School of Women's and Children's Health, University of New South Wales, Kensington, New South Wales, Australia.
Qual Health Res. 2012 Aug;22(8):1102-13. doi: 10.1177/1049732312448542. Epub 2012 Jun 6.
In this study we explored the psychosocial experiences of melanoma survivors at high risk of developing new primary disease. A total of 20 survivors (9 men, 11 women, mean age 57.6 years) completed a semistructured telephone interview, exploring melanoma-related beliefs and experiences, psychological adjustment to melanoma risk, and supportive care needs. Participants perceived melanoma as potentially terminal and reported persistent worries about the possibility of developing new or metastatic disease. Fear of developing a new melanoma endured for years after treatment completion and, for some, created a pervasive sense of uncertainty. Still, not a single participant sought formal emotional support to address his or her melanoma-related concerns. Belief in the benefits of early intervention, including self- and clinical skin examination, provided a sense of control and a recommended course of action in an otherwise uncontrollable situation. The expertise of the High Risk Clinic physicians was perceived as instrumental in creating a sense of reassurance.
在这项研究中,我们探讨了高发性原发性疾病风险的黑色素瘤幸存者的社会心理体验。共有 20 名幸存者(9 名男性,11 名女性,平均年龄 57.6 岁)完成了半结构化电话访谈,探讨了与黑色素瘤相关的信念和经验、对黑色素瘤风险的心理调整以及支持性护理需求。参与者认为黑色素瘤可能是致命的,并报告说他们一直担心可能会患上新的或转移性疾病。对治疗后新黑色素瘤发展的恐惧持续了数年,对某些人来说,这造成了一种普遍的不确定性。尽管如此,没有一个参与者寻求正式的情感支持来解决他或她与黑色素瘤相关的问题。相信早期干预的好处,包括自我和临床皮肤检查,在这种无法控制的情况下提供了一种控制感和建议的行动方案。高危诊所医生的专业知识被认为是产生安慰感的关键因素。