CYTOMEGALOVIRUS AND ITS ASSOCIATION WITH HEPATIC-ARTERY THROMBOSIS AFTER LIVER-TRANSPLANTATION

Citation
C. Madalosso et al., CYTOMEGALOVIRUS AND ITS ASSOCIATION WITH HEPATIC-ARTERY THROMBOSIS AFTER LIVER-TRANSPLANTATION, Transplantation, 66(3), 1998, pp. 294-297
Citations number
33
Categorie Soggetti
Transplantation,Surgery,Immunology
Journal title
ISSN journal
00411337
Volume
66
Issue
3
Year of publication
1998
Pages
294 - 297
Database
ISI
SICI code
0041-1337(1998)66:3<294:CAIAWH>2.0.ZU;2-1
Abstract
Background Hepatic artery thrombosis (HAT) is a cause of morbidity and graft loss in approximately 7% of patients after an orthotopic liver transplantation (OLT). Although technical problems are often thought t o be the cause of HAT, in general the etiology remains unclear. Becaus e cytomegalovirus (CMV) can infect endothelial cells in vitro and lead to a rapid procoagulant response, it can be hypothesized that, in the absence of CMV antibodies, latent CMV in an allograft may become acti vated and promote or contribute to vascular thrombosis. Therefore, the purpose of this study was to examine the relationship between CMV ser ology of the donor and recipient with the development of HAT after OLT . Methods, Between July 1988 and November 1995 (University of Wisconsi n era), 490 OLTs were performed in 413 patients. Subsequently, four pa tients were excluded in whom the CMV serology results of the donor wer e not available. Sixteen of the 409 patients developed HAT within 30 d ays after liver transplantation. The control group consisted of the ot her 393 patients. Results, The incidence of HAT was 12.5% in 64 CMV DR- patients and 0% in 52 CMV D-R- patients. However, in the other comb inations (D+R+ and D-R+), the incidence was only 2.8% (P=0.005). Eight of the 16 patients with HAT belonged to the CMV D+R- group. Conclusio ns. We conclude that CMV-seronegative patients receiving a seropositiv e allograft may be at risk for early HAT. Seropositivity of the donor alone and of the recipient alone was not significantly related to the incidence of HAT. Prophylactic treatment with ganciclovir and/or antic oagulation should be evaluated to prevent this complication.