Evidence mapPaperPMID 38414539Full record

ArticleInternational journal of population data science2023

Using novel data linkage of congenital heart disease biobank data with administrative health data to identify cardiovascular outcomes to inform genomic analysis.

Samantha J Lain, Gillian M Blue, Bridget R O'Malley, David S Winlaw, Gary Sholler, Sally L Dunwoodie, Natasha Nassar, Congenital Heart Disease Synergy Study group

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In one paragraph

Article in International journal of population data science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Samantha J LainChild Population and Translational Health Research, Children's Hospital at Westmead Clinical School, The University of Sydney, NSW, Australia, 2006.
Gillian M BlueHeart Centre for Children, Sydney Children's Hospital Network, Children's Hospital at Westmead, NSW, Australia.
Bridget R O'MalleyHeart Centre for Children, Sydney Children's Hospital Network, Children's Hospital at Westmead, NSW, Australia.
David S WinlawCincinnati Children's Hospital Medical Centre, Heart Institute, and University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Gary ShollerChild Population and Translational Health Research, Children's Hospital at Westmead Clinical School, The University of Sydney, NSW, Australia, 2006.
Sally L DunwoodieVictor Chang Cardiac Research Institute, Sydney, New South Wales, Australia.
Natasha NassarChild Population and Translational Health Research, Children's Hospital at Westmead Clinical School, The University of Sydney, NSW, Australia, 2006.
Congenital Heart Disease Synergy Study group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Contemporary care of congenital heart disease (CHD) is largely standardised, however there is heterogeneity in post-surgical outcomes that may be explained by genetic variation. Data linkage between a CHD biobank and routinely collected administrative datasets is a novel method to identify outcomes to explore the impact of genetic variation. Objective: Use data linkage to identify and validate patient outcomes following surgical treatment for CHD. Methods: Data linkage between clinical and biobank data of children born from 2001-2014 that had a procedure for CHD in New South Wales, Australia, with hospital discharge data, education and death data. The children were grouped according to CHD lesion type and age at first cardiac surgery. Children in each 'lesion/age at surgery group' were classified into 'favourable' and 'unfavourable' cardiovascular outcome groups based on variables identified in linked administrative data including; total time in intensive care, total length of stay in hospital, and mechanical ventilation time up to 5 years following the date of the first cardiac surgery. A blind medical record audit of 200 randomly chosen children from 'favourable' and 'unfavourable' outcome groups was performed to validate the outcome groups. Results: Of the 1872 children in the dataset that linked to hospital or death data, 483 were identified with a 'favourable' cardiovascular outcome and 484 were identified as having a 'unfavourable' cardiovascular outcome. The medical record audit found concordant outcome groups for 182/192 records (95%) compared to the outcome groups categorized using the linked data. Conclusions: The linkage of a curated biobank dataset with routinely collected administrative data is a reliable method to identify outcomes to facilitate a large-scale study to examine genetic variance. These genetic hallmarks could be used to identify patients who are at risk of unfavourable cardiovascular outcomes, to inform strategies for prevention and changes in clinical care.

Indexed as

Cardiac Surgical ProceduresHeart Defects, CongenitalAustraliaBiological Specimen BanksChildGenomicsHumanscardiovascular outcomecongenital heart diseasedata linkagegenetic variation

Identifiers

PMID38414539
PMCPMC10897946

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.