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The impact of developmental and epileptic encephalopathies on families: a qualitative study.
Velarde-García, Juan Francisco; Güeita-Rodríguez, Javier; Jiménez-Antona, Carmen; García-Bravo, Cristina; Aledo-Serrano, Ángel; Gómez-Sánchez, Stella Maris; Palacios-Ceña, Domingo.
  • Velarde-García JF; Red Cross Nursing School, Universidad Autónoma de Madrid, Madrid, Spain.
  • Güeita-Rodríguez J; Research Nursing Group of Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • Jiménez-Antona C; Research Group of Humanities and Qualitative Research in Health Science of Universidad Rey Juan Carlos (Hum&QRinHS), Alcorcón, Madrid, Spain.
  • García-Bravo C; Research Group of Humanities and Qualitative Research in Health Science of Universidad Rey Juan Carlos (Hum&QRinHS), Alcorcón, Madrid, Spain. javier.gueita@urjc.es.
  • Aledo-Serrano Á; Department of Physical Therapy, Occupational Therapy, Rehabilitation and Physical Medicine, Universidad Rey Juan Carlos, Alcorcón, Madrid, Spain. javier.gueita@urjc.es.
  • Gómez-Sánchez SM; Research Group of Humanities and Qualitative Research in Health Science of Universidad Rey Juan Carlos (Hum&QRinHS), Alcorcón, Madrid, Spain.
  • Palacios-Ceña D; Department of Physical Therapy, Occupational Therapy, Rehabilitation and Physical Medicine, Universidad Rey Juan Carlos, Alcorcón, Madrid, Spain.
Eur J Pediatr ; 183(9): 4103-4110, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38965081
ABSTRACT
Developmental and epileptic encephalopathies (DEEs) cause disability and dependence affecting both children and the family. The aim of the study was to describe the perspective of parents of children with DEEs regarding the impact of the disease on the family. We carried out a qualitative study based on the interpretivist paradigm. Twenty-one participants were selected using purposive sampling. Parents of children with DEEs of SCN1A, KCNQ2, CDKL5, PCDH19, and GNAO1 variants were included. In-depth interviews and researcher notes were used for data collection. A thematic analysis was performed on the data. Three themes were identified in the

results:

(a) Assuming conflicts and changes within the couple, causing them to distance themselves, reducing their time and intimacy and leading them to reconsider having more children; (b) impact of the disorder on siblings and grandparents, where siblings perceived DEE as a burden in their lives, felt neglected, and needed to grow and mature alone; conversely, the grandparents suffered for their grandchildren and the parents, in addition to perceiving that their health worsened, and (c) reconciling the care of the child with family life and work; this led the parents to share tasks, abandon or reduce working hours and ask for help.

Conclusions:

Caring for a child with DEE can result in neglect of social, psychological, emotional, recreational, educational, or occupational needs and obligations that ultimately impact all family members. What is Known • Children with DEE may develop seizures and experience developmental and cognitive problems. • Caring for a child with DEE has a social and psychological impact on the entire family.
Caring for a child with DEE has a social and psychological impact on the entire family.
What is New • Within the couple, there are tensions due to a lack of time, which could be alleviated by alternating childcare duties. • It is necessary to implement programs that address the physical and mental needs of the couple, as well as cater to the needs of siblings and alleviate the suffering of grandparents.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Padres / Investigación Cualitativa Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Padres / Investigación Cualitativa Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article