PT - JOURNAL ARTICLE AU - Thomas A Willis AU - Suzanne Hartley AU - Liz Glidewell AU - Amanda Farrin AU - Michelle Collinson AU - Michael Holland AU - Paul Carder AU - Cheryl Hunter AU - David Meads AU - Claire Hulme AU - Robbie Foy TI - A cluster-randomised evaluation of an adaptable implementation strategy targeting ‘high impact’ indicators in primary care AID - 10.3399/bjgp18X696917 DP - 2018 Jun 01 TA - British Journal of General Practice PG - bjgp18X696917 VI - 68 IP - suppl 1 4099 - http://bjgp.org/content/68/suppl_1/bjgp18X696917.short 4100 - http://bjgp.org/content/68/suppl_1/bjgp18X696917.full SO - Br J Gen Pract2018 Jun 01; 68 AB - Background Recognised gaps between evidence and practice in primary care present particular implementation challenges when addressing multiple priorities.Aim To evaluate the effectiveness of a multifaceted, adaptable implementation package targeting four different ‘high impact’ indicators.Method We undertook two parallel, pragmatic cluster randomised trials using balanced incomplete block designs with parallel process evaluation. General practices in West Yorkshire, UK, were recruited using an ‘opt out’ process. The adaptable implementation package included audit and feedback, educational outreach visits and computerised support with embedded behaviour change techniques tailored to each indicator. Practices were randomised to packages targeting either type 2 diabetes control or risky prescribing of non-steroidal anti-inflammatory drugs, or packages targeting either anticoagulation in atrial fibrillation or blood pressure control in patients at high risk of cardiovascular events. Respective primary endpoints comprised: achievement of all recommended levels of haemoglobin A1c, blood pressure and cholesterol; risky prescribing levels; anticoagulation prescribing; and achievement of recommended blood pressure levels. Outcomes at 11 months used routinely collected data.Results 178 out of 244 eligible practices participated. The implementation package reduced risky prescribing (odds ratio 0.82; 97.5% confidence interval 0.67 to 0.99). There was no effect on other primary endpoints.Conclusion This highly pragmatic, robust evaluation suggests the value of targeting risky prescribing, given predictable population reductions in avoidable morbidity, deaths and hospital admissions. However, in broad terms, an adapted ‘one-size-fits-all’ approach did not consistently work, with no improvement for other targeted indicators.