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STANDING Collaboration: a study protocol for developing clinical standards

INTRODUCTION: Despite widespread availability of clinical practice guidelines (CPGs), considerable gaps continue between the care that is recommended (‘appropriate care’) and the care provided. Problems with current CPGs are commonly cited as barriers to providing ’appropriate care'. Our study...

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Autores principales: Wiles, Louise K, Hibbert, Peter D, Stephens, Jacqueline H, Coiera, Enrico, Westbrook, Johanna, Braithwaite, Jeffrey, Day, Ric O, Hillman, Ken M, Runciman, William B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652459/
https://www.ncbi.nlm.nih.gov/pubmed/29025823
http://dx.doi.org/10.1136/bmjopen-2016-014048
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author Wiles, Louise K
Hibbert, Peter D
Stephens, Jacqueline H
Coiera, Enrico
Westbrook, Johanna
Braithwaite, Jeffrey
Day, Ric O
Hillman, Ken M
Runciman, William B
author_facet Wiles, Louise K
Hibbert, Peter D
Stephens, Jacqueline H
Coiera, Enrico
Westbrook, Johanna
Braithwaite, Jeffrey
Day, Ric O
Hillman, Ken M
Runciman, William B
author_sort Wiles, Louise K
collection PubMed
description INTRODUCTION: Despite widespread availability of clinical practice guidelines (CPGs), considerable gaps continue between the care that is recommended (‘appropriate care’) and the care provided. Problems with current CPGs are commonly cited as barriers to providing ’appropriate care'. Our study aims to develop and test an alternative method to keep CPGs accessible and up to date. This method aims to mitigate existing problems by using a single process to develop clinical standards (embodied in clinical indicators) collaboratively with researchers, healthcare professionals, patients and consumers. A transparent and inclusive online curated (purpose-designed, custom-built, wiki-type) system will use an ongoing and iterative documentation process to facilitate synthesis of up-to-date information and make available its provenance. All participants are required to declare conflicts of interest. This protocol describes three phases: engagement of relevant stakeholders; design of a process to develop clinical standards (embodied in indicators) for ‘appropriate care’ for common medical conditions; and evaluation of our processes, products and feasibility. METHODS AND ANALYSIS: A modified e-Delphi process will be used to gain consensus on ‘appropriate care’ for a range of common medical conditions. Clinical standards and indicators will be developed through searches of national and international guidelines, and formulated with explicit criteria for inclusion, exclusion, time frame and setting. Healthcare professionals and consumers will review the indicators via the wiki-based modified e-Delphi process. Reviewers will declare conflicts of interest which will be recorded and managed according to an established protocol. The provenance of all indicators and suggestions included or excluded will be logged from indicator inception to finalisation. A mixed-methods formative evaluation of our research methodology will be undertaken. ETHICS AND DISSEMINATION: Human Research Ethics Committee approval has been received from the University of South Australia. We will submit the results of the study to relevant journals and offer national and international presentations.
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spelling pubmed-56524592017-10-27 STANDING Collaboration: a study protocol for developing clinical standards Wiles, Louise K Hibbert, Peter D Stephens, Jacqueline H Coiera, Enrico Westbrook, Johanna Braithwaite, Jeffrey Day, Ric O Hillman, Ken M Runciman, William B BMJ Open Health Informatics INTRODUCTION: Despite widespread availability of clinical practice guidelines (CPGs), considerable gaps continue between the care that is recommended (‘appropriate care’) and the care provided. Problems with current CPGs are commonly cited as barriers to providing ’appropriate care'. Our study aims to develop and test an alternative method to keep CPGs accessible and up to date. This method aims to mitigate existing problems by using a single process to develop clinical standards (embodied in clinical indicators) collaboratively with researchers, healthcare professionals, patients and consumers. A transparent and inclusive online curated (purpose-designed, custom-built, wiki-type) system will use an ongoing and iterative documentation process to facilitate synthesis of up-to-date information and make available its provenance. All participants are required to declare conflicts of interest. This protocol describes three phases: engagement of relevant stakeholders; design of a process to develop clinical standards (embodied in indicators) for ‘appropriate care’ for common medical conditions; and evaluation of our processes, products and feasibility. METHODS AND ANALYSIS: A modified e-Delphi process will be used to gain consensus on ‘appropriate care’ for a range of common medical conditions. Clinical standards and indicators will be developed through searches of national and international guidelines, and formulated with explicit criteria for inclusion, exclusion, time frame and setting. Healthcare professionals and consumers will review the indicators via the wiki-based modified e-Delphi process. Reviewers will declare conflicts of interest which will be recorded and managed according to an established protocol. The provenance of all indicators and suggestions included or excluded will be logged from indicator inception to finalisation. A mixed-methods formative evaluation of our research methodology will be undertaken. ETHICS AND DISSEMINATION: Human Research Ethics Committee approval has been received from the University of South Australia. We will submit the results of the study to relevant journals and offer national and international presentations. BMJ Publishing Group 2017-10-11 /pmc/articles/PMC5652459/ /pubmed/29025823 http://dx.doi.org/10.1136/bmjopen-2016-014048 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Health Informatics
Wiles, Louise K
Hibbert, Peter D
Stephens, Jacqueline H
Coiera, Enrico
Westbrook, Johanna
Braithwaite, Jeffrey
Day, Ric O
Hillman, Ken M
Runciman, William B
STANDING Collaboration: a study protocol for developing clinical standards
title STANDING Collaboration: a study protocol for developing clinical standards
title_full STANDING Collaboration: a study protocol for developing clinical standards
title_fullStr STANDING Collaboration: a study protocol for developing clinical standards
title_full_unstemmed STANDING Collaboration: a study protocol for developing clinical standards
title_short STANDING Collaboration: a study protocol for developing clinical standards
title_sort standing collaboration: a study protocol for developing clinical standards
topic Health Informatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652459/
https://www.ncbi.nlm.nih.gov/pubmed/29025823
http://dx.doi.org/10.1136/bmjopen-2016-014048
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