Evidence map›Paper›PMID 37233944›Full record

ArticleForensic science, medicine, and pathology2024

Cardiovascular-related death in infancy and childhood: a clinicopathological study of two referral institutions in England.

Fu Chuen Kon, Irene Scheimberg, Mohammad Haini, Marta C Cohen

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Forensic science, medicine, and pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 18% of its field
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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Sudden Cardiac Death in Childhood: Peaks in Teenagers.Circulation. Arrhythmia and electrophysiology · 2025
    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

4 authors at 2 institutions in 1 country.

Fu Chuen KonDepartment of Pathology, Sheffield Children's Hospital NHS F.T., University of Sheffield, Western Bank, Sheffield, UK.
Irene Scheimberg *Department of Pathology, Royal London Hospital, Barts Health NHS T., Tower Hamlets, London, UK.
Mohammad HainiDepartment of Pathology, Royal London Hospital, Barts Health NHS T., Tower Hamlets, London, UK.
Marta C CohenDepartment of Pathology, Sheffield Children's Hospital NHS F.T., University of Sheffield, Western Bank, Sheffield, UK. Marta.Cohen@nhs.net.ORCID 0000-0001-5534-444X
Barts Health NHS Trust · GBSheffield Children's Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To review post-mortem findings among deaths presenting as sudden and/or unexpected deaths in two centers in the UK during a 16-year period in order to identify those related to cardiovascular conditions. The post-mortem databases of two tertiary referral institutions were searched, and all reports were reviewed. Histological features and results of ancillary investigations were noted. All cases of sudden and/or unexpected cardiac deaths (SCD) between 2003 and 2018 were identified. The study was PRISMA compliant and approved by clinical governance. 68/1129 cases of SCD (6.0%) were identified in one center and 83/753 cases (11%) in the other. These 151 cases constituted the study cohort. The mean annual incidence of SCD was 0.3 per 100,000 persons/annum. The three most prevalent groups of cardiac pathology were cardiac malformations (51/151; 33.8%), cardiomyopathies (32/151; 21.2%), and myocarditis (31/151; 20.5%). Mean age at death was 3.4 years. Prematurity was predominantly associated with deaths related to cardiac malformations (p < 0.001). Symptoms had been present for a mean of 3.8, 3.0, and 3.5 days before death for myocarditis, cardiomyopathy, and cardiac malformations/complications post-surgery. This retrospective comparative study represents the largest autopsy series of SCD in infants and children in the UK. Some entities are very infrequent. Several diseases could have been identified earlier in life allowing for the possibility of intervention. Limitation includes the retrospective nature of the study and that, as arrhythmogenic gene mutations are not yet routinely performed in unexplained deaths, the incidence of SCD in infants and children is most likely underestimated.

Indexed as

Death, Sudden, CardiacMyocarditisAdolescentCardiomyopathiesCardiovascular DiseasesCause of DeathChildChild, PreschoolEnglandFemaleHeart Defects, CongenitalHumansIncidenceInfantInfant, NewbornMaleCardiac malformationsMyocarditisRepaired-heart malformationsSudden cardiac deaths in children

Identifiers

PMID37233944
PMCPMC10214348
OpenAlexW4378349311

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.