Et Tu, Bare Metal Stent?
2007; Lippincott Williams & Wilkins; Volume: 116; Issue: 21 Linguagem: Alemão
10.1161/circulationaha.107.736918
ISSN1524-4539
AutoresDavid O. Williams, J. Dawn Abbott,
Tópico(s)Cardiac Valve Diseases and Treatments
ResumoHomeCirculationVol. 116, No. 21Et Tu, Bare Metal Stent? Free AccessEditorialPDF/EPUBAboutView PDFView EPUBSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toFree AccessEditorialPDF/EPUBEt Tu, Bare Metal Stent? David O. Williams and J. Dawn Abbott David O. WilliamsDavid O. Williams From the Division of Cardiology, Department of Medicine, Rhode Island Hospital, The Warren Alpert School of Medicine, Brown University, Providence, RI. and J. Dawn AbbottJ. Dawn Abbott From the Division of Cardiology, Department of Medicine, Rhode Island Hospital, The Warren Alpert School of Medicine, Brown University, Providence, RI. Originally published20 Nov 2007https://doi.org/10.1161/CIRCULATIONAHA.107.736918Circulation. 2007;116:2363–2365When performing percutaneous coronary revascularization, physicians nearly always supplement balloon angioplasty with a stent.1 This decision is based on evidence that stent implantation enhances the procedural success and durability of angioplasty. Benefits of stenting, compared with balloon angioplasty, include a reduction in the incidence of lesion recurrence, manifested as reduced need for repeat revascularization and lower rates of periprocedural myocardial infarction (MI).2–5 The major shortcoming of bare metal stents (BMS) is that ≈20% of native vessel and 30% of saphenous vein graft patients develop angiographic restenosis from neointimal hyperplasia. About half of these patients will have clinical restenosis and require repeat revascularization. In contrast to the favorable results of stents in de novo lesions, stenting of in-stent restenotic lesions with BMS results in more restenosis. Before the drug-eluting stent (DES) era, of multiple therapies investigated, only intracoronary brachytherapy was effective in preventing recurrent in-stent restenosis.6,7Article p 2391Fortunately, the DES was developed to suppress neointimal hyperplasia, and several randomized, double-blind, clinical trials demonstrated the ability of DES to substantially reduce the incidence of in-stent restenosis.8–10 Within a short time after commercialization, DES nearly replaced BMS in the United States, and the number of patients requiring repeat revascularization fell substantially.1As clinical restenosis became infrequent, another potential and untoward event related to stents became more exposed—namely, stent thrombosis. This disorder can cause abrupt coronary occlusion and frequently clinically manifests as acute MI or death. Although stent thrombosis was common during the early years of BMS use, improvements in the technique of stent implantation and the administration of both aspirin and a thienopyridine (dual antiplatelet therapy) reduced the incidence of acute stent thrombosis to clinically acceptable levels.11,12 More recently, however, some investigators have suggested that the incidence of stent thrombosis in patients treated with DES was excessive and greater than that of patients treated with BMS.13 The initial randomized trials comparing DES with BMS in patients with noncomplex coronary disease do not support this contention.14,15 What does appear to be a valid concern, however, is that DES patients must take dual antiplatelet therapy for an extended period of time to achieve outcomes equivalent to BMS patients, and that when stent thrombosis is observed in DES patients, it may occur late (ie, >1 year after implantation).16 Moreover, there has been a general perception that the risk of stent thrombosis in BMS is limited to the first few weeks and that there is no need for dual antiplatelet therapy beyond 1 month. Accordingly, clinicians now favor BMS for patients who cannot take uninterrupted dual antiplatelet therapy for at least a year and accept the increased risk that such patients will experience restenosis.16Doyle et al17 suggest in this issue of Circulation that some of our perceptions about the safety of BMS may be incorrect. In a retrospective analysis of a percutaneous coronary revascularization database, these investigators analyzed the frequency and outcomes of stent thrombosis and restenosis during extended follow-up in 4503 patients treated with at least 1 BMS. The primary findings, which have been reported but are underappreciated, are that late (>30 days) and very late (>1 year) stent thrombosis do occur with BMS and are associated with MI and death, and