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Further Validation of the Uterine Fibroid Symptom and Quality-of-Life Questionnaire

Abstract Objective To further examine the reliability, validity and responsiveness of the uterine fibroid symptom and quality-of-life (UFS-QOL) questionnaire among women with and without uterine fibroids. Methods A multicenter, non-randomized, prospective study was conducted with women undergoing tr...

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Published in:Value in health 2012-01, Vol.15 (1), p.135-142
Main Authors: Coyne, Karin S., PhD, MPH, Margolis, Mary Kay, MPH, MHA, Bradley, Linda D., MD, Guido, Richard, MD, Maxwell, G. Larry, MD, MC, Spies, James B., MD, MPH
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container_title Value in health
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creator Coyne, Karin S., PhD, MPH
Margolis, Mary Kay, MPH, MHA
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Guido, Richard, MD
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Spies, James B., MD, MPH
description Abstract Objective To further examine the reliability, validity and responsiveness of the uterine fibroid symptom and quality-of-life (UFS-QOL) questionnaire among women with and without uterine fibroids. Methods A multicenter, non-randomized, prospective study was conducted with women undergoing treatment for uterine fibroids (fibroid treatment group [FTG]) and normal controls (normal control group [NCG]). Women in the FTG were recruited when they were scheduled for treatment; women in the NCG were recruited during their annual exam. Participants completed the UFS-QOL and a short form 36 health survey (SF-36) at enrollment and at 6 and 12 months. Descriptive statistics, Cronbach's alpha, Spearman's correlations, t tests, and general linear models were used to analyze the internal consistency and test–retest reliability, concurrent and discriminant validity, and responsiveness of the UFS-QOL. Results There were 89 NCG and 234 FTG women who completed the study. Mean age was 43.1 years for FTG and 40.8 for NCG ( P < 0.001). The FTG reported significantly greater symptom severity and worse health-related quality of life (HRQL) than the NCG (all UFS-QOL subscales P < 0.001). The UFS-QOL subscales were significantly correlated in the expected direction and magnitude with each SF-36 subscale in the FTG, indicating acceptable concurrent validity. Cronbach's alphas were 0.73 to 0.97, reflecting adequate internal consistency. Each UFS-QOL subscale was responsive to changes after treatment in the FTG with effect sizes ranging between 1.1 and −2.35. The UFS-QOL remained stable in the NCG during the 1 year follow-up. Conclusion The UFS-QOL is a valid and reliable measure to assess symptoms and HRQL in women with uterine fibroids and is highly responsive to treatment-related changes.
doi_str_mv 10.1016/j.jval.2011.07.007
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Larry, MD, MC ; Spies, James B., MD, MPH</creator><creatorcontrib>Coyne, Karin S., PhD, MPH ; Margolis, Mary Kay, MPH, MHA ; Bradley, Linda D., MD ; Guido, Richard, MD ; Maxwell, G. Larry, MD, MC ; Spies, James B., MD, MPH</creatorcontrib><description>Abstract Objective To further examine the reliability, validity and responsiveness of the uterine fibroid symptom and quality-of-life (UFS-QOL) questionnaire among women with and without uterine fibroids. Methods A multicenter, non-randomized, prospective study was conducted with women undergoing treatment for uterine fibroids (fibroid treatment group [FTG]) and normal controls (normal control group [NCG]). Women in the FTG were recruited when they were scheduled for treatment; women in the NCG were recruited during their annual exam. Participants completed the UFS-QOL and a short form 36 health survey (SF-36) at enrollment and at 6 and 12 months. Descriptive statistics, Cronbach's alpha, Spearman's correlations, t tests, and general linear models were used to analyze the internal consistency and test–retest reliability, concurrent and discriminant validity, and responsiveness of the UFS-QOL. Results There were 89 NCG and 234 FTG women who completed the study. Mean age was 43.1 years for FTG and 40.8 for NCG ( P &lt; 0.001). The FTG reported significantly greater symptom severity and worse health-related quality of life (HRQL) than the NCG (all UFS-QOL subscales P &lt; 0.001). The UFS-QOL subscales were significantly correlated in the expected direction and magnitude with each SF-36 subscale in the FTG, indicating acceptable concurrent validity. Cronbach's alphas were 0.73 to 0.97, reflecting adequate internal consistency. Each UFS-QOL subscale was responsive to changes after treatment in the FTG with effect sizes ranging between 1.1 and −2.35. The UFS-QOL remained stable in the NCG during the 1 year follow-up. Conclusion The UFS-QOL is a valid and reliable measure to assess symptoms and HRQL in women with uterine fibroids and is highly responsive to treatment-related changes.