Evidence map›Paper›PMID 40643661›Full record

ArticleInnere Medizin (Heidelberg, Germany)2025

[Molecular autopsy: post-mortem genetic testing following sudden cardiac death].

Tina Jenewein, Britt-Maria Beckmann, Stefanie Scheiper-Welling, Silke Kauferstein

Abstract readEnglish Abstract
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In one paragraph

Article in Innere Medizin (Heidelberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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.

Tina JeneweinInstitut für Rechtsmedizin, Zentrum für plötzlichen Herztod und Kardiogenetik, Universitätsklinikum Frankfurt, Kennedyallee 104, 60590, Frankfurt, Deutschland.
Britt-Maria BeckmannInstitut für Rechtsmedizin, Zentrum für plötzlichen Herztod und Kardiogenetik, Universitätsklinikum Frankfurt, Kennedyallee 104, 60590, Frankfurt, Deutschland.
Stefanie Scheiper-WellingInstitut für Rechtsmedizin, Zentrum für plötzlichen Herztod und Kardiogenetik, Universitätsklinikum Frankfurt, Kennedyallee 104, 60590, Frankfurt, Deutschland.
Silke KaufersteinInstitut für Rechtsmedizin, Zentrum für plötzlichen Herztod und Kardiogenetik, Universitätsklinikum Frankfurt, Kennedyallee 104, 60590, Frankfurt, Deutschland. kauferstein@em.uni-frankfurt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSudden cardiac death (SCD) is an unexpected natural death with a suspected cardiac cause, accounting for approximately 20% of all cardiovascular deaths in Germany. A significant proportion of SCD in young people (< 50 years) are caused by hereditary arrhythmogenic diseases.

methodsThe European Society of Cardiology (ESC) guidelines recommend autopsy in all cases of unexpected sudden death, especially in young people, and post-mortem genetic testing (molecular autopsy) if a hereditary heart disease is suspected. Several studies show that molecular autopsy reveals a clinically relevant sequence variant associated with an inherited arrhythmogenic disease in about 20% of cases. Clinical cardiological and genetic testing of biologically related relatives of the deceased can reduce the risk of further deaths within affected families. RESULTS AND

conclusionBased on molecular autopsy and clinical and genetic examination of relatives, therapeutic and preventive measures can be taken within families affected by SCD. This requires a structured approach to an SCD case by various medical disciplines within a financial and legal framework that has yet to be established in the German healthcare system.

Indexed as

Death, Sudden, CardiacGenetic TestingAdultArrhythmias, CardiacAutopsyFemaleGermanyHumansMaleMiddle AgedFamily screeningHeart diseases, hereditaryMultidisciplinary carePreventionSudden cardiac death

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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.