Major Recommendations
The American College of Cardiology/American Heart Association (ACC/AHA) Classification of the recommendations for patient evaluation and treatment (Classes I-III) and the levels of evidence (A-C) are defined at the end of the "Major Recommendations" field.
Procedural Considerations
Intraoperative Considerations
Anesthetic Considerations
Class I
- Anesthetic management directed toward early postoperative extubation and accelerated recovery of low- to medium-risk patients undergoing uncomplicated coronary artery bypass grafting (CABG) is recommended (Hawkes, Dhileepan, & Foxcroft, 2003; Myles et al., 2003; van Mastrigt et al., 2006). (Level of Evidence: B)
- Multidisciplinary efforts are indicated to ensure an optimal level of analgesia and patient comfort throughout the perioperative period (Bainbridge, Martin, & Cheng, 2006; Brennan, Carr, & Cousins, 2007; Lahtinen, Kokki, & Hynynen, 2006; Serfontein, 2010; Taillefer et al., 2006). (Level of Evidence: B)
- Efforts are recommended to improve interdisciplinary communication and patient safety in the perioperative environment (e.g., formalized checklist-guided multidisciplinary communication) (Martinez et al., 2010; Wadhera et al., 2010; Neily et al., 2010; Haynes et al., 2009). (Level of Evidence: B)
- A fellowship-trained cardiac anesthesiologist (or experienced board-certified practitioner) credentialed in the use of perioperative transesophageal echocardiography (TEE) is recommended to provide or supervise anesthetic care of patients who are considered to be at high risk (Cahalan et al., 2002; Mathew et al., 2006; Thys, 2009). (Level of Evidence: C)
Class IIa
- Volatile anesthetic-based regimens can be useful in facilitating early extubation and reducing patient recall (Myles et al., 2003; Dowd et al., 1998; Groesdonk, et al., 2010; Cheng et al., "Early," 1996). (Level of Evidence: A)
Class IIb
- The effectiveness of high thoracic epidural anesthesia/analgesia for routine analgesic use is uncertain (Horlocker et al., 2010; Murphy et al., 2003; Nygard et al., 2005; Tenenbein et al., 2008). (Level of Evidence: B)
Class III: HARM
- Cyclooxygenase-2 inhibitors are not recommended for pain relief in the postoperative period after CABG (Nussmeier et al., 2005; Ott et al., 2003). (Level of Evidence: B)
- Routine use of early extubation strategies in facilities with limited backup for airway emergencies or advanced respiratory support is potentially harmful. (Level of Evidence: C)
Bypass Graft Conduit
Class I
- If possible, the left internal mammary artery (LIMA) should be used to bypass the left anterior descending (LAD) artery when bypass of the LAD artery is indicated (Boylan et al., 1994; Cameron et al., 1996; Loop et al., 1986; Sabik et al., 2005). (Level of Evidence: B)
Class IIa
- The right internal mammary artery (IMA) is probably indicated to bypass the LAD artery when the LIMA is unavailable or unsuitable as a bypass conduit. (Level of Evidence: C)
- When anatomically and clinically suitable, use of a second IMA to graft the left circumflex or right coronary artery (when critically stenosed and perfusing left ventricle [LV] myocardium) is reasonable to improve the likelihood of survival and to decrease reintervention (Lytle et al., 1999; Lytle et al., 2004; Sabik et al., 2006; Sabik et al., 2008; Stevens et al., 2004). (Level of Evidence: B)
Class IIb
- Complete arterial revascularization may be reasonable in patients less than or equal to 60 years of age with few or no comorbidities. (Level of Evidence: C)
- Arterial grafting of the right coronary artery may be reasonable when a critical (≥90%) stenosis is present (Sabik et al., 2005; Sabik et al., 2008; Sabik et al., 2003). (Level of Evidence: B)
- Use of a radial artery graft may be reasonable when grafting left-sided coronary arteries with severe stenoses (>70%) and right-sided arteries with critical stenoses (≥90%) that perfuse LV myocardium (Acar et al., 1998; Maniar et al., 2002; Moran et al., 2001; Possati et al., 1998; Royse et al., 2000; Desai, et al., 2004). (Level of Evidence: B)
Class III: HARM
- An arterial graft should not be used to bypass the right coronary artery with less than a critical stenosis (<90%) (Sabik et al., 2005). (Level of Evidence: C)
Intraoperative TEE
Class I
- Intraoperative TEE should be performed for evaluation of acute, persistent, and life-threatening hemodynamic disturbances that have not responded to treatment (Eltzschig et al., 2008; Savage et al., 1997). (Level of Evidence: B)
- Intraoperative TEE should be performed in patients undergoing concomitant valvular surgery (Eltzschig et al., 2008; American Society of Anesthesiologists and Society of Cardiovascular Anesthesiologists, 2010). (Level of Evidence: B)
Class IIa
- Intraoperative TEE is reasonable for monitoring of hemodynamic status, ventricular function, regional wall motion, and valvular function in patients undergoing CABG (Savage, et al., 1997; Bergquist, Bellows, & Leung, 1996; Moises et al., 1998; Qaddoura et al., 2004; Swaminathan et al., 2007; Wang et al., 2004; Zimarino et al., 2004). (Level of Evidence: B)
Preconditioning/Management of Myocardial Ischemia
Class I
- Management targeted at optimizing the determinants of coronary arterial perfusion (e.g., heart rate, diastolic or mean arterial pressure, and right ventricular or LV end-diastolic pressure) is recommended to reduce the risk of perioperative myocardial ischemia and infarction (Slogoff & Keats, 1985; Dyub et al., 2008; Heusch, 2008; Gibbons et al., 2002; Lavana et al., 2010). (Level of Evidence: B)
Class IIa
- Volatile-based anesthesia can be useful in reducing the risk of perioperative myocardial ischemia and infarction (Landoni et al., "Desflurane," 2007; Lucchinetti et al., 2007; Yao & Li, 2009; Yu & Beattie, 2006). (Level of Evidence: A)
Class IIb
- The effectiveness of prophylactic pharmacological therapies or controlled reperfusion strategies aimed at inducing preconditioning or attenuating the adverse consequences of myocardial reperfusion injury or surgically induced systemic inflammation is uncertain (Rabi et al., 2010; Buckberg, 2010; MEND-CABG II Investigators et al., 2008; Mangano, 1997; Mangano et al., 2006; Shernan et al., 2004; Smith et al., 2011; Testa et al., 2008). (Level of Evidence: A)
- Mechanical preconditioning might be considered to reduce the risk of perioperative myocardial ischemia and infarction in patients undergoing off-pump CABG (Laurikka et al., 2002; Penttila et al., 2003; Walsh et al., 2008). (Level of Evidence: B)
- Remote ischemic preconditioning strategies using peripheral-extremity occlusion/reperfusion might be considered to attenuate the adverse consequences of myocardial reperfusion injury (Hausenloy et al., 2007; Rahman et al., 2010; Venugopal et al., 2009). (Level of Evidence: B)
- The effectiveness of postconditioning strategies to attenuate the adverse consequences of myocardial reperfusion injury is uncertain (Luo et al., 2008; Ovize et al., 2010). (Level of Evidence: C)
Clinical Subsets
CABG in Patients with Acute Myocardial Infarction (MI)
Class I
- Emergency CABG is recommended in patients with acute MI in whom 1) primary percutaneous coronary intervention (PCI) has failed or cannot be performed, 2) coronary anatomy is suitable for CABG, and 3) persistent ischemia of a significant area of myocardium at rest and/or hemodynamic instability refractory to nonsurgical therapy is present (Alexiou et al., 2008; Chiu et al., 2009; DeWood et al., 1983; Donatelli et al., 1997; Filizcan et al., 2011). (Level of Evidence: B)
