利福布汀联合氯法齐明、异烟肼和乙胺丁醇治疗机会性分枝杆菌感染的临床观察

B. Dautzenberg , Ch. Truffot , A. Mignon , W. Rozenbaum , C. Katlama , Ch. Perronne , R. Parrot , J. Grosset , GETIM (Groupe d'Etude et de Traitement des Infections à Mycobacteries Résistantes)
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引用次数: 29

摘要

对96例发热伴细菌学镜检抗酸杆菌或培养分离分枝杆菌的艾滋病患者,每日给予7 ~ 10 mg/kg利福布汀、5 mg/kg异烟肼、20 mg/kg乙胺丁醇和100 mg氯法齐明4种药物联合治疗。46例患者被排除在疗效评估之外:13例患者在治疗前或第一天内死亡,5例初始培养阴性,14例结核分枝杆菌阳性,4例堪萨斯分枝杆菌阳性,1例黄分枝杆菌阳性,1例戈登分枝杆菌阳性,7例失访,1例未接受瑞福布汀治疗。在其余50例患者中,31例因鸟分枝杆菌胞内复合体(MAIC)而播散性疾病,19例因明显的局部疾病,MAIC 15例,xenopi分枝杆菌4例。副作用导致异烟肼1例停药(肝酶升高),利福布汀1例停药(血小板减少)。治疗1个月后,发热由38.4±0.6°C降至37.7±0.5°C (p <0.01),患者体重停止下降。治疗3个月后,只有37例患者存活并仍在接受治疗。有细菌学资料的23例患者中有16例培养呈阴性(14例弥散性疾病患者中有9例,9例局部疾病患者中有7例),4例患者死前复发。34例患者在治疗结束前死亡。5例死亡被认为与分枝杆菌感染有关。我们的结论是,这四种药物的组合是安全的,在某些情况下,它似乎是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rifabutin in combination with clofazimine, isoniazid and ethambutol in the treatment of AIDS patients with infections due to opportunist mycobacteria

96 AIDS patients with fever and either acid-fast bacilli on microscopic examination of bacteriological samples or mycobacteria isolated by culture were treated with a daily 4-drug combination of 7–10 mg/kg rifabutin, 5 mg/kg isoniazid, 20 mg/kg ethambutol and 100 mg clofazimine.

46 patients were excluded from efficacy assessment: 13 died before or within the first days of treatment, 5 had negative initial cultures, 14 had initial cultures positive for M. tuberculosis, 4 for M. kansasii, 1 for M. flavescens, 1 for M. gordonae, 7 were lost to follow-up and 1 received no rifabutin.

In the 50 remaining patients, 31 had disseminated disease due to M. avium intracellulare complex (MAIC) and 19 had apparently localised disease, due to MAIC in 15 cases and to M. xenopi in 4 cases. Side-effects led to withdrawal of isoniazid in 1 case (hepatic enzymes increased) and rifabutin in another (thrombocytopenia). After 1 month of treatment, fever decreased from 38.4 ± 0.6 °C to 37.7 ± 0.5 °C (p < 0.01) and patients stopped losing weight. After 3 months treatment, only 37 patients were alive and still under treatment. Cultures became negative in 16 of 23 patients with available bacteriological data (9 of 14 patients with disseminated disease and 7 of 9 patients with localised disease), relapse occurred before death in 4 patients. 34 patients died before treatment was completed. Death was considered to be related to mycobacterial infection in 5 cases.

We conclude that the 4-drug combination is safe and, in some cases, it appears to be effective.

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