ACC/AHA PRACTICE GUIDELINES
ACC/AHA guidelines for percutaneous coronary intervention (revision of the 1993 PTCA guidelines)executive summary2,2
A report of the American College of Cardiology/American Heart Association Task Force on practice guidelines (Committee to revise the 1993 guidelines for percutaneous transluminal coronary angioplasty) endorsed by the Society for Cardiac Angiography and Interventions
Sidney C. Smith, Jr, MD, FACC, Chair, Committee Member,
James T. Dove, MD, FACC, Committee Member,
Alice K. Jacobs, MD, FACC, Committee Member,
J. Ward Kennedy, MD, MACC, Committee Member,
Dean Kereiakes, MD, FACC, Committee Member,
Morton J. Kern, MD, FACC, Committee Member,
Richard E. Kuntz, MD, FACC, Committee Member,
Jeffery J. Popma, MD, FACC, Committee Member,
Hartzell V. Schaff, MD, FACC, Committee Member,
David O. Williams, MD, FACC, Committee Member,
Raymond J. Gibbons, MD, FACC, Chair, Task Force Member,
Joseph P. Alpert, MD, FACC, Task Force Member,
Kim A. Eagle, MD, FACC, Task Force Member,
David P. Faxon, MD, FACC, Task Force Member,
Valentin Fuster, MD, PhD, FACC, Task Force Member,
Timothy J. Gardner, MD, FACC, Task Force Member,
Gabriel Gregoratos, MD, FACC, Task Force Member,
Richard O. Russell, MD, FACC, Task Force Member and
Sidney C. Smith, MD, Jr, FACC, Task Force Member
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Table of contents
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- Introduction......2216
- General Considerations and Background......2217
- Outcomes............2217
- Definitions of PCI Success......2217
- Angiographic Success......2217
- Procedural Success......2217
- Clinical Success......2218
- Definitions of Procedural Complications......2218
- Acute Outcome......2219
- Long-Term Outcome and Restenosis......2219
- Predictors of Success/Complications......2220
- Anatomic Factors......2220
- Clinical Factors......2220
- Risk of Death......2220
- Women......2221
- The Elderly Patient......2221
- Diabetes Mellitus......2221
- Coronary Angioplasty After Coronary Artery Bypass Surgery......2222
- Specific Technical Considerations......2222
- Issues of Hemodynamic Support in High-Risk Angioplasty......2222
- Comparison With Bypass Surgery......2222
- Comparison With Medicine......2223
- Institutional and Operator Competency......2223
- Quality Assurance......2223
- Operator and Institutional Volume......2223
- On-Site Cardiac Surgical Backup......2225
- Primary PCI Without On-Site Cardiac Surgery......2225
- Elective PCI Without On-Site Surgery......2225
- Indications......2226
- Asymptomatic or Mild Angina......2227
- Angina Class II to IV or Unstable Angina......2228
- Myocardial Infarction......2229
- PCI in Thrombolytic-Ineligible Patients......2230
- Post Thrombolysis PCI......2230
- Rescue PCI......2231
- PCI for Cardiogenic Shock......2231
- PCI Hours to Days After Thrombolysis......2231
- PCI After Thrombolysis in Selected Patient Subgroups......2231
- Young and Elderly Post-Infarct Patients.......2231
- Patients With Prior Myocardial Infarction.......2231
- Percutaneous Intervention in Patients With Prior Coronary Bypass Surgery......2232
- Early Ischemia after CABG......2232
- Late Ischemia after CABG......2233
- Early and Late Outcomes of Percutaneous Intervention......2233
- Surgery Versus Percutaneous Reintervention......2233
- Use of Adjunctive Technology (Intracoronary Ultrasound Imaging, Flow Velocity and Pressure)......2234
- Intravascular Ultrasound Imaging (IVUS)......2234
- Coronary Flow Velocity and Coronary Vasodilatory Reserve......2234
- Coronary Artery Pressure and Fractional Flow Reserve......2234
- Management of Patients Undergoing PCI......2235
- Experience With New Technologies......2235
- Acute Results......2235
- Late-Term Results......2235
- Antiplatelet and Antithrombotic Therapies and Coronary Angioplasty......2235
- Aspirin, Ticlopidine, Clopidogrel......2235
- Glycoprotein IIb/IIIa Inhibitors......2235
- Heparin......2235
- Post-PCI Management......2236
- Post-Procedure Evaluation of Ischemia......2236
- Risk Factor Modifications......2236
- Exercise Testing After PCI......2237
- Special Considerations......2237
- Ad Hoc AngioplastyPCI at the Time of Initial Cardiac Catheterization......2237
- PCI in Cardiac Transplant Patients......2237
- Management of Clinical Restenosis......2237
- Restenosis After Stent Implantation (Instent Restenosis)......2237
- Cost-Effectiveness Analysis for PCI......2237
- Future Directions......2238
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I. Introduction
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The American College of Cardiology/American Heart Association (ACC/AHA) Task Force on Practice Guidelines was formed to gather information and make recommendations about appropriate use of technology for the diagnosis and treatment of patients with cardiovascular disease. Percutaneous coronary interventions (PCI) are an important group of technologies in this regard. Although initially limited to PTCA, and termed percutaneous transluminal coronary angioplasty (PTCA), PCI now includes other new techniques capable of relieving coronary narrowing. Accordingly, in this document, rotational atherectomy, directional atherectomy, extraction atherectomy, laser angioplasty, implantation of intracoronary stents and other catheter devices for treating coronary atherosclerosis are considered components of PCI. In this context PTCA will be used to refer to those studies using primarily PTCA while PCI will refer to the broader group of percutaneous techniques. These new technologies have impacted the effectiveness and safety profile initially established for PTCA. Moreover, important advances have occurred in the use of adjunctive medical therapies such as glycoprotein (GP) IIb/IIIa receptor blockers. In addition, since publication of the previous Guidelines in 1993, greater experience in the performance of PCI in patients with acute coronary syndromes and in community hospital settings has been gained. In view of these developments, further review and revision of the guidelines is warranted. This document reflects the opinion of the third ACC/AHA committee charged with revising the guidelines for PTCA to include the broader group of technologies now termed PCI.
