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  1. 紀要

看護師が捉える膠原病患者の体験

https://jrccn.repo.nii.ac.jp/records/39
https://jrccn.repo.nii.ac.jp/records/39
74300f30-c2f1-4fcd-a9a7-44e37836a547
名前 / ファイル ライセンス アクション
本文.pdf 本文 (646.4 kB)
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Item type 紀要論文 / Departmental Bulletin Paper(1)
公開日 2019-04-22
タイトル
タイトル 看護師が捉える膠原病患者の体験
言語 ja
タイトル
タイトル Nurses' perspectives on experience of collagen disease patients
言語 en
言語
言語 jpn
キーワード
言語 ja
主題Scheme Other
主題 膠原病
キーワード
言語 ja
主題Scheme Other
主題 看護師
キーワード
言語 ja
主題Scheme Other
主題 患者
キーワード
言語 ja
主題Scheme Other
主題 体験
キーワード
言語 ja
主題Scheme Other
主題 看護師―患者関係
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
著者 泉, 貴子

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ja 泉, 貴子

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著者別名
識別子Scheme WEKO
識別子 39
姓名 IZUMI, Atsuko
言語 en
抄録
内容記述タイプ Abstract
内容記述 The present study aimed to describe' the experiences considered to be unique to collagen disease patients from the perspective of nurses and the characteristic experiences of each stage of the disease, and to consider the points of commonality and difference with the experience of the patients themselves. Semistructured interviews were conducted on three nurses who had experience nursing collagen disease patients.
The nurses said that collagen disease patients in general have the feeling that while their disease is not fatal, it is something they will have to live with for their entire lives, and that they had experienced their disease affecting all parts of their lives. In addition, they were depicted as always having heavy anxiety or big anxiety from the repeated flare-ups and remissions.
The period of exacerbating symptoms and reactivation was depicted as a period of passivity and stagnation in which the patients can't think of anything and simply endure the symptoms.
The period during which patients are recovering from the period of exacerbated symptoms was depicted as a time when they feel their outlook is brighter, but at the same wonder what will happen next and are anxious about returning to their normal lives, and have a positive anxiety while seeking for something.
The period of recovery was depicted as one in which the patients feel physical lightness that makes them think their disease is nothing special, while also harboring anxiety about a recurrence.
Based on the present findings, the experience of patients as seen by nurses was of a disease that will be with one for life, an image that was common with the image of patients themselves as shown in an earlier study. In addition, the nurses felt that patients thought their disease was difficult and something they had to work to maintain their resolve. The nurses also felt that there were few occasions for them to be consulted. The previous study showed that patients felt that they cannot explain the disease well because it is difficult one, and that since they look healthy, they sense that people do not understand their situation. These differences in opinion suggest the need for nurses to have a better understanding of patients and to offer them a more supportive voice.
言語 en
書誌情報 ja : 日本赤十字看護大学紀要
en : Bulletin of the Japanese Red Cross College of Nursing

号 24, p. 24-33, 発行日 2010-03-10
出版者
出版者 日本赤十字看護大学
言語 ja
ISSN
収録物識別子タイプ PISSN
収録物識別子 09142444
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AN10078861
権利
言語 ja
権利情報 日本赤十字看護大学
フォーマット
内容記述タイプ Other
内容記述 application/pdf
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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