Publication Name	World Journal of Transplantation
Manuscript ID	68379
Country	Greece

Received	2021-05-20 22:04
Peer-Review Started	2021-05-20 22:08
To Make the First Decision
Return for Revision	2021-06-17 05:32
Revised	2021-06-26 13:11
Second Decision	2021-08-17 03:30
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2021-08-18 06:27
Articles in Press	2021-08-18 06:27
Publication Fee Transferred
Edit the Manuscript by Language Editor	2021-08-27 21:20
Typeset the Manuscript	2021-09-13 04:32
Publish the Manuscript Online	2021-09-15 06:29

ISSN	2220-3230 (online)
Open Access	This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.
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Category	Transplantation
Manuscript Type	Minireviews
Article Title	Management of biliary atresia: To transplant or not to transplant
Manuscript Source	Invited Manuscript
All Author List	Christos Dimitrios Kakos, Ioannis A Ziogas, Sophoclis P Alexopoulos and Georgios Tsoulfas
ORCID	Author(s) ORCID Number Christos Dimitrios Kakos http://orcid.org/0000-0002-2269-9014 Ioannis A Ziogas http://orcid.org/0000-0002-6742-6909 Sophoclis P Alexopoulos http://orcid.org/0000-0001-8785-7469 Georgios Tsoulfas http://orcid.org/0000-0001-5043-7962
Funding Agency and Grant Number
Corresponding Author	Georgios Tsoulfas, FACS, FICS, MD, PhD, Associate Professor, Department of Transplant Surgery, Aristotle University School of Medicine, 66 Tsimiski Street, Thessaloniki 54622, Greece. tsoulfasg@gmail.com
Key Words	Biliary atresia; Kasai procedure; Portoenterostomy; Native liver survival; Liver transplantation
Core Tip	Timely diagnosis of biliary atresia (BA) is critical to optimizing the outcomes of Kasai procedure (KP), which should be performed as early as possible. Children with a delayed diagnosis of BA at high risk of early KP failure or those presenting with clear evidence of decompensated cirrhosis should be considered for primary liver transplantation (LT). Early KP failure requiring salvage LT within the first 2-3 years of life occurs in nearly half of all children with BA but even those with a successful KP need life-long monitoring for progression of liver disease that may require salvage LT.
Publish Date	2021-09-15 06:29
Citation	Kakos CD, Ziogas IA, Alexopoulos SP, Tsoulfas G. Management of biliary atresia: To transplant or not to transplant. World J Transplant 2021; 11(9): 400-409
URL	https://www.wjgnet.com/2220-3230/full/v11/i9/400.htm
DOI	https://dx.doi.org/10.5500/wjt.v11.i9.400

Full Article (PDF)	WJT-11-400.pdf
Full Article (Word)	WJT-11-400.docx
Manuscript File	68379-Review-FilipodiaCL.docx
Answering Reviewers	68379-Answering reviewers.pdf
Audio Core Tip	68379-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	68379-Conflict-of-interest statement.pdf
Copyright License Agreement	68379-Copyright license agreement.pdf
Peer-review Report	68379-Peer-review(s).pdf
Scientific Misconduct Check	68379-Bing-Gao CC-1.jpg
Scientific Misconduct Check	68379-Bing-Wang JJ-2.png
Scientific Misconduct Check	68379-Scientific misconduct check.pdf
Scientific Editor Work List	68379-Scientific editor work list.pdf