Reliability of patient-reported outcome instruments in US adults with hemophilia: the Pain, Functional Impairment and Quality of life
Background: Hemophilia is marked by frequent joint bleeding, resulting in pain and functional impairment. Objective: This study aimed to assess the reliability of five patient-reported outcome (PRO) instruments in people with hemophilia (PWH) in a non-bleeding state. Methods: Adult male PWH of any s...
Gespeichert in:
| Veröffentlicht in: | Patient preference and adherence 2017-01, Vol.11, p.1603 |
|---|---|
| Hauptverfasser: | , , , , , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | |
|---|---|
| container_issue | |
| container_start_page | 1603 |
| container_title | Patient preference and adherence |
| container_volume | 11 |
| creator | Kulkarni, Roshni Cooper, David L Iyer, Neeraj N Recht, Michael Soni, Amit Kempton, Christine L Batt, Katharine Shapiro, Amy D Buckner, Tyler W Wang, Michael Neff, Anne |
| description | Background: Hemophilia is marked by frequent joint bleeding, resulting in pain and functional impairment. Objective: This study aimed to assess the reliability of five patient-reported outcome (PRO) instruments in people with hemophilia (PWH) in a non-bleeding state. Methods: Adult male PWH of any severity and inhibitor status, with a history of joint pain or bleeding, completed a pain history and five PRO instruments (EQ-5D-5L, Brief Pain Inventory v2 [BPI], International Physical Activity Questionnaire [IPAQ], Short Form 36 Health Survey v2 [SF-36v2], and Hemophilia Activities List [HAL]) during their routine comprehensive care visit. Patients were approached to complete the PRO instruments again at the end of their visit while in a similar non-bleeding state. Concordance of individual questionnaire items and correlation between domain scores were assessed using intra-class correlation coefficient (ICC). Results: Participants completing the retest (n=164) had a median age of 33.9 years. Median time for completion of the initial survey with PRO instruments was 36.0 minutes and for the five PRO instruments, median retest time was 21.0 minutes. The majority of participants had hemophilia A (74.4%), were white and non-Hispanic (72.6%), and self-reported arthritis/bone/joint problems (61%). Median/mean test-retest concordance was EQ-5D-5L 80.0%/79.1%, BPI 54.5%/58.9%, IPAQ 100%/100%, SF-36v2 77.8%/76.4%, and HAL 77.4%/75.9%. ICCs for test-retest reliability were EQ-5D-5L index 0.890; BPI--severity 0.950; BPI--interference 0.920; IPAQ total activity 0.940; SF-36v2 overall health 0.910; HAL total score 0.970. Conclusion: All five PRO scales showed acceptable test-retest reliability in adult PWH. Therefore, the choice of instrument to be used for research or clinical care should be driven by instrument characteristics other than reliability. Keywords: hemophilia, pain, patient-reported outcome, reliability |
| format | Article |
| fullrecord | <record><control><sourceid>gale</sourceid><recordid>TN_cdi_gale_healthsolutions_A534235804</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A534235804</galeid><sourcerecordid>A534235804</sourcerecordid><originalsourceid>FETCH-gale_healthsolutions_A5342358043</originalsourceid><addsrcrecordid>eNqNTctqwkAUHURBW_sPd9VVA4nxkXZXSsXu7Au6k1tz41y5mQmZOxQ_wP9uBAtdujrncF49M8qyxSIpivuv_j8-NFch7NN0ns8n2cgc30gYv1lYD-AraFCZnCYtNb5VKsFH3fqagF3QNtadFzoOn--AZZRO_LBasFT7xnYr-ABqCdbI7g6W0W2VvUOBl7pBbk91QFfCa8S_R-GKxmZQoQS6OeO1uV0-fzytkh0KbSyhqA1e4mksbB5n-XSSz4p0ml8c_AX13FbF</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Reliability of patient-reported outcome instruments in US adults with hemophilia: the Pain, Functional Impairment and Quality of life</title><source>DOAJ Directory of Open Access Journals</source><source>Dove Press Free</source><source>PubMed Central Open Access</source><source>Access via Taylor & Francis (Open Access Collection)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Kulkarni, Roshni ; Cooper, David L ; Iyer, Neeraj N ; Recht, Michael ; Soni, Amit ; Kempton, Christine L ; Batt, Katharine ; Shapiro, Amy D ; Buckner, Tyler W ; Wang, Michael ; Neff, Anne</creator><creatorcontrib>Kulkarni, Roshni ; Cooper, David L ; Iyer, Neeraj N ; Recht, Michael ; Soni, Amit ; Kempton, Christine L ; Batt, Katharine ; Shapiro, Amy D ; Buckner, Tyler W ; Wang, Michael ; Neff, Anne</creatorcontrib><description>Background: Hemophilia is marked by frequent joint bleeding, resulting in pain and functional impairment. Objective: This study aimed to assess the reliability of five patient-reported outcome (PRO) instruments in people with hemophilia (PWH) in a non-bleeding state. Methods: Adult male PWH of any severity and inhibitor status, with a history of joint pain or bleeding, completed a pain history and five PRO instruments (EQ-5D-5L, Brief Pain Inventory v2 [BPI], International Physical Activity Questionnaire [IPAQ], Short Form 36 Health Survey v2 [SF-36v2], and Hemophilia Activities List [HAL]) during their routine comprehensive care visit. Patients were approached to complete the PRO instruments again at the end of their visit while in a similar non-bleeding state. Concordance of individual questionnaire items and correlation between domain scores were assessed using intra-class correlation coefficient (ICC). Results: Participants completing the retest (n=164) had a median age of 33.9 years. Median time for completion of the initial survey with PRO instruments was 36.0 minutes and for the five PRO instruments, median retest time was 21.0 minutes. The majority of participants had hemophilia A (74.4%), were white and non-Hispanic (72.6%), and self-reported arthritis/bone/joint problems (61%). Median/mean test-retest concordance was EQ-5D-5L 80.0%/79.1%, BPI 54.5%/58.9%, IPAQ 100%/100%, SF-36v2 77.8%/76.4%, and HAL 77.4%/75.9%. ICCs for test-retest reliability were EQ-5D-5L index 0.890; BPI--severity 0.950; BPI--interference 0.920; IPAQ total activity 0.940; SF-36v2 overall health 0.910; HAL total score 0.970. Conclusion: All five PRO scales showed acceptable test-retest reliability in adult PWH. Therefore, the choice of instrument to be used for research or clinical care should be driven by instrument characteristics other than reliability. Keywords: hemophilia, pain, patient-reported outcome, reliability</description><identifier>ISSN: 1177-889X</identifier><identifier>EISSN: 1177-889X</identifier><language>eng</language><publisher>Dove Medical Press Limited</publisher><subject>Analysis ; Care and treatment ; Hemophilia ; Pain management ; Patient outcomes ; Quality of life</subject><ispartof>Patient preference and adherence, 2017-01, Vol.11, p.1603</ispartof><rights>COPYRIGHT 2017 Dove Medical Press Limited</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Kulkarni, Roshni</creatorcontrib><creatorcontrib>Cooper, David L</creatorcontrib><creatorcontrib>Iyer, Neeraj N</creatorcontrib><creatorcontrib>Recht, Michael</creatorcontrib><creatorcontrib>Soni, Amit</creatorcontrib><creatorcontrib>Kempton, Christine L</creatorcontrib><creatorcontrib>Batt, Katharine</creatorcontrib><creatorcontrib>Shapiro, Amy D</creatorcontrib><creatorcontrib>Buckner, Tyler W</creatorcontrib><creatorcontrib>Wang, Michael</creatorcontrib><creatorcontrib>Neff, Anne</creatorcontrib><title>Reliability of patient-reported outcome instruments in US adults with hemophilia: the Pain, Functional Impairment and Quality of life</title><title>Patient preference and adherence</title><description>Background: Hemophilia is marked by frequent joint bleeding, resulting in pain and functional impairment. Objective: This study aimed to assess the reliability of five patient-reported outcome (PRO) instruments in people with hemophilia (PWH) in a non-bleeding state. Methods: Adult male PWH of any severity and inhibitor status, with a history of joint pain or bleeding, completed