Care Process Model MONTH JUNE 2015 2020

DEVELOPMENTDIAGNOSIS AND AND MANAGEMENT DESIGN OF OF CareACUTE Process CORONARY Models SYNDROME (ACS) 2015 Update 2020 Update

These guidelines were developed by Intermountain Healthcare’s Cardiovascular WHAT’S INSIDE? Clinical Program to guide the diagnosis and treatment of patients presenting to Intermountain Healthcare’s emergency departments (ED) with signs and ALGORITHM 1: DIAGNOSIS OF ACUTE symptoms suggestive of acute coronary syndrome (ACS). Recommendations CORONARY SYNDROME (ACS) . . . . 2 are based on ACS-probability categories and capabilities of individual facilities. TABLE 1: MANAGEMENT OF ACUTE They may need to be adapted to meet the needs of a specific patient and should CORONARY SYNDROME...... 4 not replace clinical judgment. TABLES 2 – 7: TESTING AND MEDICATION GUIDELINES ...... 5 BIBLIOGRAPHY...... 8 Why Focus ON ACS? REFERENCES...... 8 RESOURCES...... 8 • Incidence and mortality . In 2018, it was expected that nearly 720,000 Americans would experience their first (MI) or die from coronary heart . BEN • Cost . Between 2012 and 2014, more than $361 billion in direct and PROGRAM GOALS & indirect costs (14 % of total health expenditures) were attributed MEASUREMENTS to coronary vascular disease and . Direct medical costs of (CVD) are projected to increase from $318 billion  Time from ED arrival to PCI for all to $749 billion between 2015 and 2035. BEN STEMI patients • Outcomes are improved when key processes are followed . GOAL: < 90 minutes from ED arrival to intervention

Successful reperfusion (percutaneous coronary intervention [PCI] in 60 < 90 minutes OR fibrinolytic infusion in < 30 minutes) usually results in  % cTroponin-I testing at 0 and preserved left ventricle function, reduced mortality, and fewer 2 – 3 hours after arrival when long-term complications. AMS appropriate  % HEART score assessment of NSTEMI patients

What’s new in this update?  % of eligible ED patients treated • Updated algorithm for the diagnosis and treatment of ACS (see page 2). with fibrinolytics within 30 minutes of arrival • Use of the HEART score, instead of in MI (TIMI), to determine the risk of major adverse cardiac events (MACE) (see page 3).  % Lipid and HbA1c testing on eligible patients • HbA1c monitoring of all STEMI (ST-elevation MI) patients and those with a moderate-to-high probability of ACS or definite unstable (seepage 2). Indicates an Intermountain measure • More frequent monitoring of -I (see pages 2-3).

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ALGORITHM 1: DIAGNOSIS OF ACUTE CORONARY SYNDROME (ACS)

Patient presents with symptoms of ACS (a)

PERFORM ECG (b) Goal: Within 5 min . of arrival at ED

INITIATE site-specific STEMI protocol STEMI? yes Goal: Reperfusion < 90 min . from ED arrival no

ASSESS HEART Risk Score (c)

CONSULT Is initial cTn-l ≥ 2? yes NSTEMI ADMIT for urgent reperfusion MANAGE according to TABLE 1 no

Low Risk Moderate Risk* High Risk* (score 0 – 3) (score 4 – 6) (score ≥ 7)

no Is initial cTn-I yes * If patient remains > 0.04? symptomatic, strongly consider serial ECG every 15 min.

