Favorable Vasomotor Function after Drug-Coated Balloon-Only Angioplasty of De Novo Native Coronary Artery Lesions.
Favorable Vasomotor Function after Drug-Coated Balloon-Only Angioplasty of De Novo Native Coronary Artery Lesions.
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原发性冠状动脉病变药物涂层血管成形术后良好的血管功能。
DOI:
10.3390/jcm11020299
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发表时间:
2022-01-07
影响因子:
3.9
通讯作者:
Song WH
中科院分区:
文献类型:
--
作者:
Kim S;Lee JS;Kim YH;Kim JS;Lim SY;Kim SH;Kim M;Ahn JC;Song WH
Balloon-injured coronary segments are known to harbor abnormal vasomotion. We evaluated whether de novo coronary lesions treated using drug-coated balloon (DCB) are prone to vasospasm and how they respond to ergonovine and nitrate. Among 132 DCB angioplasty recipients followed, 89 patients underwent ergonovine provocation test at 6–9 months follow-up. Within-subject ergonovine- and nitrate-induced diameter changes were compared among three different sites: DCB-treated vs. angiographically normal vs. segment showing prominent vasoreactivity (spastic). No patient experienced clinically refractory vasospastic angina or symptom-driven revascularization during follow-up. Ergonovine induced vasospasm in seven patients; all were multifocal spasm either involving (n = 2) or rather sparing DCB-treated segments (n = 5). None showed focal spasm that exclusively involved DCB-treated lesions. Among 27 patients with vasospastic features, DCB-treated segments showed less vasoconstriction than spastic counterparts (p < 0.001). A total of 110 DCB-treated lesions were analyzed to assess vasomotor function. Vasomotor function, defined as a combined constrictor and dilator response, was comparable between DCB-treated and angiographically normal segments (p = 0.173), while significant differences were observed against spastic counterparts (p < 0.001). In our study, DCB-treated lesions were not particularly vulnerable to vasospasm and were found to have vasomotor function similar to angiographically normal segments, supporting safety of DCB-only strategy in treating de novo native coronary lesions.
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影响因子:
56.9
作者:
COHEN, RA;SHEPHERD, JT;VANHOUTTE, PM
通讯作者:
VANHOUTTE, PM
DOI:
10.1016/s0735-1097(83)80327-1
发表时间:
1983-01-01
影响因子:
24
作者:
HOLLMAN, J;AUSTIN, GE;KING, SB
通讯作者:
KING, SB
影响因子:
24
作者:
Yasue, Hirofumi;Mizuno, Yuji;Saito, Yoshihiko
通讯作者:
Saito, Yoshihiko
影响因子:
37.8
作者:
LAM, JYT;CHESEBRO, JH;FUSTER, V
通讯作者:
FUSTER, V
影响因子:
37.8
作者:
FISCHELL, TA;DERBY, G;STADIUS, ML
通讯作者:
STADIUS, ML