Department of Physiotherapy, Monash University, Melbourne, Victoria, Australia.
Department of Psychology, University of British Columbia, Vancouver, British Columbia, Canada.
Psychooncology. 2018 Aug;27(8):1979-1986. doi: 10.1002/pon.4754. Epub 2018 May 16.
The population of adult survivors of childhood cancers (ASCCs) is growing, resulting in unique long-term challenges. This study explored experiences of perceived unmet ASCC survivorship needs.
We invited ASCCs to complete surveys sent through the cancer registry. Four open-ended questions allowed participants to write in comments. We analyzed responses to these open-ended questions thematically, employing a process of constant comparison.
Our sample included 94 ASCCs who completed open-ended questions (61 female; aged 20-78 years, mean age = 34.47, SD = 11.84, mean = 23.27 years post diagnosis). Identified themes included (1) overlooked experiences of distress; (2) lack of counseling: system, patient, and family barriers; (3) difficulty negotiating future life milestones exacerbated by lack of knowledge; and (4) dissatisfaction with service provision: past and present. Prevalent issues identified by participants included lack of supportive care to address needs, distress due to missed developmental milestones as a result of cancer, lack of knowledge about late-term and long-term effects of cancer treatment, and concern over absence of organized long-term follow-up.
Adult survivors of childhood cancers continue to experience unmet needs during their cancer diagnosis, treatment, and long into survivorship due to the treatment for cancer and ongoing side effects. Solutions could focus on addressing the needs of survivors to bridge system gaps and barriers. Specifically, there is a need to improve psychological interventions and transitions from pediatric to adult-care facilities.
儿童癌症幸存者(ASCC)的人口不断增加,导致了独特的长期挑战。本研究探讨了感知到的未满足的 ASCC 生存需求的经验。
我们邀请 ASCC 通过癌症登记处完成发送的调查。四个开放式问题允许参与者写入评论。我们对这些开放式问题进行了主题分析,采用了不断比较的过程。
我们的样本包括 94 名完成开放式问题的 ASCC(61 名女性;年龄 20-78 岁,平均年龄=34.47,标准差=11.84,平均诊断后 23.27 年)。确定的主题包括(1)被忽视的痛苦经历;(2)缺乏咨询:系统、患者和家庭障碍;(3)由于缺乏知识,难以协商未来的生活里程碑,这加剧了困难;(4)对服务提供的不满:过去和现在。参与者确定的普遍问题包括缺乏支持性护理来满足需求、由于癌症而错过发展里程碑的痛苦、缺乏对癌症治疗晚期和长期影响的了解,以及对缺乏有组织的长期随访的担忧。
由于癌症的治疗和持续的副作用,儿童癌症幸存者在癌症诊断、治疗和长期生存期间仍继续经历未满足的需求。解决方案可以集中在满足幸存者的需求上,以弥合系统差距和障碍。具体来说,需要改善心理干预和从儿科到成人护理机构的过渡。