a pain history and five PRO instruments (EQ-5D-5L, Brief Pain Inventory v2 [BPI], International Physical Activity Questionnaire [IPAQ], Short Form 36 Health Survey v2 [SF-36v2], and Hemophilia Activities List [HAL]) during their routine comprehensive care visit. Patients were approached to complete the PRO instruments again at the end of their visit while in a similar non-bleeding state. Concordance of individual questionnaire items and correlation between domain scores were assessed using intra-class correlation coefficient (ICC). Results: Participants completing the retest (n=164) had a median age of 33.9 years. Median time for completion of the initial survey with PRO instruments was 36.0 minutes and for the five PRO instruments, median retest time was 21.0 minutes. The majority of participants had hemophilia A (74.4%), were white and non-Hispanic (72.6%), and self-reported arthritis/bone/joint problems (61%). Median/mean test-retest concordance was EQ-5D-5L 80.0%/79.1%, BPI 54.5%/58.9%, IPAQ 100%/100%, SF-36v2 77.8%/76.4%, and HAL 77.4%/75.9%. ICCs for test-retest reliability were EQ-5D-5L index 0.890; BPI--severity 0.950; BPI--interference 0.920; IPAQ total activity 0.940; SF-36v2 overall health 0.910; HAL total score 0.970. Conclusion: All five PRO scales showed acceptable test-retest reliability in adult PWH. Therefore, the choice of instrument to be used for research or clinical care should be driven by instrument characteristics other than reliability. Keywords: hemophilia, pain, patient-reported outcome, reliability</description><subject>Analysis</subject><subject>Care and treatment</subject><subject>Hemophilia</subject><subject>Pain management</subject><subject>Patient outcomes</subject><subject>Quality of life</subject><issn>1177-889X</issn><issn>1177-889X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqNTctqwkAUHURBW_sPd9VVA4nxkXZXSsXu7Au6k1tz41y5mQmZOxQ_wP9uBAtdujrncF49M8qyxSIpivuv_j8-NFch7NN0ns8n2cgc30gYv1lYD-AraFCZnCYtNb5VKsFH3fqagF3QNtadFzoOn--AZZRO_LBasFT7xnYr-ABqCdbI7g6W0W2VvUOBl7pBbk91QFfCa8S_R-GKxmZQoQS6OeO1uV0-fzytkh0KbSyhqA1e4mksbB5n-XSSz4p0ml8c_AX13FbF</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Kulkarni, Roshni</creator><creator>Cooper, David L</creator><creator>Iyer, Neeraj N</creator><creator>Recht, Michael</creator><creator>Soni, Amit</creator><creator>Kempton, Christine L</creator><creator>Batt, Katharine</creator><creator>Shapiro, Amy D</creator><creator>Buckner, Tyler W</creator><creator>Wang, Michael</creator><creator>Neff, Anne</creator><general>Dove Medical Press Limited</general><scope/></search><sort><creationdate>20170101</creationdate><title>Reliability of patient-reported outcome instruments in US adults with hemophilia: the Pain, Functional Impairment and Quality of life</title><author>Kulkarni, Roshni ; Cooper, David L ; Iyer, Neeraj N ; Recht, Michael ; Soni, Amit ; Kempton, Christine L ; Batt, Katharine ; Shapiro, Amy D ; Buckner, Tyler W ; Wang, Michael ; Neff, Anne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-gale_healthsolutions_A5342358043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Analysis</topic><topic>Care and treatment</topic><topic>Hemophilia</topic><topic>Pain management</topic><topic>Patient outcomes</topic><topic>Quality of life</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kulkarni, Roshni</creatorcontrib><creatorcontrib>Cooper, David L</creatorcontrib><creatorcontrib>Iyer, Neeraj N</creatorcontrib><creatorcontrib>Recht, Michael</creatorcontrib><creatorcontrib>Soni, Amit</creatorcontrib><creatorcontrib>Kempton, Christine L</creatorcontrib><creatorcontrib>Batt, Katharine</creatorcontrib><creatorcontrib>Shapiro, Amy D</creatorcontrib><creatorcontrib>Buckner, Tyler W</creatorcontrib><creatorcontrib>Wang, Michael</creatorcontrib><creatorcontrib>Neff, Anne</creatorcontrib><jtitle>Patient preference and adherence</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kulkarni, Roshni</au><au>Cooper, David