Diagnostic Accuracy of Diastolic Fractional Flow Reserve for Functional Evaluation of Coronary Stenosis: DIASTOLE Study.
FFR, fractional flow reserve
IQR, interquartile range
LAD, left anterior descending artery
LCX, left circumflex artery
MPS, myocardial perfusion scintigraphy
RCA, right coronary artery
ROC, receiver-operating characteristic
SDS, summed difference score
SRS, summed rest score
SSS, summed stress score
dPR, diastolic pressure ratio
fractional flow reserve
iFR, instantaneous wave-free ratio
myocardial ischemia
myocardial perfusion scintigraphy
stable coronary artery disease
Journal
JACC. Asia
ISSN: 2772-3747
Titre abrégé: JACC Asia
Pays: United States
ID NLM: 9918452380106676
Informations de publication
Date de publication:
Sep 2021
Sep 2021
Historique:
received:
10
05
2021
revised:
28
06
2021
accepted:
08
07
2021
entrez:
7
11
2022
pubmed:
21
9
2021
medline:
21
9
2021
Statut:
epublish
Résumé
In the resting conditions, narrowing the window of coronary pressure measurements from the whole cardiac cycle to diastole improves diagnostic performance of coronary pressure-derived physiological index. However, whether this also applies to the hyperemic conditions has not yet been thoroughly evaluated. The purpose of this study was to assess whether diastolic fractional flow reserve (diastolic FFR) has better diagnostic performance in identifying ischemia-causing coronary lesions than conventional FFR in a prospective, multicenter, and independent core laboratory-based environment. In this prospective multicenter registry at 29 Japanese centers, we compared the diagnostic performance of FFR, diastolic FFR, resting distal to aortic coronary pressure (Pd/Pa), and diastolic pressure ratio (dPR) using myocardial perfusion scintigraphy (MPS) as the reference standard in 378 patients with single-vessel coronary disease. Inducible myocardial ischemia was found on MPS in the relevant myocardial territory of the target vessel in 85 patients (22%). In the receiver-operating curve analyses, diastolic FFR had comparable area under the curve (AUC) compared with FFR (AUC Diastolic FFR showed a similar diagnostic performance to FFR as compared with MPS. This result reaffirms the use of FFR as the most accurate invasive physiological lesion assessment. (Diagnostic accuracy of diastolic fractional flow reserve (d-FFR) for functional evaluation of coronary stenosis; UMIN000015906).
Sections du résumé
Background
UNASSIGNED
In the resting conditions, narrowing the window of coronary pressure measurements from the whole cardiac cycle to diastole improves diagnostic performance of coronary pressure-derived physiological index. However, whether this also applies to the hyperemic conditions has not yet been thoroughly evaluated.
Objectives
UNASSIGNED
The purpose of this study was to assess whether diastolic fractional flow reserve (diastolic FFR) has better diagnostic performance in identifying ischemia-causing coronary lesions than conventional FFR in a prospective, multicenter, and independent core laboratory-based environment.
Methods
UNASSIGNED
In this prospective multicenter registry at 29 Japanese centers, we compared the diagnostic performance of FFR, diastolic FFR, resting distal to aortic coronary pressure (Pd/Pa), and diastolic pressure ratio (dPR) using myocardial perfusion scintigraphy (MPS) as the reference standard in 378 patients with single-vessel coronary disease.
Results
UNASSIGNED
Inducible myocardial ischemia was found on MPS in the relevant myocardial territory of the target vessel in 85 patients (22%). In the receiver-operating curve analyses, diastolic FFR had comparable area under the curve (AUC) compared with FFR (AUC
Conclusions
UNASSIGNED
Diastolic FFR showed a similar diagnostic performance to FFR as compared with MPS. This result reaffirms the use of FFR as the most accurate invasive physiological lesion assessment. (Diagnostic accuracy of diastolic fractional flow reserve (d-FFR) for functional evaluation of coronary stenosis; UMIN000015906).
