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Dr. Ihab Suliman
Ingrowth of tissue may cause bare-metal stents to
become obstructed, resulting in the need for a second
procedure. Drug-eluting stents inhibit this
process, but uncovered struts may be prone to
thrombosis after discontinuation of antiplatelet
therapy.
Perioperative coronary stent thrombosis is a

    catastrophic complicationthat can occur in
    patients receiving both bare-metal and drug-
    elutingstents.
    Noncardiac surgery appears to increase the

    risk that recently-placed stents
    thrombose, especially when surgery
    is performed early after stenting, and
    particularly if dual antiplatelet therapy is
    discontinued.
In patients with a bare metal coronary stent

    who require surgery within 6 weeks of stent
    placement, we recommend continuing aspirin
    and clopidogrel in the perioperative period
    (Grade 1C);
     In patients with a drug-eluting coronary

    stent who require surgery within 12 months
    of stent placement, we recommend
    continuing aspirin and clopidogrel in the
    perioperative period (Grade 1C).
The optimal duration of clopidogrel required

    to prevent late DES thrombosis is unknown.
    an observational study showed reduced risk

    of death or MI when clopidogrel was
    continued up to 2 years after DES
    implantation
• Continue dual antiplatelet therapy during
and after surgery
• Discontinue clopidogrel but quot;bridgequot; the
patient to surgery using a short-acting
antiplatelet agent with a glycoprotein IIb/IIIa
inhibitor or an antithrombin, and restart
clopidogrel as soon as possible after surgery
• Discontinue clopidogrel before surgery and
restart it as soon as possible after surgery
some clinicians quot;bridgequot; the patient to

    surgery using a short-acting antiplatelet agent or
    an anticoagulant. Because stent thrombosis is
    primarily a platelet-mediated
    phenomenon, platelet inhibitors might be a more
    logical choice if such a strategy is pursued.
    Furthermore, the cessation of heparin in a patient
    not on aspirin or other antiplatelet agents has
    been shown to cause platelet activation and a
    rebound phenomenon which may actually
    increase the likelihood of perioperative stent
    thrombosis compared to if no heparin bridging
    had been performed.
However, it must be emphasized that

    admitting a patient to a hospital before
    surgery to bridge them to surgery does not
    offer complete protection because the
    greatest risk of stent thrombosis is actually
    during or after surgery.
We systematically searched Medline for

    reported cases of late stent thrombosis and
    very late stent thrombosis published between
    January 2001 and July 2008. We restricted our
    search to Academic Research Consortium–
    defined definite cases. We identified 161
    cases of late stent thrombosis or very late
    stent thrombosis from 84 articles (
79 from case reports, 61 from registries, and 21

    from randomized clinical trials). Patients had a
    mean age of 58.4±13.4 years, and 88% were
    male. A total of 19 cases occurred in
    patients who were receiving dual antiplatelet
    therapy at the time of the event. If patients
    stopped both antiplatelet agents
    simultaneously, the median time to event was 7
    days. If patients had previouslystopped a
    thienopyridine with no ill effect and
    subsequently stopped acetylsalicylic acid, the
    median time to event was also 7 days from the
    time of acetylsalicylic acid cessation.
If the thienopyridine was stopped but

    acetylsalicylic acid was maintained, the
    median time to event was 122 days. Among
    the 48 patients who stopped both agents, 36
    cases (75%) occurred within 10 days. Among
    the 94 patients who discontinued a
    thienopyridine but continued acetylsalicylic
    acid, only 6 cases (6%) occurred within 10
    days.
If acetylsalicylic acid therapy is

    maintained, short-term discontinuation of a
    thienopyridine may be relatively safe in
    patients with drug-eluting stents.
The real-world use of the CYPHER stent is safer than

    was shown in clinical trials.
    According to the MATRIX Registry, which is

    sponsored by Cordis, CYPHER's manufacturer, rates
    of stent thrombosis at one year were lower than
    clinical trials reported.
     Most patients in the MATRIX Registry, up to 80%,

    have chronic conditions such as diabetes that would
    have disqualified them from clinical trials, and
    therefore received stents off-label. MATRIX
    investigators also found that many patients had
    trouble maintaining the clopidogrel regimen and that
    one-third were no longer taking the drug as
    recommended at one year.
Found that off-label use of sirolimus-eluting

    stents led to low two-year rates of
    complications and thrombosis.
    Of 1,521 patients, 34% had diabetes, 45% had

    prior percutaneous coronary
    intervention, 21% had prior coronary artery
    bypass grafting, 33% had prior MI and 46%
    had acute cardiac syndrome at baseline.
Two years after stenting, rates of cardiac

    death, non-cardiac death, MI, target lesion
    revascularization and target vessel
    revascularization were 1.1%, 1.7%, 4%, 9% and
    12%, respectively.

