Documenting Patient Outcomes with Questionnaires
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This document discusses the importance of documenting outcomes using patient-reported questionnaires in prostate cancer treatment. It outlines how patient-centered outcomes like health-related quality of life are as important as objective clinical measures. It also describes several validated questionnaires that are used to measure quality of life domains affected by prostate cancer and its treatment, such as urinary, sexual, and bowel function as well as general physical and mental health. Principles for documenting outcomes include using validated instruments, relying on patient self-assessment, tracking outcomes longitudinally, and interpreting changes from a patient's own baseline.
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Documenting Patient Outcomes with Questionnaires
- 12. Doctor or patient perspective Physician vs Patient perception of QOL impairment Sonn, J Urol 2009 n = 1,366
- 13. Doctor or patient perspective Physician vs Patient perception of QOL impairment Sonn, J Urol 2009 n = 1,366
- 14. National longitudinal QOL Cohort Sanda, NEJM 2008 n = 1,201
- 15. UCLA longitudinal QOL cohort SF-36 Physical Composite Litwin, Cancer 2007 n = 580
- 16. UCLA longitudinal QOL cohort PCI Sexual Function % Return to baseline Litwin, Cancer 2007 n = 580
- 18. Websites for further information on patient-reported outcomes proqolid.org outcomes.cancer.gov sf-36.org
Notas do Editor
- Again, the SF-36 scales run from 0-100 with higher scores representing better outcomes. Physical function was similar between groups.
- Men undergoing brachytherapy had substantially worse AUASI scores that persisted, even a year after treatment.