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頁籤選單縮合
題 名 | 肝癌病患家屬參加教育心理團體成效探討=The Outcomes of the Family of Patients with Hepatocellular Carcinoma Participating in Psychoeducational Groups |
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作 者 | 胡麗霞; 蔡欣玲; 溫明寰; 莊琴英; | 書刊名 | 榮總護理 |
卷 期 | 15:2 1998.06[民87.06] |
頁 次 | 頁206-213 |
分類號 | 419.77 |
關鍵詞 | 肝癌; 家屬; 教育心理團體; Hepatocellular carcinoma; Family; Psychoeducational groups; |
語 文 | 中文(Chinese) |
中文摘要 | 相關研究顯示,癌症病患家屬以獲得資訊和心理方面的需求最多,為了滿足家屬 知的需求,成立了肝癌病患家屬教育心理團體。本研究之目的為探討肝癌病患家屬參加教育心 理團體後對肝癌的知識與焦慮的影響。研究採前實驗設計法,研究工具以肝癌知識量表及鍾思 嘉的情境-特質焦慮量表為評量指標。以某一級醫學中心胃腸科病房之肝癌病患家屬為研究對 象,在參加教育心理團體常先做前測,給予衛教及討論後再做後測,共有四個主題-疾病的認 識、病患的照護、營養及經驗分享,全程參與者有34人,所得資料以SPSS PC軟體分析處理 之。研究結果顯示:肝癌病惠家屬參加教育心理團體後對肝癌的知識有顯著的增進,以病患照 護方面的知識增進最多,其次為疾病的認識;在情境焦慮上有顯著的降低;而肝癌的知識增進 與焦慮降低未呈現相關。對教育心理團體的滿意度,以Likert 5分法計分,滿意度皆在4.3 分以上;100%家屬認為常要此團體之支持,其中64.7%的家屬認為非常需要。肝癌病患家屬所 面臨的問題依序為(1)對中藥、偏方、草藥的疑惑(2)是否告知病情(3)不忍見病人痛苦。家屬 的因應方式:(1)經由醫療小組人員獲得正確的資訊(2)信仰宗教使心靈有個寄託(3)家人或親 友的互相支持。研究結果可提供臨床專業人員面對肝癌病患家屬之照護方向。 |
英文摘要 | Many research findings show that the most important things to the family of those cancer patients were to obtain the information and support in psychology, but these were the most unsatisfactory affairs too. Psychoeducatinal Groups for the Family of Hepatocel-lular Carcinoma Patients (PGFHP) were just setup for the above reasons to help the families face the disease and death of their relatives. The purpose of the study was to understand the effects on the knowledge of Hepatocellular Carcinoma (H. C. C.) and the anxiety of the families which have joined the PGFHP. A pre-experimental study design was used. The research tool was evaluated and then pointed by the measuring questionaire of the knowledge to the H. C. C. and the anxiety measuring questionaire of State-Trait Anxiety Inventory. The research subjects were the families of H. C. C patients in the gas-tro-intestinal wards of a medical center. The families took a pre-test before joining the PGFHP and then took a post-test after learning and discussing sanitary knowledge. There were four topics in the course, 1st to realize the disease, 2nd to take care of the patients, 3rd the nutrition and 4th to share experiences. 34 people took both tests and participated in every activity. The results indicated that the families' knowledge about H. C. C. was obviously increased. Among these, the knowledge of technique in taking care of the H. C. C. patients was increased mostly and their recognition to the H. C. C. disease was right behind. The situation anxiety was evidently reduced, it seemed to have no relationship to the increase of knowledge of H. C. C. As to the satisfaction to the PGFHP, all of (100%) the families accounted that they needed support from this group and 64.7% of the families thought that this support was very necessary. The results of this research will point the direction that health teams can use to help the families take care of their H. C. C. relatives or friends in a better way. |
本系統中英文摘要資訊取自各篇刊載內容。