Editor-In-Chief: C. Michael Gibson, M.S., M.D. [7] Associate Editor(s)-in-Chief: Anahita Deylamsalehi, M.D.[8] Muhammad Saad, M.B.B.S.[9]
Overview
Overview
There are several steps involved in preparing patients for PCI, which include shared decision-making and informed consent, preprocedural documentation and history and physical examination, preprocedural laboratory testing, preprocedural fasting and sedation, antiplatelet and anticoagulant premedication, vascular access site selection, management of patients on oral anticoagulants, prevention of contrast-induced acute kidney injury, management of allergies and potential anaphylactoid reactions, preprocedural timeout and safety checklists, use of statins, assessment of bleeding risk, evaluation of on-site surgical backup services, and consideration of same-day discharge eligibility. A Heart Team approach is recommended for complex revascularization decisions.
Preparation of the Patient for PCI
Preparation of the Patient for PCI
- Revascularization decisions should be patient centered — considerate of the patient’s preferences and goals, cultural beliefs, health literacy, and social determinants of health — and made in collaboration with the patient’s support system (Class 1, LOE C-LD).[1] Adequate information about benefits, risks, therapeutic consequences, and potential alternatives should be given, when feasible, with sufficient time for informed decision-making (Class 1, LOE C-LD).[1]
- Consent procedures should include:[1][2]
- Plain language and teach-back documentation
- Trained interpreter when needed
- Patient-specific short- and long-term risks
- Information on operator expertise and facility volume
- The need for continued medical therapy and lifestyle modifications
- The potential for emergency surgery
- Preprocedural Documentation, History and Physical Examination
- All patients must have a history and physical (H&P) examination prior to the procedure, performed by either a physician or an advanced practice professional (APP).[3] For outpatient procedures, a timed and dated H&P within 30 days is acceptable, with a focused update by the attending physician within 24 hours prior to the procedure. For inpatients, an H&P should be performed within 24 hours of admission.[3]
- At a minimum, the H&P should include:[3][4]
- History of present illness, CCS angina and NYHA heart failure classes
- Relevant medications (including those received within the last 48 hours)
- Relevant comorbidities
- Review of systems (renal, gastrointestinal, peripheral vascular, neurological, pulmonary)
- History of contrast reaction or other allergies
- Potential issues related to antiplatelet or anticoagulant therapy
- Barriers to long-term DAPT adherence
- Prior airway or sedation issues
- Physical examination should focus on the cardiopulmonary and vascular system and document peripheral pulses.[3] Procedural indications should be well documented and reconciled with published appropriate use criteria (AUC).[3] Risk scores and calculators (e.g., SCAI PCI Risk App) for predicting complications (mortality, bleeding, contrast-induced nephropathy) should be documented.[3]
- For patients who have had prior catheterization or coronary/peripheral bypass surgery, every effort should be made to review procedural reports and prior cardiovascular angiograms.[4]
Preprocedural Laboratory Testing
Sources: SCAI 2021 Expert Consensus Update[3]; SCAI 2016 Best Practices[4]; 2012 ACCF/SCAI Expert Consensus Document[2]
Preprocedural Fasting and Sedation
The ASA 2017 guidelines recommend clear liquids up to 2 hours prior and light meals up to 6 hours prior (8 hours for heavier meals).[3] NPO instructions are typically waived for emergency procedures.[3] Moderate sedation/analgesia is frequently sufficient for coronary artery procedures; anxiolysis or pain control alone may suffice. Physicians in the cardiac catheterization laboratory should be credentialed for providing moderate sedation.[3]
Emerging evidence on nonfasting: The SCOFF trial (multicenter RCT, n=716) randomized patients to fasting vs. no fasting before cardiac catheterization procedures with conscious sedation. The primary composite outcome (aspiration pneumonia, hypotension, hyperglycemia, hypoglycemia) occurred in 19.1% of fasting vs. 12.0% of no-fasting patients, confirming non-inferiority (posterior probability >99.5%) and superiority (posterior probability 99.1%) of no fasting. Patient satisfaction scores were significantly better with no fasting (posterior mean difference 4.02 points).[5] The TONIC trial similarly supported the safety of nonfasting before interventional coronary procedures under local anesthesia with moderate sedation.[6] These findings are not yet incorporated into formal guidelines but represent a potential practice change.
