Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy

The North Star ambulatory assessment (NSAA) is a functional motor outcome measure in Duchenne muscular dystrophy (DMD), widely used in clinical trials and natural history studies, as well as in clinical practice. However, little has been reported on the minimal clinically important difference (MCID)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2023-04, Vol.18 (4), p.e0283669-e0283669
Hauptverfasser: Ayyar Gupta, Vandana, Pitchforth, Jacqueline M, Domingos, Joana, Ridout, Deborah, Iodice, Mario, Rye, Catherine, Chesshyre, Mary, Wolfe, Amy, Selby, Victoria, Mayhew, Anna, Mazzone, Elena S, Ricotti, Valeria, Hogrel, Jean-Yves, Niks, Erik H, de Groot, Imelda, Servais, Laurent, Straub, Volker, Mercuri, Eugenio, Manzur, Adnan Y, Muntoni, Francesco
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e0283669
container_issue 4
container_start_page e0283669
container_title PloS one
container_volume 18
creator Ayyar Gupta, Vandana
Pitchforth, Jacqueline M
Domingos, Joana
Ridout, Deborah
Iodice, Mario
Rye, Catherine
Chesshyre, Mary
Wolfe, Amy
Selby, Victoria
Mayhew, Anna
Mazzone, Elena S
Ricotti, Valeria
Hogrel, Jean-Yves
Niks, Erik H
de Groot, Imelda
Servais, Laurent
Straub, Volker
Mercuri, Eugenio
Manzur, Adnan Y
Muntoni, Francesco
description The North Star ambulatory assessment (NSAA) is a functional motor outcome measure in Duchenne muscular dystrophy (DMD), widely used in clinical trials and natural history studies, as well as in clinical practice. However, little has been reported on the minimal clinically important difference (MCID) of the NSAA. The lack of established MCID estimates for NSAA presents challenges in interpreting the significance of the results of this outcome measure in clinical trials, natural history studies and clinical practice. Combining statistical approaches and patient perspectives, this study estimated MCID for NSAA using distribution-based estimates of 1/3 standard deviation (SD) and standard error of measurement (SEM), an anchor-based approach, with six-minute walk distance (6MWD) as the anchor, and evaluation of patient and parent perception using participant-tailored questionnaires. The MCID for NSAA in boys with DMD aged 7 to 10 years based on 1/3 SD ranged from 2.3-2.9 points, and that on SEM ranged from 2.9-3.5 points. Anchored on the 6MWD, the MCID for NSAA was estimated as 3.5 points. When the impact on functional abilities was considered using participant response questionnaires, patients and parent perceived a complete loss of function in a single item or deterioration of function in one to two items of the assessment as an important change. Our study examines MCID estimates for total NSAA scores using multiple approaches, including the impact of patient and parent perspective on within scale changes in items based on complete loss of function and deterioration of function, and provides new insight on evaluation of differences in these widely used outcome measure in DMD.
