Multiple sclerosis national registry system in Iran: Validity and reliability of a minimum data set
•The S-CVI values of the relevance, clarity, and simplicity for the whole form were 0.92, 0.96, and 0.93, respectively.•The presented minimum data set had a significantly high content validity in terms of relevance, clarity, and simplicity.•The Persian version of minimum data set found to be valid a...
Gespeichert in:
Veröffentlicht in: | Multiple sclerosis and related disorders 2019-08, Vol.33, p.158-161 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 161 |
---|---|
container_issue | |
container_start_page | 158 |
container_title | Multiple sclerosis and related disorders |
container_volume | 33 |
creator | Shahin, Sarvenaz Eskandarieh, Sharareh Moghadasi, Abdorreza Naser Razazian, Nazanin Baghbanian, Seyed Mohammad Ashtari, Fereshteh bayati, Asghar Manouchehrinia, Ali Beiki, Omid Mohebi, Farnam Dezfuli, Mahdieh Mokhber Sahraian, Mohammad Ali |
description | •The S-CVI values of the relevance, clarity, and simplicity for the whole form were 0.92, 0.96, and 0.93, respectively.•The presented minimum data set had a significantly high content validity in terms of relevance, clarity, and simplicity.•The Persian version of minimum data set found to be valid and reliable in national MS registry system of Iran.
As the prevalence and incidence of Multiple Sclerosis (MS) are increasing remarkably in Iran, gathering standardized information regarding the individual's diagnosis, care, and outcomes through a uniform registry system would enable policy-makers to systematically plan for care quality improvements.
To design a valid and reliable Persian version of a minimum data set to be utilized and integrated into the national MS registry system of Iran.
The minimum data set consisted of six domains including patient identification, family history of MS, diagnosis, disease course, disability status, and medications. The content validity was assessed based on 27 experts’ opinions. Item-Content Validity Index (I-CVI) and Scale-Content Validity Index (S-CVI) were used to assess the questions and their validities. Reliability was evaluated using the intra-class correlation coefficient (ICC) of the test-retest results.
For validity appraisal, 27 experts reviewed the developed minimum data set. All the items had I-CVI values higher than the critical value of 0.78 in terms of relevance, clarity, and simplicity, except for “medication start date” and “medication end date” in relevance (I-CVI = 0.75 and 0.73, respectively) and “MS type” in simplicity (I-CVI = 0.76). The total S-CVI scores for relevance, clarity, and simplicity were higher than 0.9. In reliability assessment, 27 patients (out of 74 interviewed patients) were re-interviewed to assess the test-retest reliability. All ICCs were higher than the critical value of 0.7 (in 14 items out of 16), except for “progression to secondary-progressive MS” with the ICC = 0.68 and “the reason for medication discontinuance” with the ICC = 0.64.
The use of standardized validated minimum data set has the potential to enable the researchers and policy-makers to systematically compare and analyze patient information. The Persian version of the minimum data set found to be valid and reliable in Iran. |
doi_str_mv | 10.1016/j.msard.2019.06.009 |
format | Article |
