Detecting disability using self-reported and clinical assessments in early-stage relapsing-remitting multiple sclerosis: Looking for a complementary approach
Disability accrual is mainly driven by progression independent of relapse activity, which is present even in early stages of relapsing-remitting multiple sclerosis (RRMS) and sometimes overlooked. This multicenter, non-interventional study evaluated whether patient-reported outcomes measures (PROMs)...
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Published in | Multiple sclerosis journal - experimental, translational and clinical Vol. 9; no. 2; p. 20552173231169475 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London, England
SAGE Publications
01.04.2023
Sage Publications Ltd |
Subjects | |
Online Access | Get full text |
ISSN | 2055-2173 2055-2173 |
DOI | 10.1177/20552173231169475 |
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Abstract | Disability accrual is mainly driven by progression independent of relapse activity, which is present even in early stages of relapsing-remitting multiple sclerosis (RRMS) and sometimes overlooked. This multicenter, non-interventional study evaluated whether patient-reported outcomes measures (PROMs) could capture disability in 189 early-stage RRMS patients (mean age: 36.1 ± 9.4 years, 71.4% female, mean disease duration: 1.4 ± 0.8 years, median EDSS: 1.0). The 9-Hole Peg Test (9-HPT), NeuroQoL Upper Extremity (NeuroQoL-UE), Timed 25-Foot Walk (T25-FW), Multiple Sclerosis Walking Scale (MSWS-12), Symbol Digit Modalities Test (SDMT), and Perceived Deficits Questionnaire (PDQ-5) were used to assess hand function, gait, and cognition, respectively. These functions were at least mildly affected in this early-stage population, finding significant correlations between PROMs and clinical assessments. PROMs could enable early-stage RRMS patients to communicate their perceived disability in different domains, assisting clinicians in disease monitoring and decision making. |
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AbstractList | Disability accrual is mainly driven by progression independent of relapse activity, which is present even in early stages of relapsing-remitting multiple sclerosis (RRMS) and sometimes overlooked. This multicenter, non-interventional study evaluated whether patient-reported outcomes measures (PROMs) could capture disability in 189 early-stage RRMS patients (mean age: 36.1 ± 9.4 years, 71.4% female, mean disease duration: 1.4 ± 0.8 years, median EDSS: 1.0). The 9-Hole Peg Test (9-HPT), NeuroQoL Upper Extremity (NeuroQoL-UE), Timed 25-Foot Walk (T25-FW), Multiple Sclerosis Walking Scale (MSWS-12), Symbol Digit Modalities Test (SDMT), and Perceived Deficits Questionnaire (PDQ-5) were used to assess hand function, gait, and cognition, respectively. These functions were at least mildly affected in this early-stage population, finding significant correlations between PROMs and clinical assessments. PROMs could enable early-stage RRMS patients to communicate their perceived disability in different domains, assisting clinicians in disease monitoring and decision making.Disability accrual is mainly driven by progression independent of relapse activity, which is present even in early stages of relapsing-remitting multiple sclerosis (RRMS) and sometimes overlooked. This multicenter, non-interventional study evaluated whether patient-reported outcomes measures (PROMs) could capture disability in 189 early-stage RRMS patients (mean age: 36.1 ± 9.4 years, 71.4% female, mean disease duration: 1.4 ± 0.8 years, median EDSS: 1.0). The 9-Hole Peg Test (9-HPT), NeuroQoL Upper Extremity (NeuroQoL-UE), Timed 25-Foot Walk (T25-FW), Multiple Sclerosis Walking Scale (MSWS-12), Symbol Digit Modalities Test (SDMT), and Perceived Deficits Questionnaire (PDQ-5) were used to assess hand function, gait, and cognition, respectively. These functions were at least mildly affected in this early-stage population, finding significant correlations between PROMs and clinical assessments. PROMs could enable early-stage RRMS patients to communicate their perceived disability in different domains, assisting clinicians in disease monitoring and decision making. Disability accrual is mainly driven by progression independent of relapse activity, which is present even in early stages of relapsing-remitting multiple sclerosis (RRMS) and sometimes overlooked. This multicenter, non-interventional study evaluated whether patient-reported outcomes measures (PROMs) could capture disability in 189 early-stage RRMS patients (mean age: 36.1 ± 9.4 years, 71.4% female, mean disease duration: 1.4 ± 0.8 years, median EDSS: 1.0). The 9-Hole Peg Test (9-HPT), NeuroQoL Upper Extremity (NeuroQoL-UE), Timed 25-Foot Walk (T25-FW), Multiple Sclerosis Walking Scale (MSWS-12), Symbol Digit Modalities Test (SDMT), and Perceived Deficits Questionnaire (PDQ-5) were used to assess hand function, gait, and cognition, respectively. These functions were at least mildly affected in this early-stage population, finding significant correlations between PROMs and clinical assessments. PROMs could enable early-stage RRMS patients to communicate their perceived disability in different domains, assisting clinicians in disease monitoring and decision making. Disability accrual is mainly driven by progression independent of relapse activity, which is present even in early stages of relapsing-remitting multiple sclerosis (RRMS) and sometimes overlooked. This multicenter, non-interventional study evaluated whether patient-reported outcomes measures (PROMs) could capture disability in 189 early-stage RRMS patients (mean age: 36.1 ± 9.4 years, 71.4% female, mean disease duration: 1.4 ± 0.8 years, median EDSS: 1.0). The 9-Hole Peg Test (9-HPT), NeuroQoL Upper Extremity (NeuroQoL-UE), Timed 25-Foot Walk (T25-FW), Multiple Sclerosis Walking Scale (MSWS-12), Symbol Digit Modalities Test (SDMT), and Perceived Deficits Questionnaire (PDQ-5) were used to assess hand function, gait, and cognition, respectively. These functions were at least mildly affected in this early-stage population, finding significant correlations between PROMs and clinical assessments. PROMs could enable early-stage RRMS patients to communicate their perceived disability in different domains, assisting clinicians in disease monitoring and decision making. |
Author | Barrero-Hernández, Francisco J Sotoca, Javier Borrega, Laura Sánchez-Menoyo, José L Carmona, Olga Blasco-Quílez, María R Campo-Amigo, María del Castillo-Triviño, Tamara Forero, Lucía Navarro-Cantó, Laura Medrano, Nicolás Hervàs, Mariona Dotor García-Soto, Julio Gabaldón-Torres, Laura Gómez-Ballesteros, Rocío Agüera, Eduardo Borges, Mónica Garcés-Redondo, Moisés Calles, Carmen Martín-Martínez, Jesús Alonso, Ana Brieva, Luis Sainz de la Maza, Susana Caminero, Ana B Maurino, Jorge |
Author_xml | – sequence: 1 givenname: Susana surname: Sainz de la Maza fullname: Sainz de la Maza, Susana organization: , Universidad de Alcalá, Madrid, Spain – sequence: 2 givenname: Rocío orcidid: 0000-0001-9582-9230 surname: Gómez-Ballesteros fullname: Gómez-Ballesteros, Rocío organization: Medical Department, Roche Farma, Madrid, Spain – sequence: 3 givenname: Mónica surname: Borges fullname: Borges, Mónica organization: , Sevilla, Spain – sequence: 4 givenname: Jesús surname: Martín-Martínez fullname: Martín-Martínez, Jesús organization: , Zaragoza, Spain – sequence: 5 givenname: Javier surname: Sotoca fullname: Sotoca, Javier organization: , Terrassa, Spain – sequence: 6 givenname: Ana orcidid: 0000-0002-7337-8384 surname: Alonso fullname: Alonso, Ana