Shear wave elastography as a screening modality for liver fibrosis in a comprehensive sickle cell disease clinic

Marissa Solow1, Anas Samman2, Dawn Goodyear1,3

  • 1Division of Hematology and Hematological Malignancies, Department of Medicine, University of Calgary, Calgary, AB, Canada.

Insights

Shear wave elastography (SWE) identified significant liver fibrosis in 8% of sickle cell disease (SCD) patients. This noninvasive ultrasound method may help detect hepatic complications in SCD.

Area of Science:

  • Hepatology
  • Hematology
  • Medical Imaging

Background:

  • Sickle cell disease (SCD) patients face risks of liver fibrosis and cirrhosis due to chronic hemolysis, intrahepatic sickling, and iron overload.
  • Current screening for liver fibrosis in SCD lacks standardization.
  • Shear wave elastography (SWE), a noninvasive ultrasound technique, offers a potential solution for assessing liver stiffness and fibrosis.

Purpose of the Study:

  • To determine the prevalence of liver fibrosis in adults with SCD using SWE.
  • To explore clinical and laboratory factors associated with SWE-detected fibrosis in SCD patients.

Main Methods:

  • A retrospective cohort study involving adults with SCD who underwent SWE between 2021 and 2025.
  • Liver fibrosis was staged using METAVIR-equivalent scores (F0-F4), with ≥F2 considered clinically significant.
  • Clinical, laboratory, and imaging data were collected within six months of the SWE procedure.

Main Results:

  • Out of 219 eligible patients, 153 (70%) underwent SWE.
  • Clinically significant fibrosis (≥F2) was detected in 8% (12 patients) of the cohort.
  • Abnormal SWE findings correlated with elevated bilirubin, GGT, and ferritin levels.

Conclusions:

  • SWE identified significant liver fibrosis in 8% of adults with SCD.
  • This noninvasive ultrasound technique shows promise for detecting previously unrecognized hepatic involvement in SCD patients.
  • The findings suggest SWE could be a valuable tool for routine screening and management of liver complications in SCD.
Abstract