Dreps Douglas, Hyndman Bruce, Shepherd Marvin
Mercy Clinical Engineering Services, St. Louis, USA.
J Healthc Risk Manag. 2007;27(1):13-7. doi: 10.1002/jhrm.5600270104.
The quality of a device-related, accident investigation is largely determined by the clinical and technical data available to the investigators. After an event, traditional legal conflicts have tended to prevent full information sharing between the manufacturer and the risk manager of the healthcare facility. We propose that, under the guidance of a risk manager, a healthcare clinical engineer partner with an engineer from the manufacturer and each partner provide maximum information and focused attention on the investigation. The synergy of the partnership should provide a more effective investigation and an increased patient safety in the healthcare delivery system.
与设备相关的事故调查质量在很大程度上取决于调查人员可获得的临床和技术数据。事件发生后,传统的法律冲突往往会阻碍制造商与医疗机构风险管理者之间的全面信息共享。我们建议,在风险管理者的指导下,医疗机构的临床工程师与制造商的工程师合作,每个合作伙伴都提供最大程度的信息,并对调查给予重点关注。这种合作关系的协同效应应能在医疗服务系统中提供更有效的调查,并提高患者安全性。