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Letters
To the Editor: In Australia, an estimated 11 000 people become infected with hepatitis C virus (HCV) each year.1 Most are injecting drug users.
The Early Hepatitis C Intervention Project was a collaboration between the STD Services Surveillance Unit, Drug and Alcohol Resource Unit and Infectious Diseases Unit at the Royal Adelaide Hospital, Adelaide, South Australia. Its objectives were to manage people who had seroconverted in the preceding 12 months and to provide standard treatments for drug use and dependence. Services included information and education on HCV, referral, counselling, psychosocial support and three-monthly clinical evaluation. The project was approved by the Ethics Committee of the Royal Adelaide Hospital and funded by the Department of Human Services for 18 months.
The attendance rate was low. Of 88 people with HCV seroconversion who were identified as eligible for enrolment by the Surveillance Unit (from the mandatory notification scheme), 57 agreed to further contact by mail or telephone, and 12 attended for risk assessment. Of these, eight enrolled in the project (10% of those eligible).
Despite demographic variation within the group, similarities included difficulties with accommodation, finances, mental health and social integration. Seven of the eight participants had injecting drug use as the risk factor for HCV infection. Most participants also used alcohol and cannabis. During the program, half decreased their risk-taking behaviour: four reduced injecting drug use, and four reduced alcohol use, reaching low risk levels. Characteristics of participants at their last interview are summarised in the Box. Two participants are maintaining regular contact with the Drug and Alcohol Resource Unit.
Despite encouragement, few of the target group engaged in the program. We do not know why so few people who agreed to attend a first appointment failed to do so. We did not have their permission or the resources to contact them again. Maintaining contact with participants also proved challenging, and was in part unsuccessful because of complex, multifaceted social issues aside from HCV infection (Box). These included unstable accommodation, use of health services only when in crisis, mental health problems, financial difficulties, polydrug use and continued risk-taking behaviours despite harm-reduction information.
In conclusion, the Australian epidemic of HCV infection, driven by injecting drug use, is likely to continue unless a new approach to harm minimisation is developed. Such an approach will recognise that comorbidities and social dislocation influence risk of infection. Unless treatment programs address coexisting problems, it will be futile to offer definitive treatment for HCV infection.2
Within the limited objectives and resources of this project, we were unable to support these people comprehensively. We believe that a "one-stop shop" that includes active and intensive case management by a flexible, multidisciplinary team and deals with social, economic and mental health issues may be a more effective approach to the care of people with recent HCV infection.
Characteristics of participants in the Early Hepatitis C Intervention Project at last interview
Place of residence |
Current mental illness* |
Attendances |
|||||||||
Age, sex |
Employ-ment |
Polydrug use |
At 5 nominated appointments |
Total† |
IDU change‡ |
Persistent viraemia‡ |
|||||
19, F |
No |
Yes |
NFA |
Yes |
3 |
6 |
Reduced IDU |
Yes |
|||
21, F |
Part-time |
Yes |
NFA |
Yes |
3 |
5 |
Reduced IDU |
No |
|||
21, M |
No |
Yes |
NFA |
Yes |
3 |
4 |
No IDU at enrolment |
Yes |
|||
24, M |
Voluntary |
No |
Rental |
Yes |
1 |
1 |
Denied IDU ever |
Yes |
|||
30, M |
Casual |
Yes |
NFA |
No |
2 |
4 |
No IDU |
Yes |
|||
36, M |
No |
Yes |
Parents |
Yes |
1 |
4 |
Unknown |
Yes |
|||
38, M |
Full-time |
Yes |
NFA |
Yes |
2 |
3 |
Reduced IDU |
No |
|||
43, M |
Full-time |
No |
Rental |
Unknown |
1 |
1 |
Unknown |
No |
|||
IDU = injecting drug use. NFA = no fixed abode. * Mainly depression, anxiety and personality disorder. † Includes self-initiated visits. ‡ Determined by polymerase chain reaction. |
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Royal Adelaide Hospital, Adelaide, SA.
Katrein Depraetere, Medical Officer, STD Services; Shelley J Toepfer, RN, RPN, Nurse Counsellor, Drug and Alcohol Resource Unit; Joy G Copland, MSc, Senior Project Officer, STD Services; Matthew D Gaughwin, PhD FAFPHM, Director, Drug and Alcohol Resource Unit; David R Shaw, FRACP, Director, Infectious Diseases Unit; Russell G Waddell, FACSHP, Clinical Manager, STD Services.Correspondence: Dr Matthew D Gaughwin, Royal Adelaide Hospital, North Terrace, Adelaide, SA 5000. mgaughwiATmedicine.adelaide.edu.au
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©The Medical Journal of Australia 2002 www.mja.com.au PRINT ISSN: 0025-729X ONLINE ISSN: 1326-5377