fullrecord | <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_479052</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2211034819302500</els_id><sourcerecordid>2242114907</sourcerecordid><originalsourceid>FETCH-LOGICAL-c397t-2d22bd519dc6eedecdf0140d2aa17241033316e4f21042adb87b1adfd11cacc63</originalsourceid><addsrcrecordid>eNp9kU9v1DAQxS0EolXpJ0BCPnJJ6rG9ToPEAVX8qVTEBbhaE3uCvDjJYjtF--3xsssemcs8W7-Zkd5j7CWIFgSYm207ZUy-lQL6VphWiP4Ju5QSoBFqY56etb69YNc5b0UtswFt4Dm7UCCFqvqSuc9rLGEXiWcXKS05ZD5jCcuMkSf6EXJJe573udDEw8zvE85v-HeMwYey5zj7SsWAQ4iH9zJy5FOYw7RO3GNBnqm8YM9GjJmuT_2Kffvw_uvdp-bhy8f7u3cPjVN9VxrppRz8BnrvDJEn50cBWniJCJ3UIJRSYEiPEoSW6IfbbgD0owdw6JxRV6w57s2_abcOdpfChGlvFwz29PWzKrK668VGVv71kd-l5ddKudgpZEcx4kzLmq2Uunqoe9FVVB1RVy3KicbzchD2EIjd2r-B2EMgVhhbA6lTr04H1mEif575Z38F3h4BqrY8Bko2u0CzIx8SuWL9Ev574A9xj57n</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2242114907</pqid></control><display><type>article</type><title>Multiple sclerosis national registry system in Iran: Validity and reliability of a minimum data set</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Shahin, Sarvenaz ; Eskandarieh, Sharareh ; Moghadasi, Abdorreza Naser ; Razazian, Nazanin ; Baghbanian, Seyed Mohammad ; Ashtari, Fereshteh ; bayati, Asghar ; Manouchehrinia, Ali ; Beiki, Omid ; Mohebi, Farnam ; Dezfuli, Mahdieh Mokhber ; Sahraian, Mohammad Ali</creator><creatorcontrib>Shahin, Sarvenaz ; Eskandarieh, Sharareh ; Moghadasi, Abdorreza Naser ; Razazian, Nazanin ; Baghbanian, Seyed Mohammad ; Ashtari, Fereshteh ; bayati, Asghar ; Manouchehrinia, Ali ; Beiki, Omid ; Mohebi, Farnam ; Dezfuli, Mahdieh Mokhber ; Sahraian, Mohammad Ali</creatorcontrib><description>•The S-CVI values of the relevance, clarity, and simplicity for the whole form were 0.92, 0.96, and 0.93, respectively.•The presented minimum data set had a significantly high content validity in terms of relevance, clarity, and simplicity.•The Persian version of minimum data set found to be valid and reliable in national MS registry system of Iran.
As the prevalence and incidence of Multiple Sclerosis (MS) are increasing remarkably in Iran, gathering standardized information regarding the individual's diagnosis, care, and outcomes through a uniform registry system would enable policy-makers to systematically plan for care quality improvements.
To design a valid and reliable Persian version of a minimum data set to be utilized and integrated into the national MS registry system of Iran.
The minimum data set consisted of six domains including patient identification, family history of MS, diagnosis, disease course, disability status, and medications. The content validity was assessed based on 27 experts’ opinions. Item-Content Validity Index (I-CVI) and Scale-Content Validity Index (S-CVI) were used to assess the questions and their validities. Reliability was evaluated using the intra-class correlation coefficient (ICC) of the test-retest results.
For validity appraisal, 27 experts reviewed the developed minimum data set. All the items had I-CVI values higher than the critical value of 0.78 in terms of relevance, clarity, and simplicity, except for “medication start date” and “medication end date” in relevance (I-CVI = 0.75 and 0.73, respectively) and “MS type” in simplicity (I-CVI = 0.76). The total S-CVI scores for relevance, clarity, and simplicity were higher than 0.9. In reliability assessment, 27 patients (out of 74 interviewed patients) were re-interviewed to assess the test-retest reliability. All ICCs were higher than the critical value of 0.7 (in 14 items out of 16), except for “progression to secondary-progressive MS” with the ICC = 0.68 and “the reason for medication discontinuance” with the ICC = 0.64.
