期刊论文详细信息
BMC Public Health
Mortality among British Columbians testing for hepatitis C antibody
Mel Krajden3  Jane A Buxton4  Darrel A Cook2  John J Spinelli1  Amanda Yu4 
[1] BC Cancer Agency, Vancouver, BC, Canada;BC Centre for Disease Control, 655 West 12th Avenue, Vancouver, BC, V5Z 4R4, Canada;Department of Pathology & Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada;School of Population & Public Health, University of British Columbia, Vancouver, BC, Canada
关键词: Data linkage;    Injection drug use;    Chronic hepatitis;    Mortality;    Hepatitis C virus;   
Others  :  1162389
DOI  :  10.1186/1471-2458-13-291
 received in 2012-08-21, accepted in 2013-02-13,  发布年份 2013
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【 摘 要 】

Background

Hepatitis C virus (HCV) infection is a major preventable and treatable cause of morbidity and mortality. The ability to link population based centralized laboratory HCV testing data with administrative databases provided a unique opportunity to compare mortality between HCV seronegative and seropositive individuals. Through the use of laboratory testing patterns and results, the objective of this study was to differentiate the viral effects of mortality due to HCV infection from risk behaviours/activities that are associated with acquisition of HCV infection.

Methods

Serological testing data from the British Columbia (BC) Centre for Disease Control Public Health Microbiology and Reference Laboratory from 1992–2004 were linked to the BC Vital Statistics Agency death registry. Four groups of HCV testers were defined by their HCV antibody (anti-HCV) testing patterns: single non-reactive (SNR); serial multiple tested non-reactive (MNR); reactive at initial testing (REAC); and seroconverter (SERO) (previously seronegative followed by reactive, a marker for incident infection). Standardized mortality ratios (SMRs) were calculated to compare the relative risk of all cause and disease specific mortality to that of the BC population for each serological group. Time dependent Cox proportional hazard regression was used to compare hazard ratios (HRs) among HCV serological groups.

Results

All anti-HCV testers had higher SMRs than the BC population. Referent to the SNR group, the REAC group had higher risks for liver (HR: 9.62; 95% CI=8.55-10.87) and drug related mortality (HR: 13.70; 95% CI=11.76-16.13). Compared to the REAC group, the SERO group had a lower risk for liver (HR: 0.53; 95% CI=0.24-0.99), but a higher risk for drug related mortality (HR: 1.54; 95% CI=1.12-2.05).

Conclusions

These findings confirm that individuals who test anti-HCV positive have increased mortality related to progressive liver disease, and that a substantial proportion of the mortality is attributable to drug use and risk behaviours/activities associated with HCV acquisition. Mortality reduction in HCV infected individuals will require comprehensive prevention programming to reduce the harms due to behaviours/activities which relate to HCV acquisition, as well as HCV treatment to prevent progression of chronic liver disease.

【 授权许可】

   
2013 Yu et al.; licensee BioMed Central Ltd.

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