Application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophrenia
<p>Abstract</p> <p>Background</p> <p>Most tools for estimating utilities use clinical trial data from general health status models, such as the 36-Item Short-Form Health Survey (SF-36). A disease-specific model may be more appropriate. The objective of this study was to...
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doaj-1b4e9cad4ba84227955fc10d19a0d1302020-11-25T00:37:15ZengBMCHealth and Quality of Life Outcomes1477-75252005-09-01315710.1186/1477-7525-3-57Application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophreniaRupnow Marcia FTLenert Leslie AElnitsky Christine<p>Abstract</p> <p>Background</p> <p>Most tools for estimating utilities use clinical trial data from general health status models, such as the 36-Item Short-Form Health Survey (SF-36). A disease-specific model may be more appropriate. The objective of this study was to apply a disease-specific utility mapping function for schizophrenia to data from a large, 1-year, open-label study of long-acting risperidone and to compare its performance with an SF-36-based utility mapping function.</p> <p>Methods</p> <p>Patients with schizophrenia or schizoaffective disorder by DSM-IV criteria received 25, 50, or 75 mg long-acting risperidone every 2 weeks for 12 months. The Positive and Negative Syndrome Scale (PANSS) and SF-36 were used to assess efficacy and health-related quality of life. Movement disorder severity was measured using the Extrapyramidal Symptom Rating Scale (ESRS); data concerning other common adverse effects (orthostatic hypotension, weight gain) were collected. Transforms were applied to estimate utilities.</p> <p>Results</p> <p>A total of 474 patients completed the study. Long-acting risperidone treatment was associated with a utility gain of 0.051 using the disease-specific function. The estimated gain using an SF-36-based mapping function was smaller: 0.0285. Estimates of gains were only weakly correlated (r = 0.2). Because of differences in scaling and variance, the requisite sample size for a randomized trial to confirm observed effects is much smaller for the disease-specific mapping function (156 versus 672 total subjects).</p> <p>Conclusion</p> <p>Application of a disease-specific mapping function was feasible. Differences in scaling and precision suggest the clinically based mapping function has greater power than the SF-36-based measure to detect differences in utility.</p> http://www.hqlo.com/content/3/1/57 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rupnow Marcia FT Lenert Leslie A Elnitsky Christine |
spellingShingle |
Rupnow Marcia FT Lenert Leslie A Elnitsky Christine Application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophrenia Health and Quality of Life Outcomes |
author_facet |
Rupnow Marcia FT Lenert Leslie A Elnitsky Christine |
author_sort |
Rupnow Marcia FT |
title |
Application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophrenia |
title_short |
Application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophrenia |
title_full |
Application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophrenia |
title_fullStr |
Application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophrenia |
title_full_unstemmed |
Application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophrenia |
title_sort |
application of a disease-specific mapping function to estimate utility gains with effective treatment of schizophrenia |
publisher |
BMC |
series |
Health and Quality of Life Outcomes |
issn |
1477-7525 |
publishDate |
2005-09-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Most tools for estimating utilities use clinical trial data from general health status models, such as the 36-Item Short-Form Health Survey (SF-36). A disease-specific model may be more appropriate. The objective of this study was to apply a disease-specific utility mapping function for schizophrenia to data from a large, 1-year, open-label study of long-acting risperidone and to compare its performance with an SF-36-based utility mapping function.</p> <p>Methods</p> <p>Patients with schizophrenia or schizoaffective disorder by DSM-IV criteria received 25, 50, or 75 mg long-acting risperidone every 2 weeks for 12 months. The Positive and Negative Syndrome Scale (PANSS) and SF-36 were used to assess efficacy and health-related quality of life. Movement disorder severity was measured using the Extrapyramidal Symptom Rating Scale (ESRS); data concerning other common adverse effects (orthostatic hypotension, weight gain) were collected. Transforms were applied to estimate utilities.</p> <p>Results</p> <p>A total of 474 patients completed the study. Long-acting risperidone treatment was associated with a utility gain of 0.051 using the disease-specific function. The estimated gain using an SF-36-based mapping function was smaller: 0.0285. Estimates of gains were only weakly correlated (r = 0.2). Because of differences in scaling and variance, the requisite sample size for a randomized trial to confirm observed effects is much smaller for the disease-specific mapping function (156 versus 672 total subjects).</p> <p>Conclusion</p> <p>Application of a disease-specific mapping function was feasible. Differences in scaling and precision suggest the clinically based mapping function has greater power than the SF-36-based measure to detect differences in utility.</p> |
url |
http://www.hqlo.com/content/3/1/57 |
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