The use of standardized validated minimum data set has the potential to enable the researchers and policy-makers to systematically compare and analyze patient information. The Persian version of the minimum data set found to be valid and reliable in Iran.</description><identifier>ISSN: 2211-0348</identifier><identifier>EISSN: 2211-0356</identifier><identifier>DOI: 10.1016/j.msard.2019.06.009</identifier><identifier>PMID: 31203146</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Datasets as Topic - standards ; Humans ; Iran - epidemiology ; Minimum data set ; Multiple sclerosis ; Multiple Sclerosis - epidemiology ; Registries - standards ; Registry system ; Reliability ; Reproducibility of Results ; Validity</subject><ispartof>Multiple sclerosis and related disorders, 2019-08, Vol.33, p.158-161</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c397t-2d22bd519dc6eedecdf0140d2aa17241033316e4f21042adb87b1adfd11cacc63</citedby><cites>FETCH-LOGICAL-c397t-2d22bd519dc6eedecdf0140d2aa17241033316e4f21042adb87b1adfd11cacc63</cites><orcidid>0000-0002-8138-7504 ; 0000-0002-3224-8807 ; 0000-0002-8942-9983 ; 0000-0003-4857-5762 ; 0000-0002-8598-0911 ; 0000-0002-6181-2008</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31203146$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:141393294$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Shahin, Sarvenaz</creatorcontrib><creatorcontrib>Eskandarieh, Sharareh</creatorcontrib><creatorcontrib>Moghadasi, Abdorreza Naser</creatorcontrib><creatorcontrib>Razazian, Nazanin</creatorcontrib><creatorcontrib>Baghbanian, Seyed Mohammad</creatorcontrib><creatorcontrib>Ashtari, Fereshteh</creatorcontrib><creatorcontrib>bayati, Asghar</creatorcontrib><creatorcontrib>Manouchehrinia, Ali</creatorcontrib><creatorcontrib>Beiki, Omid</creatorcontrib><creatorcontrib>Mohebi, Farnam</creatorcontrib><creatorcontrib>Dezfuli, Mahdieh Mokhber</creatorcontrib><creatorcontrib>Sahraian, Mohammad Ali</creatorcontrib><title>Multiple sclerosis national registry system in Iran: Validity and reliability of a minimum data set</title><title>Multiple sclerosis and related disorders</title><addtitle>Mult Scler Relat Disord</addtitle><description>•The S-CVI values of the relevance, clarity, and simplicity for the whole form were 0.92, 0.96, and 0.93, respectively.•The presented minimum data set had a significantly high content validity in terms of relevance, clarity, and simplicity.•The Persian version of minimum data set found to be valid and reliable in national MS registry system of Iran.
As the prevalence and incidence of Multiple Sclerosis (MS) are increasing remarkably in Iran, gathering standardized information regarding the individual's diagnosis, care, and outcomes through a uniform registry system would enable policy-makers to systematically plan for care quality improvements.
To design a valid and reliable Persian version of a minimum data set to be utilized and integrated into the national MS registry system of Iran.
The minimum data set consisted of six domains including patient identification, family history of MS, diagnosis, disease course, disability status, and medications. The content validity was assessed based on 27 experts’ opinions. Item-Content Validity Index (I-CVI) and Scale-Content Validity Index (S-CVI) were used to assess the questions and their validities. Reliability was evaluated using the intra-class correlation coefficient (ICC) of the test-retest results.
For validity appraisal, 27 experts reviewed the developed minimum data set. All the items had I-CVI values higher than the critical value of 0.78 in terms of relevance, clarity, and simplicity, except for “medication start date” and “medication end date” in relevance (I-CVI = 0.75 and 0.73, respectively) and “MS type” in simplicity (I-CVI = 0.76). The total S-CVI scores for relevance, clarity, and simplicity were higher than 0.9. In reliability assessment, 27 patients (out of 74 interviewed patients) were re-interviewed to assess the test-retest reliability. All ICCs were higher than the critical value of 0.7 (in 14 items out of 16), except for “progression to secondary-progressive MS” with the ICC = 0.68 and “the reason for medication discontinuance” with the ICC = 0.64.
