Search academic texts

Information × Registration Number 0220U100019, 0117U004538 , R & D reports Title To work out and implement the system of medical-psychological support for newborn infants from risk group for developing chronic diseases, disability and developmental delay popup.stage_title Head Antipkin Yuri G., Доктор медичних наукZnamenska Tetiana K., Доктор медичних наук Registration Date 03-01-2020 Organization State Institution "Institute of pediatrics, obstetrics and gynecology named after acad. O.M. Luk'yanova of National academy of medical sciences of Ukraine" popup.description2  The study found that specialized tools for assessing the neural and behavioral development of premature babies simultaneously allow us to evaluate both the child's development and to identify the components of developmental care that are subject to correction. Implementation of the Psychomotor Development Scale (INFANIB) allows to identify 3 adaptive components: neurological, motor and rehabilitation. Developing a concept of quality of life for preterm infants fits the current biopsychosocial model of health. As a result of research and development, a comprehensive methodology for determining the quality of life of preterm infants was offered while in intensive care and post-intensive care and during the first 3 years of life on the Munich Functional Diagnosis of Early Childhood Scale. For practical use, it is recommended to use the INFANIB scale, the Munich Functional Diagnosis Scale for infants, the neonatal pain assessment scale, the NIDCAP method, and the adapted QUALIN questionnaire for children VITN and VTPIN. The decline in indicators by the results of a comprehensive analysis of the scales indicates the need for a detailed analysis of the child's environment, the creation of conditions for individual care and involvement of the family in the care of premature infants. The study revealed reliable associations between the AGT2R1 gene polymorphism and the development of hypotension syndrome in premature infants, which are part of cerebral lesions due to cerebral hypoxia and cerebral circulation disorders. Thus, the scientific analysis of the association between glutathione-S- transferase and renin - angiotensin gene polymorphism will help in the in-depth study of perinatal pathology in newborns, as well as provide an opportunity to predict the course of organ dysfunction, shorten the duration of treatment in the wards and further assistance in creating a patient's genetic passport. Product Description popup.authors Vorobiova Olga V. Hryshyna Tamara O. Zbrozhyk Yevheniya V. Znamenska Tetyana K. Kaniovska Valentyna A. Klymchuk Juliya K. Marchuk Oleksandr O. Myratova Oksana V. Nikulina Lyudmyla I. Nesterenko Tetyana M. Pokhylko Valeriy I. Rossokha Zoya Ivanivna Rossokha Zoya I. Slysareva Anastasiya V. Tsvirenko Svitlana M. Chernyavska Julia I. Shveykina Viktoriya B. Shpylova Iryna V. popup.nrat_date 2020-04-02 Close