Peppa, M;
Minassian, C;
Mangtani, P;
Thomas, SL;
(2021)
The identification and validity of congenital malformation diagnoses in UK electronic health records: A systematic review.
Pharmacoepidemiology & Drug Safety
, 30
(7)
pp. 875-898.
10.1002/pds.5251.
Preview |
Text
Peppa_Pharmacoepidemiology and Drug - 2021 - Peppa - The identification and validity of congenital malformation diagnoses in UK.pdf - Published Version Download (2MB) | Preview |
Abstract
PURPOSE: To describe the methods used to identify and validate congenital malformation diagnoses recorded in UK electronic health records, and the results of validation studies. METHODS: Medline and Embase were searched for publications between 1987 and 2019 that involved identifying congenital malformations from UK electronic health records using diagnostic codes. The methods and code-lists used to identify congenital malformations, and the methods and results of validations, were examined. RESULTS: We retrieved 54 eligible studies; 36 identified congenital malformations from primary care data and 18 from secondary care data alone or in combination with birth and/or death records. Identification in secondary care data relied on codes from the 'Q' chapter for congenital malformations in ICD-10. In contrast, studies using primary care data frequently used additional codes outside of the 'P' chapter for congenital malformation diagnoses in Read, although the exact codes used were not always clear. Eight studies validated diagnoses identified in primary care data. The positive predictive value was highest (80-100%) for congenital malformations overall, major malformations, and heart defects although the validity of the reference standard used was often uncertain. It was lowest for neural tube defects (71%) and developmental hip dysplasia (56%). CONCLUSIONS: Studies identifying congenital malformations from primary care data provided limited details about the methods used. The few validation studies were limited to diagnoses recorded in primary care. Further assessments of all measures of validity in both data sources and of other malformation subgroups are needed, using robust reference standards and adhering to reporting guidelines. This article is protected by copyright. All rights reserved.
Type: | Article |
---|---|
Title: | The identification and validity of congenital malformation diagnoses in UK electronic health records: A systematic review |
Location: | England |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1002/pds.5251 |
Publisher version: | https://doi.org/10.1002/pds.5251 |
Language: | English |
Additional information: | Copyright © 2021 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
Keywords: | congenital abnormalities, electronic health records, pharmacoepidemiology, systematic review, United Kingdom, validation study |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Population, Policy and Practice Dept |
URI: | https://discovery-pp.ucl.ac.uk/id/eprint/10126834 |
Archive Staff Only
![]() |
View Item |