Literature DB >> 27323334

Influence of hepatorenal syndrome on outcome of living donor liver transplantation: A single-center experience in 357 patients.

Yusuke Okamura1, Koichiro Hata1, Osamu Inamoto1, Toyonari Kubota1, Hirofumi Hirao1, Hirokazu Tanaka1, Yasuhiro Fujimoto1, Kohei Ogawa1, Akira Mori1, Hideaki Okajima1, Toshimi Kaido1, Shinji Uemoto1.   

Abstract

AIM: Liver transplantation is the only curative treatment for hepatorenal syndrome (HRS); however, the influence of HRS on the patient and renal outcome after living donor liver transplantation (LDLT) is still unclear. The aim of the present study was to evaluate the influence of HRS on the outcome of LDLT.
METHODS: We retrospectively analyzed 357 consecutive adult patients who underwent primary LDLT between January 2005 and March 2013 at Kyoto University Hospital. The outcome of the patients with HRS was compared with those without HRS.
RESULTS: A total of 29 patients (8%) were diagnosed as HRS (Group-HRS) preoperatively, and the other 328 patients (92%) were not diagnosed as HRS (Group-Non-HRS). Group-HRS showed a significantly lower preoperative estimated glomerular filtration rate (22.1 vs 78.3 mL/min/1.73m2 , P < 0.001) and higher Child-Pugh-Turcotte score (13 vs 10, P < 0.001) than Group-non-HRS. After a median follow up of 60 months, the 1-, 3- and 5-year recipients' survival were 60.7%, 57.1% and 57.1% in Group-HRS, and 83.7%, 79.4% and 76.2% in Group-Non-HRS, respectively (P = 0.030). Concomitant HRS significantly elongated postoperative hospital stays (75 vs 50 days, P = 0.003), as well as predisposed patients to higher in-hospital mortality (41% vs 18%, P = 0.005). Multivariate analysis showed that preoperative renal dysfunction (estimated glomerular filtration rate on admission <40 mL/min/1.73m2 , OR 2.106, P = 0.03) was an independent risk factor for 1-year recipients' survival after LDLT, in addition to donor age ≥38 years (OR 3.114, P < 0.001), Child-Pugh-Turcotte score ≥13 (OR 2.929, P < 0.001) and left lobe graft (OR 2.225, P = 0.004).
CONCLUSION: Coincidence of HRS is associated with significantly worse outcome after LDLT, especially in the early post-transplant period.
© 2016 The Japan Society of Hepatology.

Entities:  

Keywords:  hepatorenal syndrome; liver transplantation; living donor

Year:  2016        PMID: 27323334     DOI: 10.1111/hepr.12764

Source DB:  PubMed          Journal:  Hepatol Res        ISSN: 1386-6346            Impact factor:   4.288


  3 in total

1.  Disruption of Renal Arginine Metabolism Promotes Kidney Injury in Hepatorenal Syndrome in Mice.

Authors:  Zoltan V Varga; Katalin Erdelyi; Janos Paloczi; Resat Cinar; Zsuzsanna K Zsengeller; Tony Jourdan; Csaba Matyas; Balazs Tamas Nemeth; Adrien Guillot; Xiaogang Xiang; Adam Mehal; György Haskó; Isaac E Stillman; Seymour Rosen; Bin Gao; George Kunos; Pal Pacher
Journal:  Hepatology       Date:  2018-10       Impact factor: 17.425

2.  Impact of Advanced Renal Dysfunction on Posttransplant Outcomes After Living Donor Liver Transplantation in the United States.

Authors:  Therese Bittermann; Peter L Abt; Kim M Olthoff; Navpreet Kaur; Julie K Heimbach; Juliet Emamaullee
Journal:  Transplantation       Date:  2021-12-01       Impact factor: 5.385

3.  Development and validation of a prognostic model for patients with hepatorenal syndrome: A retrospective cohort study.

Authors:  Xin-Yu Sheng; Fei-Yan Lin; Jian Wu; Hong-Cui Cao
Journal:  World J Gastroenterol       Date:  2021-05-28       Impact factor: 5.742

  3 in total

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