Lanza Michele, Leone Angelo, Scognamiglio Gabriele, Serra Luigi, Iodice Clemente Maria, Melillo Paolo, Simonelli Francesca
Dipartimento di Specialità Mediche, Chirurgiche ed Odontoiatriche, Università della Campania Luigi Vanvitelli, 80131 Napoli, Italy.
J Clin Med. 2022 Oct 19;11(20):6166. doi: 10.3390/jcm11206166.
Background: To investigate the efficacy interval of the topical therapies available for primary open-angle glaucoma (POAG) and the ocular and systemic features potentially associated. Methods: This retrospective study included 190 patients with POAG undergoing first topical therapy, throughout a follow-up of 15 years. The patients started one topical intraocular pressure (IOP)-lowering drug within single molecules such betablockers, prostaglandin or dorzolamide, or fixed combinations such as betablockers + prostaglandin, betablockers + dorzolamide, or betablockers + brimonidine. Efficacy duration was measured as the time between the start of the therapy and the change due to IOP increase or visual field worsening. For each patient, ocular and systemic features and comorbidities were analysed to detect any significant correlation with the length of effectiveness of every drug used. Results: The molecules explored showed some discrepancies in terms of mean duration of efficacy; however, no significant differences were demonstrated (p > 0.05). Furthermore, when evaluating the overall cohort, no systemic or ocular features correlated significantly with the effectiveness of the molecules explored. However, the same analysis carried out upon stratifying the different groups according to the IOP-lowering drops they received, demonstrated that the drug efficacy could be influenced by several ocular and systemic features. Conclusion: Data observed in this study suggest that there is no difference in using one of the medications evaluated as first choice of treatment of POAG if the patients are accurately evaluated and the most recent guidelines are adopted.
研究原发性开角型青光眼(POAG)可用局部治疗方法的疗效间隔以及可能相关的眼部和全身特征。方法:这项回顾性研究纳入了190例接受首次局部治疗的POAG患者,随访时间为15年。患者开始使用单分子局部降眼压药物,如β受体阻滞剂、前列腺素或多佐胺,或固定组合,如β受体阻滞剂+前列腺素、β受体阻滞剂+多佐胺或β受体阻滞剂+溴莫尼定。疗效持续时间以治疗开始至因眼压升高或视野恶化而发生变化的时间来衡量。对每位患者的眼部和全身特征及合并症进行分析,以检测与所用每种药物疗效持续时间的任何显著相关性。结果:所研究的分子在平均疗效持续时间方面存在一些差异;然而,未显示出显著差异(p>0.05)。此外,在评估整个队列时,没有全身或眼部特征与所研究分子的疗效显著相关。然而,根据他们接受的降眼压滴眼液对不同组进行分层后进行的相同分析表明,药物疗效可能受多种眼部和全身特征的影响。结论:本研究观察到的数据表明,如果对患者进行准确评估并采用最新指南,作为POAG首选治疗药物之一使用时没有差异。