Several issues relevant to the Committees process and the interpretation of the Guidelines have been noted previously and are worthy of restatement. First, PCI is a technique that has been continually refined and modified; hence continued, periodic Guideline revision is anticipated. Second, these guidelines are to be viewed as broad recommendations to aid in the appropriate application of PCI. Under unique circumstances, exceptions may exist. These Guidelines are intended to complement, not replace, sound medical judgment and knowledge. They are intended for operators who possess the cognitive and technical skills for performing PCI and assume that facilities and resources required to properly perform PCI are available. As in the past, the indications are categorized as Class I, II, or III based on a multifactorial assessment of risk as well as expected efficacy viewed in the context of current knowledge and the relative strength of this knowledge. Initially, this document describes the background information that forms the foundation for specific indications. Topics fundamental to coronary intervention are reviewed followed by separate discussions relating to unique technical and operational issues. Formal recommendations for the use of angioplasty are included in Section V. Indications are organized according to clinical presentation. This format is designed to enhance the usefulness of this document for the assessment and care of patients with coronary artery disease (CAD).
This document employs the ACC/AHA style classification as Class I, II, or III. These classes summarize the indications for PCI as follows: - Class I: Conditions for which there is evidence for and/or general agreement that the procedure or treatment is useful and effective.
- Class II: Conditions for which there is conflicting evidence and/or a divergence of opinion about the usefulness/efficacy of a procedure or treatment.
- Class IIa: Weight of evidence/opinion is in favor of usefulness/efficacy.
- Class IIb: Usefulness/efficacy is less well established by evidence/opinion.
- Class III: Conditions for which there is evidence and/or general agreement that the procedure/treatment is not useful/effective, and in some cases may be harmful.
The weight of evidence in support of the recommendation for each listed indication is presented as follows: - Level of Evidence A: Data derived from multiple randomized clinical trials.
- Level of Evidence B: Data derived from a single randomized trial or nonrandomized studies.
- Level of Evidence C: Consensus opinion of experts.
The ACC/AHA Task Force on Practice Guidelines makes every effort to avoid any actual or potential conflicts of interest that might arise as a result of an outside relationship or personal interest of a member of the writing panel. Specifically, all members of the writing panel are asked to provide disclosure statements of all such relationships that might be perceived as real or potential conflicts of interest. These statements are reviewed by the parent task force, reported orally to all members of the writing panel at the first meeting, and updated as changes occur.
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II. General considerations and background
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More than 500,000 PCI procedures are performed yearly in the U.S., and it has been estimated that more than 1,000,000 procedures are performed annually worldwide. New coronary devices have expanded the clinical and anatomical indications for revascularization initially limited by balloon catheter angioplasty. For example, stents reduce both the acute risk of major complications and late-term restenosis. The success of new coronary devices in meeting these goals is in part represented by the less frequent use of PTCA alone (<30%) and the high (>70%) penetration of coronary stenting in the current practice of interventional cardiology. Atherectomy devices and stenting, associated with improved acute angiographic and clinical outcomes compared to PTCA, in specific subsets, continue to be applied to a wider patient domain that includes multivessel disease and complex coronary anatomy. However, strong evidence (level A data from multiple randomized clinical trials) is only available for stenting in selected patients undergoing single-vessel PCI. These Guidelines will focus on the Food and Drug Administration (FDA) approved balloon-related and nonballoon coronary revascularization devices.
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III. Outcomes
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The outcomes of coronary interventional procedures are measured in terms of success and complications and are related to the mechanisms of the employed devices, as well as the clinical and anatomic patient-related factors. With increased operator experience, new technology, and adjunctive pharmacotherapy, the overall success and complication rates of angioplasty have improved.
A. Definitions of PCI success.
The success of a PCI procedure may be defined by angiographic, procedural, and clinical criteria.
1. Angiographic success
A successful PCI produces substantial enlargement of the lumen at the target site. The consensus definition prior to the widespread use of stents was the achievement of a minimum stenosis diameter reduction to <50% in the presence of grade 3 TIMI flow (assessed by angiography). However, with the advent of advanced adjunct technology, including coronary stents, a minimum stenosis diameter reduction to <20% has been the clinical benchmark of an optimal angiographic result.
2. Procedural success
A successful PCI should achieve angiographic success without in-hospital major clinical complications (e.g., death, myocardial infarction [MI], emergency coronary artery bypass surgery [CABG]) during hospitalization. Although the occurrence of emergency artery coronary bypass surgery and death are easily identified end points, the definition of procedure-related MI has been debated. The development of Q-waves in addition to a threshold value of CK elevation has been commonly used. However, the significance of enzyme elevations in the absence of Q-waves remains a subject of investigation and debate. Several reports have identified nonQ-wave MIs with CK-MB elevations 3 to 5 times the upper limit of normal as having clinical significance. Thus a significant increase in CK-MB without Q-waves is considered by most to qualify as an associated complication of PCI.
If serial determinations are performed after PCI, an abnormally high value (CK-MB >1 times normal) can be expected in 10 to 15% of PTCA procedures, 15 to 20% of stent procedures, 25 to 35% of atherectomy procedures, and >25% for any device used in saphenous vein grafts (SVGs) or long lesions with a high atherosclerotic burden, even in the absence of other signs and symptoms of MI. There is no accepted consensus on what level of CK-MB index (with or without clinical or electrocardiographic [ECG] findings) is indicative of a clinically important MI following the interventional procedure. Cardiac troponin T and I have now been introduced as measurements of myocardial necrosis and have been proven to be more sensitive and specific than CK-MB. However, prognostic criteria after PCI based on troponin T and I have not yet been developed. The Writing Committee recommends that CK-MB determination be performed on all patients who have signs or symptoms suggestive of MI following the procedure or in patients in whom there is angiographic evidence of abrupt vessel closure, important side branch occlusion, or new and persistent slow coronary flow. In patients in whom a clinically driven CK-MB determination is made, a CK-MB of >3 times the upper limit of normal would constitute a clinically significant MI.
