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Efficacy and safety of prostaglandin analogues in patients with predominantly primary open-angle glaucoma or ocular hypertension: a meta-analysis

机译:前列腺素类似物在主要原发性开角型青光眼或高眼压患者中的疗效和安全性:一项荟萃分析

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Background: First-line therapy for primary open-angle glaucoma and ocular hypertension generally involves prostaglandin analogue therapy. The relative efficacy of differing prostaglandin therapy is disputed.Methods: A meta-analysis was conducted of head-to-head randomized trials of prostaglandin therapies. We included randomized trials assessing head-to-head evaluations of prostaglandin analogues travoprost, latanoprost and bimatoprost in patients with predominantly primary open-angle glaucoma or ocular hypertension. Findings were interpreted in light of equivalence margins.Results: Our search identified 16 eligible trials, of which 15 were included in the meta-analysis. Trials were, in general, poorly reported. We pooled 9 trials assessing IOP-lowering effects of travoprost vs latanoprost (total n = 1098, weighted mean difference [WMD], –0.24 mmHg, 95% CI, –0.87 to 0.38, P = 0.45, I2 = 56%, 95% CI, 0 to 0.77, heterogeneity P = 0.01). Eight trials assessed travoprost vs bimatoprost (total n = 714, WMD, 0.88 mmHg, 95% CI, 0.13 to 1.63, P = 0.02, I2 = 56%, 95% CI, 0% to 78%, heterogeneity P = 0.02). And 8 trials assessed latanoprost vs bimatoprost (total n = 943, WMD, 0.73 mmHg, 95% CI, 0.10 to 1.37, P = 0.02, I2 = 47%, 95% CI, 0% to 74%, heterogeneity P = 0.06). Travoprost was associated with greater incidence of conjunctival hyperemia than latanoprost (RR 5.71, 95% CI, 1.81 to 18.02, P ≤ 0.001, I2 = 97%, 95% CI, 95 to 98, P ≤ 0.001). Five trials assessing latanoprost and bimatoprost revealed an elevated risk of conjunctival hyperemia with bimatoprost (RR 1.59, 95% CI, 1.02 to 2.48, P = 0.04, I2 = 76%, 95% CI, 16 to 88, P = 0.002).Conclusion: Randomized head-to-head evaluations of prostaglandin therapy demonstrate similar efficacy effects, but differing hyperemia effects.
机译:背景:用于原发性开角型青光眼和高眼压症的一线治疗通常涉及前列腺素类似物治疗。方法:对前列腺素疗法的头对头随机试验进行荟萃分析。我们纳入了随机对照试验,以评估主要患有原发性开角型青光眼或高眼压症患者中前列腺素类似物特拉沃前列素,拉坦前列素和比马前列素的并列评价。结果:我们的搜索结果确定了16项符合条件的试验,其中15项纳入荟萃分析。一般而言,审判报告不多。我们汇总了9项评估travoprost与latanoprost降低IOP的试验(总n = 1098,加权平均差[WMD],-0.24 mmHg,95%CI,-0.87至0.38,P = 0.45,I2 = 56%,95% CI,0至0.77,异质性P = 0.01)。八项试验评估了travoprost vs bimatoprost(总n = 714,WMD,0.88 mmHg,95%CI,0.13至1.63,P = 0.02,I2 = 56%,95%CI,0%至78%,异质性P = 0.02)。有8个试验评估了拉坦前列素与比马前列素(总n = 943,WMD,0.73 mmHg,95%CI,0.10至1.37,P = 0.02,I2 = 47%,95%CI,0%至74%,异质性P = 0.06) 。与拉坦前列素相比,曲妥前列素与结膜充血的发生率更高(RR 5.71,95%CI,1.81至18.02,P≤0.001,I2 = 97%,95%CI,95至98,P≤0.001)。五项评估拉坦前列素和比马前列素的试验显示,比马前列素导致结膜充血的风险升高(RR 1.59,95%CI,1.02至2.48,P = 0.04,I2 = 76%,95%CI,16至88,P = 0.002)。 :前列腺素疗法的随机头对头评估显示出相似的功效效果,但充血效果不同。

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