1Program in Medicine and Human Values, California Pacific Medical Center, San Francisco, CA. 2Lorry I. Lokey Graduate School of Business, and School of Public Policy, Mills College, Oakland, CA. 3Department of Family and Preventive Medicine, University of California, San Diego, CA. 4Department of Medical History and Ethics, University of Washington School of Medicine, Seattle, WA.
Crit Care Med. 2014 Apr;42(4):824-30. doi: 10.1097/CCM.0000000000000034.
To investigate whether the proactive intervention of a clinical ethicist in cases of prolonged lengths of stay in a critical care setting reduces nonbeneficial treatment while increasing perceived patient/surrogate and provider satisfaction and reducing associated costs. Nonbeneficial treatment is defined here as the use of life-sustaining treatments delivered to patients who had been in the ICU for 5 days and did not survive to discharge.
Prospective randomized exploratory trial from October 2007 to February 2010 in the adult ICU of a large, urban, not-for-profit community hospital.
Medical/surgical ICU of California Pacific Medical Center, a large tertiary not-for-profit hospital in San Francisco, CA.
Three hundred eighty-four patients with ICU lengths of stay of five days or greater. Patients were randomized to either an intervention arm (Proactive Ethics Intervention) (n = 174) or control arm (n = 210). There were 56 patients in the intervention arm and 52 patients in the control arm who did not survive to discharge.
Proactive ethics intervention involves a trained bioethicist in the care of all ICU patients with a length of stay greater than or equal to 5 days. The intervention used a nine step process model designed to look for manifest or latent ethics conflicts and address them.
The primary outcome measures were days in the ICU; overall length of hospital stay; mortality; nonbeneficial treatments, for example, provision of nutritional support; surrogate and survivor satisfaction, and cost. The intervention and control arms showed no significant difference in mortality. Proactive Ethics Intervention, at the 95% CI, was not associated with reductions of overall length of stay (23 d for intervention and 21 d for control, p = 0.74), ICU days (11 in each arm, p = 0.91), life-sustaining treatments (days on ventilator: intervention, 14.6; control, 13.7; p = 0.74; days receiving artificial nutrition and hydration: intervention, 16.5; control, 15.9; p = 0.85), or cost ($167,350.00 for intervention and $164,670.00 for control, p =0.92) in patients who did not survive to discharge. Perceptions of quality of care by patients and providers showed no difference between intervention and control arms.
Our study finds that Proactive Ethics Intervention, provided to all patients in a critical care setting for 5 days, and before an ethical conflict has been recognized, is ineffective in reducing overall length of hospital stay, ICU days, nonbeneficial treatments, or hospital costs. It is also not effective in increasing perceptions of quality of care by patients or providers.
探讨在重症监护病房(ICU)中,临床伦理学家主动干预是否可以减少无益治疗,同时提高患者/代理人和医护人员满意度,并降低相关成本,从而降低患者的住院时间。无益治疗是指对 ICU 住院时间超过 5 天且未存活出院的患者使用生命支持治疗。
2007 年 10 月至 2010 年 2 月在加利福尼亚太平洋医疗中心的成人 ICU 进行的前瞻性随机探索性试验。
位于加利福尼亚州旧金山的大型非营利性社区医院——加州太平洋医疗中心的内科/外科 ICU。
384 名 ICU 住院时间为 5 天或更长的患者。将患者随机分为干预组(主动伦理干预)(n=174)或对照组(n=210)。干预组中有 56 名患者和 52 名患者未存活出院。
主动伦理干预涉及对 ICU 中所有住院时间大于或等于 5 天的患者进行培训。该干预措施使用了九步流程模型,旨在发现明显或潜在的伦理冲突并加以解决。
主要结局指标为 ICU 住院天数、总住院天数、死亡率、无益治疗(例如提供营养支持)、代理人和幸存者满意度以及成本。干预组和对照组的死亡率无显著差异。主动伦理干预组(95%置信区间)与降低总住院时间(干预组 23 天,对照组 21 天,p=0.74)、ICU 住院时间(每组 11 天,p=0.91)、生命支持治疗(呼吸机使用天数:干预组 14.6 天,对照组 13.7 天,p=0.74;接受人工营养和水合治疗的天数:干预组 16.5 天,对照组 15.9 天,p=0.85)或成本(干预组 167350.00 美元,对照组 164670.00 美元,p=0.92)之间无显著差异。未存活出院的患者对医护人员的护理质量感知无组间差异。
我们的研究发现,在重症监护病房中,对所有住院时间超过 5 天的患者,在识别到伦理冲突之前,提供主动伦理干预并不能降低总住院时间、ICU 住院时间、无益治疗或住院费用。它也不能增加患者或医护人员对护理质量的感知。