Mabilangan Curtis, Preiksaitis Jutta K, Cervera Carlos
Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Transpl Infect Dis. 2019 Feb;21(1):e13015. doi: 10.1111/tid.13015. Epub 2018 Nov 19.
Some studies have shown that pre-transplant cytomegalovirus (CMV) serostatus is associated with heart transplant patient survival while others have not. We analyzed the relationship between pre-transplant donor/recipient CMV serostatus and long-term mortality in a retrospective cohort of heart transplant recipients at our center.
Adult (Age >17 years) heart recipients transplanted between July 1985-December 2015 were analyzed. Variables included age, sex, pre-transplant donor (D)/recipient (R) serostatus [D-/R-, D-/R+, D+/R+, D+/R-], CMV infection within 2 years of transplant and transplant eras divided by changes in CMV prevention strategies: Era 1 (Pre-ganciclovir, July 1985-April 1998), Era 2 (Oral ganciclovir, May 1998-December 2004), Era 3 (Valganciclovir, January 2005-December 2015). Survival analysis and Cox regression were performed at 10 years.
A total of 620 heart transplants were included in our analysis; 20% were CMV mismatched pre-transplant. Thirty-eight percent of patients were infected with CMV within the first two post-transplant years. Survival analysis showed D/R CMV serostatus did not significantly impact survival of heart recipients at 10 years (P = 0.11). Survival was significantly different across eras for D-/R+, D+/R+, and D+/R+ (P = 0.043) but not D-/R- patients (P = 0.8). Cox regression revealed that patients transplanted in the valganciclovir era have an estimated 29% reduced risk of death (P = 0.047) compared to patients transplanted in the pre-ganciclovir era after controlling for age at transplantation, D/R CMV serostatus and CMV infection.
Our review of the impact of CMV managed differently across eras suggests in heart transplantation there is no influence of D/R CMV serostatus on 10 year survival.
一些研究表明,移植前巨细胞病毒(CMV)血清学状态与心脏移植患者的生存率相关,而其他研究则未发现此关联。我们分析了本中心心脏移植受者回顾性队列中移植前供体/受体CMV血清学状态与长期死亡率之间的关系。
对1985年7月至2015年12月期间接受移植的成年(年龄>17岁)心脏受者进行分析。变量包括年龄、性别、移植前供体(D)/受体(R)血清学状态[D-/R-、D-/R+、D+/R+、D+/R-]、移植后2年内的CMV感染情况以及根据CMV预防策略变化划分的移植时代:时代1(更昔洛韦之前,1985年7月至1998年4月)、时代2(口服更昔洛韦,1998年5月至2004年12月)、时代3(缬更昔洛韦,2005年1月至2015年12月)。在10年时进行生存分析和Cox回归。
我们的分析共纳入620例心脏移植;20%在移植前CMV血清学不匹配。38%的患者在移植后的头两年内感染了CMV。生存分析显示,D/R CMV血清学状态在10年时对心脏受者的生存率没有显著影响(P = 0.11)。对于D-/R+、D+/R+和D+/R+患者,不同时代的生存率有显著差异(P = 0.043),但D-/R-患者无显著差异(P = 0.8)。Cox回归显示,在控制了移植时的年龄、D/R CMV血清学状态和CMV感染后,与在更昔洛韦之前时代接受移植的患者相比,在缬更昔洛韦时代接受移植的患者死亡风险估计降低29%(P = 0.047)。
我们对不同时代CMV管理影响的回顾表明,在心脏移植中,D/R CMV血清学状态对10年生存率没有影响。