Brinkmann Lisa, Schuetzmann Karsten, Richter-Appelt Hertha
Institute for Sex Research and Forensic Psychiatry, Center for Psychosocial Medicine, University Hospital Hamburg-Eppendorf, D-20246 Hamburg, Germany.
J Sex Med. 2007 Jul;4(4 Pt 1):964-80. doi: 10.1111/j.1743-6109.2007.00524.x.
Until now, there are only few studies that focus on the specific treatment experiences of people with intersexuality and evaluate their outcome in terms of psychological, physical, and social well-being. Further, the presentation of the patients' perspective is often neglected in research.
Overview of preliminary results of the Hamburg-Intersex-Study on gender assignment and medical history of adult subjects with intersexuality (disorders of sex development), as well as the patients retrospectively stated thoughts and feelings regarding these interventions.
Medical records from participants of the study were analyzed. The subjective attitudes and evaluation of the treatment measures were assessed with a self-constructed questionnaire. Data on psychological well-being were measured with the Brief Symptom Inventory.
In total, 37 adult participants (mean age 30.6 years) with following diagnosis were included: congenital adrenal hyperplasia, complete and partial androgen insensitivity syndrome, gonadal dysgenesis and disturbances of the androgen biosynthesis, such as 5 alpha reductase deficiency and 17 beta hydroxysteroid deficiency.
The majority of participants had (often multiple) genital surgery to correct the appearance of their genitalia and/or to enable sexual functioning. The diagnostic groups differ not only in amount and invasiveness of experienced surgical and medical treatment but also in the subjective and retrospective evaluation of the treatment measures and in the amount of reported psychological distress.
Many subjects stated to have experienced the medical procedures and care very negatively, whereby the aspects of secrecy, untruthfulness, and concealment were stated as most difficult and burdening.
到目前为止,仅有少数研究关注双性人的具体治疗经历,并从心理、身体和社会福祉方面评估其结果。此外,患者的观点在研究中常常被忽视。
概述汉堡双性人研究关于双性人(性发育障碍)成年受试者的性别指定和病史的初步结果,以及患者对这些干预措施的回顾性陈述的想法和感受。
分析研究参与者的病历。使用自行编制的问卷评估对治疗措施的主观态度和评价。使用简明症状量表测量心理健康数据。
总共纳入了37名成年参与者(平均年龄30.6岁),诊断如下:先天性肾上腺皮质增生症、完全和部分雄激素不敏感综合征、性腺发育不全以及雄激素生物合成障碍,如5α还原酶缺乏症和17β羟类固醇缺乏症。
大多数参与者接受了(通常是多次)生殖器手术,以矫正其生殖器外观和/或实现性功能。诊断组不仅在经历的手术和医疗治疗的数量和侵入性方面存在差异,而且在对治疗措施的主观和回顾性评价以及报告的心理困扰程度方面也存在差异。
许多受试者表示对医疗程序和护理的体验非常负面,其中保密、不诚实和隐瞒方面被认为是最困难和负担最重的。