(Circulation. 2001;104:2620.)
© 2001 American Heart Association, Inc.
Clinical Cardiology: New Frontiers |
From the Division of Cardiovascular Diseases (P.S.T.), Scripps Clinic, La Jolla, Calif; and the Divisions of Clinical Biometrics and Cardiology (R.E.K.), Brigham and Womens Hospital, Boston, Mass.
Correspondence to Paul S. Teirstein, MD, Division of Cardiovascular Diseases, Scripps Clinic, 10666 North Torrey Pines Road, La Jolla, CA 92037. E-mail Radman@scrippsclinic.com
Key Words: radioisotopes restenosis stents angioplasty
| Introduction |
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The treatment of restenosis with vascular radiation appears to work through inhibition of smooth muscle cell proliferation. The energy emitted from an active isotope is believed to block mitosis by causing a double-stranded break in the cells DNA (Figure 1).3,4 Thus, by performing surgery on the vascular smooth muscle cells DNA, radiation prevents the proliferative ingrowth of tissue that often reblocks the vessel lumen after a successful angioplasty. The United States Food and Drug Administrations recent premarket approval of two radiation devices has now propelled this first effective antiproliferative treatment into the mainstream of patient care. This report provides an overview of the basic laboratory and clinical data supporting the effectiveness of brachytherapy as well as some of the challenges and controversies surrounding its integration into clinical practice.
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