性别和性别差异在持续体征症状的公众污名化:一个系统的审查
Aranka V Ballering1, Peter L B J Lucassen2, Donald G van Tol3
1University of Groningen, University Medical Center Groningen, Department of Psychiatry, Groningen, the Netherlands; Ghent University, Faculty of Political and Social Sciences, Department of Sociology, Ghent, Belgium.
Social science & medicine (1982)
|July 12, 2025
概括
关于公众对持续体征症状 (PSS) 的耻辱感的研究表明,由于质量不佳的研究,没有明显的性别或性别差异. 需要更严格的研究来理解PSS的耻辱感.
科学领域:
- 医学社会学 医学社会学
- 精神病学是一个精神病学.
- 性别研究是性别研究.
背景情况:
- 持续的身体症状 (PSS) 往往会受到公众的耻辱.
- 了解性别和性别如何影响这种污名化至关重要,但研究不足.
研究的目的:
- 系统地审查和评估关于性别和性别差异的研究质量,以公开污名化PSS.
- 综合现有证据,并确定文献中的空白.
主要方法:
- 在六个主要数据库中进行系统的文献审查.
- 从2664个记录中包含12项研究 (10个定量标签,2个定性/混合方法).
- 系统的数据提取和质量评估由两个独立审查员进行.
主要成果:
- 关于PSS公共污名化的性别和/或性别差异没有确定一致的模式.
- 在测量PSS,性别,性别和污名化方面观察到显著的异质性.
- 大多数被纳入的研究质量低,偏差风险高.
结论:
- 关于PSS公众耻辱感中的性别和性别差异的高质量研究很少.
- 测量的异质性阻碍了确定一致的模式.
- 未来的研究应该采用强大的方法,验证的措施,并考虑交叉性和跨文化背景.
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