罗马尼亚患者不孕经历的现象学研究:女性视角

Ioana Silistraru, Anamaria Ciubară, R. Soroceanu, Ș. Roșca, A. Ciubotaru, Gabriela Simionescu
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引用次数: 0

摘要

最近的定性研究表明,不孕症的主观体验、患者叙述中的情绪、想法和问题表明,不孕症对社会心理的影响是真实存在的,患者需要长期的支持。本文从接受体外受精怀孕的患者角度出发,探讨了患者被诊断为女性或男性不孕症的经历。样本包括 17 名参与者,他们都是罗马尼亚雅西一家私人生殖健康和生育诊所的患者。根据半结构化访谈指南对患者进行了访谈,以获得有关不孕不育经历的信息,包括从诊断到试管婴儿手术的整个过程,无论采用哪种治疗方法。我们从定性的角度,采用现象学的方法对所获得的数据进行分析,从患者的角度描述和解释不孕不育的经历,以理解和加深诊断对个人、社会和夫妻生活的影响。从收集到的数据中发现了六个主题群,分别涉及对孕产的定义、个人不孕故事、一系列已确定的情绪、夫妻动态、感知到的社会支持和应对策略。大量文献越来越关注不孕症的生物医学方面。但是,如果能将与患者生活背景和主题相关的信息补充完整,就能为治疗的成功提供相关数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phenomenological Study of the Experience of Infertility in Romanian Patients: The Female Perspective
The subjective experience of infertility, the emotions, thoughts and problems stated in the patients' narratives show that thepsycho-social impact of infertility is real, and patients need permanent support, the recent qualitative studies suggest. Thepresent paper explores the patients' experiences with a diagnosis of female or male infertility from the perspective ofpatients undergoing IVF to become pregnant. The sample included 17 participants, patients of a private reproductivehealth and fertility clinic in Iasi, Romania. Patients were interviewed based on a semi-structured interview guide to obtaininformation about the infertility experience, from diagnosis to IVF procedures, regardless of the therapeutic approach.The data was enriched through observation notes. The data obtained were analyzed from a qualitative perspective, with aphenomenological approach, to describe and interpret the experience of infertility from the patient's perspective tounderstand and deepen the diagnosis's effect on personal, social and couple life. Six theme clusters emerged from thecollected data related to the perceived definition of maternity, the personal infertility story, the array of identifiedemotions, couple dynamics, perceived social support and coping strategies. The body of literature gives increased interestto the biomedical aspect of infertility. However, its completion with information related to the patient's life context and themeanings attributed to it provides relevant data for therapeutic success.
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