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Two decades after legislation on identifiable donors in Sweden: are recipient couples ready to be open about using gamete donation?

机译:瑞典关于可识别的捐赠者的立法颁布后的二十年:受赠夫妇是否准备好接受使用配子捐赠的开放性?

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BACKGROUND Two decades after the introduction of Swedish legislation that allows children born as a result of gamete donation access to identifying information about the donor, a nationwide multicentre study on the psychosocial consequences of this legislation for recipients and donors of gametes was initiated in 2005. The aim of the present study was to investigate recipient couples' attitudes and behaviour regarding disclosure to offspring and others, attitudes towards genetic parenthood and perceptions of information regarding parenthood after donation. METHODS The present study is part of the prospective longitudinal 'Swedish study on gamete donation', including all fertility clinics performing donation treatment in Sweden. A consecutive cohort of 152 heterosexual recipient couples of donated oocytes (72% response) and 127 heterosexual recipient couples of donated sperm (81% response) accepted participation in the study. In connection with the donation treatment, male and female participants individually completed two questionnaires with study-specific instruments concerning disclosure, genetic parenthood and informational aspects. RESULTS About 90% of participants (in couples receiving anonymous donated gametes) supported disclosure and openness to the offspring concerning his/her genetic origin. Only 6% of all participants had not told other people about their donation treatment. Between 26 and 40% of participants wanted additional information/support about parenthood following donation treatment. CONCLUSIONS Two decades after the Swedish legislation of identifiable gamete donors, recipient couples of anonymously donated sperm and oocytes are relatively open about their treatment and support disclosure to offspring. Recipient couples may benefit from more information and support regarding parenthood after gamete donation. Further studies are required to follow-up on the future parents' actual disclosure behaviour directed to offspring.
机译:背景技术在瑞典立法允许通过配子捐赠而出生的孩子获得有关捐赠者身份的信息的立法出台后的二十年,这项立法对配子的接受者和捐赠者的心理社会后果的全国性多中心研究于2005年启动。本研究的目的是调查接受者夫妇对后代和其他人披露的态度和行为,对遗传父母的态度以及捐赠后对父母的信息的看法。方法本研究是前瞻性纵向“瑞典关于配子捐赠的研究”的一部分,包括瑞典所有进行捐赠治疗的生育诊所。连续的152例捐赠卵母细胞的异性受体对夫妇(72%应答)和127例捐赠精子的异性受体受体对(81%应答)接受了该研究。在捐赠治疗方面,男性和女性参与者分别完成了两份问卷调查表,其中包括披露,遗传育儿和信息方面的研究专用工具。结果大约90%的参与者(在接受匿名捐赠配子的夫妇中)支持对其后代的公开和公开性。所有参与者中只有6%的人没有告诉其他人有关他们的捐赠治疗的信息。 26%至40%的参与者希望在捐赠治疗后获得有关父母身份的其他信息/支持。结论在瑞典确定配子配体的立法出台后的二十年,匿名捐赠的精子和卵母细胞的接受者夫妇对治疗的态度相对开放,并向后代公开信息。配子捐赠后,接收夫妇可能会从有关父母的更多信息和支持中受益。需要进一步的研究来跟踪未来父母针对后代的实际披露行为。

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