that restenosis can occur late (>1 year) and uncommonly presents as MI (2.1%), but in these patients the death rate is increased. With regard to the occurrence of late BMS thrombosis, the majority of events occurred within the first year, and there was a steady incidence of stent thrombosis out to 10 years, albeit at a very low rate. Many similarities between BMS and DES are highlighted in the study by Doyle et al,17 including the common use of stents for off-label indications, risk factors for late stent thrombosis (such as acute MI as procedural indication), and the clinical presentation of stent thrombosis. As recently reported with DES, stent thrombosis was more common among patients with an off-label indication18,19; however, in the study by Doyle et al17 the findings were driven by saphenous vein graft interventions. The authors concluded that BMS may not be as safe as initially considered and share some of the risks for untoward events noted among DES-treated patients.Strengths of this report include the size and consecutive enrollment of the study cohort; the duration of follow-up; the use of standardized definitions, including the most contemporary definition of stent thrombosis; and the methodologies used for data collection and analysis. On the other hand, the reported cohort reflects the practice patterns of only 1 medical center, and follow-up was available for only 93% of patients, some of whom may not have been contacted in ≤2 years. Accordingly, the ability to generalize these findings broadly may be limited, and the rates of death and MI may be underestimated.What are the clinical implications of this report? First, as noted by the authors, in-stent restenosis must be considered more than just a nuisance disorder because it can present as MI. Although infrequent (87 cases), these events accounted for more absolute MI events than did stent thrombosis (74 cases) in the report by Doyle et al.17 Accordingly, one might postulate that in-stent restenosis–related MI would be observed less commonly among DES-treated patients than BMS-treated patients. Such a finding may offset any increase in MI associated with late DES thrombosis and help explain the lack of difference in rates of death and MI observed during extended follow-up of the original BMS versus DES randomized trials14,15 and large prospective observational studies.Second, use of a BMS does not protect against the occurrence of late or very late stent thrombosis. Therefore, this mechanism of coronary occlusion should be considered in BMS-treated patients, even if it occurs years after the BMS procedure, in addition to progression of coronary disease. Also, one might wonder about the possible impact of extended dual antiplatelet therapy on the stent thrombosis and MI event rates in this population. The findings of Doyle et al17 suggest that dual antiplatelet therapy might be of special value for patients who receive a BMS for lesions located in coronary saphenous bypass grafts, but this remains untested.Third, not mentioned by the authors is the prominent disparity between the overall rates of death and MI in their study and those attributable to either stent thrombosis or restenosis. At 10 years, the overall rate of death or MI was 39.9%. The rate of MI attributable to restenosis was 2.1%, and the total rate of stent thrombosis was 2.0%. At worst, the combined rate of death/MI attributable to either event was <5%. Thus, the contribution of the stented lesion to major adverse cardiac events is comparatively small. This observation highlights the need to investigate further other mechanisms of death and MI among patients who undergo percutaneous coronary revascularization and to initiate more aggressive therapies to reduce the occurrence of these events.Not limited to the present report from Doyle et al17 is a general concern about our ability to accurately identify the incidence of stent thrombosis during extended patient follow-up. For example, in this report, all cases of late stent thrombosis presented with MI, and a subset of MI events were attributed to restenosis. Can we be certain of the mechanism of these events given the limitation of angiography and intravascular ultrasound for determining the pathophysiology of an event? Ideally, stent thrombosis should be counted only when the criteria of definite stent thrombosis are satisfied. Including patients with probable stent thrombosis tends to overestimate its frequency because mechanisms other than stent thrombosis, such as disease progression, can cause MI in the distribution of the stented artery. On