Cytomegalovirus infection and kidney transplantation- A retrospective study of risk factors and long-term clinical outcome

被引:1
|
作者
Rajendiran, Aravinth Kumar [1 ]
Jeyachandran, Dhanapriya [1 ]
Gopalakrishnan, Natarajan [1 ]
Arumugam, Venkatesh [1 ]
Thanigachalam, Dineshkumar [1 ]
Ramanathan, Sakthirajan [1 ]
机构
[1] Madras Med Coll & Govt Gen Hosp, Inst Nephrol, Chennai 600003, Tamil Nadu, India
关键词
Allograft rejection; cytomegalovirus infection; long-term graft survival; new-onset diabetes after transplantation; DIABETES-MELLITUS; CMV DISEASE; RECIPIENTS; IMPACT; PROPHYLAXIS; MANAGEMENT;
D O I
10.4103/ijot.ijot_116_20
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Aim: The aim was to study the clinical characteristics of postrenal transplant cytomegalovirus (CMV) infection and analyze its risk factors and its impact on graft and patient survival. Materials and Methods: We reviewed medical records of 739 renal transplant patients over 17 years (2002-2018). The demographic characteristics of patients were collected and compared with and without CMV infection. Multiple logistic regression analysis was done to identify risk factors for posttransplant CMV infection. Kaplan-Meier survival curve analysis was performed to analyze graft and patient survival by CMV infection. Results: The prevalence of CMV infection in our center was 12.4%. The most common presentation of CMV infection posttransplant is CMV syndrome. The use of antirejection therapy (hazard ratio [HR] 4.2, 95% confidence interval [CI] 2.6-6.9, P = 0.00), and new-onset diabetes after transplantation (NODAT) (HR 5.95, 95% CI 3.4-10, P = 0.00) was independently associated with postrenal transplant CMV infection. In Kaplan-Meier survival analysis, death-censored graft survival was significantly superior in patients without CMV infection/disease (CMV group: 55.4% vs. non-CMV group: 70.6% at 140 months P = 0.046). Patient survival was also significantly superior in patients without CMV infection (CMV group :59.8% vs. non-CMV group: 75.9% at 140 months P = 0.016). Conclusions: The use of antirejection therapy and NODAT are strong risk factors for developing CMV infection. Posttransplant CMV infection has a significant negative impact on graft and patient survival.
引用
收藏
页码:125 / 130
页数:6
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