doi_str_mv 10.1371/journal.pone.0283669
format Article
fullrecord <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_2806443033</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A747087094</galeid><doaj_id>oai_doaj_org_article_21885a505e0b4afe9114a65409bbe906</doaj_id><sourcerecordid>A747087094</sourcerecordid><originalsourceid>FETCH-LOGICAL-c638t-d1eb988d53b1abbb59739851ed3b7f015d068a180b908144b788dbf1d881f3073</originalsourceid><addsrcrecordid>eNptUk1v1DAUjBCIlsI_QGCJSznsYsdxYp9Q1PJRqSqHwtmynZddr5w42EnR_gz-Md7dtOqiygdbzzPz3htNlr0leEloRT5t_BR65ZaD72GJc07LUjzLTomg-aLMMX3-6H2SvYpxgzGjvCxfZie0wkIwQk6zv5cwQuhsb_sV2l2dcsi49DDKuS2y3eDDqPoRNbZtIUBvICLbo3EN6CZ9rdHtqAKqOz05NfqwRXWMEGMHiXN-c1vXH1HrAxrUaFMpoj82cS4ns4a-B9RN0SRiQM02jsEP6-3r7EWrXIQ3832W_fr65efF98X1j29XF_X1wpSUj4uGgBacN4xqorTWTFRUcEagobpqMWENLrkiHGuBOSkKXSWwbknDOWkpruhZ9v6gOzgf5exmlDnHZVFQTGlCXB0QjVcbOYTkTdhKr6zcF3xYSRVGaxzInHDOFMMMsC5UC4KQQpWswEJrELhMWp_nbpPuoDHJiqDckejxT2_XcuXvJMGE5oyLpEAPCs7CClJ3beVdvmfu35NL4xip0zB5ySXNC8F2W57PfYP_PUEcZWejAedUD36a12U8jZ-gH_6DPm3KjFqptLftW5_GNTtRWVdFhXmKVpFQyydQ6TTQWZMS29pUPyIUB4IJPsYA7YM1BMtd3u-Hkbu8yznvifbusa0PpPuA038L8v5k</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2806443033</pqid></control><display><type>article</type><title>Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Public Library of Science (PLoS)</source><creator>Ayyar Gupta, Vandana ; Pitchforth, Jacqueline M ; Domingos, Joana ; Ridout, Deborah ; Iodice, Mario ; Rye, Catherine ; Chesshyre, Mary ; Wolfe, Amy ; Selby, Victoria ; Mayhew, Anna ; Mazzone, Elena S ; Ricotti, Valeria ; Hogrel, Jean-Yves ; Niks, Erik H ; de Groot, Imelda ; Servais, Laurent ; Straub, Volker ; Mercuri, Eugenio ; Manzur, Adnan Y ; Muntoni, Francesco</creator><contributor>Alway, Stephen E</contributor><creatorcontrib>Ayyar Gupta, Vandana ; Pitchforth, Jacqueline M ; Domingos, Joana ; Ridout, Deborah ; Iodice, Mario ; Rye, Catherine ; Chesshyre, Mary ; Wolfe, Amy ; Selby, Victoria ; Mayhew, Anna ; Mazzone, Elena S ; Ricotti, Valeria ; Hogrel, Jean-Yves ; Niks, Erik H ; de Groot, Imelda ; Servais, Laurent ; Straub, Volker ; Mercuri, Eugenio ; Manzur, Adnan Y ; Muntoni, Francesco ; iMDEX Consortium and the U.K. NorthStar Clinical Network ; on behalf of the iMDEX Consortium and the U.K. NorthStar Clinical Network ; Alway, Stephen E</creatorcontrib><description>The North Star ambulatory assessment (NSAA) is a functional motor outcome measure in Duchenne muscular dystrophy (DMD), widely used in clinical trials and natural history studies, as well as in clinical practice. However, little has been reported on the minimal clinically important difference (MCID) of the NSAA. The lack of established MCID estimates for NSAA presents challenges in interpreting the significance of the results of this outcome measure in clinical trials, natural history studies and clinical practice. Combining statistical approaches and patient perspectives, this study estimated MCID for NSAA using distribution-based estimates of 1/3 standard deviation (SD) and standard error of measurement (SEM), an anchor-based approach, with six-minute walk distance (6MWD) as the anchor, and evaluation of patient and parent perception using participant-tailored questionnaires. The MCID for NSAA in boys with DMD aged 7 to 10 years based on 1/3 SD ranged from 2.3-2.9 points, and that on SEM ranged from 2.9-3.5 points. Anchored on the 6MWD, the MCID for NSAA was estimated as 3.5 points. When the impact on functional abilities was considered using participant response questionnaires, patients and parent perceived a complete loss of function in a single item or deterioration of function in one to two items of the assessment as an important change. Our study examines MCID estimates for total NSAA scores using multiple approaches, including the impact of patient and parent perspective on within scale changes in items based on complete loss of function and deterioration of function, and provides new insight on evaluation of differences in these widely used outcome measure in DMD.