3. Clinical success
In the short term, a clinically successful PCI includes anatomic and procedural success with relief of signs and/or symptoms of myocardial ischemia after the patient recovers from the procedure. The long-term clinical success requires that the short-term clinical success remains durable and that the patient has persistent relief of signs and symptoms of myocardial ischemia for more than 6 months after the procedure. Restenosis is the principal cause of lack of long-term clinical success when a short-term clinical success has been achieved.
B. Definitions of procedural complications.
As outlined in the 1998 coronary interventional document, procedural complications are divided into six basic categories: death, MI, emergency CABG, stroke, vascular access site complications, and contrast agent nephropathy. Key data elements and definitions to measure the clinical management and outcomes of patients undergoing diagnostic catheterization and/or PCI have been defined in the Clinical Data Standards document and the ACC-National Cardiovascular Data RegistryTM Catheterization Laboratory Module version 2.0. These rigorous definitions for key adverse events are endorsed by this Writing Committee for inclusion in the present PCI Guidelines (Table 1).
C. Acute outcome.
Improvements in balloon technology coupled with the increased use of nonballoon devices, particularly stents (which are effective in treating abrupt vessel closure) and GP IIb/IIIa platelet receptor antagonists have favorably influenced acute procedural outcome. This combined balloon/device/pharmacologic approach to coronary intervention in elective procedures has resulted in angiographic success rates of 96 to 99%, with Q-wave MI rates of 1 to 3%, emergency coronary bypass surgery rates of 0.2 to 3%, and unadjusted in-hospital mortality rates of 0.5 to 1.4%.
D. Long-term outcome and restenosis.
Although improvements in technology, including stents and new pharmacologic therapy, have resulted in an improved acute outcome of the procedure, the impact of these changes on long-term (5 to 10 years) outcome may be less dramatic where factors such as advanced age, reduced left ventricular (LV) function, and complex multivessel disease in patients currently undergoing PCI may have a more important influence. In addition, available data on long-term outcome are mostly limited to patients undergoing PTCA. Ten-year follow-up of the initial cohort of patients treated with PTCA revealed an 89.5% survival rate (95% in patients with single-vessel disease, 81% in patients with multivessel disease). In patients within the 19851986 NHLBI PTCA Registry, 5-year survival was 92.9% for patients with single-vessel disease, 88.5% for those with 2-vessel disease, and 86.5% for those with 3-vessel disease. In patients with multivessel disease undergoing PTCA in BARI, 5-year survival was 86.3% and infarct-free survival was 78.7%. Specifically, 5-year survival was 84.7% in patients with 3-vessel disease and 87.6% in patients with 2-vessel disease.
In addition to the presence of multivessel disease, other clinical factors adversely impact late mortality. In randomized patients with treated diabetes in BARI, the 5-year survival was 65.5%, and the cardiac mortality was 20.6% in comparison to 5.8% cardiac mortality in patients without treated diabetes, although among eligible but not randomized diabetic patients, the 5-year cardiac mortality was 7.5%. In the 19851986 NHLBI PTCA Registry, 4-year survival was significantly lower in women (89.2%) in comparison to men (93.4%). In addition, although LV dysfunction was not associated with an increase in in-hospital mortality or nonfatal MI in patients undergoing PTCA in the same registry, it was an independent predictor of a higher long-term mortality.
A major determinant of event-free survival following coronary intervention is the incidence of restenosis which had, until the development of stents, remained fairly constant, despite multiple pharmacologic and mechanical approaches to limit this process (Table 2). Depending on the definition, (i.e., whether clinical or angiographic restenosis or target lesion revascularization is measured), the incidence of restenosis following coronary intervention had been 30 to 40%, and higher in certain clinical and angiographic subsets.
Although multiple clinical factors (diabetes, unstable angina, acute MI, prior restenosis), angiographic factors (proximal left anterior descending artery, small vessel diameters, total occlusion, long lesion length, SVG), and procedural factors (higher post-procedure percent diameter stenosis, smaller minimal lumen diameter, and smaller acute gain), have been associated with an increased incidence of restenosis, the ability to integrate these factors and predict the risk of restenosis in individual patients following the procedure remains difficult. The most promising potential approaches to favorably impact the restenosis process relate to: 1) the ability to decrease elastic recoil and remodeling using intracoronary stents, and 2) to the ability to reduce intimal hyperplasia using catheter-based ionizing radiation. More than 6,300 patients have been studied in 12 randomized clinical trials to assess the efficacy of PTCA vs. stents to reduce restenosis (Table 3).
In addition, randomized studies in patients with in-stent restenosis have shown that both intracoronary gamma and beta radiation significantly reduced the rate of subsequent angiographic and clinical restenosis by 30 to 50%.
E. Predictors of success/complications.
1. Anatomic factors
The risk of PTCA in the pre-stent era relative to anatomic subsets has been identified in previous NHLBI PTCA Registry data and by the ACC/AHA Task Force. The lesion classification based on severity of characteristics proposed in the past has been principally altered using the present PCI techniques, which capitalize on the ability of stents to manage initial and subsequent complications of coronary interventions. As a result the Committee has revised the previous ACC/AHA lesion classification system to reflect low, moderate, and high risk (Table 4) in accordance with the PCI Clinical Data Standards from the ACC-National Cardiovascular Data RegistryTM.
2. Clinical factors
Coexistent clinical conditions can increase the complication rates for any given anatomic risk factor. The clinical risk factors associated with in-hospital adverse events have been further evaluated with additional experience during the PCI era and summarized based on odds ratio >2.0 or results of multivariate analysis (Table 5).
3. Risk of death
In the majority of patients undergoing elective PCI, death as a result of PCI is directly related to the occurrence of coronary artery occlusion and is most frequently associated with pronounced LV failure. The clinical and angiographic variables associated with increased mortality include advanced age, female gender, diabetes, prior MI, multivessel disease, left main or equivalent coronary disease, a large area of myocardium at risk, pre-existing impairment of LV or renal function, and collateral vessels supplying significant areas of myocardium that originate distal to the segment to be dilated (Table 5).