- Emergency CABG is recommended in patients undergoing surgical repair of a postinfarction mechanical complication of MI, such as ventricular septal rupture, mitral valve insufficiency because of papillary muscle infarction and/or rupture, or free wall rupture (Chevalier et al., 2004; Lemery et al., 1992; Russo et al., 2008; Shamshad et al., 2010; Tavakoli et al., 2002). (Level of Evidence: B)
- Emergency CABG is recommended in patients with cardiogenic shock and who are suitable for CABG irrespective of the time interval from MI to onset of shock and time from MI to CABG (Donatelli et al., 1997; Hochman et al., 1999; Mehta et al., 2010; White et al., 2005). (Level of Evidence: B)
- Emergency CABG is recommended in patients with life-threatening ventricular arrhythmias (believed to be ischemic in origin) in the presence of left main stenosis greater than or equal to 50% and/or 3-vessel coronary artery disease (CAD) (Ngaage et al., 2008). (Level of Evidence: C)
Class IIa
- The use of CABG is reasonable as a revascularization strategy in patients with multivessel CAD with recurrent angina or MI within the first 48 hours of ST segment elevation myocardial infarction (STEMI) presentation as an alternative to a more delayed strategy (Alexiou, et al., 2008; DeWood et al., 1983; Filizcan et al., 2011; Parikh et al., 2010). (Level of Evidence: B)
- Early revascularization with PCI or CABG is reasonable for selected patients greater than 75 years of age with ST-segment elevation or left bundle branch block who are suitable for revascularization irrespective of the time interval from MI to onset of shock (Lim et al., 2009; Amin et al., 2009; Migliorini et al., 2006; Hochman, et al., 2000; Dzavik et al., 2003). (Level of Evidence: B)
Class III: HARM
- Emergency CABG should not be performed in patients with persistent angina and a small area of viable myocardium who are stable hemodynamically. (Level of Evidence: C)
- Emergency CABG should not be performed in patients with no-reflow (successful epicardial reperfusion with unsuccessful microvascular reperfusion). (Level of Evidence: C)
Life-Threatening Ventricular Arrhythmias
Class I
- CABG is recommended in patients with resuscitated sudden cardiac death or sustained ventricular tachycardia thought to be caused by significant CAD (≥50% stenosis of left main coronary artery and/or ≥70% stenosis of 1, 2, or all 3 epicardial coronary arteries) and resultant myocardial ischemia (Ngaage et al., 2008; Every et al., 1992; Kelly et al., 1990). (Level of Evidence: B)
Class III: HARM
- CABG should not be performed in patients with ventricular tachycardia with scar and no evidence of ischemia. (Level of Evidence: C)
Emergency CABG After Failed PCI
Class I
- Emergency CABG is recommended after failed PCI in the presence of ongoing ischemia or threatened occlusion with substantial myocardium at risk (Barakate et al., 2003; Roy et al., 2009). (Level of Evidence: B)
- Emergency CABG is recommended after failed PCI for hemodynamic compromise in patients without impairment of the coagulation system and without a previous sternotomy (Barakate et al., 2003; Craver et al., 1992; Stamou et al., 2006). (Level of Evidence: B)
Class IIa
- Emergency CABG is reasonable after failed PCI for retrieval of a foreign body (most likely a fractured guidewire or stent) in a crucial anatomic location. (Level of Evidence: C)
- Emergency CABG can be beneficial after failed PCI for hemodynamic compromise in patients with impairment of the coagulation system and without previous sternotomy. (Level of Evidence: C)
Class IIb
- Emergency CABG might be considered after failed PCI for hemodynamic compromise in patients with previous sternotomy. (Level of Evidence: C)
Class III: HARM
- Emergency CABG should not be performed after failed PCI in the absence of ischemia or threatened occlusion. (Level of Evidence: C)
- Emergency CABG should not be performed after failed PCI if revascularization is impossible because of target anatomy or a no-reflow state. (Level of Evidence: C)
CABG in Association with Other Cardiac Procedures
Class I
- CABG is recommended in patients undergoing noncoronary cardiac surgery with greater than or equal to 50% luminal diameter narrowing of the left main coronary artery or greater than or equal to 70% luminal diameter narrowing of other major coronary arteries. (Level of Evidence: C)
Class IIa
- The use of the LIMA is reasonable to bypass a significantly narrowed LAD artery in patients undergoing noncoronary cardiac surgery (Level of Evidence: C)
- CABG of moderately diseased coronary arteries (>50% luminal diameter narrowing) is reasonable in patients undergoing noncoronary cardiac surgery. (Level of Evidence: C)
CAD Revascularization
Heart Team Approach to Revascularization Decisions
Class I
- A Heart Team approach to revascularization is recommended in patients with unprotected left main or complex CAD (Serruys et al., 2009; Feit et al., 2000; King et al., 1997).(Level of Evidence: C)
Class IIa
- Calculation of the Society of Thoracic Surgeons (STS) and SYNTAX scores is reasonable in patients with unprotected left main and complex CAD (Morice et al., 2010; Serruys et al., 2009; Chakravarty et al., 2011; Grover et al., 2001; Kim et al., 2010; Shahian et al., 2009; Shahian et al., 2010; Welke et al., 2007). (Level of Evidence: B)
Revascularization to Improve Survival: Left Main CAD Revascularization
Class I
- CABG to improve survival is recommended for patients with significant (≥50% diameter stenosis) left main coronary artery stenosis (Caracciolo et al., 1995; Chaitman et al., 1981; Dzavik et al., 2001; Takaro et al., 1976; Takaro et al., 1982; Taylor et al., 1989; Yusuf et al., 1994). (Level of Evidence: B)
Class IIa
- PCI to improve survival is reasonable as an alternative to CABG in selected stable patients with significant (≥50% diameter stenosis)unprotected left main CAD with: 1) anatomic conditions associated with a low risk of PCI procedural complications and a high likelihood of good long-term outcome (e.g., a low SYNTAX score [≤22], ostial or trunk left main CAD); and 2) clinical characteristics that predict a significantly increased risk of adverse surgical outcomes (e.g., STS-predicted risk of operative mortality ≥5%) (Morice et al., 2010; Chakravarty et al., 2011; Kim et al., 2010; Buszman et al., 2008; Capodanno et al., 2011; Hannan et al., 2008; Ellis et al., 1997; Biondi-Zoccai et al., 2008; Boudriot et al., 2011; Brener et al., 2008; Chieffo et al., 2006; Chieffo et al., 2010; Lee et al., 2006; Makikallio et al., 2008; Naik et al., 2009; Palmerini et al., 2006; Park et al., 2010; Rodes-Cabau et al., 2008; Sanmartin et al., 2007; Kappetein et al., 2011; Seung et al., 2008; White et al., 2008). (Level of Evidence: B)
- PCI to improve survival is reasonable in patients with unstable angina/non-ST segment elevation myocardial infarction (UA/NSTEMI) when an unprotected left main coronary artery is the culprit lesion and the patient is not a candidate for CABG (Morice et al., 2010; Brener et al., 2008; Chieffo et al., 2006; Chieffo et al., 2010; Lee et al., 2006; Rodes-Cabau et al., 2008; Sanmartin et al., 2007; Seung et al., 2008; White et al., 2008; Montalescot et al., 2009). (Level of Evidence: B)
