Literature DB >> 33750299

Liver transplantation in adult polycystic liver disease: the Ontario experience.

Mohammed Alsager1, Shuet Fong Neong2, Radhika Gandhi1, Anouar Teriaky1, Ephraim Tang2, Anton Skaro2, Karim Qumosani1, Les Lilly2, Zita Galvin2, Nazia Selzner2, Mamatha Pallavi Bhat2, Klajdi Puka3, Mayur Brahmania4,5.   

Abstract

BACKGROUND: Liver transplantation (LT) remains the curative treatment for symptomatic Polycystic Liver Disease (PCLD) patients and is associated with excellent survival rates. The aim of the study is to review the Ontario experience in LT for PCLD.
METHODS: A retrospective study was performed from pre-existing LT databases from the LT Units at Toronto General Hospital and London Health Sciences Center, which are the two LT programs in Ontario, Canada. This database contains demographic, clinical parameters and follow-up of all patients transplanted for PCLD. Data was extracted for patients who underwent LT between January 2000-April 2017 and included follow up until December 31st, 2018.
RESULTS: A total of 3560 patients underwent LT, of whom 51 (1.4%) had PCLD and met inclusion criteria. 43 (84%) of these patients were female. The median physiologic Model for End Stage Liver Disease (MELD-Na) score at time of referral was 13 (IQR = 7-22), however all patients required MELD-Na exception points to receive LT. The median age of transplant was 62 years (IQR = 59-64) for male vs. 52 (IQR = 45-56) for female patients. 33 (65%) of our cohort had PCLD while 9 (17.5%) had ADPKD and 9 (17.5%) had both diseases. 39 (76%) had LT due to symptoms of mass effect, while 8 (16%) had portal hypertensive complications. After a median follow-up of 6.3 (IQR = 2.9-12.5) years, the probability of survival was 96% (95% CI: 90%, 100%). Log-rank test, comparing survival analysis between males and females did not show a statistically significant difference (p = 0.26).
CONCLUSION: Most patients underwent LT for PCLD due to symptoms of mass effect with women being more likely than men to undergo LT. LT for PCLD had excellent long-term survival.

Entities:  

Keywords:  Liver transplantation; PCLD outcome; Polycystic liver disease

Mesh:

Year:  2021        PMID: 33750299      PMCID: PMC7941890          DOI: 10.1186/s12876-021-01703-x

Source DB:  PubMed          Journal:  BMC Gastroenterol        ISSN: 1471-230X            Impact factor:   3.067


  21 in total

1.  Evolution of indications and results of liver transplantation in Europe. A report from the European Liver Transplant Registry (ELTR).

Authors:  René Adam; Vincent Karam; Valérie Delvart; John O'Grady; Darius Mirza; Jurgen Klempnauer; Denis Castaing; Peter Neuhaus; Neville Jamieson; Mauro Salizzoni; Stephen Pollard; Jan Lerut; Andreas Paul; Juan Carlos Garcia-Valdecasas; Fernando San Juan Rodríguez; Andrew Burroughs
Journal:  J Hepatol       Date:  2012-05-16       Impact factor: 25.083

2.  Excellent survival after liver transplantation for isolated polycystic liver disease: an European Liver Transplant Registry study.

Authors:  Loes van Keimpema; Frederik Nevens; René Adam; Robert J Porte; Panagiotis Fikatas; Thomas Becker; Preben Kirkegaard; Herold J Metselaar; Joost P H Drenth
Journal:  Transpl Int       Date:  2011-09-29       Impact factor: 3.782

3.  Extended liver resection for polycystic liver disease can challenge liver transplantation.

Authors:  Béatrice Aussilhou; Ghislaine Douflé; Catherine Hubert; Claire Francoz; Catherine Paugam; Valérie Paradis; Olivier Farges; Valérie Vilgrain; François Durand; Jacques Belghiti
Journal:  Ann Surg       Date:  2010-11       Impact factor: 12.969

4.  Polycystic liver disease: a critical appraisal of hepatic resection, cyst fenestration, and liver transplantation.

Authors:  Thomas Schnelldorfer; Vicente E Torres; Shaheen Zakaria; Charles B Rosen; David M Nagorney
Journal:  Ann Surg       Date:  2009-07       Impact factor: 12.969

5.  Ethical Dilemmas in Liver Transplant Organ Allocation: Is it Time for a New Mathematical Model?

Authors:  Aaron Ahearn
Journal:  AMA J Ethics       Date:  2016-02-01

6.  Canadian liver transplant allocation for hepatocellular carcinoma.

Authors:  Mayur Brahmania; Vladimir Marquez; Norman M Kneteman; Mamatha Bhat; Denis Marleau; Philip Wong; Kevork M Peletekian; Kelly W Burak; Stephen E Congly
Journal:  J Hepatol       Date:  2019-09-05       Impact factor: 25.083

Review 7.  Systematic review: the pathophysiology and management of polycystic liver disease.

Authors:  F Temmerman; L Missiaen; B Bammens; W Laleman; D Cassiman; C Verslype; J van Pelt; F Nevens
Journal:  Aliment Pharmacol Ther       Date:  2011-07-26       Impact factor: 8.171

8.  Autosomal dominant polycystic liver disease: a second family.

Authors:  G Berrebi; R P Erickson; B W Marks
Journal:  Clin Genet       Date:  1982-05       Impact factor: 4.438

Review 9.  Polycystic liver disease: a clinical review.

Authors:  Natasha Chandok
Journal:  Ann Hepatol       Date:  2012 Nov-Dec       Impact factor: 2.400

Review 10.  Gastrointestinal Manifestations of Autosomal-Dominant Polycystic Kidney Disease.

Authors:  Adam E Mikolajczyk; Helen S Te; Arlene B Chapman
Journal:  Clin Gastroenterol Hepatol       Date:  2016-06-29       Impact factor: 11.382

View more
  1 in total

1.  Massive Polycystic Liver with a Poor Performance Status Successfully Treated by ABO-incompatible Adult Living-donor Liver Transplantation While Overcoming Complications.

Authors:  Satoshi Takakusagi; Yuichi Masuda; Hitoshi Takagi; Yozo Yokoyama; Kazuko Kizawa; Kyoko Marubashi; Takashi Kosone; Yuji Soejima
Journal:  Intern Med       Date:  2021-09-04       Impact factor: 1.271

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.