Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]

Detalhes bibliográficos
Autor(a) principal: Meyer, A
Data de Publicação: 2018
Outros Autores: Scirè, CA, Talarico, R, Alexander, T, Amoura, Z, Avcin, T, Barsotti, S, Beretta, L, Blagojevic, J, Burmester, G, Cavazzana, I, Cherrin, P, Damian, L, Doria, A, Fonseca, JE, Furini, F, Galetti, I, Houssiau, F, Krieg, T, Maddalena, L, Launay, D, Campanilho-Marques, R, Martin, T, Matucci-Cerinic, M, Moinzadeh, P, Montecucco, C, Moraes-Fontes, MF, Mouthon, L, Neri, R, Paolino, S, Piette, Y, Rednic, S, Tamirou, F, Tincani, A, Toplak, N, Bombardieri, S, Hachulla, E, Mueller-Ladner, U, Schneider, M, Smith, V, Vieira, A, Cutolo, M, Mosca, M, Cavagna, L
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.17/3546
Resumo: Idiopathic inflammatory myopathies (IIMs) encompass a heterogeneous group of rare autoimmune diseases characterised by muscle weakness and inflammation, but in antisynthetase syndrome arthritis and interstitial lung disease are more frequent and often inaugurate the disease. Clinical practice guidelines (CPGs) have been proposed for IIMs, but they are sparse and heterogeneous. This work aimed at identifying: i) current available CPGs for IIMs, ii) patients ' and clinicians' unmet needs not covered by CPGs. It has been performed in the framework of the European Reference Network on rare and complex connective tissue and musculoskeletal diseases (ReCONNET), a network of centre of expertise and patients funded by the European Union's Health Programme. Fourteen original CPGs were identified, notably recommending that: i) extra-muscular involvements should be assessed; ii) corticosteroids and methotrexate or azathioprine are first-line therapies of IIMs. ii) IVIG is a treatment of resistant-DM that may be also used in other resistant-IIMs; iii) physical therapy and sun protection (in DM patients) are part of the treatment; v) tumour screening for patients with DM include imaging of chest, abdomen, pelvis and breast (in woman) along with colonoscopy (in patients over 50 years); vi) disease activity and damages should be monitor using standardised and validated tools. Yet, only half of these CPGs were evidence-based. Crucial unmet needs were identified both by patients and clinicians. In particular, there was a lack of large multidisciplinary working group and of patients ' preferences. The following fields were not or inappropriately targeted: diagnosis; management of extra-muscular involvements other than skin; co-morbidities and severe manifestations.
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spelling Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]Idiopathic inflammatory myopathiesState of the artClinical practice guidelinesHCC DAUTOIMIdiopathic inflammatory myopathies (IIMs) encompass a heterogeneous group of rare autoimmune diseases characterised by muscle weakness and inflammation, but in antisynthetase syndrome arthritis and interstitial lung disease are more frequent and often inaugurate the disease. Clinical practice guidelines (CPGs) have been proposed for IIMs, but they are sparse and heterogeneous. This work aimed at identifying: i) current available CPGs for IIMs, ii) patients ' and clinicians' unmet needs not covered by CPGs. It has been performed in the framework of the European Reference Network on rare and complex connective tissue and musculoskeletal diseases (ReCONNET), a network of centre of expertise and patients funded by the European Union's Health Programme. Fourteen original CPGs were identified, notably recommending that: i) extra-muscular involvements should be assessed; ii) corticosteroids and methotrexate or azathioprine are first-line therapies of IIMs. ii) IVIG is a treatment of resistant-DM that may be also used in other resistant-IIMs; iii) physical therapy and sun protection (in DM patients) are part of the treatment; v) tumour screening for patients with DM include imaging of chest, abdomen, pelvis and breast (in woman) along with colonoscopy (in patients over 50 years); vi) disease activity and damages should be monitor using standardised and validated tools. Yet, only half of these CPGs were evidence-based. Crucial unmet needs were identified both by patients and clinicians. In particular, there was a lack of large multidisciplinary working group and of patients ' preferences. The following fields were not or inappropriately targeted: diagnosis; management of extra-muscular involvements other than skin; co-morbidities and severe manifestations.BMJ OpenRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEMeyer, AScirè, CATalarico, RAlexander, TAmoura, ZAvcin, TBarsotti, SBeretta, LBlagojevic, JBurmester, GCavazzana, ICherrin, PDamian, LDoria, AFonseca, JEFurini, FGaletti, IHoussiau, FKrieg, TMaddalena, LLaunay, DCampanilho-Marques, RMartin, TMatucci-Cerinic, MMoinzadeh, PMontecucco, CMoraes-Fontes, MFMouthon, LNeri, RPaolino, SPiette, YRednic, STamirou, FTincani, AToplak, NBombardieri, SHachulla, EMueller-Ladner, USchneider, MSmith, VVieira, ACutolo, MMosca, MCavagna, L2021-01-22T16:46:03Z20182018-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/3546engRMD Open. 2019 Feb 26;4(Suppl 1):e00078410.1136/rmdopen-2018-000784info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:43:31Zoai:repositorio.chlc.min-saude.pt:10400.17/3546Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:20:51.442351Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]
title Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]
spellingShingle Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]
Meyer, A
Idiopathic inflammatory myopathies
State of the art
Clinical practice guidelines
HCC DAUTOIM
title_short Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]
title_full Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]
title_fullStr Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]
title_full_unstemmed Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]
title_sort Idiopathic Inflammatory Myopathies: State of the Art on Clinical Practice Guidelines [corrected]
author Meyer, A
author_facet Meyer, A
Scirè, CA
Talarico, R
Alexander, T
Amoura, Z
Avcin, T
Barsotti, S
Beretta, L
Blagojevic, J
Burmester, G
Cavazzana, I
Cherrin, P
Damian, L
Doria, A
Fonseca, JE
Furini, F
Galetti, I
Houssiau, F
Krieg, T
Maddalena, L
Launay, D
Campanilho-Marques, R
Martin, T
Matucci-Cerinic, M
Moinzadeh, P
Montecucco, C
Moraes-Fontes, MF
Mouthon, L
Neri, R
Paolino, S
Piette, Y
Rednic, S
Tamirou, F
Tincani, A
Toplak, N
Bombardieri, S
Hachulla, E
Mueller-Ladner, U
Schneider, M
Smith, V
Vieira, A
Cutolo, M
Mosca, M
Cavagna, L
author_role author
author2 Scirè, CA
Talarico, R
Alexander, T
Amoura, Z
Avcin, T
Barsotti, S
Beretta, L
Blagojevic, J
Burmester, G
Cavazzana, I
Cherrin, P
Damian, L
Doria, A
Fonseca, JE
Furini, F
Galetti, I
Houssiau, F
Krieg, T
Maddalena, L
Launay, D
Campanilho-Marques, R
Martin, T
Matucci-Cerinic, M
Moinzadeh, P
Montecucco, C
Moraes-Fontes, MF
Mouthon, L
Neri, R
Paolino, S
Piette, Y
Rednic, S
Tamirou, F
Tincani, A
Toplak, N
Bombardieri, S
Hachulla, E
Mueller-Ladner, U
Schneider, M
Smith, V
Vieira, A
Cutolo, M
Mosca, M
Cavagna, L
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE
dc.contributor.author.fl_str_mv Meyer, A
Scirè, CA
Talarico, R
Alexander, T
Amoura, Z
Avcin, T
Barsotti, S
Beretta, L
Blagojevic, J
Burmester, G
Cavazzana, I
Cherrin, P
Damian, L
Doria, A
Fonseca, JE
Furini, F
Galetti, I
Houssiau, F
Krieg, T
Maddalena, L
Launay, D
Campanilho-Marques, R
Martin, T
Matucci-Cerinic, M
Moinzadeh, P
Montecucco, C
Moraes-Fontes, MF
Mouthon, L
Neri, R
Paolino, S
Piette, Y
Rednic, S
Tamirou, F
Tincani, A
Toplak, N
Bombardieri, S
Hachulla, E
Mueller-Ladner, U
Schneider, M
Smith, V
Vieira, A
Cutolo, M
Mosca, M
Cavagna, L
dc.subject.por.fl_str_mv Idiopathic inflammatory myopathies
State of the art
Clinical practice guidelines
HCC DAUTOIM
topic Idiopathic inflammatory myopathies
State of the art
Clinical practice guidelines
HCC DAUTOIM
description Idiopathic inflammatory myopathies (IIMs) encompass a heterogeneous group of rare autoimmune diseases characterised by muscle weakness and inflammation, but in antisynthetase syndrome arthritis and interstitial lung disease are more frequent and often inaugurate the disease. Clinical practice guidelines (CPGs) have been proposed for IIMs, but they are sparse and heterogeneous. This work aimed at identifying: i) current available CPGs for IIMs, ii) patients ' and clinicians' unmet needs not covered by CPGs. It has been performed in the framework of the European Reference Network on rare and complex connective tissue and musculoskeletal diseases (ReCONNET), a network of centre of expertise and patients funded by the European Union's Health Programme. Fourteen original CPGs were identified, notably recommending that: i) extra-muscular involvements should be assessed; ii) corticosteroids and methotrexate or azathioprine are first-line therapies of IIMs. ii) IVIG is a treatment of resistant-DM that may be also used in other resistant-IIMs; iii) physical therapy and sun protection (in DM patients) are part of the treatment; v) tumour screening for patients with DM include imaging of chest, abdomen, pelvis and breast (in woman) along with colonoscopy (in patients over 50 years); vi) disease activity and damages should be monitor using standardised and validated tools. Yet, only half of these CPGs were evidence-based. Crucial unmet needs were identified both by patients and clinicians. In particular, there was a lack of large multidisciplinary working group and of patients ' preferences. The following fields were not or inappropriately targeted: diagnosis; management of extra-muscular involvements other than skin; co-morbidities and severe manifestations.
publishDate 2018
dc.date.none.fl_str_mv 2018
2018-01-01T00:00:00Z
2021-01-22T16:46:03Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.17/3546
url http://hdl.handle.net/10400.17/3546
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv RMD Open. 2019 Feb 26;4(Suppl 1):e000784
10.1136/rmdopen-2018-000784
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv BMJ Open
publisher.none.fl_str_mv BMJ Open
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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