Literature DB >> 25142950

Parents of children with haemophilia at an early age: assessment of perceived stress and family functioning.

A Torres-Ortuño1, R Cuesta-Barriuso, J Nieto-Munuera.   

Abstract

Haemophilia is a chronic disease that requires a multidisciplinary approach for proper management and control of its clinical manifestations. The perception and management of parents of children with haemophilia can be affected by stressful situations as a result of treatment or disease progression. The aim of this study was to evaluate the perception of stress and family functioning in parents of children with haemophilia 1-7 years. This is an observational clinical study involving 49 parents of children with haemophilia 1-7 years who attended the VIII Workshop for Parents of Children with haemophilia, organized by the Spanish Federation of Hemophilia in La Charca, Murcia (Spain). After obtaining parental consent, the questionnaires was applied to them, FACES III (family functioning) and Pediatric Inventory for Parents (perceived stress), and a record of data on the clinical characteristics and treatment. Significant differences in the perception of stressors by gender of parents were found. A family history of haemophilia, the use of port-a-cath, inhibitor development and gender of the parents were the descriptive variables most correlated with dependents variables. These variables, together with the type of haemophilia affect significantly in the parental stress and family functioning. Parents have difficulty adjusting to disease management, perceiving many stressors. Gender and family history, can hinder the proper compliance with treatments, reducing its effectiveness.
© 2014 John Wiley & Sons Ltd.

Entities:  

Keywords:  early age; family functioning; haemophilia; parents; stress

Mesh:

Year:  2014        PMID: 25142950     DOI: 10.1111/hae.12471

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  5 in total

1.  The Association of Parental Coping and Childhood Injury.

Authors:  Mariann Nocera; Annie Gjelsvik; Robyn Wing; Siraj Amanullah
Journal:  Matern Child Health J       Date:  2016-11

2.  "It was a lot Tougher than I Thought It would be". A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier.

Authors:  Charlotte von der Lippe; Jan C Frich; Anna Harris; Kari Nyheim Solbrække
Journal:  J Genet Couns       Date:  2017-05-26       Impact factor: 2.537

3.  Health-related quality of life in paediatric haemophilia B patients treated with rIX-FP.

Authors:  Sylvia von Mackensen; Jinesh Shah; Wilfried Seifert; Gili Kenet
Journal:  Haemophilia       Date:  2018-11-14       Impact factor: 4.287

4.  The impact of extended half-life versus conventional factor product on hemophilia caregiver burden.

Authors:  Carolyn E Schwartz; Victoria E Powell; Jun Su; Jie Zhang; Adi Eldar-Lissai
Journal:  Qual Life Res       Date:  2018-02-01       Impact factor: 4.147

5.  A brief version of the Pediatric Inventory for Parents (PIP) in Spanish population: Stress of main family carers of chronic paediatric patients.

Authors:  Sara Casaña-Granell; Laura Lacomba-Trejo; Selene Valero-Moreno; Vicente Prado-Gasco; Inmaculada Montoya-Castilla; Marián Pérez-Marín
Journal:  PLoS One       Date:  2018-07-26       Impact factor: 3.240

  5 in total

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