Two-dimensional shear wave elastography predicts survival in advanced chronic liver disease
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Multicenter Study, Observational Study, Research Support, Non-U.S. Gov't
PubMed
33479052
PubMed Central
PMC8761995
DOI
10.1136/gutjnl-2020-323419
PII: gutjnl-2020-323419
Knihovny.cz E-resources
- Keywords
- chronic liver disease, clinical decision making, liver cirrhosis, liver failure, portal hypertension,
- MeSH
- Algorithms MeSH
- Chronic Disease MeSH
- Adult MeSH
- Elasticity Imaging Techniques * MeSH
- Middle Aged MeSH
- Humans MeSH
- Survival Rate MeSH
- Liver Diseases diagnosis etiology mortality MeSH
- Predictive Value of Tests MeSH
- Retrospective Studies MeSH
- ROC Curve MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
- Research Support, Non-U.S. Gov't MeSH
OBJECTIVE: Liver stiffness measurement (LSM) is a tool used to screen for significant fibrosis and portal hypertension. The aim of this retrospective multicentre study was to develop an easy tool using LSM for clinical outcomes in advanced chronic liver disease (ACLD) patients. DESIGN: This international multicentre cohort study included a derivation ACLD patient cohort with valid two-dimensional shear wave elastography (2D-SWE) results. Clinical and laboratory parameters at baseline and during follow-up were recorded. LSM by transient elastography (TE) was also recorded if available. The primary outcome was overall mortality. The secondary outcome was the development of first/further decompensation. RESULTS: After screening 2148 patients (16 centres), 1827 patients (55 years, 62.4% men) were included in the 2D-SWE cohort, with median liver SWE (L-SWE) 11.8 kPa and a model for end stage liver disease (MELD) score of 8. Combination of MELD score and L-SWE predict independently of mortality (AUC 0.8). L-SWE cut-off at ≥20 kPa combined with MELD ≥10 could stratify the risk of mortality and first/further decompensation in ACLD patients. The 2-year mortality and decompensation rates were 36.9% and 61.8%, respectively, in the 305 (18.3%) high-risk patients (with L-SWE ≥20 kPa and MELD ≥10), while in the 944 (56.6%) low-risk patients, these were 1.1% and 3.5%, respectively. Importantly, this M10LS20 algorithm was validated by TE-based LSM and in an additional cohort of 119 patients with valid point shear SWE-LSM. CONCLUSION: The M10LS20 algorithm allows risk stratification of patients with ACLD. Patients with L-SWE ≥20 kPa and MELD ≥10 should be followed closely and receive intensified care, while patients with low risk may be managed at longer intervals.
Bern University Hospital Bern Switzerland
CHU Bordeaux and INSERM U1053 Bordeaux University Bordeaux France
Department of Gastroenterology and Hepatology Odense University Hospital Odense Denmark
Department of Gastroenterology Hepatology Antwerp University Hospital Antwerp Belgium
Department of Internal Medicine 1 Frankfurt University Hospital Frankfurt am Main Hessen Germany
Department of Radiology Beaujon University Hospital Clichy France
Department of Radiology Saint Jean Hospital Perpignan France
European Foundation for the Study of Chronic Liver Failure Barcelona Catalunya Spain
Fédération des Spécialités Digestives Hôpital Edouard Herriot Lyon France
Internal Medicine 1 University of Bonn Bonn Germany
Paris Cochin University Hopital Paris France
University Hospital and HIFIH Lab Angers France
University hospital Dubrava University of Zagreb School of Medicine Zagreb Zagreb Croatia
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