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阿育吠陀药物Brahmi vati和Saraswatarista治疗广泛性焦虑症的疗效——一项随机对照试验

Efficacy of ayurveda medications, Brahmi vati and Saraswatarista, in generalized anxiety disorder- a randomized controlled trial.

作者信息

Gonugade Varsha B, Chate Sameeran S, Tubaki Basavaraj R, Thakur Rajat

机构信息

Department of Kayachikitsa, BVVS Ayurved Medical College & Hospital Bagalkot, Karnataka, India. 587101.

Department of Psychiatry, J N Medical College, A Constituent Unit of KLE Academy of Higher Education & Research, Belagavi, Karnataka, India, 590016.

出版信息

J Ayurveda Integr Med. 2024 Nov-Dec;15(6):101033. doi: 10.1016/j.jaim.2024.101033. Epub 2024 Dec 2.

Abstract

BACKGROUND

Ayurvedic intervention (Brahmi Vati with Saraswatarista) is explored for their possible role in management of Generalized Anxiety Disorder (GAD), a common psychiatric disorder.

OBJECTIVE

The objective of the study was to evaluate the efficacy of Brahmi Vati and Saraswatarista in GAD.

METHODS

Study is a randomized controlled clinical trial. Patients (n = 50) of GAD (Diagnostic and Statistical Manual of Mental Disorders (DSM-5 criteria), 18-60 years of age, either sex participated in the study. Participants were randomly divided into two groups. Group A, received escitalopram 10 mg/day for first 10 days followed by 20 mg/day for next 50 days. Group B, received Ayurvedic intervention (Brahmi Vati 500 mg thrice a day (TID) and Saraswatarista 10 ml TID) for 60 days. Assessments were with clinical parameters like Hamilton Anxiety Rating Scale (HARS), GAD 7 scale (GAD 7), Beck Depression Inventory scale (BDI), Epworth sleepiness scale (ESS), Pittsburgh Sleep Quality Index (PSQI), WHO Quality of Life- BREF (WHOQOL-BREF), Clinical Global Improvement scale (CGI) and UKU-Side effect scale (UKU). These clinical assessments were measured on every 15th day during the intervention. Haemoglobin, liver function test (LFT), serum creatinine, serum urea were assessed before and after the study.

RESULTS

Study results indicate that both the groups were comparable in HARS, GAD7, BDI, WHOQOL-Bref and CGI-Severity. Group B was better in PSQI (standard mean difference = 0.87, 95% CI: 0.28, 1.43), ESS (standard mean difference = 1.42, 95% CI: 0.78, 2.02), CGI [global improvement (standard mean difference = 0.82, 95% CI: 0.23,1.28) and efficacy index (standard mean difference = 0.97, 95% CI: 0.37,1.54)] and had better adverse events profile (standard mean difference = 0.79, 95% CI: 0.21, 1.36). Both the groups had a good safety profile assessed through liver and renal profiles.

CONCLUSION

Ayurveda interventions has additional advantages likes improvements in sleep profile, lesser adverse events and better global improvement in management of GAD. CTRI Registration Number is CTRI/2020/09/027750.

摘要

背景

阿育吠陀干预措施(含有 Saraswatarista 的婆罗米丸)被探索在广泛性焦虑障碍(一种常见的精神疾病)管理中可能发挥的作用。

目的

本研究的目的是评估婆罗米丸和 Saraswatarista 对广泛性焦虑障碍的疗效。

方法

本研究为随机对照临床试验。符合广泛性焦虑障碍(《精神疾病诊断与统计手册》(DSM - 5 标准))的患者(n = 50),年龄在 18 - 60 岁之间,男女均可参与研究。参与者被随机分为两组。A 组,前 10 天每天服用艾司西酞普兰 10 毫克,接下来 50 天每天服用 20 毫克。B 组,接受阿育吠陀干预措施(每天三次,每次服用婆罗米丸 500 毫克及 Saraswatarista 10 毫升),持续 60 天。评估采用临床参数,如汉密尔顿焦虑量表(HARS)、广泛性焦虑障碍 7 项量表(GAD 7)、贝克抑郁量表(BDI)、爱泼华嗜睡量表(ESS)、匹兹堡睡眠质量指数(PSQI)、世界卫生组织生活质量简表(WHOQOL - BREF)、临床总体改善量表(CGI)和 UKU 副作用量表(UKU)。在干预期间,每 15 天进行一次这些临床评估。在研究前后评估血红蛋白、肝功能检查(LFT)、血清肌酐、血清尿素。

结果

研究结果表明,两组在 HARS、GAD7、BDI、WHOQOL - Bref 和 CGI - 严重程度方面具有可比性。B 组在 PSQI(标准平均差 = 0.87,95%置信区间:0.28,1.43)、ESS(标准平均差 = 1.42,95%置信区间:0.78,2.02)、CGI[总体改善(标准平均差 = 0.82,95%置信区间:0.23,1.2)和疗效指数(标准平均差 = 0.97,95%置信区间:0.37,1.54)]方面表现更好,且不良事件情况更佳(标准平均差 = 0.79,95%置信区间:0.21,1.36)。通过肝脏和肾脏指标评估,两组均具有良好的安全性。

结论

阿育吠陀干预措施具有额外的优势,如改善睡眠状况、不良事件较少以及在广泛性焦虑障碍管理中总体改善更好。临床试验注册编号为 CTRI/2020/09/027750。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3343/11652770/2ac52a4b0397/gr1.jpg

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