Clinical, economic, and health‐related quality of life burden associated with von Willebrand disease in adults and children: Systematic and targeted literature reviews

Abstract Introduction Debilitating clinical complications in von Willebrand disease (VWD) can affect health‐related quality of life (HRQoL), increase healthcare costs and cause long‐lasting consequences. However, the magnitude of these burdens needs to be more fully explored. Aim To estimate the prevalence and burden of clinical complications, the impact on HRQoL and the economic burden associated with VWD. Methods Embase ® , MEDLINE ® , the Cochrane Library and conference proceedings were searched for studies on VWD evaluating clinical complications, HRQoL and cost and resource use. Results Among 16 studies assessing clinical complications in VWD, the most prevalent bleeding symptoms were menorrhagia (2%–95% [ n = 7 studies]), epistaxis (12%–80% [ n = 6]) and easy bruising (46%–65% [ n = 2]). Among 17 studies evaluating HRQoL, the most common assessment scales were the generic SF‐36 ( n = 8 studies) and the EQ‐5D ( n = 2). Bleeding symptoms were associated with reduced QoL in six of seven studies, and of six studies evaluating treatment impact, four reported improvements in one or more HRQoL components. Among 25 studies on cost and resource use, key observations included higher post‐surgery healthcare costs in VWD versus non‐VWD patients ( n = 1 study) and higher costs and resource use in VWD patients with bleeding complications versus those without ( n = 1). Conclusion Although limited, available evidence suggests that VWD patients experience a high burden of clinical complications, reduced QoL and high healthcare costs. Haemarthrosis is more common in severe VWD than is often assumed, and bleeds (including haemarthrosis) can reduce QoL. Research efforts to improve QoL and other outcomes should be prioritized.