use of heparin-coated stents improves short-term clinical outcomes

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Inpharma 1438 - 22 May 2004 Use of heparin-coated rather than noncoated stents may improve short-term clinical outcomes in patients undergoing percutaneous coronary intervention for acute myocardial infarction (MI), say researchers from Israel. This nonrandomised study included 238 patients who underwent intracoronary stent implantation, either using a heparin-coated [HepaCoat] stent (n = 124) or a non-heparin-coated stent. * Patients were prospectively followed for a total of 180 days. Clinical outcomes at 30 days, such as in- hospital death, recurrent acute MI and stent thrombosis, were significantly better among patients receiving heparin-coated stents, compared with those receiving non-heparin-coated stents (0% vs 4.4%, 1.6% vs 7% and 0.8% vs 6.1%, respectively). However, there were no significant differences in clinical outcomes between the two groups at 180 days. * During the procedure, patients received unfractionated IV heparin, a bolus of 70 U/kg, adjusted to achieve an activated clotting time of 225–300 sec. Most patients also received GPIIb/IIIa inhibitors. After the procedure, all patients received aspirin 200 mg/day and a loading dose of oral clopidogrel 300mg followed by 75 mg/day orally for one month, followed by aspirin alone at a dosage of 100 mg/day. Lev EI, et al. Comparison of outcomes up to six months of heparin-coated with noncoated stents after percutaneous coronary intervention for acute myocardial infarction. American Journal of Cardiology 93: 741-743, No. 6, 15 Mar 2004 800976581 1 Inpharma 22 May 2004 No. 1438 1173-8324/10/1438-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

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Inpharma 1438 - 22 May 2004

■ Use of heparin-coated rather than noncoatedstents may improve short-term clinical outcomes inpatients undergoing percutaneous coronaryintervention for acute myocardial infarction (MI), sayresearchers from Israel. This nonrandomised studyincluded 238 patients who underwent intracoronarystent implantation, either using a heparin-coated[HepaCoat] stent (n = 124) or a non-heparin-coatedstent.* Patients were prospectively followed for a totalof 180 days. Clinical outcomes at 30 days, such as in-hospital death, recurrent acute MI and stentthrombosis, were significantly better among patientsreceiving heparin-coated stents, compared with thosereceiving non-heparin-coated stents (0% vs 4.4%, 1.6%vs 7% and 0.8% vs 6.1%, respectively). However, therewere no significant differences in clinical outcomesbetween the two groups at 180 days.* During the procedure, patients received unfractionated IVheparin, a bolus of 70 U/kg, adjusted to achieve an activatedclotting time of 225–300 sec. Most patients also received GPIIb/IIIainhibitors. After the procedure, all patients received aspirin200 mg/day and a loading dose of oral clopidogrel 300mg followedby 75 mg/day orally for one month, followed by aspirin alone at adosage of 100 mg/day.

Lev EI, et al. Comparison of outcomes up to six months of heparin-coatedwith noncoated stents after percutaneous coronary intervention for acutemyocardial infarction. American Journal of Cardiology 93: 741-743, No. 6, 15Mar 2004 800976581

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Inpharma 22 May 2004 No. 14381173-8324/10/1438-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved