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Tail Vein Transection Bleeding Model in Fully Anesthetized Hemophilia A Mice
Published on: September 30, 2021
Tailored versus standard dose prophylaxis in children with hemophilia A
Cristina Santoro1, Erminia Baldacci, Caterina Mercanti
1Division of Hematology, Department of Cellular Biotechnology and Hematology, Sapienza University of Rome, Rome, Italy.
Insights
Tailored prophylaxis for hemophilia modifies standard dosing for better outcomes. New methods for measuring joint damage and coagulation are improving personalized treatment strategies.
Area of Science:
- Hematology
- Pharmacology
Background:
- Prophylaxis is the standard treatment for hemophilia.
- Tailored prophylaxis involves modifying standard weight-based dosing regimens.
- Various tailored regimens are being evaluated for efficacy and patient acceptance.
Purpose of the Study:
- To review current approaches to tailored prophylaxis in hemophilia.
- To discuss methods for evaluating treatment outcomes, particularly arthropathy.
- To explore novel tools for individualizing prophylaxis regimens.
Main Methods:
- Review of existing literature on hemophilia prophylaxis.
- Discussion of imaging techniques (MRI, ultrasound) for arthropathy assessment.
- Exploration of pharmacokinetic-driven and global coagulation assays.
Main Results:
- Tailored low-dose frequent regimens may be cost-effective but less patient-accepted.
- Escalating dose regimens show promise in preventing bleeding and arthropathy, with long-term data pending.
- Advanced imaging and global assays offer potential for reliable outcome measurement and regimen individualization.
Conclusions:
- Sensitive tools are crucial for evaluating tailored prophylaxis efficacy.
- Pharmacokinetic and global coagulation assays can aid in personalizing hemophilia treatment.
- Future strategies aim for less frequent, more comfortable, and cost-effective prophylaxis.
Abstract:
Prophylaxis is universally recognized as the treatment of choice in people with hemophilia, and tailored prophylaxis is the consistent modification of the standard weight-based dosing regimen. A large number of factors guide the choice of a specific tailored regimen, and different regimens are under evaluation. Tailored low-dose frequent regimens are likely to be cost-effective, but they are less accepted by patients. Escalating dose regimens seem to be quite effective in preventing bleedings and, consequently, arthropathy, although data on long-term outcomes are still not available. Pharmacokinetic-driven approaches have been also proposed. Sensitive and validated tools able to reliably measure the different outcomes are necessary in this setting. With regard to the evaluation of arthropathy, magnetic resonance imaging and ultrasound are promising imaging techniques in detecting early joint damage. Factor VIII trough levels can be considered a measure of the efficacy of FVIII infused, although other factors influence the bleeding pattern. Global assays of coagulation could provide more complete information on the hemostatic potential of a sample and predict bleeding phenotype. These techniques are also promising for the individualization of prophylaxis regimens, potentially resulting in less frequent dosing, more comfortable and less expensive approaches.
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