کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4258136 | 1284554 | 2010 | 7 صفحه PDF | دانلود رایگان |

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 ≥50/4 × 105 leukocytes after kidney transplantation. The 634 recipients were allocated into 2 groups according to the peak CMV antegenemia: group A, CMV antigenemia titer <50/4 × 105 (n = 550); and group B, ≥50/40 × 105 (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 ≥50/4 × 105 leukocytes can be considered an appropriate guideline for preemptive anti-CMV therapy.
Journal: Transplantation Proceedings - Volume 42, Issue 3, April 2010, Pages 804–810