Evidence map›Paper›PMID 39713572›Full record

ArticleInternational journal of cardiology. Congenital heart disease2023

Algorithmic complexity stratification for congenital heart disease patients.

Jason Chami, Geoff Strange, David Baker, Rachael Cordina, Leeanne Grigg, David S Celermajer, Calum Nicholson

Abstract read
In one paragraph

Article in International journal of cardiology. Congenital heart disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Living with congenital heart disease: a qualitative study to explore psychosocial impacts in adulthood.International journal of cardiology. Congenital heart disease · 2025
    Article
  5. A national Australian Congenital Heart Disease registry; methods and initial results.International journal of cardiology. Congenital heart disease · 2024
    Article
  6. Article
  7. 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

7 authors.

Jason ChamiSydney Medical School, The University of Sydney, Camperdown, Australia.
Geoff StrangeHeart Research Institute, Newtown, Australia.
David BakerRoyal Prince Alfred Hospital, Camperdown, Australia.
Rachael CordinaRoyal Prince Alfred Hospital, Camperdown, Australia.
Leeanne GriggRoyal Melbourne Hospital, Parkville, Australia.
David S CelermajerSydney Medical School, The University of Sydney, Camperdown, Australia.
Calum NicholsonHeart Research Institute, Newtown, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Congenital Heart Disease (CHD) encompasses a huge variety of rare diagnoses that range in complexity and comorbidity. To help build clinical guidelines, plan health services and conduct statistically powerful research on such a disparate set of diseases there have been various attempts to group pathologies into mild, moderate, or severe disease. So far, however, these complexity scores have required manual specialist input for every case, and are therefore missing in large databases where this is impractical, or quickly outdated when guidelines are revised. Methods: We used the up-to-date European Society of Cardiology guidelines to create an algorithm to assign complexity scores to CHD patients using only their diagnosis list. Two CHD specialists then independently assigned complexity scores to a random sample of patients. Results: Our algorithm was 96% accurate where both specialists agreed on a complexity score; this occurred 68% of the time overall, and 79% of the time in moderate or complex CHD. The algorithm "failed" mainly when diagnoses were insufficiently specific, usually for septal defects (where size was unspecified), or where complexity depends on the procedure performed (e.g. atrial/arterial switch for transposition of the great arteries). Conclusions: We were able to algorithmically determine the complexity scores of a majority of patients with CHD based on their diagnosis list alone. This could allow for automatic complexity scoring of most patients in large CHD databases, for example our own Registry of the Congenital Heart Alliance of Australia and New Zealand. This will facilitate targeted research into the management, outcomes and burden of CHD.

Indexed as

Adult congenital heart diseaseCongenital heart diseaseQuality of care

Identifiers

PMID39713572
PMCPMC11657542

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.