题名

遺傳疾病對護理的衝擊及挑戰

并列篇名

Impact and Challenges of Genetic Disorders on Nursing

DOI

10.6224/JN.000065

作者

王瑤華(Yao-Hua Wang)

关键词

遺傳疾病 ； 護理 ； 衝擊 ； 挑戰 ； genetic disorders ； nursing ； impact ； challenge

期刊名称

護理雜誌

卷期/出版年月

64卷5期（2017 / 10 / 01）

页次

24 - 29

内容语文

繁體中文
中文摘要

遺傳疾病對個人生活型態及家庭都可能產生巨大影響，提供接受遺傳檢測之個案，護理人員應於檢驗前後給予諮詢與衛教。目前對於接受遺傳檢測的態度趨向提高婦女或夫婦的自主性，提供充分資訊，讓他們自行決定可以接受的檢驗，並及早準備迎接有特殊照護需求的新生兒。另外，對於已被檢測為失智症高危險羣之民眾應給予合適諮詢，以協助其瞭解結果代表的意義及心理支持。而目前政府對於遺傳檢驗機構之管理，遺傳疾病患者治療費用之保險或補助，以及倘若因檢測產生醫療糾紛，政府如何給予受檢者及檢驗機構公平審理等，皆未有清楚之標準。民眾對於引起遺傳疾病的因素所知有限，對於相關診斷、治療也存在許多不確定性，這雖是醫療照護者的限制，但對於民眾來說則風險更大，護理人員應儘早發現此項趨勢及護理需求，訂定合適方針以因應遺傳疾病帶給民眾的衝擊及挑戰。
英文摘要

Genetic disorders greatly impact human life. Nursing staffs should provide counseling and health education before and after patients receive genetic testing. Current attitudes toward women who receive genetic tests emphasize respect patient autonomy and allowing the patient to make her own decisions regarding the tests she wants to take and her reproductive planning. For patients whose results include them in the high-risk group for dementia, providing mental support and counseling to assist them to understand the meaning of these results is important. One issue that deserves particular attention is the supervision of genetic testing agencies. Although the credibility, testing fees, and professionalism of these agencies must be verified, no government agency currently has executive authority in this area. Because genetic disorders often require huge expenditures to help patients live with dementia, health insurance is necessary. As Taiwan currently offers universal healthcare under the National Health Insurance program, dementia is currently and will continue to be an immense challenge to both the government and the nursing profession. Currently, medical knowledge related to genetic diseases and the ability of health professionals to provide effective treatments are still very limited. The nursing profession should be aware of the trends and challenges related to genetic disorders and devise appropriate policies in order to response the challenges.
主题分类 醫藥衛生 > 預防保健與衛生學
醫藥衛生 > 社會醫學
参考文献
  1. 蔡甫昌、朱怡康、黃天祥(2007)。遺傳檢測與諮詢的倫理議題與執業準則—罹病傾向之遺傳檢測：以BRCA檢驗為例。醫學教育，11(1)，69-88。
    連結：
  2. 內政部戶政司（無日期）．出生數按生母年齡及胎次．取自http://www.ris.gov.tw/fr/346 [Department of Household Registration, Ministry of the Interior, Taiwan, ROC. (n.d.). Live births, by mother's age. Retrieved from http://www.ris.gov.tw/fr/346]
  3. 中華民國人類遺傳學會（無日期）．遺傳檢驗及諮詢一般倫理準則． 取自http://www.genes-at-taiwan.com.tw/News/03.pdf [Taiwan Human Genetics Society. (n.d.). Ethical guidelines for genetic testing and counseling. Retrieved from http://www.genes-at-taiwan.com.tw/News/03.pdf]
  4. 台灣失智症協會（無日期）．失智人口知多少．取自http://www.tada2002.org.tw/tada_know_02.html [Taiwan Alzheimer Disease Association. (n.d.). Population with dementia. Retrieved from http://www.tada2002.org.tw/tada_know_02.html]
  5. Benn, P.,Chapman, A. R.,Erickson, K.,DeFrancesco, M. S.,Wilkins-Haug, L.,Egan, J. F. X.,Schulkin, J.(2014).Obstetricians and gynecologists' practice and opinions of expanded carrier testing prenatal testing.Prenatal Diagnosis,34(2),145-152.
  6. Camak, D. J.(2016).Increasing importance of genetics in nursing.Nurse Education Today,44,86-91.
  7. de Jong, A.,Maya, I.,van Lith, J. M. M.(2015).Prenatal screening: Current practice, new developments, ethical challenges.Bioethics,29(1),1-8.
  8. Paneque, M.,Mendes, Á.,Guimarães, L.,Sequeiros, J.,Skirton, H.(2015).Genetics health professionals' views on quality of genetic counseling service provision for presymptomatic testing in late-onset neurological diseases in Portugal: Core components, specific challenges and the need for assessment tools.Journal of Genetic Counseling,24(4),616-625.
  9. Paz De Jesus, M.,Mitchel, M.(2016).Today's nurses need genetics education.Nursing,46(10),68.
  10. Prince, M.,Wimo, A.,Guerchet, M.,Ali, G.-C.,Wu, Y. T.,Prina, M.(2015).World Alzheimer report 2015-The global impact of dementia: An analysis of prevalence, incidence, cost and trends.London, England:Alzheimer's Disease International.
  11. Steinbart, E. J.,Smith, C. O.,Poorkaj, P.,Bird, T. D.(2001).Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia.Archives of Neurology,58(11),1828-1831.
  12. Taylor, J. Y.,Wright, M. L.,Hickey, K. T.,Housman, D. E.(2017).Genome sequencing technologies and nursing: What are the roles of nurses and nurse scientists?.Nursing Research,66(2),198-205.
  13. 洪成志、廖敏華、王正如、鄭之雅(2011)。遺傳性失智症的基因檢測與諮詢。臺灣醫界，54(9)，10-18。
  14. 蔡甫昌、許毓仁、陳晶瑩、黃宗正、邱銘章(2016)。失智症之遺傳檢驗暨諮詢倫理議題。台灣醫學，20(5)，517-527。
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