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0283669</identifier><identifier>PMID: 37099511</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Age ; Ambulatory assessment ; Biology and Life Sciences ; Care and treatment ; Clinical medicine ; Clinical trials ; Diagnosis ; Duchenne muscular dystrophy ; Duchenne's muscular dystrophy ; Dystrophy ; Error analysis ; Estimates ; Evaluation ; Human health sciences ; Humans ; Male ; Medicine and Health Sciences ; Minimal Clinically Important Difference ; Multidisciplinary ; Muscular dystrophy ; Muscular Dystrophy, Duchenne ; Mutation ; Natural history ; Patients ; Pediatrics ; Physical Sciences ; Physical Therapy Modalities ; Pédiatrie ; Questionnaires ; Research and Analysis Methods ; Sciences de la santé humaine ; Standard error ; Surveys and Questionnaires ; Walking ; Walking - physiology</subject><ispartof>PloS one, 2023-04, Vol.18 (4), p.e0283669-e0283669</ispartof><rights>Copyright: © 2023 Ayyar Gupta et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Ayyar Gupta et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Ayyar Gupta et al 2023 Ayyar Gupta et al</rights><rights>2023 Ayyar Gupta et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c638t-d1eb988d53b1abbb59739851ed3b7f015d068a180b908144b788dbf1d881f3073</citedby><cites>FETCH-LOGICAL-c638t-d1eb988d53b1abbb59739851ed3b7f015d068a180b908144b788dbf1d881f3073</cites><orcidid>0000-0001-5892-5143 ; 0000-0001-9046-3540 ; 0000-0003-3022-4307</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132589/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132589/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37099511$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Alway, Stephen E</contributor><creatorcontrib>Ayyar Gupta, Vandana</creatorcontrib><creatorcontrib>Pitchforth, Jacqueline M</creatorcontrib><creatorcontrib>Domingos, Joana</creatorcontrib><creatorcontrib>Ridout, Deborah</creatorcontrib><creatorcontrib>Iodice, Mario</creatorcontrib><creatorcontrib>Rye, Catherine</creatorcontrib><creatorcontrib>Chesshyre, Mary</creatorcontrib><creatorcontrib>Wolfe, Amy</creatorcontrib><creatorcontrib>Selby, Victoria</creatorcontrib><creatorcontrib>Mayhew, Anna</creatorcontrib><creatorcontrib>Mazzone, Elena S</creatorcontrib><creatorcontrib>Ricotti, Valeria</creatorcontrib><creatorcontrib>Hogrel, Jean-Yves</creatorcontrib><creatorcontrib>Niks, Erik H</creatorcontrib><creatorcontrib>de Groot, Imelda</creatorcontrib><creatorcontrib>Servais, Laurent</creatorcontrib><creatorcontrib>Straub, Volker</creatorcontrib><creatorcontrib>Mercuri, Eugenio</creatorcontrib><creatorcontrib>Manzur, Adnan Y</creatorcontrib><creatorcontrib>Muntoni, Francesco</creatorcontrib><creatorcontrib>iMDEX Consortium and the U.K. NorthStar Clinical Network</creatorcontrib><creatorcontrib>on behalf of the iMDEX Consortium and the U.K. NorthStar Clinical Network</creatorcontrib><title>Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The North Star ambulatory assessment (NSAA) is a functional motor outcome measure in Duchenne muscular dystrophy (DMD), widely used in clinical trials and natural history studies, as well as in clinical practice. However, little has been reported on the minimal clinically important difference (MCID) of the NSAA. The lack of established MCID estimates for NSAA presents challenges in interpreting the significance of the results of this outcome measure in clinical trials, natural history studies and clinical practice. Combining statistical approaches and patient perspectives, this study estimated MCID for NSAA using distribution-based estimates of 1/3 standard deviation (SD) and standard error of measurement (SEM), an