Clinical outcomes of fractional flow reserve-guided percutaneous coronary intervention by coronary flow capacity status in stable lesions

被引:2
|
作者
Hamaya, Rikuta [1 ,2 ]
Lee, Joo Myung [3 ]
Hoshino, Masahiro [1 ]
Yonetsu, Taishi [4 ]
Koo, Bon-Kwon [5 ,6 ,7 ]
Escaned, Javier [8 ,9 ]
Kakuta, Tsunekazu [1 ]
机构
[1] Tsuchiura Kyodo Gen Hosp, Div Cardiovasc Med, 4-4-1 Otsuno, Tsuchiura, Ibaraki 3000028, Japan
[2] Harvard TH Chan Sch Publ Hlth, Boston, MA USA
[3] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Cardiol,Dept Internal Med,Heart Vasc Stroke I, Seoul, South Korea
[4] Tokyo Med & Dent Univ, Dept Cardiovasc Med, Tokyo, Japan
[5] Seoul Natl Univ Hosp, Dept Internal Med, Seoul, South Korea
[6] Seoul Natl Univ Hosp, Cardiovasc Ctr, Seoul, South Korea
[7] Seoul Natl Univ, Inst Aging, Seoul, South Korea
[8] Hosp Clin San Carlos, Cardiovasc Inst, Madrid, Spain
[9] Ctr Nacl Invest Cardiovasc Carlos III CNIC, Madrid, Spain
关键词
clinical research; fractional flow reserve; stable angina; RESISTANCE;
D O I
10.4244/EIJ-D-20-00401
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Coronary flow capacity (CFC) provides integrated information about coronary flow reserve (CFR) and hyperaemic coronary flow and is useful for identifying coronary flow limitation. Aims: The aim of this study was to investigate the effect of percutaneous coronary intervention (PCI) on vessel-related major adverse cardiovascular events (MACE) according to CFC status in stable coronary lesions. Methods: From a global, multicentre registry of comprehensive physiological assessment, a total of 1,397 patients (1,694 vessels) were analysed. Low CFC was defined for lesions with reduced CFR and inverse of hyperaemic mean transit time (1/hTmn). A predefined definition of CFC (CFR <2.0 and 1/hTmn less than the corresponding percentile) was assessed first in a multivariable marginal Cox proportional model with the interaction term between CFC status and PCI (performed or not), and then the optimal definition of CFC was explored. Results: We observed a significant interaction between predefined low CFC and PCI (p=0.067). With the optimal definition of CFC (CFR <3.2 and 1/hTmn <2.8), the HR (95% CI) of PCI was 0.278 (0.103-0.751) and 1.393 (0.783-2.478) in lesions with low and normal CFC, respectively. If lesions with fractional flow reserve (FFR) <0.8 and normal CFC had been deferred, the number of PCI would have decreased by 64%. Conclusions: FFR-guided PCI for low CFC lesions was associated with reduced incidence of MACE in low CFC but not in normal CFC lesions. Our results suggest the potential use of CFC in combination with FFR for optimising the indication for PCI by reducing potentially unbeneficial PCI. Clinical Trials Registration: https://clinicaltrials.gov/ct2/show/NCT03690713
引用
收藏
页码:E301 / +
页数:16
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