</description><identifier>ISSN: 1098-3015</identifier><identifier>EISSN: 1524-4733</identifier><identifier>DOI: 10.1016/j.jval.2011.07.007</identifier><identifier>PMID: 22264981</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Comorbidity ; Female ; Fibroids ; Health Status ; health-related quality of life ; Humans ; Internal Medicine ; Leiomyoma - physiopathology ; Leiomyoma - psychology ; Magnitude ; Mental Health ; Middle Aged ; Patient-reported outcomes ; Prospective Studies ; Psychometrics ; Quality of Life ; Reproducibility of Results ; Responsiveness ; Socioeconomic Factors ; Surveys and Questionnaires ; Symptoms ; Uterine fibroids ; Women</subject><ispartof>Value in health, 2012-01, Vol.15 (1), p.135-142</ispartof><rights>International Society for Pharmacoeconomics and Outcomes Research (ISPOR)</rights><rights>2012 International Society for Pharmacoeconomics and Outcomes Research (ISPOR)</rights><rights>Copyright © 2012 International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-cd5de5c803a65412c9d3c3fd229d80726a58b4acf6a2fcb676f7e68b9dc30e1a3</citedby><cites>FETCH-LOGICAL-c487t-cd5de5c803a65412c9d3c3fd229d80726a58b4acf6a2fcb676f7e68b9dc30e1a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912,30987</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22264981$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Coyne, Karin S., PhD, MPH</creatorcontrib><creatorcontrib>Margolis, Mary Kay, MPH, MHA</creatorcontrib><creatorcontrib>Bradley, Linda D., MD</creatorcontrib><creatorcontrib>Guido, Richard, MD</creatorcontrib><creatorcontrib>Maxwell, G. Larry, MD, MC</creatorcontrib><creatorcontrib>Spies, James B., MD, MPH</creatorcontrib><title>Further Validation of the Uterine Fibroid Symptom and Quality-of-Life Questionnaire</title><title>Value in health</title><addtitle>Value Health</addtitle><description>Abstract Objective To further examine the reliability, validity and responsiveness of the uterine fibroid symptom and quality-of-life (UFS-QOL) questionnaire among women with and without uterine fibroids. Methods A multicenter, non-randomized, prospective study was conducted with women undergoing treatment for uterine fibroids (fibroid treatment group [FTG]) and normal controls (normal control group [NCG]). Women in the FTG were recruited when they were scheduled for treatment; women in the NCG were recruited during their annual exam. Participants completed the UFS-QOL and a short form 36 health survey (SF-36) at enrollment and at 6 and 12 months. Descriptive statistics, Cronbach's alpha, Spearman's correlations, t tests, and general linear models were used to analyze the internal consistency and test–retest reliability, concurrent and discriminant validity, and responsiveness of the UFS-QOL. Results There were 89 NCG and 234 FTG women who completed the study. Mean age was 43.1 years for FTG and 40.8 for NCG ( P &lt; 0.001). The FTG reported significantly greater symptom severity and worse health-related quality of life (HRQL) than the NCG (all UFS-QOL subscales P &lt; 0.001). The UFS-QOL subscales were significantly correlated in the expected direction and magnitude with each SF-36 subscale in the FTG, indicating acceptable concurrent validity. Cronbach's alphas were 0.73 to 0.97, reflecting adequate internal consistency. Each UFS-QOL subscale was responsive to changes after treatment in the FTG with effect sizes ranging between 1.1 and −2.35. The UFS-QOL remained stable in the NCG during the 1 year follow-up. Conclusion The UFS-QOL is a valid and reliable measure to assess symptoms and HRQL in women with uterine fibroids and is highly responsive to treatment-related changes.