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This publication is distributed under a CC ____________ license. ____________________________________________________ Downloaded from http://bmjopen.bmj.com/ on January 9, 2018 - Published by group.bmj.com Open Access Research Process evaluation of the Data-driven Quality Improvement in Primary Care (DQIP) trial: case study evaluation of adoption and maintenance of a complex intervention to reduce high-risk primary care prescribing Aileen Grant,1 Tobias Dreischulte,2,3 Bruce Guthrie3 To cite: Grant A, ABSTRACT Strengths and limitations of this study Dreischulte T, Guthrie B. Objective: To explore how different practices Process evaluation of the responded to the Data-driven Quality Improvement in ▪ Data-driven Quality This is a comprehensive, preplanned process Primary Care (DQIP) intervention in terms of their Improvement in Primary Care evaluation which includes a third of all practices (DQIP) trial: case study adoption of the work, reorganisation to deliver the which participated in the Data-driven Quality evaluation of adoption and intended change in care to patients, and whether Improvement in Primary Care (DQIP) stepped- maintenance of a complex implementation was sustained over time. wedge cluster-randomised trial. intervention to reduce high- Design: Mixed-methods parallel process evaluation of ▪ The evaluation sampled four practices which risk primary care prescribing. a cluster trial, reporting the comparative case study of rapidly implemented the intervention and all six BMJ Open 2017;7:e015281. purposively selected practices. practices which failed to implement the interven- doi:10.1136/bmjopen-2016- Setting: Ten (30%) primary care practices tion to some degree. 015281 participating in the trial from Scotland, UK. ▪ A strength of the study is the use of qualitative Results: Four practices were sampled because they data from interviews and observational field ▸ Prepublication history and had large rapid reductions in targeted prescribing. They notes, and quantitative data about key trial pro- additional material is all had internal agreement that the topic mattered, cesses and practice-level effectiveness to available. To view please visit made early plans to implement including assigning examine implementation in detail. the journal (http://dx.doi.org/ ▪ 10.1136/bmjopen-2016- responsibility for work and regularly evaluated A limitation is that we did not collect any data 015281). progress. However, how they internally organised the from practices prior to them receiving the work varied. Six practices were sampled because they intervention. had initial implementation failure. Implementation Received 25 November 2016 failure occurred at different stages depending on Revised 7 February 2017 practice context, including internal disagreement about care to patients in ways which suited their context, Accepted 14 February 2017 whether the work was worthwhile, and intention but emphasising the importance of flexibility in any future lack of capacity to implement or sustain widespread implementation. implementation due to unfilled posts or sickness. Trial registration number: NCT01425502. Practice context was not fixed, and most practices with initial failed implementation adapted to deliver at least some elements. All interviewed participants valued the intervention because it was an innovative way to address on an important aspect of safety (although 1School of Health Sciences one of the non-interviewed general practitioners in one BACKGROUND and Sport, University of practice disagreed with this). Participants felt that High-risk prescribing in primary care is a reviewing existing prescribing did influence their future Stirling, Stirling, UK major concern for healthcare systems inter- 2Medicines Governance Unit, initiation of targeted drugs, but raised concerns about NHS Tayside, Dundee, UK sustainability. nationally. Between 2% and 4% of emer- 3Population Health Sciences gency hospital admissions are caused by Conclusions: Variation in implementation and 12 Division, Medical Research effectiveness was associated with differences in how preventable adverse drug events (ADEs), fi 34 Institute, University of practices valued, engaged with and sustained the work at signi cant cost to healthcare systems. Dundee, Dundee, UK required. Initial implementation failure varied with A large proportion of these admissions Correspondence to practice context, but was not static, with most are caused by commonly prescribed drugs, Dr Aileen Grant; practices at least partially implementing by the end of with non-steroidal anti-inflammatory drugs [email protected] the trial. Practices organised their delivery of changed (NSAIDs) and antiplatelets being frequently Grant A, et al. BMJ Open 2017;7:e015281. doi:10.1136/bmjopen-2016-015281 1 Downloaded from http://bmjopen.bmj.com/ on January 9, 2018 - Published by group.bmj.com Open Access implicated, causing gastrointestinal, cardiovascular and ulcer or bleeding (risk ratio (RR) 0.66, 95% CI 0.51 to – renal adverse events.5 7 0.86) and heart failure (RR 0.73, 95% CI 0.56 to 0.95).12 The Data-driven Quality Improvement in Primary Care Alongside the main trial, we designed a mixed- (DQIP) intervention was systematically developed and methods process evaluation,13 14 based on a cluster- – optimised8 10 and comprised three intervention compo- randomised trial process evaluation framework which we nents: (1) professional education about the risks of developed.15 Our framework emphasises the importance NSAIDs and antiplatelets via an outreach visit by a of considering two levels of intervention delivery and pharmacist; (2) financial incentives to review patients at response that often characterise cluster-randomised the highest risk of NSAID and antiplatelet ADEs, split trials of behaviour change interventions (although their into a participation fee of £350 and £15 per patient importance will depend on intervention design). The reviewed and (3) access to a web-based IT tool to iden- first is the intervention that is delivered to clusters, tify such patients and support structured review. The which respond by adopting (or not) the intervention intervention was evaluated in a pragmatic stepped-wedge and integrating it with existing work. The second is the cluster-randomised controlled trial11 in 33 practices change in care which the cluster professionals deliver to from one Scottish health board, where all participating patients. In DQIP, the delivery of the intervention to pro- practices received the intervention but were randomised fessionals was predefined, intended to be delivered with to one of 10 different start dates.8 Across all practices, high fidelity across all practices by the research team, targeted high-risk prescribing fell from 3.7% immedi- whereas the intervention delivered to patients was at the ately before to 2.2% at the end of the intervention discretion of practices, who decided whether and how period (adjusted OR 0.63 (95% CI 0.57 to 0.68), they reviewed patients and whether to change prescrib- p<0.0001). The intervention only incentivised review of ing. We used this framework to structure our parallel ongoing high-risk prescribing, but led to reductions in process evaluation, mapping data collection to a logic ongoing (adjusted OR 0.60, 95% CI 0.53 to 0.67) and model of how the DQIP intervention was expected to ‘new’ high-risk prescribing (adjusted OR 0.77, 95% CI work (figure 1). 0.68 to 0.87). Notably, reductions in high-risk prescrib- The aim of this analysis is to examine how different ing were sustained in the year after financial incentives practices responded to the intervention delivered to stopped. In addition, there were significant reductions them by the research team in terms of their adoption of in emergency hospital admissions with gastrointestinal the work, their reorganisation to deliver the intended Figure 1 DQIP process evaluation framework. DQIP, Data-driven Quality Improvement in Primary Care. 2 Grant A, et al. BMJ Open 2017;7:e015281. doi:10.1136/bmjopen-2016-015281 Downloaded from http://bmjopen.bmj.com/ on January 9, 2018 - Published by group.bmj.com Open Access change in care to patients and whether implementation were field notes made by AG during the educational out- was sustained over time. reach visits (EOV), detailing response to the educational component and informatics tool training. Data gener- ation took place between September 2011 and METHODS December 2013 in parallel with intervention implemen- The design was a mixed-method comparative case study, 16 17 tation. All data have been anonymised, including by with general practices the

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