Robin Christine, Hémery François, Dindorf Christel, Thillard Julien, Cabanne Ludovic, Redjoul Rabah, Beckerich Florence, Rodriguez Christophe, Pautas Cécile, Toma Andrea, Maury Sébastien, Durand-Zaleski Isabelle, Cordonnier Catherine
Department of Hematology, Assistance Publique-Hopitaux de Paris (APHP), Henri Mondor Teaching Hospital, 94010, Créteil, France.
University Paris-Est Créteil (UPEC), 94000, Créteil, France.
BMC Infect Dis. 2017 Dec 5;17(1):747. doi: 10.1186/s12879-017-2854-2.
Cytomegalovirus (CMV) infection and disease (CMV episodes) are global concerns after allogeneic hematopoietic stem cell transplantation (HSCT). They affect survival, both by direct and indirect effects. Due to safety issues of current anti-CMV antivirals, long-term CMV prophylaxis is poorly tolerated and the most common strategy to decrease the incidence of CMV disease is preemptive. New, less toxic, molecules are currently being assessed for CMV prophylaxis which should replace or considerably decrease the preemptive approach. The aim of this study was to assess the economic burden of CMV episodes after HSCT with a preemptive approach.
We analyzed data from 208 consecutive adults transplanted in our institution, between 2008 and 2013. Hospital resource utilization was retrieved via the linked hospital admissions and Diagnostic Related Groups for the period of conditioning to 12 months after transplant.
CMV episodes occurred in 70 patients (34%) over the first 12 months following HSCT, after a mean of 75 days (median: 46 (7-334)). The mean total length of stay was significantly associated with the occurrence of a CMV episode (113.9 vs. 87.5 days, p = 0.0002) but was associated neither with the pre-transplant CMV serology of donors/recipients nor with survival. The mean cost of transplant was €104,016 (SD = €37,281) after 12 months. Bivariate and multivariate analyses indicated that the occurrence of >1 CMV episode increased the costs of allogeneic HSCT by 25-30% (p < 0.0001).
Our study, which is the largest, single-institution cost study of allogeneic HSCT in Europe, shows that two or more CMV episodes significantly increased the transplant cost. New prophylactic strategies to prevent CMV infection and disease should decrease transplant costs.
巨细胞病毒(CMV)感染及疾病(CMV发作)是异基因造血干细胞移植(HSCT)后全球关注的问题。它们通过直接和间接影响来影响生存率。由于当前抗CMV抗病毒药物的安全性问题,长期CMV预防耐受性差,而降低CMV疾病发生率的最常见策略是抢先治疗。目前正在评估毒性较小的新型分子用于CMV预防,有望取代或大幅减少抢先治疗方法。本研究的目的是评估采用抢先治疗方法的HSCT后CMV发作的经济负担。
我们分析了2008年至2013年期间在我们机构连续接受移植的208名成年患者的数据。通过关联的医院入院记录和诊断相关分组检索移植预处理至移植后12个月期间的医院资源利用情况。
在HSCT后的前12个月内,70名患者(34%)发生了CMV发作,平均发作时间为75天(中位数:46天(7 - 334天))。平均总住院时间与CMV发作显著相关(113.9天对87.5天,p = 0.0002),但与供体/受体移植前的CMV血清学以及生存率均无关。移植12个月后的平均费用为104,016欧元(标准差 = 37,281欧元)。双变量和多变量分析表明,发生1次以上CMV发作会使异基因HSCT的费用增加25 - 30%(p < 0.0001)。
我们的研究是欧洲最大的关于异基因HSCT的单机构成本研究,表明两次或更多次CMV发作会显著增加移植成本。预防CMV感染和疾病的新预防策略应能降低移植成本。