Oftalmol Zh. 2013; 5: 51-6.

https://doi.org/10.31288/oftalmolzh201355156

Clinical and neurofunctional criteria for prognosing the development of primary open angle glaucoma

Stotska LM

Ivano-Frankivsk, Ukraine 

odjusa@email.ua

Introduction. The etiology and pathogenesis of primary open-angle glaucoma remain controversial, causing considerable difficulties in its early diagnosis. Purpose. To study the clinical and neurofunctional criteria for prognosing the development of primary open-angle glaucoma (POAG)

Material and Methods. A clinical and functional examination was made in 119 patients with primary open angle glaucoma, the average age (51.8 + 3.2) years old; 46.8 % male and 53.2 % female, and 30 patients of a study group without POAG with diseases as follows: vegetative — vascular dystonia, migraine, hypertension, hypotension; mean age 52.4 + 3.1, 48.3 % and 51.7 % males and females respectively. We used neurophysiological methods: visual sensory-motor reaction according to standard procedure, the critical flicker fusion frequency (CFFF) was studied using the diagnostic module ophthalmic stimulator KNSO2— 91 «phosphene», allowing to detect functional changes in the visual analyzer at its different levels.

Results. We received priority data regarding aspects of neurofunctional status in patients with primary open angle glaucoma: a statistically significant changes in the imbalance between excitation and inhibition, namely, the increase in the difference values of the latent periods of simple and complex visual sensorimotor reactions, reducing the lability of the nervous system that meet the clinical and morphological changes of glaucomatous optic neuropathy at appropriate stages.

Conclusions. With the help of multivariate analysis it was established clinical criteria of neurofunctional early diagnosis and prognosis of primary open angle glaucoma: an increase in the difference between the latent periods of simple and complex visual sensorimotor reactions exceeds the standard value of 145 ms by 20 % or more; a decrease of the lability of the nervous system (in blue) from 31.01 Hz when volume is reduced neuroretinal rim from 0.36 mm 3.

Key words: primary open angle glaucoma, nervous system lability, visual sensory-motor reactions            

References

1.Alekseev VN, Nikitin VN, Gazizov IR. Changes of the central parts of the visual analyzer in primary open angle glaucoma. Proceedings of sscientific prctical conference of ophthalmologists with international participation; 24-25 May 2012; Odessa.

2.Zavgorodnyaya NG, Pasyechnikova NV. Primary glaucoma. A new look at the old problem. Zaporozhie-Odessa; 2010. 185 p.

3.Mantrova IN. Methodological guidance for psychophysi-ological and psychological diagnostics. Russia, Ivanovo; 1992. 248 p.

4.Nesterov AP. Glaucoma. M.: Meditsina; 2008. 255 p.

5.Nikadrov VV. Psychomotor system. Work book. StP.: Rech; 2004. 104 p.

6.Nil T Choplin, Landi SD. Glaucoma. Moscow: Logosfera; 2011. 354 p.

7.Novokhatskii AS, Ponomarchuk VS. Eye diseases in pathology of vegetative nervous system. Odessa: Astroprint; 2008. 128 p.

8.Ponomarchuk VS, Krizhanovskii GI, Ruseev VV. Disorders of ophthalmotonus regulation in creating a generator of pathological excitation in the hippocampus. Eksperimen-talnaya biologia i meditsina. 1983; 1: 14-7.

9.Stotska LM, Degtyarenko TV. Method of early diagnosis of glaucoma using the results of the simple and complex visu-al sensorimotor reaction. Patent (11) 55961. (51) MPK — 2011.01 A 61 F 9 / 00 // 27.12.2010 Bul. № 24. 2010. 4 p.

10.Ronald S Harwerth, RhD, Harry A Quigley. Visual field defects and retinal ganglion cell losses in patients with glau-coma. Arch ophthalmol. 2006; 124: 853- 9.
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