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J Am Coll Cardiol, 2001; 37:856-862
© 2001 by the American College of Cardiology Foundation
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CLINICAL STUDY: INTERVENTIONAL CARDIOLOGY

Coronary artery stenting in the aged

Manish S. Chauhan, MD* {ddagger}, Richard E. Kuntz, MD, MSc{dagger} {ddagger}, Kalon K. L. Ho, MD, MSc, FACC* {ddagger}, David J. Cohen, MD, MSc*, Jeffrey J. Popma, MD, FACC{dagger}, Joseph P. Carrozza, Jr, MD, FACC*, Donald S. Baim, MD, FACC{dagger} and Donald E. Cutlip, MD, FACC{ddagger}

* Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA
{dagger} Brigham and Women’s Hospital, Boston, Massachusetts, USA
{ddagger} Harvard Clinical Research Institute and Cardiovascular Data Analysis Center, Boston, Massachusetts, USA

Manuscript received April 12, 2000; revised manuscript received October 16, 2000, accepted November 17, 2000.

Reprint requests and correspondence: Dr. Manish S. Chauhan, Interventional Cardiology Section, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, Massachusetts 02215
mchauhan{at}caregroup.harvard.edu


    Abstract
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 Methods
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 Discussion
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OBJECTIVES

The study compared the safety and efficacy of coronary artery stenting in aged and nonaged patients and identified predictors of adverse clinical outcomes.

BACKGROUND

Limited data are available on the outcomes of stenting in the aged (≥80 years) compared to nonaged patients.

METHODS

The study was a pooled analysis of 6,186 patients who underwent coronary artery stenting in six recent multicenter trials. A clinical events committee adjudicated clinical end points, and quantitative angiography was performed by an independent core laboratory.

RESULTS

There were 301 (4.9%) aged patients (≥80 years). Compared to nonaged patients, aged patients had a higher prevalence of multivessel disease (16.5% vs. 9.6%, p = 0.001), unstable angina (50.8% vs. 42.1%, p = 0.003), moderate to severe target lesion calcification (30.4% vs. 15.3%, p = 0.001) and smaller reference vessel diameter (2.90 mm vs. 2.98 mm, p = 0.004). Procedural success rate (97.4% vs. 98.5%, p = 0.14) was similar in the two groups. In-hospital mortality (1.33% vs. 0.10%, p = 0.001), bleeding complications (4.98% vs. 1.00%, p < 0.001) and one-year mortality (5.65% vs. 1.41%, p < 0.001) were significantly higher for the aged patients. Clinical restenosis was similar for the two groups (11.19% vs. 11.93%, p = 0.78). Advanced age, diabetes, prior myocardial infarction and presence of three-vessel disease were independent predictors of long-term mortality.

CONCLUSIONS

Coronary artery stenting can be performed safely in patients ≥80 years of age, with excellent acute results and a low rate of clinical restenosis, albeit with higher incidences of in-hospital and long-term mortality, and vascular and bleeding complications compared to nonaged patients.

Abbreviations and Acronyms
  CABG = coronary artery bypass graft
  EPISTENT = Evaluation of Platelet IIb/IIIa Inhibitor for Stenting Trial
  Gp = glycoprotein
  MI = myocardial infarction
  PCI = percutaneous coronary intervention
  QCA = quantitative coronary angiography
  QMI = Q-wave myocardial infarction
  STARS = Stent Antithrombotic Regimen Study
  TLR = target lesion revascularization
  TVR = target vessel revascularization


The aged (≥80 years) form the most rapidly growing segment of the U.S. population (1). Because the prevalence of coronary artery disease is higher in older patients, more of them are presenting for percutaneous coronary interventions (PCIs). These patients are more likely to have multivessel coronary artery disease and heavy calcification of the vessels, as well as other co-morbid conditions that place them at a higher risk for peri-procedural complications (2–4). At the same time, the use of coronary stents is steadily increasing to include high-risk indications, including older patients, and this currently constitutes over 60% of all coronary interventional procedures.

Earlier studies have reported a low rate of procedure success (<50% diameter stenosis without death, myocardial infarction [MI], or emergent bypass surgery) and high rates of major complications in older patients undergoing balloon angioplasty, including up to 8.4% 30-day mortality and 14% incidence of MI (2–14). In addition, older age has previously been reported to be a predictor of in-hospital mortality, as well as major ischemic and vascular complications in various small single-center angioplasty and stent studies. Data on the safety, efficacy and clinical outcomes of coronary stenting in the aged using modern deployment techniques and newer stent designs are limited.

