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Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy
BACKGROUND: Reports on the clinical meaningfulness of outcome measures in spinal muscular atrophy (SMA) are rare. In this two-part study, our aim was to explore patients’ and caregivers’ views on the clinical relevance of the Hammersmith Functional Motor Scale Expanded- (HFMSE). METHODS: First, we u...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324197/ https://www.ncbi.nlm.nih.gov/pubmed/28231823 http://dx.doi.org/10.1186/s12883-017-0790-9 |
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author | Pera, Maria C. Coratti, Giorgia Forcina, Nicola Mazzone, Elena S. Scoto, Mariacristina Montes, Jacqueline Pasternak, Amy Mayhew, Anna Messina, Sonia Sframeli, Maria Main, Marion Lofra, Robert Muni Duong, Tina Ramsey, Danielle Dunaway, Sally Salazar, Rachel Fanelli, Lavinia Civitello, Matthew de Sanctis, Roberto Antonaci, Laura Lapenta, Leonardo Lucibello, Simona Pane, Marika Day, John Darras, Basil T. De Vivo, Darryl C. Muntoni, Francesco Finkel, Richard Mercuri, Eugenio |
author_facet | Pera, Maria C. Coratti, Giorgia Forcina, Nicola Mazzone, Elena S. Scoto, Mariacristina Montes, Jacqueline Pasternak, Amy Mayhew, Anna Messina, Sonia Sframeli, Maria Main, Marion Lofra, Robert Muni Duong, Tina Ramsey, Danielle Dunaway, Sally Salazar, Rachel Fanelli, Lavinia Civitello, Matthew de Sanctis, Roberto Antonaci, Laura Lapenta, Leonardo Lucibello, Simona Pane, Marika Day, John Darras, Basil T. De Vivo, Darryl C. Muntoni, Francesco Finkel, Richard Mercuri, Eugenio |
author_sort | Pera, Maria C. |
collection | PubMed |
description | BACKGROUND: Reports on the clinical meaningfulness of outcome measures in spinal muscular atrophy (SMA) are rare. In this two-part study, our aim was to explore patients’ and caregivers’ views on the clinical relevance of the Hammersmith Functional Motor Scale Expanded- (HFMSE). METHODS: First, we used focus groups including SMA patients and caregivers to explore their views on the clinical relevance of the individual activities included in the HFMSE. Then we asked caregivers to comment on the clinical relevance of possible changes of HFMSE scores over time. As functional data of individual patients were available, some of the questions were tailored according to their functional level on the HFMSE. RESULTS: Part 1: Sixty-three individuals participated in the focus groups. This included 30 caregivers, 25 patients and 8 professionals who facilitated the discussion. The caregivers provided a comparison to activities of daily living for each of the HFMSE items. Part 2: One hundred and forty-nine caregivers agreed to complete the questionnaire: in response to a general question, 72% of the caregivers would consider taking part in a clinical trial if the treatment was expected to slow down deterioration, 88% if it would stop deterioration and 97% if the treatment was expected to produce an improvement. Caregivers were informed of the first three items that their child could not achieve on the HFMSE. In response 75% indicated a willingness to take part in a clinical trial if they could achieve at least one of these abilities, 89% if they could achieve two, and 100% if they could achieve more than 2. CONCLUSIONS: Our findings support the use of the HFMSE as a key outcome measure in SMA clinical trials because the individual items and the detected changes have clear content validity and clinical meaningfulness for patients and their caregivers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12883-017-0790-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5324197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53241972017-03-01 Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy Pera, Maria C. Coratti, Giorgia Forcina, Nicola Mazzone, Elena S. Scoto, Mariacristina Montes, Jacqueline Pasternak, Amy Mayhew, Anna Messina, Sonia Sframeli, Maria Main, Marion Lofra, Robert Muni Duong, Tina Ramsey, Danielle Dunaway, Sally Salazar, Rachel Fanelli, Lavinia Civitello, Matthew de Sanctis, Roberto Antonaci, Laura Lapenta, Leonardo Lucibello, Simona Pane, Marika Day, John Darras, Basil T. De Vivo, Darryl C. Muntoni, Francesco Finkel, Richard Mercuri, Eugenio BMC Neurol Research Article BACKGROUND: Reports on the clinical meaningfulness of outcome measures in spinal muscular atrophy (SMA) are rare. In this two-part study, our aim was to explore patients’ and caregivers’ views on the clinical relevance of the Hammersmith Functional Motor Scale Expanded- (HFMSE). METHODS: First, we used focus groups including SMA patients and caregivers to explore their views on the clinical relevance of the individual activities included in the HFMSE. Then we asked caregivers to comment on the clinical relevance of possible changes of HFMSE scores over time. As functional data of individual patients were available, some of the questions were tailored according to their functional level on the HFMSE. RESULTS: Part 1: Sixty-three individuals participated in the focus groups. This included 30 caregivers, 25 patients and 8 professionals who facilitated the discussion. The caregivers provided a comparison to activities of daily living for each of the HFMSE items. Part 2: One hundred and forty-nine caregivers agreed to complete the questionnaire: in response to a general question, 72% of the caregivers would consider taking part in a clinical trial if the treatment was expected to slow down deterioration, 88% if it would stop deterioration and 97% if the treatment was expected to produce an improvement. Caregivers were informed of the first three items that their child could not achieve on the HFMSE. In response 75% indicated a willingness to take part in a clinical trial if they could achieve at least one of these abilities, 89% if they could achieve two, and 100% if they could achieve more than 2. CONCLUSIONS: Our findings support the use of the HFMSE as a key outcome measure in SMA clinical trials because the individual items and the detected changes have clear content validity and clinical meaningfulness for patients and their caregivers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12883-017-0790-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-23 /pmc/articles/PMC5324197/ /pubmed/28231823 http://dx.doi.org/10.1186/s12883-017-0790-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Pera, Maria C. Coratti, Giorgia Forcina, Nicola Mazzone, Elena S. Scoto, Mariacristina Montes, Jacqueline Pasternak, Amy Mayhew, Anna Messina, Sonia Sframeli, Maria Main, Marion Lofra, Robert Muni Duong, Tina Ramsey, Danielle Dunaway, Sally Salazar, Rachel Fanelli, Lavinia Civitello, Matthew de Sanctis, Roberto Antonaci, Laura Lapenta, Leonardo Lucibello, Simona Pane, Marika Day, John Darras, Basil T. De Vivo, Darryl C. Muntoni, Francesco Finkel, Richard Mercuri, Eugenio Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy |
title | Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy |
title_full | Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy |
title_fullStr | Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy |
title_full_unstemmed | Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy |
title_short | Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy |
title_sort | content validity and clinical meaningfulness of the hfmse in spinal muscular atrophy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324197/ https://www.ncbi.nlm.nih.gov/pubmed/28231823 http://dx.doi.org/10.1186/s12883-017-0790-9 |
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