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

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...

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Detalles Bibliográficos
Autores principales: Konkle, Barbara A., Skinner, Mark, Iorio, Alfonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462740/
https://www.ncbi.nlm.nih.gov/pubmed/31011702
http://dx.doi.org/10.1002/rth2.12195
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author Konkle, Barbara A.
Skinner, Mark
Iorio, Alfonso
author_facet Konkle, Barbara A.
Skinner, Mark
Iorio, Alfonso
author_sort Konkle, Barbara A.
collection PubMed
description 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.
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spelling pubmed-64627402019-04-22 Hemophilia trials in the twenty‐first century: Defining patient important outcomes Konkle, Barbara A. Skinner, Mark Iorio, Alfonso Res Pract Thromb Haemost Review Articles 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. John Wiley and Sons Inc. 2019-03-12 /pmc/articles/PMC6462740/ /pubmed/31011702 http://dx.doi.org/10.1002/rth2.12195 Text en © 2019 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Konkle, Barbara A.
Skinner, Mark
Iorio, Alfonso
Hemophilia trials in the twenty‐first century: Defining patient important outcomes
title Hemophilia trials in the twenty‐first century: Defining patient important outcomes
title_full Hemophilia trials in the twenty‐first century: Defining patient important outcomes
title_fullStr Hemophilia trials in the twenty‐first century: Defining patient important outcomes
title_full_unstemmed Hemophilia trials in the twenty‐first century: Defining patient important outcomes
title_short Hemophilia trials in the twenty‐first century: Defining patient important outcomes
title_sort hemophilia trials in the twenty‐first century: defining patient important outcomes
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462740/
https://www.ncbi.nlm.nih.gov/pubmed/31011702
http://dx.doi.org/10.1002/rth2.12195
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