Literature DB >> 21083689

Siblings of children with cystic fibrosis: quality of life and the impact of illness.

T Havermans1, L Wuytack, J Deboel, A Tijtgat, A Malfroot, C De Boeck, M Proesmans.   

Abstract

OBJECTIVE: To asses self-reported quality of life (QoL) and perception of impact of illness on siblings of children with cystic fibrosis (CF).
METHODS: The Child Health Questionnaire was used to assess QoL. The Sibling Perception Questionnaire was used to assess impact of illness.
RESULTS: Siblings of children with CF (n= 39) rated their QoL higher than siblings of healthy children on most QoL domains (e.g. Physical Functioning, Behavior, Mental Health). Siblings older than the child with CF reported a higher impact of CF than younger siblings. Perceived impact of illness was higher when the child with CF had been hospitalized or was intermittent or chronically infected with Pseudomonas aeruginosa.
CONCLUSIONS: Siblings of children with CF reported a good QoL. QoL and impact of illness were related to indices of CF severity. Insight into sibling-issues helps CF teams to provide family-oriented care.
© 2010 Blackwell Publishing Ltd.

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Year:  2010        PMID: 21083689     DOI: 10.1111/j.1365-2214.2010.01165.x

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  5 in total

1.  Parental Communication and Experiences and Knowledge of Adolescent Siblings of Children with 22q11.2 Deletion Syndrome.

Authors:  Rebecca Okashah; Kelly Schoch; Stephen R Hooper; Vandana Shashi; Nancy Callanan
Journal:  J Genet Couns       Date:  2014-12-27       Impact factor: 2.537

2.  Psychological wellbeing and quality-of-life among siblings of paediatric CFS/ME patients: A mixed-methods study.

Authors:  Sophie Velleman; Simon M Collin; Lucy Beasant; Esther Crawley
Journal:  Clin Child Psychol Psychiatry       Date:  2015-09-22       Impact factor: 2.544

3.  Health-Related Quality of Life and mental health of families with children and adolescents affected by rare diseases and high disease burden: the perspective of affected children and their siblings.

Authors:  Silke Wiegand-Grefe; Anna Liedtke; Lydia Morgenstern; Antonia Hoff; Anikó Csengoe-Norris; Jessika Johannsen; Jonas Denecke; Claus Barkmann; Benjamin Grolle; Anne Daubmann; Karl Wegscheider; Johannes Boettcher
Journal:  BMC Pediatr       Date:  2022-10-14       Impact factor: 2.567

4.  Health-Related Quality of Life in Children and Adolescents with Hereditary Bleeding Disorders and in Children and Adolescents with Stroke: Cross-Sectional Comparison to Siblings and Peers.

Authors:  Bruno Neuner; Sylvia von Mackensen; Susanne Holzhauer; Stephanie Funk; Robert Klamroth; Karin Kurnik; Anne Krümpel; Susan Halimeh; Sarah Reinke; Michael Frühwald; Ulrike Nowak-Göttl
Journal:  Biomed Res Int       Date:  2016-05-15       Impact factor: 3.411

5.  Caregiver burden in cystic fibrosis: a systematic literature review.

Authors:  Conor Daly; Philip Ruane; Karl O'Reilly; Louise Longworth; Gabriela Vega-Hernandez
Journal:  Ther Adv Respir Dis       Date:  2022 Jan-Dec       Impact factor: 4.031

  5 in total

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