Assessment of pharmacotherapy efficacy for the treatment of exacerbations of chronic obstructive pulmonary disease associated with viral infection

L. A. Shpagina, O. Kotova, I. Shpagin, G. V. Kuznetsova, E. Loktin, A. Rukavitsyna, S. Karmanovskaya, L. Panacheva, E. Anikina
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Abstract

   Justification. Knowledge of the differences in response to therapy between phenotypes of exacerbations of chronic obstructive pulmonary disease (COPD) is necessary to improve treatment outcomes.   Objective: to determine the most effective additional pharmacological methods for virus-associated exacerbations of COPD.   Material and methods. The study included patients hospitalized with exacerbations of COPD with viral (n = 60) and viral-bacterial (n = 60) infections, and a comparison group with exacerbations of COPD with bacterial infection (n = 60). The diagnosis of COPD was based on spirometric criteria, viral infection — according to the results of PCR-RV of sputum for RNA of respiratory viruses. Treatment was carried out in real clinical practice. The groups were comparable in the use of systemic glucocorticoids, short-acting bronchodilators. Dyspnea was assessed using the TDI index (primary endpoint), lung function (spirometry, diffusion capacity for carbon monoxide), exercise tolerance (6-minute walk test), length of hospital stay (secondary endpoints). The сorrelations were determined with the use of Cox proportional hazards model.   Results. In the groups with virus-associated and viral-bacterial exacerbations, unlike bacterial exacerbations, the following types of treatment were associated with achieving TDI +1 (odds ratio — OR, 95 % confidence interval — CI): fixed triple combination (OR 2.69; 95 % CI 1.48–4.90; p = 0.010 and OR 2.74; 95 % CI 1.29–3.80; p = 0.031), inhalation of 3 % sodium chloride solution (OR 3.64; 95 % CI 1.45–5.42; p = 0.001 and OR 3.23; 95 % CI 2.15–5.43;\ p = 0.042), antiviral drugs (OR 2.91; 95 % CI 1.15–3.62; p = 0.009 and OR 2.76; 95 % CI 1.31–3.90; p = 0.008). As a result of treatment, an increase in DLco/Va, SpO2 after a 6-minute walk, and a decrease in the length of hospital stay were observed.   Conclusion. Detection of virus-associated infections is a promising marker for determining indications for prescribing long-acting anticholinergic drugs and beta-adrenomimetics, inhaled corticosteroids, inhalations of hypertonic sodium chloride solution, and antiviral drugs for exacerbations of COPD.
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评估药物疗法治疗与病毒感染相关的慢性阻塞性肺病恶化的疗效
理由。有必要了解慢性阻塞性肺疾病(COPD)加重表型之间对治疗反应的差异,以改善治疗效果。 目的:确定治疗病毒相关慢性阻塞性肺疾病加重的最有效的附加药物治疗方法。 材料和方法。研究对象包括慢性阻塞性肺疾病加重期病毒感染(n = 60)和病毒细菌感染(n = 60)住院患者,以及慢性阻塞性肺疾病加重期细菌感染对比组(n = 60)。慢性阻塞性肺病的诊断依据是肺活量测定标准,病毒感染的诊断依据是痰中呼吸道病毒 RNA 的 PCR-RV 检测结果。治疗在真实的临床实践中进行。两组在使用全身性糖皮质激素和短效支气管扩张剂方面具有可比性。呼吸困难通过 TDI 指数(主要终点)、肺功能(肺活量测定、一氧化碳弥散能力)、运动耐量(6 分钟步行测试)和住院时间(次要终点)进行评估。利用考克斯比例危险模型确定了相关性。 结果显示在病毒相关性和病毒细菌性病情恶化组中,与细菌性病情恶化不同,以下治疗类型与达到 TDI +1 相关(几率比 - OR,95 % 置信区间 - CI):固定三联疗法(OR 2.69; 95 % CI 1.48-4.90; p = 0.010 和 OR 2.74; 95 % CI 1.29-3.80; p = 0.031),吸入 3 % 氯化钠溶液(OR 3.64; 95 % CI 1.45-5.42; p = 0.001 和 OR 3.23; 95 % CI 2.15-5.43;p = 0.042)、抗病毒药物(OR 2.91; 95 % CI 1.15-3.62; p = 0.009 和 OR 2.76; 95 % CI 1.31-3.90; p = 0.008)。经过治疗后,DLco/Va、6 分钟步行后的 SpO2 均有所提高,住院时间也有所缩短。 结论检测与病毒有关的感染是一个很有前景的指标,可用于确定慢性阻塞性肺疾病加重期的长效抗胆碱能药物和β-拟肾上腺素药物、吸入皮质类固醇、吸入高渗氯化钠溶液和抗病毒药物的处方适应症。
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