Efficacy and safety of decamethoxin in complex treatment of patients with group III viral-bacterial community-acquired pneumonia

O. Bororova
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引用次数: 2

Abstract

BACKGROUND. There are many unsolved medical problems and, of course, pneumonia is one of them. Communityacquired pneumonia (CAP) is a multifactorial disease, but the role of viruses as causative agents is constantly growing. Specific antiviral therapy for CAP is limited. Therefore, the search for drugs with virucidal activity remains relevant. An antimicrobial agent with a broad spectrum of action – decamethoxin – is successfully used today for treatment of patients with infectious exacerbations of bronchial asthma and chronic bronchitis. At the same time efficacy of decamethoxin in CAP patients was not studied. OBJECTIVE. To evaluate the effectiveness and safety of the inhaled antimicrobial drug decamethoxin in the complex treatment of patients with group III viral-bacterial CAP. MATERIALS AND METHODS. There was enrolled 62 patients with group III viral-bacterial CAP. All patients received the same sequential antibiotic therapy: protected aminopenicillin with macrolide or III generation cephalosporin with macrolide. Patients of the main group were prescribed inhalations through a nebulizer of the antiseptic drug decamethoxin in addition to antibacterial therapy from the first day of treatment for 5-7 days. RESULTS AND DISCUSSION. No adverse events were detected in any of the patients during treatment. In all cases, recovery was diagnosed. At the same time, the term of achieving positive results in the main group was 12.2±0.7 days, and in the control – 17.2±0.7 (р <0,05). The average duration of antibiotic use was different in main and control groups: respectively 9.4±0.4 and 10.7±0.4 days (р <0,05). There were no infectious complications in the patients of the main group, while 24 (72 %) patients of the control group were diagnosed with acute rhinopharyngitis (47.0 % of cases), lateral pharyngitis (13 %) and sinusitis (9 %), other complications (otitis, infectious exudative pericarditis). In 22 (66 %) cases there was one complication and in 2 (6 %) cases there were two complications. CONCLUSIONS. For patients with group III viral-bacterial CAP additional inclusion in the empirical sequential antibiotic therapy of inhaled decamethoxin can significantly reduce the frequency of infectious complications, duration of antibiotic therapy, as well as the duration of positive treatment results.
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十甲氧辛复合治疗III型病毒-细菌社区获得性肺炎的疗效和安全性
背景。有许多尚未解决的医疗问题,当然,肺炎就是其中之一。社区获得性肺炎(CAP)是一种多因素疾病,但病毒作为病原体的作用不断增强。针对CAP的特异性抗病毒治疗是有限的。因此,寻找具有杀病毒活性的药物仍然具有重要意义。一种具有广谱作用的抗菌剂——十甲氧辛,目前已成功用于治疗支气管哮喘和慢性支气管炎的感染性加重患者。同时,对十甲虫灵在CAP患者中的疗效没有进行研究。目标。目的:评价吸入抗菌药物十甲氧恶素复合治疗III型病毒-细菌感染患者的有效性和安全性。纳入62例III组病毒-细菌性CAP患者。所有患者均接受相同的序贯抗生素治疗:保护性氨霉素联合大环内酯或第三代头孢菌素联合大环内酯。主组患者自治疗第一天起,在抗菌治疗的基础上,通过雾化器吸入抗菌药物十甲氧辛,持续5-7天。结果和讨论。治疗期间未发现任何患者出现不良事件。在所有病例中,都被诊断为康复。同时,主治疗组达到阳性结果的时间为12.2±0.7天,对照组达到阳性结果的时间为- 17.2±0.7天(p < 0.05)。主要组和对照组的平均抗生素使用时间分别为9.4±0.4和10.7±0.4 d,差异有统计学意义(p < 0.05)。主组患者无感染性并发症,对照组24例(72%)出现急性鼻咽炎(47.0%)、侧咽炎(13%)、鼻窦炎(9%)及其他并发症(中耳炎、感染性渗出性心包炎)。22例(66%)出现1例并发症,2例(6%)出现2例并发症。结论。对于III组病毒-细菌性CAP患者,在吸入性十甲氧恶素经年性序贯抗生素治疗中增加纳入,可显著减少感染并发症的发生频率、抗生素治疗的持续时间以及治疗结果阳性的持续时间。
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