Literature DB >> 28691134

Seizure disorders and developmental disorders: impact on life of affected families-a structured interview.

Ulrike Petra Spindler1, Lena Charlott Hotopp1, Vivien Angela Bach1, Frauke Hornemann1, Steffen Syrbe1,2, Anna Andreas1, Andreas Merkenschlager1, Wieland Kiess1, Matthias Karl Bernhard1, Thilo Bertsche3, Martina Patrizia Neininger3, Astrid Bertsche4.   

Abstract

Seizure disorder and developmental disorder are two of the most common chronic disorders in childhood. Data on perceived parental burden and specific effects on daily life is scarce. We performed a structured interview, consecutively talking to all parents of pediatric outpatients of our university hospital diagnosed with seizure or developmental disorder. Three hundred seven parents (of 317 affected children: 53 with seizure disorder, 44 with specific developmental disorder, 35 with learning disorder, 71 with intellectual disability, 15 with seizure + specific developmental disorder, 23 with seizure + learning disorder, 76 with seizure disorder + intellectual disability) were interviewed. Parents of children with both seizure disorder and intellectual disability stated the highest constraints in daily life, regarding friends, hobbies, emotional pressure, occupation, partnership, habitation, and financial burden. Due to diagnosis of seizure or developmental disorder, 155/307 (51%) parents reduced their working hours/stopped working, 62/307 (20%) changed their habitation, and 46/307 (15%) broke up. As judged by parents, 148/317 (47%) children are being discriminated against, even own family/friends and educators are held responsible.
CONCLUSION: Parents perceive changes in their daily life and discrimination of their children due to their children's seizure and developmental disorders. An intellectual disability combined with seizure disorder caused the highest constraint. What is Known: • Seizure and/or developmental disorders of children may adversely influence quality of life for affected parents. • Caring for a child with special health care needs can take complete attention and own parental needs may therefore be difficult to meet. What is New: • Two out of three parents stated changes of their daily life such as quitting work, change of habitation, or breakup of partnership due to their child's diagnosis. • As judged by the parents, one in two children with developmental disorder of any kind is being discriminated against, even teachers and own family are held responsible.

Entities:  

Keywords:  Developmental disorder; Discrimination; Epilepsy; Parental constraint; Patient perspective; Seizure disorder

Mesh:

Year:  2017        PMID: 28691134     DOI: 10.1007/s00431-017-2958-0

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  27 in total

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7.  Effects of child health on parents' relationship status.

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8.  [Psycho-emotional impact of a child's disability on parents].

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Journal:  Arch Pediatr       Date:  2012-12-20       Impact factor: 1.180

9.  Mental Health of Parents as Caregivers of Children with Disabilities: Based on Japanese Nationwide Survey.

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10.  Impairment of quality of life in parents of children and adolescents with pervasive developmental disorder.

Authors:  Diego Mugno; Liliana Ruta; Valentina Genitori D'Arrigo; Luigi Mazzone
Journal:  Health Qual Life Outcomes       Date:  2007-04-27       Impact factor: 3.186

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  8 in total

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Journal:  Eur J Pediatr       Date:  2019-08-02       Impact factor: 3.183

2.  Screening Effects of the National Health Screening Program on Developmental Disorders.

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Journal:  Eur J Pediatr       Date:  2018-07-03       Impact factor: 3.183

4.  How do pediatric patients perceive adverse drug events of anticonvulsant drugs? A survey.

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5.  Quality of Life and Concerns in Parent Caregivers of Adult Children Diagnosed with Intellectual Disability: A Qualitative Study.

Authors:  María Inmaculada Fernández-Ávalos; María Nieves Pérez-Marfil; Rosario Ferrer-Cascales; Francisco Cruz-Quintana; Violeta Clement-Carbonell; Manuel Fernández-Alcántara
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6.  TELEmedicine for EPIlepsy Care (TELE-EPIC): protocol of a randomised, open controlled non-inferiority clinical trial.

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7.  Why do children and adolescents with epilepsy disclose or not disclose their condition to their friends?

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Journal:  Eur J Pediatr       Date:  2020-05-05       Impact factor: 3.183

8.  Parent Mental Health and Family Coping over Two Years after the Birth of a Child with Acute Neonatal Seizures.

Authors:  Linda S Franck; Renée A Shellhaas; Monica E Lemmon; Julie Sturza; Marty Barnes; Trisha Brogi; Elizabeth Hill; Katrina Moline; Janet S Soul; Taeun Chang; Courtney J Wusthoff; Catherine J Chu; Shavonne L Massey; Nicholas S Abend; Cameron Thomas; Elizabeth E Rogers; Charles E McCulloch; Hannah C Glass
Journal:  Children (Basel)       Date:  2021-12-22
  8 in total

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