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异烟肼、利福平不同剂型对肺结核病患者的临床疗效 被引量:14

Clinical Analysis of Isoniazid and Rifampicin in Different Dosage Forms for Patients with Pulmonary Tuberculosis
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摘要 目的比较不同剂型异烟肼、利福平治疗肺结核的有效性及安全性,指导临床合理用药。方法对2016年5月至2017年6月昆明市第三人民医院住院的128例初治肺结核患者随机分为注射异烟肼、利福平组和口服异烟肼、利福平组,其中注射组65例,口服组63例,治疗方案统一采用规范2HREZ/4HR。观察不同剂型在肺结核患者治疗中临床疗效及副反应有无差异性。结果注射组痰菌阴转率高于口服组,但治疗1月末和2月末2组痰菌阴转率均差异无统计学意义(χ2=1.422,2.652;P>0.05);治疗2月末的注射组和口服组病灶显吸率分别为57.1%,33.3%,差异有统计学意义(χ2=7.025,P=0.008<0.01);治疗2月末的注射组和口服组的空洞闭合率分别为55.0%和29.4%,2组差异无统计学意义(χ2=2.451,P=0.117>0.05);2组治疗1月和2月后的病灶和空洞变化无效率均差异无统计学意义(P>0.05);注射组的胃肠道反应发生率3.4%,明显低于口服组的12.7%,注射组肝功能损害的发生率12.3%,高于口服组7.9%,但2组不良反应各指标比较差异无统计学意义(P>0.05);注射组总不良反应发生率为23.1%,口服组总不良反应发生率为30.2%,2组比较差异无统计学意义(χ2=0.823,P>0.05)。结论注射组异烟肼、利福平治疗肺结核疗效高于口服组,安全性相似。 Objective To compare the effectivity and safety of isoniazide and rifampicin with different dosage forms in the treatment of pulmonary tuberculosis and to guide clinical rational drug use.Methods 128 initially treated patients with pulmonary tuberculosis admitted into the Third People's Hospital of Kunming City from May 2016 to June 2017 were randomly divided into isoniazid-injection group and isoniazid oral-administration group,65 patients in the injection group and 63 in the oral administration group.The standard 2HREZ#4HR was uniformly adopted in the therapeutic schedules.The existence of differences in the clinical effectiveness and side effects of different dosage forms in the treatment of pulmonary tuberculosis were observed.ResultThe negative rate of sputum necrosis in the injection group was higher than that in the oral administration group,but there was no statistic difference in the negative rates of sputum necrosis in the two groups after one-month and two-month treatment(x2=1.422,2.652;all P >0.05);Inhalation rate in the injection group and the oral administration group after 2 months of treatment were 57.1%and 33.3%respectively,and there were statistic differences(χ^2=7.025,P=0.008<0.01).The cavity closure rates in the injection group and the oral administration group after 2 months of treatment were 55.0%and 29.4%respectively,and there were no statistic differences between the two groups(χ^2=2.451,P=0.117 >0.05);there was no difference in the ineffectiveness rate in the changes of nidus and cavities between the two groups after two months of treatment(P >0.05);The incidence of gastrointestinal reactions of 3.4%in the injection group was significantly lower than that of 12.7%in the oral administration group.The incidence of hepatic impairment in the injection group was 12.3%,higher than that of 7.9%in the oral administration group,but there was no statistic difference in the comparison between adverse reaction indicators in the two groups(P >0.5);The total incidence of adverse reactions in the injection group was 23.1%,and that in the oral administration group was 30.2%.There was no statistic difference of the comparison between that of the two groups(χ^2=0.823,P >0.05).Conclusion The effectiveness of isoniazid and rifampicin in the treatment of pulmonary tuberculosis in the injection group was higher than that in the oral administration group,and the safety was similar.
作者 李明武 马萌 张瑞雨 赖明红 朱惠琼 万荣 LI Ming-wu;MA Meng;ZHANG Rui-yu;LAI Ming-hong;ZHU Hui-qiong;WAN Rong(Dept.of Drug Resistance and Severe Tuberculosis,The Third People's Hospital of Kunming,Kunming Yunnan 650041;Physical and Chemical Laboratory,Kunming City Center for Disease Control and Prevention,Kunming Yunnan 650000,China)
出处 《昆明医科大学学报》 CAS 2019年第1期105-108,共4页 Journal of Kunming Medical University
基金 昆明市科技计划基金资助项目(2015-2-S-01429)
关键词 异烟肼 利福平 注射剂 口服剂 临床疗效 Isoniazid Rifampin Injection Oral administration Clinical effect
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