Evidence map›Paper›PMID 42481157›Full record

ArticleOpen heart2026

Percutaneous coronary interventions improve phasic cardiac-coronary interaction in chronic coronary syndromes as assessed by wave intensity analysis.

Ahmet Taş, Yaren Alan, Alp Ozcan, Ilke Kara Taş, Nehir Taş, Irem Sezer, Tim P van de Hoef, Kim H Parker, Murat Sezer, Jan J Piek

Abstract read
In one paragraph

Article in Open heart, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Ahmet TaşCardiovascular Sciences, Amsterdam UMC Locatie AMC, Amsterdam, Netherlands a.tas@amsterdamumc.nl.ORCID http://orcid.org/0000-0002-1944-2576
Yaren AlanDepartment of Cardiology, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkey.
Alp OzcanDepartment of Cardiology, Koc University School of Medicine, Istanbul, Turkey.
Ilke Kara TaşDepartment of Pathology, Istanbul Training and Research Hospital, Istanbul, Turkey.
Nehir TaşIstanbul Medipol University International School of Medicine, Beykoz, Turkey.
Irem SezerNational Amyloidosis Centre, Royal Free Hospital, London, UK.
Tim P van de HoefCardiology, University Medical Centre Utrecht, Utrecht, Netherlands.
Kim H ParkerDepartment of Bioengineering, Imperial College London, London, UK.
Murat SezerDepartment of Cardiology, Acıbadem International Hospital, Istanbul, Turkey.ORCID http://orcid.org/0000-0001-9614-1614
Jan J PiekCardiovascular Sciences, Amsterdam UMC Locatie AMC, Amsterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinical benefit of percutaneous coronary intervention (PCI) in chronic coronary syndromes (CCS) remains controversial. Coronary wave intensity analysis (WIA) provides mechanistic insights into cardiac-coronary coupling.

objectivesTo assess peri-PCI WIA changes at rest and during hyperaemia, and to identify features associated with improvements in epicardial and microvascular resistance.

methodsIntracoronary Doppler and pressure measurements were analysed in 27 CCS patients undergoing elective PCI. Haemodynamics (fractional flow reserve (FFR), basal and hyperaemic stenosis resistance (bSR, hSR), coronary flow reserve (CFR), basal and hyperaemic microvascular resistance (bMR, hMR)) and WIA metrics (forward compression wave (FCW), backward compression wave (BCW), forward expansion wave (FEW), backward expansion wave (BEW), wave speed) were quantified at rest and hyperaemia.

resultsPCI reduced bSR and hSR (p<0.001), increased FFR (0.58±0.18 to 0.87±0.09; p<0.001) and CFR (1.68±0.47 to 2.79±0.62; p<0.001), and lowered hMR (2.22 (1.67-3.10) to 1.49 (1.18-1.74); p<0.001). At rest, PCI increased FCW (40.3±48.9 to 89.3±64.8; p=0.022), FEW (24.5 (7.2-42.8) to 58.8 (24.0-93.1); p=0.001) and BEW (57.6±70.6 to 82.1±51.8; p=0.017). Hyperaemic backward wave peaks augmented significantly (BCW: 77.8±53.3 to 172.8±112.3; BEW: 60.5±47.5 to 126.7±66.2; both p<0.001). WIA time-to-peaks occurred earlier post-PCI. Reduced resting wave speed (41±21 to 25±10 m/s; p<0.001) correlated with hMR decreases (r=0.77; p<0.001). Increased resting BEW correlated with total vascular resistance reductions (hSR+hMR; r=-0.76; p<0.001).

conclusionsElective PCI restores phasic cardiac-coronary coupling. Resting BEW and coronary wave speed provide complementary physiological endpoints reflecting microvascular and epicardial recovery, warranting larger prospective evaluation.

Indexed as

Coronary CirculationCoronary VesselsFractional Flow Reserve, MyocardialHemodynamicsPercutaneous Coronary InterventionAgedChronic DiseaseEchocardiography, DopplerFemaleHumansMaleMicrocirculationMiddle AgedTreatment OutcomeVascular ResistanceCoronary Artery DiseaseCoronary VesselsPercutaneous Coronary Intervention

Identifiers

PMID42481157
PMCPMC13404420

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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.