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Factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey

OBJECTIVES: While national quality registries (NQRs) are suggested to provide opportunities for systematic follow-up and learning opportunities, and thus clinical improvements, features in registries and contexts triggering such processes are not fully known. This study focuses on one of the world&#...

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Autores principales: Eldh, Ann Catrine, Wallin, Lars, Fredriksson, Mio, Vengberg, Sofie, Winblad, Ulrika, Halford, Christina, Dahlström, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128910/
https://www.ncbi.nlm.nih.gov/pubmed/28128099
http://dx.doi.org/10.1136/bmjopen-2016-011562
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author Eldh, Ann Catrine
Wallin, Lars
Fredriksson, Mio
Vengberg, Sofie
Winblad, Ulrika
Halford, Christina
Dahlström, Tobias
author_facet Eldh, Ann Catrine
Wallin, Lars
Fredriksson, Mio
Vengberg, Sofie
Winblad, Ulrika
Halford, Christina
Dahlström, Tobias
author_sort Eldh, Ann Catrine
collection PubMed
description OBJECTIVES: While national quality registries (NQRs) are suggested to provide opportunities for systematic follow-up and learning opportunities, and thus clinical improvements, features in registries and contexts triggering such processes are not fully known. This study focuses on one of the world's largest stroke registries, the Swedish NQR Riksstroke, investigating what aspects of the registry and healthcare organisations facilitate or hinder the use of registry data in clinical quality improvement. METHODS: Following particular qualitative studies, we performed a quantitative survey in an exploratory sequential design. The survey, including 50 items on context, processes and the registry, was sent to managers, physicians and nurses engaged in Riksstroke in all 72 Swedish stroke units. Altogether, 242 individuals were presented with the survey; 163 responded, representing all but two units. Data were analysed descriptively and through multiple linear regression. RESULTS: A majority (88%) considered Riksstroke data to facilitate detection of stroke care improvement needs and acknowledged that their data motivated quality improvements (78%). The use of Riksstroke for quality improvement initiatives was associated (R(2)=0.76) with ‘Colleagues’ call for local results’ (p=<0.001), ‘Management Request of Registry data’ (p=<0.001), and it was said to be ‘Simple to explain the results to colleagues’ (p=0.02). Using stepwise regression, ‘Colleagues’ call for local results’ was identified as the most influential factor. Yet, while 73% reported that managers request registry data, only 39% reported that their colleagues call for the unit's Riksstroke results. CONCLUSIONS: While an NQR like Riksstroke demonstrates improvement needs and motivates stakeholders to make progress, local stroke care staff and managers need to engage to keep the momentum going in terms of applying registry data when planning, performing and evaluating quality initiatives.
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spelling pubmed-51289102016-12-02 Factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey Eldh, Ann Catrine Wallin, Lars Fredriksson, Mio Vengberg, Sofie Winblad, Ulrika Halford, Christina Dahlström, Tobias BMJ Open Health Services Research OBJECTIVES: While national quality registries (NQRs) are suggested to provide opportunities for systematic follow-up and learning opportunities, and thus clinical improvements, features in registries and contexts triggering such processes are not fully known. This study focuses on one of the world's largest stroke registries, the Swedish NQR Riksstroke, investigating what aspects of the registry and healthcare organisations facilitate or hinder the use of registry data in clinical quality improvement. METHODS: Following particular qualitative studies, we performed a quantitative survey in an exploratory sequential design. The survey, including 50 items on context, processes and the registry, was sent to managers, physicians and nurses engaged in Riksstroke in all 72 Swedish stroke units. Altogether, 242 individuals were presented with the survey; 163 responded, representing all but two units. Data were analysed descriptively and through multiple linear regression. RESULTS: A majority (88%) considered Riksstroke data to facilitate detection of stroke care improvement needs and acknowledged that their data motivated quality improvements (78%). The use of Riksstroke for quality improvement initiatives was associated (R(2)=0.76) with ‘Colleagues’ call for local results’ (p=<0.001), ‘Management Request of Registry data’ (p=<0.001), and it was said to be ‘Simple to explain the results to colleagues’ (p=0.02). Using stepwise regression, ‘Colleagues’ call for local results’ was identified as the most influential factor. Yet, while 73% reported that managers request registry data, only 39% reported that their colleagues call for the unit's Riksstroke results. CONCLUSIONS: While an NQR like Riksstroke demonstrates improvement needs and motivates stakeholders to make progress, local stroke care staff and managers need to engage to keep the momentum going in terms of applying registry data when planning, performing and evaluating quality initiatives. BMJ Publishing Group 2016-11-09 /pmc/articles/PMC5128910/ /pubmed/28128099 http://dx.doi.org/10.1136/bmjopen-2016-011562 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 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 Services Research
Eldh, Ann Catrine
Wallin, Lars
Fredriksson, Mio
Vengberg, Sofie
Winblad, Ulrika
Halford, Christina
Dahlström, Tobias
Factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey
title Factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey
title_full Factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey
title_fullStr Factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey
title_full_unstemmed Factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey
title_short Factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey
title_sort factors facilitating a national quality registry to aid clinical quality improvement: findings of a national survey
topic Health Services Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128910/
https://www.ncbi.nlm.nih.gov/pubmed/28128099
http://dx.doi.org/10.1136/bmjopen-2016-011562
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