Coronary Artery Disease
Immediate and Long-Term Results of Drug-Eluting Stents in Mammary Artery Grafts

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Percutaneous intervention of a coronary graft is the treatment of choice when the graft fails. The objective is to report the long-term results of drug-eluting stents (DES) in mammary artery grafts (MAG). Patients who had been treated with DES for MAG in 27 centers were selected. The baseline and procedural clinical data were included prospectively, and the follow-up was performed with the patients, families, and medical records. Two hundred and sixty-eight patients were included: age 65.5 ± 10.1 years, diabetes 47.8%, ejection fraction 55.5 ± 14.9%. Indication: stable angina 28.4%, unstable angina 38.1%, non–ST-elevation myocardial infarction 21.6%, ST-elevation myocardial infarction 5.3%, and heart failure 6.7%; 1.19 ± 0.59 stents/patient were implanted measuring 18.8 ± 8.8 mm in length and 2.68 ± 0.35 mm in diameter. Rapamycin was used in 78 cases (29.1%), paclitaxel in 77 (28.7%), everolimus in 70 (26.1%), zotarolimus in 34 (12.7%), and biolimus in 9 (3.4%). All cases were successful except for 1 in which the patient died 30 minutes after the procedure. There were no other inhospital events. After a follow-up of 41 months (Q25: 23.7 to Q75: 57.8), 24 patients (9%) died of heart-related causes and 20 (7.5%) of noncardiac causes. Repeat revascularization was necessary in 31 cases, and in 1 additional patient, there was total occlusion, which was not treated. These 32 patients represented 11.9% of the total. In conclusion, the implantation of DES in MAG shows very high procedural success and also low long-term event rates.

Section snippets

Methods

An observational study of a cohort of patients treated consecutively with at least 1 DES in a lesion affecting an MAG. Twenty-seven centers were contacted in Spain to obtain the data of patients treated from 2003 to 2011.

We selected all the patients who had received at least 1 DES in an MAG on the date indicated from 27 centers in Spain. The clinical and procedural characteristics had been introduced prospectively at the time of PCI. The data relating to follow-up were obtained from the medical

Results

A total of 268 patients aged 65.5 ± 10.1 years was included. Table 1 provides the patient characteristics and Table 2 provides the characteristics of the lesions and the data relating to the procedure. None of the patients had 2 different types of DES.

The procedure was successful in 263 patients (98.2%), whereas in 1 case, there was final Thrombolysis In Myocardial Infarction (TIMI) flow grade 0, in 2 cases TIMI flow grade 1, and in another 2 TIMI flow grade 2. The TIMI 0 patient died half an

Discussion

Existing data on DESs in MAG are scarce, and they are limited to clinical case reports or studies on a small number of patients. Our study represents the largest series of patients with implantation of DESs in MAG.

Although current literature on these devices in saphenous veins is very detailed, the results cannot be extrapolated to MAG because of their different characteristics. Therefore, although the latter only measure 1.9 to 2.6 mm in diameter, compared with the 3.1 to 8.5 mm of the venous

Disclosures

Dr. de la Torre is a consultant of Abbott, Boston Scientific, Biotronik, Volcano, Medtronic, IHT, Astra, and Lilly. None of the other authors have any conflict of interest.

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