Hemophilia trials in the twenty-first century: Defining patient important outcomes.

bleeding coagulation factor gene therapy hemophilia outcomes research

Journal

Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 06 01 2019
accepted: 01 02 2019
entrez: 24 4 2019
pubmed: 24 4 2019
medline: 24 4 2019
Statut: epublish

Résumé

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.

Identifiants

pubmed: 31011702
doi: 10.1002/rth2.12195
pii: S2475-0379(22)01543-6
pmc: PMC6462740
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

184-192

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Auteurs

Barbara A Konkle (BA)

Bloodworks Northwest Seattle Washington.
Department of Medicine University of Washington Seattle Washington.

Mark Skinner (M)

Institute for Policy Advancement, Ltd. Washington District of Columbia.
Department of Health Resource Methods, Evidence, and Impact McMaster University Hamilton Canada.

Alfonso Iorio (A)

Department of Health Resource Methods, Evidence, and Impact McMaster University Hamilton Canada.
Department of Medicine McMaster University Hamilton Canada.

Classifications MeSH