4. Women
In comparison to men, women undergoing PCI are older and have a higher incidence of hypertension, diabetes mellitus, hypercholesterolemia, and comorbid disease. Early reports of patients undergoing PTCA revealed a lower procedural success rate in women; however, more recent studies have noted similar angiographic outcome and incidence of MI and emergency coronary bypass surgery in women and men. Although reports have been inconsistent, in several large-scale registries, in-hospital mortality is significantly higher in women and an independent effect of gender on acute mortality following PCI persists after adjustments for the baseline higher-risk profile in women.
5. The elderly patient
Age >75 years is one of the major clinical variables associated with increased risk of complications. In the elderly population, the morphologic and clinical variables are compounded by advanced years with the very elderly having the highest-risk of adverse outcomes. In the stent era, procedural success rates and short-term outcomes are comparable to those for nonoctogenarians. Thus, with rare exception (primary PCI for cardiogenic shock for patients >75 years), a separate category has not been created in these Guidelines for the elderly. However, their higher incidence of comorbidities should be taken into account when considering the need for PCI.
6. Diabetes mellitus
In the TIMI-IIB study of MI, patients with diabetes mellitus had significantly higher 6-week (11.6% vs. 4.7%), 1-year (18.0% vs. 6.7%), and 3-year (21.6% vs. 9.6%) mortality rates compared to nondiabetic patients. The BARI trial, in which stents and abciximab were not used, showed that survival was better for patients with treated diabetes undergoing CABG with an arterial conduit than for those undergoing angioplasty. Stenting decreases the need for target revascularization procedures in diabetic patients compared with PTCA. The efficacy of stenting with GP IIb/IIIa inhibitors was assessed in the diabetic population compared to those without diabetes in a substudy of the EPISTENT trial. Irrespective of revascularization strategy abciximab significantly reduced 6-month death and MI rates in patients with diabetes for all strategies. Likewise, 6-month target-vessel revascularization was reduced in the stent/abciximab group approach.
7. Coronary angioplasty after coronary artery bypass surgery
Although speculated to be at higher risk, patients having PCI of native vessels after prior coronary bypass surgery have, in recent years, nearly equivalent interventional outcomes and complication rates compared to patients having similar interventions without prior surgery. For PCI of SVG, studies indicate that the rate of successful angioplasty exceeds 90%, death <1.2%, Q-wave MI <2.5%. The incidence of nonQ-wave MI may be higher than that associated with native coronary arteries.
Use of GP IIb/IIIa blockers has not been shown to improve results of angioplasty in vein grafts. The native vessels should be treated with PCI if feasible. Patients with older and/or severely diseased SVGs may benefit from elective repeat coronary artery bypass graft surgery rather than PCI.
8. Specific technical considerations
Certain outcomes of PCI may be specifically related to the technology utilized for coronary recanalization. Antecedent unstable angina appears to be a clinical predictor of slow flow and periprocedural infarction following ablative technologies and direct platelet activation has been demonstrated to occur with both directional and rotational atherectomy.
Coronary perforation may occur more commonly following the use of ablative technologies including rotational, directional or extraction atherectomy, and excimer laser coronary angioplasty. Coronary perforation complicates PCI more frequently in the elderly and in women. While 20% of perforations may be secondary to the coronary guidewire, most are related to the specific technology used.
9. Issues of hemodynamic support in high-risk angioplasty
Elective high-risk PCI can be performed safely without intra-aortic balloon pump (IABP) or cardiopulmonary support (CPS) in most circumstances. Emergency high-risk PCI such as direct PCI for acute MI can usually be performed without IABP or CPS. CPS for high-risk PCI should be reserved only for patients at the extreme end of the spectrum of hemodynamic compromise, such as those patients with extremely depressed LV function and patients in cardiogenic shock. However, it should be noted that in patients with borderline hemodynamics, ongoing ischemia, or cardiogenic shock, insertion of an intra-aortic balloon just prior to coronary instrumentation has been associated with improved outcomes. Furthermore, it is reasonable to obtain vascular access in the contralateral femoral artery prior to the procedure in patients in whom the risk of hemodynamic compromise is high, thereby facilitating intra-aortic balloon insertion, if necessary.
In patients having a higher-risk profile, consideration of alternative therapies, particularly CABG, formalized surgical standby, or periprocedural hemodynamic support should be addressed before proceeding with PCI.
F. Comparison with bypass surgery.
The major advantage of PCI is its relative ease of use, avoiding general anesthesia, thoracotomy, extracorporeal circulation, CNS complications, and prolonged convalescence. Repeat PCI can be performed more easily than repeat bypass surgery, and revascularization can be achieved more quickly in emergency situations. The disadvantages of PCI are early restenosis and the inability to relieve many totally occluded arteries and/or those vessels with extensive atherosclerotic disease.
Coronary artery bypass surgery has the advantages of greater durability (graft patency rates exceeding 90% at 10 years with arterial conduits) and more complete revascularization irrespective of the morphology of the obstructing atherosclerotic lesion. Generally speaking, the greater the extent of coronary atherosclerosis and its diffuseness, the more compelling the choice of CABG, particularly if LV function is depressed. Patients with lesser extent of disease and localized lesions are good candidates for endovascular approaches.
Percutaneous transluminal coronary angioplasty and CABG have been compared in many nonrandomized and randomized studies. The most accurate comparisons of outcomes are best made from prospective randomized trials of patients suitable for either treatment. Although results of these trials provide useful information for selection of therapy in several patient subgroups, prior studies of PTCA may not reflect outcome of current PCI practice, which includes frequent use of stents and antiplatelet drugs. Similarly, many previous studies of CABG may not reflect outcome of current surgical practice in which arterial conduits are used whenever practicable. Beating heart bypass operations are also employed for selected patients with single-vessel disease with reduced morbidity. In addition, patients are selected for PCI (with or without stenting) because of certain lesion characteristics, and these anatomical criteria are not required for CABG.
Despite these limitations, some generalizations can be made from comparative trials of PTCA and CABG. First, for most patients with single-vessel disease, late survival is similar with either revascularization strategy, and this might be expected given the generally good prognosis of most patients with single-vessel disease managed medically.
