Dhiman K S, Adhoor Veeranagouda S, Agarwal Riju, Mehta Amit J
Department of Shalakya, Institute of Post Graduate Teaching and Research In Ayurveda, Gujarat Ayurveda University, Jamnagar, Gujarat, India.
Department of Shalakya, Chaudhary Brahm Prakash Ayurved Charak Sansthan, Guru Gobind Singh Indraprastha University, New Delhi, India.
Ayu. 2016 Apr-Jun;37(2):125-134. doi: 10.4103/ayu.AYU_30_16.
Primary open angle glaucoma is an insidious and chronic vision-threatening eye ailment due to neuro-retino-optic nerve degeneration, which may be due to the raised intraocular pressure (IOP) or due to independent factors. Management of glaucoma is mainly concentrated on lowering IOP that requires lifetime topical medication, different ocular medicaments for lowering of IOP, and surgical interventions, but it has its own limitations to control the progression of glaucomatous optic neuropathy (GON), and this is the reason behind the use of alternative neuroprotective adjuvants.
To evaluate the neuroprotective effect of Ayurvedic line of management of progressive GON.
Ingredients of trial drug Vara Fort powder () were procured from the Institute Pharmacy, except , which was purchased from Dhootapapeshwar Pharmaceuticals. The patients fulfilling inclusion criteria, attending outpatient and inpatient departments, irrespective of their sex, race, religion, occupation, etc., were selected and divided into two groups with open-labeled randomization. In Group A, in addition to betaxolol (0.1%) or timolol (0.5%) (non-iobrim), 6 g/day orally with and honey along with (body-microchannel clearing treatment) protocol was tried. (oleation through nasal route) with and (eye satiation) with were also performed. In Group B (control), brimonidine (iobrim) 0.2% eye drop was used for 3 months.
Significant improvement was observed in subjective parameters in Group A such as blurred vision, frequent change of presbyopic glasses, and delayed dark adaptation.
, if administered in a systematic approach along with a modern topical betaxolol or timolol eye drops, has a definite role in improving the lost retinal sensitivity as much as up to 12 dB in 3 months duration.
原发性开角型青光眼是一种隐匿性慢性眼病,可威胁视力,病因是神经视网膜视神经变性,这可能是由于眼压升高或独立因素所致。青光眼的治疗主要集中在降低眼压,这需要终身使用局部药物、不同的降低眼压的眼部药物以及手术干预,但在控制青光眼性视神经病变(GON)的进展方面有其自身的局限性,这就是使用替代神经保护佐剂的原因。
评估阿育吠陀疗法对进行性GON的神经保护作用。
试验药物Vara Fort散剂()的成分从研究所药房采购,除外,从Dhootapapeshwar制药公司购买。符合纳入标准、在门诊和住院部就诊的患者,不论其性别、种族、宗教、职业等,均被选中并通过开放标签随机分组分为两组。在A组中,除了倍他洛尔(0.1%)或噻吗洛尔(0.5%)(非碘必殊)外,尝试口服6克/天的,并与蜂蜜一起配合(身体微通道清理疗法)方案。还进行了(经鼻途径的润滑)和(用眼饱足)。在B组(对照组)中,使用0.2%的溴莫尼定(碘必殊)滴眼液,持续3个月。
A组的主观参数如视力模糊、老花镜频繁更换和暗适应延迟有显著改善。
如果与现代局部倍他洛尔或噻吗洛尔滴眼液一起系统给药,在3个月的时间内,在改善丧失的视网膜敏感度方面有明确作用,可提高多达12分贝。