anchor-based approach, with six-minute walk distance (6MWD) as the anchor, and evaluation of patient and parent perception using participant-tailored questionnaires. The MCID for NSAA in boys with DMD aged 7 to 10 years based on 1/3 SD ranged from 2.3-2.9 points, and that on SEM ranged from 2.9-3.5 points. Anchored on the 6MWD, the MCID for NSAA was estimated as 3.5 points. When the impact on functional abilities was considered using participant response questionnaires, patients and parent perceived a complete loss of function in a single item or deterioration of function in one to two items of the assessment as an important change. Our study examines MCID estimates for total NSAA scores using multiple approaches, including the impact of patient and parent perspective on within scale changes in items based on complete loss of function and deterioration of function, and provides new insight on evaluation of differences in these widely used outcome measure in DMD.</description><subject>Age</subject><subject>Ambulatory assessment</subject><subject>Biology and Life Sciences</subject><subject>Care and treatment</subject><subject>Clinical medicine</subject><subject>Clinical trials</subject><subject>Diagnosis</subject><subject>Duchenne muscular dystrophy</subject><subject>Duchenne's muscular dystrophy</subject><subject>Dystrophy</subject><subject>Error analysis</subject><subject>Estimates</subject><subject>Evaluation</subject><subject>Human health sciences</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine and Health Sciences</subject><subject>Minimal Clinically Important Difference</subject><subject>Multidisciplinary</subject><subject>Muscular dystrophy</subject><subject>Muscular Dystrophy, Duchenne</subject><subject>Mutation</subject><subject>Natural history</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Physical Sciences</subject><subject>Physical Therapy Modalities</subject><subject>Pédiatrie</subject><subject>Questionnaires</subject><subject>Research and Analysis Methods</subject><subject>Sciences de la santé humaine</subject><subject>Standard error</subject><subject>Surveys and Questionnaires</subject><subject>Walking</subject><subject>Walking - physiology</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAUjBCIlsI_QGCJSznsYsdxYp9Q1PJRqSqHwtmynZddr5w42EnR_gz-Md7dtOqiygdbzzPz3htNlr0leEloRT5t_BR65ZaD72GJc07LUjzLTomg-aLMMX3-6H2SvYpxgzGjvCxfZie0wkIwQk6zv5cwQuhsb_sV2l2dcsi49DDKuS2y3eDDqPoRNbZtIUBvICLbo3EN6CZ9rdHtqAKqOz05NfqwRXWMEGMHiXN-c1vXH1HrAxrUaFMpoj82cS4ns4a-B9RN0SRiQM02jsEP6-3r7EWrXIQ3832W_fr65efF98X1j29XF_X1wpSUj4uGgBacN4xqorTWTFRUcEagobpqMWENLrkiHGuBOSkKXSWwbknDOWkpruhZ9v6gOzgf5exmlDnHZVFQTGlCXB0QjVcbOYTkTdhKr6zcF3xYSRVGaxzInHDOFMMMsC5UC4KQQpWswEJrELhMWp_nbpPuoDHJiqDckejxT2_XcuXvJMGE5oyLpEAPCs7CClJ3beVdvmfu35NL4xip0zB5ySXNC8F2W57PfYP_PUEcZWejAedUD36a12U8jZ-gH_6DPm3KjFqptLftW5_GNTtRWVdFhXmKVpFQyydQ6TTQWZMS29pUPyIUB4IJPsYA7YM1BMtd3u-Hkbu8yznvifbusa0PpPuA038L8v5k</recordid><startdate>20230426</startdate><enddate>20230426</enddate><creator>Ayyar Gupta, Vandana</creator><creator>Pitchforth, Jacqueline M</creator><creator>Domingos, Joana</creator><creator>Ridout, Deborah</creator><creator>Iodice, Mario</creator><creator>Rye, Catherine</creator><creator>Chesshyre, Mary</creator><creator>Wolfe, Amy</creator><creator>Selby, Victoria</creator><creator>Mayhew, Anna</creator><creator>Mazzone, Elena S</creator><creator>Ricotti, Valeria</creator><creator>Hogrel, Jean-Yves</creator><creator>Niks, Erik H</creator><creator>de Groot, Imelda</creator><creator>Servais, Laurent</creator><creator>Straub, Volker</creator><creator>Mercuri, Eugenio</creator><creator>Manzur, Adnan Y</creator><creator>Muntoni, Francesco</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>Q33</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5892-5143</orcidid><orcidid>https://orcid.org/0000-0001-9046-3540</orcidid><orcidid>https://orcid.org/0000-0003-3022-4307</orcidid></search><sort><creationdate>20230426</creationdate><title>Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy</title><author>Ayyar