In the ARTS trial, the first trial to compare stenting with surgery, there was no significant difference in mortality between PCI and surgical groups at one year. The main difference compared to previous PTCA and CABG trials was an approximate 50% reduction in the need for repeat revascularization in a group randomized to PCI with stent placement.
Direct comparison of initial strategies of PCI or CABG in patients with multivessel coronary disease is possible only by randomized trials because of selection criteria of patients for PCI. There have been five large (>300 patients) randomized trials of PTCA versus CABG and two smaller studies. These trials demonstrate that in appropriately selected patients with multivessel coronary disease, an initial strategy of standard PTCA yields similar overall outcomes (e.g., death, MI) compared to initial revascularization with coronary artery bypass.
An important exception to the conclusion of the relative safety of PCI in multivessel disease is the subgroup of patients with treated diabetes mellitus. Among treated diabetic patients in BARI assigned to PTCA, 5-year survival was 65.5% compared to 80.6% for patients having CABG (p = 0.003); the improved outcome with CABG was due to reduced cardiac mortality (5.8% vs. 20.6%, p = 0.0003), which was confined to those receiving at least one internal mammary artery graft.
G. Comparison with medicine.
There has been a considerable effort made to evaluate the relative effectiveness of bypass surgery as compared to PCI for coronary artery revascularization. In contrast to this, very little effort has been directed toward comparing medical therapy with PCI for the management of stable and unstable angina.
Based on the limited data available from randomized trials (Table 6) comparing medical therapy with PTCA, it seems prudent to consider medical therapy for the initial management of most patients with Canadian Cardiovascular Society Classification Class I and II and reserve PTCA and CABG for those patients with more severe symptoms and ischemia. The symptomatic individual patient who wishes to remain physically active, regardless of age, will more often require PCI. The results of the ACIP trial indicate that higher-risk patients with asymptomatic ischemia and significant CAD who undergo complete revascularization with CABG or PTCA may have a better outcome as compared to those with medical management.
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IV. Institutional and operator competency
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A. Quality assurance.
A mechanism for valid peer review must be established and ongoing at each institution performing PCI. Interventional cardiology procedures are associated with complications that in general are inversely related to operator and institutional volume. The mechanism for institutional review should provide an opportunity for interventionalists as well as physicians who do not perform angioplasty, but are knowledgeable about it, to review overall results of the program on a regular basis. The responsible supervising authority should monitor the following issues as outlined in Table 7.
The institutional credentialing committee should document that an interventionalist wishing to start practice meets the established training criteria, including those of the ACC Task Force on Training in Cardiac Catheterization and Interventional Cardiology. This Writing Committee agrees with the ACC Task Force recommendations for the Assessment and Maintenance of Proficiency in Coronary Interventional Procedures. Institutions performing PCI should meet the following standards as outlined in Tables 8 and 9.
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Table 10 Patient Selection for Angioplasty and Emergency Aortocoronary Bypass at Hospitals Without On-Site Cardiac Surgery
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B. Operator and institutional volume.
The proliferation of small angioplasty or small surgical programs to support such angioplasty programs is strongly discouraged. Several studies have identified procedural volume as a determining factor for frequency of complications with PCI.
Although some investigators have suggested that low procedure volume does not contribute to poor outcomes, these studies are small in number and underpowered for analysis. Development of small cardiovascular surgical programs to support angioplasty is a poor use of resources that will likely lead to suboptimal results.
Given the concerns regarding operator volume and surgical standby, it is recommended that PCI be performed by higher volume operators ( 75 cases/year) with advanced technical skills (e.g., subspecialty certification) at institutions with fully equipped interventional laboratories and experienced support staff. This setting will most often be in a high-volume center (>400 cases/year) associated with an on-site cardiovascular surgical program. Similar concerns have been identified and supported by the Task Force for Practice Guidelines for Coronary Angiography.
This Committee acknowledges that not every cardiologist desiring to do PCI should perform these procedures and not every hospital anxious to have an interventional program should start one. This caveat is particularly true where there are high-volume programs and operators nearby. In these situations, operators should be subspecialty board certified.
Recommendations for PCI Institutional and Operator Volumes at Centers With On-Site Cardiac Surgery
Class I - PCI done by operators with acceptable volume (
75) at high-volume centers (>400). (Level of Evidence: B)
Class IIa - PCI done by operators with acceptable volume (
75) at low-volume centers (200 to 400). (Level of Evidence: C)
- PCI done by low volume operators (<75) at high-volume centers (>400). Note: Ideally operators with annual procedure volume <75 should only work at institutions with an activity level of >600 procedures/year.* (Level of Evidence: C)
Class III - PCI done by low volume operators (<75) at low-volume centers (200 to 400). Note: An institution with a volume <200 procedures/year, unless in a region that is underserved because of geography, should carefully consider whether it should continue to offer service.* (Level of Evidence: C)
C. On-site cardiac surgical backup.
Cardiac surgical backup for PCI has evolved from the formal surgical standby in the 1980s to an informal arrangement of first available operating room and, in some cases, off-site surgical backup. With the advent of intracoronary stenting, there has been a decrease in the need for emergency coronary bypass, ranging between 0.4 and 2%.
1. Primary PCI without on-site cardiac surgery
Although thrombolytic trials demonstrated that early reperfusion saves myocardium and reduces mortality, the superiority and greater applicability of primary PCI for the treatment of acute MI has raised the question of whether primary PCI should be performed at institutions with diagnostic cardiac catheterization laboratories that do not perform elective PCI or have on-site cardiac surgery. For this reason, the establishment of PCI programs at institutions without on-site cardiovascular surgery has been promoted as necessary to maintain quality of care. It must be realized that PCI in the early phase of an acute MI can be difficult and requires even more skill and experience than routine PCI in the stable patient. The need for an experienced operator and experienced laboratory technical support with availability of a broad range of catheters, guidewires, stents, and other devices (e.g., IABP) that are required for optimum results in an acutely ill patient is of major importance (Table 9). If these complex patients are treated by interventionalists with limited experience at institutions with low volume, then the gains of early intervention may be lost because of increased complications. In such circumstances, transfer to a center that routinely performs complex PCI will often be a more effective and efficient course of action. Thrombolysis is still an acceptable form of therapy and is preferable to acute PCI by an inexperienced team.
