Literature DB >> 31844391

Family functioning among adolescents with narcolepsy.

Arpita Parmar1,2, Eluen Ann Yeh2,3, Daphne J Korczak2,4, Shelly K Weiss2,3, Zihang Lu2, Allison Zweerink1,2, Alene Toulany2,5, Brian J Murray2,6, Indra Narang1,2.   

Abstract

BACKGROUND: Narcolepsy is a sleep disorder with no cure with onset typically during adolescence. Caring for an adolescent with a lifelong medical condition can negatively impact family structure, cohesion, relationships, and overall functioning. The primary objective of this study was to evaluate family functioning in a cohort of adolescents with narcolepsy using the PedsQL Family Impact Module. The secondary objective was to compare family functioning in adolescents with narcolepsy to adolescents with chronic pain based on published data.
METHODS: This was a cross-sectional study of adolescents (aged 10 to 18 years) with narcolepsy. The narcolepsy group was recruited from The Hospital for Sick Children in Toronto, Canada. Family functioning was assessed by the PedsQL family impact module total scores, which was completed by the patient's caregiver. The PedsQL family impact module yields a total scale which encompasses parent health-related quality of life, daily activities, family relationships, communication, and worry subscales. Lower scores suggest poorer family functioning. Secondary data analyses were used to compare participants' family functioning to a cohort of adolescents with chronic pain.
RESULTS: Thirty adolescents with narcolepsy participated (mean age=13.8 ± 2.2 years, 76.7% male). Family functioning was impaired in this cohort of adolescents with narcolepsy and similar to adolescents with chronic pain (64.0 ± 19.8 versus 64.7 ± 19.5; P=0.849).
CONCLUSION: Family functioning is impaired in adolescents with narcolepsy. Clinical teams should assess family functioning at routine clinic visits by asking about concerns and challenges related to caring for an adolescent with narcolepsy and providing resources and support as needed.
© The Author(s) 2019. Published by Oxford University Press on behalf of the Canadian Paediatric Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Adolescents; Caregivers; Family; Narcolepsy

Year:  2019        PMID: 31844391      PMCID: PMC6901168          DOI: 10.1093/pch/pxy192

Source DB:  PubMed          Journal:  Paediatr Child Health        ISSN: 1205-7088            Impact factor:   2.253


  24 in total

1.  The impact of pediatric chronic pain on parents' health-related quality of life and family functioning: reliability and validity of the PedsQL 4.0 Family Impact Module.

Authors:  Kristen E Jastrowski Mano; Kimberly Anderson Khan; Renee J Ladwig; Steven J Weisman
Journal:  J Pediatr Psychol       Date:  2009-11-10

Review 2.  The diagnosis and treatment of pediatric narcolepsy.

Authors:  Sona Nevsimalova
Journal:  Curr Neurol Neurosci Rep       Date:  2014-08       Impact factor: 5.081

3.  Psychosocial Profile and Quality of Life in Children With Type 1 Narcolepsy: A Case-Control Study.

Authors:  Francesca Letizia Rocca; Elena Finotti; Fabio Pizza; Francesca Ingravallo; Michela Gatta; Oliviero Bruni; Giuseppe Plazzi
Journal:  Sleep       Date:  2016-07-01       Impact factor: 5.849

4.  Narcolepsy in the pediatric population.

Authors:  Erick N Viorritto; Suraiya A Kureshi; Judith A Owens
Journal:  Curr Neurol Neurosci Rep       Date:  2012-04       Impact factor: 5.081

Review 5.  Delayed diagnosis of narcolepsy: characterization and impact.

Authors:  Michael J Thorpy; Ana C Krieger
Journal:  Sleep Med       Date:  2014-02-15       Impact factor: 3.492

6.  Family impact of acquired brain injury in children and youth.

Authors:  Arend J de Kloet; Suzanne A M Lambregts; Monique A M Berger; Frederike van Markus; Ron Wolterbeek; Thea P M Vliet Vlieland
Journal:  J Dev Behav Pediatr       Date:  2015-06       Impact factor: 2.225

7.  A multilevel analysis of whole family functioning using the McMaster Family Assessment Device.

Authors:  Katholiki Georgiades; Michael H Boyle; Jennifer M Jenkins; Mark Sanford; Ellen Lipman
Journal:  J Fam Psychol       Date:  2008-06

8.  The health and psychosocial functioning of caregivers of children with neurodevelopmental disorders.

Authors:  Lucyna M Lach; Dafna E Kohen; Rochelle E Garner; Jamie C Brehaut; Anton R Miller; Anne F Klassen; Peter L Rosenbaum
Journal:  Disabil Rehabil       Date:  2009       Impact factor: 3.033

9.  Increased incidence and clinical picture of childhood narcolepsy following the 2009 H1N1 pandemic vaccination campaign in Finland.

Authors:  Markku Partinen; Outi Saarenpää-Heikkilä; Ismo Ilveskoski; Christer Hublin; Miika Linna; Päivi Olsén; Pekka Nokelainen; Reija Alén; Tiina Wallden; Merimaaria Espo; Harri Rusanen; Jan Olme; Heli Sätilä; Harri Arikka; Pekka Kaipainen; Ilkka Julkunen; Turkka Kirjavainen
Journal:  PLoS One       Date:  2012-03-28       Impact factor: 3.240

Review 10.  Caregiving process and caregiver burden: conceptual models to guide research and practice.

Authors:  Parminder Raina; Maureen O'Donnell; Heidi Schwellnus; Peter Rosenbaum; Gillian King; Jamie Brehaut; Dianne Russell; Marilyn Swinton; Susanne King; Micheline Wong; Stephen D Walter; Ellen Wood
Journal:  BMC Pediatr       Date:  2004-01-14       Impact factor: 2.125

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