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United Kingdom Haemophilia Centre Doctors' Organisation (UKHCDO)
|Subject Keywords:||Haemophilia Database|
Primary Data Sources
The National Haemophilia Database (NHD) is a register of patients with bleeding disorders living in the UK, originally established in Oxford in 1968. This database collects data from haemophilia centres. Every quarter Haemophilia Centres are required to submit information to the NHD about the treatment issued to patients, including products delivered to the patient’s home. Information collected includes:
The United Kingdom Haemophilia Centre Doctors' Organisation (UKHCDO) is required by the Department of Health to collect data on diagnosis, management and complications of bleeding disorders. This information is kept in the NHD which is managed by the Data Management Working Party of UKHCDO.
|Rights:||© United Kingdom Haemophilia Centre Doctors' Organisation|
United Kingdom Haemophilia Centre Doctors' Organisation (UKHCDO). (2012) The National Haemophilia Database [Online]. Available from: http://www.thehealthwell.info/node/113372 [Accessed: 24th March 2017].
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