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(Circulation. 2007;116:e378-e382.)
© 2007 American Heart Association, Inc.
Clinician Update |
From the Services de Cardiologie (J.W.R., M.H.), Chirurgie Digestive (L.C.), and Anesthesiologie (B.P.), University Hospital of Caen, Normandy, France.
Correspondence to Professor Martial Hamon, Service des Maladies du Coeur et des Vaisseaux, UF Soins Intensifs Cardiologiques, Centre Hospitalier Universitaire de Caen, Ave Côte de Nacre 14033 Caen, Normandy, France. E-mail hamon-m{at}chu-caen.fr
Key Words: angioplasty stents surgery thrombosis
| Introduction |
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| Noncardiac Surgery and Stent Thrombosis |
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The timing and definition of stent thrombosis vary between studies, which has led to a call for standardizing definitions.5 In addition, although most of the trials have included low-risk patients and coronary lesions, the use of DES in the real world is much less controlled, potentially increasing the risk of stent thrombosis.6,7
It has been well established that patients who undergo noncardiac surgery soon after stent implantation are at increased risk for stent thrombosis.8–10 The reasons for this increased risk may include nonendothelialization of the stent, interruption of dual OAA therapy, and the potentially prothrombotic state associated with surgery itself.
The risks of surgery after coronary stenting have been described in 8 observational, mainly retrospective, studies8–15 (summarized in Table 1). The mortality rate in such patients ranged from 2.5% to 21.4%.
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Noncardiac surgery performed in patients who have had recent coronary stenting exposes them to an increased risk of major cardiac events in the perioperative period, especially if the OAA therapy is interrupted. Good theoretical reasons exist for delaying elective noncardiac surgery after coronary stenting, thereby allowing the stents to endothelialize.
| Likely Clinical Settings |
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60% percutaneous coronary intervention versus 40% CABG. A reanalysis of this trial comparing percutaneous coronary intervention with CABG suggested that percutaneous coronary intervention offered no benefit but that coronary artery bypass graft surgery (CABG) might.18 More recently, the Dutch Echocardiographic Cardiac Risk Evaluation Applying Stress Echo V (DECREASE-V) pilot study, a randomized trial of coronary revascularization or not in high-risk patients with demonstrable ischemia, including 3-vessel disease and left main stem disease, before major vascular surgery, showed no benefit for the patients who underwent preoperative revascularization.19 Again, the method of revascularization strategy was not randomized and was 65% percutaneous coronary intervention versus 35% CABG. Although these data are limited, they suggest that preoperative revascularization in general is not beneficial. They also suggest that if preoperative revascularization is to be performed, methods that do not involve stenting such as balloon angioplasty or CABG may be preferable. The second situation, which is becoming increasingly common, occurs when a patient with previous coronary stenting requires noncardiac surgery. In this situation, it is important to know the indication for stenting, the date of implantation, and the type(s) of stent(s) used, as well as the patients current OAA therapy and proposed duration. An assessment of the risks of the proposed surgery by the surgeon and anesthetist and of the likelihood and importance of possible stent thrombosis, preferably in conjunction with a cardiologist (ideally the cardiologist who implanted the stent), then needs to be undertaken. As an aid to this assessment, we have adapted a table from Albaladejo et al20 and incorporated the latest recommendations (Table 2). This table and the accompanying algorithm (the Figure) are based on consensus opinion and therefore may change as further data become available.
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When possible, surgery should be delayed until the patient is outside the recommended period of dual antiplatelet therapy, as determined by the stent and lesion characteristics. This would mean that surgery should be delayed until 6 weeks after implantation of a bare-metal stent and 1 year after implantation of a DES. In reality, the recommendation for a 6-week delay with a bare-metal stent is to ensure that the patient completes a 4-week course of dual antiplatelet therapy because the patient will need 5 to 10 days (depending on the platelet half-life) for the effect of the antiplatelet agents to wear off before surgery.21 Patients in whom noncardiac surgery is carried out within these time periods are deemed at high risk of stent thrombosis. Patients in whom noncardiac surgery is performed outside these time periods may still be at high risk of stent thrombosis, depending on factors related to their coronary anatomy and their clinical characteristics. Stent thrombosis is more likely to occur in patients who have had stenting of ostial lesions, bifurcation lesions, lesions in small vessels, multiple lesions, or long lesions. In addition, patients with diabetes mellitus or renal impairment or patients in whom the indication for stenting was an acute myocardial infarction or an acute coronary syndrome are at higher risk of stent thrombosis.
When assessing the bleeding risk for an operative procedure, one needs to consider not only the actual blood loss associated with the procedure in terms of anemia and need for transfusion but also the consequences of the bleeding in terms of its site. For instance, even minor bleeding may be intolerable during or after certain ophthalmologic and intracranial surgery. Often, the decision to operate while antiplatelet agents are continued will be a matter of personal judgment. For many operative procedures, there is no evidence and no recommendations to aid in this decision.22 Dual OAA therapy usually consists of aspirin and a thienopyridine (most frequently clopidogrel). It is generally accepted that there are more perioperative bleeding problems with thienopyridines than aspirin23; therefore, if 1 OAA is stopped, it is generally the thienopyridine.
When possible, OAAs should be continued throughout the perioperative period, and if stopped, they should be stopped for as short a period as possible before surgery and restarted as soon as possible after surgery. In addition, for patients at high risk of stent thrombosis, consideration should be given to substituting oral agents with a shorter-acting, intravenous glycoprotein IIb/IIIa inhibitor during the perioperative period. However, the evidence for this use of alternative antiplatelet agents is largely anecdotal.24 In patients for whom noncardiac surgery is planned soon but preoperative revascularization is considered essential, consideration should first be given to modes of revascularization that do not involve stents such as CABG25 or balloon angioplasty,26 although the latter may necessitate stenting if there is a complication. If stenting is deemed necessary, there may be a place for newer stents that encourage rapid endothelialization,27 thereby possibly allowing surgery to be performed earlier. However, there is no evidence yet that these theoretical benefits will be realized. Along the same lines, absorbable stents are currently in development.28 However, although they may remove the risk of late thrombosis, they probably will not solve the problem of the risk of early surgery. If, despite all of the above precautions, stent thrombosis should occur during the perioperative period, the correct treatment is almost certainly urgent percutaneous coronary intervention29 because recent surgery usually rules out the use of thrombolytic therapy.
| How Should We Manage Our Patients Antiplatelet Therapy? |
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| Conclusions |
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| Acknowledgments |
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None.
| References |
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3. Lagerqvist B, James SK, Stenestrand U, Lindback J, Nilsson T, Wallentin L. Long-term outcomes with drug-eluting stents versus bare-metal stents in Sweden. N Engl J Med. 2007; 356: 1009–1019.
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29. Berger PB, Bellot V, Bell MR, Horlocker TT, Rihal CS, Hallett JW, Dalzell C, Melby SJ, Charnoff NE, Holmes DR Jr. An immediate invasive strategy for the treatment of acute myocardial infarction early after noncardiac surgery. Am J Cardiol. 2001; 87: 1100–1102, A1106, A1109.
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