PERFORM patient-provider shared admission decision

no Admit to hospital? yes

REPEAT cTn-I testing at 2 hours

ADMIT for further workup no Repeat cTn-I ≥ 0.04 yes AND > 50 % increase? MANAGE according to TABLE 1

CONSIDER outpatient imaging (for guidance use Abbreviations: cTn-I – cardiac troponin; ECG – electrocardiogram; Proven Imaging: Known or Suspected CAD CPM) STEMI – ST-elevation myocardial infarction; NSTEMI – non-ST-elevation FOLLOW UP with PCP myocardial infarction; PCP – primary care provider

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ALGORITHM NOTES (a) Symptoms of ACS High-probability ACS: STEMI Moderate-probability ACS Low-probability ACS (NSTEMI or definite UAP) Strongly suggestive of Typical of or consistent with / infarction Strongly suggestive of ischemia Suggestive but atypical for ischemia ischemia / infarction (b) ECG Findings High-probability ACS: STEMI Moderate-probability ACS Low-probability ACS (NSTEMI or definite UAP) Ischemic ST elevation at the J point in 2 or more New ST depression ≥ 1 mm Normal or non-specific, with or Normal or non-specific, with or contiguous leads (≥ 2 mm in men or ≥ 1.5 mm OR without pain. without pain. in women in leads V2 – V3 or ≥ 1 mm in other Deep T-wave inversion contiguous chest leads or limb leads) OR Note: Must be normal at 0 Note: Must be normal at 0 hours ST depression in ≥ 2 leads (V1 – V4) (may indicate and at 3 to 6 hours from ED arrival. Note: If symptoms persist, strongly and 3 hours from ED arrival, acute posterior MI) If abnormal, continue with consider serial ECG every 15 minutes. and consider ECG at 6, 12, OR “High-probability ACS” column. New or presumably new left and 18 hours. If abnormal, (LBBB) that obscures ST-segment analysis, with continue with “High-probability MI symptoms ACS” column. OR Rarely, hyperacute T-waves (in very early phase of STEMI, before ST elevation develops)

Note: Multilead ST depression combined with ST elevation in lead aVR has been noted in left main or proximal left anterior descending (LAD) occlusion. (c) HEART Risk Score for NSTEMI / UAPFRI This score predicts the short-term risk of subsequent mortality, new / recurrent MI, or severe ischemia for patients with NSTEMI or pectoris (UAP). A higher score may warrant a higher ACS probability and more aggressive treatment. Diagnosis of STEMI is primarily based on ECG findings, and rapid reperfusion is the goal for all STEMI patients, regardless of estimated mortality . HEART Score How to score: composition Highly suspicious 2 Scores 0 – 3: 0.9 – 1.7 % MACE over next 6 weeks Low Risk History Moderately suspicious 1 Scores 4 – 6: 12 – 16.6 % MACE over next 6 weeks Moderate Risk Slightly suspicious 0 Scores ≥ 7: 50 – 65 % MACE over next 6 weeks High Risk Significant ST depression 2 ECG Nonspecific polarization disturbance 1 Notes: Normal 0 •• Critical actions: Do not use this classification if new ST elevation requiring immediate intervention or clinically unstable patient. ≥ 65 years 2 •• MACE is defined as all-cause mortality, MI, or coronary Age 45 – 64 1 . ≤ 44 0 •• Risk factors: mellitus (DM), current or recent (< 1 month) smoker, hypertension, hyperlipidemia, family history of coronary artery ≥ 3 risk factors or history of atherosclerotic disease 2 disease (CAD), and obesity. Risk factors 1 – 2 risk factors 1 No risk factors 0 > 2 x normal limit 2 Troponin-I (cTn-I) 1– 2 x normal limit 1 < normal limit 0

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TABLE 1: Management of ACS High-probability ACS STEMI Diagnosis Non-ST-elevation MI (NSTEMI) (ST-elevation MI) OR definite unstable angina pectoris (UAP) Admit status Cath lab / CCU / ICU CCU / ICU Goal Urgent reperfusion Rapid reperfusion

For onsite urgent Elective invasive intervention or early invasive or transport patient (ideally If ≤ 90 minutes: If > 90 minutes: intervention Patient criteria <48 hours after onset of (< 12 hours after onset symptoms) of symptoms)