The use of standardized validated minimum data set has the potential to enable the researchers and policy-makers to systematically compare and analyze patient information. The Persian version of the minimum data set found to be valid and reliable in Iran.</description><subject>Datasets as Topic - standards</subject><subject>Humans</subject><subject>Iran - epidemiology</subject><subject>Minimum data set</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - epidemiology</subject><subject>Registries - standards</subject><subject>Registry system</subject><subject>Reliability</subject><subject>Reproducibility of Results</subject><subject>Validity</subject><issn>2211-0348</issn><issn>2211-0356</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v1DAQxS0EolXpJ0BCPnJJ6rG9ToPEAVX8qVTEBbhaE3uCvDjJYjtF--3xsssemcs8W7-Zkd5j7CWIFgSYm207ZUy-lQL6VphWiP4Ju5QSoBFqY56etb69YNc5b0UtswFt4Dm7UCCFqvqSuc9rLGEXiWcXKS05ZD5jCcuMkSf6EXJJe573udDEw8zvE85v-HeMwYey5zj7SsWAQ4iH9zJy5FOYw7RO3GNBnqm8YM9GjJmuT_2Kffvw_uvdp-bhy8f7u3cPjVN9VxrppRz8BnrvDJEn50cBWniJCJ3UIJRSYEiPEoSW6IfbbgD0owdw6JxRV6w57s2_abcOdpfChGlvFwz29PWzKrK668VGVv71kd-l5ddKudgpZEcx4kzLmq2Uunqoe9FVVB1RVy3KicbzchD2EIjd2r-B2EMgVhhbA6lTr04H1mEif575Z38F3h4BqrY8Bko2u0CzIx8SuWL9Ev574A9xj57n</recordid><startdate>20190801</startdate><enddate>20190801</enddate><creator>Shahin, Sarvenaz</creator><creator>Eskandarieh, Sharareh</creator><creator>Moghadasi, Abdorreza Naser</creator><creator>Razazian, Nazanin</creator><creator>Baghbanian, Seyed Mohammad</creator><creator>Ashtari, Fereshteh</creator><creator>bayati, Asghar</creator><creator>Manouchehrinia, Ali</creator><creator>Beiki, Omid</creator><creator>Mohebi, Farnam</creator><creator>Dezfuli, Mahdieh Mokhber</creator><creator>Sahraian, Mohammad Ali</creator><general>Elsevier B.V</general><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>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope><orcidid>https://orcid.org/0000-0002-8138-7504</orcidid><orcidid>https://orcid.org/0000-0002-3224-8807</orcidid><orcidid>https://orcid.org/0000-0002-8942-9983</orcidid><orcidid>https://orcid.org/0000-0003-4857-5762</orcidid><orcidid>https://orcid.org/0000-0002-8598-0911</orcidid><orcidid>https://orcid.org/0000-0002-6181-2008</orcidid></search><sort><creationdate>20190801</creationdate><title>Multiple sclerosis national registry system in Iran: Validity and reliability of a minimum data set</title><author>Shahin, Sarvenaz ; Eskandarieh, Sharareh ; Moghadasi, Abdorreza Naser ; Razazian, Nazanin ; Baghbanian, Seyed Mohammad ; Ashtari, Fereshteh ; bayati, Asghar ; Manouchehrinia, Ali ; Beiki, Omid ; Mohebi, Farnam ; Dezfuli, Mahdieh Mokhber ; Sahraian, Mohammad Ali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-2d22bd519dc6eedecdf0140d2aa17241033316e4f21042adb87b1adfd11cacc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Datasets as Topic - standards</topic><topic>Humans</topic><topic>Iran - epidemiology</topic><topic>Minimum data set</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - epidemiology</topic><topic>Registries - standards</topic><topic>Registry system</topic><topic>Reliability</topic><topic>Reproducibility of Results</topic><topic>Validity</topic><toplevel>online_resources</toplevel><creatorcontrib>Shahin, Sarvenaz</creatorcontrib><creatorcontrib>Eskandarieh, Sharareh</creatorcontrib><creatorcontrib>Moghadasi, Abdorreza Naser</creatorcontrib><creatorcontrib>Razazian, Nazanin</creatorcontrib><creatorcontrib>Baghbanian, Seyed Mohammad</creatorcontrib><creatorcontrib>Ashtari, Fereshteh</creatorcontrib><creatorcontrib>bayati, Asghar</creatorcontrib><creatorcontrib>Manouchehrinia, Ali</creatorcontrib><creatorcontrib>Beiki, Omid</creatorcontrib><creatorcontrib>Mohebi, Farnam</creatorcontrib><creatorcontrib>Dezfuli, Mahdieh Mokhber</creatorcontrib><creatorcontrib>Sahraian, Mohammad Ali</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>Multiple sclerosis and related disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shahin, Sarvenaz</au><au>Eskandarieh, Sharareh</au><au>Moghadasi, Abdorreza Naser</au><au>Razazian, Nazanin</au><au>Baghbanian, Seyed Mohammad</au><au>Ashtari, Fereshteh</au><au>bayati, Asghar</au><au>Manouchehrinia, Ali</au><au>Beiki, Omid</au><au>Mohebi, Farnam</au><au>Dezfuli, Mahdieh Mokhber</au><au>Sahraian, Mohammad Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiple sclerosis national registry system in Iran: Validity and reliability of a minimum data set</atitle><jtitle>Multiple sclerosis and related disorders</jtitle><addtitle>Mult Scler Relat Disord</addtitle><date>2019-08-01</date><risdate>2019</risdate><volume>33</volume><spage>158</spage><epage>161</epage><pages>158-161</pages><issn>2211-0348</issn><eissn>2211-0356</eissn><abstract>•The S-CVI values of the relevance, clarity, and simplicity for the whole form were 0.92, 0.96, and 0.93, respectively.•The presented minimum data set had a significantly high content validity in terms of relevance, clarity, and simplicity.•The Persian version of minimum data set found to be valid and reliable in national MS registry system of Iran.
