新诊断肺结核合并多药耐药合并慢性阻塞性肺疾病患者的治疗选择:以吸入糖皮质激素为重点

N. Bagisheva, A. Mordyk, M. Moiseeva, K. Nesterova, E. Nebesnaya, S. Sitnikova
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A simple, prospective, comparative study in accordance with the inclusion criteria included 40 patients admitted to an anti-tuberculosis dispensary with newly diagnosed MDR tuberculosis with COPD. The diagnosis of TB and COPD was confirmed using radiographic, functional and laboratory research methods. Group 1, age Me (25; 75) 55.5 (46; 58) years - 22 patients with MDR + COPD tuberculosis who, simultaneously with TB chemotherapy, received a short-acting M-anticholinergic blocker, 2 inhalations 4 times a day, group 2, age 54.5 (51; 58) years - 18 patients with MDR + COPD tuberculosis, simultaneously with TB chemotherapy received a combination of ICS with a long-acting bronchodilator (beta-2-agonist (LABA)), budesonide + formoterol 160 / 4.5 μg dose - 2 inhalations 2 times a day (in an inhaler device). Duration of observation is 9 months. Results and discussion. 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引用次数: 0

摘要

介绍。由于耐药结核分枝杆菌的增长以及合并支气管肺病理的患者中结核病发病率的增加,治疗结核病的问题仍然具有相关性,这需要对这类患者进行全面管理,并对合并病理进行强制性药物纠正。的目标。本研究的目的是评估吸入糖皮质激素(布地奈德/福莫特罗160 / 4.5在吸入器装置中)对新诊断为多药耐药结核病(MDR)患者结核病治疗效果的影响,这些患者存在慢性阻塞性肺病(COPD)。材料和方法。根据纳入标准,一项简单、前瞻性、比较研究纳入了40例新诊断为耐多药结核病合并COPD的抗结核药房收治的患者。结核和慢性阻塞性肺病的诊断通过影像学、功能和实验室研究方法得到证实。第一组,年龄25岁;75) 55.5 (46;58岁- 22例MDR + COPD结核病患者,与结核病化疗同时接受短效m -抗胆碱能阻滞剂,2次吸入,每天4次,组2,年龄54.5 (51;58年- 18例MDR + COPD结核病患者,同时接受TB化疗,接受ICS联合长效支气管扩张剂(β -2激动剂(LABA)),布地奈德+福莫特罗160 / 4.5 μg剂量-2次吸入,每天2次(在吸入器装置中)。观察时间为9个月。结果和讨论。观察9个月后,1组龋齿闭合率为63.6%,2组为83.3% (χ²= 0.3;P = 0.581), 1组和2组的涂片阴性率分别为90.9%和100.0% (χ²= 0.04 P = 0.834), 1组和2组的涂片阴性率分别下降63.3%和100.0% (χ²= 0.46;P = 0.496)。在结核病化疗强化期与抗生素治疗同时使用ICS的背景下,与未接受ICS的组相比,消融和关闭蛀牙的时间有所减少。同时,在支气管疾病中,使用ICS可以快速停止支气管阻塞性综合征,提高生活质量和长期抗结核治疗的依从性。ICS的另一个非特异性抗炎作用促进了浸润性病变的主动吸收和特定过程的治愈,缩短了主要疗程的持续时间,包括耐多药患者。结论。伴有支气管肺病理的抗结核药房患者需要复杂的治疗,旨在纠正合并症,同时化疗结核病。在结核病强化治疗阶段,慢性阻塞性肺病患者除使用长效支气管扩张剂(LABA、LDAH)外,还使用ICS来纠正支气管阻塞性综合征,可缩短涂片阴性、消音和龋齿闭合的时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SELECTED ASPECTS OF TREATMENT OF PATIENTS WITH NEWLY DIAGNOSED PULMONARY TUBERCULOSIS WITH MULTIDRUG-RESISTANT COMBINATION AND CHRONIC OBSTRUCTIVE PULMONARY DISEASE: IN THE FOCUS OF INHALED GLUCOCORTICOSTEROIDS
Introduction. The problem of treating tuberculosis (TB) remains relevant, due to the growth of drug-resistant forms of mycobacterium tuberculosis and an increase in the incidence of TB in persons with comorbid bronchopulmonary pathology, which requires comprehensive management of this category of patients, with mandatory drug correction of concomitant pathology. Aim. The aim of this study was to assess the effect of inhaled glucocorticosteroids (budesonide / formoterol 160 / 4.5 in an Inhaler device) on the efficacy of TB therapy in patients with newly diagnosed multidrug-resistant tuberculosis (MDR) who developed in the presence of chronic obstructive pulmonary disease (COPD). Material and methods. A simple, prospective, comparative study in accordance with the inclusion criteria included 40 patients admitted to an anti-tuberculosis dispensary with newly diagnosed MDR tuberculosis with COPD. The diagnosis of TB and COPD was confirmed using radiographic, functional and laboratory research methods. Group 1, age Me (25; 75) 55.5 (46; 58) years - 22 patients with MDR + COPD tuberculosis who, simultaneously with TB chemotherapy, received a short-acting M-anticholinergic blocker, 2 inhalations 4 times a day, group 2, age 54.5 (51; 58) years - 18 patients with MDR + COPD tuberculosis, simultaneously with TB chemotherapy received a combination of ICS with a long-acting bronchodilator (beta-2-agonist (LABA)), budesonide + formoterol 160 / 4.5 μg dose - 2 inhalations 2 times a day (in an inhaler device). Duration of observation is 9 months. Results and discussion. After 9 months of observation, closure of decay cavities in 63.6% in group 1 and 83.3% in group 2 (χ² = 0.3; p = 0.581), smear negativity in 90.9% of cases in group 1 and in 100, 0% in group 2, respectively (χ² = 0.04 p = 0.834), abacillated 63.3% and 100.0% in groups 1 and 2, respectively (χ² = 0.46; p = 0.496). Against the background of the use of ICS in the intensive phase of TB chemotherapy simultaneously with antibiotic therapy, there was a decrease in the time of abacillation and closure of decay cavities in comparison with the group that did not receive ICS. At the same time in broncholics, the use of ICS made it possible to quickly stop the broncho-obstructive syndrome, improve the quality of life and compliance with long-term anti-tuberculosis therapy. An additional nonspecific anti-inflammatory effect of ICS promoted the active resorption of infiltrative changes and the cure of a specific process, reducing the duration of the main course of treatment, including in patients with MDR. Conclusion. Patients of the anti-tuberculosis dispensary with concomitant bronchopulmonary pathology need complex treatment aimed at correcting comorbid conditions, simultaneously with chemotherapy for tuberculosis. The use of ICS in addition to long-acting bronchodilators (LABA, LDAH) in patients with COPD for the correction of broncho-obstructive syndrome in the intensive phase of TB treatment can reduce the time of smear negativity, abacillation and closure of decay cavities.
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