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Original Research

Real-world utilities and health-related quality-of-life data in hemophilia patients in France and the United Kingdom

, , , , &
Pages 941-957 | Published online: 14 Jun 2019

Figures & data

Table 1 Population characteristics by country, treatment regimen, and hemophilia severity

Table 2 Health-utility values and health-related quality-of-life scores by country, hemophilia type, severity, and treatment regimen in the pooled sample (n=184)

Table 3 Health utility values and health-related quality-of-life scores by number of target joints, joint pain, and joint surgery occurrence in the pooled sample (n=184)

Table 4 Health-utility values and health-related quality-of-life scores by history of long hospital stays and frequency of visits tomedical professionals due to hemophilia in the pooled sample (n=184)

Table 5 US-norm–based SF-36-dimension and -component summary scores by country

Table S1 Health-utility values and health-related quality-of life-scores by country, hemophilia type, and treatment regimen in the subsample of subjects with severe hemophilia (n=130)

Table S2 Health-utility values and health-related quality-of-life scores by number of target joints, joint pain, and joint surgery occurrence in the subsample of subjects with severe hemophilia (n=130)

Table S3 Health-utility values and health-related quality-of-life scores by history of long hospital stays and frequency of visits to medical professionals due to hemophilia in subsample of subjects with severe hemophilia (n=130)