Literature DB >> 2329462

Long-term follow-up after surgery for patients with biliary atresia.

R Ohi1, M Nio, T Chiba, N Endo, M Goto, M Ibrahim.   

Abstract

Long-term results after surgery for biliary atresia (BA) in 48 patients, ranging in age from 10 to 33 years, were examined. There were 19 males and 29 females. Twelve had correctable type BA and 36 had the noncorrectable type. Forty-one cases had no jaundice; seven did. Thirty-seven of the 48 cases were leading normal lives. Among them, six cases were enjoying their lives after overcoming sequelae, such as portal hypertension. The main morbidities of the remaining 11 long-term survivors were jaundice and portal hypertension. The growth of most cases were comparable to those of the normal Japanese population. The data of liver function tests were variable and disclosed a moderate degree of abnormality in patients mainly complicated by cholangitis. Eleven cases, including six jaundice cases, required treatment for esophageal varices and/or hypersplenism. In conclusion, the cured states of most cases without jaundice are satisfactory and these former patients have achieved a favorable quality of life. Early operations are essential to obtain good short-term results as well as good long-term results.

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Year:  1990        PMID: 2329462     DOI: 10.1016/0022-3468(90)90390-u

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  20 in total

Review 1.  Liver transplantation.

Authors:  J Chiyende; A P Mowat
Journal:  Arch Dis Child       Date:  1992-09       Impact factor: 3.791

2.  Newborn Screening for Biliary Atresia.

Authors:  Kasper S Wang
Journal:  Pediatrics       Date:  2015-12       Impact factor: 7.124

3.  Jaundice at 14 days of age: exclude biliary atresia.

Authors:  M Hussein; E R Howard; G Mieli-Vergani; A P Mowat
Journal:  Arch Dis Child       Date:  1991-10       Impact factor: 3.791

4.  Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometry.

Authors:  I Mushtaq; S Logan; M Morris; A W Johnson; A M Wade; D Kelly; P T Clayton
Journal:  BMJ       Date:  1999-08-21

5.  Advanced biliary atresia: is portoenterostomy justified in all infants?

Authors:  D K Gupta; S Dave
Journal:  Indian J Pediatr       Date:  2001-05       Impact factor: 1.967

Review 6.  Earlier identification of biliary atresia and hepatobiliary disease: selective screening in the third week of life.

Authors:  A P Mowat; L L Davidson; M C Dick
Journal:  Arch Dis Child       Date:  1995-01       Impact factor: 3.791

7.  Liver transplantation in 100 children: Cambridge and King's College Hospital series.

Authors:  A Salt; G Noble-Jamieson; N D Barnes; A P Mowat; K Rolles; N Jamieson; P Johnston; P Friend; R Y Calne
Journal:  BMJ       Date:  1992-02-15

8.  Surgical treatment of biliary atresia with patent distal extra hepatic bile ducts: Is hepatic portocholecystostomy the right choice?

Authors:  V V S Chandrasekharam
Journal:  J Indian Assoc Pediatr Surg       Date:  2009-01

Review 9.  Biliary atresia.

Authors:  Giorgina Mieli-Vergani; Diego Vergani
Journal:  Semin Immunopathol       Date:  2009-06-17       Impact factor: 9.623

10.  Surgical treatment of biliary atresia in the liver transplantation era.

Authors:  R Ohi
Journal:  Surg Today       Date:  1998       Impact factor: 2.549

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