Criteria have been suggested for the performance of primary PCI at hospitals without on-site cardiac surgery (Tables 9 and 10). Of note, large-scale registries have shown an inverse relationship between the number of primary angioplasty procedures performed and in-hospital mortality. The data suggest that both door-to-balloon time and in-hospital mortality are significantly lower in institutions performing a minimum of 36 primary angioplasty procedures per year. Communities may identify a unique qualified and experienced center wherein the on-site intervention for acute MI could be performed. Suboptimal results may relate to operator/staff inexperience and capabilities and delays in performing angioplasty for logistical reasons. From clinical data and expert consensus, the Committee recommends that primary PCI for acute MI performed at hospitals without established elective PCI programs should be restricted to those institutions with a proven plan for rapid and effective PCI as well as rapid access to cardiac surgery in a nearby facility (Table 11).
2. Elective PCI without on-site surgery
Technical improvements in interventional cardiology have led to the development of elective angioplasty programs without on-site surgical coverage. Caution is warranted before endorsing an unrestricted policy for PCI in hospitals without appropriate facilities. Several outstanding and critically important clinical issues, such as timely management of ischemic complications, adequacy of specialized post-interventional care, logistics for managing cardiac surgical or vascular complications and operator/laboratory volumes, and accreditation must be addressed. At this time, the Committee, therefore, continues to support the recommendation that elective PCI should not be performed in facilities without on-site cardiac surgery (Table 11). As with many dynamic areas in interventional cardiology, these recommendations may be subject to revision as clinical data and experience increase.
Recommendations for PCI With and Without On-Site Cardiac Surgery (Table 11)
Class I - Patients undergoing elective PCI in facilities with on-site cardiac surgery. (Level of Evidence: B)
- Patients undergoing primary PCI in facilities with on-site cardiac surgery. (Level of Evidence: B)
Class IIb - Patients undergoing primary PCI in facilities without on-site cardiac surgery, but with a proven plan for rapid access (within 1 h) to a cardiac surgery operating room in a nearby facility with appropriate hemodynamic support capability for transfer. The procedure should be limited to patients with ST-segment elevation MI or new LBBB on ECG, and done in a timely fashion (balloon inflation within 90 ± 30 min of admission) by persons skilled in the procedure (
75 PCIs/year) and only at facilities performing a minimum of 36 primary PCI procedures per year. (Level of Evidence: B)
Class III - Patients undergoing elective PCI in facilities without on-site cardiac surgery. (Level of Evidence: C)
- Patients undergoing primary PCI in facilities without on-site cardiac surgery and without a proven plan for rapid access (within 1 h) to a cardiac surgery operating room in a nearby facility with appropriate hemodynamic support capability for transfer or when performed by lower skilled operators (<75 PCIs/year) in a facility performing <36 primary PCI procedures per year. (Level of Evidence: C)
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V. Indications
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A broad spectrum of clinical presentations exists wherein patients may be considered candidates for PCI, ranging from asymptomatic to severely symptomatic or unstable, with variable degrees of jeopardized myocardium. Each time that a patient is considered for revascularization, the potential risk and benefits of the particular procedure under consideration must be weighed against alternative therapies.
The initial simplicity and associated low morbidity of PCI as compared to surgical therapy is always attractive, but the patient and family must understand the limitations inherent in current PCI procedures, including a realistic presentation of the likelihood of restenosis and the potential for incomplete revascularization as compared with CABG surgery. In patients with CAD who are asymptomatic or have only mild symptoms, the potential benefit of antianginal drug therapy along with an aggressive program of risk reduction must also be understood by the patient before a revascularization procedure is performed.
A. Asymptomatic or mild angina.
In the previous ACC/AHA Guidelines for PTCA, specific recommendations were made separately for patients with single- or multivessel disease. The current techniques of PCI have matured to the point where, in patients with favorable anatomy, the competent practitioner can perform either single- or multivessel PCI at low risk and with a high likelihood of initial success. For this reason, in this revision of the Guidelines, recommendations will be made largely based upon the patients clinical condition, specific coronary lesion morphology and anatomy, LV function, and associated medical conditions, and less emphasis will be placed on the number of lesions or vessels requiring PCI. The CCS Class of angina (I to IV) is used to define the severity of symptoms. The categories described in this section refer to an initial PCI procedure in a patient without prior CABG surgery.
The Committee recognizes that the majority of patients with asymptomatic ischemia or mild angina should be treated medically. The published ACIP study casts some doubt on the wisdom of medical management for those higher-risk patients who are asymptomatic or have mild angina, but have objective evidence by both treadmill testing and ambulatory monitoring of significant myocardial ischemia and CAD. In addition, there is a substantial portion of the middle and older age populations in this country that remains physically active, participating in sports, such as tennis and skiing, or performing regular and vigorous physical exercise, such as jogging, who have CAD. For such individuals with moderate or severe ischemia and few symptoms, revascularization with PCI or CABG surgery may reduce their risk of serious or fatal cardiac events. For this reason, patients in this category of higher-risk asymptomatic ischemia or mild symptoms and severe anatomic CAD are placed in Class I or II. PCI may be considered if there is a high likelihood of success and a low risk of morbidity or mortality. The judgment of the experienced physician is deemed valuable in assessing the extent of ischemia.
