Other Liver Disease
Noninvasive assessment of the risk of esophageal variceal bleeding from noncirrhotic portal hypertension
Xu Hangfei, Wang Yu, He Fuliang, Fan Zhenhua, Liu Hui, Yang Yongping, Jia Jidong, Liu Fuquan, Ding Huiguo
Published 2022-10-20
Cite as Chin J Hepatol, 2022, 30(10): 1092-1099. DOI: 10.3760/cma.j.cn501113-20210126-00044
Abstract
ObjectiveTo verify Baveno VI criteria, Expanded-Baveno VI criteria, liver stiffness×spleen diameter-to-platelet ratio risk score (LSPS), and platelet count/spleen diameter ratio (PSR) in evaluating the severity value of esophageal varices (EV) in patients with non-cirrhotic portal hypertension (NCPH).
Methods111 cases of NCPH and 204 cases of hepatitis B cirrhosis who met the diagnostic criteria were included in the study. NCPH included 70 cases of idiopathic non-cirrhotic portal hypertension (INCPH) and 41 cases of nontumoral portal vein thrombosis (PVT). According to the severity of EV on endoscopy, they were divided into the low-bleeding-risk group (no/mild EV) and the high-bleeding-risk group (moderate/severe EV). The diagnostic value of Baveno VI and Expanded-Baveno VI criteria was verified to evaluate the value of LSPS and PSR for EV bleeding risk severity in NCPH patients. The t-test or Mann-Whitney U test was used to compare the measurement data between groups. Comparisons between counting data groups were performed using either the χ2 test or the Fisher exact probability method.
ResultsConsidering endoscopy was the gold standard for diagnosis, the missed diagnosis rates of low/high bleeding risk EVs in INCPH/PVT patients with Baveno VI and Expanded-Baveno VI criteria were 50.0%/30.0% and 53.8%/50.0%, respectively. There were no statistically significant differences in platelet count (PLT), spleen diameter, liver stiffness (LSM), LSPS, and PSR between low-bleeding-risk and high-bleeding-risk groups in INCPH patients, and the area under the receiver operating characteristic curve (AUC) of LSPS and PSR was 0.564 and 0.592, respectively (P=0.372 and 0.202, respectively). There were statistically significant differences in PLT, spleen diameter, LSPS, and PSR between the low and high-bleeding risk groups in PVT patients, and the AUCs of LSPS and PSR were 0.796 and 0.833 (P=0.003 and 0.001, respectively). In patients with hepatitis B cirrhosis, the Baveno VI and Expanded-Baveno VI criteria were used to verify the low bleeding risk EV, and the missed diagnosis rates were 0 and 5.4%, respectively. There were statistically significant differences in PLT, spleen diameter, LSM, LSPS and PSR between the low-bleeding-risk and high-bleeding-risk groups (P<0.001). LSPS and PSR AUC were 0.867 and 0.789, respectively (P<0.05).
ConclusionBaveno VI and Expanded-Baveno VI criteria have a high missed diagnosis rate for EVs with low bleeding risk in patients with INPCH and PVT, while LSPS and PSR have certain value in evaluating EV bleeding risk in PVT patients, which requires further clinical research.
Key words:
Non-cirrhotic portal hypertension; Esophageal varices; Bleeding risk; Non-invasive diagnosis
Contributor Information
Xu Hangfei
Department of Gastroenterology and Hepatology, Beijing You'an Hospital, Capital Medical University, Beijing 100069, China
Wang Yu
Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China
He Fuliang
Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China
Fan Zhenhua
Department of Interventional Therapy, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China
Liu Hui
Department of Pathology, Beijing You'an Hospital, Capital Medical University, Beijing 100069, China
Yang Yongping
Comprehensive Liver Cancer Department, the Fifth Medical Center, Chinese PLA General Hospital, Beijing 100039, China
Jia Jidong
Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China
Liu Fuquan
Department of Interventional Therapy, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China
Ding Huiguo
Department of Gastroenterology and Hepatology, Beijing You'an Hospital, Capital Medical University, Beijing 100069, China