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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 |
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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 < 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.</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 < 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.</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. Larry, MD, MC ; Spies, James B., MD, MPH</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-cd5de5c803a65412c9d3c3fd229d80726a58b4acf6a2fcb676f7e68b9dc30e1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Comorbidity</topic><topic>Female</topic><topic>Fibroids</topic><topic>Health Status</topic><topic>health-related quality of life</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Leiomyoma - physiopathology</topic><topic>Leiomyoma - psychology</topic><topic>Magnitude</topic><topic>Mental Health</topic><topic>Middle Aged</topic><topic>Patient-reported outcomes</topic><topic>Prospective Studies</topic><topic>Psychometrics</topic><topic>Quality of Life</topic><topic>Reproducibility of Results</topic><topic>Responsiveness</topic><topic>Socioeconomic Factors</topic><topic>Surveys and Questionnaires</topic><topic>Symptoms</topic><topic>Uterine fibroids</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>MEDLINE - Academic</collection><jtitle>Value in health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coyne, Karin S., PhD, MPH</au><au>Margolis, Mary Kay, MPH, MHA</au><au>Bradley, Linda D., MD</au><au>Guido, Richard, MD</au><au>Maxwell, G. 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 < 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.</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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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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