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J Am Coll Cardiol, 2007; 49:2320-2328, doi:10.1016/j.jacc.2007.02.057 (Published online 1 June 2007).
© 2007 by the American College of Cardiology Foundation
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Comparable Clinical Outcomes With Paclitaxel- and Sirolimus-Eluting Stents in Unrestricted Contemporary Practice

John Cosgrave, MD*, Gloria Melzi, MD*,{dagger}, Simon Corbett, PhD*, Giuseppe G.L. Biondi-Zoccai, MD{ddagger}, Pierfrancesco Agostoni, MD§, Rade Babic, MD*, Flavio Airoldi, MD*,{dagger}, Alaide Chieffo, MD{dagger}, Giuseppe M. Sangiorgi, MD*, Matteo Montorfano, MD{dagger}, Iassen Michev, MD*,{dagger}, Mauro Carlino, MD{dagger} and Antonio Colombo, MD, FACC*,{dagger},*

* EMO Centro Cuore Columbus, Milan, Italy
{dagger} San Raffaele Scientific Institute, Milan, Italy
{ddagger} Abano Terme Hospital, Abano Terme, Italy
§ Antwerp Cardiovascular Institute, AZ Middelheim, Antwerp, Belgium.


Figure 1
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Figure 1 Distribution of Late Loss of Both SES and PES

(A) Distribution of late loss of sirolimus-eluting stents (SES) and paclitaxel-eluting stents (PES) for the total cohort. Late loss was not normally distributed (p = 0.0001) and was higher in the PES group: 0.45 mm (interquartile ratio [IQR] 0.07 to 0.99) compared with 0.23 mm (IQR –0.02 to 0.69) after SES, p = 0.0001. (B) Distribution of late loss of both SES and PES for nonrestenotic lesions. Late loss was normally distributed and was significantly higher in the PES group: 0.32 ± 0.55 mm compared with 0.06 ± 0.52 mm, p = 0.0001. (C) Distribution of late loss of both SES and PES for restenotic lesions. Late loss was normally distributed, and there was no difference in late loss between the 2 groups: PES 1.78 ± 0.72 mm compared with SES 1.7 ± 0.69 mm, p = 0.39.

 

Figure 2
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Figure 2 Distribution of Late Loss of Both SES and PES for the Total Cohort, Demonstrating the Area of Overlap for the Nonrestenotic and Restenotic Lesions

Abbreviations as in Figure 1.

 




 
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