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患者在冷冻胚胎处置方面偏好的变化。

Changes in patient preferences in the disposal of cryopreserved embryos.

作者信息

Newton C R, Fisher J, Feyles V, Tekpetey F, Hughes L, Isacsson D

机构信息

Reproductive Endocrinology and Infertility, University Hospital, London Health Sciences Centre, London, Ontario, Canada N6A 5A5.

出版信息

Hum Reprod. 2007 Dec;22(12):3124-8. doi: 10.1093/humrep/dem287. Epub 2007 Oct 24.

Abstract

BACKGROUND

The disposal of unused cryopreserved embryos can be a difficult decision for patients and the existence of unclaimed embryos raises ethical concerns for clinics. This study examined changes in patients' preferences for disposition of unused embryos and the relevance of a two-stage process for obtaining consent.

METHODS

Patients who had not returned for cryopreserved embryos for over 5 years were contacted and asked to specify their current preferences for embryo disposition. These preferences were compared with dispositional choices made at the time of embryo freezing.

RESULTS

Over one-third of patients had not returned for cryopreserved embryos within 5 years, and 31% of these declined to provide an updated directive. Those with a live birth through treatment were more likely to provide a new directive and more likely to choose to discard rather than donate embryos for research. Prior to IVF, the majority of non-returnees had elected to donate unused embryos for research, but 59% of all couples changed their minds after treatment.

CONCLUSIONS

Changes in preferences for embryo disposition was linked to treatment outcome and highlighted the need for a two-stage process to obtain fully informed consent. In this Canadian sample, patients' affinity for research declined after treatment.

摘要

背景

对于患者而言,如何处理未使用的冷冻胚胎可能是一个艰难的决定,而无人认领的胚胎的存在也引发了诊所对伦理问题的担忧。本研究调查了患者对未使用胚胎处置偏好的变化,以及分两阶段获取同意的相关性。

方法

联系那些超过5年未前来处理冷冻胚胎的患者,要求他们明确其目前对胚胎处置的偏好。将这些偏好与胚胎冷冻时所做的处置选择进行比较。

结果

超过三分之一的患者在5年内未前来处理冷冻胚胎,其中31%拒绝提供最新的指示。通过治疗活产的患者更有可能提供新的指示,也更有可能选择丢弃胚胎而非捐赠用于研究。在体外受精之前,大多数未回来处理胚胎的患者选择捐赠未使用的胚胎用于研究,但所有夫妇中有59%在治疗后改变了主意。

结论

胚胎处置偏好的变化与治疗结果相关,并凸显了分两阶段获取充分知情同意的必要性。在这个加拿大样本中,患者在治疗后对研究的意愿降低。

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