Effect of Plantago major on cough severity in acute bronchitis: A double-blind randomized clinical trial.

Pub Date : 2024-09-07 eCollection Date: 2024-01-01 DOI:10.22088/cjim.15.4.651
Alireza Naderi, Seyyed Ali Mozaffarpur, Hoda Shirafkan, Masomeh Bayani, Zahra Memariani
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Abstract

Background: Treatments for acute bronchitis is usually a supportive care to relieve upper respiratory symptoms. This study aimed to evaluate the effect of Plantago major syrup (PMS) on cough severity in acute bronchitis.

Methods: Patients (20-75 years-old) referred to the clinic of infectious diseases in Ayatollah Rouhani Hospital, Babol, Iran with a complaint of cough and the Bronchitis Severity Scale (BSS) ≥5 entered the study. The patients randomly received PMS or placebo 30 ml/day for 10 days. Patients were visited before treatment and on days 5 and 10 after treatment. The primary outcome was BSS score and secondary outcome was the life quality that was measured by means of the Persian version of the Leicester Cough Questionnaire (LCQ) at the first visit and on the 10th day.

Results: Of the 121 patients diagnosed with acute bronchitis, 80 eligible patients (42.87±11.75 years-old) were randomly divided into PMS and placebo groups. The BSS score in the PMS group after 10 days was significantly lower than that of the placebo group (P=0.001). Frequency of cough (P=0.001), sputum production (P=0.005), and chest wall pain (P=0.008) were significantly lower in the PMS group than in the placebo group. In terms of quality of life, all items, including psychological, physical, and social domains, as well as total scores, were altered significantly in the PMS group compared to placebo. During monitoring of side effects, no significant adverse effects were stated in either group.

Conclusion: The study indicates the palliative effects of PMS in relieving the symptoms of acute bronchitis and improving quality of life.

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大车前草对急性支气管炎咳嗽严重程度的影响:双盲随机临床试验
背景:急性支气管炎的治疗通常是缓解上呼吸道症状的支持性治疗。本研究旨在评估大车前子糖浆(PMS)对急性支气管炎咳嗽严重程度的影响:方法:在伊朗巴博勒阿亚图拉-鲁哈尼医院传染病门诊就诊、主诉咳嗽且支气管炎严重程度量表(BSS)≥5 的患者(20-75 岁)参与研究。患者随机接受 PMS 或安慰剂治疗,每天 30 毫升,为期 10 天。在治疗前、治疗后第 5 天和第 10 天对患者进行访视。主要结果是 BSS 评分,次要结果是生活质量,在首次就诊时和第 10 天通过波斯语版莱斯特咳嗽问卷(LCQ)进行测量:在121名确诊为急性支气管炎的患者中,80名符合条件的患者(42.87±11.75岁)被随机分为PMS组和安慰剂组。10 天后,PMS 组的 BSS 评分明显低于安慰剂组(P=0.001)。PMS 组的咳嗽频率(P=0.001)、痰量(P=0.005)和胸壁疼痛(P=0.008)明显低于安慰剂组。在生活质量方面,与安慰剂组相比,PMS 组的所有项目,包括心理、生理和社会领域以及总分都有明显变化。在对副作用的监测中,两组均未发现明显的不良反应:研究表明,PMS 在缓解急性支气管炎症状和提高生活质量方面具有缓和作用。
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