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The development and validation of the daily electronic Endometriosis Pain and Bleeding Diary

BACKGROUND: The objective of this study was to develop and validate a daily electronic Endometriosis Pain and Bleeding Diary (EPBD) for assessing treatment-related changes in endometriosis symptoms from the patient's perspective in a clinical trial setting. METHODS: The EPBD items were develope...

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Autores principales: Deal, Linda S, DiBenedetti, Dana Britt, Williams, Valerie SL, Fehnel, Sheri E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908571/
https://www.ncbi.nlm.nih.gov/pubmed/20598144
http://dx.doi.org/10.1186/1477-7525-8-64
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author Deal, Linda S
DiBenedetti, Dana Britt
Williams, Valerie SL
Fehnel, Sheri E
author_facet Deal, Linda S
DiBenedetti, Dana Britt
Williams, Valerie SL
Fehnel, Sheri E
author_sort Deal, Linda S
collection PubMed
description BACKGROUND: The objective of this study was to develop and validate a daily electronic Endometriosis Pain and Bleeding Diary (EPBD) for assessing treatment-related changes in endometriosis symptoms from the patient's perspective in a clinical trial setting. METHODS: The EPBD items were developed based on clinician input and the results of 5 focus groups (N = 38) and 3 iterative sets of cognitive interviews (N = 22). The psychometric properties were evaluated using data collected in a usual-practice, non-intervention study conducted at 4 sites in the United States. Existing questionnaires were also administered to explore the construct validity of the EPBD. The development and validation processes were consistent with the recommendations in the 2009 FDA Patient Reported Outcomes Guidance to Industry. RESULTS: Focus group participants described 2 distinct types of pain (intermittent and continuous), which they felt were relevant and important to monitor. Participants also indicated that pain and bleeding/spotting associated with intercourse were important symptoms related to endometriosis. Cognitive interviews with additional endometriosis patients served to optimize item content, wording, and response options. Psychometric analyses found the EPBD items to behave as expected, for example, item-level means for subjects with severe endometriosis symptoms were higher (i.e., worse) compared with subjects with mild symptoms. Item-total correlations for the EPBD pain items (range 0.40-0.89) indicated that the items were related but not redundant. EPBD pain ratings correlated highly with the modified Brief Pain Inventory-Short Form Pain Intensity score (range 0.46-0.61). Women with severe endometriosis symptoms reported significantly higher intermittent and continuous dysmenorrhea and intermittent and continuous pelvic pain ratings and greater interference with daily activities compared with women with mild symptoms (all p < 0.01). CONCLUSIONS: The results of this study show that the 17-item EPBD reliably and validly characterizes the types of pain that endometriosis patients identified as being important. As a daily patient-reported assessment, it overcomes the significant potential for intra- and inter-rater variability and rater and recall bias that is inherent in the Biberoglu and Behrman Scale. Additional studies are required to confirm the dimensionality and optimal scoring of the EPBD, to corroborate the present results, and to assess other important measurement properties, such as responsiveness.
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spelling pubmed-29085712010-07-23 The development and validation of the daily electronic Endometriosis Pain and Bleeding Diary Deal, Linda S DiBenedetti, Dana Britt Williams, Valerie SL Fehnel, Sheri E Health Qual Life Outcomes Research BACKGROUND: The objective of this study was to develop and validate a daily electronic Endometriosis Pain and Bleeding Diary (EPBD) for assessing treatment-related changes in endometriosis symptoms from the patient's perspective in a clinical trial setting. METHODS: The EPBD items were developed based on clinician input and the results of 5 focus groups (N = 38) and 3 iterative sets of cognitive interviews (N = 22). The psychometric properties were evaluated using data collected in a usual-practice, non-intervention study conducted at 4 sites in the United States. Existing questionnaires were also administered to explore the construct validity of the EPBD. The development and validation processes were consistent with the recommendations in the 2009 FDA Patient Reported Outcomes Guidance to Industry. RESULTS: Focus group participants described 2 distinct types of pain (intermittent and continuous), which they felt were relevant and important to monitor. Participants also indicated that pain and bleeding/spotting associated with intercourse were important symptoms related to endometriosis. Cognitive interviews with additional endometriosis patients served to optimize item content, wording, and response options. Psychometric analyses found the EPBD items to behave as expected, for example, item-level means for subjects with severe endometriosis symptoms were higher (i.e., worse) compared with subjects with mild symptoms. Item-total correlations for the EPBD pain items (range 0.40-0.89) indicated that the items were related but not redundant. EPBD pain ratings correlated highly with the modified Brief Pain Inventory-Short Form Pain Intensity score (range 0.46-0.61). Women with severe endometriosis symptoms reported significantly higher intermittent and continuous dysmenorrhea and intermittent and continuous pelvic pain ratings and greater interference with daily activities compared with women with mild symptoms (all p < 0.01). CONCLUSIONS: The results of this study show that the 17-item EPBD reliably and validly characterizes the types of pain that endometriosis patients identified as being important. As a daily patient-reported assessment, it overcomes the significant potential for intra- and inter-rater variability and rater and recall bias that is inherent in the Biberoglu and Behrman Scale. Additional studies are required to confirm the dimensionality and optimal scoring of the EPBD, to corroborate the present results, and to assess other important measurement properties, such as responsiveness. BioMed Central 2010-07-02 /pmc/articles/PMC2908571/ /pubmed/20598144 http://dx.doi.org/10.1186/1477-7525-8-64 Text en Copyright ©2010 Deal et al; 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
Deal, Linda S
DiBenedetti, Dana Britt
Williams, Valerie SL
Fehnel, Sheri E
The development and validation of the daily electronic Endometriosis Pain and Bleeding Diary
title The development and validation of the daily electronic Endometriosis Pain and Bleeding Diary
title_full The development and validation of the daily electronic Endometriosis Pain and Bleeding Diary
title_fullStr The development and validation of the daily electronic Endometriosis Pain and Bleeding Diary
title_full_unstemmed The development and validation of the daily electronic Endometriosis Pain and Bleeding Diary
title_short The development and validation of the daily electronic Endometriosis Pain and Bleeding Diary
title_sort development and validation of the daily electronic endometriosis pain and bleeding diary
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908571/
https://www.ncbi.nlm.nih.gov/pubmed/20598144
http://dx.doi.org/10.1186/1477-7525-8-64
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