Developing routinely recorded clinical data from electronic patient records as a national resource to improve neonatal health care: the Medicines for Neonates research programme

Developing routinely recorded clinical data from electronic patient records as a national resource to improve neonatal health care: the Medicines for Neonates research programme

Background: Clinical data offer the potential to advance patient care. Neonatal specialised care is a high-cost NHS service received by approximately 80,000 newborn infants each year. Objectives: (1) To develop the use of routinely recorded operational clinical data from electronic patient records (...

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Bibliographic Details
Main Authors: Neena Modi, Deborah Ashby, Cheryl Battersby, Peter Brocklehurst, Zoe Chivers, Kate Costeloe, Elizabeth S Draper, Victoria Foster, Jacquie Kemp, Azeem Majeed, Joanna Murray, Stavros Petrou, Katherine Rogers, Shalini Santhakumaran, Sonia Saxena, Yevgeniy Statnikov, Hilary Wong, Alys Young
Format: Article
Language:English
Published: NIHR Journals Library 2019-09-01
Series:Programme Grants for Applied Research
Subjects:
ELECTRONIC PATIENT RECORDS
CLINICAL DATA
DATABASE
PERSONAL HEALTH DATA
DATA LINKAGE
NECROTISING ENTEROCOLITIS
PRETERM MORTALITY
HOSPITAL EPISODES STATISTICS
PUBLIC–PATIENT INVOLVEMENT
REGISTRIES
HEALTH ECONOMICS
BIRTH COHORTS
Online Access:https://doi.org/10.3310/pgfar07060

Internet

https://doi.org/10.3310/pgfar07060

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