1. Use and acceptability of an asthma diagnosis clinical decision support system for primary care clinicians: an observational mixed methods study.
- Author
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Daines L, Canny A, Donaghy E, Murray V, Campbell L, Stonham C, Milne H, Price D, Buchner M, Nelson L, Mair FS, Sheikh A, Bush A, McKinstry B, and Pinnock H
- Subjects
- Adolescent, Adult, Child, Child, Preschool, Female, Humans, Male, Young Adult, Attitude of Health Personnel, England, Primary Health Care, Qualitative Research, Scotland, Asthma diagnosis, Decision Support Systems, Clinical
- Abstract
There is uncertainty about how best to diagnose asthma, especially in primary care where mis-diagnosis is common. To address this, we developed a clinical decision support system (CDSS) for asthma diagnosis in children and young people (aged 5-25 years). This study explored the feasibility and acceptability of the CDSS in UK primary care. We recruited general practices from England and Scotland. The CDSS was available for use during routine consultations for six months. We analysed CDSS usage and, toward the end of the study, undertook qualitative interviews with clinicians who had used the CDSS. Within the 10 practices who completed the study, the CDSS was used by 75 out of 94 clinicians. 11 clinicians from 8 practices were interviewed. The CDSS was acceptable to participants who particularly commented on the ease of use and auto-population of information from the patient record. Barriers to use included the inability to record findings directly into the patient notes and a sense that, whilst possibly useful for trainees and junior colleagues, the CDSS would not necessarily lead to a change in their own practice. The CDSS was generally well received by primary care clinicians, though participants felt it would be most useful for trainees and less experienced colleagues., Competing Interests: Competing interests: C.S. reports unconditional honoraria via a Limited company for consultancy and delivery of education from AstraZeneca, Bedfont, Boehringer Inglehieim, Cheisi, GSK, Teva, and Trudell; policy lead PCRS and Co-chair of Early and Accurate Diagnosis working group of Taskforce for Lung Health. D.P. has advisory board membership with AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Novartis, Viatris, Teva Pharmaceuticals; consultancy agreements with AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Novartis, Viatris, Teva Pharmaceuticals; grants and unrestricted funding for investigator-initiated studies (conducted through Observational and Pragmatic Research Institute Pte Ltd.) from AstraZeneca, Chiesi, Viatris, Novartis, Regeneron Pharmaceuticals, Sanofi Genzyme, and UK National Health Service; payment for lectures/speaking engagements from AstraZeneca, Boehringer Ingelheim, Chiesi, Cipla, Inside Practice, GlaxoSmithKline, Medscape, Viatris, Novartis, Regeneron Pharmaceuticals and Sanofi Genzyme, Teva Pharmaceuticals; payment for travel/accommodation/meeting expenses from AstraZeneca, Boehringer Ingelheim, Novartis, Medscape, Teva Pharmaceuticals.; owns 74% of the social enterprise Optimum Patient Care Ltd. (Australia and UK) and 92.61% of Observational and Pragmatic Research Institute Pte Ltd. (Singapore); 5% shareholding in Timestamp which develops adherence monitoring technology; is peer reviewer for grant committees of the UK Efficacy and Mechanism Evaluation programme, and Health Technology Assessment; and was an expert witness for GlaxoSmithKline. H.P. has received fees for non-promotional talks in sponsored symposia from Teva and Sandoz Pharmaceuticals. The remaining authors declare no competing interests., (© 2024. The Author(s).)
- Published
- 2024
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