Failure mode and effects analysis: too little for too much?

被引:79
作者
Franklin, Bryony Dean [1 ,2 ,3 ]
Shebl, Nada Atef [3 ]
Barber, Nick [1 ,3 ]
机构
[1] UCL Sch Pharm, Ctr Medicat Safety & Serv Qual, London W6 8RF, England
[2] Imperial Coll Healthcare NHS Trust, Charing Cross Hosp, Dept Pharm, London W6 8RF, England
[3] UCL Sch Pharm, Dept Practice & Policy, London W6 8RF, England
关键词
D O I
10.1136/bmjqs-2011-000723
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Failure mode and effects analysis (FMEA) is a structured prospective risk assessment method that is widely used within healthcare. FMEA involves a multidisciplinary team mapping out a high-risk process of care, identifying the failures that can occur, and then characterising each of these in terms of probability of occurrence, severity of effects and detectability, to give a risk priority number used to identify failures most in need of attention. One might assume that such a widely used tool would have an established evidence base. This paper considers whether or not this is the case, examining the evidence for the reliability and validity of its outputs, the mathematical principles behind the calculation of a risk prioirty number, and variation in how it is used in practice. We also consider the likely advantages of this approach, together with the disadvantages in terms of the healthcare professionals' time involved. We conclude that although FMEA is popular and many published studies have reported its use within healthcare, there is little evidence to support its use for the quantitative prioritisation of process failures. It lacks both reliability and validity, and is very time consuming. We would not recommend its use as a quantitative technique to prioritise, promote or study patient safety interventions. However, the stage of FMEA involving multidisciplinary mapping process seems valuable and work is now needed to identify the best way of converting this into plans for action.
引用
收藏
页码:607 / 611
页数:5
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