アラシ ヒロユキ
Arashi Hiroyuki
嵐 弘之 所属 医学部 医学科(附属足立医療センター) 職種 教授 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Lesion characteristics of coronary arteries associated with a mismatch between angiographic severity of stenosis and fractional flow reserve. |
掲載誌名 | 正式名:Cardiovascular intervention and therapeutics 略 称:Cardiovasc Interv Ther ISSNコード:18684300/18684297 |
掲載区分 | 国内 |
出版社 | Springer Japan |
巻・号・頁 | 32(2),pp.120-126 |
著者・共著者 | ARASHI Hiroyuki†, YAMAGUCHI Junichi*, NAKAZAWA Mayui, OOTSUKI Hisao, HARUKI Shintaro, NAKAO Masashi, KAMISHIMA Kazuho, JUJO Kentaro, MINAMI Yuichiro, TAKAGI Atsushi, OGAWA Hiroshi, HAGIWARA Nobuhisa |
担当区分 | 筆頭著者 |
発行年月 | 2017/04 |
概要 | We aimed to clarify the relationships between angiographic lesion characteristics and values of fractional flow reserve (FFR) on intermediate coronary artery stenosis. The clinical meaning and assessment for "visual-functional mismatches," including regular-mismatches [defined as angiographic percent diameter stenosis (%DS) ≥50 % and FFR >0.80] and reverse-mismatches (defined as angiographic %DS <50 %, FFR ≤0.80) remains unresolved in contemporary practice. We retrospectively enrolled 140 consecutive patients who underwent coronary angiography and FFR measurement. One hundred fifty-seven cases of intermediate coronary artery stenosis were evaluated. The relationship between clinical/lesion characteristics and regular- or reverse-mismatches were examined. Lesions in the left anterior descending artery (LAD) showed significantly lower frequency of regular-mismatch than did non-LAD lesions (26.7 vs. 73.3 %, respectively; p < 0.001). Conversely, almost all reverse-mismatches were observed in LAD lesions (93.8 %). The best cut-off value of %DS, derived from receiver operating characteristic (ROC) curve analysis, to predict FFR ≤0.8 was 45.0 % in LAD lesions and 67.5 % in non-LAD lesions. FFR measurement should be considered in LAD intermediate lesions to avoid residual functional ischemia and in non-LAD lesions to avoid unnecessary coronary intervention. |
DOI | 10.1007/s12928-016-0399-8 |
PMID | 27236812 |