Identifiants
pubmed: 36338166
doi: 10.1016/j.jacasi.2021.07.008
pii: S2772-3747(21)00077-6
pmc: PMC9627917
doi:
Types de publication
Journal Article
Langues
eng
Pagination
230-241Investigateurs
Y Shiono
(Y)
Y Katayama
(Y)
K Hironori
(K)
T Kubo
(T)
T Akasaka
(T)
N Tanaka
(N)
J Yamashita
(J)
H Fujita
(H)
A Matsuo
(A)
H Matsuo
(H)
Y Kawase
(Y)
I Kawamura
(I)
T Kakuta
(T)
M Hoshino
(M)
T Sugano
(T)
H Takashima
(H)
T Amano
(T)
H Yokoi
(H)
Y Yamamoto
(Y)
Y Nozaki
(Y)
M Machida
(M)
M Kobori
(M)
T Kikuchi
(T)
H Ohira
(H)
H Yoshino
(H)
H Ishiguro
(H)
Y Wakabayashi
(Y)
T Kondo
(T)
H Terai
(H)
T Suwa
(T)
T Kimura
(T)
T Kawajiri
(T)
A Hirohata
(A)
S Uemura
(S)
Y Neishi
(Y)
T Sakamoto
(T)
M Yamada
(M)
K Okeie
(K)
K Hishikari
(K)
M Oguri
(M)
T Uetani
(T)
T Saegusa
(T)
F Yamamoto
(F)
M Yamada
(M)
Informations de copyright
© 2021 The Authors.
Déclaration de conflit d'intérêts
This study was supported by a grant from NPO Association for Thinking about the Future of the Heart Angioplasty and JSPS KAKENHI Grant Number JP15K09093; however, these entities were not involved in the design and execution of this study. Drs Akasaka and Kubo have received lecture fees and research grants from Abbott Vascular. Dr Tanaka has received lecture fees and research grants from Abbott Vascular, Philips, and Boston Scientific Japan. Dr Matsuo has received lecture fees from Phillips, Abbott Vascular, and Boston Scientific Japan, and consultant fees from Zeon Medical. Drs Yokoi and Shiono have received lecture fees from Abbott Vascular and Philips. All other authors have no relationships relevant to the contents of this paper to disclose.
Références
Circulation. 2000 Nov 7;102(19):2371-7
pubmed: 11067791
N Engl J Med. 1996 Jun 27;334(26):1703-8
pubmed: 8637515
J Am Coll Cardiol. 2003 Jul 16;42(2):226-33
pubmed: 12875756
J Am Coll Cardiol. 2017 Oct 24;70(17):2114-2123
pubmed: 29050558
J Am Coll Cardiol. 2012 Mar 20;59(12):1045-57
pubmed: 22421298
J Am Coll Cardiol. 1998 Dec;32(7):1987-95
pubmed: 9857883
Circ Cardiovasc Interv. 2018 Jan;11(1):e004613
pubmed: 29326150
Circulation. 1994 Sep;90(3):1215-24
pubmed: 8087931
Eur Heart J. 2018 Dec 7;39(46):4072-4081
pubmed: 30452609
N Engl J Med. 2010 Mar 11;362(10):886-95
pubmed: 20220183
J Am Coll Cardiol. 2013 Apr 2;61(13):1409-20
pubmed: 23500218
J Am Coll Cardiol. 2017 Dec 26;70(25):3088-3096
pubmed: 29268922
J Am Coll Cardiol. 2012 Apr 10;59(15):1392-402
pubmed: 22154731
Circulation. 2002 Jan 29;105(4):539-42
pubmed: 11815441
Circ Res. 1982 Sep;51(3):261-70
pubmed: 7116578
EuroIntervention. 2018 Sep 20;14(7):806-814
pubmed: 29790478
N Engl J Med. 2018 Jul 19;379(3):250-259
pubmed: 29785878
J Am Coll Cardiol. 2014 Apr 8;63(13):1253-1261
pubmed: 24211503
Circulation. 2013 Dec 17;128(24):2557-66
pubmed: 24141255
Circ Cardiovasc Interv. 2012 Aug 1;5(4):508-14
pubmed: 22787017
Eur Heart J. 2019 Jan 7;40(2):87-165
pubmed: 30165437
Circulation. 1989 Oct;80(4):941-50
pubmed: 2791252
Circulation. 2000 Nov 7;102(19):2365-70
pubmed: 11067790
EuroIntervention. 2015 Dec;11(8):914-25
pubmed: 25169594
Circ Cardiovasc Interv. 2014 Aug;7(4):492-502
pubmed: 24987048