High prevalence and incidence of hepatitis C virus infections among dialysis patients in the East-Centre of Tunisia

被引:24
作者
Ben Othman, S
Bouzgarrou, N
Achour, A
Boulet, T
Pozzetto, B
Trabelsi, A
机构
[1] Univ St Etienne, Lab Bacteriol Virol Hyg, Fac Med Jacques Lisfranc, F-42055 St Etienne 02, France
[2] Fac Pharm, Lab Maladies Transmissibles & Subst Biologiquemen, MDT01, Monastir, Tunisia
[3] CHU Fattouma Bourguiba, Serv Nephrol, Monastir, Tunisia
来源
PATHOLOGIE BIOLOGIE | 2004年 / 52卷 / 06期
关键词
hepatitis c virus; hemodialysis; nosocomial infection; Tunisia;
D O I
10.1016/j.patbio.2003.07.001
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Hemodialysed patients are recognised as a group at increased risk of infection with hepatitis C virus (HCV). The aim of this study was to determine the prevalence and incidence of HCV infection among dialysis patients of the east-centre part of Tunisia. Two hundred and seventy-six patients dialysed until 2001 were recruited within seven hemodialysis units located in the cities of Sousse, Monastir and Mahdia. The serum markers of HCV infection were tested over the period of March 2000-December 2002, by a 3rd generation ELISA test for antibodies and by qualitative RT-PCR technique for viral RNA. The prevalence of anti-HCV antibodies and of HCV RNA was 32.6% (90 patients) and 25.7% (71 patients), respectively. Between 1998 and 2002, 20 new infections were documented in five of the seven dialysis units corresponding to an incidence of 2.34% per year, with an average time of contamination after the beginning of dialysis of 4.6 years. If all the infections are assessed to have occurred during dialysis, the density of incidence of HCV contamination was 4.4% per year of dialysis. A high correlation was noticed between the presence of HCV markers in serum and the duration of dialysis (F = 34.15, P < 0.0001). In the absence of other risk factors (transfusion, drug-addiction), these results plead for the nosocomial transmission of the observed HCV infections. A phylogenetic analysis of the E2 hypervariable region of the viral genome is in progress to confirm this assumption. (C) 2003 Elsevier SAS. Tous droits reserves.
引用
收藏
页码:323 / 327
页数:5
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