Hemophilia trials in the twenty-first century: Defining patient important outcomes
- PMID: 31011702
- PMCID: PMC6462740
- DOI: 10.1002/rth2.12195
Hemophilia trials in the twenty-first century: Defining patient important outcomes
Abstract
Treatment for hemophilia has advanced dramatically over the past 5 decades. Success of prophylactic therapy in preventing bleeding and decreasing associated complications has established a new standard of care. However, with the advent of gene therapy and treatments that effectively mimic sustained coagulation factor replacement, outcome measures that worked well for assessing factor replacement therapies in past clinical trials need to be reassessed. In addition, while therapies have advanced, so has the science of outcome assessment, including recognition of the importance of patient important and patient reported outcomes. This manuscript reviews strengths and limitations of outcome measures used in hemophilia from both a provider and patient perspective.
Keywords: bleeding; coagulation factor; gene therapy; hemophilia; outcomes research.
References
-
- Hoag S, Johnson FF, Robinson JA, Aggeler PM. Treatment of hemophilia B with a new clotting factor concentrate. N Engl J Med. 1969;280:581–6. - PubMed
-
- Dallman PR, Pool JG. Treatment of hemophilia with factor eight concentrates. N Engl J Med. 1968;278:199–202. - PubMed
-
- White GC, Courter S, Bray GL, Lee M, Gomperts ED, White G, et al. A multicenter study of recombinant factor VIII (Recombinate(TM)) in previously treated patients with hemophilia A. Thromb Haemost. 1997;77:660–7. - PubMed
-
- Lusher JM. First and second generation recombinant factor VIII concentrates in previously untreated patients: recovery, safety, efficacy, and inhibitor development. Semin Thromb Hemost. 2002;28:273–6. - PubMed
Publication types
LinkOut - more resources
Full Text Sources
Miscellaneous