As the prevalence and incidence of Multiple Sclerosis (MS) are increasing remarkably in Iran, gathering standardized information regarding the individual's diagnosis, care, and outcomes through a uniform registry system would enable policy-makers to systematically plan for care quality improvements.
To design a valid and reliable Persian version of a minimum data set to be utilized and integrated into the national MS registry system of Iran.
The minimum data set consisted of six domains including patient identification, family history of MS, diagnosis, disease course, disability status, and medications. The content validity was assessed based on 27 experts’ opinions. Item-Content Validity Index (I-CVI) and Scale-Content Validity Index (S-CVI) were used to assess the questions and their validities. Reliability was evaluated using the intra-class correlation coefficient (ICC) of the test-retest results.
For validity appraisal, 27 experts reviewed the developed minimum data set. All the items had I-CVI values higher than the critical value of 0.78 in terms of relevance, clarity, and simplicity, except for “medication start date” and “medication end date” in relevance (I-CVI = 0.75 and 0.73, respectively) and “MS type” in simplicity (I-CVI = 0.76). The total S-CVI scores for relevance, clarity, and simplicity were higher than 0.9. In reliability assessment, 27 patients (out of 74 interviewed patients) were re-interviewed to assess the test-retest reliability. All ICCs were higher than the critical value of 0.7 (in 14 items out of 16), except for “progression to secondary-progressive MS” with the ICC = 0.68 and “the reason for medication discontinuance” with the ICC = 0.64.
The use of standardized validated minimum data set has the potential to enable the researchers and policy-makers to systematically compare and analyze patient information. The Persian version of the minimum data set found to be valid and reliable in Iran.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31203146</pmid><doi>10.1016/j.msard.2019.06.009</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-8138-7504</orcidid><orcidid>https://orcid.org/0000-0002-3224-8807</orcidid><orcidid>https://orcid.org/0000-0002-8942-9983</orcidid><orcidid>https://orcid.org/0000-0003-4857-5762</orcidid><orcidid>https://orcid.org/0000-0002-8598-0911</orcidid><orcidid>https://orcid.org/0000-0002-6181-2008</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2211-0348 |
ispartof | Multiple sclerosis and related disorders, 2019-08, Vol.33, p.158-161 |
issn | 2211-0348 2211-0356 |
language | eng |
recordid | cdi_swepub_primary_oai_swepub_ki_se_479052 |
source | MEDLINE; Alma/SFX Local Collection |
subjects | Datasets as Topic - standards Humans Iran - epidemiology Minimum data set Multiple sclerosis Multiple Sclerosis - epidemiology Registries - standards Registry system Reliability Reproducibility of Results Validity |
title | Multiple sclerosis national registry system in Iran: Validity and reliability of a minimum data set |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T02%3A31%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Multiple%20sclerosis%20national%20registry%20system%20in%20Iran:%20Validity%20and%20reliability%20of%20a%20minimum%20data%20set&rft.jtitle=Multiple%20sclerosis%20and%20related%20disorders&rft.au=Shahin,%20Sarvenaz&rft.date=2019-08-01&rft.volume=33&rft.spage=158&rft.epage=161&rft.pages=158-161&rft.issn=2211-0348&rft.eissn=2211-0356&rft_id=info:doi/10.1016/j.msard.2019.06.009&rft_dat=%3Cproquest_swepu%3E2242114907%3C/proquest_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2242114907&rft_id=info:pmid/31203146&rft_els_id=S2211034819302500&rfr_iscdi=true |