Evidence map›Paper›PMID 39219198›Full record

ArticleCroatian medical journal2024

Strong and weak points in the quality of life of school-age children with newly diagnosed uncomplicated epilepsy over the first six months: golden hours for prevention.

Željka Rogač, Dimitrije Nikolić, Aleksandar Dimitrijević, Ivana Andrić, Goran Milošević, Dejan Stevanović

Abstract read
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Article in Croatian medical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Željka RogačŽeljka Rogač, Clinical Centre of Montenegro - Institute for Children's Diseases, Moskovska 111, 81000 Podgorica, Montenegro, zeljka.rogac89@gmail.com.
Dimitrije Nikolić
Aleksandar Dimitrijević
Ivana Andrić
Goran Milošević
Dejan Stevanović

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo determine changes in the quality of life associated with epilepsy in school-age children with newly diagnosed uncomplicated epilepsy over the first six months after diagnosis to find points relevant for the early prevention of deterioration in quality of life.

methodsThis prospective follow-up study, performed in University Children's Hospital in Belgrade, enrolled 60 school-aged children with recently diagnosed epilepsy, along with their parents. The respondents completed the Children with Epilepsy Quality of Life immediately following the diagnosis of epilepsy and six months later.

resultsSignificant decline was observed in the domains related to intrapersonal/emotional relationships by both children (P<0.001) and their parents (P=0.03), and in the need to keep epilepsy a secret as observed by parents (P = 0.04). Significant improvement was found in the Interpersonal/Social domain as rated by parents (P=0.001). Total quality-of-life scores, as assessed by children and parents, did not change significantly.

conclusionBearing in mind that stigma and intrapersonal struggles are the major factors affecting the quality of life in children with epilepsy, psychological and social support is highly recommended in the first six months following an epilepsy diagnosis. Since intrapersonal relationships improved over six months, compensating for other deteriorations in the quality of life, children with epilepsy should be encouraged to socialize with their peers and to join organizations and actions that encourage social contact.

Indexed as

EpilepsyQuality of LifeAdolescentChildFemaleFollow-Up StudiesHumansMaleParentsProspective StudiesSocial SupportSurveys and Questionnaires

Identifiers

PMID39219198
PMCPMC11399723

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.