Evidence map›Paper›PMID 34514746›Full record

Observational studyESC heart failure2021

Shortening of time-to-peak left ventricular pressure rise (Td) in cardiac resynchronization therapy.

Hans Henrik Odland, Manuel Villegas-Martinez, Stian Ross, Torbjørn Holm, Richard Cornelussen, Espen W Remme, Erik Kongsgard

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in ESC heart failure, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06103539 (Pacertool-Study - Safety and Performance of the Presens-Catheter and the Pacer Software), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

NCT06103539 unknown statusnot on this mapstarted 2023, after this paper: background citation

Pacertool-Study - Safety and Performance of the Presens-Catheter and the Pacer Software

TypeobservationalSponsorPacertool ASRan2023 to 2024Enrolled50ConditionsHeart Failure With Reduced Ejection Fraction, Dyssynchrony, Medical Device PerformanceArmsCardiac catheterization and evoked response to cardiac stimulation
3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Pulse arrival time variation as a non-invasive marker of acute response to cardiac resynchronization therapy.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2023
    Article
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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

7 authors.

Hans Henrik OdlandDepartment of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, 0027, Norway.ORCID 0000-0002-0868-4457
Manuel Villegas-MartinezIntervention Center, Oslo University Hospital, Rikshospitalet, Oslo, 0027, Norway.
Stian RossDepartment of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, 0027, Norway.
Torbjørn HolmDepartment of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, 0027, Norway.
Richard CornelussenBakken Research Centre, Medtronic Plc, Maastricht, The Netherlands.
Espen W RemmeIntervention Center, Oslo University Hospital, Rikshospitalet, Oslo, 0027, Norway.
Erik KongsgardDepartment of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, 0027, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsWe tested the hypothesis that shortening of time-to-peak left ventricular pressure rise (Td) reflect resynchronization in an animal model and that Td measured in patients will be helpful to identify long-term volumetric responders [end-systolic volume (ESV) decrease >15%] in cardiac resynchronization therapy (CRT).

methodsTd was analysed in an animal study (n = 12) of left bundle-branch block (LBBB) with extensive instrumentation to detect left ventricular myocardial deformation, electrical activation, and pressures during pacing. The sum of electrical delays from the onset of pacing to four intracardiac electrodes formed a synchronicity index (SI). Pacing was performed at baseline, with LBBB, right and left ventricular pacing and finally with biventricular pacing (BIVP). We then studied Td at baseline and with BIVP in a clinical observational study in 45 patients during the implantation of CRT and followed up for up to 88 months.

resultsWe found a strong relationship between Td and SI in the animals (R = 0.84, P < 0.01). Td and SI increased from narrow QRS at baseline (Td = 95 ± 2 ms, SI = 141 ± 8 ms) to LBBB (Td = 125 ± 2 ms, SI = 247 ± 9 ms, P < 0.01), and shortened with biventricular pacing (BIVP) (Td = 113 ± 2 ms and SI = 192 ± 7 ms, P < 0.01). Prolongation of Td was associated with more wasted deformation during the preejection period (R = 0.77, P < 0.01). Six patients increased ESV by 2.5 ± 18%, while 37 responders (85%) had a mean ESV decrease of 40 ± 15% after more than 6 months of follow-up. Responders presented with a higher Td at baseline than non-responders (163 ± 26 ms vs. 121 ± 19 ms, P < 0.01). Td decreased to 156 ± 16 ms (P = 0.02) with CRT in responders, while in non-responders, Td increased to 148 ± 21 ms (P < 0.01). A decrease in Td with BIVP to values similar or below what was found at baseline accurately identified responders to therapy (AUC 0.98, P < 0.01). Td at baseline and change in Td from baseline was linear related to the decrease in ESV at follow-up. All-cause mortality was high among six non-responders (n = 4), while no patients died in the responder group during follow-up.

conclusionsProlongation of Td is associated with cardiac dyssynchrony and more wasted deformation during the preejection period. Shortening of a prolonged Td with CRT in patients accurately identifies volumetric responders to CRT with incremental value on top of current guidelines and practices. Thus, Td carries the potential to become a biomarker to predict long-term volumetric response in CRT candidates.

Indexed as

Cardiac Resynchronization TherapyHeart FailureAnimalsArrhythmias, CardiacBundle-Branch BlockHumansVentricular PressureCardiac resynchronization therapyReverse volumetric remodellingTime-to-peak dP/dt

Identifiers

PMID34514746
PMCPMC8712829

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Registered trials

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.