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The Impact of Bleeding Disorders on the Socioeconomic Status of Adult Patients.

HAMOSTASEOLOGIE(2018)

Cited 7|Views19
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Abstract
The impact of inherited bleeding disorders on the socioeconomic status (SES) of affected individuals is not clear. The SES of adult patients with congenital bleeding disorders (PWBD) from a centre in Germany (age 42.3 ± 15.0 years) was compared to that of a gender- and age-matched control group of patients with thrombophilia or a thrombotic event (PWT). Patients completed a questionnaire including aspects of SES, impact of the disease on their lives, and health-related quality of life (HRQoL). Forty-five patients were enrolled in each group; 71 % of PBWD had a severe form of the bleeding disorder (FVIII/IX activity < 1 % or VWD type 3), and 60 % of all PWBD were treated on-demand. PWBD had a lower monthly income ( = 0.029) and a worse occupational status ( = 0.047) than PWT, but there was no difference regarding the project-specific SES index. PWBD also reported a worse HRQoL in the physical summary component score of the SF-36 ( < 0.001). More PWBD (69.8 %) reported a high impact of the disease on their lives than PWT (33.3 %,  < 0.001). In summary, PWBD had a worse occupational status, monthly income, health behaviour, HRQoL, and impact of the disease on their lives compared to PWT, but not a significantly different SES in general.
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Key words
haemophilia,von Willebrand disease,socioeconomic status,quality of life,outcomes
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