Gupta, Vandana ; Pitchforth, Jacqueline M ; Domingos, Joana ; Ridout, Deborah ; Iodice, Mario ; Rye, Catherine ; Chesshyre, Mary ; Wolfe, Amy ; Selby, Victoria ; Mayhew, Anna ; Mazzone, Elena S ; Ricotti, Valeria ; Hogrel, Jean-Yves ; Niks, Erik H ; de Groot, Imelda ; Servais, Laurent ; Straub, Volker ; Mercuri, Eugenio ; Manzur, Adnan Y ; Muntoni, Francesco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c638t-d1eb988d53b1abbb59739851ed3b7f015d068a180b908144b788dbf1d881f3073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Age</topic><topic>Ambulatory assessment</topic><topic>Biology and Life Sciences</topic><topic>Care and treatment</topic><topic>Clinical medicine</topic><topic>Clinical trials</topic><topic>Diagnosis</topic><topic>Duchenne muscular dystrophy</topic><topic>Duchenne's muscular dystrophy</topic><topic>Dystrophy</topic><topic>Error analysis</topic><topic>Estimates</topic><topic>Evaluation</topic><topic>Human health sciences</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine and Health Sciences</topic><topic>Minimal Clinically Important Difference</topic><topic>Multidisciplinary</topic><topic>Muscular dystrophy</topic><topic>Muscular Dystrophy, Duchenne</topic><topic>Mutation</topic><topic>Natural history</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Physical Sciences</topic><topic>Physical Therapy Modalities</topic><topic>Pédiatrie</topic><topic>Questionnaires</topic><topic>Research and Analysis Methods</topic><topic>Sciences de la santé humaine</topic><topic>Standard error</topic><topic>Surveys and Questionnaires</topic><topic>Walking</topic><topic>Walking - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ayyar Gupta, Vandana</creatorcontrib><creatorcontrib>Pitchforth, Jacqueline M</creatorcontrib><creatorcontrib>Domingos, Joana</creatorcontrib><creatorcontrib>Ridout, Deborah</creatorcontrib><creatorcontrib>Iodice, Mario</creatorcontrib><creatorcontrib>Rye, Catherine</creatorcontrib><creatorcontrib>Chesshyre, Mary</creatorcontrib><creatorcontrib>Wolfe, Amy</creatorcontrib><creatorcontrib>Selby, Victoria</creatorcontrib><creatorcontrib>Mayhew, Anna</creatorcontrib><creatorcontrib>Mazzone, Elena S</creatorcontrib><creatorcontrib>Ricotti, Valeria</creatorcontrib><creatorcontrib>Hogrel, Jean-Yves</creatorcontrib><creatorcontrib>Niks, Erik H</creatorcontrib><creatorcontrib>de Groot, Imelda</creatorcontrib><creatorcontrib>Servais, Laurent</creatorcontrib><creatorcontrib>Straub, Volker</creatorcontrib><creatorcontrib>Mercuri, Eugenio</creatorcontrib><creatorcontrib>Manzur, Adnan Y</creatorcontrib><creatorcontrib>Muntoni, Francesco</creatorcontrib><creatorcontrib>iMDEX Consortium and the U.K. NorthStar Clinical Network</creatorcontrib><creatorcontrib>on behalf of the iMDEX Consortium and the U.K. NorthStar Clinical Network</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Université de Liège - Open Repository and Bibliography (ORBI)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ayyar Gupta, Vandana</au><au>Pitchforth, Jacqueline M</au><au>Domingos, Joana</au><au>Ridout, Deborah</au><au>Iodice, Mario</au><au>Rye, Catherine</au><au>Chesshyre, Mary</au><au>Wolfe, Amy</au><au>Selby, Victoria</au><au>Mayhew, Anna</au><au>Mazzone, Elena S</au><au>Ricotti, Valeria</au><au>Hogrel, Jean-Yves</au><au>Niks, Erik H</au><au>de Groot, Imelda</au><au>Servais, Laurent</au><au>Straub, Volker</au><au>Mercuri, Eugenio</au><au>Manzur, Adnan Y</au><au>Muntoni, Francesco</au><au>Alway, Stephen E</au><aucorp>iMDEX Consortium and the U.K. NorthStar Clinical Network</aucorp><aucorp>on behalf of the iMDEX Consortium and the U.K. NorthStar Clinical