Prevalence and Clinical Outcomes of Discordant Lesions Between Fractional Flow Reserve and Nonhyperemic Pressure Ratios in Clinical Practice: The J-PRIDE Registry
Abstract
BACKGROUND: Limited large-scale, real-world data exist on the prevalence and clinical impact of discordance between fractional flow reserve (FFR) and nonhyperemic pressure ratios (NHPRs). METHODS: The J-PRIDE registry (Clinical Outcomes of Japanese Patients With Coronary Artery Disease Assessed by Resting Indices and Fractional Flow Reserve: A Prospective Multicenter Registry) prospectively enrolled 4304 lesions in 3200 patients from 20 Japanese centers. The lesions were classified into FFR+/NHPR−, FFR−/NHPR+, FFR+/NHPR+, or FFR−/NHPR groups according to cutoff values of 0.89 for NHPRs and 0.80 for FFR. The primary study end point was the cumulative 1-year incidence of target vessel failure (a composite of cardiac death, target vessel–related myocardial infarction, and clinically driven target vessel revascularization) on a lesion basis. RESULTS: An NHPR cutoff value of 0.89, determined using online software, predicted an FFR of 0.80 across various NHPR types. Discordance between FFR and NHPRs was observed in 20% of lesions (FFR+/NHPR−, 11.2%; FFR−/NHPRs+, 8.8%). Revascularization was deferred in 42.9% and 88.4% of the FFR+/NHPR− and FFR−/NHPR+ groups, respectively. In deferred vessels, the FFR+/NHPR− and FFR−/NHPR+ groups showed a higher 1-year incidence of target vessel failure compared with the FFR−/NHPR− group (7.9% versus 5.5% versus 1.7%; for FFR+/NHPR−, adjusted hazard ratio [aHR], 4.89 [95% CI, 2.68–8.91]; P <0.001; for FFR−/NHPR+, aHR, 2.64 [95% CI, 1.49–4.69]; P <0.001). In revascularized vessels, the 1-year target vessel failure rate was numerically higher in the FFR−/NHPR+ group than in the FFR+/NHPR+ group (9.6% versus 3.4%; aHR, 2.27 [95% CI, 0.70–7.34]; P =0.17), although with similar outcomes between the FFR+/NHPR− and FFR+/NHPR+ groups (2.3% versus 3.4%; aHR, 0.96 [95% CI, 0.37–2.38]; P =0.93). The FFR+/NHPR− group benefited from revascularization compared with medical treatment (aHR, 0.26 [95% CI, 0.08–0.86]; P =0.027); the FFR−/NHPR+ group did not (aHR, 2.39 [95% CI, 0.62–9.21]; P =0.20). CONCLUSIONS: Discordance between FFR and NHPRs was noted in 20% of lesions, and discordant deferred lesions resulted in worse outcomes than concordant negative lesions. Although the outcomes after deferring revascularization were comparable between the FFR+/NHPR− and FFR−/NHPR+ lesions, only FFR+/NHPR− lesions showed a benefit from revascularization compared with medical treatment, suggesting that an FFR-guided strategy is superior to an NHPR-guided strategy in discordant lesions. REGISTRATION: URL: https://www.umin.ac.jp ; Unique identifier: UMIN000038403.
Article Details
Authors (40)
Tomohiro Shinozaki
Tsutomu Fujita
Masashi Iwabuchi
Department of Cardiovascular Medicine, Nephrology and Neurology, Graduate School of Medicine, University of Ryukyus, Okinawa, Japan (M.I.).
Hiroyoshi Yokoi
Department of Cardiology, Fukuoka Sanno Hospital, Japan (H.Y.).
Takashi Akasaka
Department of Cardiovascular Medicine, Nishinomiya Watanabe Cardiovascular Center, Japan (T. Akasaka).
Hirohiko Ando
Department of Cardiology, Aichi Medical University, Aichi, Japan (H.A., T. Amano).
Hirofumi Ohashi
Tetsuya Amano
Yuetsu Kikuta
Department of Cardiology, Fukuyama Cardiovascular Hospital, Japan (Y. Kikuta).
Hitoshi Matsuo
Department of Cardiovascular Medicine, Gifu Heart Center, Gifu, Japan
Yoshiaki Kawase
Department of Cardiovascular Medicine, Gifu Heart Center, Japan (Y. Kawase, H.M.).
Yuki Nakashima
Akinori Sugano
Department of Cardiology, Ibaraki Prefectural Central Hospital, Tomobe, Japan (A.S.).
Jun Shiraishi
Department of Cardiology, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan (J.S.).
Hidenobu Terai
Department of Cardiology, Kanazawa Cardiovascular Hospital, Kanazawa, Japan (H.T.).
Yohei Yakuta
Shinichiro Yamada
Toru Tagashira
Department of Cardiology, Kita-Harima Medical Center, Ono, Japan (T.T.).
Hiromasa Otake
Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan
Takayoshi Toba
Takenori Domei
Department of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan (T.D.).
Toru Morofuji
Tomoaki Ito
kazutaka nogi
Nara Medical University, Kashihara, Japan
Atsushi Iwai
Graduate School of Pharmaceutical Sciences, Synthetic Organic Chemistry Lab
Shoichi Kuramitsu
Department of Cardiovascular Medicine, Sapporo Cardiovascular Clinic, Sapporo Heart Center, Japan (S.K., U.K., T.F.).
Umihiko Kaneko
Department of Cardiovascular Medicine, Sapporo Cardiovascular Clinic, Sapporo Heart Center, Japan (S.K., U.K., T.F.).
Kazunori Horie
Department of Cardiovascular Medicine, Sendai Kousei Hospital, Japan (K.H.).
Futoshi Yamanaka
Department of Cardiology, Shonan Kamakura General Hospital, Kanagawa, Japan (F.Y.).
Taku Asano
Department of Cardiovascular Medicine, St Luke’s International Hospital, Tokyo, Japan (T. Asano).
Kotaro Miyata
Nobuhiro Tanaka
Department of Cardiology, Tokyo Medical University Hachioji Medical Center, Japan (T. Kubo, N.T.).
Takashi Kubo
Department of Chemistry, Graduate School of Science, The University of Osaka, 1-1 Machikaneyama, Osaka 560-0043, Japan
Tsunekazu Kakuta
Masahiro Hada
Hidetaka Nishina
Department of Cardiology, Tsukuba Medical Center, Japan (H.N.).
Reo Anai
The Second Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan (R.A.).
Yutaro Naka
Yasutsugu Shiono
Department of Cardiovascular Medicine, Wakayama Medical University, Japan (A. Taruya, S.O., Y.S., T.Y., M.T., H.K., A. Tanaka).
Daisuke Higashioka