Abstract

Premature infants with extremely low birth weight are at high risk of developing severe disabling forms of retinopathy of prematurity. Nonsurgical therapy methods of treatment of retinopathy in prematurity are ineffective. Taking into consideration the multifactoriality of retinopathy in prematurity, studies aimed at analyzing accessory risk factors aiding the progression of active retinopathy of prematurity and the development in their pharmacological therapy are relevant for practical healthcare. Effective prevention of retinopathy of prematurity and prevention of severe disabling stages in premature infants at risk require timely diagnosis of the form and severity of anemia. This is the neonatologist’s task. The ophthalmologist should inform the neonatologist about the possibility of developing retinopathy of prematurity in a baby’s eye and about the necessity for diagnostic and remedial measure to treat anemia. The purpose of this study was to assess the impact of early anemia of prematurity on the frequency and severity of retinopathy of prematurity in infants at risk and the effectiveness of its treatment with erythropoietin. The frequency of anemia in preterm risk group (total 1603 children) and its treatment with the degree of prematurity were analyzed. Anemia was manifested in 99–100 % of children with retinopathy of prematurity. The comparative frequency and severity of retinopathy of prematurity was observed in three groups of infants: with extremely low birth weight and gestational age up to 28 weeks of pregnancy (245 children) group I, with gestational age 29–31 weeks of pregnancy (471 children) group II, and more than 31 weeks (581 children) group III. It was found that without treatment in group I retinopathy of prematurity developed in 100 % of cases and ended with adverse outcomes (IV–V degree of retinopathy of prematurity) in 13.64 %, which is significantly higher ( p < 0.01) than after treatment (1.78 %). Similar index was found in groups II and III. Conclusion. We traced the importance of early premature anemia in the pathogenesis of retinopathy of prematurity. It helped us to conclude that the lower the gestational age of the child at the time of birth stronger linked with the dependence of anemia and retinopathy of prematurity. Both of them are associated with the imperfection of the protective mechanisms of preterm infants. Early prescription of erythropoietin significantly improves the clinical course of retinopathy of prematurity and its prognosis.

Highlights

  • В связи с этим изучение роли анемии как одного из факторов риска развития ретинопатии недоношенных (РН), а также влияния ле‐ чения эритропоэтином на развитие РН представляется весьма актуальным

  • Цель исследования: оценить влияние анемии и эффективность лечения эритропоэтином на частоту и тяжесть РН недоношенных группы риска по разви‐ тию РН

  • СВЕДЕНИЯ ОБ АВТОРАХКГБУЗ «Алтайская краевая офтальмологическая больница» Лебедев Владимир Ильич заведующий 2-м офтальмологическим отделением ул

Read more

Summary

ПАЦИЕНТЫ И МЕТОДЫ

Исследование проведено на базе отделения вы‐ хаживания недоношенных новорожденных КГБУЗ «Алтайская краевая клиническая детская больница». Были проанализированы истории болезни 1603 мла‐ денцев, находившихся на лечении в КГБУЗ «Алтайская краевая клиническая детская больница» за 11 лет (с 2006 по 2016 г.). Всем недоношенным младенцам группы риска по РН было проведено офтальмологическое обследо‐ вание по стандартной методике и включало: визуаль‐ ный осмотр, осмотр оптических сред в проходящем свете, прямую и обратную офтальмоскопию глазного дна в условиях максимального мидриаза с использова‐ нием налобного бинокулярного офтальмоскопа Heine, линз 20 и 30 диоптрий, векоподъемников и крючков для склерокомпрессии. Лечение анемии эритропоэтином проводили в соот‐ ветствии с протоколом применения рекомбинантного человеческого эритропоэтина для лечения ранней ане‐ мии недоношенных [11]. Одновременно вводили пре‐ парат железа — мальтофер в виде капель в дозе 2,5 мг/кг массы, при снижении гемоглобина ниже 110 г/л дозу увеличивали до 5 мг/кг.

РЕЗУЛЬТАТЫ И ОБСУЖДЕНИЕ
Findings
СВЕДЕНИЯ ОБ АВТОРАХ

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.