Lived experience of Silver-Russell syndrome: implications for management during childhood and into adulthood.


Journal

Archives of disease in childhood
ISSN: 1468-2044
Titre abrégé: Arch Dis Child
Pays: England
ID NLM: 0372434

Informations de publication

Date de publication:
01 2019
Historique:
received: 09 02 2018
revised: 28 05 2018
accepted: 03 06 2018
pubmed: 30 6 2018
medline: 23 10 2019
entrez: 30 6 2018
Statut: ppublish

Résumé

There is limited information on the psychosocial impact of growing up with Silver-Russell syndrome (SRS), characterised by slow growth in utero leading to short stature in adulthood. Such information could aid families in making difficult treatment decisions and guide management strategies for health professionals. We aimed to explore the lived experience of people with SRS across the lifespan. In-depth, semi-structured interviews were conducted between January 2015 and October 2016 with a sample of 15 adults (six women) with genetically confirmed SRS from the UK. Qualitative interviews were transcribed and coded to identify similarities and differences: codes were then grouped to form overarching themes. Four themes were identified from participant accounts: (1) appearance-related concerns extending beyond height; (2) strategies to deal with real and perceived threats; (3) women's experiences of pain, disability and feeling older than their years; and (4) feeling overlooked in romantic relationships. These themes show that other factors, beyond short stature, affect patient well-being and indicate a mismatch between patient need and healthcare provision. Challenges in SRS during childhood and adolescence were central to the psychosocial impact of SRS, and were not limited to height. These challenges, as well as symptoms such as pain and fatigue for women, have not previously been documented. To help individuals with SRS develop strategies to manage psychosocial issues, we recommend clinicians incorporate psychological services as an integral part of multidisciplinary teams managing individuals with SRS during childhood, adolescence and adulthood.

Identifiants

pubmed: 29954740
pii: archdischild-2018-314952
doi: 10.1136/archdischild-2018-314952
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

76-82

Subventions

Organisme : Medical Research Council
ID : MC_UP_A620_1017
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12011/4
Pays : United Kingdom
Organisme : Department of Health
ID : PB-PG-1111-26003
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2019. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Déclaration de conflit d'intérêts

Competing interests: JHD has received travel bursaries from Novo Nordisk, SANDOZ, Ferring and Pfizer. HI reports grants from the UK National Institute for Health Research and UK Medical Research Council (the latter for her salary) during the conduct of the study. OLS reports grants from the National Institute of Health Research during the conduct of the study.

Auteurs

Lisa Marie Ballard (LM)

Faculty of Medicine, Clinical Ethics and Law, University of Southampton, Southampton, UK.

Elizabeth Jenkinson (E)

Faculty of Health and Applied Sciences, University of the West of England, Bristol, UK.

Christopher D Byrne (CD)

Nutrition and Metabolism Unit, University of Southampton, Southampton, UK.
Southampton National Institute for Health Research, Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Jenny C Child (JC)

Membership and Communications, Child Growth Foundation, Sutton Coldfield, UK.

Justin Huw Davies (JH)

Department of Endocrinology, University Hospital Southampton NHS Foundation Trust, Southampton Children's Hospital, Southampton, UK.

Hazel Inskip (H)

MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
NIHR Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Oluwakemi Lokulo-Sodipe (O)

Faculty of Medicine, Human Development and Health, University of Southampton, Southampton, UK.
Wessex Clinical Genetics Service, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Deborah J G Mackay (DJG)

Faculty of Medicine, University of Southampton, Southampton, UK.

Emma L Wakeling (EL)

North West Thames Regional Genetics Service, London North West Healthcare NHS Trust, London, UK.

I Karen Temple (IK)

Wessex Clinical Genetics Service, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
Faculty of Medicine, Human Development and Health, University of Southampton, Southampton, UK.

Angela Fenwick (A)

Faculty of Medicine, Clinical Ethics and Law, University of Southampton, Southampton, UK.

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