Expanding the Baveno VI criteria for the screening of varices in patients with compensated advanced chronic liver disease

医学 置信区间 内科学 慢性肝病 队列 人口 肝病 胃肠病学 外科 肝硬化 环境卫生
作者
Salvador Augustín,Mònica Pons,James Maurice,Christophe Bureau,Horia Ștefănescu,Michel Ney,Hélène Blasco,Bogdan Procopeț,Emmanuel Tsochatzis,Rachel Westbrook,Jaime Bosch,Annalisa Berzigotti,Juan G. Abraldeṣ,Joan Genescà
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:66 (6): 1980-1988 被引量:253
标识
DOI:10.1002/hep.29363
摘要

Patients with compensated advanced chronic liver disease (cACLD) can safely avoid screening endoscopy with a platelet count >150 × 109 cells/L and a liver stiffness measurement (LSM) <20 kPa (Baveno VI criteria). However, the total number of avoided endoscopies using this rule is relatively low. We aimed at expanding the Baveno VI criteria and validating them in additional cohorts. Patients from the Anticipate cohort (499 patients with cACLD of different etiologies) were used to study the performance of different thresholds of platelets and LSM for the identification of patients at very low risk (<5%) of having varices needing treatment (VNT). The new criteria (Expanded-Baveno VI) were validated in two additional cohorts from London (309 patients) and Barcelona (117 patients). The performance of the new criteria by etiology of cACLD was also assessed. The best new expanded classification rule was platelet count >110 × 109 cells/L and LSM <25 kPa. This was validated in the two additional cohorts. Overall, the Expanded-Baveno VI criteria would potentially spare 367 (40%) endoscopies (21% with Baveno VI criteria) with a risk of missing VNT of 1.6% (95% confidence interval, 0.7%-3.5%) in patients within the criteria and 0.6% (95% confidence interval, 0.3%-1.4%) in the overall population of 925 patients evaluated. The Expanded-Baveno VI criteria performed well in patients with cACLD with hepatitis C virus and alcoholic and nonalcoholic steatohepatitis.The new Expanded-Baveno VI criteria spare more endoscopies than the original criteria with a minimal risk of missing VNT in most of the main etiologies of cACLD. (Hepatology 2017;66:1980-1988).
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