•• PERFORM ECG. •• PERFORM ECG. •• PERFORM serial ECG •• PERFORM serial ECG every every 15 minutes. 15 minutes. •• ARRANGE •• GIVE fibrinolytic in Initial for immediate ≤ 30 minutes (see TABLE 3). •• ARRANGE for possible •• TRANSFER to interventional diagnostics percutaneous Do not give GPI (GP percutaneous coronary center immediately if ongoing coronary IIb / IIIa inhibitor) intervention (PCI) pain or within 24 hours and with fibrinolytic . (immediately for therapeutics intervention (PCI).1 (≤ 12 hours preferred). •• TRANSFER immediately ongoing (See STEMI Power to interventional center or hemodynamic Plan in iCentra.) for PCI. instability).

Emergency •• , NTG, and O2 •• Aspirin, NTG and O2 •• Aspirin, NTG, and O2 •• Aspirin, NTG, and O2 Department •• (80 mg) •• Atorvastatin (80 mg) •• Atorvastatin (80 mg) •• Atorvastatin (80 mg) •• bolus only •• : •• Heparin bolus only •• Enoxaparin (see TABLE 5) or (see TABLE 4) –– Age <75: 300 mg PO (see TABLE 4) Heparin (see TABLE 6) Drugs •• PRN –– Age ≥75: 75 mg PO •• Morphine PRN 5 •• Tirofiban or agent •• Enoxaparin (see TABLE 5) per cardiologist (see TABLE 7) Contraindications •• Morphine PRN •• Morphine PRN (see pages 6 – 7) •• GPI or anticoagulant per cardiologist (e.g., for high clot burden) GPI is contraindicated with TNKase .

SELECT one: SELECT one: SELECT one: •• Clopidogrel 600 mg •• Clopidogrel 600 mg •• Clopidogrel 600 mg •• 180 mg •• Ticagrelor 180 mg •• Ticagrelor 180 mg •• 2 60 mg PO •• Prasugrel 2 60 mg PO •• Prasugrel 2 60 mg PO (loading doses) (loading doses) (loading doses) 2 Cath Lab Drugs AND AND AND •• Anticoagulant: •• Anticoagulant: heparin •• Additional enoxaparin heparin or bivalirudin or bivalirudin per guideline May consider GPI per May consider GPI per cardiologist (e.g., for cardiologist (e.g., high clot high clot burden) burden Diagnosis STEMI, NSTEMI, and UAP

• PERFORM ECG at 6, 12, and 18 hours after admission. Initial • •• PERFORM troponin-I testing at 6, 12, and 18 hours after admission. testing •• SCHEDULE lipid and HbA1c for morning after admission. Hospital- Based Care 3 •• Aldosterone blocker: CONSIDER if EF <40% and •• Oral beta blocker : PRESCRIBE at discharge post-MI or symptomatic or diabetes are present. CONSIDER if ejection fraction (EF) < 40 % Drugs as contraindications and follow up. • ACE inhibitor (ACEI) or ARB: PRESCRIBE when blood 4 • •• P2Y12 inhibitor for at least 12 months : PRESCRIBE one of the needed pressure becomes stable (required for EF < 40 %). following: clopidogrel (75 -150 mg / day for 1 week followed • Aspirin: PRESCRIBE 81 mg per day. by 75 mg / day) OR ticagrelor (90 mg twice daily) OR prasugrel • (10 mg / day) 2.

1. Immediate Cath / PCI: On-site cath lab or transferable to interventional center in < 60 minutes from ED to receiving hospital cath lab. REFER to STEMI orders: Primary PCI or STEMI orders: Fibrinolytic Pathway. 2. Clopidogrel, prasugrel, and ticagrelor: CONSIDER platelet function testing for all ACS and high-risk elective PCI patients; see Antiplatelet Guidelines. Prasugrel: CONSIDER delay until after for NSTEMI / UAP. AVOID if cerebrovascular accident (CVA) or transient ischemic attack (TIA) history. Can use for patients < 75 years and > 60 kg. (CONSIDER 5 mg daily for patients > 75 years or < 60 kg.) 3. Oral beta blocker (BB): GIVE within 24 hours for patients without signs of heart failure (HF), low-output, risk for cardiogenic shock, or other relative contraindications. AVOID IV BB except in STEMI patients with or tachyarrythmias and without signs of HF, low-output, risk for cardiogenic shock, or other relative contraindications.

