Cytomegalovirus PP65 antigenemia monitoring as a guide for preemptive therapy: A cost effective strategy for prevention of cytomegalovirus disease inadult liver transplant recipients

Citation
S. Kusne et al., Cytomegalovirus PP65 antigenemia monitoring as a guide for preemptive therapy: A cost effective strategy for prevention of cytomegalovirus disease inadult liver transplant recipients, TRANSPLANT, 68(8), 1999, pp. 1125-1131
Citations number
62
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
TRANSPLANTATION
ISSN journal
00411337 → ACNP
Volume
68
Issue
8
Year of publication
1999
Pages
1125 - 1131
Database
ISI
SICI code
0041-1337(19991027)68:8<1125:CPAMAA>2.0.ZU;2-D
Abstract
Background The aim of the study was to assess the incidence of cytomegalovi rus (CMV) infection and disease in adult liver transplant recipients, using routine preemptive therapy guided by the pp65 antigenemia test. Methods. Antigenemia was monitored weekly after liver transplantation (OLTX ) for the first 3 months, and once a month for another 3 months. CMV serone gative recipients were treated preemptively for the first positive antigene mia, Seropositive recipients were treated only when their antigenemia count reached a threshold of greater than or equal to 100 positive cells per 200 ,000 leukocytes. Results. A total of 144 patients were included between June 1994 and April 1995, of which 137 (95%) were primary OLTX, The percentage of positive anti genemia and CMV disease was 55 and 8%, respectively, Seventy-eight (54%) pa tients were protocol-monitored for the entire follow-up (group 1) and recei ved appropriate preemptive therapy, although 66 (46%) patients had protocol violation by having missed blood samples or blood drawn at unscheduled tim es (group 2), Using Cox's proportional hazards model, patients with a first antigenemia count of >11 leukocytes had a significantly higher rate of CMV disease compared to patients with an antigenemia count less than or equal to 11 leukocytes (RR=7.3, 95% confidence interval = 2.2 to 24.5), In a mult ivariate Cox regression analysis, adjustments were made to control for: gro up 1 versus group 2, use of OKT3, and serology risk categories. This analys is showed that the relative rate of CMV disease was still significantly hig her among patients with antigenemia count >11 leukocytes (adjusted RR=4.9, 95% confidence interval=1.3 to 18.1). The estimated cost of preemptive ther apy was less than that of prophylaxis with i.v. (14-day course) or oral (90 -day course) ganciclovir. Conclusions. Preemptive therapy guided by pp65 antigenemia is a useful and cost effective strategy for prevention of CMV disease.