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Physical, Social, and Psychological Consequences of Treatment for Hepatitis C

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Listed:
  • M. Manos
  • Chanda Ho
  • Rosemary Murphy
  • Valentina Shvachko

Abstract

Patient perspectives can help formulate and refine HCV treatment support programs. Effective support programs for diverse populations are crucial as the complexities and costs of HCV treatment increase. The call for greater support from peers, providers, and employers demands new systems such as patient-centered care teams. Copyright Springer International Publishing Switzerland 2013

Suggested Citation

  • M. Manos & Chanda Ho & Rosemary Murphy & Valentina Shvachko, 2013. "Physical, Social, and Psychological Consequences of Treatment for Hepatitis C," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 6(1), pages 23-34, March.
    • Handle: RePEc:spr:patien:v:6:y:2013:i:1:p:23-34
    DOI: 10.1007/s40271-013-0005-4
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    References listed on IDEAS

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    1. Krieger, N., 1992. "Overcoming the absence of socioeconomic data in medical records: Validation and application of a census-based methodology," American Journal of Public Health, American Public Health Association, vol. 82(5), pages 703-710.
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