| Literature DB >> 20430177 |
G O Jung1, S-J Kim, G-S Choi, J I Moon, J M Kim, M J Sin, E Y Kim, C H D Kwon, J W Joh, S-K Lee.
Abstract
There is some controversy regarding the exact cytomegalovirus (CMV) antigenemia titer that should be used as a guideline for preemptive anti-CMV therapy. We performed 634 consecutive kidney transplantations between January 2000 and June 2007. Preemptive therapy employed intravenous gancyclovir treatment when the CMV antigenemia titer was >or=50/4x10(5) leukocytes after kidney transplantation. The 634 recipients were allocated into 2 groups according to the peak CMV antegenemia: group A, CMV antigenemia titer<50/4x10(5) (n=550); and group B, >or=50/40x10(5) (n=84). Among the 634 recipients, 264 were positive for CMV antigenemia, and 61 developed symptomatic CMV infections. The incidence of symptomatic CMV infections in group B was significantly higher than in group A. Two cases in both groups developed tissue-proven CMV disease: group A CMV colitis and CMV nephritis, and group B, 2 cases of CMV colitis. Graft and patient survival rates in groups A and B at 5 years posttransplantation were not different. The authors concluded that a CMV antigenemia titer of >or=50/4x10(5) leukocytes can be considered an appropriate guideline for preemptive anti-CMV therapy. Copyright (c) 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20430177 DOI: 10.1016/j.transproceed.2010.02.040
Source DB: PubMed Journal: Transplant Proc ISSN: 0041-1345 Impact factor: 1.066