首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Cytomegalovirus Serostatus Pairing and Deceased Donor Kidney Transplant Outcomes in Adult Recipients With Antiviral Prophylaxis
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Cytomegalovirus Serostatus Pairing and Deceased Donor Kidney Transplant Outcomes in Adult Recipients With Antiviral Prophylaxis

机译:成人接受抗病毒预防的巨细胞病毒血清配对和捐赠者肾脏移植死因的减少

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Background. The objectives of this study are to investigate the impact of cytomegalovirus (CMV) donor (D)/recipient (R) serostatus on kidney transplant outcomes in recipients who received CMV prophylaxis and to investigate the association of individual antiviral agents (acyclovir, ganciclovir, and valganciclovir) with outcomes in high-risk recipients (D+/R-). Methods. By using the Organ Procurement and Transplant Network/United Network for Organ Sharing database, 25,058 deceased donor kidney recipients (>=18 years, 2004-2008) who received CMV prophylaxis were stratified into four groups: D+/R+ (11,875), D-/R+ (6046), D+/R- (4555), and D-/R- (2582). The impact of CMV D/R serostatus on acute rejection (6 months and 1 year posttransplant) and long-term outcomes of death-censored graft failure and mortality were compared. The impact of the individual antiviral agent on long-term outcome was further evaluated in the high-risk group (D+/R-). Results. In multivariate analysis, CMV D/R status was not associated with acute rejection. Compared with D -/ R-, D+/R- was associated with an increased risk for death-censored graft failure (hazard ratio= 1.28, P=0.01), all-cause mortality(hazard ratio = 1.36, P=0.003), and mortality because of viral infection (hazard ratio = 8.36, P=0.04). In the D + /R- group, valganciclovir usage was associated with a decreased risk for death-censored graft failure (hazard ratio = 0.65, P=0.007) and mortality because of viral infection (hazard ratio = 0.22, P=0.03) compared with ganciclovir usage. Conclusions. CMV mismatch (D+/R-) was no longer a risk factor for acute rejection in kidney recipients who received antiviral prophylaxis but was still an independent risk factor for death-censored graft failure, all-cause mortality, and viral infection-related mortality.
机译:背景。这项研究的目的是调查巨细胞病毒(CMV)供体(D)/受体(R)血清状况对接受CMV预防的接受者的肾脏移植结局的影响,并研究各个抗病毒药物(阿昔洛韦,更昔洛韦和缬更昔洛韦)在高危接受者(D + / R-)中有预后。方法。通过使用器官采购和移植网络/器官共享联合网络数据库,将接受CMV预防的25,058例死者的供体肾脏接受者(> = 18岁,2004-2008年)分为四类:D + / R +(11,875),D- / R +(6046),D + / R-(4555)和D- / R-(2582)。比较了CMV D / R血清状况对急性排斥反应(移植后6个月和1年)的影响以及以死亡为检查对象的移植失败和死亡率的长期结果。在高风险组(D + / R-)中进一步评估了个别抗病毒药物对长期预后的影响。结果。在多变量分析中,CMV D / R状态与急性排斥反应无关。与D-/ R-相比,D + / R-与死亡检查的移植失败风险增加(危险比= 1.28,P = 0.01),全因死亡率(危险比= 1.36,P = 0.003)有关,病毒感染造成的死亡和死亡(危险比= 8.36,P = 0.04)。在D + / R-组中,与使用缬更昔洛韦治疗相比,与病毒检查相关的死亡率降低(以死亡为原因的移植失败(危险比= 0.65,P = 0.007)和死亡率降低)(危险比= 0.22,P = 0.03)更昔洛韦用法。结论。在接受抗病毒预防的肾脏接受者中,CMV不匹配(D + / R-)不再是急性排斥反应的危险因素,但仍然是死亡检查的移植失败,全因死亡率和与病毒感染相关的死亡率的独立危险因素。

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