Have I argued with my family this week?": What questions do those with lived experience choose to monitor their bipolar disorder?

Bipolar disorder Longitudinal Mood monitoring Online data collection Patient perspective

Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
15 02 2021
Historique:
received: 25 05 2020
revised: 25 09 2020
accepted: 07 11 2020
pubmed: 26 11 2020
medline: 24 4 2021
entrez: 25 11 2020
Statut: ppublish

Résumé

Electronic self-report mood monitoring tools for individuals with bipolar disorder (BD) are rapidly emerging and predominately employ predefined symptom-based questions. Allowing individuals to additionally choose what they monitor in relation to their BD offers the unique opportunity to capture and gain a deeper insight into patient priorities in this context. In addition to monitoring mood symptoms with two standardised self-rated questionnaires, 308 individuals with BD participating in the Bipolar Disorder Research Network True Colours electronic mood-monitoring tool for research chose to create and complete additional personalised questions. A content analysis approach was used to analyse the content of these questions. 35 categories were created based on the personalised questions with the most common being physical activity and exercise, anxiety and panic, sleep and coping/stress levels. The categories were grouped into six overarching themes 1) mental health; 2) behaviour and level of functioning; 3) physical wellbeing; 4) health behaviours; 5) active self-management; and, 6) interpersonal. The average age of the sample was around 50 years meaning our findings may not be generalisable to younger individuals with BD. Aspects of BD important to patients in relation to longitudinal monitoring extend well beyond mood symptoms, highlighting the limitations of solely relying on standardised questions/mood rating scales based on symptoms primarily used for diagnosis. Additional symptoms and aspects of life not necessarily useful diagnostically for BD may be more important for individuals themselves to monitor and have more meaning in capturing their own experience of changes in BD severity.

Sections du résumé

BACKGROUND
Electronic self-report mood monitoring tools for individuals with bipolar disorder (BD) are rapidly emerging and predominately employ predefined symptom-based questions. Allowing individuals to additionally choose what they monitor in relation to their BD offers the unique opportunity to capture and gain a deeper insight into patient priorities in this context.
METHODS
In addition to monitoring mood symptoms with two standardised self-rated questionnaires, 308 individuals with BD participating in the Bipolar Disorder Research Network True Colours electronic mood-monitoring tool for research chose to create and complete additional personalised questions. A content analysis approach was used to analyse the content of these questions.
RESULTS
35 categories were created based on the personalised questions with the most common being physical activity and exercise, anxiety and panic, sleep and coping/stress levels. The categories were grouped into six overarching themes 1) mental health; 2) behaviour and level of functioning; 3) physical wellbeing; 4) health behaviours; 5) active self-management; and, 6) interpersonal.
LIMITATIONS
The average age of the sample was around 50 years meaning our findings may not be generalisable to younger individuals with BD.
CONCLUSIONS
Aspects of BD important to patients in relation to longitudinal monitoring extend well beyond mood symptoms, highlighting the limitations of solely relying on standardised questions/mood rating scales based on symptoms primarily used for diagnosis. Additional symptoms and aspects of life not necessarily useful diagnostically for BD may be more important for individuals themselves to monitor and have more meaning in capturing their own experience of changes in BD severity.

Identifiants

pubmed: 33234286
pii: S0165-0327(20)32964-5
doi: 10.1016/j.jad.2020.11.034
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

918-925

Subventions

Organisme : Wellcome Trust
ID : 102616/Z
Pays : United Kingdom

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Katherine Gordon-Smith (K)

Psychological Medicine, University of Worcester, Henwick Grove, Worcester, WR2 6AJ, UK.

Kate Ea Saunders (KE)

University of Oxford Department of Psychiatry, Warneford Hospital, Oxford, OX3 7JX, UK; Oxford Health NHS Foundation Trust, Warneford Hospital, Oxford, OX3 7JX, UK.

Julia Savage (J)

Expert by Lived Experience, Worcester, UK.

Nick Craddock (N)

Division of Psychiatry and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, CF24 4HQ, UK.

Ian Jones (I)

Division of Psychiatry and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, CF24 4HQ, UK.

Lisa Jones (L)

Psychological Medicine, University of Worcester, Henwick Grove, Worcester, WR2 6AJ, UK. Electronic address: lisa.jones@worc.ac.uk.

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Classifications MeSH