Impact of post-dilation on the acute and one-year clinical outcomes of a large cohort of patients treated solely with the Absorb Bioresorbable Vascular Scaffold

被引:19
作者
Costa, Jose De Ribamar, Jr. [1 ]
Abizaid, Alexandre [1 ]
Bartorelli, Antonio L. [2 ]
Whitbourn, Robert [3 ]
van Geuns, Robert Jan [4 ]
Chevalier, Bernard [5 ]
Perin, Marcos [6 ]
Seth, Ashok [7 ]
Botelho, Roberto [8 ]
Serruys, Patrick W. [4 ]
机构
[1] Inst Cardiol Dante Pazzanese, Sao Paulo, Brazil
[2] Univ Milan, Ctr Cardiol Monzino, IRCCS, Milan, Italy
[3] Si Vincents Hosp, Fitzroy, Vic, Australia
[4] Erasmus Univ, Thoraxctr, Med Ctr, NL-3000 DR Rotterdam, Netherlands
[5] Inst Cardiovasc Paris Sud, Massy, France
[6] Hosp Israelita Albert Einstein, Sao Paulo, Brazil
[7] Fortis Escorts Heart Inst, New Delhi, India
[8] Inst Cardiol Triangulo Mineiro, Uberaha, MG, Brazil
关键词
bioresorbable scaffold; coronary artery disease; percutaneous coronary intervention; post-dilation; ELUTING STENT IMPLANTATION; INTRAVASCULAR ULTRASOUND; REGISTRY; THROMBOSIS; TRIALS;
D O I
10.4244/EIJY15M05_06
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Aims: We sought to determine the impact of post-dilation (PD) on clinical outcomes in a large cohort of patients treated only with the Absorb Bioresorbable Vascular Scaffold (BVS). Methods and results: We evaluated all consecutive patients enrolled in the multicentre, single-arm ABSORB EXTEND study up to June 2013. The study allowed treatment of up to two coronaries (diameter 2.0 to 3.8 mm) and the use of overlapping (lesion length <= 28 mm). Patients with severe lesion calcification/tortuosity were excluded. Aggressive lesion predilation (balloon to artery ratio of 0.9-1.0) was mandatory, and PD was left to the operator's discretion. Patients were grouped according to whether PD was performed or not, and the one-year incidences of MACE and scaffold thrombosis were compared. A total of 768 patients were enrolled in the study; PD was performed in 526(68.4%). There were no significant differences between the PD group and non-PD group in the majority of baseline characteristics, including the presence of moderate calcification and of B2/C lesions. Lesion length was similar (12.3 +/- 5.1 mm vs. 12.1 +/- 5.3 mm, p=0.6), as was RVD (2.6 mm for both groups, p=0.2). Residual in-scaffold stenosis (15.5 +/- 6.4% with PD, 15.0 +/- 6% without PD, p=0.3) and the need for bail-out scaffold/stent (4.2% with PD, 4.6% without PD, p=0.8) were comparable. Acute gain was higher in the non-PD group (1.14 +/- 0.3 mm vs. 1.21 +/- 0.4 mm, p=0.02). Clinical device success was 98.9% in both groups. At one year, there was no difference in MACE (5.4% in the PD group vs. 2.5% in the non-PD group, p=0.1). All individual components of TLR, death, and MI were similar as well as definite/probable scaffold thrombosis between the two groups. Conclusions: These results reflect very similar final angiographic and clinical results achieved with or without post-dilation in the treatment of low to moderately complex coronary lesions. Therefore, post-dilation should be performed whenever needed to optimise acute results.
引用
收藏
页码:141 / 148
页数:8
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