The prognostic value of HVPG-response to non-selective beta-blockers in patients with NASH cirrhosis and varices. Issue 4 (April 2022)

• Record Type: Journal Article
• Authors: Paternostro, Rafael; Becker, Jeannette; Hofer, Benedikt Silvester; Panagl, Vera; Schiffke, Helena; Simbrunner, Benedikt; Semmler, Georg; Schwabl, Philipp; Scheiner, Bernhard; Bucsics, Theresa; Bauer, David; Binter, Teresa; Trauner, Michael; Mandorfer, Mattias; Reiberger, Thomas
• Is Part Of: Digestive and liver disease. Volume 54:Issue 4(2022)
• Page Start: 500
• Page End: 508
• Publication Date: 2022-04
• Subjects: Cirrhosis -- Non-selective beta blockers -- Nash -- Portal hypertension -- Varices; Digestive organs -- Diseases -- Periodicals; Liver -- Diseases -- Periodicals; 616.33005
• DOI: 10.1016/j.dld.2021.09.009
• Languages: English
• ISSNs: 1590-8658

Abstract

Abstract: Background and Aims: Non-alcoholic steatohepatitis has become a leading cause of cirrhosis. The prognostic value of (HVPG)-guided NSBB prophylaxis remains to be investigated in the setting of NASH cirrhosis. Methods: Patients with NASH cirrhosis and varices undergoing HVPG-guided NSBB therapy were included. HVPG-response to NSBBs was evaluated within a median 52 (IQR:28–71) days after baseline measurement. HVPG-Response was defined as a decrease of ≥10% from baseline or below <12 mmHg. The composite endpoint was defined as variceal bleeding, decompensation, and liver-related death. Results: Thirtyeight patients were included: Child-A/B:33(87%), Child-C:5(13%) median HVPG:19.7 ± 4.7 mmHg. 21(55.3%) patients achieved HVPG-response to NSBB. Presence of diabetes(aOR:0.16, p = 0.038) and arterial blood pressure (aOR:1.07, p = 0.044) were independently associated with NSBB-response. While NSBB-HVPG-responders showed fewer decompensations within 90 days ( n = 1(5%) vs. n = 3(29%), p = 0.172), only Child-Pugh stage B/C ( p = 0.001), MELD ≥ 15( p = 0.021) and HVPG ≥ 20 mmHg( p = 0.011) predicted the composite endpoint at 90 days. Similarly, after 2years of follow-up, only Child-Pugh stage (B: p = 0.001, C: p < 0.001), MELD ≥ 15 ( p = 0.021), HVPG≥20 mmHg ( p = 0.011) predicted the composite endpoint. Importantly, all bleeding events occurred in HVPG-NSBB non-responders. Conclusion: HVPG-response to NSBB was achieved in 55.3% of NASH patients with varices and this seemed to protect from variceal bleeding. However, only baseline HVPG ≥ 20 mmHg, Child-Pugh stage B/C and MELD ≥ 15 were predictors of decompensation/death in patients with NASH cirrhosis and varices.