Comparison between Escitalopram and Pregabalin for Generalized Anxiety Disorder Treatment

Muhammad Shoaib Zafar, Nazish Idrees Chaudhary
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Abstract

Objective: To facilitate the emerging need for investigating the efficacy of escitalopram compared to pregabalin for treating generalized anxiety disorders. Methods: This quasi-experimental study with pre and post-test design was carried out for twelve weeks in the year 2019 between January to June where 90 patients visiting Mayo Hospital in Lahore, within the age range of 18 to 60 years were divided into 2 equal groups by purposive sampling. The 20 mg dose of escitalopram per day was given to the participants of group A while a dose of 150-200mg per day of pregabalin was given to group B and the level of anxiety before and after the experiment was measured by Hamilton Anxiety Baseline. A record of all clinical signs and symptoms was also maintained throughout the time of medication. After 12 weeks, follow-up data was taken from the patients and the scores were compared with the baseline. Results: Efficacy, defined as ≥2% reduction in the scores of anxiety among the participants after 12 weeks was significantly higher in Escitalopram group A than in Pregabalin group B: (92.8% vs. 82.5%) with p-value= 0.003. Gastrointestinal symptoms were seen in 11.9% of patients in Group A and 27.5% of patients in Group B. In Group A 14.2% of patients reported headaches, as compared to 22.5% of patients in Group B. Sleep disturbances, were reported by 10% of patients in Group A and 15% of patients in Group B. Sweating was seen by 19% of patients in Group A and 50% patients in Group B. Urinary symptoms were experienced by 4.7% patients in Group A and 7.5% patients in Group B. Conclusion: Escitalopram is a better option and efficacious for the Pakistani population in treating psychological issues including depression, bipolar and other affective disorders despite the minor side effects compared to Pregabalin.  
艾司西酞普兰与普瑞巴林治疗广泛性焦虑障碍的比较
目的:探讨艾司西酞普兰与普瑞巴林治疗广泛性焦虑障碍的疗效。方法:采用准实验设计,于2019年1月至6月对在拉合尔梅奥医院就诊的年龄在18岁至60岁之间的90例患者进行为期12周的准实验研究,采用目的抽样法将其分为两组。A组给予艾司西酞普兰20 mg /天,B组给予普瑞巴林150 ~ 200mg /天,采用汉密尔顿焦虑基线测定实验前后的焦虑水平。所有临床体征和症状的记录也在整个药物治疗期间保持。12周后,从患者中获取随访数据,并将得分与基线进行比较。结果:艾司西酞普兰A组的疗效(定义为12周后参与者焦虑评分降低≥2%)显著高于普瑞巴林B组(92.8%对82.5%),p值= 0.003。胃肠道症状被认为在A组11.9%的患者和27.5%的患者组b组中14.2%的患者报告头痛,相比在b组22.5%的患者睡眠障碍,据报道,10%的患者在A组和b组15%的患者出汗被组19%的患者,50%的患者在b组尿症状是有经验的4.7%患者组和7.5%病人在b组的结论:尽管与普瑞巴林相比,艾司西酞普兰的副作用较小,但在治疗包括抑郁症、双相情感障碍和其他情感障碍在内的心理问题方面,艾司西酞普兰是巴基斯坦人口更好的选择和有效的选择。
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