a Centre for Health Research, University of Western Sydney , Sydney , Australia .
Psychol Health. 2013;28(12):1370-90. doi: 10.1080/08870446.2013.811242. Epub 2013 Jun 28.
There is consistent evidence that health care professionals (hcps) are not addressing the sexual information and support needs of people with cancer. Thirty-eight Australian hcps across a range of professions working in cancer care were interviewed, to examine constructions of sexuality post-cancer, the subject positions adopted in relation to sexual communication, and the ways in which discourses and subject positions shape information provision and communication about sexuality. Participants constructed sexual changes post-cancer in physical, psychological and relational terms, and positioned such changes as having the potential to significantly impact on patient and partner well-being. This was associated with widespread adoption of a discourse of psychosocial support, which legitimated discussion of sexual changes within a clinical consultation, to alleviate distress, dispel myths and facilitate renegotiation of sexual practices. However, this did not necessarily translate into patient-centred practice outcomes, with the majority of participants positioning personal, patient-centred and situational factors as barriers to the discussion of sex within many clinical consultations. This included: absence of knowledge, confidence and comfort; positioning sex as irrelevant or inappropriate for some people; and limitations of the clinical context. In contrast, those who did routinely discuss sexuality adopted a subject position of agency, responsibility and confidence.
有确凿的证据表明,医疗保健专业人员(hcps)并未满足癌症患者的性信息和支持需求。我们采访了 38 名来自澳大利亚不同癌症护理专业的 hcps,以研究癌症后对性的构建、与性交流相关的主体位置以及话语和主体位置如何塑造有关性的信息提供和交流。参与者从身体、心理和关系方面构建了癌症后的性变化,并将这些变化定位为有可能对患者和伴侣的健康产生重大影响。这与广泛采用心理社会支持话语有关,该话语使在临床咨询中讨论性变化合法化,以减轻痛苦,消除误解并促进重新协商性行为。然而,这并不一定转化为以患者为中心的实践结果,大多数参与者将个人、以患者为中心和具体情况的因素定位为在许多临床咨询中讨论性的障碍。这包括:缺乏知识、信心和舒适度;将性定位为对某些人来说不相关或不适当;以及临床环境的限制。相比之下,那些经常讨论性的人则采取了主动、责任和自信的主体位置。