2025 ACC/AHA/ACEP/NAEMSP/SCAI ACS Guideline Updates
2025 ACC/AHA/ACEP/NAEMSP/SCAI ACS Guideline Updates
Aspirin should be initiated with a loading dose (162-325 mg, nonenteric coated, chewed) in patients with ACS as soon as possible on presentation.[7] Ticagrelor or prasugrel is recommended in preference to clopidogrel in patients with ACS undergoing PCI.[7] DAPT with aspirin and an oral P2Y12 inhibitor is indicated for at least 12 months as the default strategy in patients with ACS who are not at high bleeding risk.[7]
Antiplatelet Dosing Table
| Agent
|
Loading Dose
|
Maintenance Dose
|
| Aspirin
|
162-325 mg (nonenteric coated, chewed)
|
75-100 mg daily
|
| Clopidogrel (NSTE-ACS/STEMI without fibrinolytic)
|
300 or 600 mg
|
75 mg daily
|
| Clopidogrel (STEMI with fibrinolytic, age ≤75 y)
|
300 mg
|
75 mg daily
|
| Clopidogrel (STEMI with fibrinolytic, age >75 y)
|
75 mg (no loading)
|
75 mg daily
|
| Prasugrel (NSTE-ACS/STEMI, undergoing PCI)
|
60 mg
|
10 mg daily (≥60 kg, <75 y); 5 mg daily (<60 kg or ≥75 y)
|
| Ticagrelor (NSTE-ACS/STEMI)
|
180 mg
|
90 mg twice daily
|
Source: 2025 ACC/AHA/ACEP/NAEMSP/SCAI ACS Guideline[7]
Timing of P2Y12 Loading
When PCI is planned or anticipated, loading with aspirin 324 mg po (chewed) should be performed before the procedure if the patient is not already on daily aspirin.[3] Loading before the procedure with a P2Y12 inhibitor is reasonable, although there is no evidence that pre-loading decreases ischemic complications compared to loading at the time of PCI or at its conclusion. Delaying P2Y12 loading until anatomy is known may prevent delays if anatomy demonstrates a need for CABG.[3]
Intravenous P2Y12 Inhibition (Cangrelor)
[1][7]
Cangrelor is a potent, direct, reversible, short-acting IV P2Y12 inhibitor with rapid onset and restoration of platelet function within 1 hour of discontinuation. No studies have compared cangrelor with a loading dose of ticagrelor or prasugrel given at the time of PCI.[1]
Glycoprotein IIb/IIIa Inhibitors
Glycoprotein IIb/IIIa inhibitors (GPIs) are generally only recommended for selected cases at high, life-threatening risk for ischemic complications or for bail-out situations.[8] A pooled patient-level analysis from 3 phase 3 CHAMPION trials demonstrated that cangrelor‘s reduction in periprocedural ischemic complications was maintained irrespective of GPI use, while GPI use was associated with substantially higher bleeding rates regardless of randomization to cangrelor or clopidogrel.[9]
Periprocedural Anticoagulation
[1]
[1]
[1]
Fondaparinux is no longer recommended as the only anticoagulant in PCI because of a higher incidence of guiding-catheter thrombosis.[1]
Anticoagulant Dosing Table
| Drug
|
No Previous Anticoagulant
|
Previous Anticoagulant
|
| UFH
|
70-100 U/kg bolus (target ACT 250-300 s)
|
Additional UFH as needed (2000-5000 U) to achieve ACT 250-300 s
|
| Enoxaparin
|
0.5-0.75 mg/kg IV bolus
|
If last SC dose 8-12 h prior: 0.3 mg/kg IV; if <8 h: no additional dose
|
| Bivalirudin
|
0.75 mg/kg bolus, 1.75 mg/kg/h infusion
|
If prior UFH: repeat ACT; if not therapeutic: 0.75 mg/kg bolus + infusion
|
| Argatroban
|
350 μg/kg bolus, 15 μg/kg/min infusion
|
200 μg/kg bolus, 15 μg/kg/min infusion
|
Target ACTs shown for HemoTec or I-Stat devices. For Hemochron ACT devices, ACT goals are 50 s higher. In CTO or ACS, consider higher target ACT. If IV GPI planned, target ACT 200-250 s. Source: 2021 ACC/AHA/SCAI Guideline[1]
Vascular Access Site Selection
