透過您的圖書館登入
IP:18.222.121.170

摘要


Background: Although it is now possible to achieve permanent remission in a large percentage of gynecologic cancer (GC) cases, many GC patients in remission experience side effects or complications that influence their physical function and family relationships. Compared with other types of cancer patients, survivors of GC face greater challenges in terms of physical and psychological adaptations, and many of these do not receive sufficient assistance. An in-depth understanding of the lived experiences and demands of GC survivors is key to constructing comprehensive related healthcare services. Purpose: The aim of this study was to understand the lived experience of GC survivors in Taiwan to help their return to a healthy life. Methods: This was a phenomenological study. Twenty-three survivors of GC participated in semistructured interviews that were held in a private environment. The transcripts were based on synchronous recordings from the interviews. Giorgi's phenomenology analysis was adopted for data analysis. Results: Three themes with six subthemes were extracted from the data, including (a) the inner struggle of living with cancer and recurrence: repeatedly exploring the causes of cancer and treatment and facing a fear of cancer recurrence, (b) the interpretation and adjustment to cancer treatment: filled with fluctuating physical and mental distress and working to adopt a different perspective, and (c) the long passage of finding a desirable lifestyle: adjusting to long-term coexistence with side effects and realizing the strength of society, body, and mind. Conclusions/Implications for Practice: The journey of rehabilitation for GC survivors is very long. The participants in this study faced different respective challenges during the diagnosis, treatment, and adjustment phases. Conventional disease-oriented medical care cannot satisfy the requirements of cancer patients because of patient-decentralized services. Our results indicate that GC survivors face diverse problems, both physically and mentally. Healthcare professionals should work to facilitate the psychological adjustment of cancer survivors and provide timely professional advice in combination with social resources. These results may serve as a reference for cancer care professionals who are navigating healthcare services.

參考文獻


Abayomi, J.,Kirwan, J.,Hackett, A.,Bagnall, G.(2005).A study to investigate women's experiences of radiation enteritis following radiotherapy for cervical cancer.Journal of Human Nutrition and Dietetics.18(5),353-363.
Akyüz, A.,Güvenó, G.,Üstünsöz, A.,Kaya, T.(2008).Living with gynecologic cancer: Experience of women and their partners.Journal of Nursing Scholarship.40(3),241-247.
Ashing-Giwa, K. T.,Kagawa-Singer, M.,Padilla, G. V.,Tejero, J. S.,Hsiao, E.,Chhabra, R.,Tucker, M. B.(2004).The impact of cervical cancer and dysplasia: A qualitative, multiethnic study.Psycho-Oncology.13(10),709-728.
Booth, K.,Beaver, K.,Kitchener, H.,O'Neill, J.,Farrell, C.(2005).Women's experiences of information, psychological distress and worry after treatment for gynaecological cancer.Patient Education and Counseling.56(2),225-232.
Burns, M.,Costello, J.,Ryan-Woolley, B.,Davidson, S.(2007).Assessing the impact of late treatment effects in cervical cancer: An exploratory study of women's sexuality.European Journal of Cancer Care (English Language Edition).16(4),364-372.

被引用紀錄


葉月珍、黃曉峰、呂建興(2019)。婦癌婦女焦慮憂鬱及生活品質之相關因素探討護理雜誌66(6),43-53。https://doi.org/10.6224/JN.201912_66(6).07
TSAI, L. Y., WANG, K. L., TSAI, J. M., & TSAY, S. L. (2019). Chinese Version of the Assessment of Survivor Concerns Scale for Gynecological Cancer Survivors: A Psychometric Study in Taiwan. The Journal of Nursing Research, 27(5), 1-7-003. https://doi.org/10.1097/jnr.0000000000000323

延伸閱讀