Literature DB >> 9186254

Social adjustment and competence 35 years after onset of childhood epilepsy: a prospective controlled study.

M Jalava1, M Sillanpää, C Camfield, P Camfield.   

Abstract

PURPOSE: To study the effect of childhood-onset epilepsy without other neurologic deficit on adult social adjustment and competence.
METHODS: Social competence was studied in a prospective, population-based cohort of childhood-onset epilepsy after a mean follow-up of 35 years. One hundred patients (60% of the total cohort) had no other neurologic problems ("epilepsy only"), and for each patient, two matched controls, a "random" control and an "employee" control were chosen.
RESULTS: Good social outcome was significantly reduced in the "epilepsy only" cohort compared with random controls: education [cumulative odds ratio (COR), 2.4; 95% confidence interval (CI), 1.4-4.1]; employability (COR, 7.3; 95% CI, 2.7-20.0); and marriage rate (COR, 3.7; 95% CI, 1.9-7.3). The patients with epilepsy rated their own ability to control their lives as "poor or missing" four times more frequently than the employee controls. Patients receiving antiepileptic polytherapy, but not monotherapy, were significantly less satisfied with their present life (OR, 6.7; 95% CI, 1.9-24.1) and felt their general health was significantly poorer (OR, 5.1; 95% CI, 1.2-21.3) than did the employee controls. Furthermore, patients with continuing seizures were significantly less satisfied with their present life (OR, 4.1; 95% CI, 1.1-15.1) than were employee controls.
CONCLUSIONS: Many patients with "epilepsy only" beginning in childhood have persistent and significant social-adjustment and competence problems in adulthood.

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Year:  1997        PMID: 9186254     DOI: 10.1111/j.1528-1157.1997.tb01241.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  20 in total

Review 1.  Health-related quality of life in youth with epilepsy: theoretical model for clinicians and researchers. Part I: the role of epilepsy and co-morbidity.

Authors:  Lucyna M Lach; Gabriel M Ronen; Peter L Rosenbaum; Charles Cunningham; Michael H Boyle; Shauna Bowman; David L Streiner
Journal:  Qual Life Res       Date:  2006-09-13       Impact factor: 4.147

2.  Growing up with epilepsy: a two-year investigation of cognitive development in children with new onset epilepsy.

Authors:  Bruce P Hermann; Jana E Jones; Raj Sheth; Monica Koehn; Tara Becker; Jason Fine; Chase A Allen; Michael Seidenberg
Journal:  Epilepsia       Date:  2008-09-10       Impact factor: 5.864

Review 3.  Starting at the beginning: the neuropsychological status of children with new-onset epilepsies.

Authors:  Bruce P Hermann; Jana E Jones; Daren C Jackson; Michael Seidenberg
Journal:  Epileptic Disord       Date:  2012-03       Impact factor: 1.819

4.  Cognitive Outcome in Childhood-Onset Epilepsy: A Five-Decade Prospective Cohort Study.

Authors:  Mira Karrasch; Petri Tiitta; Bruce Hermann; Juho Joutsa; Shlomo Shinnar; Juha Rinne; Anu Anttinen; Matti Sillanpää
Journal:  J Int Neuropsychol Soc       Date:  2017-01-10       Impact factor: 2.892

5.  Cognitive outcomes in children who present with a first unprovoked seizure.

Authors:  Yoshimi Sogawa; David Masur; Christine O'Dell; Solomon L Moshe; Shlomo Shinnar
Journal:  Epilepsia       Date:  2010-09-24       Impact factor: 5.864

6.  Psychosocial functioning following surgical treatment for intractable epilepsy in childhood.

Authors:  Yolanda G Korneluk; Sally M Kuehn; Daniel L Keene; Enrique C G Ventureyra
Journal:  Childs Nerv Syst       Date:  2003-02-18       Impact factor: 1.475

7.  Language and social functioning in children and adolescents with epilepsy.

Authors:  Anna W Byars; Ton J deGrauw; Cynthia S Johnson; Susan M Perkins; Philip S Fastenau; David W Dunn; Joan K Austin
Journal:  Epilepsy Behav       Date:  2014-01-14       Impact factor: 2.937

8.  What is new in paediatric epilepsy?

Authors:  Peter Camfield; Carol Camfield
Journal:  Paediatr Child Health       Date:  2003-11       Impact factor: 2.253

9.  Transition from pediatric to adult epilepsy care: a difficult process marked by medical and social crisis.

Authors:  Peter Camfield; Carol Camfield; Bernd Pohlmann-Eden
Journal:  Epilepsy Curr       Date:  2012-07       Impact factor: 7.500

10.  Validation of the German version of the Pediatric Quality of Life Inventory (PedsQL) in childhood cancer patients off treatment and children with epilepsy.

Authors:  R Felder-Puig; E Frey; K Proksch; J W Varni; H Gadner; R Topf
Journal:  Qual Life Res       Date:  2004-02       Impact factor: 4.147

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