Sears Samuel F, Conti Jamie B
Am J Cardiol. 2006 Aug 15;98(4):565-7. doi: 10.1016/j.amjcard.2006.02.066. Epub 2006 Jul 7.
The product recall of an implantable cardioverter defibrillator (ICD) creates a potentially stressful event for patients. This study briefly describes the psychological adjustment of patients with implantable devices and makes recommendations for the management of device recalls and adverse outcomes to minimize psychological distress. Because the occurrence of ICD-specific fears and symptoms of anxiety are the most common psychological symptoms experienced by ICD recipients, a comprehensive care plan to attend to recall procedures and patient distress is needed. It is suggested that recalls do not affect all ICD patients equally, with risk factors for poor psychological adjustment to ICDs including younger age (< 50 years), shock experience, and female gender that may be associated with increased recall anxiety. Specific recommendations for device recall management include formalizing clinic responses to recall before and after implantation and innovative uses of patient support systems to communicate recall responses.
植入式心脏复律除颤器(ICD)的产品召回对患者来说是一个潜在的压力事件。本研究简要描述了植入式设备患者的心理调适情况,并就设备召回及不良后果的管理提出建议,以尽量减少心理困扰。由于ICD特定恐惧和焦虑症状的出现是ICD接受者最常见的心理症状,因此需要一个全面的护理计划来处理召回程序和患者困扰。研究表明,召回对所有ICD患者的影响并不相同,心理调适不佳的风险因素包括年龄较小(<50岁)、电击经历以及女性性别,这些因素可能与召回焦虑增加有关。设备召回管理的具体建议包括规范植入前后诊所对召回的应对措施,以及创新利用患者支持系统来传达召回应对措施。