RATAJOVA, Katerina, Jan BLATNÝ, Iva SOLCOVA POLACKOVA, Zdenek MEIER, Tekla HORNAKOVA, Robert BRNKA a Peter TAVEL. Social support and resilience in persons with severe haemophilia: An interpretative phenomenological analysis. Haemophilia. Hoboken: Wiley-Blackwell, 2020, roč. 26, č. 3, s. "E74"-"E80", 7 s. ISSN 1351-8216. Dostupné z: https://dx.doi.org/10.1111/hae.13999.
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Základní údaje
Originální název Social support and resilience in persons with severe haemophilia: An interpretative phenomenological analysis
Autoři RATAJOVA, Katerina (203 Česká republika, garant), Jan BLATNÝ (203 Česká republika, domácí), Iva SOLCOVA POLACKOVA (203 Česká republika), Zdenek MEIER (203 Česká republika), Tekla HORNAKOVA (203 Česká republika), Robert BRNKA (203 Česká republika) a Peter TAVEL (203 Česká republika).
Vydání Haemophilia, Hoboken, Wiley-Blackwell, 2020, 1351-8216.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30205 Hematology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 4.287
Kód RIV RIV/00216224:14110/20:00116021
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1111/hae.13999
UT WoS 000525836000001
Klíčová slova anglicky group therapy; haemophilia; individual therapy; resilience; social support
Štítky 14110321, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 17. 7. 2020 08:54.
Anotace
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.
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