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Pathogenetic approach to the treatment of functional disorders of the gastrointestinal tract and their intersection: results of the Russian observation retrospective program COMFORT

机译:治疗胃肠道功能性疾病的致病方法及其交叉路口:俄罗斯观察结果的结果舒适

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The aim of this study was to investigate the efficacy and safety of the novel complex drug, consisting of released-active form of antibodies to S-100 protein, tumor necrosis factor-α and histamine, (Kolofort) under outpatient conditions in patients with functional dyspepsia (FD), irritable bowel syndrome (IBS), and FD-IBS overlap. The subjects of the observational noninterventional retrospective program were the data of 14,362 outpatient records of patients with diagnosed FD, IBS, and/or overlap, who were observed by gastroenterologists from November 01, 2017, through March 30, 2018, who received the drug Kolofort in monotherapy for 12?weeks, 2 tablets twice a day. To assess the presence and severity of symptoms of functional gastrointestinal disorders (FGID), the “7*7” questionnaire developed by a working group from the Russian Gastroenterological Association was used. The evaluated parameters included the proportion of patients: who had a 50% or more reduction in the total score; who have switched to the less severe category of the condition; who have switched to the “healthy” or “borderline ill” severity categories; and the change in the score in domains 1–7. The final efficacy analysis included data from 9254 patients. A decrease in the total score by 50% or more was observed in 80.45% of patients with FD, 79.02% of patients with IBS, and in 83% of patients with both IBS and FD. Switch to a lower severity category of the condition at the end of therapy was noted in 93.35% of patients with FD, in 93.80% of cases in patients with IBS, and in 96.17% of cases in patients with a combination of IBS and FD. A total of 94 adverse events (AEs) were reported in 80 patients (0.65%). The COMFORT program has demonstrated the positive effect of treatment in the majority of patients with IBS and FD and their combination in real clinical practice.
机译:本研究的目的是探讨新型复杂药物的疗效和安全性,由函数患者的门诊病症下的S-100蛋白,肿瘤坏死因子-α和组胺的抗体的释放活性形式,(Kolofort)组成。消化不良(FD),肠易激综合征(IBS)和FD-IBS重叠。观察性非事实无主的回顾性计划的主题是2017年11月1日从2017年11月30日期间观察的患有FD,IBS和/或重叠患者的14,362名门诊记录,2018年3月30日,他们接受了毒品Kolofort在单疗法中为12个?周,每天两片2片。为了评估功能性胃肠病症(FGID)的症状的存在和严重程度,使用了由俄罗斯胃肠学协会的工作组开发的“7 * 7”调查问卷。评估的参数包括患者的比例:谁的总分减少50%或更高;谁已切换到不太严重的条件;谁已切换到“健康”或“边界生病”严重程度类别;和域名1-7中得分的变化。最终的疗效分析包括来自9254名患者的数据。在80.45%的FD,79.02%的IBS患者中,患者的80%或更多的总分或更多的减少,患有IBS和FD的83%的患者。在93.35%的FD患者中,在93.35%的患者中,在患有IBS患者的93.35%的患者中,在治疗结束时切换到较低的严重程度范畴,以IBS和FD组合的患者患者的96.17%。报告80例患者共有94例不良事件(AES)(0.65%)。舒适计划已经证明了在大多数IBS和FD患者中治疗的积极作用及其在真正的临床实践中的组合。

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