TREATMENT OF EPILEPSY IN INFANTS BORN PRETERM WITH EXTREMELY LOW BODY WEIGHT
About the author:
Makedonska I. V.
Heading:
CLINICAL AND EXPERIMENTAL MEDICINE
Type of article:
Scentific article
Annotation:
It is difficult to treat young child with epilepsy. Even greater difficulties arise if a child suffering from epilepsy is born premature with extremely low birth weight. Development of technologies of nursing severely preterm infants has led not only to a decrease in mortality and improved survival of premature infants with extremely low birth weight, but also to the development of a number of diseases which significantly worsen the child’s condition not only during the acute phase but also in the long-term period. Treatment of epilepsy in preterm infants remains a challenge. The main purpose of the antiepileptic drug therapy is to achieve the absence of seizures in patients. In 40-50% of patients the seizure control can be achieved already when using the first anticonvulsant. However, about a third of patients have drug-resistant forms of epilepsy. The largest number of drug-resistant forms are found in childhood which is primarily due to the faster maturation of the excitatory glutamatergic system and belated formation of the brake GABAergic system. So it is in early childhood that the maximum number of epileptic encephalopathies with resistance to the ongoing anticonvulsant therapy and symptomatic forms of epilepsy resulting from perinatal pathology (symptoms of hypoxic-ischemic lesion of the central nervous system, congenital infections, malformations of brain development) are found. This leads to the emergence of many serious complications, including delayed psycho and motor development of a child, high frequency of attacks, their sequence, a combination of several types of seizures, the occurrence of status epilepticus, disruption of the drug remission, as well as the increased risk of death of the patient. Therefore, a timely and adequate anti-epileptic treatment, especially in the early stages of the disease, can stop this process and improve the condition of patients. Also, the initial occurrence of epilepsy in children deserves special attention because the boundary for convulsive readiness in children is higher than in adults. The lower the age, the lower is the seizure threshold. One of the features of the childhood period is the continuous development process of the structures and functions of the whole body, including the central nervous system which is responsible for the child’s adaptation to the environmental impact. The evolution of epilepsy and transformation of seizures in children are in most cases affected by the formation of the nervous system, perinatal brain injury, genetic factors and hormonal changes. One of the priority directions in the study of epilepsy in children is to find new opportunities for projecting the disease course and its complications which are determined by the degree of involvement of brain structures in the pathological process. The dynamics of the patients’ condition in the course of treatment may be a clinical criterion for evaluating its effectiveness. In connection with the presented problem, a great importance for the clinical management is placed on the determination of the methodological approaches, selection and justification of adequate diagnostic and treatment methods. The development of seizures in the child at an early age leads to her disability, even when seizures are capable of being treated. However, treatment of seizures is one of many aspects of the problem of epilepsy therapy in children born premature with extremely low birth weight. As a result of neonatal diseases, as well as intensive (intensive care, infusion), massive antibiotic therapy, such children can suffer from continuously maintained dysfunction of the gastrointestinal tract, liver and urinary excretory system. Prolonged mechanical ventilation can cause eye damage, as well as malfunctions of the respiratory and cardiovascular system. Therefore, the study of somatic condition (comorbid background) for delicate use of anticonvulsants will help to preserve the quality of life of these children. Elimination of seizures in children with epilepsy, who were born premature with extremely low birth weight, may not be the purpose of the treatment. Principles of treatment should be based on tailoring the adequacy of anticonvulsant therapy to the needs of the patient in each case, as well as the development of an integrated approach to the treatment strategies for children born prematurely with epilepsy. In an attempt to eliminate the clinical manifestations of epilepsy, it is very important to clearly identify the extent to which other organs and systems of the patient are able to tolerate anticonvulsant therapy.
Tags:
epilepsy, preterm infants, extreme weight, anticonvulsant therapy
Bibliography:
- 1. Айвазян С.О. Современные возможности лечения фармакорезистентной эпилепсии у детей / С.О. Айвазян, Е.Г. Лукьянова, Ю.С. Ширяев // Эпилепсия. — 2014. — № 1. — С. 34-43.
- 2. Белоусова Е. Не ошибиться в выборе. Экспертный консенсус по сравнительной оценке противоэпилептических препаратов, применяемых в России / Е. Белоусова, П. Власов, А. Ермаков, Л. Зенков [и др.] // Медицинская газета. — 2005. — № 66. — С. 7-9.
- 3. Брусенцов А.И. Эффективность финлепсина при терапевтически резистентных случаях эпилепсии / А.И. Брусенцов, Л.С. Годлевский // Украинский вестник психоневрологии. — Харьков 1996. — 4: 5: 12: С. 147-153.