Recommendations for PCI in Asymptomatic or Class I Angina Patients
Class I - Patients who do not have treated diabetes with asymptomatic ischemia or mild angina with 1 or more significant lesions in 1 or 2 coronary arteries suitable for PCI with a high likelihood of success and a low risk of morbidity and mortality. The vessels to be dilated must subtend a large area of viable myocardium (Table 12). (Level of Evidence: B)
Class IIa - The same clinical and anatomic requirements for Class I, except the myocardial area at risk is of moderate size or the patient has treated diabetes. (Level of Evidence: B)
Class IIb - Patients with asymptomatic ischemia or mild angina with
3 coronary arteries suitable for PCI with a high likelihood of success and a low risk of morbidity and mortality. The vessels to be dilated must subtend at least a moderate area of viable myocardium. In the physicians judgment, there should be evidence of myocardial ischemia by ECG exercise testing, stress nuclear imaging, stress echocardiography or ambulatory ECG monitoring, or intracoronary physiologic measurements. (Level of Evidence: B)
Class III - Patients with asymptomatic ischemia or mild angina who do not meet the criteria as listed under Class I or Class II and who have:
- Only a small area of viable myocardium at risk.
- No objective evidence of ischemia.
- Lesions that have a low likelihood of successful dilation.
- Mild symptoms that are unlikely to be due to myocardial ischemia.
- Factors associated with increased risk of morbidity or mortality.
- Left main disease.
- Insignificant disease <50%. (Level of Evidence: C)
B. Angina Class II to IV or unstable angina.
Many patients with moderate or severe stable angina or unstable angina do not respond adequately to medical therapy and often have significant coronary artery stenoses that are suitable for revascularization with CABG surgery or PCI. In addition, a proportion of these patients have reduced LV systolic function which places them in a group that is known to have improved survival with CABG surgery and possibly with revascularization by PCI. In nondiabetic patients with 1- or 2-vessel disease in whom angioplasty of 1 or more lesions has a high likelihood of initial success, PCI is the preferred approach. In a minority of such patients, CABG surgery may be preferred, particularly for those in whom the left anterior descending coronary artery can be revascularized with the internal mammary artery or in those with left main coronary disease. In patients with unstable angina or nonQ-wave MI, intensive medical therapy should be initiated prior to revascularization with PCI or CABG surgery. Patients with unstable angina and nonST-segment elevation MI have been randomized to medical therapy or PCI in the FRISC II and TACTICS TIMI 18 trials. These trials utilizing stenting as the primary therapy have favored the invasive approach.
The indications for coronary angiography are summarized in the ACC/AHA Coronary Angiography Guidelines and recommendations for PCI are summarized in the ACC/AHA Unstable Angina Guidelines. Indications for PCI for patients with angina Class II to IV, unstable angina, or nonQ-wave infarction follow.
Recommendations for Patients With Moderate or Severe Symptoms (Angina Class II to IV, Unstable Angina or NonST-Elevation MI) With Single- or Multivessel Coronary Disease on Medical Therapy
Class I - Patients with 1 or more significant lesions in 1 or more coronary arteries suitable for PCI with a high likelihood of success and low risk of morbidity or mortality (Table 5). The vessel(s) to be dilated must subtend a moderate or large area of viable myocardium and have high risk (Table 12). (Level of Evidence: B)
Class IIa - Patients with focal saphenous vein graft lesions or multiple stenoses who are poor candidates for reoperative surgery. (Level of Evidence: C)
Class IIb - Patient has 1 or more lesions to be dilated with reduced likelihood of success (Table 5) or the vessel(s) subtend a less than moderate area of viable myocardium. Patients with 2- or 3-vessel disease, with significant proximal LAD CAD and treated diabetes or abnormal LV function. (Level of Evidence: B)
Class III - Patient has no evidence of myocardial injury or ischemia on objective testing and has not had a trial of medical therapy, or has:
- Only a small area of myocardium at risk.
- All lesions or the culprit lesion to be dilated with morphology with a low likelihood of success.
- A high risk of procedure-related morbidity or mortality. (Level of Evidence: C)
- Patients with insignificant coronary stenosis (e.g., <50% diameter). (Level of Evidence: C)
- Patients with significant left main CAD who are candidates for CABG. (Level of Evidence: B)
It is recognized by the Committee that the assessment of risk of unsuccessful PCI or serious morbidity or mortality must always be made with consideration of the alternative therapies available for the patient, including more intensive or prolonged medical therapy or surgical revascularization (Table 13) , especially in patients with unstable angina pectoris.
When CABG surgery is a poor option because of high risk due to special considerations or other organ system disease, patients otherwise in Class IIb may be appropriately managed with PCI. Under these special circumstances formal surgical consultation is recommended.
C. Myocardial infarction.
The results of randomized clinical trials of intravenous thrombolysis and subsequent management strategies of immediate, delayed, and deferred PCI have established the benefits of early pharmacologic and mechanical reperfusion therapies for patients with acute MI.
Percutaneous coronary intervention is a very effective method for re-establishing coronary perfusion and is suitable for 90% of patients. Considerable data support the use of PCI for patients with acute MI. Reported rates of achieving TIMI 3 flow, the goal of reperfusion therapy, range from 70 to 90%. Late follow-up angiography demonstrates that 87% of infarct arteries remain patent. Although most evaluations of PCI have been in patients who are eligible to receive thrombolytic therapy, considerable experience supports the value of PCI for patients who may not be suitable for thrombolytic therapy due to an increased risk of bleeding.
Intracoronary stents appear to augment the results of PCI for MI (Table 14). Preliminary results suggest that stenting achieves a better immediate angiographic result with a larger arterial lumen, less reclosure of the infarct-related artery, and fewer subsequent ischemic events than PTCA alone. Results from a randomized clinical trial suggest that stenting enhances late clinical outcomes (reduction in composite end point attributable to a decrease in target-vessel revascularization) when compared to PTCA alone. However an increase in mortality at 1 year among the stent group has been reported in the Stent-PAMI trial.
Primary PTCA performed without routine stenting has been compared to thrombolytic therapy in several randomized clinical trials. These investigations consistently demonstrate that PTCA-treated patients experience less recurrent ischemia or infarction than those treated by thrombolysis. Trends favoring a survival benefit with PTCA are noted. Two meta-analyses showed superiority of PCI over thrombolysis for mortality with risk reductions of 0.34 and 0.56. It is important to note that these results of PCI have been achieved in medical centers with experienced providers and under circumstances where angioplasty can be performed immediately following patient presentation.