4. P2Y12 inhibitor: May discontinue earlier, especially for bare metal , if patient is at high bleeding risk. 5. Tirofiban: CONSIDER discontinuing 4 – 6 hours after clopidrogrel load or 2 – 4 hours after prasugrel / ticagrelor OR CONSIDER infusing up to 18 hours for highest risk cases. ©2008 - 2020 INTERMOUNTAIN HEALTHCARE. ALL RIGHTS RESERVED. 4 DIAGNOSIS AND MANAGEMENT OF ACS JUNE 2020

TABLE 1: Management of ACS (continued) Diagnosis Moderate-probability ACS Low-probability ACS

•• Outpatient care • PERFORM serial ECG every 15 minutes. • •• REFER to Proven Imaging: •• ORDER cTroponin-I. Known or Suspected CAD •• ADMIT for further workup. CPM to determine if imaging is appropriate.

•• MANAGE symptoms. • OBSERVE telemetry for . Initial • Diagnostics and •• If ongoing chest pain, MANAGE as definite UAP inTABLE 1. Therapeutics •• OBTAIN serial troponin-I as described in TABLE 2 below to determine if more invasive treatment or imaging may be indicated.

•• Aspirin, , and O2. • Enoxaparin (see TABLE 5) or heparin (see TABLE 6). Initial drugs • •• Oral beta blocker 2. Hospital-Based Care •• Morphine PRN. •• . •• ACE inhibitor (or ARB) when blood pressure becomes stable (required for EF < 40 %). •• Aldosterone blocker if EF < 40 % and symptomatic HF or DM.

Ongoing drugs •• If PCI, P2Y12 inhibitor for at least 12 months for bare metal stent or drug-eluting stent.3 Dosing:1 (SELECT one) –– Clopidogrel (75 mg / day) –– Ticagrelor (90 mg twice daily) –– Prasugrel (10 mg / day) 1

1. Clopidogrel, prasugrel, and ticagrelor: CONSIDER platelet function testing for all ACS and high-risk elective PCI patients; see Antiplatelet Guidelines. Prasugrel: CONSIDER delay until after angiography for NSTEMI / UAP. AVOID if CVA or TIA history. Can use for patients < 75 years and > 60 kg. (CONSIDER 5 mg daily for patients > 75 years or < 60 kg.) 2. Oral beta blocker (BB): GIVE within 24 hours for patients without signs of HF, low-output, risk for cardiogenic shock, or other relative contraindications. AVOID IV BB except in STEMI patients with hypertension or tachyarrhythmias and without signs of HF, low-output, risk for cardiogenic shock, or other relative contraindications.