- PCI to improve survival is reasonable in patients with acute STEMI when an unprotected left main coronary artery is the culprit lesion, distal coronary flow is less than Thrombolysis In Myocardial Infarction grade 3, and PCI can be performed more rapidly and safely than CABG (Ellis et al., 1997; Lee et al., 2008; Lee et al., 2010). (Level of Evidence: C)
Class IIb
- PCI to improve survival may be reasonable as an alternative to CABG in selected stable patients with significant (≥50% diameter stenosis) unprotected left main CAD with: 1) anatomic conditions associated with a low to intermediate risk of PCI procedural complications and an intermediate to high likelihood of good long-term outcome (e.g., low–intermediate SYNTAX score of <33, bifurcation left main CAD); and 2) clinical characteristics that predict an increased risk of adverse surgical outcomes (e.g., moderate–severe chronic obstructive pulmonary disease, disability from previous stroke, or previous cardiac surgery; STS-predicted risk of operative mortality >2%) (Morice et al., 2010; Chakravarty et al., 2011; Kim et al., 2010; Buszman et al., 2008; Capodanno et al., 2011; Hannan et al., 2008; Ellis, et al., 1997; Biondi-Zoccai et al., 2008; Boudriot et al., 2011; Brener et al., 2008; Chieffo et al., 2006; Chieffo et al., 2010; Lee et al., 2006; Makikallio et al., 2008; Naik et al., 2009; Palmerini et al., 2006; Park et al., 2010; Rodes-Cabau et al., 2008; Sanmartin et al., 2007; Kappetein et al., 2011; Seung et al., 2008; White et al., 2008; Park et al., 2011). (Level of Evidence: B)
Class III: HARM
- PCI to improve survival should not be performed in stable patients with significant (≥50% diameter stenosis) unprotected left main CAD who have unfavorable anatomy for PCI and who are good candidates for CABG (Morice et al., 2010; Chakravarty et al., 2011; Kim et al., 2010; Caracciolo et al., 1995; Chaitman et al., 1981; Dzavik et al., 2001; Takaro et al., 1976; Takaro et al., 1982; Taylor et al., 1989; Yusuf et al., 1994; Capodanno et al., 2011; Hannan et al., 2008). (Level of Evidence: B)
Non–Left Main CAD Revascularization
Class I
- CABG to improve survival is beneficial in patients with significant (≥70% diameter) stenoses in 3 major coronary arteries (with or without involvement of the proximal LAD artery) or in the proximal LAD plus 1 other major coronary artery (Dzavik et al., 2001; Yusuf et al., 1994; Jones et al., "Long-term," 1996; Myers er al., 1989; Smith et al., 2006; Varnauskas, 1988). (Level of Evidence: B)
- CABG or PCI to improve survival is beneficial in survivors of sudden cardiac death with presumed ischemia-mediated ventricular tachycardia caused by significant (≥70% diameter) stenosis in a major coronary artery. (CABG Level of Evidence: B [Every et al., 1992; Borger van der Burg et al., 2003; Kaiser et al., 1975]; PCI Level of Evidence: C [Borger van der Burg et al., 2003])
Class IIa
- CABG to improve survival is reasonable in patients with significant (≥70% diameter) stenoses in 2 major coronary arteries with severe or extensive myocardial ischemia (e.g., high-risk criteria on stress testing, abnormal intracoronary hemodynamic evaluation, or >20% perfusion defect by myocardial perfusion stress imaging) or target vessels supplying a large area of viable myocardium (Di Carli et al., 1998; Hachamovitch et al., 2003; Sorajja et al., 2005; Davies et al., 1997). (Level of Evidence: B)
- CABG to improve survival is reasonable in patients with mild-moderate LV systolic dysfunction (EF 35% to 50%) and significant (≥70% diameter stenosis) multivessel CAD or proximal LAD coronary artery stenosis, when viable myocardium is present in the region of intended revascularization (Yusuf et al., 1994; Alderman et al., 1983; O'Connor et al., 2002; Phillips, O'Connor, & Rogers, 2007; Tarakji et al., 2006; Tsuyuki et al., 2006). (Level of Evidence: B)
- CABG with a LIMA graft to improve survival is reasonable in patients with significant (≥70% diameter) stenosis in the proximal LAD artery and evidence of extensive ischemia (Cameron et al., 1996; Loop et al., 1986; Yusuf et al., 1994; Smith et al., 2006). (Level of Evidence: B)
- It is reasonable to choose CABG over PCI to improve survival in patients with complex 3-vessel CAD (e.g., SYNTAX score >22), with or without involvement of the proximal LAD artery, who are good candidates for CABG (Hannan et al., 2008; Kappetein et al., 2011; Smith et al., 2006; Brener et al., 2004; Hannan et al., 2005). (Level of Evidence: B)
- CABG is probably recommended in preference to PCI to improve survival in patients with multivessel CAD and diabetes mellitus, particularly if a LIMA graft can be anastomosed to the LAD artery (Sorajja et al., 2005; "Influence of diabetes," 1997; BARI Investigators, 2007; Banning et al., 2010; Hoffman et al., 2003; Hueb et al., 2007; Malenka et al., 2005; Niles et al., 2001; Weintraub et al., 1998). (Level of Evidence: B)
Class IIb
- The usefulness of CABG to improve survival is uncertain in patients with significant (≥70%) stenoses in 2 major coronary arteries not involving the proximal LAD artery and without extensive ischemia (Smith et al., 2006). (Level of Evidence: C)
- The usefulness of PCI to improve survival is uncertain in patients with 2- or 3-vessel CAD (with or without involvement of the proximal LAD artery) or 1-vessel proximal LAD disease (Dzavik et al., 2001; Jones et al., "Long-term," 1996; Smith et al., 2006; Boden et al., 2007). (Level of Evidence: B)
- CABG might be considered with the primary or sole intent of improving survival in patients with silent ischemic heart disease (SIHD) with severe LV systolic dysfunction (EF <35%) whether or not viable myocardium is present (Yusuf et al., 1994; Alderman et al., 1983; O'Connor et al., 2002; Phillips, O'Connor, & Rogers, 2007; Tarakji et al., 2006; Tsuyuki et al., 2006; Bonow et al., 2011; Velazquez et al., 2011). (Level of Evidence: B)
- The usefulness of CABG or PCI to improve survival is uncertain in patients with previous CABG and extensive anterior wall ischemia on noninvasive testing (Brener et al., 2006; Gurfinkel et al., 2007; Lytle et al., 1993; Morrison et al., 2001; Pfautsch et al., 1999; Sergeant, "First," et al., 1998; Stephan et al., 1996; Subramanian et al., 2009; Weintraub et al., 1997). (Level of Evidence: B)
Class III: HARM
- CABG or PCI should not be performed with the primary or sole intent to improve survival in patients with SIHD with 1 or more coronary stenoses that are not anatomically or functionally significant (e.g., <70% diameter non–left main coronary artery stenosis, fractional flow reserve >0.80, no or only mild ischemia on noninvasive testing), involve only the left circumflex or right coronary artery, or subtend only a small area of viable myocardium (Yusuf et al., 1994; Jones et al., "Long-term," 1996; Di Carli et al., 1998; Hachamovitch et al., 2003; Shaw et al., 2008; Cashin et al., 1984; Pijls NH et al., 1996; Tonino et al., 2009; Sawada et al., 2003). (Level of Evidence: B)
Revascularization to Improve Symptoms
Class I
- CABG or PCI to improve symptoms is beneficial in patients with 1 or more significant (≥70% diameter) coronary artery stenoses amenable to revascularization and unacceptable angina despite guideline-directed medical therapy (GDMT) (Boden et al., 2007; TIME Investigators, 2001; Benzer, Hofer, & Oldridge, 2003; Bonaros et al., 2005; Bucher et al., 2000; Favarato et al., 2007; Hueb et al., 2010; Pocock et al., 1996; Pocock et al., 2000; Weintraub et al., 2008; Wijeysundera et al., 2010). (Level of Evidence: A)
