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首页> 外文期刊>Transplant international : >Six months anti-viral prophylaxis significantly decreased cytomegalovirus disease compared with no anti-viral prophylaxis following renal transplantation.
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Six months anti-viral prophylaxis significantly decreased cytomegalovirus disease compared with no anti-viral prophylaxis following renal transplantation.

机译:与肾脏移植后未进行抗病毒预防相比,抗病毒预防六个月显着降低了巨细胞病毒病的发生。

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摘要

We followed up 550 primary kidney transplant recipients in an observational retrospective cohort to evaluate the impact of three consecutive cytomegalovirus (CMV) prevention strategies. In period 1 (1996-2000; n = 190), no anti-CMV prophylaxis was given; in period 2 (2000-2004; n = 173), 6-month valacyclovir was given and in period 3 (>2004; n = 187), 6-month valganciclovir was given. Cytomegalovirus disease significantly decreased from 33.2% in period 1 to 13.9% in period 2 and to 8.6% in period 3; onset was significantly prolonged with valganciclovir (228 days) compared with valacyclovir (93 days) and with no prophylaxis (33 days). After Cox regression adjustments, both valganciclovir and valacyclovir were similarly protective factors for CMV disease. Cytomegalovirus diseases encountered in both valacyclovir and valganciclovir groups were primary infections (79.2 and 93.8% respectively) as compared with a significant low number (39.7%) in the nonprophylaxis group. Two cases of valganciclovir resistance were recorded in the valganciclovir group and no resistance was seen with valacyclovir. A significantly reduced incidence of other herpes viruses was only observed with valganciclovir. Valganciclovir was better tolerated than valacyclovir and this long-term prophylaxis was applicable to 85% of patients. Longer follow-up of valganciclovir or valacyclovir prophylaxis is still required to appreciate its impact on graft and patient survivals, as well as other indirect effects, in the mycophenolate mofetil and calcineurin inhibitor immunosuppressive era.
机译:我们在一项观察性回顾性队列研究中随访了550名原发性肾脏移植受者,以评估三种连续巨细胞病毒(CMV)预防策略的影响。在第1阶段(1996年至2000年; n = 190)中,未进行任何抗CMV预防措施;在第2阶段(2000-2004; n = 173),给予6个月的伐昔洛韦;在第3阶段(> 2004; n = 187),给予6个月的缬更昔洛韦。巨细胞病毒病从第1阶段的33.2%下降到第2阶段的13.9%和第3阶段的8.6%;与伐昔洛韦(93天)相比,缬更昔洛韦(228天)显着延长了发作时间,而无预防措施(33天)。在Cox回归调整后,缬更昔洛韦和伐昔洛韦都同样是CMV疾病的保护因素。在伐昔洛韦和缬更昔洛韦组中都遇到的巨细胞病毒疾病是主要感染(分别为79.2和93.8%),相比之下,非预防组的感染率很低(39.7%)。在伐昔洛韦组中记录了2例伐昔洛韦耐药性,伐昔洛韦未见耐药性。仅使用缬更昔洛韦观察到其他疱疹病毒的发病率显着降低。缬更昔洛韦比伐昔洛韦耐受性更好,这种长期预防适用于85%的患者。在霉酚酸酯和钙调神经磷酸酶抑制剂的免疫抑制时代,仍然需要对缬更昔洛韦或伐昔洛韦预防进行更长的随访,以了解其对移植物和患者生存的影响以及其他间接影响。

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