J 2020

Social support and resilience in persons with severe haemophilia: An interpretative phenomenological analysis

RATAJOVA, Katerina, Jan BLATNÝ, Iva SOLCOVA POLACKOVA, Zdenek MEIER, Tekla HORNAKOVA et. al.

Basic information

Original name

Social support and resilience in persons with severe haemophilia: An interpretative phenomenological analysis

Authors

RATAJOVA, Katerina (203 Czech Republic, guarantor), Jan BLATNÝ (203 Czech Republic, belonging to the institution), Iva SOLCOVA POLACKOVA (203 Czech Republic), Zdenek MEIER (203 Czech Republic), Tekla HORNAKOVA (203 Czech Republic), Robert BRNKA (203 Czech Republic) and Peter TAVEL (203 Czech Republic)

Edition

Haemophilia, Hoboken, Wiley-Blackwell, 2020, 1351-8216

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30205 Hematology

Country of publisher

United States of America

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 4.287

RIV identification code

RIV/00216224:14110/20:00116021

Organization unit

Faculty of Medicine

DOI

UT WoS

000525836000001

Keywords in English

group therapy; haemophilia; individual therapy; resilience; social support

Tags

Tags

International impact, Reviewed
Změněno: 17/7/2020 08:54, Mgr. Tereza Miškechová

Abstract

V originále

Introduction Haemophilia is a hereditary haemorrhagic disorder characterized by deficiency or dysfunction of coagulation factors. Recurrent joint and muscle bleeds lead to progressive musculoskeletal damage. Haemophilia affects patients physically but also socially and psychologically. Traumatic experiences, chronic stress and illnesses can lead to mental disorders, but many persons with haemophilia maintain a highly positive outlook. Aim To explore qualitatively which coping mechanisms persons with haemophilia use and in what way they help them to live with their diagnosis. Methods We recruited five adults with haemophilia and conducted semi-structured face-to-face interviews. Transcripts were analysed using interpretative phenomenological analysis (IPA). Results Two core themes emerged from the analysis: social support as an external factor and resilience as an internal factor of coping with the disease. Persons with haemophilia usually need help with health-related complications, and this affects the social support they require. Their wider support network tends to involve family and friends but also healthcare professionals and other specialists. This network provides practical help but also functions as an important psychological protective factor. An unexpected finding was that persons with haemophilia want not only to receive support but are also keen to offer support to others. Conclusion These findings can help identify persons who provide most support to people suffering from haemophilia. Haemophilic centres should include in their teams psychologists and social workers and offer individual and group therapy to their clients, group meetings for friends and families of persons with haemophilia, provide learning resources to teachers aiming to incorporate children with haemophilia in their peer group, and organize Balint groups for physicians, psychologists and other healthcare professionals.