3. P2Y12 inhibitor: May discontinue earlier, especially for bare metal stent, if patient is at high bleeding risk.

TABLE 2 . Inpatient Serial Troponin Guideline

May or may not be elevated at 0 hours; typically Initial cTn-I (ng / mL) AMI = Acute Myocardial Infarction elevated at 6 hours post-event onset. Initial diagnosis and reperfusion ≥ 2.0 ng / mL 0.1 to < 2.0 ng / mL 0.04 to < 0.1 ng / mL < 0.04 ng / mL decision must be made immediately, before troponin-I results are available . Retest cTn-I in 2 – 3 hours Retest cTn-I in 2 – 3 hours Retest cTn-I in 2 – 3 hours AMI Non-AMI causes of elevated cTn-I The conditions below can also elevate cTn-I. Increase Increase Increase Increase Elevated cTn-I, even with a non-AMI cause, ≥ 0.1 ng / mL 0.04 to < 0.1 ng / mL < 0.04 ng / mL ≥ 20 % < 20 % ≥ 50 % < 50 % brings higher clinical risk. •• Heart failure •• Malignancy • Viral or stress • Pulmonary Retest cTn-I in 2 – 3 hours • • 2 AMI Imaging2 AMI AMI Imaging •• , •• Infiltrative ≥ 0.1 ng / mL <0.1 ng / mL pericarditis •• Toxicity or sepsis Early invasive •• Trauma •• Renal failure strategy 1 2 •• Stroke •• Ablation recommended Imaging •• Subarachnoid procedures hemorrhage 1 ADMIT to hospital . Begin aspirin and enoxaparin therapy. CONSIDER: Beta blocker, tirofiban (if ongoing chest pain), left heart catheterization. 2 SELECT most appropriate imaging test based on patient-specific factors. SeeProven Imaging for Known or Suspected CAD CPM.

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TABLE 3 . TNKase Dosing Instructions (see Tenecteplase (TNKase) clinical guideline) Dose (IV bolus Weight (kg) Notes Indications Contraindications over 5 seconds) • ECG showing ANY of the following: • Previous hemorrhagic stroke < 60 30 mg •• Do not give if GPI (GP IIb / IIIa inhibitor) was ––Ischemic ST elevation (> 1 mm) at any time; other or given (e.g., abciximab, eptifibatide, in 2 or more contiguous leads cerebrovascular events 60 – 69 35 mg or tirofiban). ––Hyperacute T-waves within 1 year • Known intracranial neoplasm • Also, begin enoxaparin with TNK ––Signs of acute posterior MI or • • Active internal bleeding 70 – 79 40 mg bolus (see table 5 below). LBBB obscuring ST segment analysis with MI history (does not include menses) • Suspected aortic dissection • History of ACS 80 – 89 45 mg • Pain / symptoms within the past 24 hours with or without > 90 50 mg ongoing symptoms Cautions and relative contraindications • Severe, uncontrolled hypertension on presentation (>180 / 110 mmHg) or history • Non-compressible vascular punctures of chronic severe hypertension • Recent (within 2 – 4 weeks) internal bleeding • History of CVA or known intracerebral pathology • Age > 75 years • Current warfarin therapy (INR > 2 – 3); known bleeding diathesis • Pregnancy • Current therapy with direct oral anticoagulant (DOAC) • Active peptic ulcer • Recent trauma, prolonged CPR (> 10 minutes), or major surgery (< 3 weeks)

TABLE 4 . STEMI / NSTEMI: TABLE 5 . Enoxaparin Dosing Instructions (see Enoxaparin guideline) Unfractionated Heparin Bolus Only for Patients Going to the Cath Lab Age Fibrinolytic STEMI NSTEMI IV bolus dose (years) Weight (kg) CrCl > 30 mL / min CrCl < 30 mL / min CrCl > 30 mL / min CrCl < 30 mL / min (60 units / kg) 30 mg IV bolus 30 mg IV bolus 1 mg / kg subcut 1 mg / kg subcut < 46 2500 units followed 15 min. later followed 15 min. later every 12 hours once daily by 1 mg / kg subcut by 1 mg / kg subcut 46 – 52 3000 units < 75 every 12 hours (max once daily (max 53 – 61 3500 units 100 mg first 2 doses) 100 mg first 2 doses)

