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Helen E Harris Public Health Laboratory Service Communicable
Disease Surveillance Centre, London NW9 5EQ
Correspondence to: H E Harris hharris{at}phls.nhs.uk
Objective:
To determine the clinical course of
hepatitis C virus in the first decade of infection in a group of
patients who acquired their infections on a known date.
What is already known on this topic
Studies that follow patients from disease onset are rare because most
HCV infections are asymptomatic What this study adds
Infected patients have an increased risk of dying from a liver related
cause, particularly if they consumed excess alcohol
Design:
Cohort study.
Setting:
Clinical centres throughout the United Kingdom.
Participants:
924 transfusion recipients infected
with the hepatitis C virus (HCV) traced during the HCV lookback
programme and 475 transfusion recipients who tested negative for
antibodies to HCV (controls).
Main outcome measures:
Clinical evidence of liver
disease and survival after 10 years of infection.
Results:
All cause mortality was not
significantly different between patients and controls (Cox's hazards
ratio 1.41, 95% confidence interval 0.95 to 2.08). Patients were more
likely to be certified with a death related to liver disease than were controls (12.84, 1.73 to 95.44), but although the risk of death directly from liver disease was higher in patients than controls this
difference was not significant (5.78, 0.72 to 46.70). Forty per cent of
the patients who died directly from liver disease were known to have
consumed excess alcohol. Clinical follow up of 826 patients showed that
liver function was abnormal in 307 (37.2%), and 115 (13.9%) reported
physical signs or symptoms of liver disease. Factors associated with
developing liver disease were testing positive for HCV ribonucleic acid
(odds ratio 6.44, 2.67 to 15.48), having acquired infection when older
(at age
40 years; 1.80, 1.14 to 2.85), and years since transfusion
(odds ratio 1.096 per year, 1.00 to 1.20). For patients with severe disease, sex was also significant (odds ratio for women 0.38, 0.17 to
0.88). Of the 362 patients who had undergone liver biopsy, 328 (91%)
had abnormal histological results and 35 (10%) of these were cirrhotic.
Conclusions:
Hepatitis C virus infection did not
have a great impact on all cause mortality in the first decade of
infection. Infected patients were at increased risk of dying directly
from liver disease, particularly if they consumed excess alcohol, but this difference was not statistically significant.
The clinical course of HCV infection is unclear because most
information has come from studies of patients with established chronic
liver disease
HCV infection does not have a great impact on all cause mortality in
the first decade of infection
© BMJ 2002
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