Collateral presence and extent do not predict myocardial viability and ischemia in chronic total occlusions: A stress-CMR study.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
15 Jan 2023
Historique:
received: 09 03 2022
revised: 05 08 2022
accepted: 26 09 2022
pubmed: 2 10 2022
medline: 15 12 2022
entrez: 1 10 2022
Statut: ppublish

Résumé

Well-developed collaterals are assumed as a marker of viability and ischemia in chronic total occlusions (CTO). We aim to correlate viability and ischemia with collateral presence and extent in CTO patients by cardiac magnetic resonance (CMR). Multicentre study of 150 CTO patients undergoing stress-CMR, including adenosine if normal systolic function, high-dose-dobutamine for patients with akinetic/>2 hypokinetic segments and EF ≥35%, otherwise low-dose-dobutamine (LDD); all patients underwent late gadolinium enhancement (LGE) imaging. Viability was defined as mean LGE transmurality ≤50% for adenosine, as functional improvement for dobutamine-stress-test, ischemia as ≥1.5 segments with perfusion defects outside the scar zone. Rentrop 3/CC 2 defined well-developed (WD, n = 74) vs poorly-developed collaterals (PD, n = 76). Viability was equally prevalent in WD vs PD: normo-functional myocardium with ≤50% LGE in 52% vs 58% segments, p = 0.76, functional improvement by LDD in 48% vs 52%, p = 0.12. Segments with none, 1-25%,26-50%,51-75% LGE showed viability by LDD in 90%,84%,81%,61% of cases, whilst in 12% if 76-100% LGE (p < 0.01). There was no difference in WD vs PD for ischemia presence (74% vs 75%, p = 0.99) and extent (2.7 vs 2.8 segments, p = 0.77). In a large cohort of CTO patients, presence and extent of collaterals did not predict viability and ischemia by stress-CMR. Scar extent up to 75% LGE was still associated with viability, whereas ischemia was undetectable in 25% of patients, suggesting that the assessment of CTO patients with CMR would lead to a more comprehensive evaluation of viability and ischemia to guide revascularization.

Sections du résumé

BACKGROUND BACKGROUND
Well-developed collaterals are assumed as a marker of viability and ischemia in chronic total occlusions (CTO). We aim to correlate viability and ischemia with collateral presence and extent in CTO patients by cardiac magnetic resonance (CMR).
METHODS METHODS
Multicentre study of 150 CTO patients undergoing stress-CMR, including adenosine if normal systolic function, high-dose-dobutamine for patients with akinetic/>2 hypokinetic segments and EF ≥35%, otherwise low-dose-dobutamine (LDD); all patients underwent late gadolinium enhancement (LGE) imaging. Viability was defined as mean LGE transmurality ≤50% for adenosine, as functional improvement for dobutamine-stress-test, ischemia as ≥1.5 segments with perfusion defects outside the scar zone.
RESULTS RESULTS
Rentrop 3/CC 2 defined well-developed (WD, n = 74) vs poorly-developed collaterals (PD, n = 76). Viability was equally prevalent in WD vs PD: normo-functional myocardium with ≤50% LGE in 52% vs 58% segments, p = 0.76, functional improvement by LDD in 48% vs 52%, p = 0.12. Segments with none, 1-25%,26-50%,51-75% LGE showed viability by LDD in 90%,84%,81%,61% of cases, whilst in 12% if 76-100% LGE (p < 0.01). There was no difference in WD vs PD for ischemia presence (74% vs 75%, p = 0.99) and extent (2.7 vs 2.8 segments, p = 0.77).
CONCLUSIONS CONCLUSIONS
In a large cohort of CTO patients, presence and extent of collaterals did not predict viability and ischemia by stress-CMR. Scar extent up to 75% LGE was still associated with viability, whereas ischemia was undetectable in 25% of patients, suggesting that the assessment of CTO patients with CMR would lead to a more comprehensive evaluation of viability and ischemia to guide revascularization.

Identifiants

pubmed: 36181950
pii: S0167-5273(22)01421-8
doi: 10.1016/j.ijcard.2022.09.071
pii:
doi:

Substances chimiques

Contrast Media 0
Gadolinium AU0V1LM3JT
Dobutamine 3S12J47372
Adenosine K72T3FS567

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

10-15

Informations de copyright

Copyright © 2022. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors report no relationships with Industries or other Institutions that could be construed as a conflict of interest related to the present work.

Auteurs

S Pica (S)

Multimodality Cardiac Imaging Section, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy. Electronic address: silvia.pica@grupposandonato.it.

L Di Odoardo (L)

Multimodality Cardiac Imaging Section, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.

L Testa (L)

Cardiology Department, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.

M Bollati (M)

Cardiology Department, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.

G Crimi (G)

Interventional Cardiology, Cardio Thoraco-Vascular-Department, IRCCS Policlinico San Martino, Genoa, Italy.

A Camporeale (A)

Multimodality Cardiac Imaging Section, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.

L Tondi (L)

Multimodality Cardiac Imaging Section, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.

G Pontone (G)

Cardiology Department, Centro Cardiologico Monzino, IRCCS, Milan, Italy.

M Guglielmo (M)

Cardiology Department, Centro Cardiologico Monzino, IRCCS, Milan, Italy.

D Andreini (D)

Cardiology Department, Centro Cardiologico Monzino, IRCCS, Milan, Italy.

A Squeri (A)

Cardiology Department, Villa Maria Cecilia Hospital, Cotignola, Ravenna, Italy.

L Monti (L)

Cardiology Department, Humanitas Clinical and Research Center, IRCCS Rozzano, Milan, Italy.

F Roccasalva (F)

Cardiology Department, Humanitas Clinical and Research Center, IRCCS Rozzano, Milan, Italy.

L Grancini (L)

Cardiology Department, Centro Cardiologico Monzino, IRCCS, Milan, Italy.

G L Gasparini (GL)

Cardiology Department, Humanitas Clinical and Research Center, IRCCS Rozzano, Milan, Italy.

G G Secco (GG)

Interventional Cardiology Department, A.O.Ss. Antonio e Biagio, Alessandria, Italy.

B Bellini (B)

Interventional Cardiology Department, San Raffaele Scientific Institute, Milan, Italy.

L Azzalini (L)

Division of Cardiology, VCU Health Pauley Heart Center, Virginia Commonwealth University, Richmond, VA, USA.

A Maestroni (A)

Cardiology Department, ASST Valle Olona, Busto Arsizio, Varese, Italy.

F Bedogni (F)

Cardiology Department, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.

M Lombardi (M)

Multimodality Cardiac Imaging Section, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.

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Classifications MeSH