Class IIa
- CABG or PCI to improve symptoms is reasonable in patients with 1 or more significant (≥70% diameter) coronary artery stenoses and unacceptable angina for whom GDMT cannot be implemented because of medication contraindications, adverse effects, or patient preferences. (Level of Evidence: C)
- PCI to improve symptoms is reasonable in patients with previous CABG, 1 or more significant (≥70% diameter) coronary artery stenoses associated with ischemia, and unacceptable angina despite GDMT (Gurfinkel et al., 2007; Pfautsch et al., 1999; Subramanian et al., 2009). (Level of Evidence: C)
- It is reasonable to choose CABG over PCI to improve symptoms in patients with complex 3-vessel CAD (e.g., SYNTAX score >22), with or without involvement of the proximal LAD artery, who are good candidates for CABG (Hannan et al., 2008; Kappetein et al., 2011; Smith et al., 2006; Brener et al., 2004; Hannan et al., 2005). (Level of Evidence: B)
Class IIb
- CABG to improve symptoms might be reasonable for patients with previous CABG, 1 or more significant (≥70% diameter) coronary artery stenoses not amenable to PCI, and unacceptable angina despite GDMT (Weintraub et al., 1997). (Level of Evidence: C)
- Transmyocardial laser revascularization (TMR) performed as an adjunct to CABG to improve symptoms may be reasonable in patients with viable ischemic myocardium that is perfused by arteries that are not amenable to grafting (Schofield et al., 1999; Aaberge et al., 2000; Burkhoff et al., 1999; Allen et al., 2000; Stamou et al., 2002). (Level of Evidence: B)
Class III: HARM
- CABG or PCI to improve symptoms should not be performed in patients who do not meet anatomic (≥50% left main or ≥70% non–left main stenosis) or physiological (e.g., abnormal fractional flow reserve) criteria for revascularization. (Level of Evidence: C)
Dual Anti-Platelet Therapy (DAPT) Compliance and Stent Thrombosis
Class III: HARM
- PCI with coronary stenting (bare-metal stent [BMS] or drug-eluting stent [DES]) should not be performed if the patient is not likely to be able to tolerate and comply with DAPT for the appropriate duration of treatment based on the type of stent implanted (Grines et al., 2007; Leon et al., 1998; Mauri et al., 2007; McFadden et al., 2004). (Level of Evidence: B)
Hybrid Coronary Revascularization
Class IIa
- Hybrid coronary revascularization (defined as the planned combination of LIMA-to-LAD artery grafting and PCI of ≥1 non-LAD coronary arteries) is reasonable in patients with 1 or more of the following (Bonatti et al., 2008; Gilard et al., 2007; Holzhey et al., 2008; Kon et al., 2008; Reicher et al., 2008; Vassiliades et al., 2006; Zhao et al., 2009; Angelini et al., 1996; Simoons, 1996) (Level of Evidence: B):
- Limitations to traditional CABG, such as heavily calcified proximal aorta or poor target vessels for CABG (but amenable to PCI);
- Lack of suitable graft conduits;
- Unfavorable LAD artery for PCI (i.e., excessive vessel tortuosity or chronic total occlusion).
Class IIb
- Hybrid coronary revascularization (defined as the planned combination of LIMA-to-LAD artery grafting and PCI of ≥1 non-LAD coronary arteries) may be reasonable as an alternative to multivessel PCI or CABG in an attempt to improve the overall risk–benefit ratio of the procedures. (Level of Evidence: C)
Perioperative Management
Preoperative Antiplatelet Therapy
Class I
- Aspirin (100 mg to 325 mg daily) should be administered to CABG patients preoperatively (Bybee et al., 2005; Dacey et al., 2000; Mangano, 2002). (Level of Evidence: B)
- In patients referred for elective CABG, clopidogrel and ticagrelor should be discontinued for at least 5 days before surgery (Berger et al., 2008; Held et al., 2011; Hongo et al., 2002) (Level of Evidence: B) and prasugrel for at least 7 days (Level of Evidence: C) to limit blood transfusions.
- In patients referred for urgent CABG, clopidogrel and ticagrelor should be discontinued for at least 24 hours to reduce major bleeding complications (Held et al., 2011; Firanescu et al., 2009; Herman et al., 2010; Mehta et al., 2009). (Level of Evidence: B)
- In patients referred for CABG, short-acting intravenous glycoprotein IIb/IIIa inhibitors (eptifibatide or tirofiban) should be discontinued for at least 2 to 4 hours before surgery (Bizzarri et al., 2001; Dyke et al., 2000) and abciximab for at least 12 hours beforehand (Lincoff et al., 2000) to limit blood loss and transfusions. (Level of Evidence: B)
Class IIb
- In patients referred for urgent CABG, it may be reasonable to perform surgery less than 5 days after clopidogrel or ticagrelor has been discontinued and less than 7 days after prasugrel has been discontinued. (Level of Evidence: C)
Postoperative Antiplatelet Therapy
Class I
- If aspirin (100 mg to 325 mg daily) was not initiated preoperatively, it should be initiated within 6 hours postoperatively and then continued indefinitely to reduce the occurrence of saphenous vein graft (SVG) closure and adverse cardiovascular events (Mangano, 2002; Sethi et al., 1990; Antithrombotic Trialists' Collaboration, 2002). (Level of Evidence: A)
Class IIa
- For patients undergoing CABG, clopidogrel 75 mg daily is a reasonable alternative in patients who are intolerant of or allergic to aspirin. (Level of Evidence: C)
Management of Hyperlipidemia
Class I
- All patients undergoing CABG should receive statin therapy, unless contraindicated (Campeau et al., 1997; "Third Report," 2002; Cholesterol Treatment Trialists' (CTT) Collaboration et al., 2010; Pedersen et al., 2005; LaRosa et al., 2005; Heart Protection Study Collaborative Group, 2002; Dotani et al., 2000; Mannacio et al., 2008; Liakopoulos et al., 2008; Knatterud et al., 2000; Christenson, 1999; Pascual et al., 2006; Pan et al., 2004). (Level of Evidence: A)
- In patients undergoing CABG, an adequate dose of statin should be used to reduce LDL cholesterol to less than 100 mg/dL and to achieve at least a 30% lowering of LDL cholesterol (Campeau et al., 1997; "Third Report," 2002; CTT Collaboration et al., 2010; Pedersen et al., 2005; LaRosa et al., 2005; Heart Protection Study Collaborative Group, 2002). (Level of Evidence: C)
Class IIa
- In patients undergoing CABG, it is reasonable to treat with statin therapy to lower the LDL cholesterol to less than 70 mg/dL in very high-risk* patients (CTT Collaboration et al., 2010; Pedersen et al., 2005; LaRosa et al., 2005; Cannon et al., 2004; Cannon et al., 2006; Grundy et al., 2004). (Level of Evidence: C)
- For patients undergoing urgent or emergency CABG who are not taking a statin, it is reasonable to initiate high-dose statin therapy immediately ("Food and Drug Administration [FDA] safety alert," 2011). (Level of Evidence: C)
*Presence of established cardiovascular disease plus 1) multiple major risk factors (especially diabetes), 2) severe and poorly controlled risk factors (especially continued cigarette smoking), 3) multiple risk factors of the metabolic syndrome (especially high triglycerides ≥200 mg/dL plus non–high-density lipoprotein cholesterol ≥130 mg/dL with low high-density lipoprotein cholesterol [<40 mg/dL]), and 4) acute coronary syndromes.
