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Volume 103, Issue 12, Pages 1651-1656 (15 June 2009)


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Comparison of Neointimal Hyperplasia With Drug-Eluting Stents Versus Bare Metal Stents in Patients Undergoing Intracoronary Bone-Marrow Mononuclear Cell Transplantation Following Acute Myocardial Infarction

TECAM (Terapia Celular Aplicada al Miocardio) Research GroupAdolfo Villa, MDa, Roman Arnold, MD, PhDb, Pedro L. Sánchez, MD, PhDa, Federico Gimeno, MD, PhDb, Benigno Ramos, MDb, Teresa Cantero, MDb, Maria Eugenia Fernández, PhDc, Ricardo Sanz, MDa, Oliver Gutiérrez, MDd, Pedro Mota, MDb, Javier García-Frade, MD, PhDd, José Alberto San Román, MD, PhDb, Francisco Fernández-Avilés, MD, PhDaCorresponding Author Informationemail address

Received 17 November 2008; received in revised form 5 February 2009; accepted 5 February 2009. published online 20 April 2009.

The aims of this study were to assess the safety of drug-eluting stent (DES) use and to compare the incidence of in-stent restenosis (ISR) and neointimal hyperplasia formation according to the type of stent implanted (DES vs bare-metal stents [BMS]) in patients who underwent intracoronary bone marrow mononuclear cell transplantation after acute ST elevation myocardial infarction. Fifty-nine patients with successfully revascularized ST elevation myocardial infarction (37 using BMS and 22 using DES) underwent paired angiographic examinations at baseline and 6 to 9 months after the intracoronary injection of 91 million ± 56 million autologous bone marrow mononuclear cells. A subgroup of 30 patients also underwent serial intravascular ultrasound examinations. Off-line angiographic assessment showed 4 cases of binary ISR, primarily in BMS (3 cases), and no major adverse cardiac events were associated with stent type (mean follow-up period 41 ± 10 months). At follow-up, angiographic late luminal loss was significantly lower in patients with DES than in those patients with BMS (0.35 ± 0.66 vs 0.71 ± 0.38 mm, p = 0.011). Multivariate analysis identified the use of DES (β = −0.32, 95% confidence interval [CI] −0.57 to −0.26, p = 0.03) and a smaller baseline reference vessel diameter (β = 0.29, 95% CI 0.04 to 0.54, p = 0.02) as independent predictors of lower late loss. Moreover, intravascular ultrasound showed a significant reduction of in-stent neointimal hyperplasia formation related to DES use compared with BMS use (Δ neointimal hyperplasia volume 5.4 mm3 [95% CI 2.7 to 28.1] vs 35.9 mm3 [95% CI 22.0 to 43.6], p = 0.035). In conclusion, these findings suggest that the use of DES is safe and may prevent ISR and neointimal hyperplasia formation in patients who undergo intracoronary bone marrow mononuclear cell transplantation after a successfully revascularized ST elevation myocardial infarction.

a Department of Cardiology, Hospital General Universitario Gregorio Marañón, Madrid, Spain

b Institute of Heart Sciences, Hospital Clínico Universitario, Valladolid, Spain

c Instituto de Biología y Genética Molecular, University of Valladolid, Spain

d Department of Hematology, Hospital Universitario Río Hortega, Valladolid, Spain

Corresponding Author InformationCorresponding author: Tel: 34-914265882; fax: 34-915868276

 This work was supported in part by Junta de Castilla y Leon and the networks RECAVA and TERCEL (Instituto de Salud Carlos III, Ministry of Science and Innovation, Spain).

PII: S0002-9149(09)00592-X

doi:10.1016/j.amjcard.2009.02.011


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