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Evaluation of a pharmacist-led actionable audit and feedback intervention for improving medication safety in UK primary care: An interrupted time series analysis

机译:评估药剂师LED的可操作审计和反馈干预,以改善英国初级保健治疗的药物安全性:中断时间序列分析

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Background We evaluated the impact of the pharmacist-led Safety Medication dASHboard (SMASH) intervention on medication safety in primary care. Methods and findings SMASH comprised (1) training of clinical pharmacists to deliver the intervention; (2) a web-based dashboard providing actionable, patient-level feedback; and (3) pharmacists reviewing individual at-risk patients, and initiating remedial actions or advising general practitioners on doing so. It was implemented in 43 general practices covering a population of 235,595 people in Salford (Greater Manchester), UK. All practices started receiving the intervention between 18 April 2016 and 26 September 2017. We used an interrupted time series analysis of rates (prevalence) of potentially hazardous prescribing and inadequate blood-test monitoring, comparing observed rates post-intervention to extrapolations from a 24-month pre-intervention trend. The number of people registered to participating practices and having 1 or more risk factors for being exposed to hazardous prescribing or inadequate blood-test monitoring at the start of the intervention was 47,413 (males: 23,073 [48.7%]; mean age: 60 years [standard deviation: 21]). At baseline, 95% of practices had rates of potentially hazardous prescribing (composite of 10 indicators) between 0.88% and 6.19%. The prevalence of potentially hazardous prescribing reduced by 27.9% (95% CI 20.3% to 36.8%, p 0.001) at 24 weeks and by 40.7% (95% CI 29.1% to 54.2%, p 0.001) at 12 months after introduction of SMASH. The rate of inadequate blood-test monitoring (composite of 2 indicators) reduced by 22.0% (95% CI 0.2% to 50.7%, p = 0.046) at 24 weeks; the change at 12 months (23.5%) was no longer significant (95% CI ?4.5% to 61.6%, p = 0.127). After 12 months, 95% of practices had rates of potentially hazardous prescribing between 0.74% and 3.02%. Study limitations include the fact that practices were not randomised, and therefore unmeasured confounding may have influenced our findings. Conclusions The SMASH intervention was associated with reduced rates of potentially hazardous prescribing and inadequate blood-test monitoring in general practices. This reduction was sustained over 12 months after the start of the intervention for prescribing but not for monitoring of medication. There was a marked reduction in the variation in rates of hazardous prescribing between practices.
机译:背景技术我们评估了药剂师LED安全药物仪表板(SMASH)干预对初级保健药物安全性的影响。方法和调查结果粉碎(1)培训临床药剂师,以提供干预; (2)基于Web的仪表板,提供可操作,患者级反馈; (3)药剂师审查个体风险患者,并启动补救措施或建议将全科医生做好事。它是在英国萨尔福德(大曼彻斯特)的435,595人口的43个一般性做法中实施。所有做法都开始接受2016年4月18日至2017年9月26日之间的干预。我们使用了潜在危险规定和血液试验监测不足的中断时间序列分析(患病率),比较了观察到的速度从24-外推月前介入趋势。在干预措施开始对参与实践的人数和具有1个或更多危险因素的人数为危险处方或血液试验监测不足为47,413(男性:23,073 [48.7%];意思年龄:60岁[标准差:21])。在基线时,95%的实践具有潜在危险的处方的税率(10个指标的复合材料)0.88%和6.19%。潜在危险规定的患病率降低了27.9%(95%CI 20.3%至36.8%,P <0.001),在引言后12个月后120.7%(95%CI 29.1%至54.2%,P <0.001)粉碎。血液试验监测(2个指标的复合材料)的速率不足22.0%(95%CI 0.2%至50.7%,p = 0.046); 12个月(23.5%)的变化不再有显着(95%CIα.4.5%至61.6%,P = 0.127)。 12个月后,95%的实践潜在危险规定的税率为0.74%和3.02%。研究限制包括实践不随机的事实,因此未测量的混乱可能影响了我们的发现。结论粉碎干预措施与潜在危险规定的率降低有关,并且在一般实践中血液试验监测不足。这种减少在开展后的处方后12个月内持续,但不用于监测药物。实践之间有害规定的危险率的变化有明显减少。

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