Centre for Medication Safety and Service Quality, Imperial College Healthcare NHS Trust, London, UK.
Pharmacoepidemiol Drug Saf. 2009 Nov;18(11):992-9. doi: 10.1002/pds.1811.
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.
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.
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.
In this study, each method predominantly identified different PE. A combination of methods may be required to understand the true effectiveness of different interventions.
比较同一患者队列在干预(计算机化医师医嘱录入;CPOE)前后使用四种方法检测处方错误(PE)的效果,并确定 CPOE 是否能被所有方法一致识别。
在英国一所教学医院的一个外科病房,通过(1)病房药师的前瞻性检测;(2)回顾性病历审查;(3)回顾性使用触发工具;(4)在两个独立的 4 周期间自发报告,使用这四种方法分别在干预前后识别 PE。
我们共回顾了 93 名干预前患者和 114 名干预后患者。使用这四种方法,我们在干预前识别出 135 例 PE(所有药物医嘱的 10.7%),在干预后识别出 127 例(7.9%)。不同方法检测到的 PE 几乎没有重叠:前瞻性检测在干预前识别出 48 例(所有 PE 的 36%)和 30 例(24%),在干预后;回顾性审查(RR)在干预前发现 93 例(69%)和 105 例(83%),触发工具在干预前识别出 0 例和 2 例(2%),在干预后;自发报告在干预前识别出 1 例(1%)和 1 例(1%),在干预后。使用前瞻性数据计算出的 PE 风险相对减少 50%,使用 RR 计算出的风险减少 12%,使用所有四种方法计算出的风险减少 26%。
在这项研究中,每种方法主要识别出不同的 PE。可能需要结合使用多种方法来了解不同干预措施的真正效果。