Class III: HARM
- Discontinuation of statin or other dyslipidemic therapy is not recommended before or after CABG in patients without adverse reactions to therapy (Collard et al., 2006; Kulik et al., 2008; Thielmann et al., 2007). (Level of Evidence: B)
Hormonal Manipulation
Class I
- Use of continuous intravenous insulin to achieve and maintain an early postoperative blood glucose concentration less than or equal to 180 mg/dL while avoiding hypoglycemia is indicated to reduce the incidence of adverse events, including deep sternal wound infection, after CABG (Furnary et al., 2003; Ingels et al., 2006; van den Berghe et al., 2001). (Level of Evidence: B)
Class IIb
- The use of continuous intravenous insulin designed to achieve a target intraoperative blood glucose concentration less than 140 mg/dL has uncertain effectiveness (Butterworth et al., 2005; Duncan et al., 2010; Gandhi et al., 2007). (Level of Evidence: B)
Class III: HARM
- Postmenopausal hormonal therapy (estrogen/progesterone) should not be administered to women undergoing CABG (Hulley et al., 1998; Rossouw et al., 2002; Ouyang et al., 2006). (Level of Evidence: B)
Perioperative Beta Blockers
Class I
- Beta blockers should be administered for at least 24 hours before CABG to all patients without contraindications to reduce the incidence or clinical sequelae of postoperative atrial fibrillation (AF) (Crystal et al., 2004; Connolly et al., 2003; Andrews et al., 1991; Mariscalco et al., 2008; Fuster et al., 2011; Al-Khatib et al., 2009; Silverman, Wright, & Levitsky, 1982; Ali, Sanalla, & Clark, 1997). (Level of Evidence: B)
- Beta blockers should be reinstituted as soon as possible after CABG in all patients without contraindications to reduce the incidence or clinical sequelae of AF (Crystal et al., 2004; Connolly et al., 2003; Andrews et al., 1991; Mariscalco et al., 2008; Fuster et al., 2011; Al-Khatib et al., 2009; Silverman, Wright, & Levitsky, 1982; Ali, Sanalla, & Clark, 1997). (Level of Evidence: B)
- Beta blockers should be prescribed to all CABG patients without contraindications at the time of hospital discharge. (Level of Evidence: C)
Class IIa
- Preoperative use of beta blockers in patients without contraindications, particularly in those with a left ventricular ejection fraction (LVEF) greater than 30%, can be effective in reducing the risk of in-hospital mortality (Ferguson, Coombs, & Peterson, 2002; ten Broecke et al., 2003; Weightman et al., 1999). (Level of Evidence: B)
- Beta blockers can be effective in reducing the incidence of perioperative myocardial ischemia (Chung et al., 1988; Podesser et al., 1995; Slogoff & Keats, 1988; Wiesbauer et al., 2007). (Level of Evidence: B)
- Intravenous administration of beta blockers in clinically stable patients unable to take oral medications is reasonable in the early postoperative period (Halonen et al., 2006). (Level of Evidence: B)
Class IIb
- The effectiveness of preoperative beta blockers in reducing in-hospital mortality rate in patients with LVEF less than 30% is uncertain (Ferguson, Coombs, & Peterson, 2002; Lin et al., 2010). (Level of Evidence: B)
Angiotensin-converting Enzyme (ACE) Inhibitor/Angiotensin Receptor Blocker (ARB)
Class I
- ACE inhibitors and ARBs given before CABG should be reinstituted postoperatively once the patient is stable, unless contraindicated (Goyal et al., 2007; AHA et al., 2006; Oosterga et al., 2001). (Level of Evidence: B)
- ACE inhibitors or ARBs should be initiated postoperatively and continued indefinitely in CABG patients who were not receiving them preoperatively, who are stable, and who have an LVEF less than or equal to 40%, hypertension, diabetes mellitus, or chronic kidney disease (CKD), unless contraindicated (Goyal et al., 2007; Oosterga et al., 2001; Garg & Yusuf, 1995; Yusuf et al., 2000). (Level of Evidence: A)
Class IIa
- It is reasonable to initiate ACE inhibitors or ARBs postoperatively and to continue them indefinitely in all CABG patients who were not receiving them preoperatively and are considered to be at low risk (i.e., those with a normal LVEF in whom cardiovascular risk factors are well controlled), unless contraindicated (Goyal et al., 2007; Oosterga et al., 2001; Garg & Yusuf, 1995; Yusuf et al., 2000; Fox et al., 2007; Kjoller-Hansen, Steffensen, & Grande, 2000; Rouleau et al., 2008). (Level of Evidence: B)
Class IIb
- The safety of the preoperative administration of ACE inhibitors or ARBs in patients on chronic therapy is uncertain (Arora et al., 2008; Benedetto et al., 2008; Levin et al., 2009; Miceli et al., 2009; Rader et al., 2010; White et al., 2007). (Level of Evidence: B)
- The safety of initiating ACE inhibitors or ARBs before hospital discharge is not well established (Goyal et al., 2007; Fox et al., 2007; Rouleau et al., 2008; Eagle et al., 2004). (Level of Evidence: B)
Smoking Cessation
Class I
- All smokers should receive in-hospital educational counseling and be offered smoking cessation therapy during CABG hospitalization (Hilleman, Mohiuddin, & Packard, 2004; Rigotti, Munafo, & Stead, 2008; Smith & Burgess, 2009). (Level of Evidence: A)
Class IIb
- The effectiveness of pharmacological therapy for smoking cessation offered to patients before hospital discharge is uncertain. (Level of Evidence: C)
Emotional Dysfunction and Psychosocial Considerations
Class IIa
- Cognitive behavior therapy or collaborative care for patients with clinical depression after CABG can be beneficial to reduce object measures of depression (Blumenthal et al., 2003; Connerney, et al., 2001; Freedland et al., 2009; Rollman, et al., "Telephone," 2009; Rollman et al., "The Bypassing the Blues," 2009). (Level of Evidence: B)
Cardiac Rehabilitation
Class I
- Cardiac rehabilitation is recommended for all eligible patients after CABG (Engblom et al., 1997; Hansen et al., 2009; Milani & Lavie, 1998; Taylor et al., 2004; Clark et al., 2005; Thomas et al., 2007; Walther et al., 2008). (Level of Evidence: A)
Perioperative Monitoring
Electrocardiographic Monitoring
Class I
- Continuous monitoring of the electrocardiogram for arrhythmia should be performed for at least 48 hours in all patients after CABG (Andrews et al., 1991; Drew et al., 2004; Echahidi et al., 2008). (Level of Evidence: B)
Class IIa
- Continuous ST-segment monitoring for detection of ischemia is reasonable in the intraoperative period for patients undergoing CABG (Slogoff & Keats, 1985; Gordon et al., 1991; Jain et al., 1997; Knight et al., 1988). (Level of Evidence: B)
Class IIb
- Continuous ST-segment monitoring for detection of ischemia may be considered in the early postoperative period after CABG (Podesser et al., 1995, Drew et al., 2004; Mangano et al., 1992; Zvara et al., 2000; Berry et al., 1998; Cheng et al., "Morbidity," 1996). (Level of Evidence: B)
Pulmonary Artery Catheterization
Class I