Vascular Access Site Selection
Management of Patients on Oral Anticoagulants
Management of Patients on Oral Anticoagulants
Prevention of Contrast-Induced Acute Kidney Injury
Prevention of Contrast-Induced Acute Kidney Injury
The SCAI Quality Initiatives for Prevention of CI-AKI (2025) recommend the following approach:[11]
Risk Assessment:
Use risk calculators (e.g., Mehran score) to predict risk of CI-AKI
Hydration Strategies:
- Pre- and post-procedural hydration: 1-1.5 mL/kg/hour NaCl × 3-12 hours pre-procedure; 12-24 hours post-procedure
- LVEDP-guided hydration (POSEIDON trial, n=396): 3 mL/kg 0.9% NaCl × 1 hour pre-procedure, then 5 mL/kg/h (LVEDP <13 mmHg), 3 mL/kg/h (LVEDP 13-18 mmHg), 1.5 mL/kg/h (LVEDP >18 mmHg) × 4 hours post-procedure — lowered CI-AKI by 60%
Contrast Volume Limitation:
- Risk of CI-AKI increases by 12% for every 100 mL of contrast administered
- CV/CCC ratio should be kept <3 and ideally <2
- MACD equation: 5 × body weight (kg) / serum creatinine. Contrast Ratio (contrast volume/MACD) exceeding 1 is associated with progressive increase in CI-AKI risk
Additional Measures:
Allergy Management
Allergies to latex, contrast, heparin (and history of HIT), aspirin, narcotics, antiplatelet agents, and other medications should be reviewed and documented.[3]
Contrast Allergies:
Aspirin Allergy:
If aspirin allergy is present, an aspirin desensitization protocol should be considered prior to stent placement when possible[3]
Diabetes Management:
Preprocedural Timeout and Safety Checklist
Preprocedural Timeout and Safety Checklist
- A dedicated “time out” protocol should be performed before vascular access or moderate sedation is initiated, when all members of the team are present.[3] Items reviewed during time-out include:
- Patient identity, procedure to be performed, planned primary and backup access site
- Equipment availability
- Patient allergies and pre-medication
- Special laboratory or medical conditions (INR, CKD)
- Appropriate documentation (H&P updated within 24 hours)
- Signed informed consent
- For ad-hoc coronary interventions, a “Pre-PCI time out” should be considered, including: appropriate use classification, radiation exposure and contrast dose, appropriateness of intravascular imaging or physiologic assessment, DAPT issues, adequate pre-treatment with aspirin and P2Y12 inhibitors, and baseline hemodynamics.[3]
- Additional safety measures:[3]
- All solutions on the table must be labeled in real-time (not prelabeled)
- Defibrillation pads should be placed on all STEMI patients and those at increased risk of cardiac arrest
- At least one working IV must be in place prior to the start of the procedure
Same-Day Discharge Considerations
Same-Day Discharge Considerations
- The 2021 ACC Expert Consensus Decision Pathway on Same-Day Discharge After PCI provides the following guidance:[14]
- Practice patterns regarding P2Y12 inhibitor loading and maintenance vary among physicians, with providers initiating P2Y12 inhibitors either days before the procedure, in the pre-procedural area, or in the catheterization laboratory after defining coronary anatomy
- Orders for outpatient loading and maintenance or preprocedural DAPT loading should be confirmed in the EHR and communicated between preprocedural and procedural nursing
- In addition to the DAPT loading dose, the EHR should confirm prescriptions for aspirin and statin therapy as well as a referral to cardiac rehabilitation
- Special Populations — Older Adults
