Literature DB >> 17880446

Parents of children with haemophilia--a transforming experience.

K Beeton1, D Neal, T Watson, C A Lee.   

Abstract

Owing to the improvements in the management of haemophilia, children with severe haemophilia in the United Kingdom have very different experiences of their condition compared with many adults' early experiences of haemophilia. However, haemophilia can still have physical and social effects which can impact on the quality of life, not only for a child who has the condition, but also for their parents. The purpose of this study was to undertake a qualitative exploration of the impact of haemophilia on parents. The participants included 12 parents of children with severe haemophilia who took part in interviews or focus groups. Four major themes emerged from the data which were initial experiences, managing the condition, engaging with others and developing mastery. The findings highlighted the importance of evaluating parents' experiences. Parents are deeply affected by their child's condition and their lives are transformed by the experiences of living with a child with haemophilia. Parents' responses are influenced by how well the child manages the disorder and the difficulties they experience. Further studies are required in order to develop a more complete understanding of the impact of haemophilia on parent's lives.

Entities:  

Mesh:

Year:  2007        PMID: 17880446     DOI: 10.1111/j.1365-2516.2007.01494.x

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


  13 in total

1.  Understanding of genetic inheritance among Xhosa-speaking caretakers of children with hemophilia.

Authors:  Gabriele Solomon; Jacquie Greenberg; Merle Futter; Lauraine Vivian; Claire Penn
Journal:  J Genet Couns       Date:  2012-03-10       Impact factor: 2.537

2.  Uptake of Genetic Counseling, Knowledge of Bleeding risks and Psychosocial Impact in a South African Cohort of Female Relatives of People with Hemophilia.

Authors:  Anne Gillham; Brenda Greyling; Tina-Marie Wessels; Bongi Mbele; Rosemarie Schwyzer; Amanda Krause; Johnny Mahlangu
Journal:  J Genet Couns       Date:  2015-04-02       Impact factor: 2.537

3.  The social burden and quality of life of patients with haemophilia in Italy.

Authors:  Yllka Kodra; Marianna Cavazza; Arrigo Schieppati; Marta De Santis; Patrizio Armeni; Romano Arcieri; Gabriele Calizzani; Giovanni Fattore; Lamberto Manzoli; Lorenzo Mantovani; Domenica Taruscio
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

Review 4.  Hemophilia Care in the Pediatric Age.

Authors:  Marta Bertamino; Francesca Riccardi; Laura Banov; Johanna Svahn; Angelo Claudio Molinari
Journal:  J Clin Med       Date:  2017-05-19       Impact factor: 4.241

Review 5.  The experiences and attitudes of hemophilia carriers around pregnancy: A qualitative systematic review.

Authors:  Marieke C Punt; Tanja H Aalders; Kitty W M Bloemenkamp; Mariette H E Driessens; Kathelijn Fischer; Marlies H Schrijvers; Karin P M van Galen
Journal:  J Thromb Haemost       Date:  2020-05-12       Impact factor: 5.824

6.  Newborn screening for haemophilia: The views of families and adults living with haemophilia in the UK.

Authors:  Felicity K Boardman; Rachel Hale; Philip J Young
Journal:  Haemophilia       Date:  2019-02-28       Impact factor: 4.287

7.  Pharmacokinetics and Associated Efficacy of Emicizumab in Humans: A Systematic Review.

Authors:  Anouk A M T Donners; Carin M A Rademaker; Lisanne A H Bevers; Alwin D R Huitema; Roger E G Schutgens; Toine C G Egberts; Kathelijn Fischer
Journal:  Clin Pharmacokinet       Date:  2021-08-13       Impact factor: 5.577

8.  Social participation and hemophilia: Self-perception, social support, and their influence on boys in Canada.

Authors:  Aubrey S Chiu; Victor S Blanchette; Maru Barrera; Pamela Hilliard; Nancy L Young; Audrey Abad; Brian M Feldman
Journal:  Res Pract Thromb Haemost       Date:  2021-11-30

9.  'You have to do what is best': The lived reality of having a child who is repeatedly hospitalized because of acute lower respiratory infection.

Authors:  Karen McBride-Henry; Charissa Miller; Adrian Trenholm; Tara N Officer
Journal:  Health Expect       Date:  2021-12-20       Impact factor: 3.377

10.  Psychological interventions for people with hemophilia.

Authors:  Laura Palareti; Giannino Melotti; Frederica Cassis; Sarah J Nevitt; Alfonso Iorio
Journal:  Cochrane Database Syst Rev       Date:  2020-03-18
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