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遗传咨询——咨询后阶段:I. 父母对不确定性的认知。

Genetic counseling--the postcounseling period: I. Parents' perceptions of uncertainty.

作者信息

Lippman-Hand A, Fraser F C

出版信息

Am J Med Genet. 1979;4(1):51-71. doi: 10.1002/ajmg.1320040108.

Abstract

To investigate how parents who have had genetic counseling perceive the problems created by being at risk, transcripts of open-ended, semistructured follow-up interviews with 53 counselees were analyzed qualitatively. Rate information, though recalled accurately by parents considering further childbearing, was discounted as impersonal, and subjects overwhelmingly perceived the chance of recurrence in binary form -- it either will or will not happen. By processing rates this way, they simplified probabilistic information and shifted their focus to the implications of being at risk and the potential impact of that which might or might not occur. The many uncertainties they faced, the "consequences" of being at risk that parents felt had to be resolved during the decision-making process, fell into 3 major categories: uncertainty that arose because of the ambiguous impact and meaning of having an affected child; uncertainty about how to make a choice and how others would view it, the burden of decision-making; and uncertainty about their ability to fulfill their roles as parents. These issues were perceived as part of the problem to be resolved and were consolidated into "scenarios" in which the parents "tried out the worst." This analysis of counselees' perceptions of the problems created by being at genetic risk suggests that parents may process the disparate facts of their situation in common ways that emphasize their uncertainty, and it indicates that how parents perceive factual information may be more important in orienting their deliberations than what these facts (diagnosis, prognosis, risks) actually are.

摘要

为了调查接受过遗传咨询的父母如何看待处于风险中所带来的问题,我们对53名咨询对象进行了开放式、半结构化的随访访谈,并对访谈记录进行了定性分析。尽管考虑再次生育的父母能够准确回忆发生率信息,但他们认为这些信息缺乏人情味而不予重视,而且受访者绝大多数以二元形式看待复发几率——要么会发生,要么不会发生。通过这种方式处理发生率,他们简化了概率信息,并将关注点转移到处于风险中的影响以及可能发生或不发生之事的潜在影响上。他们面临的诸多不确定性,即父母认为在决策过程中必须解决的处于风险中的“后果”,可分为三大类:因有患病子女所带来的影响和意义不明确而产生的不确定性;关于如何做出选择以及他人会如何看待该选择的不确定性,即决策负担;以及关于他们履行父母角色能力的不确定性。这些问题被视为有待解决的问题的一部分,并被整合为“情景”,在这些情景中父母“设想了最糟糕的情况”。对咨询对象对基因风险所带来问题的认知的这一分析表明,父母可能以强调自身不确定性的常见方式来处理自身情况中的不同事实,这表明在引导他们进行思考时,父母如何看待事实信息可能比这些事实(诊断、预后、风险)本身更为重要。

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