Literature DB >> 31071641

What really matters? A mixed methods study of treatment preferences and priorities among people with epilepsy in the UK.

Adele Ring1, Ann Jacoby2, Gus Baker3, Emily Holmes4, Dyfrig Hughes4, Ciara Kierans2, Anthony Marson3.   

Abstract

The widening range of treatment options for epilepsy, and their potential outcomes, mean decisions about treatment for people with epilepsy (PWE) are often complex. While antiepileptic drugs (AEDs) represent the mainstay of treatment, other potential nondrug interventions are gaining in importance. These treatments all have the potential for harming those using them, as well as bringing benefits. This study examined the views and experiences of PWE about a range of treatment options. We used both qualitative and quantitative approaches - a series of depth-narrative interviews, followed by a large-scale survey. Treatment options and healthcare priorities deemed important by at least 10% of interview participants were then addressed as a series of statements in the follow-on survey questionnaire. Quantitative responses supported healthcare priorities identified through the qualitative interviews. The key goal of treatment among study participants was to be able to live 'a normal life'. Important physical, psychological, and life benefits of treatment were identified - most being the direct consequence of improved seizure control. One psychological benefit, reduced worry, was also identified as an important treatment goal. All participants viewed AEDs as appropriate first-line treatment; and since adverse effects of AEDs had implications for individual levels of daily function and wellbeing, their appropriate management was considered important. In contrast, surgery was almost always regarded as the treatment of last resort. Despite lack of research evidence supporting their use, participants were interested in complementary therapies as adjunctive treatment and a means of coping with having epilepsy, with yoga and meditation of particular interest. An important finding was the desire for targeted services to help with memory problems, as was the call to increase availability of psychological/counseling services. Our findings emphasize the importance of providing treatment responsive to the life context of individual patients. They highlight not only the level of demand for specific treatment options, but also the need for high-quality evidence to support future investment in their provision.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Antiepileptic drugs; Complementary therapies; Life context; Patient preferences; Psychological/neuropsychological treatments; Surgery

Mesh:

Substances:

Year:  2019        PMID: 31071641     DOI: 10.1016/j.yebeh.2019.03.033

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  3 in total

1.  Neurologist prescribing versus psychiatry referral: Examining patient preferences for anxiety and depression management in a symptomatic epilepsy clinic sample.

Authors:  Heidi M Munger Clary; Rachel D Croxton; Beverly M Snively; Gretchen A Brenes; James Lovato; Fatemeh Sadeghifar; James Kimball; Cormac O'Donovan; Kelly Conner; Esther Kim; Jonathan Allan; Pamela Duncan
Journal:  Epilepsy Behav       Date:  2020-11-24       Impact factor: 2.937

2.  Subcutaneous EEG Monitoring Reveals AED Response and Breakthrough Seizures.

Authors:  Sigge Weisdorf; Ivan C Zibrandtsen; Troels W Kjaer
Journal:  Case Rep Neurol Med       Date:  2020-01-28

3.  Effects of Antiepileptic Drug Tapering on Episodic Memory as Measured by Virtual Reality Tests.

Authors:  Yvonne Höller; Christopher Höhn; Fabian Schwimmbeck; Gaën Plancher; Eugen Trinka
Journal:  Front Neurol       Date:  2020-02-20       Impact factor: 4.003

  3 in total

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