针对耐多药结核病患者的个体化抗真菌治疗方案的最佳持续时间,包括贝达喹啉和改用药物

Y. Feschenko, N. Lytvynenko, N. Grankina, M. Pogrebna, Y. Senko, L. Protsyk
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引用次数: 1

摘要

包括Y. I. Feschenko, N. a . Lytvynenko, N. V. grankina, M. V. Pogrebna, Y. O. Senko, L. M. Protsyk在内的多药耐药结核病患者抗真菌个体化治疗方案的最佳持续时间世界正处于抗生素治疗新时代的边缘,因为新药物的出现可以显著缩短结核病患者的总体治疗时间。该研究的目的是:开发一种算法,用于选择耐药结核病患者的抗真菌治疗个体化方案的最佳持续时间,包括贝达喹啉和重新使用的药物。材料和方法。一项前瞻性观察研究在2017-2021年期间对425名患者进行了治疗。患者按照WHO相同的分步原则,采用不同疗程的个体化治疗方案(ITR),包括贝达喹啉和再用途药物(不含delamanid)。结果成功的患者分为3组:第一组(176例)ITR持续时间为12个月(小于等于400天);第二组(170例):13-16个月;第三组(79例)- 16-20个月。结果和讨论。在治疗超过12个月的患者中,治疗前出现肺部常见破坏性病变(治疗6个月后保留空腔)和氟喹诺酮类药物耐药的患者明显更多,这些患者接受了二线抗细菌药物治疗。两组患者之间有明显的相关性:1组和2组患者在治疗第1 -2个月停止细菌排泄的频率显著高于对照组(p <0.05)。1、2组平均培养阴性时间分别为-(50.3±2.9)、(44.4±2.2)d,而3组平均培养阴性时间为- (61.1 + 5.0)d,差异有统计学意义(p <0.05)。结论。ITR的最佳持续时间应在治疗开始后6个月时根据主要标准(早期阴性培养)和附加标准(6个月时肺部无破坏性变化,对氟喹诺酮类药物无耐药性,既往二线抗细菌治疗史)做出决定。关键词:肺结核;个体化治疗方案
本文章由计算机程序翻译,如有差异,请以英文原文为准。
OPTIMAL DURATION OF INDIVIDUALIZED REGIMENS OF ANTIMYCOBACTERIAL THERAPY, CONTAINING BEDAQUILINE AND REPURPOSED MEDICINES, FOR PATIENTS WITH MULTIDRUG-RESISTANT TUBERCULOSIS INCLUDING
OPTIMAL DURATION OF INDIVIDUALIZED REGIMENS OF ANTIMYCOBACTERIAL THERAPY, CONTAINING BEDAQUILINE AND REPURPOSED MEDICINES, FOR PATIENTS WITH MULTIDRUG-RESISTANT TUBERCULOSIS INCLUDING Y. I. Feschenko, N. A. Lytvynenko, N. V.Grankina, M. V. Pogrebna, Y. O. Senko, L. M. Protsyk Abstract The world is on the verge of a new era of antibiotic therapy due to the emergence of new drugs that can significantly reduce the overall duration of treatment for patients with tuberculosis. Aim of the study: to develop an algorithm for selecting the optimal duration of individualized regimens of antimycobacterial therapy, containin bedaquiline and repurposed drugs for patients with drugresistant tuberculosis. Materials and methods. A prospective observational study was conducted in 425 patients treated during 2017–2021. Patients were prescribed individualized therapy regimen (ITR) which included bedaquiline and repurposed drugs (without delamanid) according to the same WHO step-by-step principle, but of different duration. Patients with successful outcome were divided into 3 groups: 1st group (176 patients) with ITR duration of 12 months (less than or equal to 400 days); 2nd group (170 patients) – 13-16 months; 3rd group (79 patients) – 16-20 months. Results and discussion. Among patients treated for more than 12 months, there were significantly more pre-treatment patients with common destructive lesions in the lungs (cavities preserved after 6 month of treatment) and fluoroquinolone resistance, treated with second line antimycobacterial medications. There was a clear relationship between patients in the comparison groups: in groups 1 and 2 a cessation of bacterial excretion was significantly more often registered at the 1st-2nd month of treatment (p <0.05). The average term of culture negativity in groups 1 and 2 was — (50.3 ± 2.9), (44.4 ± 2.2) days, respectively, vs group 3 — (61.1 + 5.0) days, (p <0.05). Conclusion. The decision on the optimal duration of ITR should be made at 6 months from the beginning of treatment, based on the main (early period of negative culture) and additional criteria (no destructive changes in the lungs at 6 months, no resistance to fluoroquinolones and history of past second line antimycobacterial treatment). Key words: tuberculosis, individualized treatment regimens
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