Interventions to optimise the outputs of national clinical audits to improve the quality of health care: a multi-method study including RCT
Autor: | Willis TA; Leeds Institute of Health Sciences, University of Leeds, Leeds, UK, Wright-Hughes A; Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK, Weller A; Centre for Human-Computer Interaction Design, City, University of London, London, UK, Alderson SL; Leeds Institute of Health Sciences, University of Leeds, Leeds, UK, Wilson S; Centre for Human-Computer Interaction Design, City, University of London, London, UK, Walwyn R; Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK, Wood S; Leeds Institute of Health Sciences, University of Leeds, Leeds, UK, Lorencatto F; Centre for Behaviour Change, University College London, London, UK, Farrin A; Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK, Hartley S; Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK, Francis J; School of Health Sciences, City, University of London, London, UK, Seymour V; School of Health Sciences, City, University of London, London, UK, Brehaut J; Ottawa Hospital Research Institute, Ottawa, ON, Canada, Colquhoun H; Department of Occupational Science and Occupational Therapy, University of Toronto, Toronto, ON, Canada, Grimshaw J; Ottawa Hospital Research Institute, Ottawa, ON, Canada, Ivers N; Women’s College Hospital, Toronto, ON, Canada, Feltbower R; Leeds Institute for Data Analytics, University of Leeds, Leeds, UK, Keen J; Leeds Institute of Health Sciences, University of Leeds, Leeds, UK, Brown BC; Centre for Health Informatics, University of Manchester, Manchester, UK; Centre for Primary Care, University of Manchester, Manchester, UK, Presseau J; Ottawa Hospital Research Institute, Ottawa, ON, Canada; School of Epidemiology and Public Health, University of Ottawa, Ottawa, ON, Canada, Gale CP; Leeds Institute for Data Analytics, University of Leeds, Leeds, UK; Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK; Department of Cardiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK, Stanworth SJ; Transfusion Medicine, NHS Blood and Transplant (NHSBT), Oxford, UK; Department of Haematology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK; Radcliffe Department of Medicine, University of Oxford, Oxford, UK; NIHR Oxford Biomedical Research Centre, Oxford, UK, Foy R; Leeds Institute of Health Sciences, University of Leeds, Leeds, UK |
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Jazyk: | angličtina |
Zdroj: | 2022 Jun. |
DOI: | 10.3310/QBBZ1124 |
Abstrakt: | Background: National clinical audit programmes aim to improve patient care by reviewing performance against explicit standards and directing action towards areas not meeting those standards. Their impact can be improved by (1) optimising feedback content and format, (2) strengthening audit cycles and (3) embedding randomised trials evaluating different ways of delivering feedback. Objectives: The objectives were to (1) develop and evaluate the effects of modifications to feedback on recipient responses, (2) identify ways of strengthening feedback cycles for two national audits and (3) explore opportunities, costs and benefits of national audit participation in a programme of trials. Design: An online fractional factorial screening experiment (objective 1) and qualitative interviews (objectives 2 and 3). Setting and Participants: Participants were clinicians and managers involved in five national clinical audits – the National Comparative Audit of Blood Transfusions, the Paediatric Intensive Care Audit Network, the Myocardial Ischaemia National Audit Project, the Trauma Audit & Research Network and the National Diabetes Audit – (objective 1); and clinicians, members of the public and researchers (objectives 2 and 3). Interventions: We selected and developed six online feedback modifications through three rounds of user testing. We randomised participants to one of 32 combinations of the following recommended specific actions: comparators reinforcing desired behaviour change; multimodal feedback; minimised extraneous cognitive load for feedback recipients; short, actionable messages followed by optional detail; and incorporating ‘the patient voice’ (objective 1). Main Outcome Measures: The outcomes were intended actions, including enactment of audit standards (primary outcome), comprehension, user experience and engagement (objective 1). Results: For objective 1, the primary analysis included 638 randomised participants, of whom 566 completed the outcome questionnaire. No modification independently increased intended enactment of audit standards. Minimised cognitive load improved comprehension (+0.1; p = 0.014) and plans to bring audit findings to colleagues’ attention (+0.13, on a –3 to +3 scale; p = 0.016). We observed important cumulative synergistic and antagonistic interactions between modifications, participant role and national audit. The analysis in objective 2 included 19 interviews assessing the Trauma Audit Research Network and the National Diabetes Audit. The identified ways of strengthening audit cycles included making performance data easier to understand and guiding action planning. The analysis in objective 3 identified four conditions for effective collaboration from 31 interviews: compromise – recognising capacity and constraints; logistics – enabling data sharing, audit quality and funding; leadership – engaging local stakeholders; and relationships – agreeing shared priorities and needs. The perceived benefits of collaboration outweighed the risks. Limitations: The online experiment assessed intended enactment as a predictor of actual clinical behaviour. Interviews and surveys were subject to social desirability bias. Conclusions: National audit impacts may be enhanced by strengthening all aspects of feedback cycles, particularly effective feedback, and considering how different ways of reinforcing feedback act together. Future Work: Embedded randomised trials evaluating different ways of delivering feedback within national clinical audits are acceptable and may offer efficient, evidence-based and cumulative improvements in outcomes. Trial Registration: This trial is registered as ISRCTN41584028. Funding Details: This project was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme and will be published in full in Health and Social Care Delivery Research ; Vol. 10, No. 15. See the NIHR Journals Library website for further project information. (Copyright © 2022 Willis et al. This work was produced by Willis et al. under the terms of a commissioning contract issued by the Secretary of State for Health and Social Care. This is an Open Access publication distributed under the terms of the Creative Commons Attribution CC BY 4.0 licence, which permits unrestricted use, distribution, reproduction and adaption in any medium and for any purpose provided that it is properly attributed. See: https://creativecommons.org/licenses/by/4.0/. For attribution the title, original author(s), the publication source – NIHR Journals Library, and the DOI of the publication must be cited.) |
Databáze: | MEDLINE |
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