The purpose of this study was to assess the success and safety of coronary artery stenting in the aged compared to the nonaged and to identify predictors of adverse outcomes using prospectively collected data from a large cohort of patients from recent multicenter clinical trials.


    Methods
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Study design.   Patients enrolled in six recent major clinical trials of coronary stenting, between September 1995 and March 1999, formed the cohort for this analysis. These included four randomized trials comparing new stent designs (MultiLink, NIR, AVE Micro II, Bard XT) with the Palmaz-Schatz stent, Crossflex stent registry and the Stent Antithrombotic Regimen Study (STARS) trial (aspirin only and aspirin plus Coumadin groups were excluded), which compared three antithrombotic regimens following successful Palmaz-Schatz coronary stenting (15–21). All these trials had similar inclusion and exclusion criteria. In general, patients were to have focal (<20 mm) lesions with 50% to 99% diameter stenosis in a vessel, with visually estimated reference diameter >3 mm, that could be covered by one to two stents. Patients with recent preprocedural MI or left ventricular ejection fraction <30% were excluded from the trials. All trials were coordinated by the Cardiovascular Data Analysis Center (CDAC, Boston, Massachusetts). Primary data as well as quantitative angiographic data (using CMS-GFT algorithm) for each of these trials were collected prospectively and entered in separate databases at the CDAC using Microsoft Access 2.0. Following data cleaning and electronic validation of data entry for each study database, standard data tables were generated and then combined into a pooled database with unique patient identification.

Study population and stenting protocol.   All patients treated within the six clinical trials who received at least one coronary stent and who were treated with aspirin and ticlopidine following the stent procedure were eligible for this analysis. The pooled data set included 6,186 patients who underwent stenting of 6,219 target lesions. The stenting protocol for each study included routine high-pressure postdilation with recommended balloon: artery ratios of 1.1–1.2. Aspirin 325 mg daily and ticlopidine 250 mg twice daily for four weeks formed the standard postprocedure antithrombotic regimen. Use of Gp (glycoprotein) IIb/IIIa inhibitors was discouraged in all of the studies, but they could be used at the discretion of the investigator and accounted for only 7.6% of patients overall. All patients were followed at prespecified points for 9 to 12 months in the individual trials, and a subgroup of patients had routine angiographic follow-up at 6 to 9 months.

Definitions.   Myocardial infarction (MI) included either Q-wave MI (QMI) (defined as presence of new regional pathologic Q-waves as reported by the blinded electrocardiogram [ECG] core laboratory) or non-QMI (defined as CK-MB [creatine kinase, MB fraction] values greater than three times normal or total CK more than two times the upper limit of normal for each respective clinical site, in the absence of new Q-waves). Vascular complications included access site-related hematoma >4 cm, pseudoaneurysm, atrioventricular (AV) fistula, retroperitoneal bleed or vascular surgical repair. Bleeding complications were reported as any procedure-related blood loss requiring transfusion. Stent thrombosis was defined as angiographic documentation of stent occlusion, sudden unexplained death within 30 days of the stenting procedure when the stent was not known to be patent, recurrent MI in the target vessel territory, or urgent target lesion revascularization (TLR). Either TLR or TVR (target vessel revascularization) required the presence of clinical or functional evidence of ischemia and >50% stenosis by quantitative coronary angiography (QCA) or the presence of a restenotic lesion >70% by QCA in the absence of documented ischemia. An independent Clinical Events Committee (CEC), blinded to the treatment assignment for randomized cohorts, adjudicated all clinical events.

Justification for pooled analyses.   These prospective studies, which were performed at the same clinical sites over a narrow time period, had nearly identical inclusion criteria, stenting protocols, similar case report forms with entry in standard databases, clinical follow-up and end point definitions as well as event adjudication by the same CEC for each study. Furthermore, the same angiographic core laboratory (Washington Hospital Center, Washington, D.C.) performed the qualitative and quantitative analyses for each study. The similarity of baseline patient and lesion characteristics across the various studies further validates the uniformity of the studies (15–21).

