Ventres W B
Department of Family and Community Medicine, University of Arizona College of Medicine, Tucson 85724.
J Am Board Fam Pract. 1993 Mar-Apr;6(2):137-41.
The Patient Self-Determination Act of 1991 implicitly encourages physicians to discuss advance directives and no-code orders with their patients. The medical literature to date, however, has done little to place resuscitative decision making in the context of how physicians, patients, and families communicate with one another. This paper investigates how interactions between involved parties affect the process and outcome of this decision making.
Participant observation and open-ended interviews were conducted with patients, their families, resident physicians, and family medicine faculty members.
This report describes three social and cultural issues that commonly influence and shape the process of do-not-resuscitate decision making: judging competency and capacity, dealing with uncertainty, and recognizing attitudes toward death.
Improved understanding of the communicative process can facilitate the establishment of meaningful, therapeutic alliances between physicians, patients, and families at an influential juncture in the family life cycle.
1991年的《患者自主决定法案》含蓄地鼓励医生与患者讨论预立医疗指示和不进行心肺复苏医嘱。然而,迄今为止的医学文献在将复苏决策置于医生、患者和家属之间如何相互沟通的背景下所做甚少。本文探讨了相关各方之间的互动如何影响这一决策的过程和结果。
对患者、其家属、住院医师和家庭医学教员进行了参与观察和开放式访谈。
本报告描述了通常影响和塑造不进行心肺复苏决策过程的三个社会和文化问题:判断能力和行为能力、应对不确定性以及认识对死亡的态度。
更好地理解沟通流程有助于在家庭生命周期中的一个关键节点上,在医生、患者和家属之间建立有意义的治疗联盟。