the other hand, this definition also fails to capture patients who experience sudden death as a result of stent thrombosis. We wish to emphasize the importance of using the end points of death and MI when comparing different types of stents. Definitions for MI are standardized and well accepted, and data to determine this end point are ascertainable. Furthermore, all-cause death can be determined without ambiguity. Clinical investigations should emphasize the importance of obtaining complete follow-up, especially for vital status, to permit a more valid comparison of interventional devices.The opinions expressed in this article are not necessarily those of the editors or of the American Heart Association.DisclosuresDr Williams receives research support form Cordis Corporation (a Johnson and Johnson Company), Boston Scientific Corporation, and Abbott Vascular Corporation, and serves as a consultant for Cordis Corporation. Dr Abbott reports no conflicts.FootnotesCorrespondence to David O. Williams, MD, APC 814, Rhode Island Hospital, 593 Eddy St, Providence, RI 02903. E-mail [email protected] References 1 Williams DO, Abbott JD, Kip KE; DEScover Investigators. Outcomes of 6906 patients undergoing percutaneous coronary intervention in the era of drug-eluting stents: report of the DEScover Registry. Circulation. 2006; 114: 2154–2162.LinkGoogle Scholar2 Srinivas VS, Brooks MM, Detre KM, Johnston J, King SB 3rd, Jacobs AK, Williams DO. A decade of improvement in the clinical outcomes of percutaneous coronary intervention for multivessel coronary artery disease. Circulation. 2003; 107: e88.LinkGoogle Scholar3 Kiemeneij F, Serruys PW, Macaya C, Rutsch W, Heyndrickx G, Albertsson P, Fajadet J, Legrand V, Materne P, Belardi J, Sigwart U, Colombo A, Goy JJ, Disco CM, Morel MA. Continued benefit of coronary stenting versus balloon angioplasty: five-year clinical follow-up of Benestent-I trial. J Am Coll Cardiol. 2001; 37: 1598–1603.CrossrefMedlineGoogle Scholar4 Serruys PW, de Jaegere P, Kiemeneij F, Macaya C, Rutsch W, Heyndrickx G, Emanuelsson H, Marco J, Legrand V, Materne P, Belardi J, Sigwart U, Colombo A, Goy JJ, van den Heuvel P, Delcan J, Morel M. A comparison of balloon-expandable-stent implantation with balloon angioplasty in patients with coronary artery disease. Benestent Study Group. N Engl J Med. 1994; 331: 489–495.CrossrefMedlineGoogle Scholar5 Fischman DL, Leon MB, Baim DS, Schatz RA, Savage MP, Penn I, Detre K, Veltri L, Ricci D, Nobuyoshi M, Cleman M, Heuser R, Almond D, Teirstein PS, Fish RD, Colombo A, Brinker J, Moses J, Shaknovich A, Hirshfeld J, Bailey S, Ellis S, Rake R, Goldberg S. A randomized comparison of coronary-stent placement and balloon angioplasty in the treatment of coronary artery disease. Stent Restenosis Study Investigators. N Engl J Med. 1994; 331: 496–501.CrossrefMedlineGoogle Scholar6 Teirstein PS, Massullo V, Jani S, Popma JJ, Russo RJ, Schatz RA, Guarneri EM, Steuterman S, Sirkin K, Cloutier DA, Leon MB, Tripuraneni P. Three-year clinical and angiographic follow-up after intracoronary radiation: results of a randomized clinical trial. Circulation. 2000; 101: 360–365.CrossrefMedlineGoogle Scholar7 Silber S, Popma JJ, Suntharalingam M, Lansky AJ, Heuser RR, Speiser B, Teirstein PS, Bass T, O'Neill W, Lasala J, Reisman M, Sharma SK, Kuntz RE, Bonan R; for the Start Investigators. Two-year clinical follow-up of 90Sr/90 Y beta-radiation versus placebo control for the treatment of in-stent restenosis. Am Heart J. 2005; 149: 689–694.CrossrefMedlineGoogle Scholar8 Morice MC, Serruys PW, Sousa JE, Fajadet J, Ban Hayashi E, Perin M, Colombo A, Schuler G, Barragan P, Guagliumi G, Molnar F, Falotico R; for the Ravel Study Group. A randomized comparison of a sirolimus-eluting stent with a standard stent for coronary revascularization. N Engl J Med. 2002; 346: 1773–1780.CrossrefMedlineGoogle Scholar9 Moses JW, Leon MB, Popma JJ, Fitzgerald PJ, Holmes DR, O'Shaughnessy C, Caputo RP, Kereiakes DJ, Williams DO, Teirstein PS, Jaeger JL, Kuntz RE; for the Sirius Investigators. Sirolimus-eluting stents versus standard stents in patients with stenosis in a native coronary artery. N Engl J Med. 2003; 349: 1315–1323.CrossrefMedlineGoogle Scholar10 Stone GW, Ellis SG, Cox DA, Hermiller J, O'Shaughnessy C, Mann JT, Turco M, Caputo R, Bergin P, Greenberg J, Popma JJ, Russell ME; Taxus-IV Investigators. One-year clinical results with the slow-release, polymer-based, paclitaxel-eluting TAXUS stent: the TAXUS-IV trial. Circulation. 