Literature DB >> 16036236

Quality of life, depression and fatigue among persons co-infected with HIV and hepatitis C: outcomes from a population-based cohort.

P Braitstein1, V Montessori, K Chan, J S G Montaner, M T Schechter, M V O'Shaughnessy, R S Hogg.   

Abstract

The objective of the study was to describe the additional burden generated by hepatitis C (HCV) infection among HIV-infected individuals as measured by self-reported quality of life, depression and fatigue. The provincial HIV/AIDS Drug Treatment Program (DTP) distributes all antiretroviral medication in the province of British Columbia. Eligibility for accessing antiretrovirals is based on published guidelines commensurate with the International AIDS Society. Each participant is asked to complete a self-administered mailed questionnaire that includes patient sociodemographic information, quality of life measures (Medical Outcomes Study-Short Form (MOS-SF), mental health issues (Centre for Epidemiological Studies Depression scale (CESD) and fatigue information. HIV-HCV co-infected individuals were compared to HIV mono-infected individuals using parametric and nonparametric methods. Multivariate logistic regression was used to examine the impact of hepatitis C on quality of life, depression and fatigue, after controlling for sociodemographics and HIV-specific clinical characteristics. Of the 4,134 individuals who were sent a HIV/AIDS DTP survey in 1999, 2000 or 2001, 484 participants both returned one and had an HCV-antibody test result on file. Of the 484 participants eligible for this analysis, 105 (22%) were HCV-positive. In comparison to the 379 (78%) patients testing negative for HCV, a larger proportion of co-infected patients were female (18% versus 3%, p<0.001), aboriginal (20% versus 3%, p<0.001), had ever injected drugs (79% versus 5%, p<0.001), were unemployed (91% versus 49%, p<0.001) and lived in unstable housing (19% versus 1%, p<0.001) at the time they completed the survey. Co-infected patients reported more symptoms consistent with depression, increased fatigue and poorer quality of life. However, using multivariate modeling, it was determined that the impact of HCV on quality of life, depression and fatigue was better explained by the sociodemographic factors related to poverty and injection drug use, than by HCV itself. In conclusion, individuals co-infected with HIV and HCV represent a patient population with significant physical and mental health challenges. Although these patients experience poorer quality of life, increased depression and fatigue, this experience appears to be primarily related to socio-economic issues rather than HCV infection.

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Year:  2005        PMID: 16036236     DOI: 10.1080/09540120412331291733

Source DB:  PubMed          Journal:  AIDS Care        ISSN: 0954-0121


  20 in total

1.  Physiological and psychosocial factors that predict HIV-related fatigue.

Authors:  Julie Barroso; Bradley G Hammill; Jane Leserman; Naima Salahuddin; James L Harmon; Brian Wells Pence
Journal:  AIDS Behav       Date:  2010-12

2.  Death rates from human immunodeficiency virus and tuberculosis among American Indians/Alaska Natives in the United States, 1990-2009.

Authors:  Brigg Reilley; Emily Bloss; Kathy K Byrd; Jonathan Iralu; Lisa Neel; James Cheek
Journal:  Am J Public Health       Date:  2014-04-22       Impact factor: 9.308

3.  Depression and aging with HIV: Associations with health-related quality of life and positive psychological factors.

Authors:  Alexandra S Rooney; Raeanne C Moore; Emily W Paolillo; Ben Gouaux; Anya Umlauf; Scott L Letendre; Dilip V Jeste; David J Moore
Journal:  J Affect Disord       Date:  2019-03-06       Impact factor: 4.839

Review 4.  Affective disorders in patients with HIV infection: impact of antiretroviral therapy.

Authors:  Gabriele Arendt
Journal:  CNS Drugs       Date:  2006       Impact factor: 5.749

Review 5.  A comparative review of health-related quality-of-life measures for use in HIV/AIDS clinical trials.

Authors:  Darren J Clayson; Diane J Wild; Paul Quarterman; Isabelle Duprat-Lomon; Maria Kubin; Stephen Joel Coons
Journal:  Pharmacoeconomics       Date:  2006       Impact factor: 4.981

6.  Somatic symptoms and the association between hepatitis C infection and depression in HIV-infected patients.

Authors:  Jeanie C Yoon; Paul K Crane; Paul S Ciechanowski; Robert D Harrington; Mari M Kitahata; Heidi M Crane
Journal:  AIDS Care       Date:  2011-05-23

7.  Validation of the MOS-HIV as a measure of health-related quality of life in persons living with HIV and liver disease.

Authors:  Wendy A Henderson; Elizabeth A Schlenk; Kevin H Kim; Colleen M Hadigan; Angela C Martino; Susan M Sereika; Judith A Erlen
Journal:  AIDS Care       Date:  2010-04

8.  The Symptom Experience of HIV/HCV-Coinfected Adults.

Authors:  Carol Bova; Carol Jaffarian; Pauline Himlan; Linda Mangini; Lisa Ogawa
Journal:  J Assoc Nurses AIDS Care       Date:  2008 May-Jun       Impact factor: 1.354

Review 9.  Health-related quality of life assessment after antiretroviral therapy: a review of the literature.

Authors:  Harleen Gakhar; Amanda Kamali; Mark Holodniy
Journal:  Drugs       Date:  2013-05       Impact factor: 9.546

10.  Assessment of factors associated with the quality of life of patients living with HIV/HCV co-infection.

Authors:  Marco Pereira; Renata Fialho
Journal:  J Behav Med       Date:  2016-08-09
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