Literature DB >> 11034868

Validation of the side effect and life satisfaction (SEALS) inventory.

R Gillham1, L Bryant-Comstock, K Kane.   

Abstract

Diminished quality of life (QOL) is a common feature of epilepsy. It is generally more severe among patients with poor seizure control but prevalent, to a clinically significant degree, even among those whose seizures are well controlled. People with epilepsy frequently report diminished socialization, negative self image, feelings of stigmatization, reduced earnings potential, and diminished hope and ambition. Problems with antiepileptic drug (AED) therapy are common, and AED therapy is recognized as an important determinant of health-related quality of life (HRQOL). A clinically efficient psychometric instrument is needed to measure its impact. The Side Effect and Life Satisfaction (SEALS) inventory is a 38-item, patient-completed questionnaire designed to measure satisfaction with AED therapy. We tested its construct validity in comparison with three widely used psychometric instruments of similar design, the Profile of Mood States (POMS), the Hospital Anxiety and Depression (HAD) scale, and the Medical Outcomes Study-Cognitive Functioning (MOS-COG) scale. All four instruments were completed by 307 epilepsy patients. A matrix of Pearson's correlations was produced for the SEALS inventory and the comparative instruments. A statistically significant correlation was found for each planned comparison. We conclude that the SEALS inventory is a valid psychometric instrument, well suited for use in clinical investigations of AED therapy and in the practical, long-term management of epilepsy. Copyright 2000 BEA Trading Ltd.

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Year:  2000        PMID: 11034868     DOI: 10.1053/seiz.2000.0446

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


  4 in total

1.  Development and validation of the Pediatric Epilepsy Side Effects Questionnaire.

Authors:  Diego A Morita; Tracy A Glauser; Avani C Modi
Journal:  Neurology       Date:  2012-08-08       Impact factor: 9.910

Review 2.  Treatment satisfaction instruments for different purposes during a product's lifecycle: keeping the end in mind.

Authors:  Diana Rofail; Fiona Taylor; Antoine Regnault; Anna Filonenko
Journal:  Patient       Date:  2011       Impact factor: 3.883

3.  Developing a Conceptual Disease Model of Patient Experiences and Identifying Patient-Reported Clinical Outcome Assessments for Use in Trials of Treatments for Focal Onset Seizures.

Authors:  Dorothee Oberdhan; Elizabeth Bacci; Jennifer N Hill; Andrew Palsgrove; Asha Hareendran
Journal:  Neuropsychiatr Dis Treat       Date:  2022-03-22       Impact factor: 2.570

Review 4.  Patient Reported Outcome (PRO) assessment in epilepsy: a review of epilepsy-specific PROs according to the Food and Drug Administration (FDA) regulatory requirements.

Authors:  Annabel Nixon; Cicely Kerr; Katie Breheny; Diane Wild
Journal:  Health Qual Life Outcomes       Date:  2013-03-11       Impact factor: 3.186

  4 in total

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