Reproducibility of bolus versus continuous thermodilution for assessment of coronary microvascular function in patients with ANOCA.


Journal

EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
ISSN: 1969-6213
Titre abrégé: EuroIntervention
Pays: France
ID NLM: 101251040

Informations de publication

Date de publication:
05 Jun 2023
Historique:
pmc-release: 05 06 2024
medline: 8 6 2023
pubmed: 23 2 2023
entrez: 22 2 2023
Statut: epublish

Résumé

A bolus thermodilution-derived index of microcirculatory resistance (IMR) has emerged as the standard for assessing coronary microvascular dysfunction (CMD). Continuous thermodilution has recently been introduced as a tool to quantify absolute coronary flow and microvascular resistance directly. Microvascular resistance reserve (MRR) derived from continuous thermodilution has been proposed as a novel metric of microvascular function, which is independent of epicardial stenoses and myocardial mass. We aimed to assess the reproducibility of bolus and continuous thermodilution in assessing coronary microvascular function. Patients with angina and non-obstructive coronary artery disease (ANOCA) at angiography were prospectively enrolled. Bolus and continuous intracoronary thermodilution measurements were obtained in duplicate in the left anterior descending artery (LAD). Patients were randomly assigned in a 1:1 ratio to undergo either bolus thermodilution first or continuous thermodilution first. A total of 102 patients were enrolled. The mean fractional flow reserve (FFR) was 0.86±0.06. Coronary flow reserve (CFR) calculated with continuous thermodilution (CFR In the assessment of coronary microvascular function, continuous thermodilution demonstrated significantly less variability on repeated measurements than bolus thermodilution.

Sections du résumé

BACKGROUND BACKGROUND
A bolus thermodilution-derived index of microcirculatory resistance (IMR) has emerged as the standard for assessing coronary microvascular dysfunction (CMD). Continuous thermodilution has recently been introduced as a tool to quantify absolute coronary flow and microvascular resistance directly. Microvascular resistance reserve (MRR) derived from continuous thermodilution has been proposed as a novel metric of microvascular function, which is independent of epicardial stenoses and myocardial mass.
AIMS OBJECTIVE
We aimed to assess the reproducibility of bolus and continuous thermodilution in assessing coronary microvascular function.
METHODS METHODS
Patients with angina and non-obstructive coronary artery disease (ANOCA) at angiography were prospectively enrolled. Bolus and continuous intracoronary thermodilution measurements were obtained in duplicate in the left anterior descending artery (LAD). Patients were randomly assigned in a 1:1 ratio to undergo either bolus thermodilution first or continuous thermodilution first.
RESULTS RESULTS
A total of 102 patients were enrolled. The mean fractional flow reserve (FFR) was 0.86±0.06. Coronary flow reserve (CFR) calculated with continuous thermodilution (CFR
CONCLUSIONS CONCLUSIONS
In the assessment of coronary microvascular function, continuous thermodilution demonstrated significantly less variability on repeated measurements than bolus thermodilution.

Identifiants

pubmed: 36809253
pii: EIJ-D-22-00772
doi: 10.4244/EIJ-D-22-00772
pmc: PMC10242662
pii:
doi:

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e155-e166

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Auteurs

Emanuele Gallinoro (E)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.
Department of Translational Medical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.

Dario Tino Bertolone (DT)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.
Department of Advanced Biomedical Sciences, University Federico II, Naples, Turin, Italy.

Estefania Fernandez-Peregrina (E)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Pasquale Paolisso (P)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.
Department of Advanced Biomedical Sciences, University Federico II, Naples, Turin, Italy.

Konstantinos Bermpeis (K)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Giuseppe Esposito (G)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.
Department of Advanced Biomedical Sciences, University Federico II, Naples, Turin, Italy.

Andrea Gomez-Lopez (A)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Alessandro Candreva (A)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.
Department of Cardiology, Zurich University Hospital, Zurich, Switzerland.
Department of Mechanical and Aerospace Engineering, PolitoBIO Med Lab, Politecnico di Torino, Italy.

Niya Mileva (N)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Marta Belmonte (M)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Takuya Mizukami (T)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Stephane Fournier (S)

Department of Cardiology, Lausanne University Hospital, Lausanne, Switzerland.

Marc Vanderheyden (M)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Eric Wyffels (E)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Jozef Bartunek (J)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Jeroen Sonck (J)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Emanuele Barbato (E)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.
Department of Advanced Biomedical Sciences, University Federico II, Naples, Turin, Italy.

Carlos Collet (C)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.

Bernard De Bruyne (B)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium.
Department of Cardiology, Lausanne University Hospital, Lausanne, Switzerland.

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