Liang Xinyun, Famure Olusegun, Li Yanhong, Kim S Joseph
1 Multi-Organ Transplant Program, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
2 Division of Nephrology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Prog Transplant. 2018 Jun;28(2):124-133. doi: 10.1177/1526924818765798. Epub 2018 Mar 20.
Valganciclovir is used not only for cytomegalovirus prophylaxis after kidney transplantation but can also induce leukopenia, thereby making patients more susceptible to other infections. The epidemiology of leukopenia in patients on valganciclovir remains poorly understood.
To determine the incidence and risk factors for leukopenia in patients receiving valganciclovir for cytomegalovirus prophylaxis after kidney transplantation.
In this single-center, retrospective, cohort study, we included kidney recipients transplanted from January 1, 2003, to December 31, 2010, to determine the incidence and risk factors for leukopenia in patients who received valganciclovir for cytomegalovirus prophylaxis. The Kaplan-Meier product limit method was used to graphically assess time to leukopenia, and risk factors were assessed using Cox proportional hazards models.
A total of 542 kidney transplant recipients were included in the study cohort. The cumulative incidence of leukopenia at 6 months posttransplant was 39.3% (11.0% for neutropenia). Low baseline white blood cell count (hazard ratio [HR] 2.34 [95% confidence interval [CI], 1.37-4.00]) and high baseline body mass index (HR 1.05 [95% CI, 1.02-1.09]) were independently associated with an increased risk of leukopenia, while higher Cockcroft-Gault creatinine clearance (HR 0.87 [95% CI, 0.78-0.97]) was significantly associated with a decreased risk of leukopenia.
These data suggest that recipient baseline white blood cell count, baseline body mass index, and kidney function are clinical predictors of new-onset leukopenia after kidney transplantation. Our results may inform the approach to cytomegalovirus prophylaxis to reduce the risk of valganciclovir-induced leukopenia in kidney transplant recipients.
缬更昔洛韦不仅用于肾移植后巨细胞病毒的预防,还可诱发白细胞减少,从而使患者更容易受到其他感染。缬更昔洛韦治疗患者白细胞减少的流行病学情况仍知之甚少。
确定肾移植后接受缬更昔洛韦预防巨细胞病毒感染的患者白细胞减少的发生率及危险因素。
在这项单中心、回顾性队列研究中,我们纳入了2003年1月1日至2010年12月31日期间接受肾移植的患者,以确定接受缬更昔洛韦预防巨细胞病毒感染的患者白细胞减少的发生率及危险因素。采用Kaplan-Meier乘积限界法以图表形式评估白细胞减少的发生时间,并使用Cox比例风险模型评估危险因素。
研究队列共纳入542例肾移植受者。移植后6个月白细胞减少的累积发生率为39.3%(中性粒细胞减少为11.0%)。基线白细胞计数低(风险比[HR]2.34[95%置信区间[CI],1.37 - 4.00])和基线体重指数高(HR 1.05[95%CI,1.02 - 1.09])与白细胞减少风险增加独立相关,而较高的Cockcroft-Gault肌酐清除率(HR 0.87[95%CI,0.78 - 0.97])与白细胞减少风险降低显著相关。
这些数据表明,受者的基线白细胞计数、基线体重指数和肾功能是肾移植后新发白细胞减少的临床预测因素。我们的结果可能为巨细胞病毒预防方法提供参考,以降低肾移植受者中缬更昔洛韦诱发白细胞减少的风险。