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The prognostic value of HVPG-response to non-selective beta-blockers in patients with NASH cirrhosis and varices
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 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 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.
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“Data from our group [87] found that 55.3% of patients with NASH cirrhosis undergoing NSBB therapy for either primary‐ or secondary prophylaxis of variceal bleeding were NSBB responders (median Propranolol dosage: 80 mg/d, median Carvedilol dosage: 12.5 mg/d).”
From Current treatment of non‐alcoholic fatty liver disease (2022) · cites this paper as [87]
In the citing paper
“Interestingly, the presence of diabetes mellitus was associated with a reduced probability of achieving NSBB response [87].”
From Current treatment of non‐alcoholic fatty liver disease (2022) · cites this paper as [87]
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Current treatment of non‐alcoholic fatty liver disease
Paternostro, R., & Trauner, M. (2022) · Journal of Internal Medicine · doi:10.1111/joim.13531 · Cited by 305
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- Authors
- Paternostro, R., Becker, J., Hofer, B. S., Panagl, V., Schiffke, H., Simbrunner, B., Semmler, G., Schwabl, P., Scheiner, B., Bucsics, T., Bauer, D., Binter, T., Trauner, M., Mandorfer, M., & Reiberger, T.
- ORCID
- Reiberger, Thomas
- Venue
- Digestive and Liver Disease
- Publisher
- Elsevier BV
- Published
- 2022-04
- Volume
- 54
- Issue
- 4
- Pages
- 500-508
- ISSN
- 1590-8658
- Cited by
- 17
- References
- 3
- Language
- en
- Licence
- Funders
- Bayer
- Medizinische Universität Graz
- Roche
- Boehringer Ingelheim
- Gilead Sciences
- AbbVie
- Meso Scale Diagnostics
- Bristol-Myers Squibb
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