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María-Vega Catalina

Researcher at Hospital General Universitario Gregorio Marañón

Publications -  52
Citations -  1617

María-Vega Catalina is an academic researcher from Hospital General Universitario Gregorio Marañón. The author has contributed to research in topics: Cirrhosis & Portal venous pressure. The author has an hindex of 18, co-authored 43 publications receiving 1408 citations. Previous affiliations of María-Vega Catalina include Carlos III Health Institute & University of Barcelona.

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Influence of hepatic venous pressure gradient on the prediction of survival of patients with cirrhosis in the MELD Era

TL;DR: HVPG has an independent effect on survival in addition to the Model for End‐Stage Liver Disease (MELD) score, and its discriminative ability is not significantly improved.
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Comparison of transcatheter arterial embolization and surgery for treatment of bleeding peptic ulcer after endoscopic treatment failure.

TL;DR: The lack of differences between these two treatment alternatives, despite the more advanced age and greater prevalence of heart disease in the embolotherapy group, provides support for future prospective randomized studies aimed to evaluate the role of embol therapy in the management of refractory peptic ulcer bleeding.
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A meta-analysis of transjugular intrahepatic portosystemic shunt versus paracentesis for refractory ascites

TL;DR: In patients with refractory ascites, a better control of ascites by TIPS does not translate into improved survival and worsens encephalopathy.
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Value of the Hepatic Venous Pressure Gradient to Monitor Drug Therapy for Portal Hypertension: A Meta-Analysis

TL;DR: Current evidence supports the validity of HVPG end points to monitor drug therapy efficacy for variceal bleeding prophylaxis and also provides valuable prognostic information.
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Rebleeding and mortality risk are increased by ACLF but reduced by pre-emptive TIPS

Jonel Trebicka, +63 more
TL;DR: This large multi-center international real-life study identified ACLF as at admission an independent predictor of rebleeding and mortality in AVB and pTIPS may be considered in ACLF patients with AVB, although the presented data need to be independently validated.