Division of Pediatric Medicine, Hospital for Sick Children, Toronto, Ontario, M5G 1X8, Canada.
Acad Pediatr. 2009 Sep-Oct;9(5):360-365.e1. doi: 10.1016/j.acap.2009.04.007. Epub 2009 Jul 28.
To quantify admission medication discrepancies in a tertiary-care, general pediatric population, to describe their clinical importance and associated factors, and to assess a screening approach to pharmacist involvement.
A total of 272 patients were studied prospectively at hospital admission. The study pharmacist performed a medication history and compared it to physicians' admission medication orders. Discrepancies between the 2 were coded as intentional but undocumented or unintentional. Unintentional discrepancies were rated for potential to cause harm by 3 physicians. Additional data collected included patients' reason for admission and presence of chronic conditions, whether physicians used a medication reconciliation form, the characteristics of patients' home medication regimen, and the time required to perform a pharmacist history and reconciliation. Interrater reliability and associations between baseline characteristics and discrepancy rates were explored.
Eighty patients (30%) had at least one undocumented intentional discrepancy (range, 0-7). At least one unintentional discrepancy (range, 0-9) was found in 59 patients (22%). Of the unintentional discrepancies, 23% had moderate and 6% had severe potential to cause discomfort or deterioration. Ratings were similar among the 3 physicians. Characteristics associated with higher risk of clinically important discrepancies were: use of the medication reconciliation form, > or =4 prescription medications, and antiepileptic drug use. Logistic regression revealed that only the variable > or =4 medications was independently associated with clinically important discrepancies.
Admission medication errors are common in this tertiary-care, general pediatric population, and nearly a third represent potential adverse events. The use of a medication reconciliation form by physicians without pharmacist involvement does not appear to reduce errors. A cutoff of > or =4 prescription medications is highly sensitive for identifying patients at risk of clinically important discrepancies.
定量分析三级保健综合儿科人群入院用药差异,描述其临床重要性及相关因素,并评估药师参与的筛选方法。
前瞻性研究 272 例入院患者。研究药师进行用药史记录并与医师入院时的用药医嘱进行比较。用药差异分为有目的但未记录和无目的。3 名医师对无目的差异进行潜在致害性评估。收集的其他数据包括患者入院原因和慢性病情况、医师是否使用用药核对单、患者家庭用药方案特征以及药师进行用药史记录和核对所需时间。探索组内一致性和基线特征与差异率之间的关系。
80 例(30%)患者至少存在 1 项未记录的有目的用药差异(范围 0-7)。59 例(22%)患者至少存在 1 项无目的用药差异(范围 0-9)。23%的无目的差异有中度潜在致害性,6%有严重潜在致害性。3 名医师的评估结果相似。与高风险临床重要差异相关的特征包括:使用用药核对单、>或=4 种处方药和使用抗癫痫药。Logistic 回归分析显示,只有>或=4 种药物这一变量与临床重要差异独立相关。
在该三级保健综合儿科人群中,入院用药错误较为常见,近三分之一的差异可能造成不良事件。医师使用未经药师参与的用药核对单似乎并未减少错误。处方药物>或=4 种是识别有临床重要差异风险患者的高度敏感指标。