常规方案条件下肺结核的短期化疗:阿尔及利亚28周和36周疗程方案的比较

Algerian working group/British medical research council cooperative study
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引用次数: 0

摘要

对阿尔及利亚30个卫生区以前未经治疗的肺结核患者进行28周(6M)和36周(8M)化疗方案的比较。在6M方案中,患者在前8周每天服用异烟肼加利福平,外加链霉素和吡嗪酰胺。在8M方案中,患者在整个治疗过程中每天服用异烟肼,前16周服用利福平,前8周服用链霉素和吡嗪酰胺。这些地区被分配对所有符合条件的患者采用6M或8M方案。然而,22%符合条件的病人没有住院,最常见的原因是地方保健中心工作人员的疏忽。共有2218例(977 m,1241 m)患者入院,结果在化疗完成日期2年后评估,无论管理是否偏离研究方案。相当大比例的患者(占6百万病例的25%,占8百万病例的29%)无法得到评估,因为他们没有参加随访或标本收集被忽视,或者标本运输到阿尔及尔参比实验室有困难,另外还有5%和4%的患者死亡。在可评估的患者中,7.31亿例患者中有7例(1%)和8.75亿例患者中有15例(2%)被归类为在化疗期间或化疗后有不良反应,因为他们有一个或多个阳性培养。此外,16例(2%)6万例和18例(2%)8万例患者因治疗失败、复发或发生非肺部病变而接受了额外的化疗,但已达到良好的状态。在1018例(488 m, 530 m)接受全敏感菌株预处理并按计划完成治疗的患者中,97%的患者在化疗结束2年后仍处于良好状态。在最初对异烟肼耐药的患者中,8M系列的结果不如6M系列好:19个6M系列中没有一个与8个8M系列中26个中的5个相比有不利的结果,这表明利福平的持续时间可能对最初对异烟肼耐药的患者很重要。8M方案的患者在化疗期间违约的比例略高(9.3%,而6M方案为6.7%),但在其他依从性指标上,两种方案之间没有差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Short-course chemotherapy for pulmonary tuberculosis under routine programme conditions: a comparison of regimens of 28 and 36 weeks duration in Algeria

Two chemotherapy regimens of 28 weeks (6M) and 36 weeks (8M) duration were compared in patients with previously untreated pulmonary tuberculosis in 30 health districts of Algeria. In the 6M regimen, patients received isoniazid plus rifampicin daily throughout with streptomycin and pyrazinamide in addition for the first 8 weeks. In the 8M regimen patients received isoniazid daily throughout plus rifampicin for the first 16 weeks and streptomycin and pyrazinamide as well for the first 8 weeks. The districts were allocated to apply either the 6M or the 8M regimen to all eligible patients. However, 22% of eligible patients were not admitted, the most common reason being oversight on the part of the personnel in the local health centres.

A total of 2218 (977 6M,1241 8M) patients was admitted and the results were assessed 2 years after the due date of completion of chemotherapy, irrespective of whether or not management had deviated from the study protocol. An appreciable proportion of patients (25% of 6M, 29% of 8M) could not be assessed because they failed to attend for follow-up or the collection of specimens was overlooked or because of difficulties in the transport of specimens to the reference laboratory in Algiers, and a further 5% and 4% of patients died. Of those who were assessable 7 (1 %) of 731 6M and 15 (2%) of 875 8M were classified as having an unfavourable response during or after chemotherapy because they had one or more positive cultures. In addition 16 (2%) 6M and 18 (2%) 8M patients had received additional chemotherapy for failure, relapse or the development of non-pulmonary lesions but had achieved a favourable status.

Of 1018 (488 6M, 530 8M) patients assessed who had fully sensitive strains pretreatment and completed treatment as planned, 97% in both series had a favourable status 2 years after their chemotherapy was due to be completed. In patients with initial strains resistant to isoniazid the results were less good in the 8M than the 6M series: none of the 19 6M compared with 5 of 26 in the 8M series having an unfavourable outcome suggesting that the duration of rifampicin may have been important in patients with initial isoniazid resistance.

A slightly higher proportion of patients on the 8M regimen defaulted during chemotherapy (9.3% compared with 6.7% in the 6M regimen) but there was no difference between the regimens in other measures of compliance.

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