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Topical carbonic anhydrase inhibition increases ocular pulse amplitude in high tension primary open angle glaucoma

机译:局部碳酸酐酶抑制作用可增加高压原发性开角型青光眼的眼搏幅度

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摘要

BACKGROUND—Ocular pulse amplitude (OPA) is reduced in normal tension primary open angle glaucoma (NTP) patients when compared with healthy age matched controls (CTL) while increased OPA appears to protect ocular hypertensive patients from visual field loss. If NTP is accompanied by vasospasm, as in roughly half of the primary open angle glaucoma (POAG) population (independent of intraocular pressure, IOP), calcium channel blockers increase OPA and thus stabilise visual fields in these patients. Current glaucoma drugs reduce IOP but do not activate (compromised) ocular perfusion.
METHODS—The influence of dorzolamide, a topical carbonic anhydrase inhibitor in standard dosage (three times daily, one eye) on OPA, IOP, blood pressure, and heart rate was investigated in a randomised, prospective, masked clinical trial assessing the acute effects of dorzolamide v placebo before and 2 days after application in 33 cataract patients with (n = 14) and without (n = 19) high tension POAG (HTP) who provided informed consent.
RESULTS—Following application of dorzolamide (D) IOP (mm Hg, mean (SEM)) in HTPD (20.2 (0.5)/16.3 (0.5)) and in CTLD (16.0 (0.5)/12.3 (0.5)) was highly significantly (p <0.001) reduced and was significantly (p<0.03) reduced in vehicle (V) treated eyes (HTPV: 20.3 (0.4)/19.0 (0.4)) and CTLV: 15.8 (0.4)/14.9 (0.3)) when compared with respective baseline measurements. OPA (mm Hg) in HTPD (2.1 (0.1)/2.5 (0.1)) and CTLD (2.2 (0.1)/2.6 (0.2)) eyes was significantly (p<0.05) increased and unaffected in vehicle treated eyes when compared with respective baseline measurements. Systemic perfusion variables were also unchanged.
CONCLUSION—Dorzolamide increased OPA in HTP and CTL. Drugs stimulating OPA may improve prognosis of POAGs.

Keywords: ocular pulse amplitude; primary open angle glaucoma; dorzolamide
机译:背景技术与健康的年龄匹配对照组(CTL)相比,正常张力原发性开角型青光眼(NTP)患者的眼压幅度(OPA)降低,而OPA的增加似乎可以保护高眼压患者免于视野丧失。如果NTP伴有血管痉挛,如大约一半的原发性开角型青光眼(POAG)人群(与眼压,IOP无关),钙通道阻滞剂会增加OPA,从而稳定这些患者的视野。当前的青光眼药物可降低IOP,但不能激活(损害)眼内灌注。
方法-多佐胺(一种标准剂量的碳酸酐酶局部抑制剂)对OPA,IOP,血压的影响(每日三次,一只眼)在一项随机,前瞻性,隐蔽的临床试验中对心率进行了研究,评估了多佐胺v安慰剂在33例患有(n = 14)和不患有(n = 19)高压POAG(HTP)的白内障患者中的急性作用),并提供知情同意。
结果-在HTPD(20.2(0.5)/16.3(0.5))和CTLD(16.0(0.5))中应用多佐胺(D)IOP(mm Hg,平均值(SEM)) /12.3(0.5))显着降低(p <0.001),显着(p <0.03)降低(VPV)治疗的眼睛(HTPV:20.3(0.4)/19.0(0.4))和CTLV:15.8(0.4 )/14.9(0.3))与相应的基线测量值进行比较。与单独治疗相比,HTPD(2.1(0.1)/2.5(0.1))和CTLD(2.2(0.1)/2.6(0.2))眼的OPA(mm Hg)显着增加(p <0.05),并且不受影响基线测量。系统性灌注变量也没有变化。
结论:多佐胺提高了HTP和CTL中的OPA。刺激OPA的药物可改善POAGs的预后。原发性开角型青光眼;多佐胺

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