Background/Objectives: The randomized SECURITY (Second-Generation Drug-Eluting Stent Implantation Followed by Six- Versus Twelve-Month Dual Antiplatelet Therapy) trial showed the non-inferiority of 6 vs. 12-month DAPT after percutaneous coronary intervention (PCI) with second-generation DES in a low-risk population. Nevertheless, diabetes mellitus (DM) remained a major predictor of adverse cardiovascular events. We aimedto assess the interaction between DAPT duration and outcome in DM patients. Methods: All diabetic patients included in the SECURITY trial treated by second-generation DES PCI were analyzed. The primary endpoint was a composite of cardiac death, myocardial infarction (MI), stroke, definiteor probable stent thrombosis (ST), or Bleeding Academic Research Consortium (BARC) type 3 or 5 bleeding at12 months. The main secondary endpoint was a composite of cardiac death, MI, stroke, definite or probable ST, or BARC type 2, 3, or 5 bleeding at 24 months. Results: Four hundred-twenty nine DM patients received either 6 (n= 206) or 12 (n= 223) months of DAPT. The primary endpoint occurred in 3.9% and 5.4% of patients in the 6 and 12-month DAPT group, respectively (logranktest p = 0.83). Similarly, no statistically significant difference in the secondary endpoint was observed between the two study groups (5.4% vs. 7.6%, p = 0.620). Stent thrombosis rate was low irrespective of DAPT duration at both 12 (0.5% vs. 0.4%; p = 0.804) and between 12 and 24 months of follow-up (0.5% vs. 0%, p = 0.291). At multivariable analysis, female gender (HR: 3.42; 95% CI 1.32–8.85; p = 0.011 and HR 2.28; 95% CI 1.09–4.75; p = 0.027) and insulin-treated diabetes mellitus (HR: 2.62; 95% CI 1.15–6.75; p = 0.004 and HR: 2.23; 95% CI 1.09–6.33; p = 0.003) were independent predictors of both primary and secondary endpoint. Conclusions: In diabetic patients treated by second-generation DES PCI, we failed to find any additional benefit of prolonging DAPT beyond 6 months, regardless of insulin-requiring status.

Optimal duration of dual antiplatelet therapy after second-generation drug-eluting stent implantation in patients with diabetes. The SECURITY (second-generation drug-eluting stent implantation followed by six- versus twelve-month dual antiplatelet therapy)-diabetes substudy / Tarantini, G., Nai Fovino, L., Tellaroli, P., Chieffo, A., Barioli, A., Menozzi, A., Frasheri, A., Garbo, R., Masotti Centol, M., Salvatella, N., Dominguez, J.F.O., Steffanon, L., Presbitero, P., Pucci, E., Fraccaro, C., Mauri, J., Giustino, G., Sardella, G., Colombo, A.. - In: INTERNATIONAL JOURNAL OF CARDIOLOGY. - ISSN 0167-5273. - 207:15 March 2016(2016), pp. 168-176. [10.1016/j.ijcard.2016.01.068]

Optimal duration of dual antiplatelet therapy after second-generation drug-eluting stent implantation in patients with diabetes. The SECURITY (second-generation drug-eluting stent implantation followed by six- versus twelve-month dual antiplatelet therapy)-diabetes substudy

SARDELLA, Gennaro;
2016

Abstract

Background/Objectives: The randomized SECURITY (Second-Generation Drug-Eluting Stent Implantation Followed by Six- Versus Twelve-Month Dual Antiplatelet Therapy) trial showed the non-inferiority of 6 vs. 12-month DAPT after percutaneous coronary intervention (PCI) with second-generation DES in a low-risk population. Nevertheless, diabetes mellitus (DM) remained a major predictor of adverse cardiovascular events. We aimedto assess the interaction between DAPT duration and outcome in DM patients. Methods: All diabetic patients included in the SECURITY trial treated by second-generation DES PCI were analyzed. The primary endpoint was a composite of cardiac death, myocardial infarction (MI), stroke, definiteor probable stent thrombosis (ST), or Bleeding Academic Research Consortium (BARC) type 3 or 5 bleeding at12 months. The main secondary endpoint was a composite of cardiac death, MI, stroke, definite or probable ST, or BARC type 2, 3, or 5 bleeding at 24 months. Results: Four hundred-twenty nine DM patients received either 6 (n= 206) or 12 (n= 223) months of DAPT. The primary endpoint occurred in 3.9% and 5.4% of patients in the 6 and 12-month DAPT group, respectively (logranktest p = 0.83). Similarly, no statistically significant difference in the secondary endpoint was observed between the two study groups (5.4% vs. 7.6%, p = 0.620). Stent thrombosis rate was low irrespective of DAPT duration at both 12 (0.5% vs. 0.4%; p = 0.804) and between 12 and 24 months of follow-up (0.5% vs. 0%, p = 0.291). At multivariable analysis, female gender (HR: 3.42; 95% CI 1.32–8.85; p = 0.011 and HR 2.28; 95% CI 1.09–4.75; p = 0.027) and insulin-treated diabetes mellitus (HR: 2.62; 95% CI 1.15–6.75; p = 0.004 and HR: 2.23; 95% CI 1.09–6.33; p = 0.003) were independent predictors of both primary and secondary endpoint. Conclusions: In diabetic patients treated by second-generation DES PCI, we failed to find any additional benefit of prolonging DAPT beyond 6 months, regardless of insulin-requiring status.
2016
diabetes; dual antiplatelet therapy; second-generation drug-eluting stent; cardiology and cardiovascular medicine
01 Pubblicazione su rivista::01a Articolo in rivista
Optimal duration of dual antiplatelet therapy after second-generation drug-eluting stent implantation in patients with diabetes. The SECURITY (second-generation drug-eluting stent implantation followed by six- versus twelve-month dual antiplatelet therapy)-diabetes substudy / Tarantini, G., Nai Fovino, L., Tellaroli, P., Chieffo, A., Barioli, A., Menozzi, A., Frasheri, A., Garbo, R., Masotti Centol, M., Salvatella, N., Dominguez, J.F.O., Steffanon, L., Presbitero, P., Pucci, E., Fraccaro, C., Mauri, J., Giustino, G., Sardella, G., Colombo, A.. - In: INTERNATIONAL JOURNAL OF CARDIOLOGY. - ISSN 0167-5273. - 207:15 March 2016(2016), pp. 168-176. [10.1016/j.ijcard.2016.01.068]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/886064
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