Sensitivity as outcome measure of androgen replacement: the AMS scale

<p>Abstract</p> <p>Background</p> <p>The capacity of the AMS scale as clinical utility and as outcome measure still needs validation.</p> <p>Methods</p> <p>An open post-marketing study was performed by office-based physicians in Germany in 2004....

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Main Authors: Dinger Juergen C, Moore Claudia, Heinemann Lothar A, Stoehr Diana
Format: Article
Language:English
Published: BMC 2006-03-01
Series:Health and Quality of Life Outcomes
Online Access:http://www.hqlo.com/content/4/1/23
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spelling doaj-91dd82c457a240aca9aee84e022d98442020-11-25T01:40:59ZengBMCHealth and Quality of Life Outcomes1477-75252006-03-01412310.1186/1477-7525-4-23Sensitivity as outcome measure of androgen replacement: the AMS scaleDinger Juergen CMoore ClaudiaHeinemann Lothar AStoehr Diana<p>Abstract</p> <p>Background</p> <p>The capacity of the AMS scale as clinical utility and as outcome measure still needs validation.</p> <p>Methods</p> <p>An open post-marketing study was performed by office-based physicians in Germany in 2004. We analysed data of 1670 androgen-deficient males who were treated with testosterone gel. The AMS scale was applied prior to and after 3 months treatment.</p> <p>Results</p> <p>The improvement of complaints under treatment relative to the baseline score was 30.7% (total score), 27.3% (psychological domain), 30.5% (somatic domain), and 30.7% (sexual domain), respectively. Patients with little or no symptoms before therapy improved by 9%, those with mild complaints at entry by 24%, with moderate by 32%, and with severe symptoms by 39% – compared with the baseline score. We showed that the distribution of complaints of testosterone deficient men before therapy almost returned to norm values after 12 weeks of testosterone treatment. Age, BMI, and total testosterone level at baseline did not modify the positive effect of androgen therapy. We also demonstrated that the AMS results can predict the independent (physician's) opinion about the individual treatment effect. Both, sensitivity (correct prediction of a positive assessment by the physician) and specificity (correct prediction of a negative assessment by the physician) were over 70%, if about 22% improvement of the AMS total score was used as cut-off point.</p> <p>Conclusion</p> <p>The AMS scale showed a convincing ability to measure treatment effects on quality of life across the full range of severity of complaints. Effect modification by other variables at baseline was not observed. In addition, results of the scale can predict the subjective clinical expert opinion on the treatment efficiency.</p> http://www.hqlo.com/content/4/1/23
collection DOAJ
language English
format Article
sources DOAJ
author Dinger Juergen C
Moore Claudia
Heinemann Lothar A
Stoehr Diana
spellingShingle Dinger Juergen C
Moore Claudia
Heinemann Lothar A
Stoehr Diana
Sensitivity as outcome measure of androgen replacement: the AMS scale
Health and Quality of Life Outcomes
author_facet Dinger Juergen C
Moore Claudia
Heinemann Lothar A
Stoehr Diana
author_sort Dinger Juergen C
title Sensitivity as outcome measure of androgen replacement: the AMS scale
title_short Sensitivity as outcome measure of androgen replacement: the AMS scale
title_full Sensitivity as outcome measure of androgen replacement: the AMS scale
title_fullStr Sensitivity as outcome measure of androgen replacement: the AMS scale
title_full_unstemmed Sensitivity as outcome measure of androgen replacement: the AMS scale
title_sort sensitivity as outcome measure of androgen replacement: the ams scale
publisher BMC
series Health and Quality of Life Outcomes
issn 1477-7525
publishDate 2006-03-01
description <p>Abstract</p> <p>Background</p> <p>The capacity of the AMS scale as clinical utility and as outcome measure still needs validation.</p> <p>Methods</p> <p>An open post-marketing study was performed by office-based physicians in Germany in 2004. We analysed data of 1670 androgen-deficient males who were treated with testosterone gel. The AMS scale was applied prior to and after 3 months treatment.</p> <p>Results</p> <p>The improvement of complaints under treatment relative to the baseline score was 30.7% (total score), 27.3% (psychological domain), 30.5% (somatic domain), and 30.7% (sexual domain), respectively. Patients with little or no symptoms before therapy improved by 9%, those with mild complaints at entry by 24%, with moderate by 32%, and with severe symptoms by 39% – compared with the baseline score. We showed that the distribution of complaints of testosterone deficient men before therapy almost returned to norm values after 12 weeks of testosterone treatment. Age, BMI, and total testosterone level at baseline did not modify the positive effect of androgen therapy. We also demonstrated that the AMS results can predict the independent (physician's) opinion about the individual treatment effect. Both, sensitivity (correct prediction of a positive assessment by the physician) and specificity (correct prediction of a negative assessment by the physician) were over 70%, if about 22% improvement of the AMS total score was used as cut-off point.</p> <p>Conclusion</p> <p>The AMS scale showed a convincing ability to measure treatment effects on quality of life across the full range of severity of complaints. Effect modification by other variables at baseline was not observed. In addition, results of the scale can predict the subjective clinical expert opinion on the treatment efficiency.</p>
url http://www.hqlo.com/content/4/1/23
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