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J Am Coll Cardiol, 2002; 39:1581-1587
© 2002 by the American College of Cardiology Foundation
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A prospective, multicenter, randomized trial of percutaneous transmyocardial laser revascularization in patients with nonrecanalizable chronic total occlusions

Gregg W. Stone, MD, FACC*,*, Paul S. Teirstein, MD, FACC{dagger}, Ronald Rubenstein, MD, FACC{ddagger}, Dwayne Schmidt, MD, FACC§, Patrick L. Whitlow, MD, FACC||, Edward J. Kosinski, MD, FACC, Gregory Mishkel, MD, FACC# and John A. Power, MD, FACC**

* Cardiovascular Research Foundation, New York, New York, USA
{dagger} Scripps Clinic and Research Institute, La Jolla, California, USA
{ddagger} Jersey Shore Medical Center, Neptune, New Jersey, USA
§ Presbyterian Hospital, Oklahoma City, Oklahoma, USA
|| Cleveland Clinic Foundation, Cleveland, Ohio, USA
St. Vincent’s Medical Center, Bridgeport, Connecticut, USA
# St. John’s Hospital and Memorial Medical Center, Springfield, Illinois, USA
** St. Francis Hospital, Lawrenceville, Pennsylvania, USA



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Figure 1 Vessel distribution of chronic total occlusions that were unsuccessfully dilated in patients randomized to percutaneous transmyocardial revascularization (PTMR) versus maximal medical therapy (MMT). LAD = left anterior descending coronary artery; LCX = left circumflex coronary artery; RCA = right coronary artery.

 


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Figure 2 Canadian Heart Association angina class at six months in the study group. PTMR = percutaneous transmyocardial revascularization; MMT = maximal medical therapy.

 


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Figure 3 Results of the pre-discharge questionnaire of treatment assignment. PTMR = percutaneous transmyocardial revascularization; MMT = maximal medical therapy.

 


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Figure 4 Improvement in exercise duration from baseline to six months in patients randomized to percutaneous transmyocardial revascularization (white bars) with the Eclipse holmium/yttrium aluminum garnet laser versus maximal medical therapy (black bars) in the present study (patients with non-revascularizable chronic total occlusions (CTOs); left bars) compared with a previous study with the same device in a different patient group (patients with end-stage ischemic heart disease with no revascularization options; right bars).

 





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