Statistical analysis.   The primary analysis consisted of comparison of parameters in the two cohorts stratified by age. Continuous variables (e.g., minimal luminal diameter) were compared using the Student t test, and categorical data were compared using the chi-square test (or the Fisher’s exact test where appropriate). A two-sided p value of p < 0.05 was required for statistical significance. Survival estimates were computed using Kaplan-Meier methods and compared using log-rank tests. Stepwise multivariable analysis using logistic regression models was performed to identify independent predictors of each end point. Several different multivariable models for predictors of death and vascular complications were constructed. Models that had a better discriminatory ability (higher c-statistic) and calibration (higher p value for the Hosmer-Lemeshow {chi}2 statistic) were used. Missing data were not imputed, and mortality rates were not different between patients with complete versus missing data for the covariates evaluated. All statistical analyses were performed using SAS for Windows (version 6.12, SAS Institute, Cary, North Carolina).


    Results
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Baseline clinical and angiographic characteristics.   Of the 6,186 patients undergoing stenting, there were 301 aged patients, which constituted 4.9% of the study population. Significant differences existed in the prevalence of many established risk factors for coronary artery disease (Table 1). Aged patients were more likely to present with unstable angina and to have multivessel disease.


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Table 1 Baseline Clinical Characteristics

 
Angiographically, the aged patients had slightly but significantly smaller reference vessel and lesion length, and they were more likely to have moderate to severely calcified target lesions (Table 2). Other angiographic characteristics including vessel treated and American College of Cardiology/American Heart Association (ACC/AHA) lesion class were not significantly different between the two age groups.


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Table 2 Baseline Angiographic Findings (per Angiographic Core Laboratory)

 
Procedural and angiographic results.   In keeping with a higher prevalence of heavily calcified lesions, aged patients were more likely to have pretreatment with rotational atherectomy. Otherwise, procedural characteristics (Table 3) were similar with nearly identical balloon:artery ratios and maximum post-stent balloon inflation pressures. Significant dissections before stenting were less common in aged patients, and aged patients required significantly shorter total stent length per treated vessel. Overall, lesion success and procedure rates were similar between the two age groups.


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Table 3 Procedural and Angiographic Data (per Angiographic Core Laboratory)

 
In-hospital major clinical events.   In-hospital mortality was significantly higher in the aged (Table 4). Peri-procedural non-QMI was nonsignificantly higher in the aged group. Aged patients also had a significantly higher incidence of vascular and bleeding complications.


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Table 4 In-Hospital Major Clinical Events

 
Clinical follow-up.   The mean follow-up time was 282 ± 85 days (Table 5). The one-year mortality in the aged group was significantly higher than in the nonaged (Fig. 1; Kaplan-Meier estimate 7.5% vs. 1.6%, log-rank p = 0.0001). There was no significant difference in the incidence of recurrent MI, TLR or TVR.


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Table 5 Long-Term Cumulative Clinical Events

 


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Figure 1 Kaplan-Meier curve of one-year survival in the aged and nonaged patients.

 
Multivariable modeling for predictors of mortality.   Older age was a significant independent predictor of one-year mortality, with a 5% increase in risk per decade of life (per decade, odds ratio [OR] 1.05; 95% confidence interval [CI] 1.03–1.07, Table 6). The other significant predictors of mortality included history of prior MI (OR 2.03; 95% CI 1.35–3.07), presence of diabetes (OR 1.97; 95% CI 1.29–3.02) and three-vessel disease (OR 1.62; 95% CI 1.25–2.10).


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Table 6 Multivariable Modeling and Predictors of Mortality at One Year

 
Multivariable modeling for predictors of vascular and bleeding complications.   In-hospital repeat revascularization (OR 9.94; 95% CI 3.93–25.15), female gender (OR 3.49; 95% CI 2.31–5.27) and older age (OR 1.06 per decade; 95% CI 1.04–1.08) were independent predictors of the occurrence of vascular or bleeding complications (Table 7).


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Table 7 Predictors of Vascular and/or Bleeding Complications

 

    Discussion
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 Results
 Discussion
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Elderly patients have traditionally been considered a high-risk population for PCIs with a higher incidence of procedural failure and complications compared to younger patients (2–14). Our study of 301 patients ≥80 years old represents the largest reported series of aged patients undergoing coronary artery stenting, and more notably in the era of new second-generation stents and routine high-pressure dilation. Aged patients in our study had >97% procedure success rate despite smaller reference vessel diameters and more prevalent calcification, albeit with a significantly higher incidence of both in-hospital and one-year mortality compared to the nonaged patients.

