Haemophilia in a real-world setting: the value of clinical experience in data collection
At the 8th Annual Congress of the European Association for Haemophilia and Allied Disorders (EAHAD) held in Helsinki, Finland, in February 2015, Pfizer sponsored a satellite symposium entitled: ‘Haemophilia in a real‐world setting: The value of clinical experience in data collection’ Co‐chaired by R...
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Veröffentlicht in: | European journal of haematology 2016-02, Vol.96 (S82), p.3-9 |
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description | At the 8th Annual Congress of the European Association for Haemophilia and Allied Disorders (EAHAD) held in Helsinki, Finland, in February 2015, Pfizer sponsored a satellite symposium entitled: ‘Haemophilia in a real‐world setting: The value of clinical experience in data collection’ Co‐chaired by Riitta Lassila (Helsinki University Central Hospital, Helsinki, Finland) and Gerry Dolan (Guy's and St Thomas’ Hospital, London, UK); the symposium provided an opportunity to explore the practical value of real‐world data in informing clinical decision‐making. Gerry Dolan provided an introduction to the symposium by describing what is meant by real‐world data (RWD), stressing the role RWD can play in optimising patient outcomes in haemophilia and highlighting the responsibility of all stakeholders to collaborate in continuous data collection. Kristian Juusola (Oulu University Hospital, Oulu, Finland) then provided personal experience as a haemophilia nurse around patient views on adherence to treatment regimes, and how collecting insights into real‐world use of treatment can shape approaches to improving adherence. The importance of elucidating pharmacokinetic parameters in a real‐world setting was then explored by Vuokko Jokela (Helsinki University, Helsinki, Finland). Finally, Alfonso Iorio (McMaster University, Hamilton, Ontario, Canada) highlighted the importance of quality data collection in translating clinical reality into scientific advances. |
doi_str_mv | 10.1111/ejh.12715 |
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Gerry Dolan provided an introduction to the symposium by describing what is meant by real‐world data (RWD), stressing the role RWD can play in optimising patient outcomes in haemophilia and highlighting the responsibility of all stakeholders to collaborate in continuous data collection. Kristian Juusola (Oulu University Hospital, Oulu, Finland) then provided personal experience as a haemophilia nurse around patient views on adherence to treatment regimes, and how collecting insights into real‐world use of treatment can shape approaches to improving adherence. The importance of elucidating pharmacokinetic parameters in a real‐world setting was then explored by Vuokko Jokela (Helsinki University, Helsinki, Finland). 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Gerry Dolan provided an introduction to the symposium by describing what is meant by real‐world data (RWD), stressing the role RWD can play in optimising patient outcomes in haemophilia and highlighting the responsibility of all stakeholders to collaborate in continuous data collection. Kristian Juusola (Oulu University Hospital, Oulu, Finland) then provided personal experience as a haemophilia nurse around patient views on adherence to treatment regimes, and how collecting insights into real‐world use of treatment can shape approaches to improving adherence. The importance of elucidating pharmacokinetic parameters in a real‐world setting was then explored by Vuokko Jokela (Helsinki University, Helsinki, Finland). 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the symposium provided an opportunity to explore the practical value of real‐world data in informing clinical decision‐making. 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subjects | Clinical Decision-Making Coagulants - pharmacokinetics Coagulants - therapeutic use collaboration Data Collection - statistics & numerical data Factor IX - pharmacokinetics Factor IX - therapeutic use Finland haemophilia Hemophilia A - drug therapy Hemophilia A - physiopathology Hemophilia A - psychology Humans outcomes Patient Compliance - psychology Patient Compliance - statistics & numerical data real-world data Terminology as Topic Treatment Outcome |
title | Haemophilia in a real-world setting: the value of clinical experience in data collection |
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