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Optimising contrast-enhanced ultrasound (CEUS) Liver Imaging Reporting and Data System (LI-RADS) for hepatocellular carcinoma diagnosis in non-cirrhotic hepatitis B virus infection patients: incorporating alpha-fetoprotein or adjusting washout criteria.

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Clinical radiology 📖 저널 OA 2.2% 2022: 0/1 OA 2024: 0/2 OA 2025: 0/13 OA 2026: 1/23 OA 2022~2026 2026 Vol.96() p. 107292 Hepatitis B Virus Studies
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PubMed DOI OpenAlex Semantic 마지막 보강 2026-04-29
OpenAlex 토픽 · Hepatitis B Virus Studies Hepatocellular Carcinoma Treatment and Prognosis Liver Disease Diagnosis and Treatment

Gong W, Gong S, Chang H, Ma C, Zhao Q, Zhou X

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[AIM] To improve the diagnostic performance of contrast-enhanced ultrasound (CEUS) Liver Imaging Reporting and Data System (LI-RADS) for hepatocellular carcinoma (HCC) in non-cirrhotic hepatitis B vir

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value P < .05
  • p-value P < .01
  • Sensitivity 52.6%
  • Specificity 93.1%

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APA Wushuang Gong, Shaofan Gong, et al. (2026). Optimising contrast-enhanced ultrasound (CEUS) Liver Imaging Reporting and Data System (LI-RADS) for hepatocellular carcinoma diagnosis in non-cirrhotic hepatitis B virus infection patients: incorporating alpha-fetoprotein or adjusting washout criteria.. Clinical radiology, 96, 107292. https://doi.org/10.1016/j.crad.2026.107292
MLA Wushuang Gong, et al.. "Optimising contrast-enhanced ultrasound (CEUS) Liver Imaging Reporting and Data System (LI-RADS) for hepatocellular carcinoma diagnosis in non-cirrhotic hepatitis B virus infection patients: incorporating alpha-fetoprotein or adjusting washout criteria.." Clinical radiology, vol. 96, 2026, pp. 107292.
PMID 41849926 ↗

Abstract

[AIM] To improve the diagnostic performance of contrast-enhanced ultrasound (CEUS) Liver Imaging Reporting and Data System (LI-RADS) for hepatocellular carcinoma (HCC) in non-cirrhotic hepatitis B virus (NC-HBV) patients by integrating serum alpha-fetoprotein (AFP) or adjusting washout thresholds.

[MATERIALS AND METHODS] A retrospective analysis included 105 pathologically confirmed focal liver lesions in NC-HBV patients. The diagnostic performance of the original CEUS LI-RADS (Criteria 1) was compared with three modified versions: reclassifying LR-M nodules with AFP > 200 ng/mL as LR-5 (Criteria 2), AFP > 400 ng/mL as LR-5 (Criteria 3), and reducing the early washout threshold for LR-M from 60 seconds to 45 seconds (Criteria 4). Sensitivity, specificity, and positive predictive value (PPV) were assessed.

[RESULTS] Criteria 1 showed high specificity (93.1%) and PPV (95.2%) but low sensitivity (52.6%) for HCC. Criteria 2, 3, and 4 significantly increased sensitivity to 68.4%, 67.1%, and 63.2%, respectively (all P < .05), without significantly reducing specificity or PPV (all P > .05). For non-HCC malignancies, the specificity of revised LR-M increased to 82.8%, 81.6%, and 82.8% with Criteria 2, 3, and 4, respectively, compared to Criterion 1 (69.0%; all P < .01), while sensitivities remained statistically unchanged (all P > .05).

[CONCLUSION] CEUS LR-5 has high specificity for characterising HCC in NC-HBV patients. Integrating AFP or modifying the early washout threshold can significantly improve the sensitivity of CEUS LR-5 for diagnosing HCC in NC-HBV patients, while maintaining high specificity and PPV.

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