L</au><au>Iyer, Neeraj N</au><au>Recht, Michael</au><au>Soni, Amit</au><au>Kempton, Christine L</au><au>Batt, Katharine</au><au>Shapiro, Amy D</au><au>Buckner, Tyler W</au><au>Wang, Michael</au><au>Neff, Anne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reliability of patient-reported outcome instruments in US adults with hemophilia: the Pain, Functional Impairment and Quality of life</atitle><jtitle>Patient preference and adherence</jtitle><date>2017-01-01</date><risdate>2017</risdate><volume>11</volume><spage>1603</spage><pages>1603-</pages><issn>1177-889X</issn><eissn>1177-889X</eissn><abstract>Background: Hemophilia is marked by frequent joint bleeding, resulting in pain and functional impairment. Objective: This study aimed to assess the reliability of five patient-reported outcome (PRO) instruments in people with hemophilia (PWH) in a non-bleeding state. Methods: Adult male PWH of any severity and inhibitor status, with a history of joint pain or bleeding, completed a pain history and five PRO instruments (EQ-5D-5L, Brief Pain Inventory v2 [BPI], International Physical Activity Questionnaire [IPAQ], Short Form 36 Health Survey v2 [SF-36v2], and Hemophilia Activities List [HAL]) during their routine comprehensive care visit. Patients were approached to complete the PRO instruments again at the end of their visit while in a similar non-bleeding state. Concordance of individual questionnaire items and correlation between domain scores were assessed using intra-class correlation coefficient (ICC). Results: Participants completing the retest (n=164) had a median age of 33.9 years. Median time for completion of the initial survey with PRO instruments was 36.0 minutes and for the five PRO instruments, median retest time was 21.0 minutes. The majority of participants had hemophilia A (74.4%), were white and non-Hispanic (72.6%), and self-reported arthritis/bone/joint problems (61%). Median/mean test-retest concordance was EQ-5D-5L 80.0%/79.1%, BPI 54.5%/58.9%, IPAQ 100%/100%, SF-36v2 77.8%/76.4%, and HAL 77.4%/75.9%. ICCs for test-retest reliability were EQ-5D-5L index 0.890; BPI--severity 0.950; BPI--interference 0.920; IPAQ total activity 0.940; SF-36v2 overall health 0.910; HAL total score 0.970. Conclusion: All five PRO scales showed acceptable test-retest reliability in adult PWH. Therefore, the choice of instrument to be used for research or clinical care should be driven by instrument characteristics other than reliability. Keywords: hemophilia, pain, patient-reported outcome, reliability</abstract><pub>Dove Medical Press Limited</pub></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1177-889X |
| ispartof | Patient preference and adherence, 2017-01, Vol.11, p.1603 |
| issn | 1177-889X 1177-889X |
| language | eng |
| recordid | cdi_gale_healthsolutions_A534235804 |
| source | DOAJ Directory of Open Access Journals; Dove Press Free; PubMed Central Open Access; Access via Taylor & Francis (Open Access Collection); EZB-FREE-00999 freely available EZB journals; PubMed Central |
| subjects | Analysis Care and treatment Hemophilia Pain management Patient outcomes Quality of life |
| title | Reliability of patient-reported outcome instruments in US adults with hemophilia: the Pain, Functional Impairment and Quality of life |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T07%3A32%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Reliability%20of%20patient-reported%20outcome%20instruments%20in%20US%20adults%20with%20hemophilia:%20the%20Pain,%20Functional%20Impairment%20and%20Quality%20of%20life&rft.jtitle=Patient%20preference%20and%20adherence&rft.au=Kulkarni,%20Roshni&rft.date=2017-01-01&rft.volume=11&rft.spage=1603&rft.pages=1603-&rft.issn=1177-889X&rft.eissn=1177-889X&rft_id=info:doi/&rft_dat=%3Cgale%3EA534235804%3C/gale%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A534235804&rfr_iscdi=true |