- Placement of a pulmonary artery catheter (PAC) is indicated, preferably before the induction of anesthesia or surgical incision, in patients in cardiogenic shock undergoing CABG. (Level of Evidence: C)
Class IIa
- Placement of a PAC can be useful in the intraoperative or early postoperative period in patients with acute hemodynamic instability (American Society of Anesthesiologists Task Force on Pulmonary Artery Catheterization, 2003; Pearson et al., 1989; Resano et al., 2006; Schwann et al., 2002; Stewart et al., 1998; Tuman et al., 1989). (Level of Evidence: B)
Class IIb
- Placement of a PAC may be reasonable in clinically stable patients undergoing CABG after consideration of baseline patient risk, the planned surgical procedure, and the practice setting (American Society of Anesthesiologists Task Force on Pulmonary Artery Catheterization, 2003; Pearson et al., 1989; Resano et al., 2006; Schwann et al., 2002; Stewart et al., 1998; Tuman et al., 1989). (Level of Evidence: B)
Central Nervous System Monitoring
Class IIb
- The effectiveness of intraoperative monitoring of the processed electroencephalogram to reduce the possibility of adverse recall of clinical events or for detection of cerebral hypoperfusion in CABG patients is uncertain (Avidan et al., 2008; Hemmerling et al., 2005; Myles et al., 2004). (Level of Evidence: B)
- The effectiveness of routine use of intraoperative or early postoperative monitoring of cerebral oxygen saturation via near-infrared spectroscopy to detect cerebral hypoperfusion in patients undergoing CABG is uncertain (Brady et al., 2010; Murkin et al., 2007; Slater et al., 2009). (Level of Evidence: B)
CABG-Associated Morbidity and Mortality: Occurrence and Prevention
Public Reporting of Cardiac Surgery Outcomes
Class I
- Public reporting of cardiac surgery outcomes should use risk-adjusted results based on clinical data (Geraci et al., 2005; Hannan et al., 1992; Hannan et al., 1997; Hartz et al., 1994; Jones et al., "Identification," 1996; Mack et al., 2005; Shahian et al., 2007; Tu, Sykora, & Naylor, 1997). (Level of Evidence: B)
Use of Outcomes or Volume as CABG Quality Measures
Class I
- All cardiac surgery programs should participate in a state, regional, or national clinical data registry and should receive periodic reports of their risk-adjusted outcomes. (Level of Evidence: C)
Class IIa
- When credible risk-adjusted outcomes data are not available, volume can be useful as a structural metric of CABG quality (Shahian et al., 2010; Hannan et al., 1995; Clark, 1996; Grumbach et al., 1995; Hannan et al., 1991; Hannan et al., 2003; Kalant & Shrier, 2004; Nallamothu et al., 2001; Peterson et al., 2004; Rathore et al., 2004; Showstack et al., 1987; Shroyer et al., 1996; Sowden, Deeks, & Sheldon, 1995; Welke et al., 2005; Wu et al., 2004; Luft, Bunker, & Enthoven, 1979; Birkmeyer et al., 2002). (Level of Evidence: B)
Class IIb
- Affiliation with a high-volume tertiary center might be considered by cardiac surgery programs that perform fewer than 125 CABG procedures annually. (Level of Evidence: C)
Adverse Events
Stroke
Use of Epiaortic Ultrasound Imaging to Reduce Stroke Rates
Class IIa
- Routine epiaortic ultrasound scanning is reasonable to evaluate the presence, location, and severity of plaque in the ascending aorta to reduce the incidence of atheroembolic complications (Nakamura et al., 2008; Rosenberger et al., 2008; Yamaguchi et al., 2009). (Level of Evidence: B)
The Role of Preoperative Carotid Artery Noninvasive Screening in CABG Patients
Class I
- A multidisciplinary team approach (consisting of a cardiologist, cardiac surgeon, vascular surgeon, and neurologist) is recommended for patients with clinically significant carotid artery disease for whom CABG is planned. (Level of Evidence: C)
Class IIa
- Carotid artery duplex scanning is reasonable in selected patients who are considered to have high-risk features (i.e., age >65 years, left main coronary stenosis, peripheral artery disease [PAD], history of cerebrovascular disease [transient ischemic attack (TIA), stroke, etc.], hypertension, smoking, and diabetes mellitus) (Durand et al., 2004; Sheiman & Janne d'Othee, 2007). (Level of Evidence: C)
- In the CABG patient with a previous TIA or stroke and a significant (50% to 99%) carotid artery stenosis, it is reasonable to consider carotid revascularization in conjunction with CABG. In such an individual, the sequence and timing (simultaneous or staged) of carotid intervention and CABG should be determined by the patient's relative magnitudes of cerebral and myocardial dysfunction. (Level of Evidence: C)
Class IIb
- In the patient scheduled to undergo CABG who has no history of TIA or stroke, carotid revascularization may be considered in the presence of bilateral severe (70% to 99%) carotid stenoses or a unilateral severe carotid stenosis with a contralateral occlusion. (Level of Evidence: C)
Mediastinitis/Perioperative Infection
Class I
- Preoperative antibiotics should be administered to all patients to reduce the risk of postoperative infection (Kreter & Woods 1992; Goodman et al., 1968; Fong, Baker, & McKee, 1979; Fekety et al., 1969; Austin et al., 1980; Kaiser et al., 1987). (Level of Evidence: A)
- A first- or second-generation cephalosporin is recommended for prophylaxis in patients without methicillin-resistant Staphylococcus aureus colonization (Kaiser et al., 1987; Bolon et al., 2004; Finkelstein, et al., 2002; Maki et al., 1992; Saginur, Croteau, & Bergeron, 2000; Salminen et al., 1999; Townsend et al., 1993; Vuorisalo, Pokela, & Syrjala, 1998; Wilson et al., 1988). (Level of Evidence: A)
- Vancomycin alone or in combination with other antibiotics to achieve broader coverage is recommended for prophylaxis in patients with proven or suspected methicillin-resistant S. aureus colonization (Maki et al., 1992; Centers for Diseases Control and Prevention [CDC], 2010; Spelman et al., 2002; Walsh, Greene, & Kirshner, 2011). (Level of Evidence: B)
- A deep sternal wound infection should be treated with aggressive surgical debridement in the absence of complicating circumstances. Primary or secondary closure with muscle or omental flap is recommended (Jurkiewicz et al., 1980; Rand et al., 1998; Wong et al., 2006). Vacuum therapy in conjunction with early and aggressive debridement is an effective adjunctive therapy (Argenta & Morykwas, 1997; Baillot et al., 2010; Cowan et al., 2005; Doss et al., 2002; Ennker et al., 2009; Fleck et al., 2006; Fleck et al., 2002; Luckraz et al., 2003; Sjogren et al., "Clinical," 2005; Sjogren et al., "The impact," 2005). (Level of Evidence: B)
- Use of a continuous intravenous insulin protocol to achieve and maintain an early postoperative blood glucose concentration less than or equal to 180 mg/dL while avoiding hypoglycemia is indicated to reduce the risk of deep sternal wound infection (van den Berghe et al., 2001; Gandhi et al., 2007; Ouattara et al., 2005; Doenst et al., 2005; Furnary & Wu, 2006; Kirdemir et al., 2008). (Level of Evidence: B)
