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題名:先天性膽道閉鎖的護理照顧
書刊名:護理雜誌
作者:張美娟 引用關係
作者(外文):Chang, M. C.
出版日期:2000
卷期:47:2
頁次:頁77-81
主題關鍵詞:先天性膽道閉鎖肝門腸道吻合術護理Congenital biliary atresiaHepatico-porto-enterostomyNursing care
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:0
  • 點閱點閱:34
     先天性膽道閉鎖是新生兒膽道系統中常見的異常,早期發現早期予以肝 門腸道吻合術治療,可增加患童存活的機率,否則會轉變為嚴重的肝病變而亡。 即使經過治療的患童成長過程中仍有許多健康問題需要特別的照護。本篇簡介先 天性膽道閉鎖的病理、臨床表徵、診斷檢查、外科處置、健康問題及護理照護, 提供相關醫護人員參考,予患童合宜且連續性的照顧,協助家庭度過危機。
期刊論文
1.Barkin, R. M.、Lilly, J. R.(1980)。Biliary atresia and the Kasai operation: Continuing care。The Journal of Pediatrics,96(6),1015-1019。  new window
2.Balistreri, M. F.、Grand, R.、Hoofnagle, J. H.、Suchy, F. J.、Ryckman, R. C.、Perlmutter, D. H.、Sokol, R. J.(1996)。Biliary atresia: Current concepts and research directions。Hepatology,23(6),1682-1691。  new window
3.Altman, R. P.、Lilly, J. R.、Greenfeld, J.、Weinberg, A.、Leeuwen, K. V.、Flanigan, L.(1997)。A multiple variable risk factor analysis of the porto-enterostomy (Kasai) procedure for biliary atresia。Annals of Surgery,226(3),348-355。  new window
4.謝一文(19851000)。新生兒膽汁滯留。臨床醫學,16(4)=94,280-285。new window  延伸查詢new window
5.張美惠(19951100)。兒童肝臟移植之適應症及轉介時機。當代醫學,22(11)=265,940-942。  延伸查詢new window
6.Booth, M.(1985)。Biliary atresia treatment options。The Candia Nurse,81(10),33-34。  new window
7.Chen, C. L.、Chen, Y. S.、Liu, P. P.、Chiang, Y. C.、Cheng, Y. C.、Cheng, Y. F.、Huang, T. L.、Eng, H. L.(1996)。Living related donor liver transplantation: The Kaohsiung experience。Transplantation Proceedings,28(4),2385-2387。  new window
8.Goss, J. A.、Shacklton, C. R.、Swenson, K.、Satou, N. L.、Nuesse, B. J.、Imagawa, D. K.、Kinkhabwala, M. M.、Seu, P.、Markowitz, J. S.、Rudich, S. M.、Mcdiarmid, S. V.、Usuttil, R. W.(1996)。Orthotopic liver transplantation for congenital biliary atresia。Annals of Surgery,224(3),276-287。  new window
9.Karrer, F. M.、Price, M. R.、Bensard, D. D.、Sokol, R. J.、Narkewicz, M. R.、Smith, D. J.、Lilly, J. R.(1996)。Long-term results with the Kasai operation for biliary atresia。Archives of Surgery,131,493-496。  new window
10.Kaufman, S. S.、Murray, N. D.、Wood, P.、Shaw, B. W.、Vanderhoof, J. A.(1987)。Nutritional support for the infant with extxahepatic biliary atresia。The Journal of Pediatrics,110(5),679-686。  new window
11.Silveria, T. R.、Salzano, F. M.、Ednard, R. H.(1991)。Congenital structural abnormalities in biliary atresia: Evidence for etiopathogenic heterogeneity and theraputic implications。Acta Pediatric Scand,80,1192-1199。  new window
12.Ohi, R.、Nio, M.、Choba, T.(1990)。Long-term follow up after surgery for patients with billiary atresia。Journal of Pediatric Surgery,25(4),442-445。  new window
13.McEvoy, C. F.、Suchy, F. J.(1996)。Biliary tract disease in children。Pediatric Clinics of North America,43(1),75-79。  new window
14.MacDonal, C. A.(1991)。Biliary atresia。Journal of Pediatric Nursing,6(6),374-383。  new window
15.Starzl, T. E.、Iwatsuki, S.、Vaw, D. D.(1984)。Evolution of liver transplantation。Hepatology,14,1075。  new window
圖書
1.Oski, F. A.(1990)。Principles and practice of pediatrics。L. B. Lippincott company。  new window
 
 
 
 
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