2021
DOI: 10.1007/s00261-021-03055-2
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Comparison of diffusion-weighted imaging and MR elastography in staging liver fibrosis: a meta-analysis

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Cited by 9 publications
(5 citation statements)
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“…CT-LSN scores may discern subtle changes of hepatic parenchymal architecture and have been suggested as valuable in liver fibrosis staging, 38,39 and may be associated with post-hepatectomy liver failure among HCC patients. 40 However, the use of different imaging parameters and variable thresholds 10,[38][39][40][41][42][43] preclude inter-study comparisons and general The intraoperative classification of the gross severity of cirrhosis was proposed as a rapid staging method to determine the extent of hepatic resection. 44 However, the single-center study was conducted using the generic term "cirrhosis", omitted external validation, and failed to present convincing evidence of liver fibrosis staging.…”
Section: Discussionmentioning
confidence: 99%
“…CT-LSN scores may discern subtle changes of hepatic parenchymal architecture and have been suggested as valuable in liver fibrosis staging, 38,39 and may be associated with post-hepatectomy liver failure among HCC patients. 40 However, the use of different imaging parameters and variable thresholds 10,[38][39][40][41][42][43] preclude inter-study comparisons and general The intraoperative classification of the gross severity of cirrhosis was proposed as a rapid staging method to determine the extent of hepatic resection. 44 However, the single-center study was conducted using the generic term "cirrhosis", omitted external validation, and failed to present convincing evidence of liver fibrosis staging.…”
Section: Discussionmentioning
confidence: 99%
“… 109 , 110 The pooled sensitivity and specificity were 0.63–0.82 and 0.78–0.86, respectively, with an AUROC of 0.79–0.88 for the staging of significant fibrosis (F ≥ 2), 0.71–0.88 and 0.68–0.84, respectively, with an AUROC of 0.81–0.89 for the staging of severe fibrosis (F ≥ 3), and 0.80–0.96 and 0.69–0.77, respectively, with an AUROC of 0.80–0.90 for the staging of cirrhosis (F4) in DWI and IVIM. 109 , 111 114 …”
Section: Clinical Needs For Diffuse Liver Diseasesmentioning
confidence: 99%
“…109,110 The pooled sensitivity and specificity were 0.63-0.82 and 0.78-0.86, respectively, with an AUROC of 0.79-0.88 for the staging of significant fibrosis (F ≥ 2), 0.71-0.88 and 0.68-0.84, respectively, with an AUROC of 0.81-0.89 for the staging of severe fibrosis (F ≥ 3), and 0.80-0.96 and 0.69-0.77, respectively, with an AUROC of 0.80-0.90 for the staging of cirrhosis (F4) in DWI and IVIM. 109,[111][112][113][114] Elastography Cirrhosis is the most important risk factor for HCC; therefore, it is important to accurately assess advanced fibrosis. For many patients, fibrosis stages are monitored using noninvasive tests, including elastography.…”
Section: Clinical Significance Of Liver Mrimentioning
confidence: 99%
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“… 85 , 86 Although a large number of studies have shown that liver fibrosis and apparent diffusion coefficient (ADC) values are inversely correlated, a recent meta-analysis reported that DWI also showed a good diagnostic performance for histological fibrosis staging but was inferior to MRE. 85 , 87 Since the liver is a highly vascularized organ, perfusion has a significant impact on diffusivity. IVIM, a biexponential model of DWI introduced by Le Bihan et al, can evaluate capillary microcirculation and water diffusion separately by analyzing the signal attenuation of multi-b-value DWI.…”
Section: Quantification Of Fibrosismentioning
confidence: 99%