[HTML][HTML] The diagnostic accuracy of liver fibrosis in non-viral liver diseases using acoustic radiation force impulse elastography: A systematic review and meta-analysis

Y Lin, H Li, C Jin, H Wang, B Jiang - PloS one, 2020 - journals.plos.org
Y Lin, H Li, C Jin, H Wang, B Jiang
PloS one, 2020journals.plos.org
Background Acoustic radiation force impulse (ARFI) imaging is an ultrasound-based
elastography method that has been studied in the staging of hepatic fibrosis, especially in
chronic hepatitis. However, the diagnostic accuracy of ARFI in non-viral hepatopathies, such
as autoimmune hepatitis and non-alcoholic fatty liver disease, has not been systematically
determined. Aim To systematically assess the diagnostic accuracy of ARFI in non-viral
hepatopathies. Methods The databases of PubMed, Embase, Cochrane Library and …
Background
Acoustic radiation force impulse (ARFI) imaging is an ultrasound-based elastography method that has been studied in the staging of hepatic fibrosis, especially in chronic hepatitis. However, the diagnostic accuracy of ARFI in non-viral hepatopathies, such as autoimmune hepatitis and non-alcoholic fatty liver disease, has not been systematically determined.
Aim
To systematically assess the diagnostic accuracy of ARFI in non-viral hepatopathies.
Methods
The databases of PubMed, Embase, Cochrane Library and clinicaltrials.gov were systematically searched for candidate studies reporting the diagnostic accuracy of ARFI for hepatic fibrosis. The pooled estimates of the sensitivity, specificity, diagnostic odds ratio, and positive and negative likelihood ratios were calculated with the summary receiver operating curve (sROC) performed using STATA software.
Results
In detail, a total of 29 diagnostic studies were included for further analysis. The quality of the included studies was relatively high using QUADAS method. The pooled sensitivity and specificity were 0.79 (0.73, 0.83) and 0.81 (0.75, 0.86), with AUROC 0.87 (0.83, 0.89) for the staging of significant fibrosis (F≥2). Meanwhile, for the staging of severe fibrosis (F≥3), the pooled sensitivity and specificity were 0.92 (0.87, 0.95) and 0.85 (0.80, 0.89), with AUROC 0.94 (0.92, 0.96). Furthermore, the pooled sensitivity and specificity were 0.89 (0.79, 0.95) and 0.89 (0.85, 0.92), with AUROC 0.94 (0.92, 0.96) for ARFI in staging cirrhosis (F = 4), which were similar to the data for severe fibrosis. No significant publication bias was present in this study.
Conclusion
This meta-analysis demonstrated that ARFI exerted satisfactory diagnostic performance in staging non-viral hepatic fibrosis, especially severe fibrosis (F≥3) and cirrhosis (F = 4).
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