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Psychological consultation before living kidney donation: finding out and handling problem cases.

机译:活体肾脏捐献前的心理咨询:发现并处理有问题的病例。

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BACKGROUND: Since 1996, a team of medical psychologists, nephrologists, and urologists at Heidelberg University Hospital has developed a family-oriented consultation procedure for donors, recipients, and family members before living kidney transplantation. Qualitative content analyses of these consultations and their follow-up histories are presented, with particular focus on "problem cases." METHODS: Sixty-seven consultation interviews were explored by rating family interaction, consultee-consultant interaction, decision-making process, and intervention strategies in problem cases. Subsequently, 33 catamnestic interviews 1 year or more after living donation were explored by qualitative content analysis for donor and recipient quality of life, quality of relationships, and health status. RESULTS: Generally, donors show themselves to be eager; recipients appear more reluctant. Expectations focus on spontaneity and a "normal life." Fears are usually expressed not about oneself but about the partner involved. Types of confrontation with possible complications are anxious avoidance, active consideration, and optimistic fatalism. Past family experiences of medical traumata may influence content and level of anxiety. Problem cases are characterized by unilaterally dependent close relationships, unrealistic expectations, anxious avoidance of problem confrontation, and negative experiences with the medical system. At follow-up, the majority are in good medical and psychological health. Few donors and recipients are suffering from disappointed expectations or unexpected treatment side effects. CONCLUSIONS: The Heidelberg consultation setting has proven useful for allowing open discussion about critical issues. In problem cases, prescribing a moratorium instead of rejecting donation helps to relax consultation anxiety. Psychological support after transplantation seems to be indicated for a minority with typical first-year problems.
机译:背景:自1996年以来,海德堡大学医院的医学心理学家,肾脏病学家和泌尿科医师团队为活体肾脏移植之前的捐赠者,接受者和家庭成员制定了面向家庭的咨询程序。提出了对这些咨询及其后续历史的定性内容分析,尤其关注“问题案例”。方法:通过评估家庭互动,被咨询者与顾问的互动,决策过程以及对问题案例的干预策略,对67个咨询访谈进行了探讨。随后,通过定性内容分析,探讨了捐献后1年或更长时间的33次连锁访谈,以分析捐赠者和接受者的生活质量,亲戚关系和健康状况。结果:总体上,捐助者表现出了自己的渴望。收件人显得更加不情愿。期望集中在自发性和“正常生活”上。恐惧通常不是针对自己,而是针对所涉及的伴侣。可能引起并发症的对抗类型包括焦虑回避,积极考虑和乐观宿命论。过去家庭遭受医疗创伤的经历可能会影响焦虑的程度和程度。问题案例的特征是单方面依赖紧密的关系,不切实际的期望,急于避免问题对抗以及对医疗系统的负面经历。随访时,大多数患者的身体和心理健康状况良好。很少有捐赠者和接受者遭受失望的期望或意外的治疗副作用。结论:海德堡咨询设置被证明对允许就关键问题进行公开讨论很有用。在有问题的情况下,开处方暂停而不是拒绝捐赠有助于缓解咨询焦虑。对于具有典型的第一年问题的少数人,似乎表明了移植后的心理支持。

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