Literature DB >> 26153504

Empowering clinical data collection at the point of care.

Andy Spencer1, Karen Horridge2, Denise Downs1.   

Abstract

Keywords:  Data Collection; ICD10; Information Technology; Neurodisability; SNOMED-CT

Mesh：

Year:  2015        PMID： 26153504     DOI： 10.1136/archdischild-2014-307972

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  3 in total

1.  Electronic capture of patient-reported and clinician-reported outcome measures in an elective orthopaedic setting: a retrospective cohort analysis.

Authors:  Karan Malhotra; Olatunbosun Buraimoh; James Thornton; Nicholas Cullen; Dishan Singh; Andrew J Goldberg
Journal:  BMJ Open       Date:  2016-06-20       Impact factor: 2.692

2.  The UK National Neonatal Research Database: using neonatal data for research, quality improvement and more.

Authors:  C Gale; I Morris
Journal:  Arch Dis Child Educ Pract Ed       Date:  2016-03-11       Impact factor: 1.309

3.  Introduction of Systematized Nomenclature of Medicine-Clinical Terms Coding Into an Electronic Health Record and Evaluation of its Impact: Qualitative and Quantitative Study.

Authors:  Tanya Pankhurst; Felicity Evison; Jolene Atia; Suzy Gallier; Jamie Coleman; Simon Ball; Deborah McKee; Steven Ryan; Ruth Black
Journal:  JMIR Med Inform       Date:  2021-11-23
  3 in total

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