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固定剂量复合剂卫非特/卫非宁治疗结核病的临床对照研究 被引量:34

Controlled clinical study on efficacy of fixed dose compounds rifater/rifinah in antituberculous chemotherapy
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摘要 目的全面评价固定剂量复合剂卫非特/卫非宁的抗结核疗效、患者合作情况和在我国应用的前景。方法将308例初治菌阳肺结核患者,以2∶1随机对照法分为治疗组(2RIFATER/4RIFINAH,227例)和对照组(2HRZ/4HR,81例)进行短程化疗。结果治疗组和对照组2个月痰菌阴转率分别达91.2%和86.4%;满疗程痰菌阴转率各为98.7%和97.5%;胸部X线明显改善,治疗组和对照组病灶吸收分别占95.2%和93.8%,两组分别有68.6%和67.9%空洞闭合;两组药物不良反应发生率均为8.9%;治疗组和对照组自动停药率分别为4.2%和7.8%。结论固定复合剂卫非特/卫非宁是一种安全、高效、易被患者接受、在中国结核病短化中有推广应用前景的抗结核药物。 Objective To assess antituberculous efficacy, patients′ compliance and application perspective of fixed dose compounds rifater/rifinah in China. Method Three hundred eight new smear positive pulmonary tuberculosis patients were randomly allocated with a ratio of 2 to 1 into treatment group (227 cases, receiving 2RIFATER/4RIFINAH regimen) and controls (81 cases, 2HRZ/4HR) for observation. Result The sputum negative conversion rates at the 2nd month in the treatment group and the controls were 91.2% and 86.4% respectively, and at the end of the chemotherapy 98.7% and 97.5%. Chest radiography showed remarkable improvement. The resolution of pulmonary lesions in the treatment group and the controls accounted for 95.2% and 93.8% respectively, with cavity closure rates of 68.6% in the treatment group and 67.9% in the controls. The drug adverse reaction rates were 8.9% in both groups, and the default rates were 4.3% and 7.8% respectively. Conclusion Fixed dose compounds rifater/rifinah show excellent therapeutic efficacy, safety and compliance in antituberculous chemotherapy, which could be recommended for wider use in tuberculosis control in China.
出处 《中华结核和呼吸杂志》 CAS CSCD 北大核心 1998年第11期645-647,共3页 Chinese Journal of Tuberculosis and Respiratory Diseases
关键词 肺结核 药物疗法 卫非特 卫非宁 Tuberculosis, pulmonary Drug therapy, combination Rifater Rifinah
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