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Erfarenheter av hur det är att leva med mild hemofili och hepatit C-infektion. En intervjustudie.
Engelsk titel: Experiences of life in patients with mild haemophilia and hepatitis C virus infection. An interview study Läs online Författare: Mattsson, Eva ; Ekholm, C ; Berntorp, E ; Bolmsjö, I Språk: Swe Antal referenser: 25 Dokumenttyp: Artikel UI-nummer: 13073259

Tidskrift

Vård i Norden 2013;33(1)25-9 ISSN 0107-4083 E-ISSN 1890-4238 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

Background: In many cases patients with mild haemophilia have received some treatment with a factor concentrate and as a result they have become infected with hepatitis C. Aim: To explore how patients with mild haemophilia experience living with the hepatitis C virus. Methods: Semi-structured interviews with nine men. The texts were analyzed using content analysis with a qualitative approach. Findings: An overall theme: «It is possible to live with hepatitis C and at the same time accept life» and three categories: «Balance – Imbalance», «Meeting with the surroundings» and «Limitation in life» were identified. All the men in the study have accepted their situation but have different experiences and needs. For some, the hepatitis C has had a considerable impact at certain stages in life, while for others it has hardly had any negative effects at all. Conclusion: It is important to have knowledge of and be experienced in meeting prejudices in society and to be able to provide good care for these patients.