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Conversion to secondary progressive multiple sclerosis: Multistakeholder experiences and needs in Italy

BACKGROUND: Conversion to secondary progressive multiple sclerosis (SPMS) is associated with a relatively poor prognosis, and SPMS is responsible for the majority of the social and economic costs associated with MS. Managing the Transition to SPMS (ManTra) is a mixed methods project conducted in Ita...

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Autores principales: Giovannetti, Ambra Mara, Pietrolongo, Erika, Borreani, Claudia, Giordano, Andrea, Schiffmann, Insa, Barabasch, Anna, Heesen, Christoph, Solari, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018010/
https://www.ncbi.nlm.nih.gov/pubmed/32053608
http://dx.doi.org/10.1371/journal.pone.0228587
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author Giovannetti, Ambra Mara
Pietrolongo, Erika
Borreani, Claudia
Giordano, Andrea
Schiffmann, Insa
Barabasch, Anna
Heesen, Christoph
Solari, Alessandra
author_facet Giovannetti, Ambra Mara
Pietrolongo, Erika
Borreani, Claudia
Giordano, Andrea
Schiffmann, Insa
Barabasch, Anna
Heesen, Christoph
Solari, Alessandra
author_sort Giovannetti, Ambra Mara
collection PubMed
description BACKGROUND: Conversion to secondary progressive multiple sclerosis (SPMS) is associated with a relatively poor prognosis, and SPMS is responsible for the majority of the social and economic costs associated with MS. Managing the Transition to SPMS (ManTra) is a mixed methods project conducted in Italy and Germany aimed to set up a user-led resource to empower and improve the quality of life of newly diagnosed SPMS patients. AIMS: To assess the experiences and the needs of Italian people who recently converted to SPMS, patient significant others (SOs), neurologists and other health professionals (HPs). METHODS: We conducted 15 personal semistructured interviews (PSIs) with SPMS patients who transitioned up to five years, and three focus group meetings (FGMs), one of SPMS SOs, one of neurologists, and one of other HPs. Participants were purposely selected from the three geographic areas of Italy, and varied in terms of gender, education and (for patients) disease severity. PSIs and FGMs were audiorecorded, transcribed and analyzed by two researchers using the framework analysis. RESULTS: One hundred sub-categories were identified, grouped into 13 categories and four themes: ‘awareness of the transition’, ‘communication of the transition’, ‘dealing with symptoms worsening’, and ‘needs’. The major unmet needs were collected in four dimensions ‘organization and management; ‘empowerment training’; ‘information’; and ‘policies’. CONCLUSIONS: Two are the main findings: first, the widespread lack of awareness around the transition; second, the need to improve the quality of the care pathway in the Italian context. It was particularly stressed the need for a holistic and multidisciplinary approach (with patients and SOs as members of the team), the development of an ad hoc plan of follow up visits with easy access to MS specialists’ consultation/treatment; specialized training for each stakeholders; more information on SPMS, daily management and changes at policy level.
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spelling pubmed-70180102020-02-26 Conversion to secondary progressive multiple sclerosis: Multistakeholder experiences and needs in Italy Giovannetti, Ambra Mara Pietrolongo, Erika Borreani, Claudia Giordano, Andrea Schiffmann, Insa Barabasch, Anna Heesen, Christoph Solari, Alessandra PLoS One Research Article BACKGROUND: Conversion to secondary progressive multiple sclerosis (SPMS) is associated with a relatively poor prognosis, and SPMS is responsible for the majority of the social and economic costs associated with MS. Managing the Transition to SPMS (ManTra) is a mixed methods project conducted in Italy and Germany aimed to set up a user-led resource to empower and improve the quality of life of newly diagnosed SPMS patients. AIMS: To assess the experiences and the needs of Italian people who recently converted to SPMS, patient significant others (SOs), neurologists and other health professionals (HPs). METHODS: We conducted 15 personal semistructured interviews (PSIs) with SPMS patients who transitioned up to five years, and three focus group meetings (FGMs), one of SPMS SOs, one of neurologists, and one of other HPs. Participants were purposely selected from the three geographic areas of Italy, and varied in terms of gender, education and (for patients) disease severity. PSIs and FGMs were audiorecorded, transcribed and analyzed by two researchers using the framework analysis. RESULTS: One hundred sub-categories were identified, grouped into 13 categories and four themes: ‘awareness of the transition’, ‘communication of the transition’, ‘dealing with symptoms worsening’, and ‘needs’. The major unmet needs were collected in four dimensions ‘organization and management; ‘empowerment training’; ‘information’; and ‘policies’. CONCLUSIONS: Two are the main findings: first, the widespread lack of awareness around the transition; second, the need to improve the quality of the care pathway in the Italian context. It was particularly stressed the need for a holistic and multidisciplinary approach (with patients and SOs as members of the team), the development of an ad hoc plan of follow up visits with easy access to MS specialists’ consultation/treatment; specialized training for each stakeholders; more information on SPMS, daily management and changes at policy level. Public Library of Science 2020-02-13 /pmc/articles/PMC7018010/ /pubmed/32053608 http://dx.doi.org/10.1371/journal.pone.0228587 Text en © 2020 Giovannetti et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Giovannetti, Ambra Mara
Pietrolongo, Erika
Borreani, Claudia
Giordano, Andrea
Schiffmann, Insa
Barabasch, Anna
Heesen, Christoph
Solari, Alessandra
Conversion to secondary progressive multiple sclerosis: Multistakeholder experiences and needs in Italy
title Conversion to secondary progressive multiple sclerosis: Multistakeholder experiences and needs in Italy
title_full Conversion to secondary progressive multiple sclerosis: Multistakeholder experiences and needs in Italy
title_fullStr Conversion to secondary progressive multiple sclerosis: Multistakeholder experiences and needs in Italy
title_full_unstemmed Conversion to secondary progressive multiple sclerosis: Multistakeholder experiences and needs in Italy
title_short Conversion to secondary progressive multiple sclerosis: Multistakeholder experiences and needs in Italy
title_sort conversion to secondary progressive multiple sclerosis: multistakeholder experiences and needs in italy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018010/
https://www.ncbi.nlm.nih.gov/pubmed/32053608
http://dx.doi.org/10.1371/journal.pone.0228587
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