Class IIa
- When blood transfusions are needed, leukocyte-filtered blood can be useful to reduce the rate of overall perioperative infection and in-hospital death (Bilgin et al., 2004; Blumberg et al., 2002; Romano et al., 2010; van de Watering et al., 1998). (Level of Evidence: B)
- The use of intranasal mupirocin is reasonable in nasal carriers of S. aureus (Konvalinka, Errett, & Fong, 2006; van Rijen et al., 2008). (Level of Evidence: A)
- The routine use of intranasal mupirocin is reasonable in patients who are not carriers of S. aureus, unless an allergy exists. (Level of Evidence: C)
Class IIb
- The use of bilateral internal mammary arteries (IMAs) in patients with diabetes mellitus is associated with an increased risk of deep sternal wound infection, but it may be reasonable when the overall benefit to the patient outweighs this increased risk. (Level of Evidence: C)
Renal Dysfunction
Class IIb
- In patients with preoperative renal dysfunction (creatinine clearance <60 mL/min), off-pump CABG may be reasonable to reduce the risk of acute kidney injury (AKI) (Ascione et al., 2001; Chukwuemeka et al., 2005; Di Mauro et al., 2007; Nigwekar et al., 2009; Sajja et al., 2007). (Level of Evidence: B)
- In patients with preexisting renal dysfunction undergoing on-pump CABG, maintenance of a perioperative hematocrit greater than 19% and mean arterial pressure greater than 60 mm Hg may be reasonable. (Level of Evidence: C)
- In patients with preexisting renal dysfunction, a delay of surgery after coronary angiography may be reasonable until the effect of radiographic contrast material on renal function is assessed (Del Duca et al., 2007; Medalion et al., 2010; Ranucci et al., 2008). (Level of Evidence: B)
- The effectiveness of pharmacological agents to provide renal protection during cardiac surgery is uncertain (Adabag et al., 2009; Amar & Fleisher, 2001; Caimmi et al., 2003; Cogliati et al., 2007; Davis & Giesecke, 2000; El-Hamamsy et al., 2007; Fansa et al., 2003; Fischer, Tossios & Mehlhorn, 2005; Friedrich et al., 2005; Haase et al., 2007; Ip-Yam et al., 1994; Landoni et al., 2007; Landoni et al., 2008; Murphy, Murray, & Shorten, 2001; Nigwekar & Hix, 2009; Piper et al., 2003; Ranucci et al., 2004; Ranucci et al., 2010; Sirivella, Gielchinsky, & Parsonnet, 2000; Tumlin et al., 2005; Vesely, 2003; Wang et al., 2011; Young, Diab & Kirsh, 1998). (Level of Evidence: B)
Perioperative Myocardial Dysfunction
Class IIa
- In the absence of severe, symptomatic aorto-iliac occlusive disease or PAD, the insertion of an intra-aortic balloon is reasonable to reduce mortality rate in CABG patients who are considered to be at high risk (e.g., those who are undergoing reoperation or have LVEF <30% or left main CAD) (Christenson et al., 2002; Christenson et al., 1999; Christenson, Licker, & Kalangos, 2003; Christenson, Schmuziger, & Simonet, 2001; Urban et al., 2004; Santa-Cruz, Cohen, & Ohman, 2006). (Level of Evidence: B)
- Measurement of biomarkers of myonecrosis (e.g., creatine kinase-MB, troponin) is reasonable in the first 24 hours after CABG (Yau et al., 2008). (Level of Evidence: B)
Transfusion
Class I
- Aggressive attempts at blood conservation are indicated to limit hemodilutional anemia and the need for intraoperative and perioperative allogeneic red blood cell transfusion in CABG patients (Koch et al., 2006; Surgenor et al., 2006; van Straten et al., "Transfusion," 2010; van Straten et al., "Risk factors," 2010). (Level of Evidence: B)
Perioperative Dysrhythmias
Class I
- Beta blockers should be administered for at least 24 hours before CABG to all patients without contraindications to reduce the incidence or clinical sequelae of postoperative AF (Crystal et al., 2004; Connolly et al., 2003; Andrews et al., 1991; Mariscalco et al., 2008; Fuster et al., 2011; Al-Khatib et al., 2009; Silverman, Wright, & Levitsky, 1982; Ali, Sanalla, & Clark, 1997). (Level of Evidence: B)
- Beta blockers should be reinstituted as soon as possible after CABG in all patients without contraindications to reduce the incidence or clinical sequelae of AF (Crystal et al., 2004; Connolly et al., 2003; Andrews et al., 1991; Mariscalco et al., 2008; Fuster et al., 2011; Al-Khatib et al., 2009; Silverman, Wright, & Levitsky, 1982; Ali, Sanalla, & Clark, 1997). (Level of Evidence: B)
Class IIa
- Preoperative administration of amiodarone to reduce the incidence of postoperative AF is reasonable for patients at high risk for postoperative AF who have contraindications to beta blockers (Daoud et al., 1997). (Level of Evidence: B)
- Digoxin and nondihydropyridine calcium channel blockers can be useful to control the ventricular rate in the setting of AF but are not indicated for prophylaxis (Andrews et al., 1991; Williams et al., 1985; Davison et al., 1985; Tyras et al., 1979; Weiner et al., 1986; Johnson et al., 1976). (Level of Evidence: B)
Perioperative Bleeding/Transfusion
Class I
- Lysine analogues are useful intra-operatively and post-operatively in patients undergoing on-pump CABG to reduce perioperative blood loss and transfusion requirements (Fergusson et al., 2008; Greilich et al., 2009; Kikura et al., 2006; Mehr-Aein, Sadeghi, & Madani-civi, 2007; Mehr-Aein, Davoodi, & Madani-civi, 2007; Murphy et al., 2006; Santos et al., 2006; Taghaddomi et al., 2009). (Level of Evidence: A)
- A multimodal approach with transfusion algorithms, point-of-care testing, and a focused blood conservation strategy should be used to limit the number of transfusions (Paone, Spencer, & Silverman, 1994; Nuttall et al., 2001; Royston & von Kier, 2001; Avidan et al., 2004; Despotis, Grishaber, & Goodnough, 1994; Shore-Lesserson et al., 1999). (Level of Evidence: A)
- In patients taking thienopyridines (clopidogrel or prasugrel) or ticagrelor in whom elective CABG is planned, clopidogrel and ticagrelor should be withheld for at least 5 days (Berger et al., 2008; Held et al., 2011; Firanescu et al., 2009; Herman et al., 2010; Kim et al., 2008; Chu et al., 2004; Englberger et al., 2004; Kapetanakis et al., 2006; Maltais, Perrault, & Do, 2008; Vaccarino et al., 2009; Yusuf et al., 2001) (Level of Evidence: B) and prasugrel for at least 7 days (Wiviott et al., 2007) (Level of Evidence: C) before surgery.
- It is recommended that surgery be delayed after the administration of streptokinase, urokinase, and tissue-type plasminogen activators until hemostatic capacity is restored, if possible. The timing of recommended delay should be guided by the pharmacodynamic half-life of the involved agent. (Level of Evidence: C)
- Tirofiban or eptifibatide should be discontinued at least 2 to 4 hours before CABG and abciximab at least 12 hours before CABG (Bizzarri et al., 2001; Dyke et al., 2000; Lincoff et al., 2000; Murphy et al., 2006; Santos et al., 2006; Renda et al., 2007; McDonald et al., 2005; Jones et al., 2002; Kincaid et al., 2003; Medalion et al., 2003). (Level of Evidence: B).
