Author Affiliations: Centre of Diaconia and Professional Practise (Ms Breistig) and Faculty of Health Sciences (Dr Tveit Sekse), VID Specialized University, Bergen; Department of Health and Caring Sciences, Western Norway University of Applied Sciences, Stord (Dr Thorkildsen); and Department of Obstetrics and Gynecology, Haukeland University Hospital, Bergen (Dr Tveit Sekse), Norway.
Cancer Nurs. 2024;47(5):E327-E335. doi: 10.1097/NCC.0000000000001252. Epub 2023 Jun 5.
Gynecological cancer survivors experience a variety of challenges after discharge from hospital treatment. Cancer support and rehabilitation are recognized as significant facilitators for quality of life in survivorship but are reported to be insufficient by gynecological cancer survivors.
To describe the lived experiences of gynecological cancer survivors and how their needs for follow-up should be met following recently completed treatment.
This study used a phenomenological hermeneutic design with individual in-depth interviews with 20 women after recently completed cancer treatment. Transcribed interviews were analyzed with the Lindseth and Norberg phenomenological hermeneutic method.
Four themes were identified: "a brutal transition to life after cancer," "fear of recurrence overshadowing the existence," "a need for professional support," and "information is not given unless asked for."
After completing gynecological cancer treatment, the fear of cancer recurrence is dominating, regardless of prognosis and diagnosis. At the same time, information and support from healthcare professionals are described as lacking. Participants expressed a need to be contacted directly as a formal routine by healthcare professionals after cancer treatment with cancer-specific information as this may alleviate the existential suffering that the cancer experience brings.
A person-centered, systematic follow-up rehabilitation is needed as a continuation of the care provided during cancer treatment. Future research is needed to explore the impact on women's quality of life when gynecologic-specific information is given in advance of hospital discharge after completing treatment.
妇科癌症幸存者在出院后会经历各种挑战。癌症支持和康复被认为是提高生存质量的重要因素,但妇科癌症幸存者报告称这些支持和康复措施不足。
描述妇科癌症幸存者的生活体验,以及在最近完成治疗后应如何满足他们的随访需求。
本研究采用现象学解释学设计,对 20 名最近完成癌症治疗的女性进行了个体深入访谈。采用林德塞和诺伯格的现象学解释学方法对转录的访谈进行分析。
确定了四个主题:“癌症后生活的残酷过渡”、“对复发的恐惧笼罩着存在”、“对专业支持的需求”和“除非询问,否则不会提供信息”。
完成妇科癌症治疗后,无论预后和诊断如何,对癌症复发的恐惧都是主导因素。同时,医疗保健专业人员的信息和支持被描述为不足。参与者表示,希望在癌症治疗结束后,直接通过医疗保健专业人员进行有针对性的、正式的常规联系,并提供癌症相关信息,这可能会减轻癌症经历带来的生存痛苦。
需要进行以人为中心的、系统的随访康复,作为癌症治疗期间提供的护理的延续。需要进一步研究,探讨在完成治疗后出院前提前提供妇科特定信息对女性生活质量的影响。