Assessing health-related quality of life in chronic hepatitis C using the Sickness Impact Profile

G L Davis1, L A Balart, E R Schiff

  • 1University of Florida, Gainesville.

Clinical Therapeutics
|March 1, 1994
PubMed

Insights

Interferon alfa-2b improved quality of life for chronic hepatitis C patients, particularly in work and recreation. However, the Sickness Impact Profile (SIP) may not be sensitive enough to detect clinically meaningful changes from this treatment.

Area of Science:

  • Hepatology
  • Clinical Trials
  • Health-Related Quality of Life Research

Background:

  • Chronic hepatitis C significantly impacts patients' health-related quality of life (HRQOL).
  • Assessing HRQOL changes during treatment is crucial for understanding therapeutic benefits.

Purpose of the Study:

  • To evaluate the impact of interferon alfa-2b on HRQOL in chronic hepatitis C patients using the Sickness Impact Profile (SIP).
  • To assess the suitability of the SIP as an instrument for measuring treatment effects on HRQOL in this population.

Main Methods:

  • A randomized controlled trial involving 160 chronic hepatitis C patients.
  • Self-administration of the SIP at baseline, end of treatment, and study endpoint.
  • Comparison of patient scores to a general population historical control group.

Main Results:

  • Pre-treatment, patients had significantly worse SIP scores than the general population, especially in work, sleep/rest, and recreation.
  • Interferon alfa-2b treatment led to significant improvements in work, sleep/rest, and recreation SIP scores.
  • Untreated patients showed no improvement or slight worsening in SIP scores; responders had the greatest improvement in work scores.

Conclusions:

  • The SIP is a reliable instrument for assessing chronic hepatitis C's impact on HRQOL.
  • The SIP may lack disease-specificity and sensitivity to detect clinically relevant HRQOL changes from interferon alfa-2b treatment.
  • Alternative or disease-specific instruments might be better suited for evaluating interferon alfa-2b's HRQOL effects in chronic hepatitis C.

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