计数。治疗持续至CMV PCR转为阴性,无论如何至少持续14天。
3例患者接受了两个疗程的抢先口服缬更昔洛韦治疗;16例患者接受了一次治疗。11例患者(57.9%)因血浆CMV PCR阳性而接受治疗;8例患者(42.1%)仅支气管肺泡灌洗中的PCR呈阳性。治疗在移植后896±1186天(范围108 - 3911天)开始,平均CMV PCR为45,536±149,294拷贝(范围426 - 706,000)。在所有病例中,经过22±10天(范围7 - 50天)的治疗后,PCR降至检测下限以下(<400拷贝)。治疗期间7例患者(36.8%)出现轻度至中度白细胞减少。没有患者出现新的其他潜在药物相关疾病,如中性粒细胞减少、贫血、肾功能恶化或胃肠道疾病。
对于肺移植后血浆或支气管肺泡灌洗中通过PCR检测到的CMV感染,口服缬更昔洛韦抢先治疗似乎有效且安全。然而,应定期进行血常规检查以检测白细胞减少的发生。