Comprehensive risk assessment in older adults should include: traditional cardiovascular risk assessment, minimum geriatric risk assessment (functional status and goals of care), and identification of high-risk clinical groups. Additional geriatric measures organized into four domains should be considered: medical conditions, cognitive and emotional health, physical function, and social environment.[15]
2021 ACC/AHA/SCAI Guideline for Coronary Artery Revascularization. GENERAL PROCEDURAL ISSUES FOR PCI (Please do not edit)
2021 ACC/AHA/SCAI Guideline for Coronary Artery Revascularization. GENERAL PROCEDURAL ISSUES FOR PCI (Please do not edit)
Radial and Femoral Approaches for PCI
| Class I
|
| “1. In patients with ACS undergoing PCI, a radial approach is indicated in preference to a femoral approach to reduce the risk of death, vascular complications, or bleeding. (Level of Evidence: A)”
|
| “2. In patients with SIHD undergoing PCI, the radial approach is recommended to reduce access site bleeding and vascular complications(Level of Evidence: A)”
|
[16] Choice of Stent Type
| Class I
|
| “1. In patients undergoing PCI, DES should be used in preference to BMS to prevent restenosis, MI, or acute stent thrombosis (Level of Evidence: A)”
|
[16]
Use of Intravascular Imaging
| Class IIa
|
| ” 1. In patients undergoing coronary stent implantation, IVUS can be useful for procedural guidance, particularly in cases of left main or complex coronary artery stenting, to reduce ischemic events. (Level of Evidence B-R)”.
|
| ” 2. In patients undergoing coronary stent implantation, OCT is a reasonable alternative to IVUS for procedural guidance, except in the ostial left main disease.(Level of Evidence B-R)”
|
| ”3. In patients with stent failure, IVUS or OCT is reasonable to determine the mechanism of stent failure.(Level of Evidence C-LD)”
|
[16]
Thrombectomy
| Class III (No Benefit)
|
| “1. In patients with STEMI, routine aspiration thrombectomy before primary PCI is not useful. (Level of Evidence:A) ”
|
Treatment of Calcified Lesions
| Class IIa
|
| ” 1. In patients with fibrotic or heavily calcified lesions, plaque modification with rotational atherectomy can be useful to improve procedural success (Level of Evidence B-R)”.
|
[16]
| Class IIb
|
| ” 2. In patients with fibrotic or heavily calcified lesions, plaque modification with orbital ather-ectomy, balloon atherotomy, laser angioplasty, or intracoronary lithotripsy may be considered to improve procedural success. (Level of Evidence B-NR)”.
|
[16]
Treatment of Saphenous Vein Graft (SVG) Disease (Previous CABG)
| Class IIa
|
| ” 1. In select patients with previous CABG undergoing PCI of an SVG, the use of an embolic protection device, when technically feasible, is reasonable to decrease the risk of distal embolization (Level of Evidence B-R)”.
|
| ” 2. In patients with previous CABG, if PCI of a diseased native coronary artery is feasible, then it is reasonable to choose PCI of the native coronary artery over PCI of the severely diseased SVG(Level of Evidence B-NR)”
|
[16]
| Class III (No Benefit)
|
| “1. In patients with a chronic occlusion of an SVG, percutaneous revascularization of the SVG should not be performed (Level of Evidence:C-LD) ”
|
[16]
Treatment of CTO
| Class IIb
|
| ” 1. In patients with suitable anatomy who have refractory angina on medical therapy, after treatment of non-CTO lesions, the benefit of PCI of a CTO to improve symptoms is uncertain. (Level of Evidence B-R)”.
