Evidence map›Paper›PMID 40838531›Full record

ArticlePacing and clinical electrophysiology : PACE2025

High-Precision Hemodynamic and Echocardiographic Assessment of Pacing in Obstructive Hypertrophic Cardiomyopathy.

Jagdeep S Mohal, Matthew J Shun-Shin, Kayla Chiew, Alejandra A Miyazawa, Florentina Simader, Pannathorn Tangkongpanich, Rahul Bahl, Ji-Jian Chow, James P Howard, Akriti Naraen and 13 more

Abstract read
In one paragraph

Article in Pacing and clinical electrophysiology : PACE, 2025. 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

23 authors.

Jagdeep S MohalNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.ORCID 0000-0002-0442-4033
Matthew J Shun-ShinNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Kayla ChiewNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Alejandra A MiyazawaNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Florentina SimaderNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Pannathorn TangkongpanichNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Rahul BahlNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Ji-Jian ChowNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
James P HowardNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Akriti NaraenNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Keenan SalehNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Jack W SamwaysNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Daniel KeeneNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
S M Afzal SohaibBarts Heart Centre, St Bartholomew's Hospital, West Smithfield, London, UK.
Mark TannerNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Kevin M W LeongNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Norman A QureshiNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
David C LefroyNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Prapa KanagaratnamNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Darrel P FrancisNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Amanda VarnavaNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Zachary I WhinnettNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.
Ahran D ArnoldNational Heart and Lung Institute, Imperial College London, Hammersmith Hospital, London, UK.ORCID 0000-0002-7597-0170

Funding

British Heart Foundation FS/CRTF/21/24171Coronary Flow TrustMedical Research Council MR/X502959/1NIHR Imperial Biomedical Research CentreRosetrees Trust IAA 2023/1
6 · The paper itself

Abstract

backgroundLeft ventricular outflow obstruction drives symptoms and outcomes in obstructive hypertrophic cardiomyopathy (oHCM). Right ventricular pacing (RVP) can desynchronize the left ventricle to relieve this and allows control of atrioventricular delay (AVD) but may impair ventricular function. We used high-precision assessment to quantify the hemodynamic and echocardiographic effects of RVP in oHCM.

methodsPatients with oHCM and implanted dual-chamber pacing devices underwent continuous recording of ECG, beat-by-beat outflow tract continuous wave Doppler, and beat-by-beat, noninvasive finger-cuff blood pressure while pacing was alternated between atrium-only pacing and AV-sequential RVP at a range of AVDs at 5 bpm above resting heart rate and 100 bpm. Changes in systolic blood pressure (∆SBP) and left ventricular outflow tract gradient (∆LVOTg) were fitted to parabolas to produce reproducible, narrow confidence interval estimates of effects.

resultsTwenty two patients were recruited (60% male, mean resting LVOTg 53 mmHg). At just above resting heart rate (mean 75 bpm), RVP produced mean peak ∆SBP from AAI to DDD of 2.47 mmHg (95% confidence interval: 0.19-4.76, p = 0.04). The mean AVD for peak ∆SBP was 173.2 ms. Mean LVOTg reduction at this AVD was 8.31 mmHg (2.43-14.18, p < 0.001). Apart from the hemodynamically optimum AVD, no other AVDs produced statistically significant increases in SBP. At 100 bpm, greater increases in SBP and reductions in LVOTg were seen at hemodynamically optimal AVD.

conclusionMultiple alternation assessment allows precise, reproducible, narrow confidence interval quantification of hemodynamic and echocardiographic pacing effects. RVP can reduce LVOTg while preserving or improving cardiac output, but AVD is a key modifier of this relationship.

Indexed as

Cardiac Pacing, ArtificialCardiomyopathy, HypertrophicEchocardiographyHemodynamicsVentricular Outflow ObstructionAgedFemaleHumansMaleMiddle AgedReproducibility of ResultsTreatment Outcomehemodynamicshypertrophic cardiomyopathyobstructive hypertrophic cardiomyopathyright ventricular pacing

Identifiers

PMID40838531
PMCPMC12504915

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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.