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DOI 10.1016/j.jcin.2014.01.158

Медицинская библиотека · JACC. Cardiovascular interventions · 2014

Pivotal trial to evaluate the safety and efficacy of the orbital atherectomy system in treating de novo, severely calcified coronary lesions (ORBIT II).

Chambers Jeffrey W, Feldman Robert L, Himmelstein Stevan I, Bhatheja Rohit, Villa Augusto E, Strickman Neil E, Shlofmitz Richard A, Dulas Daniel D, Arab Dinesh, Khanna Puneet K, Lee Arthur C, Ghali Magdi G H, Shah Rakesh R, Davis Thomas P, Kim Christopher Y, Tai Zaheed, Patel Kirit C, Puma Joseph A, Makam Prakash, Bertolet Barry D, Nseir Georges Y

Клиническое исследованиеСтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVES

The ORBIT II (Evaluate the Safety and Efficacy of OAS in Treating Severely Calcified Coronary Lesions) trial evaluated the safety and efficacy of the coronary Orbital Atherectomy System (OAS) to prepare de novo, severely calcified coronary lesions for stent placement.

BACKGROUND

Despite advances in interventional techniques, treatment of calcified coronary lesions remains a challenge. Stent placement in these lesions may result in stent underexpansion, malapposition, and procedural complications.

METHODS

ORBIT II is a prospective, multicenter, nonblinded clinical trial that enrolled 443 consecutive patients with severely calcified coronary lesions at 49 U.S. sites from May 25, 2010, to November 26, 2012. Investigators used the centrifugal action of the OAS diamond-coated crown to modify calcified lesions prior to stent placement.

RESULTS

The pre-procedure mean minimal lumen diameter of 0.5 mm increased to 2.9 mm after the procedure. The primary safety endpoint was 89.6% freedom from 30-day major adverse cardiac events compared with the performance goal of 83%. The primary efficacy endpoint (residual stenosis <50% post-stent without in-hospital major adverse cardiac events) was 88.9% compared with the performance goal of 82%. Stent delivery occurred successfully in 97.7% of cases with <50% stenosis in 98.6% of subjects. Low rates of in-hospital Q-wave myocardial infarction (0.7%), cardiac death (0.2%), and target vessel revascularization (0.7%) were reported.

CONCLUSIONS

The ORBIT II coronary OAS trial met both the primary safety and efficacy endpoints by significant margins. Preparation of severely calcified plaque with the OAS not only helped facilitate stent delivery, but improved both acute and 30-day clinical outcomes compared with the outcomes of historic control subjects in this difficult-to-treat patient population. (Evaluate the Safety and Efficacy of OAS in Treating Severely Calcified Coronary Lesions [ORBIT II]; NCT01092416).

Для цитирования: Chambers Jeffrey W, Feldman Robert L, Himmelstein Stevan I, Bhatheja Rohit, Villa Augusto E, Strickman Neil E, Shlofmitz Richard A, Dulas Daniel D, Arab Dinesh, Khanna Puneet K, Lee Arthur C, Ghali Magdi G H, Shah Rakesh R, Davis Thomas P, Kim Christopher Y, Tai Zaheed, Patel Kirit C, Puma Joseph A, Makam Prakash, Bertolet Barry D, Nseir Georges Y. Pivotal trial to evaluate the safety and efficacy of the orbital atherectomy system in treating de novo, severely calcified coronary lesions (ORBIT II).. JACC. Cardiovascular interventions. 2014. DOI: 10.1016/j.jcin.2014.01.158.

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