Watson M C, Bond C M, Johnston M, Mearns K
Department of General Practice and Primary Care, University of Aberdeen, Westburn Road, Aberdeen AB25 2AY, UK.
Qual Saf Health Care. 2006 Aug;15(4):244-50. doi: 10.1136/qshc.2005.014035.
The importance of theory in underpinning interventions to promote effective professional practice is gaining recognition. The Medical Research Council framework for complex interventions has assisted in promoting awareness and adoption of theory into study design. Human error theory has previously been used by high risk industries but its relevance to healthcare settings and patient safety requires further investigation. This study used this theory as a framework to explore non-prescription medicine supply from community pharmacies. The relevance to other healthcare settings and behaviours is discussed.
A 25% random sample was made of 364 observed consultations for non-prescription medicines. Each of the 91 consultations was assessed by two groups: a consensus group (stage 1) to identify common problems with the consultation process, and an expert group (stages 2 and 3) to apply human error theory to these consultations. Paired assessors (most of whom were pharmacists) categorised the perceived problems occurring in each consultation (stage 1). During stage 2 paired assessors from an expert group (comprising patient safety experts, community pharmacists and psychologists) considered whether each consultation was compliant with professional guidelines for the supply of pharmacy medicines. Each non-compliant consultation identified during stage 2 was then categorised as a slip/lapse, mistake, or violation using human error theory (stage 3).
During stage 1 most consultations (n = 75, 83%) were deemed deficient in information exchange. At stage 2, paired assessors varied in attributing non-compliance to specific error types. Where agreement was achieved, the error type most often selected was "violation" (n = 27, 51.9%, stage 3). Consultations involving product requests were less likely to be guideline compliant than symptom presentations (OR 0.30, 95% CI 0.10 to 0.95, p = 0.05).
The large proportion of consultations classified as violations suggests that either pharmacy staff are unaware of professional guidelines and thus do not follow them (therefore these acts would not be violations), or that they knowingly violate the guidelines due to reasons that need further research. The methods presented here could be used in other healthcare settings to explore healthcare professional behaviour and to develop strategies to promote patient safety and effective professional practice.
理论在支持促进有效专业实践的干预措施中的重要性正日益得到认可。医学研究理事会的复杂干预框架有助于提高对理论的认识,并将其纳入研究设计。人类错误理论此前已被高风险行业所采用,但其与医疗环境及患者安全的相关性仍需进一步研究。本研究以该理论为框架,探讨社区药房的非处方药供应情况,并讨论其与其他医疗环境及行为的相关性。
从364次观察到的非处方药咨询中抽取25%的随机样本。91次咨询中的每一次都由两组人员进行评估:一个共识小组(第1阶段)以确定咨询过程中的常见问题,以及一个专家小组(第2和第3阶段)将人类错误理论应用于这些咨询。配对评估人员(大多数为药剂师)对每次咨询中出现的感知问题进行分类(第1阶段)。在第2阶段,来自专家小组(由患者安全专家、社区药剂师和心理学家组成)的配对评估人员考虑每次咨询是否符合药房药品供应的专业指南。然后,使用人类错误理论将第2阶段确定的每次不符合规定的咨询分类为失误/疏忽、错误或违规行为(第3阶段)。
在第1阶段,大多数咨询(n = 75,83%)被认为在信息交流方面存在不足。在第2阶段,配对评估人员在将不符合规定归因于特定错误类型方面存在差异。达成一致意见时,最常选择的错误类型是“违规行为”(n = 27,51.9%,第3阶段)。与症状表现相比,涉及产品请求的咨询不太可能符合指南要求(比值比0.30,95%置信区间0.10至0.95,p = 0.05)。
被归类为违规行为的咨询比例很高,这表明要么药房工作人员不了解专业指南,因此没有遵循(因此这些行为不会是违规行为),要么他们出于需要进一步研究的原因故意违反指南。这里介绍的方法可用于其他医疗环境,以探索医疗专业人员的行为,并制定促进患者安全和有效专业实践的策略。