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两种为期6个月的化疗方案治疗肺结核的对照临床试验。坦桑尼亚/英国医学研究委员会研究。

Controlled clinical trial of two 6-month regimens of chemotherapy in the treatment of pulmonary tuberculosis. Tanzania/British Medical Research Council Study.

出版信息

Am Rev Respir Dis. 1985 May;131(5):727-31. doi: 10.1164/arrd.1985.131.5.727.

Abstract

Two 6-month daily regimens of chemotherapy for smear-positive pulmonary tuberculosis were compared in Tanzania. Both had the same initial 2-month intensive phase of streptomycin, isoniazid, rifampicin, and pyrazinamide, and the continuation phase was either thiacetazone plus isoniazid or isoniazid alone. All patients were hospital inpatients for 6 months, solely to ensure that chemotherapy was fully supervised throughout. The patients were followed up to 24 months after stopping chemotherapy. In patients with fully sensitive strains pretreatment, there were no failures during chemotherapy on either regimen; the bacteriologic relapse rates were 3% for the 105 patients receiving thiacetazone plus isoniazid in the continuation phase, and 11% for the 100 patients receiving isoniazid alone (p less than 0.05). Possible adverse reactions were reported in the initial phase in 5 (1.6%) of 319 patients who started treatment, and in 2 of 306 who started the continuation phase, chemotherapy being modified in 5 of the 7 patients.

摘要

在坦桑尼亚,对两种为期6个月的涂片阳性肺结核每日化疗方案进行了比较。两种方案的初始2个月强化期均使用链霉素、异烟肼、利福平和吡嗪酰胺,继续期要么是硫代乙酰胺加异烟肼,要么仅用异烟肼。所有患者均住院6个月,只是为了确保化疗全程得到充分监督。患者在停止化疗后随访至24个月。在初始菌株完全敏感的患者中,两种方案化疗期间均无治疗失败情况;继续期接受硫代乙酰胺加异烟肼治疗的105例患者细菌学复发率为3%,仅接受异烟肼治疗的100例患者为11%(p<0.05)。在开始治疗的319例患者中,有5例(1.6%)在初始阶段报告了可能的不良反应,在开始继续期治疗的306例患者中有2例出现不良反应,7例患者中有5例的化疗方案因此进行了调整。

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