Experiencias y cambios en los padres de niños con parálisis cerebral infantil: estudio cualitativo.


Autoria(s): Fernández-Alcántara, M; García-Caro, M.P.; Berrocal-Castellano, M; Benítez, A; Robles-Vizcaíno, C; Laynez-Rubio, C
Data(s)

30/04/2015

30/04/2015

01/04/2013

Resumo

BACKGROUND The diagnosis of infant cerebral palsy (ICP) is a traumatic event that can provoke multiple effects and changes in the family. The aim of the study is to discover the difficulties that parents face in the process of parenting, especially in the initial period following diagnosis. METHODS A qualitative study was carried out through semi-structured interviews. Sixteen mothers and fathers whose children were diagnosed with cerebral palsy participated in the study. Data analysis was performed with Atlas.ti 6.2 software following a strategy of open coding. RESULTS The reception of the diagnosis is perceived as an unexpected event that makes parents change expectations and hopes related to their children. The mode of relation with the child with ICP is different from that with other children as parents are more focused on the possibility of improvement and the future evolution of their child. Changes in different aspects of the lives of these parents are shown, such as demands on time, their economic and labour situation, as well as the relationship of the couple. CONCLUSIONS In providing care for children with cerebral palsy it is necessary to take the problems of the parents into account, especially in the initial period after diagnosis. The process of parenting a child with cerebral palsy entails many changes in the family so a global perspective is needed to organize interventions.

English Abstract; Journal Article;

Identificador

Fernández-Alcántara M, García-Caro M, Berrocal-Castellano M, Benítez A, Robles-Vizcaíno C, Laynez-Rubio C. Experiencias y cambios en los padres de niños con parálisis cerebral infantil: estudio cualitativo. An Sist Sanit Navar. 2013; 36(1):9-20

1137-6627 (Online)

http://hdl.handle.net/10668/1884

23648489

Idioma(s)

es

Publicador

Gobierno de Navarra. Departamento de Salud

Relação

Anales del Sistema Sanitario de Navarra

http://recyt.fecyt.es/index.php/ASSN/article/view/18165/11292

Direitos

Acceso abierto

Palavras-Chave #Cerebral palsy #Parent #Qualitative research #Family caregiving #Parálisis cerebral #Padres #Estudio cualitativo #Cuidados familiares #Medical Subject Headings::Diseases::Nervous System Diseases::Central Nervous System Diseases::Brain Diseases::Brain Damage, Chronic::Cerebral Palsy #Medical Subject Headings::Named Groups::Persons::Age Groups::Child #Medical Subject Headings::Named Groups::Persons::Age Groups::Child::Child, Preschool #Medical Subject Headings::Check Tags::Female #Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans #Medical Subject Headings::Psychiatry and Psychology::Behavior and Behavior Mechanisms::Psychology, Social::Life Style::Life Change Events #Medical Subject Headings::Check Tags::Male #Medical Subject Headings::Named Groups::Persons::Parents #Medical Subject Headings::Disciplines and Occupations::Natural Science Disciplines::Science::Research::Empirical Research::Qualitative Research #Medical Subject Headings::Named Groups::Persons::Age Groups::Adult
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/published

Artículo