Literature DB >> 8000712

International differences in psychosocial well-being: a comparative study of adults with epilepsy in three countries.

J A Collings1.   

Abstract

Whilst studies from several countries illustrate the universality of psychosocial difficulties connected with an epilepsy diagnosis, there is a marked lack of empirical research findings on the subject of how different national populations compare on the same measuring instruments. This study reports on comparisons of the psychosocial well-being of samples of adults with epilepsy drawn from Britain (n = 392), the United States (n = 420) and New Zealand (n = 138) using scales assessing self esteem, life fulfilment, social and interpersonal difficulty, general physical health, worries and emotional well-being. The Americans with epilepsy revealed significantly lower levels of well-being than both the New Zealanders and the British. Using the multivariate statistical methods of discriminant and cluster analysis, the scales which were especially predictive of nationality were shown to be life fulfilment, worries, negative affect, and (to a lesser extent) general physical health. Differences between the three national groups were not apparent with regard to self esteem, social difficulty and positive affect. Some possible explanations for the results obtained are put forward. The findings imply that nation-specific variables should be addressed in studies of quality of life and epilepsy, and their effect alongside intra-individual factors within other quality of life domains be ascertained.

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Year:  1994        PMID: 8000712     DOI: 10.1016/s1059-1311(05)80187-6

Source DB:  PubMed          Journal:  Seizure        ISSN: 1059-1311            Impact factor:   3.184


  6 in total

1.  Cross-cultural measurement equivalence of the EQ-5D-5L items for English-speaking Asians in Singapore.

Authors:  N Luo; Y Wang; C H How; K Y Wong; L Shen; E G Tay; J Thumboo; M Herdman
Journal:  Qual Life Res       Date:  2014-11-14       Impact factor: 4.147

2.  Genetic causal attribution of epilepsy and its implications for felt stigma.

Authors:  Maya Sabatello; Jo C Phelan; Dale C Hesdorffer; Sara Shostak; Jeff Goldsmith; Shawn T Sorge; Melodie R Winawer; Wendy K Chung; Ruth Ottman
Journal:  Epilepsia       Date:  2015-08-20       Impact factor: 5.864

3.  Cross-cultural differences in health-related quality of life of people with epilepsy: findings from a European study.

Authors:  D Buck; A Jacoby; G A Baker; H Ley; N Steen
Journal:  Qual Life Res       Date:  1999-12       Impact factor: 4.147

4.  Assessing the impact of cancer among Dutch non-Hodgkin lymphoma survivors compared with their American counterparts: a cross-national study.

Authors:  Simone Oerlemans; Sophia K Smith; Catherine M Crespi; Sheryl Zimmerman; Lonneke V van de Poll-Franse; Patricia A Ganz
Journal:  Psychooncology       Date:  2012-07-26       Impact factor: 3.894

Review 5.  Quality of life in children and adolescents with cystic fibrosis: implications for optimizing treatments and clinical trial design.

Authors:  Janice Abbott; Louise Gee
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

6.  Validation of the individualised neuromuscular quality of life for the USA with comparison of the impact of muscle disease on those living in USA versus UK.

Authors:  Reza Sadjadi; Kelly A Vincent; Alison J Carr; Jessica Walburn; Victoria L Brooks; Shree Pandya; John T Kissel; Carlayne E Jackson; Michael R Rose
Journal:  Health Qual Life Outcomes       Date:  2011-12-16       Impact factor: 3.186

  6 in total

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