Narrative review of European healthcare benchmarking experiences: shared goals, different focuses and formats (Preprint)

2021 ◽  
Author(s):  
Anna García-Altés ◽  
Cristina Adroher ◽  
Viky Morón ◽  
Boi Ruiz

BACKGROUND Benchmarking experiences have been flourishing in Europe during the last years with the idea of improving healthcare quality. OBJECTIVE This paper aims to review the European benchmarking experiences, analysing their main characteristics and highlighting common and differential ones. METHODS The identification of benchmarking experiences was based on the list of European countries for which there exists an electronic “HiT health system review”. Predefined variables were identified, mainly data sources, formats, topics, and target audiences. RESULTS 14 benchmarking experiences were identified. Most of them are governmental. All of them are web-based. The easiness to navigate through the websites and materials and to understand them varies among experiences. Most common data sources are registries. Few experiences include patient experience indicators. None of them explicitly mentions if they use results as the basis to start quality improvement efforts. CONCLUSIONS Benchmarking is essential for transparency and accountability, and to support improvement. To do this effectively it must reconcile important and potentially conflicting goals: meaningful accountability, requiring real consequences from underperformance, and an environment that encourages open and honest reporting. Enhancing reporting websites is needed.

2020 ◽  
Vol 19 (1) ◽  
Author(s):  
Benjamin Jones ◽  
David Heslop ◽  
Reema Harrison

Abstract Background It is well established that Aboriginal and Torres Strait Islander populations face considerable health inequities, exacerbated by poorer healthcare quality. Patient experience is recognised as a major contributing factor to healthcare quality and outcomes, therefore, enriched knowledge of the patient experiences of Aboriginal and Torres Strait Islander populations is critical to redress health inequities. This review synthesises evidence of the healthcare experiences amongst Aboriginal and Torres Strait Islander patients through a metanarrative synthesis of qualitative literature. Methods A systematic search strategy was developed and applied to six electronic databases between January 2000 and July 2019. Titles and abstracts were screened before applying the inclusion criteria to full text articles. A meta-narrative synthesis was undertaken. Results Fifty-four publications were identified from four research traditions; each with a unique conceptualisation of patient experience. Three themes emerged that demonstrate Aboriginal and Torres Strait Islander patient experiences are informed by 1) beliefs about wellbeing and healthcare provision, 2) their level of trust in the healthcare system, and 3) individual and community health system interactions. The findings highlight a range of aspects of patient experience that were important to participating Aboriginal and Torres Strait Islanders in the included studies but not captured currently in health system surveys. Conclusion This review highlights the influence of beliefs about health and wellbeing on the patient experience amongst Aboriginal and Torres Strait Islander populations in the Australian health system. Patient experiences were informed by past experience and their trust in the health system. The different factors influencing patient experience and the gravity of their influence must be considered in current approaches to capturing patient experience data collection methods. Trial registration PROSPERO (ID: CRD42019134765).


2020 ◽  
Vol 9 (4) ◽  
pp. e001104
Author(s):  
Pamela Mathura ◽  
Miriam Li ◽  
Natalie McMurtry ◽  
Narmin Kassam

2010 ◽  
Vol 19 (5) ◽  
pp. 416-419 ◽  
Author(s):  
C. Liu ◽  
J. Babigumira ◽  
A. Chiunda ◽  
A. Katamba ◽  
I. Litvak ◽  
...  

2016 ◽  
Vol 29 (5) ◽  
pp. 176-182 ◽  
Author(s):  
G. Ross Baker ◽  
Carol Fancott ◽  
Maria Judd ◽  
Patricia O’Connor

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