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題名:肌肉萎縮症患孩母親的心理社會衝擊
書刊名:護理研究
作者:黃璉華戴玉慈
作者(外文):Huang, Lian-huaDai, Yu-tzu
出版日期:1998
卷期:6:2
頁次:頁137-151
主題關鍵詞:肌肉萎縮症母親心理社會衝擊Muscular dystrophyMothersPsychosocial impact
原始連結:連回原系統網址new window
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  • 被引用次數被引用次數:期刊(1) 博士論文(0) 專書(0) 專書論文(0)
  • 排除自我引用排除自我引用:1
  • 共同引用共同引用:10
  • 點閱點閱:31
     X連鎖隱性遺傳疾病,如裘馨氏(Duchenne)肌肉萎縮症等,通常需要長時間的特殊 照護,當家庭中有這類患孩時,會對整個家庭帶來很大的衝擊。尤其對母親更是一大打擊, 因為X連鎖隱性遺傳疾病的遺傳方式是經由女性帶因者,也就是母親本身。本研究目的為瞭 解肌肉萎縮症患孩健康與行為問題,和母親的心理社會衝擊及相關因素。本研究透過肌原性 肌肉萎縮症基金會收集肌肉萎縮症個案的名冊,以郵寄問卷的方式收集資料。研究發出問卷 195份,回收之有效問卷為78份,回覆率40%。所得資料輸入電腦以SPSS處理分析。研究結果 顯示肌肉萎縮症患孩母親大多有悲傷、無助、不能接受等的情緒反應,患孩母親的焦慮程度 與患孩的健康狀況、情緒反應、和適應能力有關。患孩健康狀況與適應能力有關,而患孩適 應能力又與情緒反應有關。家庭適應狀況及患孩適應能力同時與母親的焦慮程度有關。影響 母親焦慮的因素有患孩的情緒反應和母親是否有宗教信仰。建議未來應建立國人肌肉萎縮症 發生流行病學的資料庫,提供肌肉萎縮症家庭的護理與諮詢服務,提高醫療服務的品質,並 強化家長支持團體。
     X-linked recessive diseases, such as Duchenne Muscular Dystrophy, usually require a long period of special care. For families who must face the reality of an affected son, the diagnosis marks the beginning of a long and painful process. It inevitably has a tremendous impact on the entire family, especially on the mother, the obligate carrier. The purpose of this study was understand the health and behavior problems of children with muscular dystrophy, and the psychosocial impact on the mothers with affected children. The Study sample were recruited from the Muscular Dystrophy Foundation. Mailed questionnaires were sent to 195 mothers of children with muscular dystrophy; 78 valid questionnaires were returned, which gave a response rate of 40%. Data were analyzed via SPSS computer software. Study results revealed that mothers had emotional responses such as sadness, helplessness, and denial; mothers' emotional responses were related to the child's health condition, emotional responses, and adaptability. The health condition of the sick child was found to correlate to its adaptability, and adaptability correlated to emotional responses. The adapability of the whole family and the sick child were related to mother's level of anxiety. The predictors of a mother's level of anxiety were the child's emotional responses and whether the mother had religious belief. It is recommended to establish an epidemiological data set for muscular dystrophy. Further, to provide nursing and counseling services to strengthen parents' support groups and to enhance the quality of services is also suggested.
期刊論文
1.黃璉華(19940900)。養育唐氏症兒對家庭的衝擊。護理研究,2(3),253-262。new window  延伸查詢new window
2.Thompson, R. J. J.、Zeman, J. L.、Fanurik, D.、Sirotkin-Roses, M.(1992)。The role of parent stress and coping and family functioning in parent and child adjustment to Duchenne muscular dystrophy。Journal Clinical Psychology,48(1),11-19。  new window
3.黃璉華(19950800)。生育先天性缺陷兒對家庭的影響。中華公共衛生雜誌,14(4),299-313。new window  延伸查詢new window
4.Buchanan, D.、LaBarbera, C.、Roelofs, R.、Olson, W.(1979)。Reactions of families to children with Duchenne Muscular Dystrophy。General Hospital Psychiatry,1(3),262-269。  new window
5.Beeson, D.、Golbus, M.(1985)。Decision making: Whether or not to have prenatal diagnosis and abortion for X-lmked conditions。American Journal of Medical Genetics,20(1),107-114。  new window
6.Fitzpatrick, C.、Barry, C.(1990)。Cultural differences in family commimication about Duchenne Muscular Dystrophy。Developmental Medicine & Child Neurology,32(1),967-973。  new window
7.Fitzpatrick, C.、Barry, C.(1986)。Communication with families about Duchenne Muscular Dystrophy。Developmental Medicine & Child Neurology,28(5),596-599。  new window
8.Firth, M.、Gardner-Medwin, D.、Hosking, G.、Wilkmson, E.(1983)。Interviews with parents of boys suffering from Duchenne muscular dystrophy。Developmental Medicine & Child Neurology,25(4),466-471。  new window
9.Parsons, E.、Clarke, A.(1993)。Genetic risk: Women's understanding of carrier risks in Duchenne Muscular Dystrophy。Journal of Medical Genetics,30(7),562-566。  new window
10.Kornfeld, M. S.、Siegel, I.(1980)。Parental group therapy in management of two fatal childhood diseases: A comparison。Health and Social Work,5(1),28-34。  new window
11.Hutton, E.、Thompson, M.(1976)。Carrier detection and genetic counseling in Duchenne Muscular Dystrophy: A followup study。Canadian Medical Association Journal,115(8),749-752。  new window
12.Gagliardi, B. A.(1991)。The impact of Duchenne Muscular Dystrophy on families。Orthopaedic Nursing,10(5),41-49。  new window
13.Fowler, W. M., Jr.、Abresch, R. T.、Aitkens, S.、Carter, G. T.、Johnson, E. R.、Kilmer, D. M. D.、McCrory, M. A.、Wright, N. C.(1995)。Profiles of neuromuscular diseases: design of the protocol。American Journal of Physical Medicine & Rehabilitation,74(suppl.),S62-S69。  new window
14.Witte, R.(1985)。The psychosocial impact of a progressive physical handicap in terminal illness (Duchenne muscular dystrophy) on adolescents and their families。British Journal of Medical Psychology,58(2),179-187。  new window
15.Clubb, R. L.(1991)。Chronic sorrow: Adaptation patterns of parents with chronically ill children。Pediatric Nursing,17(5),461-466。  new window
16.Fitzpatrick, C.、Barry, C.、Garvey, C.(1986)。Psychiatric disorder among boys with Duchenne muscular dystrophy。Developmental Medicine & Child Neurology,28(5),589-595。  new window
圖書
1.肌原性肌肉萎縮症基金會(1990)。肌原性肌肉萎縮症。台北:肌原性肌肉萎縮症基金會。  延伸查詢new window
 
 
 
 
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