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Portal Hypertension in Polycystic Liver Disease Patients Does Not Affect Wait-list or Immediate Post-liver Transplantation Outcomes

Overview
Specialty Gastroenterology
Date 2016 Dec 27
PMID 28018103
Citations 2
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Abstract

Aim: To establish the impact of portal hypertension (PH) on wait-list/post-transplant outcomes in patients with polycystic liver disease (PCLD) listed for liver transplantation.

Methods: A retrospective single-centre case controlled study of consecutive patients listed for liver transplantation over 12 years was performed from our centre. PH in the PCLD cohort was defined by the one or more of following parameters: (1) presence of radiological or endoscopic documented varices from our own centre or the referral centre; (2) splenomegaly (> 11 cm) on radiology in absence of splenic cysts accounting for increased imaging size; (3) thrombocytopenia (platelets < 150 × 10/L); or (4) ascites without radiological evidence of hepatic venous outflow obstruction from a single cyst.

Results: Forty-seven PCLD patients (F: M = 42: 5) were listed for liver transplantation (LT) (single organ, = 35; combined liver-kidney transplantation, = 12) with 19 patients (40.4%) having PH. When comparing the PH group with non-PH group, the mean listing age (PH group, 50.6 (6.4); non-PH group, 47.1 (7.4) years; = 0.101), median listing MELD (PH group, 12; non-PH group, 11; = 0.422) median listing UKELD score (PH group, 48; non-PH group, 46; = 0.344) and need for renal replacement therapy ( = 0.317) were similar. In the patients who underwent LT alone, there was no difference in the duration of ICU stay (PH, 3 d; non-PH, 2 d; = 0.188), hospital stay length (PH, 9 d; non-PH, 10 d; = 0.973), or frequency of renal replacement therapy (PH, 2/8; non-PH, 1/14; = 0.121) in the immediate post-transplantation period.

Conclusion: Clinically apparent portal hypertension in patients with PCLD listed for liver transplantation does not appear to have a major impact on wait-list or peri-transplant morbidity.

Citing Articles

Management of portal hypertension and ascites in polycystic liver disease.

Bernts L, Drenth J, Tjwa E Liver Int. 2019; 39(11):2024-2033.

PMID: 31505092 PMC: 6899472. DOI: 10.1111/liv.14245.


Long-term results of liver transplantation for polycystic liver disease: Single-center experience in China.

Ding F, Tang H, Zhao H, Feng X, Yang Y, Chen G Exp Ther Med. 2019; 17(5):4183-4189.

PMID: 31007749 PMC: 6468458. DOI: 10.3892/etm.2019.7449.

References
1.
Neijenhuis M, Gevers T, Hogan M, Kamath P, Wijnands T, van den Ouweland R . Development and Validation of a Disease-Specific Questionnaire to Assess Patient-Reported Symptoms in Polycystic Liver Disease. Hepatology. 2016; 64(1):151-60. PMC: 4917464. DOI: 10.1002/hep.28545. View

2.
Qian Q, Li A, King B, Kamath P, Lager D, Huston 3rd J . Clinical profile of autosomal dominant polycystic liver disease. Hepatology. 2002; 37(1):164-71. DOI: 10.1053/jhep.2003.50006. View

3.
Hogan M, Masyuk T, Bergstralh E, Li B, Kremers W, Vaughan L . Efficacy of 4 Years of Octreotide Long-Acting Release Therapy in Patients With Severe Polycystic Liver Disease. Mayo Clin Proc. 2015; 90(8):1030-7. PMC: 4928579. DOI: 10.1016/j.mayocp.2015.05.011. View

4.
van Keimpema L, Nevens F, Vanslembrouck R, van Oijen M, Hoffmann A, Dekker H . Lanreotide reduces the volume of polycystic liver: a randomized, double-blind, placebo-controlled trial. Gastroenterology. 2009; 137(5):1661-8.e1-2. DOI: 10.1053/j.gastro.2009.07.052. View

5.
Swenson K, Seu P, Kinkhabwala M, Maggard M, MARTIN P, Goss J . Liver transplantation for adult polycystic liver disease. Hepatology. 1998; 28(2):412-5. DOI: 10.1002/hep.510280218. View