Volume 42 Issue 1
Jan.  2021
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Zhi-rong ZHAO, Hai-wen LI, Ni-hong LU, Ling SHEN, Xiao-fei LI, Yong-rui YANG. A Clinical Study on the Use of Propofol Tenofovir in the Treatment of Chronic Hepatitis B[J]. Journal of Kunming Medical University, 2021, 42(1): 89-93. doi: 10.12259/j.issn.2095-610X.S20210141
Citation: Zhi-rong ZHAO, Hai-wen LI, Ni-hong LU, Ling SHEN, Xiao-fei LI, Yong-rui YANG. A Clinical Study on the Use of Propofol Tenofovir in the Treatment of Chronic Hepatitis B[J]. Journal of Kunming Medical University, 2021, 42(1): 89-93. doi: 10.12259/j.issn.2095-610X.S20210141

A Clinical Study on the Use of Propofol Tenofovir in the Treatment of Chronic Hepatitis B

doi: 10.12259/j.issn.2095-610X.S20210141
  • Received Date: 2020-06-01
    Available Online: 2021-01-26
  • Publish Date: 2021-01-26
  •   Objective  to observe the efficacy and safety in the clinic practice of Propofol Tenofavir Fumarate(TAF)as a treatment of Chronic Hepatitis B(CHB)   Method  A total of 180 Chronic-Hepatitis-B patients who had taken TDF antiviral therapy for 48 to 49 weeks were chosen between January 2018 and February 2020. They were further separated into two groups regarding to the following treatments: one continues TDF treatment while the other replaces with TAF. The comparison was made based on the clinic efficacy and renal safety from such two groups after a 48-week continuous medication.  Results  TAF group showed a statistical difference significantly better in HBV-DNA inhibition rate, ALT normalization rate, and HBeAg serum conversion with χ2 = 10.250, P = 0.001 and χ2 = 6.871, P = 0.009, and χ2 = 3.881, P = 0.049 respectively. In terms of the safety, TAF group also demonstrates a difference significantly lower in the urinary α1 microglobulin abnormal rate with χ2 = 13.703, P = 0.000. On the other hand, there was no significant difference in bloom β2 microglobulin among the groups owning to P values ≥ 0.05.  Conclusion  With the statistical comparison between TAF and TDF treatments in this clinic study, TAF is observed to have a stronger antiviral effectiveness, fewer side effects such as less induced harm to the renal function, and reduce the risks deriving from the liver cirrhosis and cancer.
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