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ACC/AHA/SCAI PCI Guidelines - British Cardiovascular Intervention ...

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ACC - www.acc.org<br />

AHA - www.americanheart.org<br />

SCAI - www.scai.org<br />

Smith et al. 2005<br />

ACC/AHA/SCAI Practice Guidelines<br />

77<br />

contrast has been used and when adequate pretreatment with<br />

aspirin or antiplatelet agents has not been achieved (814).<br />

In contrast to ad hoc angioplasty, a staged approach also<br />

has several advantages. It allows ample time to review the<br />

angiogram and plan the procedural strategy; discuss the<br />

risks, benefits, and alternatives with the patient and family;<br />

and obtain consultation from cardiothoracic surgical colleagues.<br />

It is far more difficult to adequately inform the<br />

patient of risks, benefits, and alternatives without knowledge<br />

of the anatomy and the extent of coronary disease. A staged<br />

approach also allows for optimal hydration and pretreatment<br />

with oral antiplatelet agents. Explicit and clear informed consent,<br />

especially for ad hoc PCI, should be discussed by the<br />

interventional cardiologist with the patient and family.<br />

Studies evaluating the outcome of patients undergoing ad<br />

hoc coronary intervention have reported that informed<br />

patients with suitable anatomy have a shorter hospital stay,<br />

less radiation exposure, and lower costs without an increase<br />

in procedural complications compared with patients undergoing<br />

a staged approach (812,813,816,817). In a multicenter<br />

cohort study of 35 700 patients undergoing elective coronary<br />

angioplasty between 1992 and 1995, the risk of a major complication<br />

(MI, emergency CABG, or death) from combined<br />

(“ad hoc”) versus staged procedures was 2% and 1.6%,<br />

respectively. After adjustment for clinical and angiographic<br />

differences between groups, the risk from combined procedures<br />

was not significantly different. However, patients with<br />

multivessel disease, women, patients older than 65 years, and<br />

patients undergoing multilesion coronary angioplasty were at<br />

increased risk of an adverse outcome (818). In an analysis of<br />

patients in the New York State PCI Registry, in-hospital mortality<br />

was similar in patients undergoing ad hoc and staged<br />

procedures, although patients with HF had a significantly<br />

lower mortality when undergoing staged procedures. These<br />

studies suggest that it is safe to perform PCI after diagnostic<br />

catheterization in selected patients (819).<br />

Ad hoc coronary intervention is particularly suitable for<br />

patients with clinical evidence of restenosis 6 to 12 months<br />

after the initial procedure (820), patients undergoing primary<br />

angioplasty for MI, and patients with refractory UA in need<br />

of urgent revascularization (821). Before the procedure,<br />

these patients should be treated with aspirin and clopidogrel<br />

(822) only when PCI with stent placement is highly likely,<br />

and they should give appropriate informed consent for anticipated<br />

PCI. Ad hoc PCI should be performed only in a wellinformed<br />

patient, particularly in the setting of single-vessel<br />

disease without morphologic features predictive of an<br />

adverse outcome, when it is clear that this treatment strategy<br />

is the best alternative. However, ad hoc percutaneous revascularization<br />

should not be performed in patients in whom the<br />

angiographic findings are unanticipated or in whom the indication,<br />

suitability, or preference for percutaneous revascularization<br />

is unclear (823). Patient safety should be the paramount<br />

consideration when ad hoc intervention is being considered.<br />

This Committee endorses the recommendations<br />

from the SCAI that ad hoc PCI be individualized and not be<br />

a standard or required strategy for all patients (824). The<br />

Writing Committee encourages future studies to further evaluate<br />

the outcomes associated with ad hoc angioplasty and its<br />

cost effectiveness.<br />

7.2. PCI in Cardiac Transplant Patients<br />

Allograft atherosclerosis and vasculopathy are the main<br />

cause of death in cardiac transplant recipients. Because no<br />

medical therapy is known to prevent graft atherosclerosis,<br />

and retransplantation is associated with decreased survival,<br />

palliative therapy with PCI has been proposed and performed<br />

(825). No single medical center has performed PCI in many<br />

patients, and thus, the responses and outcomes of a large<br />

cohort are unavailable for review. However, pooled information<br />

from 11 medical centers retrospectively analyzing<br />

results of coronary angioplasty in cardiac transplant patients<br />

has been reported (826). These investigators concluded that<br />

although high procedural success can be achieved and PCI<br />

may be applied in a selected cardiac transplant population<br />

with success and complication rates comparable to the routine<br />

patient population, it remains unknown whether PCI<br />

prolongs allograft survival.<br />

Coronary stenting in cardiac allograft vascular disease has<br />

been performed in small numbers of patients with favorable<br />

results (827). Heublein et al. (828) compared angioplasty and<br />

stenting in 27 patients who received 48 stents, 5.7 plus or<br />

minus 2.9 years after heart transplantation. Coronary angioplasty<br />

resulted in a minimal increase in luminal dimensions<br />

compared with stenting (2.04 plus or minus 0.36 mm for<br />

angioplasty vs 2.53 plus or minus 0.38 mm for stenting).<br />

There were no stent thromboses or bleeding complications.<br />

At a mean follow-up period of 8 plus or minus 5 months<br />

(range 2 weeks to 23 months), all patients were clinically<br />

event-free. Six of 24 stented vessels in 16 patients had<br />

restenosis greater than 50% by ultrasound or angiography 6<br />

months after the procedure. These somewhat disappointing<br />

results highlight the need for a better understanding of the<br />

mechanism of graft vasculopathy and the development of<br />

refined, specific PCI-related therapies with better outcomes.<br />

The largest reported experience of PCI in cardiac transplant<br />

recipients to date showed that PCI with stents is effective in<br />

relieving focal stenoses in patients with allograft coronary<br />

disease (829). Between 1990 and 2000, 62 patients (1.5 to 15<br />

years after transplant) underwent 151 procedures that resulted<br />

in PCI of 219 lesions. Periprocedural mortality was low at<br />

2% (4 of 151 procedures). Two-year freedom from allograft<br />

coronary disease death or graft loss was 74% for 1-vessel<br />

disease at first PCI, 75% for 2-vessel disease, and 27% for 3-<br />

vessel disease (P equals 0.009). There were no incidences of<br />

acute stent thrombosis. Freedom from repeat PCI of the same<br />

vessel ranged from 75% at 6 months to 57% at 4 years.<br />

Freedom from restenosis ranged from 95% at 1 month to<br />

57% at 6 months. Multivariate predictors of freedom from<br />

restenosis were the use of stents, higher antiproliferative<br />

immunosuppressant dose, and an era effect (e.g., procedural<br />

advances and widespread use of periprocedural GP IIb/IIIa<br />

inhibitors and thienopyridines, among others). Long-term

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