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1.
Dig Liver Dis ; 54(8): 1007-1014, 2022 08.
Article in English | MEDLINE | ID: mdl-35016859

ABSTRACT

BACKGROUND: Refractory ascites is a severe complication of liver cirrhosis and treatment options consist in large volume paracentesis, transjugular intrahepatic portosystemic shunt, alfapump®, peritoneovenous shunt and permanent indwelling peritoneal catheter. AIM: Our aim was to assess the efficacy, mortality and complications of each treatment. METHODS: We performed a systematic review using Pubmed and Embase. Frequencies were summarized with Comprehensive Meta-Analysis Software. RESULTS: Seventy-seven studies were included. In patients with transjugular intrahepatic portosystemic shunt, 1-year mortality was 33% (95% CI 0.29-0.39, I2=82.1; τ2 = 0.37; p<0.001) with lower mortality in newer studies (26% vs. 44%). At 6 months, mortality in patients with alfapump® was 24% (95% CI 0.16-0.33, I2=0.00; τ2 = 0.00; p = 0.83), 31% developed acute kidney injury (95% CI 0.18-0.48, I2=44.0; τ2 = 0.22; p = 0.15). Mortality at 12 months was 44% (95% CI 32%-58%, I2=76.7, τ2 = 0.44, p<0.001) in peritoneovenous shunts and 45% (95% CI 38%-53%, I2=61.4, τ2 = 0.18, p = 0.003) in large volume paracentesis, respectively. Overall mortality in patients with permanent indwelling catheters was 66% (95% CI 33%-89%, I2=82.5, τ2 = 1.57, p = 0.001). DISCUSSION: Mortality in patients with transjugular intrahepatic portosystemic shunt was lower in newer studies, probably due to a better patient selection. Acute kidney injury was frequent in patients with alfapump®. Permanent indwelling catheters seemed to be a good option in a palliative setting.


Subject(s)
Acute Kidney Injury , Portasystemic Shunt, Transjugular Intrahepatic , Acute Kidney Injury/complications , Ascites/etiology , Ascites/therapy , Humans , Liver Cirrhosis/complications , Paracentesis/adverse effects , Portasystemic Shunt, Transjugular Intrahepatic/adverse effects , Treatment Outcome
2.
United European Gastroenterol J ; 8(8): 961-969, 2020 10.
Article in English | MEDLINE | ID: mdl-32588789

ABSTRACT

BACKGROUND: Treatment of refractory ascites in liver cirrhosis is challenging. Transjugular intrahepatic portosystemic shunt and alfapump® have been proposed for the management, but few data comparing both exist. AIMS: The aim of this study was to evaluate the characteristics and outcomes of patients treated with transjugular intrahepatic portosystemic shunt and alfapump® for refractory ascites at our centre. METHODS: All consecutive patients were retrospectively reviewed for baseline characteristics, efficacy of treatment, complications and survival. RESULTS: In total, 19 patients with transjugular intrahepatic portosystemic shunt and 40 patients with alfapump® were included. Patients with transjugular intrahepatic portosystemic shunt had better liver function and less hepatic encephalopathy at baseline. Fifty-eight per cent of patients developed hepatic encephalopathy in the first six months after transjugular intrahepatic portosystemic shunt. In patients with alfapump®, renal function decreased and 58% developed prerenal impairment and 43% hepatorenal syndrome in the first six months. Alfapump® patients with new catheters required less reinterventions (26% versus 57% with old catheters, p = 0.049). Transplant-free survival at 1 year was 25% in alfapump® and 65% in transjugular intrahepatic portosystemic shunt. Hepatic encephalopathy predicted transplant-free survival in patients with alfapump® (hazard ratio 2.00, 95% confidence interval 0.99-4.02, p = 0.05). In a sensitivity analysis comparing patients with similar liver function, the rate of hepatorenal syndrome and prerenal impairment was higher in patients with alfapump® and these patients were hospitalised more frequently, whereas the rate of hepatic encephalopathy was similar in both treatment groups. CONCLUSIONS: Both transjugular intrahepatic portosystemic shunt and alfapump® were effective treatments for refractory ascites in cirrhosis. Patients treated with transjugular intrahepatic portosystemic shunt had a better one-year transplant-free survival but had less negative prognostic factors at baseline. Selecting patients without hepatic encephalopathy prior to implantation of an alfapump® might improve transplant-free survival.


Subject(s)
Ascites/surgery , Drainage/instrumentation , Hepatic Encephalopathy/surgery , Hepatorenal Syndrome/surgery , Liver Cirrhosis/surgery , Portasystemic Shunt, Transjugular Intrahepatic/statistics & numerical data , Aged , Ascites/etiology , Ascites/mortality , Drainage/adverse effects , Drainage/statistics & numerical data , Female , Follow-Up Studies , Hepatic Encephalopathy/epidemiology , Hepatic Encephalopathy/etiology , Hepatorenal Syndrome/epidemiology , Hepatorenal Syndrome/etiology , Humans , Liver Cirrhosis/complications , Liver Cirrhosis/mortality , Liver Transplantation/statistics & numerical data , Male , Middle Aged , Patient Selection , Peritoneal Cavity/surgery , Portasystemic Shunt, Transjugular Intrahepatic/adverse effects , Proportional Hazards Models , Reoperation/statistics & numerical data , Retrospective Studies , Risk Assessment , Risk Factors , Survival Analysis , Treatment Outcome , Urinary Bladder/surgery
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