高潮后疾病综合症及其对自尊和人际关系的影响:一项调查。

IF 2.5 3区 医学 Q2 UROLOGY & NEPHROLOGY
Luke N Maietta, Isaac Bronson, Michael Cabral, Cameron Stokes, Karla Radillo Mendoza, Olivia Johnson, Dipavo Banerjee, Anthony J Rothschild, Rachel S Rubin
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引用次数: 0

摘要

性高潮后疾病综合征(POIS)是一种罕见的医学病症,其特征是受影响个体在射精后出现一系列令人痛苦的身体和认知症状。对于影响POIS患者的自尊和关系因素之间复杂的相互作用,我们知之甚少。本研究调查了POIS对亲密关系以及孤立感和污名感的影响,包括与个人和伴侣对症状的控制有关的问题。此外,它旨在为解决这一患者群体及其伴侣的社会心理问题提供一个临床框架。83名POIS患者(76.3%白人,37.5%本科学历,73.8%中等或更高收入)完成了性功能障碍归因量表(SDAS),作为更大规模调查研究的一部分。调查通过社交媒体、在线群组和论坛进行分发,包括reddit子版块:“POIS”、Twitter和“POISCENTER”,并于5月21日至6月9日之间完成。本次调查提供了参与者的描述性、探索性和人口学数据。POIS患者很可能报告自己无法控制自己的症状(81.9%),感觉自己的症状“总是存在”(96.4%),并感觉自己应该为性功能障碍负责(60.2%)。总体而言,80.7%的人报告说他们的症状对他们的关系产生了负面影响,37.3%的人报告说他们在过去一年内没有性生活。我们的结果可以帮助提供者了解POIS患者的经历,并为他们推荐适当的资源。进一步的研究可以使用先进的分析和定性技术来更好地阐明这一群体的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-orgasmic illness syndrome and its effects on self esteem and relationships: a survey.

Post-Orgasmic Illness Syndrome (POIS) is a rare medical condition characterized by a range of distressing physical and cognitive symptoms that occur following ejaculation in affected individuals. Little is known about the complex interaction between self-esteem and relationship factors that affect those living with POIS. This study investigated the impact of POIS on intimate relationships and feelings of isolation and stigmatization, including questions related to personal and partner control over symptoms. Furthermore, it aims to provide a clinical framework for addressing the psychosocial concerns of this patient population and their partners. Eighty-three patients (76.3% white, 37.5% with Bachelor's degree, 73.8% middle income or higher) with POIS completed the Sexual Dysfunction Attribution Scale (SDAS) as part of the larger survey study. Surveys were distributed via social media, online groups, and forums including the subreddit: "POIS", Twitter, and "POISCENTER" and were completed between 05/21/24-06/09/24. Descriptive, exploratory, and demographic data of the participants are provided from this survey. Patients with POIS were likely to report feeling no personal control over their symptoms (81.9%), feeling that their symptoms would "always be present" (96.4%), and feeling that they were personally to blame for their sexual dysfunction (60.2%). Overall, 80.7% reported that their symptoms negatively affected their relationships, and 37.3% reported not having sex within the past year. Our results can help providers to understand the experiences of patients with POIS and equip them to recommend the appropriate resources. Further research may use advanced analytical and qualitative techniques to better elucidate this population's challenges.

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来源期刊
International Journal of Impotence Research
International Journal of Impotence Research 医学-泌尿学与肾脏学
CiteScore
4.90
自引率
19.20%
发文量
140
审稿时长
>12 weeks
期刊介绍: International Journal of Impotence Research: The Journal of Sexual Medicine addresses sexual medicine for both genders as an interdisciplinary field. This includes basic science researchers, urologists, endocrinologists, cardiologists, family practitioners, gynecologists, internists, neurologists, psychiatrists, psychologists, radiologists and other health care clinicians.
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