Acute bronchitis – modern possibilities of mucactive therapy

IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
A. A. Zaitsev, E. Filon, Yulia I. Storozheva
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Abstract

Aim. Analysis of the clinical effectiveness and safety of erdosteine use in comparison with standard (real practice) mucoactive therapy in patients with acute bronchitis (АВ) in adults.Materials and methods. The observational program included 100 adult patients with АВ, 50 of them (group 1) received erdosteine, the group 2 also included 50 patients who received acetylcysteine, bromhexine and other mucolytics (real clinical practice). The following were assessed: cough severity, average time for resolution of night and daytime cough, satisfaction with treatment, NO concentration in exhaled air, levels of C-reactive protein (CRP) and interleukin-6 (IL-6).Results. The average duration of relief of severe daytime cough requiring continued therapy was: in group 1 – 3.7±0.46 days, night cough – 1.14±0.94 days. In the second group, daytime cough was relieved in 3.8±0.4 days, night cough – 1.08±0.7 days. The duration of mucoactive therapy in group 1 was 5.32±0.82 days, in group 2 this figure was 8.5±1.4 days (p0.05). The number of АВ patients with a significant reduction in the severity of productive cough (1 point on cough severity scale) on the 6th day from the beginning of treatment in group 1 (erdosteine) amounted to 32 (64%), in group 2 – 27 (54%). Satisfaction with the treatment was higher in the group receiving erdosteine: according to the indicators "very satisfied" and "extremely satisfied" the patients of the group 1 – 42 – were the leaders in comparison with the group 2, where these positions were marked by 28 patients. The level of CRP in patients with АВ in group 1 was 24.7±21.24 mg/l, in group 2 – 16.37±16.5 mg/l, which indicates the viral etiology of the process and no need in the prescription of antimicrobial drugs. For the first time in Russian practice, the following were determined: the level of IL-6, which in the group 1 was 10.3±6.7 pc/ml; in the group 2 – 10.03±3.94 pc/ml; the level of exhaled NO in group 1 was 16.5±5.1 ppb, in group 2 – 14.9±4.6 ppb (the norm is up to 25 ppb). These indicators, against the background of mucoactive therapy, decreased to normal values by 6th day.Conclusion. The findings expand our understanding of АВ in adults. New results have been obtained on the role of CRP, IL-6 and NO in exhaled air during АВ. The use of erdosteine was accompanied by a significant mucoactive effect in the form of a pronounced regression of cough in patients with АВ compared to the comparison group in shorter term.
急性支气管炎--粘液活性疗法的现代可能性
目的分析在成人急性支气管炎(АВ)患者中使用厄洛斯汀与标准(实际操作)粘液活性疗法的临床有效性和安全性。观察项目包括 100 名成年АВ患者,其中 50 人(第 1 组)接受厄多司汀治疗,第 2 组也包括 50 名接受乙酰半胱氨酸、溴己新和其他粘液溶解剂治疗的患者(真实临床实践)。对以下内容进行了评估:咳嗽严重程度、夜间和白天咳嗽的平均缓解时间、治疗满意度、呼出气体中的 NO 浓度、C 反应蛋白(CRP)和白细胞介素-6(IL-6)水平。需要继续治疗的严重白天咳嗽的平均缓解时间为:第一组--3.7±0.46 天,夜间咳嗽--1.14±0.94 天。第二组白天咳嗽缓解时间为 3.8±0.4 天,夜间咳嗽缓解时间为 1.08±0.7 天。第一组的粘液活性治疗时间为 5.32±0.82 天,第二组为 8.5±1.4 天(P0.05)。从治疗开始的第 6 天起,АВ 患者的有痰咳嗽严重程度明显减轻(咳嗽严重程度量表 1 分)的人数在第 1 组(厄多司汀)为 32 人(64%),在第 2 组为 27 人(54%)。接受厄哚司汀治疗组的患者对治疗的满意度更高:根据 "非常满意 "和 "非常满意 "的指标,第 1 组有 42 名患者,领先于第 2 组的 28 名患者。第 1 组АВ患者的 CRP 水平为 24.7±21.24 毫克/升,第 2 组为 16.37±16.5 毫克/升。在俄罗斯的临床实践中首次测定了以下指标:IL-6 水平,第 1 组为 10.3±6.7 pc/ml,第 2 组为 10.03±3.94 pc/ml;呼出氮氧化物水平,第 1 组为 16.5±5.1ppb,第 2 组为 14.9±4.6ppb(正常值为 25ppb)。这些指标在接受粘液活性治疗的背景下,在第 6 天降至正常值。这些研究结果拓展了我们对成人АВ的认识。我们对АВ期间呼出气体中 CRP、IL-6 和 NO 的作用有了新的认识。与对比组相比,АВ患者在较短时间内使用厄多司汀会产生明显的粘液活性效应,即咳嗽明显减轻。
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来源期刊
Terapevticheskii Arkhiv
Terapevticheskii Arkhiv 医学-医学:内科
CiteScore
1.40
自引率
33.30%
发文量
171
审稿时长
3-8 weeks
期刊介绍: Терапевтический архив The journal was founded by the prominent Russian therapists M.P. Konchalovsky and G.F. Lang in 1923. Then its editors-in-chief were Professors V.N. Vinogradov and A.G. Gukasyan. Since 1972, E.I. Chazov, Academician of the Russian Academy of Sciences, has been heading the editorial board of the journal. Over 90 years, there have been more than 1000 issues where the authors and editorial staff have done their best for readers to keep abreast of current advances in medical science and practice and for physicians to master the advanced principles of recognition and treatment of a wide spectrum of visceral diseases. The papers published in the journal (editorials, original articles, lectures, reviews, etc.) cover both current scientific achievements and practical experience in diagnosing, treating, and preventing visceral diseases. The authors of publications are not only Russian, but also foreign scientists and physicians. All papers are peer-reviewed by highly qualified Russian specialists. The journal is published monthly. Traditionally, each issue has predominantly certain thematic areas covering individual therapy specializations. Every year, one of the issues is devoted to related problems in practical medicine (allergology and immunology, neurology and psychiatry, obstetrics, oncology, etc.). This all draws the attention of the reading public to the journal. The journal is indexed in RSCI (Russian Science Citation Index), PubMed/Medline, Index Medicus, Scopus/EMBASE, Web of Science Core Collection (Science Citation Index Expanded), Web of Science (Russian Science Citation Index - RSCI, Current Contents Connect, BIOSIS Previews), Google Scholar, Ulrich''s Periodicals Directory. The journal is included in the list of periodicals recommended by the Higher Attestation Committee for publishing the papers containing the basic materials of doctoral and candidate dissertations. By the decision of the Presidium of the Russian Academy of Medical Sciences, the “Therapevticheskiy Arkhiv” was awarded the Botkin medal. It was admitted to the European Association of Sciences Editors (EASE). The journal was honored with the Golden Press Fund decoration at the 13th International Press Professional Exhibition.
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