青光眼的视网膜保护治疗

Q4 Medicine
A. Makarova
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The patients were split into 2 groups, each group consisting of 15 individuals, who received a different number of intramuscular (IM) injections of a neuroprotective drug, 5.0 mg: 10 injections in group 1 and 20 injections group 2. A comprehensive examination of patients was carried out at the beginning of the follow-up period, and at 3 and 6 months after the completion of the course of treatment with the drug. It included visometry, tonometry, static perimetry and optical coherence tomography of the retina and optic nerve. Results: based on the DBPM, the normal circadian BP pattern was disturbed in 27 (90%) patients. During the entire follow-up period, both groups demonstrated an improvement in visual acuity. The results of static perimetry indicated the stabilization of the glaucoma process in group 1 patients, while in group 2 where the treatment course with the neuroprotective drug lasted twice longer, it was possible to achieve an improvement in photosensitivity of the retina, as proven by the positive trends in MD and PSD indices. The results of the functional studies fully correlated with the morphological findings as demonstrated by a reliable stabilization of the status of the retinal nerve fiber layer and ganglion complex, as well as the volume of the optic nerve head. At the same time, a longer course of therapy with the drug was accompanied not only by a significant increase in the above parameters, but also by a decline in the volume of excavation of the optic nerve disc. 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引用次数: 0

摘要

背景:血压波动,尤其是夜间低血压是导致青光眼视神经病变进展的关键不利因素。目的:通过监测视网膜和视神经的形态学和功能参数,研究神经保护药物(一种水溶性多肽复合物)对不稳定型原发性开角型青光眼和归一化眼动症的疗效。患者和方法:这项为期六个月的研究包括30例(60只眼)原发性开角2期或3期代偿性青光眼,病程不稳定。在研究的第一阶段,对所有患者使用每日血压监测(DBPM)来评估全身血流动力学的变化。将患者分为2组,每组15人,给予不同次数的神经保护药物肌肉注射,1组10次,2组20次,注射剂量为5.0 mg。在随访期开始时以及药物疗程结束后3个月和6个月对患者进行全面检查。它包括粘度测量、眼压测量、静态视野测量和视网膜和视神经的光学相干断层扫描。结果:根据DBPM, 27例(90%)患者的正常昼夜血压模式受到干扰。在整个随访期间,两组患者的视力都有所改善。静态视距检查结果表明,1组患者青光眼病程稳定,而2组患者使用神经保护药物治疗的时间延长了一倍,视网膜光敏性有可能得到改善,MD和PSD指数呈阳性趋势。功能研究的结果与形态学结果完全相关,视网膜神经纤维层和神经节复合体的状态以及视神经头的体积都得到了可靠的稳定。与此同时,较长的药物治疗过程不仅伴随着上述参数的显着增加,而且还伴随着视神经盘挖掘体积的下降。结论:原发性开角型青光眼进展伴全身血流动力学改变的患者应用神经保护药物可达到稳定和改善视觉功能的目的。关键词:青光眼,全身血压,肽制剂,视网膜神经节细胞,神经保护,视网膜保护。引用本文:Makarova A.S.青光眼的视网膜保护治疗。俄罗斯临床眼科学杂志,2022;22(4):210-215。DOI: 10.32364 / 2311-7729-2022-22-4-210-215。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retinoprotective therapy of glaucoma
Background: a fluctuating blood pressure (BP) and particularly an overnight hypotension is the key adverse factor leading to the progression of glaucomatous optic neuropathy. Aim: to study the effectiveness of a neuroprotective drug (a complex of water-soluble polypeptide fractions) in patients with unstable primary open-angle glaucoma and normalized ophthalmotonus by monitoring the morphological and functional parameters of the retina and optic nerve. Patients and Methods: this six-month study included 30 patients (60 eyes) with primary open-angle stage 2 or 3 compensated glaucoma and unstable course. At the first stage of the study, a daily blood pressure monitoring (DBPM) was used for all patients to assess changes in systemic hemodynamics. The patients were split into 2 groups, each group consisting of 15 individuals, who received a different number of intramuscular (IM) injections of a neuroprotective drug, 5.0 mg: 10 injections in group 1 and 20 injections group 2. A comprehensive examination of patients was carried out at the beginning of the follow-up period, and at 3 and 6 months after the completion of the course of treatment with the drug. It included visometry, tonometry, static perimetry and optical coherence tomography of the retina and optic nerve. Results: based on the DBPM, the normal circadian BP pattern was disturbed in 27 (90%) patients. During the entire follow-up period, both groups demonstrated an improvement in visual acuity. The results of static perimetry indicated the stabilization of the glaucoma process in group 1 patients, while in group 2 where the treatment course with the neuroprotective drug lasted twice longer, it was possible to achieve an improvement in photosensitivity of the retina, as proven by the positive trends in MD and PSD indices. The results of the functional studies fully correlated with the morphological findings as demonstrated by a reliable stabilization of the status of the retinal nerve fiber layer and ganglion complex, as well as the volume of the optic nerve head. At the same time, a longer course of therapy with the drug was accompanied not only by a significant increase in the above parameters, but also by a decline in the volume of excavation of the optic nerve disc. Conclusions: the use of the neuroprotective drug in patients with the progression of primary open-angle glaucoma co-occurring with the changes in systemic hemodynamics enabled to achieve stabilization and improvement of the visual functions. Keywords: glaucoma, systemic blood pressure, peptide preparation, retinal ganglion cells, neuroprotection, retinoprotection. For citation: Makarova A.S. Retinoprotective therapy of glaucoma. Russian Journal of Clinical Ophthalmology. 2022;22(4):210–215 (in Russ.). DOI: 10.32364/2311-7729-2022-22-4-210-215.
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