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Coronary Stent Thrombosis Risks After Surgery

  • 2. Ingrowth of tissue may cause bare-metal stents to become obstructed, resulting in the need for a second procedure. Drug-eluting stents inhibit this process, but uncovered struts may be prone to thrombosis after discontinuation of antiplatelet therapy.
  • 3. Perioperative coronary stent thrombosis is a  catastrophic complicationthat can occur in patients receiving both bare-metal and drug- elutingstents. Noncardiac surgery appears to increase the  risk that recently-placed stents thrombose, especially when surgery is performed early after stenting, and particularly if dual antiplatelet therapy is discontinued.
  • 4.
  • 5. In patients with a bare metal coronary stent  who require surgery within 6 weeks of stent placement, we recommend continuing aspirin and clopidogrel in the perioperative period (Grade 1C); In patients with a drug-eluting coronary  stent who require surgery within 12 months of stent placement, we recommend continuing aspirin and clopidogrel in the perioperative period (Grade 1C).
  • 6. The optimal duration of clopidogrel required  to prevent late DES thrombosis is unknown. an observational study showed reduced risk  of death or MI when clopidogrel was continued up to 2 years after DES implantation
  • 7. • Continue dual antiplatelet therapy during and after surgery • Discontinue clopidogrel but quot;bridgequot; the patient to surgery using a short-acting antiplatelet agent with a glycoprotein IIb/IIIa inhibitor or an antithrombin, and restart clopidogrel as soon as possible after surgery • Discontinue clopidogrel before surgery and restart it as soon as possible after surgery
  • 8. some clinicians quot;bridgequot; the patient to  surgery using a short-acting antiplatelet agent or an anticoagulant. Because stent thrombosis is primarily a platelet-mediated phenomenon, platelet inhibitors might be a more logical choice if such a strategy is pursued. Furthermore, the cessation of heparin in a patient not on aspirin or other antiplatelet agents has been shown to cause platelet activation and a rebound phenomenon which may actually increase the likelihood of perioperative stent thrombosis compared to if no heparin bridging had been performed.
  • 9. However, it must be emphasized that  admitting a patient to a hospital before surgery to bridge them to surgery does not offer complete protection because the greatest risk of stent thrombosis is actually during or after surgery.
  • 10. We systematically searched Medline for  reported cases of late stent thrombosis and very late stent thrombosis published between January 2001 and July 2008. We restricted our search to Academic Research Consortium– defined definite cases. We identified 161 cases of late stent thrombosis or very late stent thrombosis from 84 articles (
  • 11. 79 from case reports, 61 from registries, and 21  from randomized clinical trials). Patients had a mean age of 58.4±13.4 years, and 88% were male. A total of 19 cases occurred in patients who were receiving dual antiplatelet therapy at the time of the event. If patients stopped both antiplatelet agents simultaneously, the median time to event was 7 days. If patients had previouslystopped a thienopyridine with no ill effect and subsequently stopped acetylsalicylic acid, the median time to event was also 7 days from the time of acetylsalicylic acid cessation.
  • 12. If the thienopyridine was stopped but  acetylsalicylic acid was maintained, the median time to event was 122 days. Among the 48 patients who stopped both agents, 36 cases (75%) occurred within 10 days. Among the 94 patients who discontinued a thienopyridine but continued acetylsalicylic acid, only 6 cases (6%) occurred within 10 days.
  • 13. If acetylsalicylic acid therapy is  maintained, short-term discontinuation of a thienopyridine may be relatively safe in patients with drug-eluting stents.
  • 14. The real-world use of the CYPHER stent is safer than  was shown in clinical trials. According to the MATRIX Registry, which is  sponsored by Cordis, CYPHER's manufacturer, rates of stent thrombosis at one year were lower than clinical trials reported. Most patients in the MATRIX Registry, up to 80%,  have chronic conditions such as diabetes that would have disqualified them from clinical trials, and therefore received stents off-label. MATRIX investigators also found that many patients had trouble maintaining the clopidogrel regimen and that one-third were no longer taking the drug as recommended at one year.
  • 15. Found that off-label use of sirolimus-eluting  stents led to low two-year rates of complications and thrombosis. Of 1,521 patients, 34% had diabetes, 45% had  prior percutaneous coronary intervention, 21% had prior coronary artery bypass grafting, 33% had prior MI and 46% had acute cardiac syndrome at baseline.
  • 16. Two years after stenting, rates of cardiac  death, non-cardiac death, MI, target lesion revascularization and target vessel revascularization were 1.1%, 1.7%, 4%, 9% and 12%, respectively.