Procedural results and acute clinical outcomes.   Although the lesion complexity by ACC/AHA classification was not significantly different in the aged patients, the reference vessel diameter was significantly smaller, and heavily calcified lesions were more frequent, accounting for the associated greater use of pre-stenting rotational atherectomy. Similar findings have been reported in prior studies (4,5). Despite these unfavorable characteristics, the lesion success rate was high. The frequency of procedure success (defined as lesion success in the absence of death, MI or emergent coronary artery bypass graft [CABG]) was also no different from nonaged patients and was somewhat higher than that reported by DeGregorio et al. (4) in their recent single-center study of 137 patients ≥75 years (90% vs. 93%, p = NS). This difference may reflect a healthier population enrolled in the representative clinical trials. Of note, dissections prior to stenting were slightly less frequent in aged patients, and this accounts in part for the significantly shorter stent lengths that were required.

Mortality and aged patients.   The aged patients had a higher incidence of in-hospital mortality (1.33% vs. 0.10%, p = 0.001) compared to the nonaged patients, although this incidence was still lower than the 2.2% to 3.1% in-hospital mortality previously reported (2,4). Not surprisingly, age was an independent predictor of overall mortality at one year, with an increased risk of 5% per decade of life. This increase was driven primarily by the continued increased risk for death more than 30 days after the index procedure (Fig. 1). Aged patients had a higher frequency of multivessel coronary artery disease, and the worse prognosis is likely a reflection of the expected poorer outcomes of patients with more severe and diffuse disease. There are limited comparative data on the long-term mortality in aged patients undergoing stenting, but the available studies have shown similar results. Abizaid et al. (2) reported 4.8% one-year mortality after stenting in subjects >80 years old. Among 137 stented patients >75 years old, DeGregorio et al. (4) reported a procedural mortality rate of 2.2% and an overall 7.3% mortality rate through one year of follow-up.

Myocardial infarction and aged patients.   An increased risk for peri-procedural MI has been associated with increased plaque burden and extent of coronary artery disease (22,23). Certainly, in this aged population with higher frequency of multivessel disease and smaller reference vessel size it is likely that overall plaque burden was also increased. Furthermore, greater use of rotational atherectomy in the aged patients places them at a higher risk for peri-procedural MI (24). Previous reports have suggested an incidence of 0.4% to 2.2% for postprocedural MI in older patients (2–4,6). In our study no significant difference was seen in the incidence of MI in the aged patients compared to the nonaged patients (9.63% vs. 7.56%, p = 0.18), although the overall higher incidence of peri-procedural MI in both age groups may be due to the greater use of rotational atherectomy as well as routine and complete ascertainment of cardiac enzyme data following PCIs.

Vascular complications and aged patients.   Along with the change in stent designs and high-pressure dilation, there has been a dramatic change in antithrombotic regimens following stent implantation, as oral antiplatelet therapy with aspirin and thienopyridines has replaced more aggressive anticoagulation protocols. Although the overall incidence of vascular complications has decreased with improvement in antithrombotic protocols and improved sheath management, older patients and women continue to have a higher incidence (4,6,13,15). Aged patients in our study similarly had more frequent postprocedural vascular and bleeding complications. Plausible explanations include more aggressive anticoagulation of these patients with complex lesion morphology, different pharmacodynamic effects of heparin in the elderly, and increased risk for vascular injury due to underlying peripheral vascular disease (25).

Because the overall use of platelet GpIIb/IIIa inhibitors was limited in our study (7.6%), we cannot assess the effects of these agents in the aged cohort. Certainly, the EPISTENT (Evaluation of Platelet IIb/IIIa Inhibitor for Stenting Trial) study has recently shown a reduction in peri-procedural non-QMI and one-year mortality with use of abciximab combined with coronary stenting compared to stenting without abciximab and balloon angioplasty with abciximab (26,27). Bleeding was not increased with use of abciximab in that study, but given the increased serious bleeding complications in aged patients in our study predominantly not receiving GpIIb/IIIa inhibitors, use of these agents in aged patients will require careful consideration of the benefits and risks.