62 – 70 4000 units No bolus . 0.75 mg / kg No bolus . 1 mg / kg subcut every 12 subcut once daily 71 – 80 5000 units ≥ 75 hours (max 75 mg (max 75 mg first first 2 doses) 2 doses) 81 – 90 5500 units Notes: > 90 6000 units max if PCI with GPI; (based on kg) 8000 units max if PCI without GPI •• Contraindications: Hemodialysis; active major bleeding; recent or planned epidural or dural anesthesia; known or suspected HIT; weight > 190 kg or women <45 kg and men < 57 kg. Notes: •• Lab monitoring: Draw a baseline BMP, aPTT STAT (include CBC, PT / INR if not done in last 24 •• UFH (unfractionated heparin) hours); draw CBC every other day while hospitalized; monitor BMP if clinical situation suggests risk contraindications: Active major of renal function decline. bleeding; recent or planned epidural anesthesia; •• Cautions: Thrombocytopenia (platelet count < 100,000 / mm3) or known bleeding diathesis; known or suspected heparin-induced recent internal bleeding or uncontrollable active bleeding (hospital admission or transfusion in last thrombocytopenia (HIT). For HIT, DO NOT use 30 days); recent (within the previous 2 weeks) surgery, major trauma, or thrombotic stroke; acute heparin or low-molecular-weight heparin (LMWH); peptic ulcer disease. use a direct thrombin inhibitor. •• Cautions: Thrombocytopenia (platelets < 100,000 / mm3) or bleeding diathesis; recent internal bleeding or uncontrollable active bleeding (admission or transfusion in past 30 days); recent surgery (within the past 2 weeks), major trauma or thrombotic stroke; acute peptic ulcer disease.

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TABLE 6 . Unfractionated Heparin (NSTEMI) Initial dosage and infusion rate of unfractionated heparin (standard concentration of 100 units / mL) in NSTEMI Weight (kg) Bolus dose (units) Infusion rate (units / hour) < 46 2500 500 46 – 52 3000 600 53 – 61 3500 700 62 – 70 4000 800 70 – 77 4000 900 Over 77 kg 4000 1000 Monitoring and adjustment of unfractionated heparin in NSTEMI Steps •• Draw baseline aPTT* STAT (include CBC, PT / INR if not done in last 24 hours). •• Give initial dosage as directed in top half of this table (above). •• Use aPTT testing to monitor and adjust dose as per table below. aPTT (in sec) Heparin Infusion rate Labs < 40 Bolus 3000 units Increase by 100 units / hour aPTT every 6 hours x 2 40 – 49 None Increase by 50 units / hour 50 – 70 None No change aPTT per protocol** 71 – 85 None Decrease by 50 units / hour 86 – 100 Hold for 30 minutes Decrease by 100 units / hour aPTT every 6 hours x 2 101 – 150 Hold for 30 minutes Decrease by 150 units / hour Over 150 Hold for 1 hour Decrease by 300 units / hour *aPPT= activated partial thromboplastin time ** After 2 consecutive aPTTs in the therapeutic range of 50 – 70 seconds, draw aPTT daily in AM.

TABLE 7 . Tirofiban (Aggrastat) Dosing for ACS or PCI Treatment Creatinine clearance Dosing regimen name Bolus dose1,2 Infusion dose ≥ 60 mL / min Standard dose 25 mcg / kg over 2 – 5 minutes 0.15 mcg / kg / min < 60 mL / min Renal dose 25 mcg / kg over 2 – 5 minutes 0.075 mcg / kg / min

1. The pump library is set up to deliver the bolus and maintenance infusion. 2. Obtain platelet count 3 hours after initial tirofiban bolus. 3. Consider discontinuing 4 – 6 hours after clopidogrel load or 2 – 4 hours after prasugrel / ticagrelor OR CONSIDER infusing up to 18 hours for highest risk cases. Notes: Contraindications: •• Active internal bleeding or bleeding diathesis in past 30 days •• History of intracerebral hemorrhage (ICH), arteriovenous malformation (AVM), aneurysm, intracranial neoplasm, or thrombocytopenia after prior tirofiban exposure •• Stroke in past 30 days or any history of hemorrhagic stroke •• Severe hypertension (systolic > 180 or diastolic > 110) •• Major surgery or trauma in past 30 days •• Concurrent use of other parenteral GB IIB / IIIA inhibitors and / or thrombolytics •• Acute •• History or signs of aortic dissection

