Psychosocial aspects of living with hepatitis C

Hepatitis C is a blood-borne virus infecting over 170 million people worldwide. About 200 000 people in Australia are estimated to have chronic infection, with about 10 000 new infections yearly (Ministerial Advisory Committee, 2006). The most common cause of transmission (around 80%) is injecting drug use. Other causes include blood transfusions and other medical and dental procedures, either in Australia or overseas. Since 1990, when screening of blood for hepatitis C was implemented, causes other than drug injecting have become rarer. Hepatitis C infection has an uncertain disease course that varies from person to person. The most common symptom is fatigue, both mental and physical. Other symptoms include nausea, joint pain, depression and irritability.

[1]  L. Fraenkel,et al.  Patients' experiences related to anti-viral treatment for hepatitis C. , 2006, Patient education and counseling.

[2]  C. Treloar,et al.  The Experience of Interferon-Based Treatments for Hepatitis C Infection , 2005, Qualitative health research.

[3]  R. Hays,et al.  Impact of hepatitis C on health related quality of life: A systematic review and quantitative assessment , 2005, Hepatology.

[4]  D. Jolley,et al.  Australian men's experiences of living with hepatitis C virus: Results from a cross‐sectional survey , 2005, Journal of gastroenterology and hepatology.

[5]  J. Crowe,et al.  Evaluation of a Brief Group Based Psychological/Educational Treatment Programme for Women with an Iatrogenic Chronic Hepatitis C Virus Infection , 2004, Journal of Clinical Psychology in Medical Settings.

[6]  Belinda Crockett,et al.  “Eyes Wide Shut”: Narratives of Women Living with Hepatitis C in Australia , 2004, Women & health.

[7]  C. Treloar,et al.  Infection control in the context of hepatitis C disclosure: implications for education of healthcare professionals. , 2004, Education for health.

[8]  M. Pitts,et al.  Making decisions about Hepatitis C treatment , 2004 .

[9]  C. Banwell,et al.  Australian women's experiences of living with hepatitis C virus: Results from a cross‐sectional survey , 2003, Journal of gastroenterology and hepatology.

[10]  Evelyn Y. Ho,et al.  "They treated me like a leper". Stigmatization and the quality of life of patients with hepatitis C. , 2003, Journal of general internal medicine.

[11]  J. Crowe,et al.  Psychological well-being and quality of life in women with an iatrogenic hepatitis C virus infection. , 2002, British journal of health psychology.

[12]  D. Shaw,et al.  Quality of life in HCV‐infection: lack of association with ALT levels , 2001, Australian and New Zealand journal of public health.

[13]  J. Beard,et al.  Hepatitis C virus infection: impact on behaviour and lifestyle , 1998, Australian and New Zealand journal of public health.

[14]  Loff,et al.  The Next Plague: Stigmatization and Discrimination Related to Hepatitis C Virus Infection in Australia. , 1997, Health and human rights.

[15]  G. Krug HEPATITIS C , 1995 .