Network</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2023-04-26</date><risdate>2023</risdate><volume>18</volume><issue>4</issue><spage>e0283669</spage><epage>e0283669</epage><pages>e0283669-e0283669</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The North Star ambulatory assessment (NSAA) is a functional motor outcome measure in Duchenne muscular dystrophy (DMD), widely used in clinical trials and natural history studies, as well as in clinical practice. However, little has been reported on the minimal clinically important difference (MCID) of the NSAA. The lack of established MCID estimates for NSAA presents challenges in interpreting the significance of the results of this outcome measure in clinical trials, natural history studies and clinical practice. Combining statistical approaches and patient perspectives, this study estimated MCID for NSAA using distribution-based estimates of 1/3 standard deviation (SD) and standard error of measurement (SEM), an anchor-based approach, with six-minute walk distance (6MWD) as the anchor, and evaluation of patient and parent perception using participant-tailored questionnaires. The MCID for NSAA in boys with DMD aged 7 to 10 years based on 1/3 SD ranged from 2.3-2.9 points, and that on SEM ranged from 2.9-3.5 points. Anchored on the 6MWD, the MCID for NSAA was estimated as 3.5 points. When the impact on functional abilities was considered using participant response questionnaires, patients and parent perceived a complete loss of function in a single item or deterioration of function in one to two items of the assessment as an important change. Our study examines MCID estimates for total NSAA scores using multiple approaches, including the impact of patient and parent perspective on within scale changes in items based on complete loss of function and deterioration of function, and provides new insight on evaluation of differences in these widely used outcome measure in DMD.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>37099511</pmid><doi>10.1371/journal.pone.0283669</doi><orcidid>https://orcid.org/0000-0001-5892-5143</orcidid><orcidid>https://orcid.org/0000-0001-9046-3540</orcidid><orcidid>https://orcid.org/0000-0003-3022-4307</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2023-04, Vol.18 (4), p.e0283669-e0283669
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_2806443033
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS)
subjects Age
Ambulatory assessment
Biology and Life Sciences
Care and treatment
Clinical medicine
Clinical trials
Diagnosis
Duchenne muscular dystrophy
Duchenne's muscular dystrophy
Dystrophy
Error analysis
Estimates
Evaluation
Human health sciences
Humans
Male
Medicine and Health Sciences
Minimal Clinically Important Difference
Multidisciplinary
Muscular dystrophy
Muscular Dystrophy, Duchenne
Mutation
Natural history
Patients
Pediatrics
Physical Sciences
Physical Therapy Modalities
Pédiatrie
Questionnaires
Research and Analysis Methods
Sciences de la santé humaine
Standard error
Surveys and Questionnaires
Walking
Walking - physiology
title Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T21%3A49%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Determining%20minimal%20clinically%20important%20differences%20in%20the%20North%20Star%20Ambulatory%20Assessment%20(NSAA)%20for%20patients%20with%20Duchenne%20muscular%20dystrophy&rft.jtitle=PloS%20one&rft.au=Ayyar%20Gupta,%20Vandana&rft.aucorp=iMDEX%20Consortium%20and%20the%20U.K.%20NorthStar%20Clinical%20Network&rft.date=2023-04-26&rft.volume=18&rft.issue=4&rft.spage=e0283669&rft.epage=e0283669&rft.pages=e0283669-e0283669&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0283669&rft_dat=%3Cgale_plos_%3EA747087094%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2806443033&rft_id=info:pmid/37099511&rft_galeid=A747087094&rft_doaj_id=oai_doaj_org_article_21885a505e0b4afe9114a65409bbe906&rfr_iscdi=true