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BIBLIOGRAPHY CPM DEVELOPMENT TEAM 1. Bhatt DL, Taqueti, VR. Out with the old rule-out: Raising the bar for acute chest pain evaluation with randomized trials of cardiac imaging. JACC Cardiovasc Imaging. 2017;10(3):350-353. • Bilal Aijaz, MD 2. Januzzi Jr JL, McCarthy CP. Evaluating chest pain in the emergency department: Searching for the optimal gatekeeper. • Joseph Bledsoe, MD J Am Coll Cardiol. 2018;71(6):617-619. 3. Mark DG, Huang J, Chettipally U, et al, on behalf of the Kaiser Permanente CREST Network Investigators. • Jason Buckway, RN, MBA Performance of coronary risk scores among patients with chest pain in the emergency department. J Am Coll Cardiol. • Reuben Evans, MSN, MHA 2018;71(6);606-616. 4. Patel MR, Calhoon JH, Dehmer GJ, et al. ACC / AATS / AHA / ASE / ASNC / SCAI / SCCT / STS 2017 Appropriateness • David Jackson, MPH (Medical Writer) Criteria® for coronary revascularization in patients with stable ischemic heart disease: A report of the American • Donald Lappé, MD College of Cardiology Appropriate Use Criteria Task Force, American Association for Thoracic Surgery, American Heart Association, American Society of Echocardiography, American Society of Nuclear Cardiology, Society for • David Min, MD Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, and Society of Thoracic Surgeons. J Am Coll Cardiol. 2017;69(17);2212-2241. • J. Brent Muhlestein, MD 5. Patel MR, Calhoon JH, Dehmer GJ, et al. ACC / AATS / AHA / ASE / ASNC / SCAI / SCCT / STS 2016 Appropriate • Heidi Porter, PhD (Medical Writer) use criteria for coronary revascularization in patients with acute coronary syndromes: A report of the American College of Cardiology Appropriate Use Criteria Task Force, American Association for Thoracic Surgery, American • Wing Province, MD Heart Association, American Society of Echocardiography, American Society of Nuclear Cardiology, Society for • Colleen Roberts, MS, RN Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, and the Society of Thoracic Surgeons. J Am Coll Cardiol. 2017;69(5):570-591. • Tamara Moores Todd, MD 6. Raff GL, Hoffmann U, Udelson JE. Trials of imaging use in the emergency department for acute chest pain. JACC • Aaron Weaver, MD Cardiovasc Imaging. 2017;10(5);338-349. • Zachary Williams, MD REFERENCES AMS Amsterdam EA, Brindis, RG, Wenger NK, et al. 2014 AHA / ACC guideline for the management of patients with non-ST-elevation acute coronary syndromes: Executive summary. A report of the American College of Cardiology / American Heart Association Task Force on practice guidelines. Circulation. 2014;130(25):2354-2394. BEN Benjamin EJ, Virani SS, Callaway CW, et al. Heart disease and stroke statistics-2018 update: A report from the American Heart Association. Circulation. 2018;137(12):e67-e492. OGA O'Gara PT, Kushner FG, Ascheim DD, et al. 2013 ACCF / AHA Guideline for the management of ST-elevation myocardial infarction. A report of the American College of Cardiology Foundation / American Heart Association Task Force on Practice Guidelines. JACC. 2013;61(4):e78-e140. PATIENT AND PROVIDER RESOURCES Physicians can order Intermountain patient education booklets and fact sheets (available in English and Spanish) for distribution to their patients from Print It!.

