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Article

Bioresorbable stents: The future of interventional cardiology?

Stephen G. Ellis, MD and Haris Riaz, MD
Cleveland Clinic Journal of Medicine November 2016, 83 (11 suppl 2) S18-S23; DOI: https://doi.org/10.3949/ccjm.83.s2.03
Stephen G. Ellis
Department of Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic
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  • For correspondence: [email protected]
Haris Riaz
Resident, Department of Internal Medicine, Cleveland Clinic
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  • FIGURE 1
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    FIGURE 1

    Reduction of restenosis rates by stent type.

  • FIGURE 2
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    FIGURE 2

    Second- vs first-generation drug-eluting stents.

    Reprinted from JACC: Cardiovascular Interventions (Gada H, et al. 5-Year results of a randomized comparison of XIENCE V everolimus-eluting and TAXUS paclitaxel-eluting stents: final results from the SPIRIT III trial (clinical evaluation of the XIENCE V everolimus eluting coronary stent system in the treatment of patients with de novo native coronary artery lesions). JACC: Cardiovasc Interv 2013; 6:1263–1266) with permission from Elsevier. © The American College of Cardiology Foundation. http://www.sciencedirect.com/science/journal/19368798

  • FIGURE 3
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    FIGURE 3

    Components of drug-eluting and bioresorbable stents.

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    FIGURE 4

    ABSORB learnings: MICAT. Pre-dilation with noncompliant balloon sized 1:1 to normal vessel with complete balloon expansion; post-dilation at 14–16 atmospheres.

    Reprinted from the Journal of the American College of Cardiology (Puricel S, et al. Bioresorbable coronary scaffold thrombosis: multicenter comprehensive analysis of clinical presentation, mechanisms, and predictors. JACC 2016; 67:921–931) with permission from Elsevier. © The American College of Cardiology Foundation. http://www.sciencedirect.com/science/journal/07351097

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    TABLE 1

    Construction of first- and second-generation drug-eluting stents (DES) and proposed pathophysiological mechanism of late adverse events

    ConstructionMechanism
    First-generation DESThick struts
    Uneven polymer distribution with poor integrity and thick coating of durable polymers
    High drug dose
    Uncovered struts
    Hypersensitivity
    Malapposition from fibrin deposition
    Stent fracture
    Neoatherosclerosis (especially for second-generation DES)
    Second-generation
    DES
    Thinner struts
    More biocompatible polymer (durable)
    Reduced drug dose
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    TABLE 2

    Key elements of technique with the Absorb scaffold

    Properly choose the lesion
    • Definitely ≥ 2.5–3.75 mm in diameter (if in doubt, check intravascular ultrasound or optical coherence tomography)

    • No excessive tortuosity or calcium proximal

    Prepare the lesion by 1:1 predilation and confirm < 40% diameter residual stenosis
    Post-dilate with 1:1 noncompliant balloon at ≥ 14 atmospheres
    Pay attention to expansion limits
    • Oversizing the scaffold by a balloon > 0.5 mm the scaffold diameter risks strut fracture

    Prescribe dual antiplatelet therapy
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Cleveland Clinic Journal of Medicine: 83 (11 suppl 2)
Cleveland Clinic Journal of Medicine
Vol. 83, Issue 11 suppl 2
1 Nov 2016
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Bioresorbable stents: The future of interventional cardiology?
Stephen G. Ellis, Haris Riaz
Cleveland Clinic Journal of Medicine Nov 2016, 83 (11 suppl 2) S18-S23; DOI: 10.3949/ccjm.83.s2.03

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Bioresorbable stents: The future of interventional cardiology?
Stephen G. Ellis, Haris Riaz
Cleveland Clinic Journal of Medicine Nov 2016, 83 (11 suppl 2) S18-S23; DOI: 10.3949/ccjm.83.s2.03
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  • Article
    • ABSTRACT
    • STENT DESIGN
    • WHAT CAUSES STENT THROMBOSIS AND RESTENOSIS?
    • CAN WE SOLVE THE PROBLEM?
    • STENTS WITH BIORESORBABLE POLYMERS
    • STENTS WITHOUT POLYMERS
    • BIORESORBABLE STENTS
    • CONCLUSION AND THE WAY FORWARD
    • Footnotes
    • REFERENCES
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