Class IIa
- It is reasonable to consider off-pump CABG to reduce perioperative bleeding and allogeneic blood transfusion (Khan et al., 2004; Angelini et al., 2002; Cheng et al., 2005; Czerny et al., 2001; Puskas et al., 2003; Raja & Dreyfuss, 2006; van Dijk et al., 2001). (Level of Evidence: A)
Specific Patient Subsets
Anomalous Coronary Arteries
Class I
- Coronary revascularization should be performed in patients with:
- A left main coronary artery that arises anomalously and then courses between the aorta and pulmonary artery (Basso et al., 2000; Thomas et al., 1991; Krasuski et al., 2011). (Level of Evidence: B)
- A right coronary artery that arises anomalously and then courses between the aorta and pulmonary artery with evidence of myocardial ischemia (Basso et al., 2000; Thomas et al., 1991; Krasuski et al., 2011; Frommelt et al., 2011). (Level of Evidence: B)
Class IIb
- Coronary revascularization may be reasonable in patients with a LAD coronary artery that arises anomalously and then courses between the aorta and pulmonary artery. (Level of Evidence: C)
Patients with Chronic Obstructive Pulmonary Disease/Respiratory Insufficiency
Class IIa
- Preoperative intensive inspiratory muscle training is reasonable to reduce the incidence of pulmonary complications in patients at high risk for respiratory complications after CABG (Hulzebos et al., 2006). (Level of Evidence: B)
Class IIb
- After CABG, noninvasive positive pressure ventilation may be reasonable to improve pulmonary mechanics and to reduce the need for reintubation (Haeffener et al., 2008; Zarbock et al., 2009). (Level of Evidence: B)
- High thoracic epidural analgesia may be considered to improve lung function after CABG (Liu, Block, & Wu, 2004; Kofidis et al., 2008). (Level of Evidence: B)
Patients with End-Stage Renal Disease on Dialysis
Class IIb
- CABG to improve survival rate may be reasonable in patients with end-stage renal disease undergoing CABG for left main coronary artery stenosis of greater than or equal to 50% (Hemmelgarn et al., 2004). (Level of Evidence: C)
- CABG to improve survival rate or to relieve angina despite GDMT may be reasonable for patients with end-stage renal disease with significant stenoses (≥70%) in 3 major vessels or in the proximal LAD artery plus 1 other major vessel, regardless of LV systolic function (Liu et al., 2000). (Level of Evidence: B)
Class III: HARM
- CABG should not be performed in patients with end-stage renal disease whose life expectancy is limited by noncardiac issues. (Level of Evidence: C)
Patients with Concomitant Valvular Disease
Class I
- Patients undergoing CABG who have at least moderate aortic stenosis should have concomitant aortic valve replacement (Filsoufi et al., 2002; Smith et al., 2004; Pereira et al., 2005; Gillinov & Garcia, 2005). (Level of Evidence: B)
- Patients undergoing CABG who have severe ischemic mitral valve regurgitation not likely to resolve with revascularization should have concomitant mitral valve repair or replacement at the time of CABG (Gillinov et al., 2001; Aklog et al., 2001; Trichon et al., 2003; Fattouch et al., 2009; Fattouch et al., 2010; Zoghbi & Sarano, 2003). (Level of Evidence: B)
Class IIa
- In patients undergoing CABG who have moderate ischemic mitral valve regurgitation not likely to resolve with revascularization, concomitant mitral valve repair or replacement at the time of CABG is reasonable (Gillinov et al., 2001; Aklog et al., 2001; Trichon et al., 2003; Fattouch et al., 2009; Fattouch et al., 2010; Zoghbi & Sarano, 2003). (Level of Evidence: B)
Class IIb
- Patients undergoing CABG who have mild aortic stenosis may be considered for concomitant aortic valve replacement when evidence (e.g., moderate–severe leaflet calcification) suggests that progression of the aortic stenosis may be rapid and the risk of the combined procedure is acceptable. (Level of Evidence: C)
Patients with Previous Cardiac Surgery
Class IIa
- In patients with a patent LIMA to the LAD artery and ischemia in the distribution of the right or left circumflex coronary arteries, it is reasonable to recommend reoperative CABG to treat angina if GDMT has failed and the coronary stenoses are not amenable to PCI (Subramanian et al., 2009; Sergeant, Blackstone, & Meyns, 1998). (Level of Evidence: B)
Definitions:
Applying Classification of Recommendations and Level of Evidence
|
Size of Treatment Effect |
|
CLASS I
Benefit >>> Risk
Procedure/Treatment
SHOULD be performed/administered |
CLASS IIa
Benefit >> Risk
Additional studies with focused objectives needed
IT IS REASONABLE to perform procedure/administer treatment |
CLASS IIb
Benefit ≥ Risk
Additional studies with broad objectives needed; additional registry data would be helpful
Procedure/Treatment
MAY BE CONSIDERED |
CLASS III No Benefit
or Class III Harm |
|
Procedure/Test |
Treatment |
COR III:
No benefit |
Not helpful |
No proven benefit |
COR III:
Harm |
Excess Cost without Benefit or Harmful |
Harmful to Patients |
Estimate of Certainty (Precision) of Treatment Effect |
LEVEL A
Multiple populations evaluated*
Data derived from multiple randomized clinical trials or meta-analyses |
- Recommendation that procedure or treatment is useful/effective
- Sufficient evidence from multiple randomized trials or meta-analyses
|
- Recommendation in favor of treatment or procedure being useful/effective
- Some conflicting evidence from multiple randomized trials or meta-analyses
|
- Recommendation's usefulness/efficacy less well established
- Greater conflicting evidence from multiple randomized trials or meta-analyses
|
- Recommendation that procedure or treatment is not useful/effective and may be harmful
- Sufficient evidence from multiple randomized trials or meta-analyses
|
LEVEL B
Limited populations evaluated*
Data derived from a single randomized clinical trials or nonrandomized studies |
- Recommendation that procedure or treatment is useful/effective
- Evidence from single randomized trial or nonrandomized studies
|
- Recommendation in favor of treatment or procedure being useful/effective
- Some conflicting evidence from single randomized trial or nonrandomized studies
|
- Recommendation's usefulness/efficacy less well established
- Greater conflicting evidence from single randomized trial or nonrandomized studies
|
- Recommendation that procedure or treatment is not useful/effective and may be harmful
- Evidence from single randomized trial or nonrandomized studies
|
LEVEL C
Very limited populations evaluated*
Only consensus opinion of experts, case studies or standard of care |
- Recommendation that procedure or treatment is useful/effective
- Only expert opinion, case studies, or standard of care
|
- Recommendation in favor of treatment or procedure being useful/effective
- Only diverging expert opinion, case studies, or standard of care
|
- Recommendation's usefulness/efficacy less well established
- Only diverging expert opinion, case studies, or standard of care
|
- Recommendation that procedure or treatment is not useful/effective and may be harmful
- Only expert opinion, case studies, or standard of care
|
A recommendation with Level of Evidence B or C does not imply that the recommendation is weak. Many important clinical questions addressed in the guidelines do not lend themselves to clinical trials. Although randomized trials are unavailable, there may be a very clear clinical consensus that a particular test or therapy is useful or effective.
*Data available from clinical trials or registries about the usefulness/efficacy in different subpopulations, such as gender, age, history of diabetes, history of prior myocardial infarction, history of heart failure, and prior aspirin use. A recommendation with Level of Evidence B or C does not imply that the recommendation is weak. Many important clinical questions addressed in the guidelines do not lend themselves to clinical trials. Even though randomized trials are not available, there may be a very clear clinical consensus that a particular test or therapy is useful or effective.
|