- 4. Дзяк Л.А. Эпилепсия / Л.А. Дзяк, Л.С. Годлевский. — К.: Книга-плюс, 2001. – 168 с.
- 5. Евтушенко С.К. Гіпоксичні ушкодження головного мозку у новонароджених / С.К. Евтушенко, О.С. Евтушенко, О.П. Шестова, Т.М. Морозова, О.П. Перфілов, В.Ю. Мартинюк, В.М. Здвижкова. — Київ: Інтермед, 2003. – 104 с.
- 6. Калинин В.А. Оптимизация диагностики и лечения эпилепсии у детей раннего возраста / В.А. Калинин // Известия Самарского научного центра Российской академии наук. – Т. 12. — № 1 (7). — 2010. – 1673 с.
- 7. Карлов В.А. Эффективность депакина при терапевтически резистентной эпилепсии / В.А. Карлов // Журнал невропатологии и психиатрии. — 1993. — № 1. — С. 33-36.
- 8. Литовченко Т.А. Проблема лечения фармакорезистентной эпилепсии / Т.А. Литовченко // Кафедра невропатологии и детской неврологии Харьковской медицинской академии последипломного образования. – 2015. — С. 23.
- 9. Мартинюк В.Ю. Лікування епілепсії, епілептичних синдромів у дітей / В.Ю. Мартинюк, Т.В. Коноплянко, В.О. Свистільник, С.К. Евтушенко, А.А. Омельяненко. — Київ, 2012. – 18 с.
- 10. Мухин К.Ю. Диагностика и лечение парциальных форм эпилепсии / К.Ю. Мухин, A.C. Петрухин, A.A. Алиханов, Э.Г. Меликян. — М: РГМУ, 2002, — 56 с.
- 11. Наказ МОЗ України від 17.04.2014 р. № 276 «Уніфікований клінічний протокол первинної, екстреної, вторинної (спеціалізованої) та третинної (високоспеціалізованої) медичної допомоги епілепсії у дітей». — 40 с.
- 12. Онегин Е.В. Алгоритм диагностики и лечения фармакорезистентных эпилепсий у детей / Е.В. Онегин // Журнал ГрГМУ. — 2010. — № 1. — С. 20-21.
- 13. Петрухин А.С. Клиническая детская неврология / А.С. Петрухин // Руководство. – М.: ОАО «Издательство: «Медицина», 2008. – 1088 с.
- 14. Таранущенко Т.Е. Амбулаторное наблюдение недоношенных детей с ЭНМТ и ОНМТ при рождении: учебно-методическое пособие для системы послевузовского профессионального образования участковых педиатров / Т.Е. Таранущенко, С.И. Устинова, Н.Г. Киселева [и др.]. – Красноярск, 2014. — 16 с.
- 15. Шалькевич Л.В. Медикаментозная терапия генерализованных судорог у детей первых лет жизни / Л.В. Шалькевич // Рецепт. — 2007. – № 5 – 55 с.
- 16. Aicardi J. Intractable epilepsy / J. Aicardi, S. Shorvon // Epilepsy. A Comprehensive Textbook. Eds. J. Engel (Jr.), T.A. Pedley. Philadelphia. — 1997. — Р. 1325-1330.
- 17. Andres M. Human cortical dysplasia and epilepsy an ontogenesis hypothesis
- based on volumetric MRI and NeuN neuronal densityand size measurements / M. Andres, V. Andre, S. Nguyen, N. Salamon, C. Cepeda, M.S. Levine, J.P. Leite, L. Neder, H.V. Vinter, G.W. Mathern // Cereb. Cortex. – 2005. – № 15. — Р. 194-210
- 18. Kwan P. Combination Therapy in Epilepsy / P. Kwan, J. Martin // Brodie Drags. — 2006. — № 66 (14). — Р. 1817-1820.
- 19. Fily A.N. Factors associated with neurodevelopment outcome at 2 years after verypretern birth the population based Nord – Pas – de – Calais Epipage cohort / A.N. Fily // Pediatrics. — 2006. — Vol. 117. № 2. — P. 357-366.
- 20. Lee B.N. Neurodevelopmental Outcomes of Extremely Low Birth Weith Infants Exposed Prenatally to Dexamethasone Versus Betamethasone / B.N. Lee // Pediatrics. — 2008. — Vol. 121. № 2. – P. 289-296.
Publication of the article:
«Bulletin of problems biology and medicine» Issue 1 part 2 (127), 2016 year, 91-95 pages, index UDK 616.853-063.32:616-009.6-08