BPG is committed to discovery and dissemination of knowledge
Articles Published Processes
11/20/2017 4:03:35 AM | Browse: 1162 | Download: 2540
 |
Received |
|
2017-06-09 00:37 |
 |
Peer-Review Started |
|
2017-06-10 00:39 |
 |
First Decision by Editorial Office Director |
|
|
 |
Return for Revision |
|
2017-07-17 11:54 |
 |
Revised |
|
2017-08-03 02:33 |
 |
Publication Fee Transferred |
|
2017-09-19 11:16 |
 |
Second Decision by Editor |
|
2017-08-15 07:54 |
 |
Second Decision by Editor-in-Chief |
|
|
 |
Final Decision by Editorial Office Director |
|
2017-08-15 15:07 |
 |
Articles in Press |
|
2017-08-15 15:07 |
 |
Edit the Manuscript by Language Editor |
|
2017-09-29 01:45 |
 |
Typeset the Manuscript |
|
2017-11-02 10:10 |
 |
Publish the Manuscript Online |
|
2017-11-20 04:03 |
| ISSN |
1007-9327 (print) and 2219-2840 (online) |
| Open Access |
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
| Copyright |
© The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
|
| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
|
| Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
| Website |
http://www.wjgnet.com |
| Category |
Gastroenterology & Hepatology |
| Manuscript Type |
Observational Study |
| Article Title |
Chronic liver disease is universal in children with biliary atresia living with native liver
|
| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Way Seah Lee, Sik Yong Ong, Hee Wei Foo, Shin Yee Wong, Chen Xi Kong, Ru Bin Seah and Ruey Terng Ng |
| ORCID |
|
| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| University Malaya High Impact Research (UM.C/625/HIR/MOHE/CHAN/13/1) from Ministry of Higher Education, Malaysia |
|
|
| Corresponding Author |
Way Seah Lee, MBBS, MD, Professor, Department of Paediatrics, University Malaya Medical Centre, Kuala Lumpur 50603, Malaysia. leews@um.edu.my |
| Key Words |
Biliary atresia; Medical status; Chronic liver disease |
| Core Tip |
Previous study showed that more than 90% of children with biliary atresia (BA) surviving with native livers have clinical and laboratory evidence of chronic liver disease (CLD). In the present cohort, we found that 71% of patients with BA living with native livers had no clinical complications of CLD and 90% had normal liver synthetic function, only 2% had ideal medical outcome. Common medical complications encountered were cholangitis, portal hypertension and bleeding oesophageal varices. Portal hypertension and bleeding oesophageal varices were seen in 12% and 6% of children younger than 5 years of age. Medical surveillance in children with BA after Kasai surgery for medical complications should start even before 5 years of age. |
| Publish Date |
2017-11-20 04:03 |
| Citation |
Lee WS, Ong SY, Foo HW, Wong SY, Kong CX, Seah RB, Ng RT. Chronic liver disease is universal in children with biliary atresia living with native liver. World J Gastroenterol 2017; 23(43): 7776-7784 |
| URL |
http://www.wjgnet.com/1007-9327/full/v23/i43/7776.htm |
| DOI |
http://dx.doi.org/10.3748/wjg.v23.i43.7776 |
All content on this site: Copyright © 1993-2026 Baishideng Publishing Group Inc, its licensors, and contributors. All rights are reserved, including those for text and data mining, AI training, and similar technologies. For all open access content, the relevant licensing terms apply.