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January 2001

 

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Research

Quality of Life Instruments Developed

For the past 5 years, a group of researchers (Gary Naglie, Jane Irvine, Paul Ritvo, Murray Krahn) have been developing instruments to evaluate health outcomes in prostate cancer. They initially developed a disease-specific instrument to measure patients’ utilities, but completing the task of utility assessment was a lengthy (1 hr.) and fairly demanding process. As part of the utility instrument, a multi-attribute health state classification system was developed. This looks like a 10 item questionnaire. Recently, another grant was successfully obtained and it will allow the team to further develop the instrument as a disease-specific health index by developing a system of utility weights similar to that used in the Health Utilities Index. The result will be what one colleague felicitously described as the “Swiss Army Knife” of quality of life Instruments. By completing a 10 item questionnaire, patients can generate valid psychometric and utility measures of health related quality of life. It is hoping that these instruments, which are all versions of the PORPUS (Patient Oriented Prostate Utility Scale) will be widely used in prostate cancer outcomes research.

From Hospital to Home and Community: A Developing Research Agenda

Major health system restructuring initiatives, technological advances and changing social values have resulted in rapid reductions in numbers of hospital beds, hospital admissions, and average lengths of hospital stay across Canada.  However, public Medicare only covers “medically necessary” services provided by doctors and in hospitals; services provided in home and community by providers other than physicians may be publicly covered, but there is no requirement to do so.  As well as changing the site of care, the ongoing shift out of hospitals thus results in an increasing proportion of care moving beyond universal public coverage.  Over the past 18 months, Professors Raisa Deber and A. Paul Williams have been working to establish the infrastructure for multidisciplinary teams of researchers, graduate students and community partners which will investigate different aspects and consequences of the ongoing shift out of hospitals for providers, consumers and governments.  For example, two major funded  research projects assess the implications for home care expenditures of different regionalization models now in place in the Atlantic provinces; and the capacity of not-for-profit community-based agencies to respond to the growing numbers of Canadians with higher levels of health care needs who now require continuing care in home and community.

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