Literature DB >> 24670246

The development and deployment of integrated electronic care records in a regional adult and paediatric cystic fibrosis unit.

D Peckham1, C Etherington1, H White1, A Mehta2, N Shaw1, A Morton1, K Pollard1, T Lee3, K Brownlee3, J Taylor3, P Whitaker1, S Conway4.   

Abstract

BACKGROUND: Electronic care records (ECRs) for cystic fibrosis (CF) provide a basis for accurate, reliable capture of clinical measures and interventions, and epidemiological trends, providing the basis for improved efficiency and patient safety.
METHODS: A primary care system was modified for hospital use and clinical codes devised for all aspects of CF care. Performance and usability were assessed.
RESULTS: Of a total of 620 patients 619 consented to their data being recorded in the system. Five hundred and twenty three new codes were created and embedded behind 60 new templates. Following introduction of ECR, completion of annual assessments increased from 43% to 92%, retrieval of drug costs rose significantly and time to correspondence with primary care fell from 34days to <2days. Staff satisfaction was high.
CONCLUSION: The system is fully operational allowing the unit to function as a paperless service. Efficiencies of staffing activity, process management and cost retrievals are evident. Sharing of coding structures is important in future care.
Copyright © 2014 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Codes; Cystic fibrosis; Electronic care records

Mesh:

Year:  2014        PMID: 24670246     DOI: 10.1016/j.jcf.2014.03.002

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  4 in total

1.  Requirements and access needs of patients with chronic disease to their hospital electronic health record: results of a cross-sectional questionnaire survey.

Authors:  H White; L Gillgrass; A Wood; D G Peckham
Journal:  BMJ Open       Date:  2016-10-14       Impact factor: 2.692

2.  Online versus paper-based screening for depression and anxiety in adults with cystic fibrosis in Ireland: a cross-sectional exploratory study.

Authors:  Jennifer Cronly; Alistair J Duff; Kristin A Riekert; Ivan J Perry; Anthony P Fitzgerald; Aine Horgan; Elaine Lehane; Barbara Howe; Muireann Ni Chroinin; Eileen Savage
Journal:  BMJ Open       Date:  2018-01-21       Impact factor: 2.692

3.  Medicons: toward clinical examination diagrams standardization in medical documentation.

Authors:  Georgios Pafitanis; Michalis Hadjiandreou; Leo Withers; Helen Dent
Journal:  Adv Med Educ Pract       Date:  2017-05-22

4.  Creating longitudinal datasets and cleaning existing data identifiers in a cystic fibrosis registry using a novel Bayesian probabilistic approach from astronomy.

Authors:  Peter Donald Hurley; Seb Oliver; Anil Mehta
Journal:  PLoS One       Date:  2018-07-09       Impact factor: 3.240

  4 in total

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