Evidence map›Paper›PMID 40931811›Full record

ArticleCirculation. Arrhythmia and electrophysiology2025

Clinical Role of the Noninvasive Abdominal Fetal ECG in the Detection and Monitoring of Fetal Tachycardia.

Sian Chivers, Nicolò Pini, Shayan Chowdhury, Ludovica Cicci, Trisha Vigneswaran, Vita Zidere, Sophie Maxwell, Grace Moriarty, William Regan, Eric Rosenthal and 9 more

Abstract read
In one paragraph

Article in Circulation. Arrhythmia and electrophysiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

19 authors.

Sian ChiversDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0000-0002-4060-2714
Nicolò PiniDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY (N.P., S. Chowdhury, W.P.F.).ORCID 0000-0002-0839-6033
Shayan ChowdhuryDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY (N.P., S. Chowdhury, W.P.F.).
Ludovica CicciDepartment of Biomedical Engineering (L.C., S.N.), Imperial College London, United Kingdom.ORCID 0000-0002-2544-9889
Trisha VigneswaranDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0000-0002-4084-4203
Vita ZidereDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0000-0001-7505-6621
Sophie MaxwellDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).
Grace MoriartyDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).
William ReganDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).
Eric RosenthalDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0000-0003-3030-9749
David F A LloydDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0000-0003-1759-6106
Thomas G DayDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0000-0001-8391-7903
Owen I MillerDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0000-0003-1448-1012
Gurleen K SharlandDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0009-0006-3780-4231
Barrie Hayes-GillFaculty of Engineering, University of Nottingham, United Kingdom (B.H.-G.).ORCID 0000-0003-4237-7001
Stephen NiedererDepartment of Biomedical Engineering (L.C., S.N.), Imperial College London, United Kingdom.
William P FiferDepartment of Women's and Children's Health (S. Chivers, W.P.F., J.M.S.), King's College London, United Kingdom.
Catherine WilliamsonInstitute of Reproductive and Developmental Biology (C.W.), Imperial College London, United Kingdom.ORCID 0000-0002-6226-7611
John M SimpsonDepartment of Congenital Heart Disease, Evelina London Children's Hospital, United Kingdom (S. Chivers, T.V., V.Z., S.M., G.M., W.R., E.R., D.F.A.L., T.G.D., O.I.M., G.K.S., J.M.S.).ORCID 0000-0002-9773-7441

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFetal tachycardias can cause adverse fetal outcomes including ventricular dysfunction, hydrops, and fetal demise. Postnatally, ECG is the gold standard, but, in fetal practice, echocardiography is used most frequently to diagnose and monitor fetal arrhythmias. Noninvasive extraction of the fetal ECG (fECG) may provide additional information about the electrophysiological mechanism and monitoring of intermittent arrhythmias. Signal processing advances could provide improved data quality impacting clinical translation. The aim of this study was to assess the fetus with known or suspected tachycardia using noninvasive abdominal fECG and correlate results with fetal echocardiography and postnatal ECG.

methodsProspective recruitment of pregnant participants with known or suspected fetal tachycardia in a tertiary fetal cardiology unit. Overnight fECG recording at home using the MonicaAN24 monitor was performed. Data processing using bespoke MATLAB scripts was undertaken to produce fetal heart rate and beat-to-beat rhythm strips. Comparison of fECG data with clinical data obtained using echocardiography and postnatal findings. Data are presented as median (interquartile range; range).

resultsFifteen participants undertook 1 to 4 fECG recordings, giving a total of 23 recordings. Gestational age was 28.9 (23.9-34.3; 21-39.1) weeks. Duration of recording was 512 (380-609; 5-1259) minutes. Intermittent tachycardia was demonstrated on fetal heart rate graphs. Rhythm strips correctly identified short-ventriculoatrial and long-ventriculoatrial tachycardia, atrial flutter, and sinus rhythm with findings correlating with echocardiography. Postnatal ECG correlation was possible in 3.

conclusionsWe have shown that rhythm strips of fECG signals can be extracted and correctly identify the electrical mechanism of arrhythmia in cases of fetal tachycardia. The potential to monitor fetal heart rate over a prolonged period is an advantage over current monitoring strategies for documentation of intermittent arrhythmias and gauging the response to medical therapy. These data will enable research to focus on improvement in signal quality, assessment of other arrhythmia subtypes, and real-time ambulatory monitoring of the fetal rhythm.

Indexed as

ElectrocardiographyFetal DiseasesFetal HeartFetal MonitoringHeart Rate, FetalTachycardiaAdultEchocardiographyFemaleGestational AgeHumansPredictive Value of TestsPregnancyProspective StudiesSignal Processing, Computer-Assistedatrial flutterdiabetes, gestationalfetusheart rate, fetaltachycardia, supraventricular

Identifiers

PMID40931811
PMCPMC12442779

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