</description><subject>Adult</subject><subject>Comorbidity</subject><subject>Female</subject><subject>Fibroids</subject><subject>Health Status</subject><subject>health-related quality of life</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Leiomyoma - physiopathology</subject><subject>Leiomyoma - psychology</subject><subject>Magnitude</subject><subject>Mental Health</subject><subject>Middle Aged</subject><subject>Patient-reported outcomes</subject><subject>Prospective Studies</subject><subject>Psychometrics</subject><subject>Quality of Life</subject><subject>Reproducibility of Results</subject><subject>Responsiveness</subject><subject>Socioeconomic Factors</subject><subject>Surveys and Questionnaires</subject><subject>Symptoms</subject><subject>Uterine fibroids</subject><subject>Women</subject><issn>1098-3015</issn><issn>1524-4733</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>7QJ</sourceid><recordid>eNp9kUuL1TAYhoMozkX_gAvpTjetuTSXgggyeEbhgMhx3IY0-YKpbXNM2oHz7005owsXs8qF5335eD6EXhHcEEzEu6EZ7s3YUExIg2WDsXyCLgmnbd1Kxp6WO-5UzTDhF-gq5wFjLBjlz9EFpVS0nSKX6LBb0_ITUvXDjMGZJcS5ir4qX9XdAinMUO1Cn2Jw1eE0HZc4VWZ21be14Mupjr7eBw_lDXnLziYkeIGeeTNmePlwXqO73afvN5_r_dfbLzcf97VtlVxq67gDbhVmRvCWUNs5Zpl3lHZOYUmF4apvjfXCUG97IYWXIFTfOcswEMOu0Ztz7zHF39sAegrZwjiaGeKadUcklx2htJBvHyUJ56rrqMKkoPSM2hRzTuD1MYXJpJMmWG_a9aA37XrTrrHURXsJvX7oX_sJ3L_IX88FeH8GoPi4D5B0tgFmC674sot2MTze_-G_uB3DHKwZf8EJ8hDXNBfTmuhMNdaHbfHb3kkp5Lxs_Q-WP6iV</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Coyne, Karin S., PhD, MPH</creator><creator>Margolis, Mary Kay, MPH, MHA</creator><creator>Bradley, Linda D., MD</creator><creator>Guido, Richard, MD</creator><creator>Maxwell, G. Larry, MD, MC</creator><creator>Spies, James B., MD, MPH</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>7X8</scope></search><sort><creationdate>20120101</creationdate><title>Further Validation of the Uterine Fibroid Symptom and Quality-of-Life Questionnaire</title><author>Coyne, Karin S., PhD, MPH ; Margolis, Mary Kay, MPH, MHA ; Bradley, Linda D., MD ; Guido, Richard, MD ; Maxwell, G. 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Larry, MD, MC</au><au>Spies, James B., MD, MPH</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Further Validation of the Uterine Fibroid Symptom and Quality-of-Life Questionnaire</atitle><jtitle>Value in health</jtitle><addtitle>Value Health</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>15</volume><issue>1</issue><spage>135</spage><epage>142</epage><pages>135-142</pages><issn>1098-3015</issn><eissn>1524-4733</eissn><abstract>Abstract Objective To further examine the reliability, validity and responsiveness of the uterine fibroid symptom and quality-of-life (UFS-QOL) questionnaire among women with and without uterine fibroids. Methods A multicenter, non-randomized, prospective study was conducted with women undergoing treatment for uterine fibroids (fibroid treatment group [FTG]) and normal controls (normal control group [NCG]). Women in the FTG were recruited when they were scheduled for treatment; women in the NCG were recruited during their annual exam. Participants completed the UFS-QOL and a short form 36 health survey (SF-36) at enrollment and at 6 and 12 months. Descriptive statistics, Cronbach's alpha, Spearman's correlations, t tests, and general linear models were used to analyze the internal consistency and test–retest reliability, concurrent and discriminant validity, and responsiveness of the UFS-QOL. Results There were 89 NCG and 234 FTG women who completed the study. Mean age was 43.1 years for FTG and 40.8 for NCG ( P &lt; 0.001). The FTG reported significantly greater symptom severity and worse health-related quality of life (HRQL) than the NCG (all UFS-QOL subscales P &lt; 0.001). The UFS-QOL subscales were significantly correlated in the expected direction and magnitude with each SF-36 subscale in the FTG, indicating acceptable concurrent validity. Cronbach's alphas were 0.73 to 0.97, reflecting adequate internal consistency. Each UFS-QOL subscale was responsive to changes after treatment in the FTG with effect sizes ranging between 1.1 and −2.35. The UFS-QOL remained stable in the NCG during the 1 year follow-up. Conclusion The UFS-QOL is a valid and reliable measure to assess symptoms and HRQL in women with uterine fibroids and is highly responsive to treatment-related changes.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22264981</pmid><doi>10.1016/j.jval.2011.07.007</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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ispartof Value in health, 2012-01, Vol.15 (1), p.135-142
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source Applied Social Sciences Index & Abstracts (ASSIA); ScienceDirect Freedom Collection
subjects Adult
Comorbidity
Female
Fibroids
Health Status
health-related quality of life
Humans
Internal Medicine
Leiomyoma - physiopathology
Leiomyoma - psychology
Magnitude
Mental Health
Middle Aged
Patient-reported outcomes
Prospective Studies
Psychometrics
Quality of Life
Reproducibility of Results
Responsiveness
Socioeconomic Factors
Surveys and Questionnaires
Symptoms
Uterine fibroids
Women
title Further Validation of the Uterine Fibroid Symptom and Quality-of-Life Questionnaire
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