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Chinese Journal of Hepatic Surgery(Electronic Edition) ›› 2026, Vol. 15 ›› Issue (01): 66-72. doi: 10.3877/cma.j.issn.2095-3232.2026.01.011

• Clinical Research • Previous Articles    

Application of avatrombopag in patients with chronic liver disease-associated thrombocytopenia undergoing high-risk invasive procedures: a single-center, prospective, non-randomized controlled trial

Bin Shi1, Lingzhan Meng2, Hu Li2, Peng Yu2, Li Cao2, Zizheng Wang2, Yanling Shao2, Jin Yan2, Zhenyu Zhu2,()   

  1. 1 Department of Organ Transplantation, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China
    2 Department of Liver Surgery, the Fifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China
  • Received:2025-07-12 Online:2026-02-10 Published:2026-02-04
  • Contact: Zhenyu Zhu

Abstract:

Objective

To evaluate clinical efficacy and safety of avatrombopag in adult patients with chronic liver disease-associated thrombocytopenia (CHRT) undergoing elective high-risk invasive procedures.

Methods

In this prospective clinical trial, 68 patients with CHRT undergoing elective invasive procedures in the PLA General Hospital were enrolled. The informed consents of all patients were obtained and the local ethical committee approval was received. Among them, 49 patients were male and 19 female, aged 50 years on average. According to different treatment regimens, they were divided into the study group (n=17) and routine group (n=51). Patients in the study group were given with avatrombopag orally at preoperative 10 to 13 d, once a day for 5 consecutive d. The dosage was selected according to platelet (Plt) count: the dosage was 60 mg/d when Plt was <40×109/L, and 40 mg/d when Plt was ranged from 40 to 50×109/L. In the routine group, observation or other Plt-elevating treatment methods were mainly used, including Plt transfusion and use of recombinant human thrombopoietin, recombinant human IL-11, eltrombopag and romiplostim, etc. The changes of Plt count, liver function indexes and the incidence of adverse reactions were observed between two groups.

Results

In the screening and baseline phases, the Plt count in the study group was (34±8)×109/L and (34±7)×109/L, significantly lower than (42±7)×109/L and (41±8)×109/L in the routine group (t=-4.134, -3.206, both P<0.05). At postoperative 10 d, the Plt count in the study group was (80±31)×109/L, significantly higher than (49±18)×109/L in the routine group (t=3.738, P<0.05). No significant differences were found in the levels of ALT, AST and TB at baseline, postoperative 1 and 10 d (all P>0.05). There was no statistical significance difference in the incidence of adverse drug reactions between two groups (P>0.05).

Conclusions

As a Plt-elevating agent, avatrombopag can elevate Plt and reduce the risk of surgery-related bleeding. In addition, it possesses high safety, showing potential clinical benefits in patients with CHRT undergoing elective high-risk invasive procedures.

Key words: Avatrombopag, Thrombocytopenia, Chronic disease, Recombinant human thrombopoietin, Invasive procedures

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