Hibberd P L, Tolkoff-Rubin N E, Conti D, Stuart F, Thistlethwaite J R, Neylan J F, Snydman D R, Freeman R, Lorber M I, Rubin R H
Infectious Disease Unit, Massachusetts General Hospital, Boston 02114, USA.
Ann Intern Med. 1995 Jul 1;123(1):18-26. doi: 10.7326/0003-4819-123-1-199507010-00002.
To determine whether preemptive ganciclovir therapy administered daily during antilymphocyte antibody therapy can prevent cytomegalovirus disease in renal transplant recipients who are positive for cytomegalovirus antibody.
Randomized, controlled, multicenter trial.
6 university-affiliated transplantation centers.
113 renal transplant recipients who were positive for cytomegalovirus antibody.
Patients were randomly assigned to receive either 1) ganciclovir, 2.5 mg/kg body weight administered intravenously on every day that antilymphocyte antibody therapy was administered or 2) no anticytomegalovirus therapy.
Patients were observed for 6 months after completion of antilymphocyte antibody therapy for development of cytomegalovirus disease and cytomegalovirus viremia.
Cytomegalovirus disease occurred in 14% of patients (9 of 64) who received preemptive ganciclovir therapy and in 33% of controls (16 of 49) (P = 0.018). Cytomegalovirus was isolated from buffy-coat specimens from 17% of patients (11 of 64) receiving preemptive ganciclovir and from 35% of controls (17 of 49) (P = 0.03). Controlling for the reason (induction or treatment of rejection) for using antilymphocyte antibodies in a Cox proportional hazards model, we found that preemptive ganciclovir still protected against cytomegalovirus disease (adjusted relative risk, 0.27; 95% CI, 0.12 to 0.64). No adverse events were attributed to preemptive ganciclovir therapy during or within 6 months of its administration.
Preemptive ganciclovir therapy administered daily during courses of treatment with antilymphocyte antibodies reduced the excessive occurrence of cytomegalovirus disease in renal transplant recipients who were positive for cytomegalovirus antibody. This approach, which links the most potent immunosuppression to intensive antimicrobial therapy, allows preventive therapy to be given to those patients at greatest risk for developing infectious complications. These patients are likely to benefit most from the preventive strategy.
确定在抗淋巴细胞抗体治疗期间每日给予抢先性更昔洛韦治疗能否预防巨细胞病毒抗体阳性的肾移植受者发生巨细胞病毒病。
随机、对照、多中心试验。
6家大学附属医院的移植中心。
113例巨细胞病毒抗体阳性的肾移植受者。
患者被随机分配接受以下两种治疗之一:1)更昔洛韦,在给予抗淋巴细胞抗体治疗的每一天,按2.5mg/kg体重静脉给药;2)不进行抗巨细胞病毒治疗。
在抗淋巴细胞抗体治疗结束后观察患者6个月,观察巨细胞病毒病和巨细胞病毒血症的发生情况。
接受抢先性更昔洛韦治疗的患者中有14%(64例中的9例)发生了巨细胞病毒病,而对照组中有33%(49例中的16例)发生了巨细胞病毒病(P = 0.018)。在接受抢先性更昔洛韦治疗的患者中,17%(64例中的11例)的血沉棕黄层标本中分离出巨细胞病毒,而对照组中这一比例为35%(49例中的17例)(P = 0.03)。在Cox比例风险模型中对使用抗淋巴细胞抗体的原因(诱导或治疗排斥反应)进行校正后,我们发现抢先性更昔洛韦仍可预防巨细胞病毒病(校正相对风险,0.27;95%CI,0.12至0.64)。在给予抢先性更昔洛韦治疗期间或治疗后六个月内,未发现任何不良事件归因于该治疗。
在抗淋巴细胞抗体治疗疗程中每日给予抢先性更昔洛韦治疗可减少巨细胞病毒抗体阳性的肾移植受者中巨细胞病毒病的过度发生。这种将最强的免疫抑制与强化抗菌治疗相结合的方法,使预防性治疗能够给予那些发生感染并发症风险最高的患者。这些患者可能从预防策略中获益最大。