Outcome in a hepatitis C (genotype 1b) single source outbreak in Germany -: a 25-year multicenter study

被引:144
作者
Wiese, M
Grüngreiff, K
Güthoff, W
Lafrenz, M
Oesen, U
Porst, H
机构
[1] Univ Leipzig, Affiliated Hosp St Georg, D-7010 Leipzig, Germany
[2] Dept Infect Dis, Potsdam, Germany
[3] Univ Rostock, Dept Internal Med, D-2500 Rostock, Germany
[4] Hosp Kuchwald, Chemnitz, Germany
[5] Hosp Friedrichstadt, Dresden, Germany
关键词
hepatitis C; HCV genotypes; natural history; outcome; fibrosis; liver cirrhosis; anti-HCV; PCR; histology; virology;
D O I
10.1016/j.jhep.2005.04.007
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The natural course of the hepatitis C virus genotype 1b (HCV-1b) infection is still unclear but important for therapeutic decisions. There are few unbiased long-term follow-up studies with known dates of infection. Methods: Between August 1978 and March 1979, 14 HCV-1b contaminated batches of anti-D immunoglobulin had been administered to 2867 women for prophylaxis of rhesus isoimmunization throughout East Germany. We reexamined 1980 women, representing 70% of the total cohort of 15 centers. Results: After application of the contaminated anti-D, 93% of the recipients developed an acute hepatitis C. After 25 years, 86% of the 1833 affected women still tested positive for hepatitis C virus antibodies and 46% for HCV RNA. Only nine (0.5%) had overt liver cirrhosis, 30 women (1.5%) developed precirrhotic stages and one HCC was diagnosed. Ten (0.5%) died of HCV related complications, half of these related to additional comorbidity. In the last 5 years, a continuous, but low increase of fibrotic scores was observed. Conclusions: Young women without comorbidity may clear HCV (1b) infection in more than half of the cases, or develop mild chronic hepatitis C. We confirmed the low risk of progression to cirrhosis in this cohort within 25 years. (c) 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:590 / 598
页数:9
相关论文
共 27 条
[1]  
[Anonymous], 1999, J Hepatol, V30, P956
[2]   The natural course of hepatitis C virus infection after 22 years in a unique homogenous cohort: spontaneous viral clearance and chronic HCV infection [J].
Barrett, S ;
Goh, J ;
Coughlan, B ;
Ryan, E ;
Stewart, S ;
Cockram, A ;
O'Keane, JC ;
Crowe, J .
GUT, 2001, 49 (03) :423-430
[3]  
DIBISCEGLIE AM, 1991, HEPATOLOGY, V14, P969, DOI 10.1016/0270-9139(91)90113-A
[4]   Is severe liver disease a common outcome for people with chronic hepatitis C? [J].
Dore, GJ ;
Freeman, AJ ;
Law, M ;
Kaldor, JM .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2002, 17 (04) :423-430
[5]   Estimating progression to cirrhosis in chronic hepatitis C virus infection [J].
Freeman, AJ ;
Dore, GJ ;
Law, MG ;
Thorpe, M ;
Von Overbeck, J ;
Lloyd, AR ;
Marinos, G ;
Kaldor, JM .
HEPATOLOGY, 2001, 34 (04) :809-816
[6]   SEQUENCE VARIABILITY IN THE ENV-CODING REGION OF HEPATITIS-C VIRUS ISOLATED FROM PATIENTS INFECTED DURING A SINGLE-SOURCE OUTBREAK [J].
HOHNE, M ;
SCHREIER, E ;
ROGGENDORF, M .
ARCHIVES OF VIROLOGY, 1994, 137 (1-2) :25-34
[7]   Global burden of disease (GBD) for hepatitis C [J].
Hutin, Y ;
Kitler, ME ;
Dore, GJ ;
Perz, JF ;
Armstrong, GL ;
Dusheiko, G ;
Ishibashi, H ;
Grob, P ;
Kew, M ;
Marcellin, P ;
Seeff, LB ;
Beutels, P ;
Nelson, C ;
Stein, C ;
Zurn, P ;
Clifford, G ;
Vranckx, R ;
Alberti, A ;
Hallaj, ZS ;
Hadler, S ;
Lavanchy, D .
JOURNAL OF CLINICAL PHARMACOLOGY, 2004, 44 (01) :20-29
[8]   HISTOLOGICAL GRADING AND STAGING OF CHRONIC HEPATITIS [J].
ISHAK, K ;
BAPTISTA, A ;
BIANCHI, L ;
CALLEA, F ;
DEGROOTE, J ;
GUDAT, F ;
DENK, H ;
DESMET, V ;
KORB, G ;
MACSWEEN, RNM ;
PHILLIPS, MJ ;
PORTMANN, BG ;
POULSEN, H ;
SCHEUER, PJ ;
SCHMID, M ;
THALER, H .
JOURNAL OF HEPATOLOGY, 1995, 22 (06) :696-699
[9]   Clinical outcomes after hepatitis C infection from contaminated anti-D immune globulin [J].
Kenny-Walsh, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (16) :1228-1233
[10]  
Keshavan P, 2002, GASTROENTEROLOGY, V122, pA242