Diagnostic accuracy of transient elastography in diagnosing clinically significant portal hypertension in patients with chronic liver disease: a systematic review and meta-analysis

被引:8
作者
Kumar, Ashish [1 ]
Maruyama, Hitoshi [2 ]
Arora, Anil [1 ]
Sharma, Praveen [1 ]
Anikhindi, Shrihari Anil [1 ]
Bansal, Naresh [1 ]
Kumar, Mandhir [1 ]
Ranjan, Piyush [1 ]
Sachdeva, Munish [1 ]
Khare, Shivam [1 ]
机构
[1] Sir Ganga Ram Hosp, Inst Liver Gastroenterol Sr Pancreat Biliary Sci, New Delhi 110060, India
[2] Juntendo Univ, Dept Gastroenterol, Tokyo, Japan
关键词
Clinically significant portal hypertension; Hepatic venous pressure gradient; Fibroscan; Elastography; Cirrhosis; VENOUS-PRESSURE GRADIENT; STIFFNESS MEASUREMENT; CIRRHOSIS; PERFORMANCE; SPLEEN; PREDICTION; FIBROSIS; VARICES; TESTS; SIZE;
D O I
10.1007/s10396-022-01239-x
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose Liver stiffness measurement using transient elastography (TE-LSM) is a promising noninvasive alternative to hepatic venous pressure gradient (HVPG) for diagnosing clinically significant portal hypertension (CSPH). However, previous studies have yielded conflicting results. We evaluated the correlation between TE-LSM and HVPG and the performance of TE-LSM in diagnosing CSPH (HVPG >= 10 mmHg). Methods We conducted a systematic review and meta-analysis by searching PubMed and Scopus databases for relevant literature evaluating the clinical usefulness of TE for diagnosing CSPH in patients with chronic liver disease. Results Twenty-six studies (4337 patients with valid TE and HVPG) met our inclusion criteria. The median correlation coefficient of TE with HVPG was 0.70 (range 0.36-0.86). The weighted mean of optimal cut-off of liver stiffness value for diagnosing CSPH was 22.8 kPa (95% CI 22.7-23.0 kPa). The summary sensitivity and specificity were 79% (95% CI 74-84%) and 88% (95% CI 84-91%), respectively. The area under the hierarchical summary receiver operating characteristic (HSROC) curve was 0.91 (95% CI 0.88-0.93) according to the bivariate model. One limitation of the study was significant heterogeneity in the results of summary sensitivity and specificity (I-2 83 and 74%, respectively). The heterogeneity could be explained by the variable liver stiffness cut-offs used in studies. The meta-regression plot revealed that as the optimal cut-off increased, the sensitivity decreased, the specificity increased, and vice versa. Conclusions Liver stiffness measurement using TE correlates well with HVPG, and a liver stiffness cut-off value of 22.8 kPa shows a high accuracy for diagnosing CSPH. Thus, use of TE should be integrated into clinical practice for noninvasive diagnosis of CSPH.
引用
收藏
页码:333 / 346
页数:14
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