|
[16]
Treatment of Patients With Stent RestenosisRecommendations
| Class I
|
| “1. In patients who develop clinical in-stent restenosis (ISR) for whom repeat PCI is planned, a DES should be used to improve outcomes if anatomic factors are appropriate and the patient is able to comply with DAPT (Level of Evidence: A)”
|
[16]
| Class IIa
|
| ” 2. In patients with symptomatic recurrent diffuse ISR with an indication for revascularization, CABG can be useful over repeat PCI to reduce recurrent events. (Level of Evidence C-EO)”.
|
[16]
| Class IIb
|
| ” 1. In patients who develop recurrent ISR, brachytherapy may be considered to improve symptoms. (Level of Evidence B-NR)”.
|
Hemodynamic Support for Complex PCI
| Class IIb
|
| ” 1. In selected high-risk patients, elective insertion of an appropriate hemodynamic support device as an adjunct to PCI may be reasonable to prevent hemodynamic compromise during PCI(Level of Evidence B-R)”.
|
[16]
2011 and 2005 ACCF/AHA/SCAI Guidelines for Percutaneous Coronary Intervention (DO NOT EDIT)[17][18]
2011 and 2005 ACCF/AHA/SCAI Guidelines for Percutaneous Coronary Intervention (DO NOT EDIT)[17][18]
Heart Team Approach to Revascularization Decisions (DO NOT EDIT)[17]
Contrast-Induced Acute Kidney Injury (DO NOT EDIT)[17]
Anaphylactoid Reactions (DO NOT EDIT)[17]
Statin Treatment (DO NOT EDIT)[17]
Bleeding Risk (DO NOT EDIT)[17]
PCI in Hospitals Without On-Site Surgical Backup (DO NOT EDIT)[17]
Role of Onsite Cardiac Surgical Back-Up (DO NOT EDIT)[18]
ACA 2021 Revascularization Guideline
ACA 2021 Revascularization Guideline
Thrombectomy
Routine rheolytic thrombectomy did not show any benefit based on trials done on patients with ST elevation myocardial infarction undergoing primary PCI even in the presence of thrombotic occlusion.[63][64][65][66][67][68]
Preprocedural Checklist Algorithm
Preprocedural Checklist Algorithm
The following algorithm summarizes the key steps in preparing a patient for PCI:[3][1][2]
| Step
|
Action
|
Key Considerations
|
| 1. Initial Assessment
|
History and physical examination; review prior catheterization and angiogram reports
|
Document CCS/NYHA class; identify allergies, bleeding history, renal function
|
| 2. Risk Stratification
|
Calculate bleeding risk (ARC-HBR, PRECISE-DAPT), ischemic risk, CI-AKI risk (Mehran score)
|
Document risk scores in the medical record
|
| 3. Laboratory Testing
|
CBC, BMP, coagulation studies (if indicated), pregnancy test (if applicable)
|
Repeat creatinine if recent contrast exposure or medication change
|
| 4. Informed Consent
|
Discuss risks, benefits, alternatives; document shared decision-making
|
Use plain language; interpreter services when needed
|
| 5. Premedications
|
Aspirin loading (162-325 mg chewed); P2Y12 inhibitor loading (timing per clinical scenario); high-dose statin
|
Consider delaying P2Y12 loading until anatomy known if CABG possible
|
| 6. Anticoagulation Plan
|
Determine periprocedural anticoagulant strategy; manage patients on oral anticoagulants
|
Hold DOACs 24-48 h for elective cases; reduced-dose UFH if on VKA
|
| 7. Allergy Prophylaxis
