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A randomized, double-blind, placebo-controlled study to assess efficacy of mirtazapine for the treatment of diarrhea predominant irritable bowel syndrome

机译:一种随机,双盲,安慰剂对照研究,评估Mirtazapine治疗腹泻优势肠易激综合征的疗效

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摘要

Abstract Background Ample evidence indicates the efficacy of serotonin type 3 (5-HT3) receptor antagonists in the treatment of patients with diarrhea-predominant irritable bowel syndrome (IBS-D). Mirtazapine is an atypical antidepressant with a well-known 5-HT3 receptor antagonist property. This study, therefore, was undertaken to investigate whether compared to placebo, mirtazapine would be efficacious and safe in the treatment of patients with IBS-D. Methods From November 2019 until July 2020, 67 patients meeting Rome IV criteria for IBS-D were randomized in a double-blind fashion into either the mirtazapine treatment group (n = 34) or the placebo treatment group (n = 33). Patients started with mirtazapine 15 mg/day at bedtime for one-week; after which the dose was increased to 30 mg/day for an additional 7-week. Outcomes included changes in the total IBS symptom severity score (IBS-SSS), Hospital anxiety and depression scale score (HADS), and IBS Quality of Life. Additionally, changes in the diary-based symptoms scores including pain, urgency of defecation, bloating, stool frequency, and stool consistency based on the 7-point Bristol Stool Form Scale (BSFS), and a number of days per week with pain, urgency, diarrhea, or bloating, once during the 1-week run-in period, and once during the last week of treatment were recorded. Results All analyses were performed on an Intention-to-Treat (ITT) analysis data set. The results showed compared to placebo, mirtazapine is more efficacious in decreasing the severity of IBS symptoms (P-value = 0.002). Further, at the end of the treatment period, all diary-derived symptoms except bloating showed significantly more improvement in the mirtazapine-treated subjects compared to the placebo-treated subjects. While was well-tolerated, mirtazapine also significantly improved the patients’ quality of life (P-value = 0.04) and anxiety symptoms (P-value = 0.005). Conclusions Overall, mirtazapine seems to have a potential benefit in the treatment of patients with IBS-D, particularly those with concomitant psychological symptoms. However, further studies are warranted to determine whether these findings are replicated. Trial registration Trial registration: Registration number at Iranian Registry of Clinical Trials: IRCT20120215009014N311 . Registration date: 2019-10-21.
机译:摘要背景充足的证据表明血清素型3(5-HT3)受体拮抗剂在治疗腹泻患者患者(IBS-D)中的疗效。 Mirtazapine是一种非典型抗抑郁药,具有众所周知的5-HT3受体拮抗剂性能。因此,本研究旨在调查与安慰剂相比,Mirtazapine在治疗IBS-D患者中是有效和安全的。方法方法从2019年11月到2020年7月,将罗马IV的67名患者IBS-D的标准以双盲方式随机分配到Mirtazapine治疗组(n = 34)或安慰剂处理组(n = 33)中。患者在睡前15毫克/天开始一周;之后,剂量增加至30mg /天,另外7周。结果包括IBS症状严重程度(IBS-SSS),医院焦虑和抑郁级别得分(HASS)和IBS生活质量的变化。此外,基于日记症状的变化,包括疼痛,排便的疼痛,膨胀,粪便频率和粪便一致性,基于7点布里斯托尔粪便形式秤(BSF),每周疼痛,紧急情况,腹泻或腹胀,一次在1周的运行期间,记录了在上一周的一次治疗期间。结果对意图(ITT)分析数据集进行了所有分析。结果表明与安慰剂相比,Mirtazapine在降低IBS症状的严重程度时更有效(P值= 0.002)。此外,在治疗期结束时,与安慰剂处理的受试者相比,除了腹胀之外的所有日记衍生的症状都显示出Mirtazapine治疗的受试者的显着更高。虽然耐受良好,但Mirtazapine也显着提高了患者的生活质量(p值= 0.04)和焦虑症状(p值= 0.005)。结论总体而言,Mirtazapine似乎对IBS-D患者的潜在益处,特别是具有伴随心理症状的患者。但是,有必要进一步研究来确定这些发现是否被复制。审判登记试验登记:临床试验中的伊朗登记处的注册号:IRCT20120215009014N311。注册日期:2019-10-21。

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