Best Practices

Best Practices: In the Management of Hemophilia

This supplement is sponsored by Shire.

 

The treatment of patients with hemophilia has rapidly evolved from one-size-fits-all factor replacement strategies to highly individualized, patient-specific care.

Faculty:

Erik Berntorp, MD, PhD

Malmö Centre for Thrombosis and Haemostasis

Lund University

Malmö, Sweden

Faculty Disclosures:

This sponsored content was prepared by Dr. Berntorp and reviewed by Shire. Dr. Berntorp discloses that he is a consultant and on the advisory boards and speakers’ bureaus for Bayer, CSL Behring, Octapharma, Shire, and Sobi. The production of this section did not involve the news or editorial staff of Frontline Medical Communications.

S28001
2/17

Click here to read the supplement

Recommended Reading

ITI protects against bleeding in hemophilia A with factor VIII inhibitors
MDedge Hematology and Oncology
Boys with severe hemophilia have good physical function
MDedge Hematology and Oncology
Solulin variants activate TAFI in vitro
MDedge Hematology and Oncology
Study highlights importance of genotyping in von Willebrand disease
MDedge Hematology and Oncology
Low inhibitor incidence seen with new generation rhFVIII
MDedge Hematology and Oncology
Specific polymorphisms excluded in hemophilic arthropathy
MDedge Hematology and Oncology
Replacement factors, bypassing agents safely manage fitusiran bleed events
MDedge Hematology and Oncology
Safety of N9-GP for hemophilia B needs further study, FDA committee agrees
MDedge Hematology and Oncology
Hemophilia A and B: An Overview
MDedge Hematology and Oncology
Drug granted fast track designation for PNH
MDedge Hematology and Oncology