|
Steroid and antihistamine premedication for prior contrast reactions
|
Shellfish allergy does NOT require pretreatment
|
| 8. Hydration Protocol
|
IV NaCl hydration for CI-AKI prevention in at-risk patients
|
Consider LVEDP-guided protocol; minimize contrast volume
|
| 9. Fasting
|
Clear liquids up to 2 hours; light meal up to 6 hours prior (per ASA guidelines)
|
Emerging evidence (SCOFF, TONIC trials) supports nonfasting under conscious sedation
|
| 10. Access Site Planning
|
Radial preferred (Class I, LOE A); femoral if mechanical circulatory support planned
|
Ensure competency in both approaches; ultrasound guidance available
|
| 11. Preprocedural Timeout
|
Verify patient identity, procedure, access site, allergies, medications, consent, equipment
|
Pre-PCI timeout for ad-hoc interventions: AUC, radiation/contrast dose, imaging plan
|
| 12. Same-Day Discharge Screening
|
Assess eligibility for same-day discharge per 2021 ACC Expert Consensus
|
Confirm DAPT prescriptions, statin, cardiac rehabilitation referral in EHR
|
References
References
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 Lawton JS, Tamis-Holland JE, Bangalore S, Bates ER, Beckie TM, Bischoff JM, Bittl JA, Cohen MG, DiMaio JM, Don CW, Fremes SE, Gaudino MF, Goldberger ZD, Grant MC, Jaswal JB, Kurlansky PA, Mehran R, Metkus TS, Nnacheta LC, Rao SV, Sellke FW, Sharma G, Yong CM, Zwischenberger BA (2022). “2021 ACC/AHA/SCAI Guideline for Coronary Artery Revascularization: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines”. J Am Coll Cardiol. 79 (2): e21–e129. doi:10.1016/j.jacc.2021.09.006. PMID 34882435 .
- ↑ 2.0 2.1 2.2 2.3 2.4 Bashore TM, Balter S, Barac A, Byrne JG, Cavendish JJ, Chambers CE, Hermiller JB, Kinlay S, Landzberg JS, Laskey WK, McKay CR, Miller JM, Moliterno DJ, Moore JW, Oliver-McNeil SM, Popma JJ, Tommaso CL (2012). “2012 American College of Cardiology Foundation/Society for Cardiovascular Angiography and Interventions Expert Consensus Document on Cardiac Catheterization Laboratory Standards Update”. J Am Coll Cardiol. 59 (24): 2221–2305. PMID 22578923.
- ↑ 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 3.11 3.12 3.13 3.14 3.15 3.16 3.17 3.18 3.19 3.20 3.21 Naidu SS, Abbott JD, Bagai J, Bates ER, Brilakis ES, Bhatt DL, Dehmer GJ, Feldman DN, Jolly SS, Kern MJ, Klein LW, Kumbhani DJ, Mahmud E, Rao SV, Swaminathan RV, Trost JC (2021). “SCAI Expert Consensus Update on Best Practices in the Cardiac Catheterization Laboratory”. Catheter Cardiovasc Interv. 98 (2): 255–276. PMID 33939260 .
- ↑ 4.0 4.1 4.2 Naidu SS, Aronow HD, Box LC, Duffy PL, Kolansky DM, Kupfer JM, Latif F, Mulukutla SR, Rao SV, Swaminathan RV, Blankenship JC (2016). “SCAI Expert Consensus Statement: 2016 Best Practices in the Cardiac Catheterization Laboratory”. Catheter Cardiovasc Interv. 88 (3): 407–423.
- ↑ Ferreira D, Hardy J, Meere W, Coughlan JJ, Arnous S, Kiernan TJ, Elzein H, Mylotte D, McFadden E, Sharif F, Maher MM, Agarwal S, Kearney P, Caplice NM (2024). “Fasting vs. No Fasting Prior to Catheterization Laboratory Procedures: The SCOFF Trial”. Eur Heart J. PMID 39217604 .
