Explores methods to enhance personalized treatment in hemophilia, suggesting a proactive shift for better outcomes.
Introduction: Hemophilia is a rare congenital bleeding disorder that requires coagulation factor replacement therapy to treat or, better, to prevent life- and limb-threatening bleeding and its complications. Personalized treatment of patients with hemophilia is crucial for improving outcomes in an environment with increasing health budget constraints.Areas covered: Unmet needs for a more effective and efficient use of factor concentrates are examined. The current approach is described with its limits and recent improvements, i.e. pharmacokinetic assessments and dosing tools/models. Future approaches to personalization were researched in the literature and discussed, including biomarkers, genotyping, decision-making tools, goal attainment tools and digital health systems.Expert opinion: A paradigm shift in hemophilia management personalization is necessary in order to improve outcome and ensure long-term sustainability in a landscape of growing and aging patient populations, increasing expectations and rising healthcare costs. Hemophilia management should gradually move from a reactive toward a more proactive approach, based on patient profiling precision, accurate treatment and outcome monitoring and a service-centered approach. This shift will require increased cooperation between clinicians, patients, caregivers and home service operators, as well as digital health systems and patient empowerment.
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Gringeri et al. (2017) studied this question.
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