Restenosis and aged patients.   The aged patients in our study had a favorable long-term clinical restenosis outcome with no difference in TLR compared with nonaged patients during one-year follow-up (8.30% vs. 10.90%); the rates of TVR were nearly identical. This is in contrast with higher TLR rates in the consecutive series of older patients reported by DiGregorio et al. (4) (28% vs. 19%, p = 0.02), but similar to the 11% versus 14% to 15% TLR rates reported by Abizaid et al. (2). This probably reflects the aggressive initial results obtained rather than a physiologic difference in the restenosis process in the different age populations. The reduced risk for restenosis associated with the shorter lesion and stent lengths in the aged patients might have also balanced other potential increased risks for restenosis (28,29).

Study limitations.   There are several limitations of this study. First, the data are pooled from several randomized trials. Because randomization by age is not possible and the number of aged patients undergoing revascularization procedures is still small, pooled analysis from similar trials was the only practical way to assess events in this group. Second, the outcome results may not be generalizable to the wider "real-world" population of aged patients undergoing stenting procedures; it is likely that "healthier" aged patients were enrolled in the clinical trials pooled for this analysis.

Conclusions.   This analysis of 301 aged patients from a pooled data set of over 6,000 patients treated with stents demonstrates that stenting can be performed safely in this high-risk group with excellent acute results and low rates of clinical restenosis, albeit with a higher incidence of in-hospital and long-term mortality and with vascular and bleeding complications. Further studies will confirm whether more aggressive risk factor modification combined with selected use of coronary stenting will improve the long-term cardiac mortality in the aged population. Although the incidence of bleeding complications was lower than previously reported, efforts such as less anticoagulation, selective use of antiplatelet regimens (especially GpIIb/IIIa agents) and use of smaller-sized sheaths should be evaluated as measures to further reduce these risks in older patients.


    Footnotes
 
The original clinical studies were supported by contracts from Cordis/Johnson and Johnson Interventional Systems, Guidant/ACS, Boston Scientific/Medinol, and Medtronics/AVE. No outside financial support was provided for performing the analyses in this report.


    References
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 Methods
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 Discussion
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1. U.S. Bureau of the Census. Current Population Reports, Special Studies, P23–190, 65+ in the United States. Available via the Internet (http://www.census.gov). Accessed 6 Sept 1999.

2. Abizaid AS, Popma JJ, Mehran R, et al. Coronary stenting in the elderly: early in-hospital and long-term clinical outcomes. (abstr)J Am Coll Cardiol. 1998;31(Suppl):234A

3. Nasser TK, Fry ET, Annan K, et al. Comparison of six-month outcome of coronary artery stenting in patients <65, 65–75, and >75 years of age. Am J Cardiol. 1997;80:998–1001[CrossRef][Medline]

4. DeGregorio JD, Kobayashi Y, Albiero R, et al. Coronary artery stenting in the elderly: short-term outcome and long-term angiographic and clinical follow-up. J Am Coll Cardiol. 1998;32:577–583[Abstract/Free Full Text]

5. Chevalier B, Guyon P, Glatt B, Royer T, Pezzano M. Coronary angioplasty in the elderly in the stenting era. (abstr)J Am Coll Cardiol. 1998;31(Suppl):234A

6. Batchelor WB, Peterson ED, Anstrom KJ, Muhlbaier LH, Grosswald RD. Does stenting benefit the very elderly? An analysis of device-specific outcomes in 3,740 octogenarians. (abstr)J Am Coll Cardiol. 1998;31(Suppl):77A

7. Lefevre T, Morice MC, Eltchaminoff H, et al. One-month results of coronary stenting in patients ≥75 years of age. Am J Cardiol. 1998;82:17–21[CrossRef][Medline]

8. Alfonso F, Azcona L, Hernandez R, et al. Coronary stenting in elderly patients: clinical and angiographic implications. (abstr)J Am Coll Cardiol. 1998;31(Suppl):78A

9. Peterson ED, Jollis JG, Bebchuk JD, et al. Changes in mortality after myocardial revascularization in the elderly: the national Medicare experience. Ann Intern Med. 1994;121:919–927[Abstract/Free Full Text]

10. Oweida SW, Roubin GS, Smith RB, Salam AA. Postcatheterization vascular complications associated with percutaneous transluminal coronary angioplasty. J Vasc Surg. 1990;12:310–315[CrossRef][Medline]