- ↑ Boukantar M, Chiaroni PM, Gallet R, Pariente A, Music V, Music V, Music V (2024). “A Randomized Controlled Trial of Nonfasting vs Fasting Before Interventional Coronary Procedures: The TONIC Trial”. JACC Cardiovasc Interv.
- ↑ 7.0 7.1 7.2 7.3 7.4 7.5 7.6 7.7 Rao SV, O’Donoghue ML, Ruel M, Bhatt DL, Cannon CP, de Winter RJ, Harrington RA, Hess CN, Kirtane AJ, Mehran R, Morrow DA, Tamis-Holland JE (2025). “2025 ACC/AHA/ACEP/NAEMSP/SCAI Guideline for the Management of Patients With Acute Coronary Syndromes”. J Am Coll Cardiol.
- ↑ 8.0 8.1 Capodanno D, Huber K, Mehran R, Lip G, Faxon DP, Granger CB, Vranckx P, Lopes RD, Montalescot G, Cannon CP, Ten Berg J, “;”; Angiolillo DJ (2019). “Management of Antithrombotic Therapy in Atrial Fibrillation Patients Undergoing PCI: JACC State-of-the-Art Review”. J Am Coll Cardiol. 74 (1): 83–99. PMID 31272561.
- ↑ Vaduganathan M, Harrington RA, Stone GW, Steg PG, Gibson CM, Hamm CW, Price MJ, Menozzi A, Prats J, Deliargyris EN, Mahaffey KW, White HD, Bhatt DL (2017). “Cangrelor With and Without Glycoprotein IIb/IIIa Inhibitors In Patients Undergoing Percutaneous Coronary Intervention”. J Am Coll Cardiol. 69 (2): 176–185. PMID 28057316.
- ↑ Kumbhani DJ, Cannon CP, Beavers CJ, Bhatt DL, Cuker A, Gluckman TJ, Marine JE, Mehran R, Messe SR, Patel NS, Peterson BE, Rosenfield KE, Spinler SA, Thourani VH (2021). “2020 ACC Expert Consensus Decision Pathway for Anticoagulant and Antiplatelet Therapy in Patients With Atrial Fibrillation or Venous Thromboembolism Undergoing Percutaneous Coronary Intervention or With Atherosclerotic Cardiovascular Disease”. J Am Coll Cardiol. 77 (5): 629–658. PMID 33338599 .
- ↑ 11.0 11.1 CIAKI2025″>“Quality Initiatives for Prevention of Contrast-Induced Acute Kidney Injury”. SCAI. 2025.
- ↑ Invalid
<ref> tag; no text was provided for refs named SCAI_CIAKI_2025
- ↑ 13.0 13.1 Invalid
<ref> tag; no text was provided for refs named pmid37532027
- ↑ Rao SV, Vidovich MI, Gilchrist IC, Gulati R, Gutierrez JA, Hess CN, Jacobs AK, Jneid H, Krucoff MW, Mehta S, Nallamothu BK, Naidu SS, Rao SV, Spertus JA, Tremmel JA (2021). “2021 ACC Expert Consensus Decision Pathway on Same-Day Discharge After Percutaneous Coronary Intervention”. J Am Coll Cardiol. 77 (6): 811–825. PMID 33478655 .
- ↑ Nanna MG, Sutton NR, Kochar A, Damluji AA, Forman DE, Gershlick AH, Singh M, Batchelor W (2023). “A Geriatric Approach to Percutaneous Coronary Interventions in Older Adults, Part II: A JACC: Advances Expert Panel”. JACC Adv. 2.
- ↑ 16.00 16.01 16.02 16.03 16.04 16.05 16.06 16.07 16.08 16.09 16.10 16.11 16.12 “Correction to: 2021 ACC/AHA/SCAI Guideline for Coronary Artery Revascularization: Executive Summary: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines”. Circulation. 145 (11): e771. 2022. doi:10.1161/CIR.0000000000001061. PMID 35286170 .
