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Methodological variability in detecting prescribing errors and consequences for the evaluation of interventions.

机译:检测处方错误和评估干预措施后果的方法学差异。

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PURPOSE: To compare four methods of detecting prescribing errors (PE) in the same patient cohorts before and after an intervention (computerised physician order entry; CPOE) and to determine whether the impact of CPOE is identified consistently by all methods. METHODS: PEs were identified using (1) prospective detection by ward pharmacist; (2) retrospective health record review; (3) retrospective use of a trigger tool and (4) spontaneous reporting over two separate 4-week periods on one surgical ward in a UK teaching hospital. RESULTS: We reviewed 93 patients pre- and 114 post-CPOE. Using all four methods, we identified 135 PE (10.7% of all medication orders) pre-CPOE, and 127 (7.9%) post-CPOE. There was little overlap in PE detected by the different methods: prospective detection identified 48 (36% of all PE) pre- and 30 (24%) post-CPOE; retrospective review (RR) revealed 93 (69%) pre- and 105 (83%) post-CPOE, trigger tool 0 pre- and 2 (2%) post-CPOE and spontaneous reporting 1 (1%) pre- and 1 (1%) post-CPOE. The calculated relative reduction in risk of PE was 50% using prospective data, 12% with RR and 26% using data from all four methods. CONCLUSIONS: In this study, each method predominantly identified different PE. A combination of methods may be required to understand the true effectiveness of different interventions.
机译:目的:比较在干预之前和之后(计算机医师订单输入; CPOE)在同一患者队列中检测处方错误(PE)的四种方法,并确定是否通过所有方法一致地确定了CPOE的影响。方法:采用以下方法鉴定PE:(1)病房药剂师的前瞻性检测; (2)回顾性健康记录审查; (3)回顾性使用触发工具,以及(4)在英国教学医院的一个外科病房中,在两个单独的4周期间内自发报告。结果:我们审查了93例CPOE之前和114例CPOE之后的患者。使用这四种方法,我们确定了CPOE前135例PE(占所有用药订单的10.7%)和CPOE后127例PE(占所有用药订单的7.9%)。通过不同方法检测到的PE几乎没有重叠:前瞻性检测发现CPOE前为48(占所有PE的36%)和CPOE后为30(占24%);回顾性审查(RR)显示,CPOE前为93(69%),CPOE后为105(83%),CPOE后触发工具为0,CPOE后为2(2%),并且自发报告1和1(1%)。 1%)。使用前瞻性数据计算得出的PE相对风险降低为50%,使用RR则为12%,使用所有四种方法的数据为26%。结论:在这项研究中,每种方法主要鉴定出不同的PE。可能需要使用多种方法来了解不同干预措施的真实有效性。

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