Год публикации:
Все года
2018
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| Название |
Дата публикации |
Коллектив авторов |
Журнал |
DOI |
Индекс цитирования |
Ссылка на источник |
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Effect of General Anesthesia Duration on Recovery of Secretion and Biochemical Properties of Tear Fluid in the Post-Anesthetic Period
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01.06.2018 |
Zernii E.
Baksheev V.
Kabanova E.
Tiulina V.
Golovastova M.
Gancharova O.
Savchenko M.
Sotikova L.
Zamyatnin A.
Filippov P.
Senin I.
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Bulletin of Experimental Biology and Medicine |
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5 |
Ссылка
© 2018, Springer Science+Business Media, LLC, part of Springer Nature. Changes in the biochemical composition of the tear film is a critical risk factor for the development of chronic perioperative dry eye syndrome, because increasing the duration of general anesthesia did not affect the dynamics of tear secretion recovery, but slowed down normalization of its structure and antioxidant activity in the post-anesthetic period.
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Secondary dry eye syndrome after keratorefractive surgeries and approaches to its treatment and prevention
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01.01.2018 |
Bubnova I.
Egorova G.
Mitichkina T.
Averich V.
Fettser E.
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Vestnik oftalmologii |
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0 |
Ссылка
The article reviews the particularities of development and pathogenesis of secondary dry eye syndrome (DES) after refractive surgeries including a complex of problems related to changes in tear film content, damage of eye surface and neurotrophic epitheliopathy. Additionally, modern algorithms of treatment and prevention of secondary DES in patients after refractive surgeries are described. Despite the transient nature of the changes, excimer-laser surgery can lead to lasting deficiencies of eye surface in some patients. Therefore, intensive and early treatment of secondary DES during the early follow-up period after refractive surgery may significantly reduce risks of tear dysfunction and neurotrophic epitheliopathy development in the long term.
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Misdiagnosed case of transthyretin amyloidosis in a fully investigated patient
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01.01.2018 |
Naumova E.
Nikitin S.
Adyan
Druzhinin D.
Varshavskiy V.
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Nervno-Myshechnye Bolezni |
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0 |
Ссылка
© 2018 ABV-Press Publishing House. All rights reserved. The DNA analysis revealed a transthyretin amyloidosis with a rare Phe53Leu mutation in a woman of 62 y.o. with the late onset progressive generalized axonal sensomotor neuropathy, dry eye syndrome, and an episode of severe unintentionally weight loss. The same mutation was found in her healthy 34 y.o. son, but not in a 42 y.o. daughter. The Congo red staining were negative in nerve and salivar gland biopsies samples. The reassessment of the transthyretin amyloidosis “red flags” showed that the patient fulfilled the criteria of the disease and the absence of amyloid deposition was not the ground to reject the hereditary cause of the condition. The reasons of the misdiagnosis are discussed.
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