- ↑ 17.0 17.1 17.2 17.3 17.4 17.5 17.6 Levine GN, Bates ER, Blankenship JC, Bailey SR, Bittl JA, Cercek B, Chambers CE, Ellis SG, Guyton RA, Hollenberg SM, Khot UN, Lange RA, Mauri L, Mehran R, Moussa ID, Mukherjee D, Nallamothu BK, Ting HH (2011). “2011 ACCF/AHA/SCAI Guideline for Percutaneous Coronary Intervention: Executive Summary A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Society for Cardiovascular Angiography and Interventions” (PDF). Journal of the American College of Cardiology. 58 (24): 2550–83. doi:10.1016/j.jacc.2011.08.006. PMID 22070837. Retrieved 2011-12-08.
- ↑ 18.0 18.1 Smith SC, Feldman TE, Hirshfeld JW, Jacobs AK, Kern MJ, King SB; et al. (2006). “ACC/AHA/SCAI 2005 guideline update for percutaneous coronary intervention: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (ACC/AHA/SCAI Writing Committee to Update 2001 Guidelines for Percutaneous Coronary Intervention)”. Circulation. 113 (7): e166–286. doi:10.1161/CIRCULATIONAHA.106.173220. PMID 16490830.
- ↑ Feit F, Brooks MM, Sopko G, Keller NM, Rosen A, Krone R et al. (2000)Long-term clinical outcome in the Bypass Angioplasty Revascularization Investigation Registry: comparison with the randomized trial. BARI Investigators. Circulation101 (24):2795-802. PMID: [1]
- ↑ King SB, Barnhart HX, Kosinski AS, Weintraub WS, Lembo NJ, Petersen JY et al. (1997) or surgery for multivessel coronary artery disease: comparison of eligible registry and randomized patients in the EAST trial and influence of treatment selection on outcomes. Emory Angioplasty versus Surgery Trial Investigators.Am J Cardiol 79 (11):1453-9. PMID:9185632
- ↑ 21.0 21.1 Serruys PW, Morice MC, Kappetein AP, Colombo A, Holmes DR, Mack MJ et al. (2009)Percutaneous coronary intervention versus coronary-artery bypass grafting for severe coronary artery disease. N Engl J Med 360 (10):961-72.DOI:10.1056/NEJMoa0804626 PMID:19228612
- ↑ Chakravarty T, Buch MH, Naik H, White AJ, Doctor N, Schapira J et al. (2011)Predictive accuracy of SYNTAX score for predicting long-term outcomes of unprotected left main coronary artery revascularization. Am J Cardiol 107 (3):360-6.DOI:10.1016/j.amjcard.2010.09.029 PMID:21256999
- ↑ Grover FL, Shroyer AL, Hammermeister K, Edwards FH, Ferguson TB, Dziuban SW et al. (2001)A decade’s experience with quality improvement in cardiac surgery using the Veterans Affairs and Society of Thoracic Surgeons national databases.Ann Surg 234 (4):464-72; discussion 472-4. PMID: 11573040
- ↑ Kim YH, Park DW, Kim WJ, Lee JY, Yun SC, Kang SJ et al. (2010)Validation of SYNTAX (Synergy between PCI with Taxus and Cardiac Surgery) score for prediction of outcomes after unprotected left main coronary revascularization. JACC Cardiovasc Interv 3 (6):612-23.DOI:10.1016/j.jcin.2010.04.004PMID:20630454
- ↑ Morice MC, Serruys PW, Kappetein AP, Feldman TE, Ståhle E, Colombo A et al. (2010)Outcomes in patients with de novo left main disease treated with either percutaneous coronary intervention using paclitaxel-eluting stents or coronary artery bypass graft treatment in the Synergy Between Percutaneous Coronary Intervention with TAXUS and Cardiac Surgery (SYNTAX) trial. Circulation 121 (24):2645-53.DOI:10.1161/CIRCULATIONAHA.109.899211 PMID:[2]
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