Literature DB >> 25552262

Paediatric multiple sclerosis: a qualitative study of families' diagnosis experiences.

Denise Hinton1, Susan Kirk1.   

Abstract

OBJECTIVE: To examine children's and parents' experiences of obtaining a diagnosis of paediatric multiple sclerosis (MS) and identify potential facilitators and barriers to early diagnosis.
DESIGN: Qualitative, semi-structured interviews conducted face-to-face in home settings with 31 parents and 21 children and adolescents (8-17 years old) with a clinical diagnosis of MS. Participants were recruited from 16 NHS Trusts and four MS voluntary organisations in the UK. Interviews were recorded and transcribed verbatim and analysed using the constant comparative method.
RESULTS: Time to diagnosis ranged from 1 to 96 months (median 11.5, mean 23.3, SD 27.3). The findings suggest that delayed presentation to healthcare services, generalists' assumptions about the nature of reported symptoms, lack of awareness of paediatric MS and delayed referral to specialists in paediatric MS were barriers to early investigation and accurate diagnosis. Children, adolescents and parents felt that their concerns about the child's health were not always taken seriously during medical consultations and that clinicians could be reluctant to diagnose MS in childhood. This created additional uncertainty about the child's condition and long-term prognosis.
CONCLUSIONS: Obtaining a diagnosis of paediatric MS can be a challenging and lengthy process with potentially adverse implications for the health of children/adolescents. Valuing families' knowledge and experience of their child's health, performing a thorough medical examination early in the disease course and organising prompt referrals may aid the early investigation and diagnosis of this disease. In view of the diagnostic challenges, children/adolescents with suspected MS would benefit from early referrals to specialists in paediatric MS. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  adolescents; children; diagnosis; paediatric multiple sclerosis; parents

Mesh:

Year:  2014        PMID: 25552262     DOI: 10.1136/archdischild-2014-306523

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  8 in total

1.  Families' Experience of Pediatric Onset Multiple Sclerosis.

Authors:  Theodore P Cross; Alane K Shanks; Lisa V Duffy; David J Rintell
Journal:  J Child Adolesc Trauma       Date:  2019-01-08

2.  Patient's Experience in Pediatric Primary Immunodeficiency Disorders: Computerized Classification of Questionnaires.

Authors:  Urs Mücke; Christian Klemann; Ulrich Baumann; Almut Meyer-Bahlburg; Xiaowei Kortum; Frank Klawonn; Werner M Lechner; Lorenz Grigull
Journal:  Front Immunol       Date:  2017-04-05       Impact factor: 7.561

3.  Progress in the Management of Paediatric-Onset Multiple Sclerosis.

Authors:  Aphra Luchesa Smith; Christina Benetou; Hayley Bullock; Adam Kuczynski; Sarah Rudebeck; Katie Hanson; Sarah Crichton; Kshitij Mankad; Ata Siddiqui; Susan Byrne; Ming Lim; Cheryl Hemingway
Journal:  Children (Basel)       Date:  2020-11-09

4.  "it's a medical condition … you need to support as much as possible": a qualitative analysis of teachers' experiences of chronic fatigue syndrome / myalgic encephalomyelitis (CFS/ME).

Authors:  Amberly Brigden; Alison Shaw; Esther Crawley
Journal:  BMC Pediatr       Date:  2021-01-04       Impact factor: 2.125

Review 5.  Needs and Experiences of Children and Adolescents with Pediatric Multiple Sclerosis and Their Caregivers: A Systematic Review.

Authors:  Shashank Ghai; Elisabeth Kasilingam; Roberta Lanzillo; Masa Malenica; Vincent van Pesch; Niamh Caitlin Burke; Antonio Carotenuto; Rebecca Maguire
Journal:  Children (Basel)       Date:  2021-05-25

6.  How do children and adolescents experience healthcare professionals? Scoping review and interpretive synthesis.

Authors:  Gail Davison; Martina Ann Kelly; Richard Conn; Andrew Thompson; Tim Dornan
Journal:  BMJ Open       Date:  2021-07-09       Impact factor: 2.692

Review 7.  Paediatric Multiple Sclerosis: A Scoping Review of Patients' and Parents' Perspectives.

Authors:  Maria Luca; Nerea Ortega-Castro; Francesco Patti
Journal:  Children (Basel)       Date:  2021-12-25

Review 8.  Intertwined like a double helix: A meta-synthesis of the qualitative literature examining the experiences of living with someone with multiple sclerosis.

Authors:  Anne Parkinson; Crystal Brunoro; Jack Leayr; Vanessa Fanning; Katrina Chisholm; Janet Drew; Jane Desborough; Christine Phillips
Journal:  Health Expect       Date:  2022-02-04       Impact factor: 3.318

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.