查詢結果分析
相關文獻
- 宜蘭縣泰雅族原住民肝硬化病患的生活品質及其相關因素之探討
- The Relatinship of Social Support to Quality of Life among Patients with Chronic Obstructive Pulmonary Disease
- 接受導管肝動脈化學藥物栓塞術肝癌病患之生活品質
- 腰椎間盤突出患者的生活品質及其相關因素之探討
- 血液透析病患生活品質及其相關因素之探討
- 技職學校原住民學生學校生活適應及其相關因素之研究--以明志技術學院為例
- 探討乳癌病人的症狀困擾、自我效能、社會支持與生活品質之關係
- 燒傷病患主要照顧者生活品質及其相關因素之探討
- 比較疼痛及非疼痛癌症病患不確定感、症狀困擾、社會支持與生活品質關係
- Quality of Life and Related Factors for People Living with HIV/AIDS in Northern Taiwan
頁籤選單縮合
題 名 | 宜蘭縣泰雅族原住民肝硬化病患的生活品質及其相關因素之探討=Quality of Life and the Associated Factors among Tayal Aboriginal Patients with Liver Cirrhosis in I-Lan |
---|---|
作 者 | 黃麗珠; 劉雪娥; 李中一; 邱愛富; | 書刊名 | 輔仁醫學期刊 |
卷 期 | 2:2 2004.06[民93.06] |
頁 次 | 頁27-37 |
分類號 | 419.73 |
關鍵詞 | 原住民; 肝硬化病患; 生活品質; 身體症狀困擾及心理狀況; 社會支持; Aboriginal; Liver cirrhosis; Quality of life; Physical symptoms and mental status; Social support; |
語 文 | 中文(Chinese) |
中文摘要 | 背景和目的:探討宜蘭縣泰雅族原住民肝硬化病患之生活品質狀況以及分析人口學變項、疾病特性、身體症狀困擾及心理狀況、社會支持與生活品質間的相關性。方法:為橫斷面描述性相關性設計,採立意取樣,以宜蘭縣二所區域教學醫院經診斷確定為肝硬化的泰雅族原住民患者(排除肝昏迷者)共30位為對象,以結構性問卷會談法收集資料,研究工具包括經過信效度驗證之生活品質量表、身體症狀困擾及心理狀況量表及社會支持量表;以百分比或平均值與標準差描述研究樣本之社會人口學特徵、疾病特性、以及在各量表的得分,並利用逐步複迴歸模式分析生活品質分數的顯著預測因子。結果:原住民肝硬化病患樣本的生活品質指標平均得分為18.5分,其中家庭因素得分最高,健康因素得分最低;對生活品質有顯著預測力之因子包括身體症狀困擾與心理狀況及疾病嚴重度等二個變項,共可解釋生活品質的變異量為63.6%。結論:身體症狀困擾與心理狀況較差以及疾病嚴重較輕之泰雅原住民肝硬化病人的生活品質較低,未來研究應著重探討可能的介入措施以有效提升泰雅原住民肝硬化病患的生活品質。 |
英文摘要 | Background and Purpose: To investigate the scale-based quality of life score (QOLS) and its potential associations with sociodemographic variables, diseases characteristics, physical symptoms and mental status, and social support among Tayal aboriginal patients with liver cirrhosis in I-Lan. Methods: A convenient sample of 30 patients (excluding those with hepatic coma) was obtained from two regional teaching hospitals in I-Lan. The study participants were personally interviewed with a structured questionnaire. Various scales with satisfactory validity and reliability were used for the collection of information on quality of life, physical symptoms and mental status, and social support. We calculated percentages or means and standard deviations of sociodemographic variables, disease characteristics, physical symptoms and mental status, and various scale-based scores. A stepwise regression model was also used to identify factors that may significantly predict the QOLS. Results: The mean score of overall QOLS was 18.5 for the study participants. Calculation of the score for each of the 5 subscales revealed that the highest and lowest score was noted for the family related subscale and the health related subscale. The stepwise regression model suggested that physical symptoms and mental status and disease severity are the two variables significantly associated with the QOLS, jointly accounted for 63.6% of the variance of QOLS. Conclusion: Tayal aboriginal liver cirrhosis patients who suffered from physical and psychological distress or experienced a relatively mild condition tended to experience a lower QOLS. Future studies may consider to exploring clinical nursing interventions that may help promote quality of life of aboriginal patients with liver cirrhosis. |
本系統中英文摘要資訊取自各篇刊載內容。