Mishin V Iu, Chukanov V I, Vylegzhanin S V
Probl Tuberk. 2001(7):13-8.
The authors evaluated the efficiency of a routine drug therapy regimen by the WHO category 1 in treating 149 new cases of destructive pulmonary tuberculosis and bacterial isolation. They used not only the WHO sputum smear negativization criterion, but the data of cultural studies and on lung cavernous closure. The specific features of the approach applied were compulsory cultural studies determining Mycobacterium sensitivities before treatment and compulsory correction of chemotherapy after there was evidence for the sensitivity. Retrospective analysis of 6-month chemotherapy has ascertained that the efficiency of the routine drug therapy regimen largely depends on the baseline extent of infiltrative and destructive changes in the lung and on the baseline resistance of Mycobacteria tuberculosis. They showed a high baseline resistance to streptomycin (20.6%) and streptomycin and isoniazid (33.1%) and a low baseline resistance to ethambutol (5.1%). In these cases, the more optimum regimen was a combination of rifampicin, pyrazanamide, and ethambutol. When Mycobacteria showed multidrug resistance, the routine regimen was ineffective and caused amplification to a larger number of drugs. A modified treatment course using the routine regimen in the intensive phase was developed. If Mycobacterial resistance was present, compulsory correction was made by using reserve agents, pathogenetic treatments, artificial pneumothorax or surgical interventions, which made it possible to abacillate 94.1% of patients by their smears and culture by months 4-5 and to close caverns in 91.3% of cases by months 8-10.
作者评估了世界卫生组织1类常规药物治疗方案在治疗149例新发性破坏性肺结核及细菌分离方面的疗效。他们不仅采用了世界卫生组织痰涂片转阴标准,还运用了培养研究数据及肺部空洞闭合情况的数据。所采用方法的具体特点包括在治疗前进行强制性培养研究以确定分枝杆菌敏感性,以及在有敏感性证据后对化疗进行强制性调整。对6个月化疗的回顾性分析确定,常规药物治疗方案的疗效很大程度上取决于肺部浸润性和破坏性改变的基线程度以及结核分枝杆菌的基线耐药性。他们发现对链霉素的基线耐药率较高(20.6%),对链霉素和异烟肼的基线耐药率为33.1%,而对乙胺丁醇的基线耐药率较低(5.1%)。在这些情况下,更优化的方案是利福平、吡嗪酰胺和乙胺丁醇的联合使用。当分枝杆菌表现出多重耐药时,常规方案无效且会导致对更多药物产生耐药。制定了在强化期使用常规方案的改良治疗疗程。如果存在分枝杆菌耐药性,则通过使用储备药物、病因治疗、人工气胸或手术干预进行强制性调整,这使得4至5个月时94.1%的患者痰涂片和培养转阴,8至10个月时91.3%的病例空洞闭合。