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Experiences of Living with Tongue Cancer Rie Hatta 1,2 , Michiko Inagaki 3 , Keiko Tasaki 3 , Tomomi Horiguchi 3 1Division of Health Sciences, Graduate School of Medical, Pharmaceutical, and Health Sciences, Kanazawa University 2Kanazawa University Hospital 3Faculty of Health Sciences, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University Keyword: 舌がん , 喪失 , 体験 , 生活 , 現象学 , tongue cancer , loss , experience , daily lives , phenomenology pp.112-120
Published Date 2021/12/31
  • Abstract
  • Reference

 The purpose of this study is to clarify how patients with tongue cancer attach meaning to their experiences up through the present after diagnosis and surgery through to the present, and to deepen medical professionals' understanding of patients, as well as to derive suggestions for future nursing practice.

 The study's design was a qualitative and descriptive study based on phenomenology: unstructured interviews were conducted with seven participants to collect data, which were analyzed based on a phenomenological method.

 As a result of the analysis, four themes were derived from ten meaning units: the difficulty of receiving recognition as a cancer patient before diagnosis, and the need for postoperative determination to protect themselves from the cancer despite already being a patient; regularly experiencing occasions that particularly remind the patient that they have tongue cancer; feeling awkward around other people due to impaired articulation caused by partial or complete removal of the tongue; and starting to try to meet the expectations of the doctor who has worked to cure the disease and to save their life.

 These themes represent the patients' feelings and behaviors as they develop and are diagnosed with tongue cancer, beginning with pain in the tongue, their embarrassment at losing their tongue, and their daily lives as tongue cancer patients, trying to adapt socially despite difficulties.

 The results suggested the importance of nurses understanding the patients' situations, and the need to assist them in living with acceptance of their status as cancer survivors, becoming accustomed to their new eating methods, and living in society in a way that involves relationships with others.


Copyright © 2021, Japanese Society of Cancer Nursing All rights reserved.

基本情報

電子版ISSN 2189-7565 印刷版ISSN 0914-6423 日本がん看護学会

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