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瑞典移植协调员对新《移植法》及实施一年后的捐赠者登记册的体验。

The Swedish Transplant Coordinators' experience of the new Transplantation Act and the donor register 1 year after implementation.

作者信息

Bergström C, Svensson L, Wolfbrandt A, Lundell M

机构信息

Department of Transplantation Surgery, University Hospital, Uppsala, Sweden.

出版信息

Transplant Proc. 1997 Dec;29(8):3232-3. doi: 10.1016/s0041-1345(97)00887-7.

Abstract

The register has been a support for the coordinators in Sweden when the relatives have said one thing and the deceased person another in regards to donation. Most of the staff are positive to the register and the safety regulations around it. Most often it has been a relief for the relatives that the deceased person's wishes also have been documented in the register or in the donor card. Most decisions are still, however, made by relatives. There is still a need for more positive information about transplantation and its value.

摘要

当亲属和逝者在器官捐赠问题上说法不一致时,该登记册为瑞典的协调员提供了支持。大多数工作人员对登记册及其相关安全规定持积极态度。对于逝者的意愿也已记录在登记册或捐赠卡中这一点,亲属们大多感到宽慰。然而,大多数决定仍然由亲属做出。仍然需要更多关于器官移植及其价值的正面信息。

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