CT-derived liver and spleen volume accurately diagnose clinically significant portal hypertension in patients with hepatocellular carcinoma

Clinically significant portal hypertension (CSPH) is a landmark in the natural history of cirrhosis, influencing clinical decisions in patients with hepatocellular carcinoma (HCC). Previous small series suggested that splanchnic volume measurements may predict portal hypertension. We aimed to evalua...

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Published inJHEP reports Vol. 5; no. 3; p. 100645
Main Authors Romero-Cristóbal, Mario, Clemente-Sánchez, Ana, Ramón, Enrique, Téllez, Luis, Canales, Elena, Ortega-Lobete, Olga, Velilla-Aparicio, Elena, Catalina, María-Vega, Ibáñez-Samaniego, Luis, Alonso, Sonia, Colón, Arturo, Matilla, Ana-María, Salcedo, Magdalena, Albillos, Agustín, Bañares, Rafael, Rincón, Diego
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.03.2023
Elsevier
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Summary:Clinically significant portal hypertension (CSPH) is a landmark in the natural history of cirrhosis, influencing clinical decisions in patients with hepatocellular carcinoma (HCC). Previous small series suggested that splanchnic volume measurements may predict portal hypertension. We aimed to evaluate whether volumetry obtained by standard multidetector computerised tomography (MDCT) can predict CSPH in patients with HCC. We included 175 patients with HCC, referred for hepatic venous pressure gradient (HVPG) evaluation, in whom contemporary MDCT was available. Liver volume, spleen volume (SV) and liver segmental volume ratio (LSVR: volume of the segments I-III/volume of the segments IV-VIII) were calculated semi-automatically from MDCT. Other non-invasive tests (NITs) were also employed. Volume parameters could be measured in almost 100% of cases with an excellent inter-observer agreement (intraclass correlation coefficient >0.950). SV and LSVR were independently associated with CSPH (HVPG ≥10 mmHg) and did not interact with aetiology. The volume Index (VI), calculated as the product of SV and LSVR, predicted CSPH (AUC 0.83; 95% CI 0.77–0.89). Similar results were observed in an external cohort (n = 23) (AUC 0.87; 95% CI 0.69–1.00). Setting a sensitivity and specificity of 98%, VI could have avoided 35.9% of HVPG measurements. The accuracy of VI was similar to that of other NITs. VI also accurately predicted HVPG greater than 12, 14, 16 and 18 mmHg (AUC 0.81 [95% CI 0.74–0.88], 0.84 [95% CI 0.77–0.91], 0.85 [95% CI 0.77–0.92] and 0.87 [95% CI 0.79–0.94], respectively). Quantification of liver and spleen volumes by MDCT is a simple, accurate and reliable method of CSPH estimation in patients with compensated cirrhosis and HCC. An increase in portal pressure strongly impacts outcomes after surgery in patients with early hepatocellular carcinoma (HCC). Direct measurement through hepatic vein catheterization remains the reference standard for portal pressure assessment, but its invasiveness limits its application. Therefore, we evaluated the ability of CT scan-based liver and spleen volume measurements to predict portal hypertension in patients with HCC. Our results indicate that the newly described index, based on quantification of liver and spleen volume, accurately predicts portal hypertension. These results suggest that a single imaging test may be used to diagnose and stage HCC, while providing an accurate estimation of portal hypertension, thus helping to stratify surgical risks. [Display omitted] •The VI predicts the presence of CSPH and severe portal hypertension in patients with compensated cirrhosis and HCC.•The accuracy of the VI for the prediction of CSPH is comparable to that of other widely used and validated NITs.•Visceral volumetric assessment by MDCT is an accessible, affordable, easy-to-perform, and accurate test.•A single imaging test can confirm the diagnosis/stage of HCC and estimate the individual risk of different degrees of portal hypertension.
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Rafael Bañares and Diego Rincón share senior authorship.
Mario Romero-Cristóbal and Ana Clemente-Sánchez share first authorship.
ISSN:2589-5559
2589-5559
DOI:10.1016/j.jhepr.2022.100645