Identification of Clinically Significant Portal Hypertension in cACLD Individuals With Spleen Stiffness Measurement

瞬态弹性成像 医学 门脉高压 脾脏 弹性成像 内科学 胃肠病学 门静脉压 超声波 放射科 肝硬化 肝纤维化
作者
Xiaofeng Zhang,Ling Zhou,Weihao Liang,Cheng Xiao,Qinjun He,Hui Li,Wenfan Luo,Jing Huang,Junying Li,Weibin Wang,Minghan Tu,Haiyu Wang,Pengcheng Ou,Biao Wen,Lushan Xiao,Damei Zhou,Vincent Wai‐Sun Wong,Jinjun Chen
出处
期刊:Liver International [Wiley]
卷期号:45 (4): e16241-e16241 被引量:5
标识
DOI:10.1111/liv.16241
摘要

BACKGROUND AND AIMS: The Baveno VII consensus recommends spleen stiffness measurement (SSM) for the detection of clinically significant portal hypertension (CSPH) in patients with compensated advanced chronic liver disease (cACLD). We aimed to evaluate the performance of SSM-based algorithms. METHODS: Consecutive cACLD individuals who underwent hepatic venous pressure gradient measurement, liver stiffness measurement (LSM), and SSM measured with the dedicated 100-Hz probe by vibration-controlled transient elastography were prospectively enrolled. RESULTS: From July 2021 to August 2024, a total of 395 patients were screened, and 185 cACLD cases were enrolled, of which 101 patients had CSPH. An SSM > 50 kPa demonstrated a positive predictive value (PPV) of 98.0% and a specificity of 98.8% for ruling in CSPH, correctly identifying 47.5% (48/101) of CSPH cases. Sensitivity analysis revealed that in 60 patients with aetiology removal or suppression, SSM > 50 kPa achieved both a PPV and specificity of 100%. Among the 125 patients with ongoing aetiologies, the PPV and specificity were 96.4% and 98.3%, respectively. Across HBV (with or without viral suppression) and non-HBV subgroups, the PPV and specificity consistently exceeded 90%. In decision curve analysis, SSM > 50 kPa provided the highest net benefit compared with other elastography-based algorithms when threshold probabilities exceeded 0.8. CONCLUSIONS: We prospectively validated that SSM > 50 kPa, measured using the spleen-dedicated probe, is sufficient for identifying CSPH in individuals with cACLD. TRIAL REGISTRATION: NCT04820166.
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