Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2007;116:1596-1601
doi: 10.1161/CIRCULATIONAHA.106.647271
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by LoGerfo, F. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by LoGerfo, F. W.
Related Collections
Right arrow Health policy and outcome research
Right arrow Other Ethics and Policy
Right arrow Restenosis
Right arrow Carotid Stenosis
Right arrow Embolic stroke
Right arrow Carotid endarterectomy
Right arrow Angioplasty and Stenting

(Circulation. 2007;116:1596-1601.)
© 2007 American Heart Association, Inc.


Controversies in Cardiovascular Medicine

Has the expanded use of carotid stents been justified?

Carotid Stents: Unleashed, Unproven

Frank W. LoGerfo, MD

From Harvard Medical School, Division of Vascular Surgery, and Beth Israel Deaconess Medical Center, Boston, Mass.

Correspondence to Frank W. LoGerfo, MD, William V. McDermott Distinguished Professor of Surgery, Harvard Medical School, Division of Vascular Surgery, Beth Israel Deaconess Medical Center, 110 Francis St, Suite 5B, Boston, MA 02215. E-mail flogerfo@bidmc.harvard.edu


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 


*    Introduction
 
Primarily on the basis of data derived from the Stenting and Angioplasty With Protection in Patients at High Risk for Endarterectomy (SAPPHIRE) trial,1 the US Food and Drug Administration (FDA) has approved the use of carotid stents (CASs) in high-risk patients. The SAPPHIRE trial was published and much heralded as a randomized trial demonstrating that CASs were not inferior to carotid endarterectomy (CEA). Yet, the more recent Endarterectomy Versus Angioplasty in Patients with Symptomatic Carotid Stenosis randomized trial of CASs compared with CEA had to be stopped because the stroke rate with stents was so high that it triggered the safety guidelines of the study design.2 How can we explain the striking difference in outcome between these 2 studies, and how did it happen that the FDA was so convinced of the quality and validity of the SAPPHIRE trial that it granted approval for CASs? An examination of the SAPPHIRE trial—its conduct, data collection and analysis, the circumstances of publication, the presentation to the FDA Advisory Panel, and its consequent approval—is the primary focus of this article. This is a case study of the flaws in our system for the evaluation and approval of medical devices that warrant serious reflection on our ability to properly create and act on accurate information and live up to our commitment to evidence-based decision making.

Response by Samuelson et al p 1601

As it now stands, existing studies leave us with the unfortunate but not unreasonable conclusion that no scientific basis exists for the . . . [Full Text of this Article]