Hyde L
Calif Med. 1972 Dec;117(6):18-21.
Rifampin is a newer semi-synthetic derivative of rifamycin. Its advantages over other derivatives are good oral absorption, high blood levels, and slower excretion rate. Rifampin has been studied in 68 patients and results can be summarized as follows:* There has been no evidence of significant toxicity.* In a randomized study of active tuberculosis patients who had not received prior chemotherapy, isoniazid-rifampin and isoniazid-aminosalicylic acid regiments were equally effective.* In retreatment patients with active, positive tuberculosis, the regimen of isoniazid, rifampin, and ethambutol proved to be very effective, especially when the two latter drugs had not been used previously.* In patients with pulmonary infections caused by atypical acid-fast bacilli, results varied with the organism isolated and the extent of disease. Rifampin is a potent, relatively non-toxic drug especially useful in the retreatment of pulmonary tuberculosis in patients who have never received this drug previously. There is little justification for its use in initial therapy except in rare cases.
利福平是利福霉素较新的半合成衍生物。它相对于其他衍生物的优点是口服吸收良好、血药浓度高且排泄速率较慢。对68例患者进行了利福平研究,结果可总结如下:
没有明显毒性的证据。
在一项针对未接受过先前化疗的活动性肺结核患者的随机研究中,异烟肼-利福平方案和异烟肼-对氨基水杨酸方案同样有效。
在活动性、结核菌素试验阳性的复治患者中,异烟肼、利福平与乙胺丁醇联合方案被证明非常有效,尤其是当后两种药物此前未使用过时。
对于由非典型抗酸杆菌引起的肺部感染患者,结果因分离出的病原体和疾病程度而异。利福平是一种强效、相对无毒的药物,特别适用于从未使用过该药的肺结核复治患者。除罕见情况外,在初始治疗中几乎没有使用它的理由。