1. PCI in thrombolytic-ineligible patients
Randomized, controlled clinical trials evaluating the outcome of PCI for patients who present with ST-segment elevation but who are ineligible for thrombolytic therapy and for patients who experience infarction without ST-segment elevation have not been performed. Nevertheless, there is a general consensus that PCI is an appropriate means for achieving reperfusion in patients who cannot receive thrombolytics because of increased risk of hemorrhage. Other reasons also exclude acute MI patients from thrombolytic therapy and the outcome of PCI in these patients may differ from those eligible for lytic therapy. For example, patients who present without ST-elevation are more often older and female and have higher in-hospital mortality than those with ST-segment elevation. Little data are available to characterize the value of primary PCI for this subset of acute MI patients (Table 15).
2. Post-thrombolysis PCI
In asymptomatic patients, the strategies of routine PCI of the stenotic infarct-related artery immediately after successful thrombolysis show no benefit with regard to salvage of jeopardized myocardium or prevention of reinfarction or death. In some studies this approach was associated with increased incidence of adverse events, which include bleeding, recurrent ischemia, emergency coronary artery surgery, and death. Routine PCI immediately after thrombolysis may increase the chance for vascular complications at the catheterization access site and hemorrhage into the infarct-related vessel wall.
3. Rescue PCI
Rescue (also known as salvage) PCI is defined as PCI after failed thrombolysis for patients with continuing or recurrent myocardial ischemia. Rescue PCI has resulted in higher rates of early infarct-artery patency, improved regional infarct zone wall motion, and greater freedom from adverse in-hospital clinical events compared to a deferred PCI strategy. The randomized evaluation of rescue PCI with combined utilization end points trial (RESCUE) demonstrated a reduction in rates of in-hospital death and combined death and congestive heart failure maintained up to 1 year after study entry for patients presenting with anterior wall MI who failed thrombolytic therapy. Improvement in TIMI grade flow from 2 to 3 may offer additional clinical benefit.
4. PCI for cardiogenic shock
Observational studies support the value of PCI for patients who develop cardiogenic shock in the early hours of MI. For patients who do not have mechanical causes of shock, such as acute mitral regurgitation or septal or free wall rupture, mortality among those having PCI is lower than those treated by medical means.
A randomized clinical trial has further clarified the role of emergency revascularization (ERV) in acute MI complicated by cardiogenic shock. This multicenter trial supports the use of ERV with PCI in appropriate candidates for patients <75 years old with acute MI complicated by cardiogenic shock. After 6 months, there was significant survival benefit to early revascularization. These data strongly support the approach that patients <75 years with acute MI complicated by cardiogenic shock should undergo emergency revascularization and support measures.
5. PCI hours to days after thrombolysis
Patients who achieve reperfusion and myocardial salvage following thrombolytic therapy may experience reocclusion of the infarct artery and recurrent MI. This concern has prompted the routine use of catheterization and PCI prior to hospital discharge to identify and dilate the culprit lesion. The SWIFT study examined 800 patients with acute MI randomly assigned to PCI within 2 to 7 days after thrombolysis or to conservative management with intervention for spontaneous or provocable ischemia. There were no differences in the two treatment strategies regarding LV function, incidence of reinfarction, in-hospital survival, or 1-year survival rate. These data indicate that routine PCI of the infarct-related artery in the absence of spontaneous or provoked ischemia is not warranted.
Initial studies of late (>6 to 12 h) PCI in asymptomatic survivors of MI indicate that opening an occluded artery does not appear to alter the process of LV dilation, the incidence of spontaneous and inducible arrhythmias, or prognosis. Although data supporting the argument to open occluded infarct-related arteries are persuasive, at least for large arteries subtending large areas of myocardium, there are few randomized trials supporting this approach. It should be noted that the overwhelming majority of trials were performed prior to the widespread use of stents and platelet IIb/IIIa receptor blockade and thus, the potential impact and benefit of these newer therapies in this clinical setting needs re-evaluation.
6. PCI after thrombolysis in selected patient subgroups
a. Young and elderly post-infarct patients
Although not supported by randomized trials, routine cardiac catheterization following thrombolytic therapy for AMI has been a frequently performed strategy in all age groups. Young (<50 years) patients often undergo cardiac catheterization after thrombolytic therapy due to a "perceived need" to define coronary anatomy and thus establish psychological as well as clinical outcomes. In contrast, older (>75 years) patients have higher in-hospital and long-term mortality rates and enhanced clinical outcomes when treated with primary PCI. Confirmatory studies to determine quality-of-life aspects of care in younger patients and to define the potential of other modes of coronary revascularization in older patient groups are not yet available. Based on the current data, with the exception of patients presenting with cardiogenic shock, PCI should be based on clinical need without special consideration of age.
b. Patients with prior myocardial infarction
A prior MI is an independent predictor of death, reinfarction, and need for urgent coronary bypass surgery. In the TIMI-II study, patients with a history of prior MI had a higher 42-day mortality (8.8% vs. 4.3%; p < 0.001), higher prevalence of multivessel CAD (60% vs. 28%; p < 0.001), and a lower LV ejection fraction (42% vs. 48%; p < 0.001) compared to patients with a first MI. Mortality tended to be lower among patients with a prior MI undergoing the invasive compared to the conservative strategy, a benefit which persisted up to 1 year following study entry.
Based on the earlier findings in this document and current practice, PCI should be based on clinical need. The presence of prior MI places the patient in a higher risk subset and should be considered in the PCI decision.
Recommendations for Primary PCI for Acute Transmural MI Patients as an Alternative to Thrombolysis
Class I - As an alternative to thrombolytic therapy in patients with AMI and ST-segment elevation or new or presumed new left bundle branch block who can undergo angioplasty of the infarct artery
12 h from the onset of ischemic symptoms or >12 h if symptoms persist, if performed in a timely fashion* by individuals skilled in the procedure and supported by experienced personnel in an appropriate laboratory environment. (Level of Evidence: A)
- In patients who are within 36 h of an acute ST elevation/Q-wave or new left bundle branch block MI who develop cardiogenic shock, are <75 years of age, and revascularization can be performed within 18 h of the onset of shock
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