organization: Department of Neurology, Hospital Regional Universitario de Málaga, Málaga, Spain – sequence: 7 givenname: Ana B surname: Caminero fullname: Caminero, Ana B organization: , Ávila, Spain – sequence: 8 givenname: Laura surname: Borrega fullname: Borrega, Laura organization: , Alcorcón, Spain – sequence: 9 givenname: José L surname: Sánchez-Menoyo fullname: Sánchez-Menoyo, José L organization: Department of Neurology, Hospital de Galdakao-Usansolo, Galdakao, Spain – sequence: 10 givenname: Francisco J surname: Barrero-Hernández fullname: Barrero-Hernández, Francisco J organization: , Granada, Spain – sequence: 11 givenname: Carmen surname: Calles fullname: Calles, Carmen organization: Department of Neurology, Hospital Universitari Son Espases, Palma de Mallorca, Spain – sequence: 12 givenname: Luis surname: Brieva fullname: Brieva, Luis organization: , Lleida, Spain – sequence: 13 givenname: María R surname: Blasco-Quílez fullname: Blasco-Quílez, María R organization: , Madrid, Spain – sequence: 14 givenname: Julio surname: Dotor García-Soto fullname: Dotor García-Soto, Julio organization: , Sevilla, Spain – sequence: 15 givenname: María del surname: Campo-Amigo fullname: Campo-Amigo, María del organization: , Pontevedra, Spain – sequence: 16 givenname: Laura surname: Navarro-Cantó fullname: Navarro-Cantó, Laura organization: , Elche, Spain – sequence: 17 givenname: Eduardo surname: Agüera fullname: Agüera, Eduardo organization: Department of Neurology, Hospital Universitario Reina Sofía, Córdoba, Spain – sequence: 18 givenname: Moisés orcidid: 0000-0002-1756-5492 surname: Garcés-Redondo fullname: Garcés-Redondo, Moisés organization: , Zaragoza, Spain – sequence: 19 givenname: Olga surname: Carmona fullname: Carmona, Olga organization: Department of Neurology, Fundació Salut Empordà, Figueres, Spain – sequence: 20 givenname: Laura surname: Gabaldón-Torres fullname: Gabaldón-Torres, Laura organization: Department of Neurology, Hospital Francesc de Borja, Gandía, Spain – sequence: 21 givenname: Lucía orcidid: 0000-0003-0256-6748 surname: Forero fullname: Forero, Lucía organization: Department of Neurology, Hospital Universitario Puerta del Mar, Cádiz, Spain – sequence: 22 givenname: Mariona surname: Hervàs fullname: Hervàs, Mariona organization: , Sabadell, Spain – sequence: 23 givenname: Nicolás surname: Medrano fullname: Medrano, Nicolás organization: Medical Department, Roche Farma, Madrid, Spain – sequence: 24 givenname: Jorge orcidid: 0000-0001-9858-3555 surname: Maurino fullname: Maurino, Jorge organization: Medical Department, Roche Farma, Madrid, Spain – sequence: 25 givenname: Tamara orcidid: 0000-0002-9249-3185 surname: Castillo-Triviño fullname: Castillo-Triviño, Tamara organization: , San Sebastián, Spain |
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Cites_doi | 10.7224/1537-2073.2015-028 10.1177/1352458517690824 10.1093/brain/awac111 10.1177/1352458515599450 10.1186/s12883-015-0296-2 10.1016/j.rehab.2021.101491 10.1016/j.msard.2022.103757 10.1093/qjmed/hcx070 10.1212/01.wnl.0000436065.97642.d2 10.1016/S1474-4422(17)30470-2 10.1001/jamaneurol.2022.4655 10.1212/WNL.60.1.31 10.1111/ene.14866 |
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Snippet | Disability accrual is mainly driven by progression independent of relapse activity, which is present even in early stages of relapsing-remitting multiple... Disability accrual is mainly driven by progression independent of relapse activity, which is present even in early stages of relapsing-remitting multiple... |
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Title | Detecting disability using self-reported and clinical assessments in early-stage relapsing-remitting multiple sclerosis: Looking for a complementary approach |
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