BMC Gastroenterology (Jul 2022)

Effects of endoscopic injection sclerotherapy for esophagogastric varices on portal hemodynamics and liver function

  • Ryuta Shigefuku,
  • Hideaki Takahashi,
  • Tsunamasa Watanabe,
  • Nobuhiro Hattori,
  • Hiroki Ikeda,
  • Kotaro Matsunaga,
  • Takuya Ehira,
  • Tatsuya Suzuki,
  • Nobuyuki Matsumoto,
  • Chiaki Okuse,
  • Motoh Iwasa,
  • Hayato Nakagawa,
  • Fumio Itoh,
  • Michihiro Suzuki

DOI
https://doi.org/10.1186/s12876-022-02422-7
Journal volume & issue
Vol. 22, no. 1
pp. 1 – 11

Abstract

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Abstract Objectives To identify patients suitable for endoscopic injection sclerotherapy (EIS) by evaluating their portal hemodynamics and liver function. Methods We selected 58 patients with esophagogastric varices (EGV) and liver cirrhosis (LC) related to either hepatitis C virus (C) (n = 19), hepatitis B virus (n = 2), alcohol (AL) (n = 20), C + AL (n = 6), non-alcoholic steatohepatitis (n = 6), others (n = 3), or non-LC (n = 2). All patients underwent EIS. We measured their portal venous tissue blood flow (PVTBF) and hepatic arterial tissue blood flow (HATBF) using xenon computed tomography before and after EIS. We classified them into increased group and decreased group according to the PVTBF to identify the predictors that contribute to PVTBF increase post-EIS. Results Low value of indocyanine green retention at 15 min (ICG-R15), the absence of paraesophageal veins, and low baseline PVTBF/HATBF (P/A) ratio predicted increased PVTBF in the multivariate logistic analysis (odds ratio (OR) 10.46, p = 0.0391; OR 12.45, p = 0.0088; OR 13.57, p = 0.0073). The protein synthetic ability improved 1 year post-EIS in increased group. Cox proportional hazards regression identified alcohol drinking (hazard ratio; 3.67, p = 0.0261) as an independent predictor of EGV recurrence. Conclusions Patients with low ICG-R15, low P/A ratio, and the absence of paraesophageal veins were probable predictors of PVTBF improvement post-EIS. In addition, the improvement of hepatic hemodynamics likely enhanced liver function following EIS.

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