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Validation of the controlled ovarian stimulation impact measure (COSI): assessing the patient perspective

BACKGROUND: Controlled Ovarian Stimulation (COS) is the first step for in vitro fertilization (IVF) treatment, a treatment often described and experienced as stressful to patients and their partners. COS also requires concerted efforts by the patients in administering medication and general complian...

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Autores principales: Brod, Meryl, Fennema, Hein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734046/
https://www.ncbi.nlm.nih.gov/pubmed/23902854
http://dx.doi.org/10.1186/1477-7525-11-130
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author Brod, Meryl
Fennema, Hein
author_facet Brod, Meryl
Fennema, Hein
author_sort Brod, Meryl
collection PubMed
description BACKGROUND: Controlled Ovarian Stimulation (COS) is the first step for in vitro fertilization (IVF) treatment, a treatment often described and experienced as stressful to patients and their partners. COS also requires concerted efforts by the patients in administering medication and general compliance to treatment protocols. Little is known about the impacts on patients that may be specific to this important first step in treatment. The absence of a conceptually sound and well-validated measure assessing patient experience and functioning during ovarian stimulation has been an obstacle to understanding the impacts of ovarian stimulation on women pursuing IVF. To address this gap, the Controlled Ovarian Stimulation Impact Measure (COSI) was developed based upon accepted methods for designing patient reported outcome (PRO) measures. The purpose of this study was to psychometrically validate the COSI. METHODS: 267 patients from three countries (Ireland, United Kingdom, United States) were administered the COSI. Psychometric validation was conducted according to an a priori statistical analysis plan. RESULTS: The final 28-item COSI was found to have robust scale structure with four domains: Interference in Daily Life (Work and Home), Injection Burden, Psychological Health and Compliance Worry. Internal consistency of all domains was adequate (between 0.80 to 0.87) as was test-retest reliability (between 0.72-0.87). All a-priori hypotheses for convergent and known-groups validity tests were met. CONCLUSIONS: There is a measurable impact of COS on patient functioning and well-being. The COSI is a well-developed and validated PRO measure of this impact. Future work should include examination of responsiveness and confirmation of concepts in non-western countries.
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spelling pubmed-37340462013-08-06 Validation of the controlled ovarian stimulation impact measure (COSI): assessing the patient perspective Brod, Meryl Fennema, Hein Health Qual Life Outcomes Research BACKGROUND: Controlled Ovarian Stimulation (COS) is the first step for in vitro fertilization (IVF) treatment, a treatment often described and experienced as stressful to patients and their partners. COS also requires concerted efforts by the patients in administering medication and general compliance to treatment protocols. Little is known about the impacts on patients that may be specific to this important first step in treatment. The absence of a conceptually sound and well-validated measure assessing patient experience and functioning during ovarian stimulation has been an obstacle to understanding the impacts of ovarian stimulation on women pursuing IVF. To address this gap, the Controlled Ovarian Stimulation Impact Measure (COSI) was developed based upon accepted methods for designing patient reported outcome (PRO) measures. The purpose of this study was to psychometrically validate the COSI. METHODS: 267 patients from three countries (Ireland, United Kingdom, United States) were administered the COSI. Psychometric validation was conducted according to an a priori statistical analysis plan. RESULTS: The final 28-item COSI was found to have robust scale structure with four domains: Interference in Daily Life (Work and Home), Injection Burden, Psychological Health and Compliance Worry. Internal consistency of all domains was adequate (between 0.80 to 0.87) as was test-retest reliability (between 0.72-0.87). All a-priori hypotheses for convergent and known-groups validity tests were met. CONCLUSIONS: There is a measurable impact of COS on patient functioning and well-being. The COSI is a well-developed and validated PRO measure of this impact. Future work should include examination of responsiveness and confirmation of concepts in non-western countries. BioMed Central 2013-07-31 /pmc/articles/PMC3734046/ /pubmed/23902854 http://dx.doi.org/10.1186/1477-7525-11-130 Text en Copyright © 2013 Brod and Fennema; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Brod, Meryl
Fennema, Hein
Validation of the controlled ovarian stimulation impact measure (COSI): assessing the patient perspective
title Validation of the controlled ovarian stimulation impact measure (COSI): assessing the patient perspective
title_full Validation of the controlled ovarian stimulation impact measure (COSI): assessing the patient perspective
title_fullStr Validation of the controlled ovarian stimulation impact measure (COSI): assessing the patient perspective
title_full_unstemmed Validation of the controlled ovarian stimulation impact measure (COSI): assessing the patient perspective
title_short Validation of the controlled ovarian stimulation impact measure (COSI): assessing the patient perspective
title_sort validation of the controlled ovarian stimulation impact measure (cosi): assessing the patient perspective
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734046/
https://www.ncbi.nlm.nih.gov/pubmed/23902854
http://dx.doi.org/10.1186/1477-7525-11-130
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