1 Intervention Center, Quang Nam Central General Hospital, Quang Nam, Vietnam.
2 Heart Research Institute, ChungAng University Hospital, Seoul, Korea.
Angiology. 2019 Sep;70(8):756-764. doi: 10.1177/0003319718822348. Epub 2019 Jan 21.
To evaluate the angiographic and intravascular ultrasound (IVUS) characteristics of coronary mismatch lesions.
Better understanding about the characteristics of mismatch lesions may help to achieve more accurate lesion assessment and, thereby, to improve the outcomes of percutaneous coronary intervention (PCI).
Angiographic and IVUS data from 1369 lesions were analyzed. Mismatch lesion was defined as the difference between proximal and distal reference lumen diameters of ≥1.0 mm or ≥30% of the distal reference lumen diameter.
The incidence of mismatch lesions was 20.1% (275/1369). Compared to nonmismatch group, mismatch group had longer lesions (21.3 [6.4] mm vs 18.4 [6.4] mm, < .001) with smaller minimum lumen diameter (0.87 [0.29] mm vs 1.10 [0.31] mm, < .001) and more severe diameter stenosis (78.8% [9.2%] vs 66.3% [10.3%], < .001). On IVUS, mismatch group had larger lumen area (18.7 [5.0] vs 15.8 [5.1] mm, < .001) but lower plaque burden at the proximal reference segment (41.0% [9.2%] vs 45.7% [9.9%], < .001) and smaller lumen area (4.83 [1.89] vs 7.36 [2.89] mm, < .001) but higher plaque burden at the distal reference segment (42.9% [10.4%] vs 41.4% [10.1%], = .023). Multivariable logistic regression analysis showed that mismatch lesions were frequently accompanied by diffuse lesions (odds ratio [OR] = 2.50; 95% confidence interval [CI]: 1.83-3.40; < .001), bifurcation lesions (OR = 5.83; 95% CI: 4.40-7.74; < .001), and lesions with a low TIMI flow grade (OR = 1.70; 95% CI: 1.08-2.67; = .022) or severe diameter stenosis (OR = 3.05; 95% CI: 2.10-4.43; < .001).
Mismatch lesions are quite common and characterized by greater lesion complexity compared with nonmismatch lesions. Further studies may be necessary to address the impact of this lesion type on the outcome of PCI.
评估冠状动脉不匹配病变的血管造影和血管内超声(IVUS)特征。
更好地了解不匹配病变的特征可能有助于更准确地评估病变,并由此改善经皮冠状动脉介入治疗(PCI)的结果。
对 1369 处病变的血管造影和 IVUS 数据进行分析。不匹配病变定义为近端和远端参考管腔直径之差≥1.0mm 或≥远端参考管腔直径的 30%。
不匹配病变的发生率为 20.1%(275/1369)。与非不匹配组相比,不匹配组的病变更长(21.3[6.4]mm 比 18.4[6.4]mm, <.001),最小管腔直径更小(0.87[0.29]mm 比 1.10[0.31]mm, <.001),直径狭窄更严重(78.8%[9.2%]比 66.3%[10.3%], <.001)。在 IVUS 上,不匹配组的管腔面积更大(18.7[5.0]mm 比 15.8[5.1]mm, <.001),但近端参考节段的斑块负荷较低(41.0%[9.2%]比 45.7%[9.9%], <.001),管腔面积较小(4.83[1.89]mm 比 7.36[2.89]mm, <.001),但远端参考节段的斑块负荷较高(42.9%[10.4%]比 41.4%[10.1%], =.023)。多变量逻辑回归分析显示,不匹配病变常伴有弥漫性病变(比值比[OR] = 2.50;95%置信区间[CI]:1.83-3.40; <.001)、分叉病变(OR = 5.83;95%CI:4.40-7.74; <.001)和 TIMI 血流分级较低的病变(OR = 1.70;95%CI:1.08-2.67; =.022)或严重的直径狭窄(OR = 3.05;95%CI:2.10-4.43; <.001)。
不匹配病变相当常见,与非不匹配病变相比,病变复杂性更大。可能需要进一步的研究来探讨这种病变类型对 PCI 结果的影响。