11. Santana JO, Haft JI, LaMarche NS, Goldstein JE. Coronary angioplasty in patients eighty years of age or older. Am Heart J. 1992;124:13–18[CrossRef][Medline]

12. Imburgia M, King TR, Soffer AD, Rich MW, Krone RJ, Salimi A. Early results and long-term outcome of percutaneous transluminal coronary angioplasty in patients age 75 years or older. Cardiology. 1989;63:1127–1129

13. Lindsay J Jr, Reddy V, Pinnow EE, Little T, Pichard AD. Morbidity and mortality rates in elderly patients undergoing percutaneous coronary transluminal angioplasty. Am Heart J. 1994;128:697–702[CrossRef][Medline]

14. Myler RK, Webb JG, Nguyen DPV, et al. Coronary angioplasty in octogenarians: comparison to coronary bypass surgery. Cathet Cardiovasc Diagn. 1991;23:3–9[Medline]

15. Leon MB, Baim DS, Popma JJ, et al. A clinical trial comparing three antithrombotic drug regimens after coronary artery stenting. N Engl J Med. 1998;338:1665–1671

16. Baim DS, Cutlip DE, Midei M, et al. Final results of a randomized trial comparing the MULTILINK stent with the Palmaz-Schatz stent for narrowings in native coronary arteries. Am J Cardiol. 2001;87:157–162[CrossRef][Medline]

17. Heuser R, Kuntz RE, Lansky A, et al. Six-month clinical and angiographic results of the SMART trial. (abstr)J Am Coll Cardiol. 1998;31(Suppl):64A

18. Heuser R, Kuntz R, Lansky A, et al. A comparison of the long AVE Micro Stent II and the Palmaz-Schatz stent: a SMART trial registry. (abst)J Am Coll Cardiol. 1998;31(Suppl):80A

19. Linnemeier T. The Rx Multi-Link stent parallel registries to the ASCENT trial. (abstr)J Inv Cardiol. 1998;10(Suppl):55B–56B

20. Baim DS, Cutlip DE, O’Shaughnessy CD, et al. Final results of a randomized trial comparing the NIR stent to the Palmaz-Schatz stent for narrowings in native coronary arteries. Am J Cardiol. 2001;87:152–156[CrossRef][Medline]

21. Carrozza JP, Kereiakes D, Caputo RP, et al. Final acute 30-day and 6-month clinical and angiographic outcome from the multicenter randomized EXTRA trial comparing the operator-mounted XT and Palmaz-Schatz coronary stent. (abstr)Circulation. 1998;98(Suppl):I661

22. Mehran R, Mintz GS, Hong MK, et al. Clinical, procedural, angiographic, and intravascular ultrasound predictors (and sequelae) of CK-MB rise (>5x normal) following catheter-based interventions. (abst)Circulation. 1998;98(Suppl):I496

23. Kini A, Marmur JD, Kini S, et al. Creatine kinase-MB elevation after coronary intervention correlates with diffuse atherosclerosis, and low-to-medium level elevation has a benign clinical course. J Am Coll Cardiol. 1999;34:663–671[Abstract/Free Full Text]

24. Califf RM, Abdelmeguid AE, Kuntz RE, et al. Myonecrosis after revascularization procedures. J Am Coll Cardiol. 1998;31:241–251[Abstract/Free Full Text]

25. EPIC Investigators. Use of a monoclonal antibody directed against the platelet glycoprotein IIb/IIIa receptor in high-risk coronary angioplasty. N Engl J Med. 1994;330:956–961[CrossRef][Medline]

26. EPISTENT Investigators. Randomised placebo-controlled and balloon-angioplasty–controlled trial to assess safety of coronary stenting with use of platelet glycoprotein-IIb/IIIa blockade. Lancet. 1998;352:87–92[Medline]

27. Evaluation of Platelet IIb/IIIa Inhibition in Stenting InvestigatorsLincoff AM, Califf RM, Moliterno DJ, et al. Complementary clinical benefits of coronary artery stenting and blockade of platelet glycoprotein IIb/IIIa receptors. N Engl J Med. 1999;341:319–327[CrossRef][Medline]

28. Kobayashi Y, De Gregorio J, Kobayashi N, et al. Stented segment length as an independent predictor of restenosis. J Am Coll Cardiol. 1999;34:651–659[Abstract/Free Full Text]

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