Combined alpha interferon and ribavirin for the treatment of hepatitis C in patients with hereditary bleeding disorders

被引:0
作者
Shields, PL
Mutimer, DJ
Muir, D
Skidmore, S
Britnell, T
Roberts, A
Wilde, JT
机构
[1] Queen Elizabeth Hosp, W Midlands Adult Comprehens Care Haemophilia Ctr, Birmingham B15 2TH, W Midlands, England
[2] Queen Elizabeth Hosp, Liver Unit, Birmingham B15 2TH, W Midlands, England
[3] Birmingham Heartlands Hosp, Publ Hlth Lab, Birmingham B9 5ST, W Midlands, England
关键词
hepatitis C virus; interferon alpha; ribavirin; hereditary bleeding disorder; therapy;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with hereditary bleeding disorders who received non-virally inactivated plasma-derived clotting factor concentrates before the mid-1980s invariably became infected with hepatitis C virus (HCV). Therapy with interferon alpha (IFN-alpha) alone has been disappointing in this group. We conducted an open-label study, using a combination of IFN-alpha 2b (3 million units three times per week) and ribavirin 1-1.2 g/d in 28 patients with hereditary bleeding disorders. Twenty-one of the 28 patients had liver biopsy-confirmed chronic hepatitis (median histological activity index 5: range 1-10) and all patients were HCV RNA positive by PCR. Virological response rate to therapy at 3 months was 82% (23 out of 28). Three HIV co-infected patients showed an early virological response with loss of HCV RNA, but two subsequently relapsed after 3 and 6 months of therapy. Four patients stopped treatment early (one at 4, one at 7 and two at 9 months) because of treatment-related side effects, although threo of these have maintained a virological response. Seventeen patients completed the 48-week course, Twenty of the 28 (71%) treated have had a durable virological response with a median follow-up of 16 months (range 1-24). Combination therapy represents a significant advance in the treatment of hepatitis C in patients with hereditary bleeding disorders.
引用
收藏
页码:254 / 258
页数:5
相关论文
共 17 条
[1]   A combined management protocol for patients with coagulation disorders infected with hepatitis C virus [J].
Ahmed, MM ;
Mutimer, DJ ;
Elias, C ;
Linin, J ;
Garrido, M ;
Hubscher, S ;
Jarvis, L ;
Simmonds, P ;
Wilde, JT .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 95 (02) :383-388
[2]   Mortality from liver cancer and liver disease in haemophilic men and boys in UK given blood products contaminated with hepatitis C [J].
Darby, SC ;
Ewart, DW ;
Giangrande, PLF ;
Spooner, RJD ;
Rizza, CR ;
Dusheiko, GM ;
Lee, CA ;
Ludlam, CA ;
Preston, FE .
LANCET, 1997, 350 (9089) :1425-1431
[3]   RIBAVIRIN AS THERAPY FOR CHRONIC HEPATITIS-C - A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL [J].
DIBISCEGLIE, AM ;
CONJEEVARAM, HS ;
FRIED, MW ;
SALLIE, R ;
PARK, Y ;
YURDAYDIN, C ;
SWAIN, M ;
KLEINER, DE ;
MAHANEY, K ;
HOOFNAGLE, JH ;
WRIGHT, D .
ANNALS OF INTERNAL MEDICINE, 1995, 123 (12) :897-&
[4]  
Eisenburg J, 1994, Fortschr Med, V112, P317
[5]   Outcome of orthotopic liver transplantation in patients with haemophilia [J].
Gordon, FH ;
Mistry, PK ;
Sabin, CA ;
Lee, CA .
GUT, 1998, 42 (05) :744-749
[6]   Interferon treatment for chronic hepatitis C infection in hemophiliacs - Influence of virus load, genotype, and liver pathology on response [J].
Hanley, JP ;
Jarvis, LM ;
Andrews, J ;
Dennis, R ;
Hayes, PC ;
Piris, J ;
Lee, R ;
Simmonds, P ;
Ludlam, CA .
BLOOD, 1996, 87 (05) :1704-1709
[7]   The antiviral compound ribavirin modulates the T helper (Th)1/Th2 subset balance in hepatitis B and C virus-specific immune responses [J].
Hultgren, C ;
Milich, DR ;
Weiland, O ;
Sällberg, M .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :2381-2391
[8]  
MAKRIS M, 1991, BLOOD, V78, P1672
[9]   The natural history of chronic hepatitis C in haemophiliacs [J].
Makris, M ;
Preston, FE ;
Rosendaal, FR ;
Underwood, JCE ;
Rice, KM ;
Triger, DR .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 94 (04) :746-752
[10]   EFFECT AND SIDE-EFFECTS OF ALPHA-INTERFERON TREATMENT IN HEMOPHILIA PATIENTS WITH CHRONIC HEPATITIS-C [J].
MAUSERBUNSCHOTEN, EP ;
BRESTERS, D ;
REESINK, HM ;
ROOSENDAAL, G ;
CHAMULEAU, RAFM ;
HAAN, E ;
JANSEN, PLM ;
VANDENBERG, HM .
HAEMOPHILIA, 1995, 1 (01) :45-53