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Chinese Journal of Antituberculosis ›› 2014, Vol. 36 ›› Issue (2): 104-108.doi: 10.3969/j.issn.1000-6621.2014.02.005

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Clinical analysis of lamivudine combined with anti-tuberculosis drugs in treating pulmonary tuberculosis complicated with hepatitis B virus carriers

DENG Guo-fang, SUN Li-zhen, LEI Jian-ping, WU Yu-qing, YE Hong   

  1. Pulmonary Department Two, Shenzhen Third People’s Hospital, Shenzhen 518112, China
  • Received:2013-07-29 Online:2014-02-10 Published:2014-04-10
  • Contact: LEI Jian-ping E-mail:lei-jianping@vip.sina.com

Abstract: Objective To explore the effect of lamivudine therapy on pulmonary tuberculosis patients with hepatitis B virus carriers based on anti-TB treatment, including the incidence of liver injury, the treatment time and long-term effects.  Methods One hundred and forty-two new pulmonary tuberculosis patients with chronic hepatitis B virus carriers who had normal liver function were randomly divided into lamivudine group (73 patients, 4 cases were lost to follow-up) and control group (69 patients, 6 cases were lost to follow-up). By the end of 18-month treatment, lamivudine would be stopped, but anti-tuberculosis drugs were not stopped until the treatment ended. All the patients of both groups were followed up for 24 months, liver injury rate within 4 weeks,the total liver injury rate, HBV-DNA negative rate, mortality, TB cure rate, failure rate were analyzed by Chi-square test or Fisher’s exact probability method. Results Patients treated with lamivudine significantly reduced liver injury. Liver injury rate within 4 weeks, the total liver injury rate and mortality of the lamivudine group were lower than the control group. There were significant differences between lamivudine group (4.3%(3/69),20.3%(14/69),0.0%(0/69); P=0.007, 0.0001, 0.023, χ2=7.064,15.176) and control group (19.0% (12/63),49.2% (31/63),7.9% (5/63)). At the end of TB treatment and the end of follow-up period, the HBV-DNA negative rate of lamivudine group (24.6%(17/69),21.7%(15/69)) was higher than control group (3.2%(2/63),3.2%(2/63)), the dif-ference was statistically significant (χ2=12.311,P=0.0005;andχ2=10.115,P=0.001). TB cure rate of lamivudine group was higher than control group (89.9% vs 73.0%) and the failure rate lamivudine group were lower than the control group (4.3% vs 17.5%), There were significant differences between 2 groups.   Conclusion Using lamivudine within 18 months is relatively safe for reducing the incidence of hepatitis B, which has a long-term effect. Our findings can provide a clinic basis for prophylactic lamivudine therapy on pulmonary tuberculosis patients with HBV infection.

Key words: Tuberculosis, pulmonary/drug therapy, Hepatitis B, Carrier state, Lamivudine, Antitubercular agents, Drug therapy, combination