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Diagnostic delay of myositis: protocol for an integrated systematic review

INTRODUCTION: Idiopathic inflammatory myopathies (IIM). described as ‘inflammatory myositis’, are a heterogeneous group of rare muscular autoimmune diseases characterised by skeletal muscle inflammation. Its complex characteristics with lack of accurate diagnostic tests, unified classification syste...

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Autores principales: Namsrai, Tergel, Desborough, Jane, Chalmers, Anita, Lowe, Christine, Cook, Matthew, Phillips, Christine, Parkinson, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196154/
https://www.ncbi.nlm.nih.gov/pubmed/35697457
http://dx.doi.org/10.1136/bmjopen-2021-060312
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author Namsrai, Tergel
Desborough, Jane
Chalmers, Anita
Lowe, Christine
Cook, Matthew
Phillips, Christine
Parkinson, Anne
author_facet Namsrai, Tergel
Desborough, Jane
Chalmers, Anita
Lowe, Christine
Cook, Matthew
Phillips, Christine
Parkinson, Anne
author_sort Namsrai, Tergel
collection PubMed
description INTRODUCTION: Idiopathic inflammatory myopathies (IIM). described as ‘inflammatory myositis’, are a heterogeneous group of rare muscular autoimmune diseases characterised by skeletal muscle inflammation. Its complex characteristics with lack of accurate diagnostic tests, unified classification system and comprehensive widely used diagnostic criteria could lead to diagnostic delay. This study will review diagnostic delay in myositis and provide an overview and clearer insight of patients’ experiences, causes and consequences of diagnostic delay in myositis. METHODS AND ANALYSIS: The literature source will be a systematic search of PubMed/MEDLINE, Scopus, ProQuest and sources of grey literature, conducted from database inception to December 2021 without restrictions on publication date. All study types (qualitative and quantitative) except review articles, examining diagnostic delay, incorrect diagnosis, missed diagnosis or slow diagnosis of all types of myositis in all ages will be included. Evidence of patients’ experiences associated with diagnostic delay will also be examined. Studies in languages other than English, German and Indonesian will be excluded. Outcomes will be diagnostic delay time, patients’ experiences, and causes and consequences associated with diagnostic delay in myositis. Two review authors will independently screen the titles and abstracts of search results against the inclusion criteria. The Mixed Methods Appraisal Tool (MMAT) will be used to appraise selected studies. Two independent authors will extract data using a prepiloted data extraction tool. If sufficient quantitative data is available, a meta-analysis will be conducted along with subgroup analysis including pooled diagnostic delay in each type of myositis. Qualitative data will be analysed in line with meta-aggregation methods. If data is insufficient, a narrative synthesis will be conducted. ETHICS AND DISSEMINATION: As this work is a systematic review, ethical approval was not required. Findings of the study will be disseminated through publications in peer-reviewed journals, conferences and symposia. PROSPERO REGISTRATION NUMBER: CRD42022289830.
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spelling pubmed-91961542022-07-08 Diagnostic delay of myositis: protocol for an integrated systematic review Namsrai, Tergel Desborough, Jane Chalmers, Anita Lowe, Christine Cook, Matthew Phillips, Christine Parkinson, Anne BMJ Open Research Methods INTRODUCTION: Idiopathic inflammatory myopathies (IIM). described as ‘inflammatory myositis’, are a heterogeneous group of rare muscular autoimmune diseases characterised by skeletal muscle inflammation. Its complex characteristics with lack of accurate diagnostic tests, unified classification system and comprehensive widely used diagnostic criteria could lead to diagnostic delay. This study will review diagnostic delay in myositis and provide an overview and clearer insight of patients’ experiences, causes and consequences of diagnostic delay in myositis. METHODS AND ANALYSIS: The literature source will be a systematic search of PubMed/MEDLINE, Scopus, ProQuest and sources of grey literature, conducted from database inception to December 2021 without restrictions on publication date. All study types (qualitative and quantitative) except review articles, examining diagnostic delay, incorrect diagnosis, missed diagnosis or slow diagnosis of all types of myositis in all ages will be included. Evidence of patients’ experiences associated with diagnostic delay will also be examined. Studies in languages other than English, German and Indonesian will be excluded. Outcomes will be diagnostic delay time, patients’ experiences, and causes and consequences associated with diagnostic delay in myositis. Two review authors will independently screen the titles and abstracts of search results against the inclusion criteria. The Mixed Methods Appraisal Tool (MMAT) will be used to appraise selected studies. Two independent authors will extract data using a prepiloted data extraction tool. If sufficient quantitative data is available, a meta-analysis will be conducted along with subgroup analysis including pooled diagnostic delay in each type of myositis. Qualitative data will be analysed in line with meta-aggregation methods. If data is insufficient, a narrative synthesis will be conducted. ETHICS AND DISSEMINATION: As this work is a systematic review, ethical approval was not required. Findings of the study will be disseminated through publications in peer-reviewed journals, conferences and symposia. PROSPERO REGISTRATION NUMBER: CRD42022289830. BMJ Publishing Group 2022-06-12 /pmc/articles/PMC9196154/ /pubmed/35697457 http://dx.doi.org/10.1136/bmjopen-2021-060312 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research Methods
Namsrai, Tergel
Desborough, Jane
Chalmers, Anita
Lowe, Christine
Cook, Matthew
Phillips, Christine
Parkinson, Anne
Diagnostic delay of myositis: protocol for an integrated systematic review
title Diagnostic delay of myositis: protocol for an integrated systematic review
title_full Diagnostic delay of myositis: protocol for an integrated systematic review
title_fullStr Diagnostic delay of myositis: protocol for an integrated systematic review
title_full_unstemmed Diagnostic delay of myositis: protocol for an integrated systematic review
title_short Diagnostic delay of myositis: protocol for an integrated systematic review
title_sort diagnostic delay of myositis: protocol for an integrated systematic review
topic Research Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196154/
https://www.ncbi.nlm.nih.gov/pubmed/35697457
http://dx.doi.org/10.1136/bmjopen-2021-060312
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