2004; 109: 1942–1947.LinkGoogle Scholar11 Leon MB, Baim DS, Popma JJ, Gordon PC, Cutlip DE, Ho KK, Giambartolomei A, Diver DJ, Lasorda DM, Williams DO, Pocock SJ, Kuntz RE. A clinical trial comparing three antithrombotic-drug regimens after coronary-artery stenting. Stent Anticoagulation Restenosis Study Investigators. N Engl J Med. 1998; 339: 1665–1671.CrossrefMedlineGoogle Scholar12 Nakamura S, Hall P, Gaglione A, Tiecco F, Di Maggio M, Maiello L, Martini G, Colombo A. High pressure assisted coronary stent implantation accomplished without intravascular ultrasound guidance and subsequent anticoagulation. J Am Coll Cardiol. 1997; 29: 21–27.CrossrefMedlineGoogle Scholar13 Camenzind E, Steg PG, Wijns W. A meta-analysis of first generation drug eluting stent programs. Presented at Hotline Session I, World Congress of Cardiology 2006, Barcelona, Spain, September 2–5, 2006. Abstract.Google Scholar14 Mauri L, Hsieh W, Massaro JM, Ho K, D'Agostino R, Cutlip DE. Stent thrombosis in randomized clinical trials of drug-eluting stents. N Engl J Med. 2007; 365: 1020–1029.Google Scholar15 Stone GW, Moses JW, Ellis SE, Schofer J, Dawkins KD, Morice MC, Colombo A, Schampaert E, Grube E, Kirtane AJ, Cutlip DE, Fahy M, Pocock SJ, Mehran R, Leon MB. Safety and efficacy of sirolimus- and paclitaxel-eluting coronary stents. N Engl J Med. 2007; 356: 998– 1008.CrossrefMedlineGoogle Scholar16 Grines CL, Bonow RO, Casey DE Jr, Gardner TJ, Lockhart PB, Moliterno DJ, O'Gara P, Whitlow P. Prevention of premature discontinuation of dual antiplatelet therapy in patients with coronary artery stents: a science advisory from the American Heart Association, American College of Cardiology, Society for Cardiovascular Angiography and Interventions, American College of Surgeons, and American Dental Association, with representation from the American College of Physicians. Circulation. 2007; 115: 813–818.LinkGoogle Scholar17 Doyle B, Rihal CS, O'Sullivan CJ, Lennon RJ, Wiste HJ, Bell M, Bresnahan JF, Holmes DR Jr. Outcomes of stent thrombosis and restenosis during extended follow-up of patients treated with bare-metal coronary stents. Circulation. 2007; 116: 2391–2398.LinkGoogle Scholar18 Beohar N, Davidson CJ, Kip KE, Goodreau L, Vlachos HA, Meyers SN, Benzuly KH, Flaherty JD, Ricciardi MJ, Bennett CL, Williams DO. Outcomes and complications associated with off-label and untested use of drug-eluting stents. JAMA. 2007; 297: 1992–2000.CrossrefMedlineGoogle Scholar19 Win HK, Caldera AE, Maresh K, Lopez J, Rihal CS, Parikh MA, Granada JF, Marulkar S, Nassif D, Cohen DJ, Kleiman NS; EVENT Registry Investigators. Clinical outcomes and stent thrombosis following off-label use of drug-eluting stents. JAMA. 2007; 297: 2001–2009.CrossrefMedlineGoogle Scholar eLetters(0)eLetters should relate to an article recently published in the journal and are not a forum for providing unpublished data. Comments are reviewed for appropriate use of tone and language. Comments are not peer-reviewed. Acceptable comments are posted to the journal website only. Comments are not published in an issue and are not indexed in PubMed. Comments should be no longer than 500 words and will only be posted online. References are limited to 10. Authors of the article cited in the comment will be invited to reply, as appropriate.Comments and feedback on AHA/ASA Scientific Statements and Guidelines should be directed to the AHA/ASA Manuscript Oversight Committee via its Correspondence page.Sign In to Submit a Response to This Article Previous Back to top Next FiguresReferencesRelatedDetailsCited By Cheong S, Kim Y, Koh Y, Shin W, Lee J, Kim W, Yoo Y and Park S (2014) Effect of Drug Eluting Uniformity for Biodegradable Stent by Solid Freeform Fabrication, Polymer Korea, 10.7317/pk.2014.38.1.93, 38:1, (93-97), Online publication date: 25-Jan-2014. Lobato E (2008) Coronary Stents and Noncardiac Surgery: Treat the Patient, Not the Stent!, Journal of Cardiothoracic and Vascular Anesthesia, 10.1053/j.jvca.2008.09.003, 22:6, (803-805), Online publication date: 1-Dec-2008. Holmes D, Teirstein P, Satler L, Sketch M, Popma J, Mauri L, Wang H, Schleckser P and Cohen S (2008) 3-Year Follow-Up of the SISR (Sirolimus-Eluting Stents Versus Vascular Brachytherapy for In-Stent Restenosis) Trial, JACC: Cardiovascular Interventions, 10.1016/j.jcin.2008.05.010, 1:4, (439-448), Online publication date: 1-Aug-2008. November 20, 2007Vol 116, Issue 21 Advertisement Article InformationMetrics https://doi.org/10.1161/CIRCULATIONAHA.107.736918PMID: 18025401 Originally publishedNovember 20, 2007 Keywordsstentscoronary diseaseEditorialsPDF download Advertisement SubjectsStent
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