Lorenz Katrin, Wasielica-Poslednik Joanna, Bell Katharina, Renieri Giulia, Keicher Alexander, Ruckes Christian, Pfeiffer Norbert, Thieme Hagen
Department of Ophthalmology, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
University Eye Clinic, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.
PLoS One. 2017 Feb 15;12(2):e0171636. doi: 10.1371/journal.pone.0171636. eCollection 2017.
To demonstrate that preoperative treatment for 28 days with topical dorzolamide/timolol is non-inferior (Δ = 4 mm Hg) to oral acetazolamide and topical dexamethasone (standard therapy) in terms of intraocular pressure (IOP) reduction 3 and 6 months after trabeculectomy in glaucoma patients.
Sixty-two eyes undergoing trabeculectomy with mitomycin C were included in this monocentric prospective randomized controlled study. IOP change between baseline and 3 months post-op was defined as the primary efficacy variable. Secondary efficacy variables included the number of 5-fluorouracil (5-FU) injections, needlings, suture lyses, preoperative IOP change, hypertension rate and change of conjunctival redness 3 and 6 months post-op. Safety was assessed based on the documentation of adverse events.
Preoperative treatment with topical dorzolamide/timolol was non-inferior to oral acetazolamide and topical dexamethasone in terms of IOP reduction 3 months after trabeculectomy (adjusted means -8.12 mmHg versus -8.30 mmHg; Difference: 0.18; 95% CI -1.91 to 2.26, p = 0.8662). Similar results were found 6 months after trabeculectomy (-9.13 mmHg versus -9.06 mmHg; p = 0.9401). Comparable results were also shown for both groups concerning the classification of the filtering bleb, corneal staining, and numbers of treatments with 5-FU, needlings and suture lyses. More patients reported AEs in the acetazolamide/dexamethasone group than in the dorzolamide/timolol group.
Preoperative, preservative-free, fixed-dose dorzolamide/timolol seems to be equally effective as preoperative acetazolamide and dexamethasone and has a favourable safety profile.
旨在证明在青光眼患者小梁切除术后3个月和6个月时,局部用多佐胺/噻吗洛尔进行28天的术前治疗在降低眼压方面不劣于口服乙酰唑胺和局部用地塞米松(标准疗法)(差异=4 mmHg)。
本单中心前瞻性随机对照研究纳入了62例行丝裂霉素C小梁切除术的患眼。基线至术后3个月的眼压变化被定义为主要疗效变量。次要疗效变量包括5-氟尿嘧啶(5-FU)注射次数、针刺次数、缝线溶解次数、术前眼压变化、高血压发生率以及术后3个月和6个月结膜充血的变化。基于不良事件记录评估安全性。
小梁切除术后3个月,局部用多佐胺/噻吗洛尔进行术前治疗在降低眼压方面不劣于口服乙酰唑胺和局部用地塞米松(调整后均值-8.12 mmHg对-8.30 mmHg;差异:0.18;95%CI -1.91至2.26,p = 0.8662)。小梁切除术后6个月也发现了类似结果(-9.13 mmHg对-9.06 mmHg;p = 0.9401)。两组在滤过泡分类、角膜染色以及5-FU治疗次数、针刺次数和缝线溶解次数方面也显示出可比结果。与多佐胺/噻吗洛尔组相比,乙酰唑胺/地塞米松组报告不良事件的患者更多。
术前无防腐剂的固定剂量多佐胺/噻吗洛尔似乎与术前乙酰唑胺和地塞米松同样有效,且具有良好的安全性。