Fact sheets:

• Cardiac Stress Testing FOLLETO INFORMATIVO PARA PACIENTES Y SUS FAMILIAS This CPM presents a model of best care based (English) / (Spanish) El electrocardiograma (ECG o EKG) ¿Qué es un electrocardiograma? Trazado (registro cardíaco) Un electrocardiograma, frecuentemente llamado ECG o EKG, es una prueba que mide la actividad eléctrica del FACT SHEET FOR PATIENTS AND FAMILIES corazón. Esta prueba es rápidaFOLLETO e indolora. INFORMATIVO Ningún tipo PARA PACIENTES Y SUS FAMILIAS de electricidad entra en su cuerpo durante el on the best available scientific evidence at procedimiento. • Electrocardiogram (ECG or EKG) Un ECG puede ser utilizado si usted tiene dolor en el pecho, si está siendo tratado por un problema cardíaco Peripheral and Stenting o simplemente como parteAngioplastia de un chequeo regular. periférica y colocación de stent ¿Cuál es el propósito de esta prueba? What is peripheral angioplasty ¿Qué es la angioplastia y la the time of publication. It is not a prescription El corazón es un músculo grande que bombea la sangre Electrodos and stenting? a través de su cuerpo. El corazóncolocación funciona de porque stent? (parches) Angioplasty Stenting Angioplastia Colocación de stent (English) / (Spanish) [AN-jee-oh-plas-tee] impulsos eléctricos que viajanLa angioplastia a través del y lamúsculo colocación dan de stent son procedimientos Angioplasty and stenting are treatments for narrowed or blocked blood vessels origen a los latidos cardíacos.para Paratratar controlar los vasos sanguíneossu salud (arterias y venas) estrechos ( and veins). cardíaca, un ECG registrau estosobstruidos. impulsos. Un electrocardiograma • Angioplasty opens a blood vessel by inflating a Un ECG se utiliza para detectar:• La angioplastia abre los vasos sanguíneos (ECGmediante or EKG) un globo es una prueba small balloon inside it. The balloon is then removed. pequeño que se infla dentro de ellos. El globorápida luego y sencilla se retira. para revisar la • Problemas de la frecuencia cardíaca salud del corazón. La máquina de • En la colocación de stent, un dispositivo en forma de for every physician or every patient, nor does • Stenting places a tube-shaped device called a ECG registra la actividad cardíaca stent in the blood vessel to keep it open. • Problemas del ritmo cardíacotubo llamado stent se introduce en el vasoen una sanguíneo copia impresa (trazado). para mantenerlo abierto. • While angioplasty can be done alone, it’s often • Daño al músculo cardíaco Peripheral Angioplasty and Stenting Aunque la angioplastia puede realizarse sola, a menudo se combined with stenting. A balloon opens up a A stent (tiny mesh tube) • Aumento del grosor del músculo cardíaco Un globo abre un vaso Un stent (pequeño tubo de combina con la colocación de stent. clogged blood vessel. holds it open. • Un técnico le colocará algunossanguíneo electrodos obstruido. (pequeñosmalla) lo mantiene abierto. Why is it done? • Deficiente flujo sanguíneo al músculo cardíaco ¿Por qué se realiza? parches adhesivos) sobre el pecho. También le Peripheral [puh-RIF-er-uhl] angioplasty and stenting are Un ECG también puede mostrar información básica, La angioplastia periférica y la colocación de pondránstent se utilizan electrodos en cada brazo y pierna. it replace clinical judgment. All statements, used to treat narrowing of the arteries that supply tal como la posición del corazón dentro de la para tratar el estrechamiento de las arterias •que El irrigantécnico los conectará un ¿Cuálescable en cada son parche los riesgos y los beneficios? PVD What are the risks and benefits? cavidad torácica. the arms and legs (a condition known as , or brazos y las piernas (conocida como enfermedad vascular adhesivo. Los cables se conectanEn la siguiente a la máquina tabla se enumeran los posibles beneficios peripheral vascular disease) and narrowing of the The table below lists the most common possible periférica [PVD, por sus siglas en inglés]) y el estrechamiento (English) / (Spanish) ¿Qué ocurre durante un ECG? de ECG. más frecuentes, los riesgos y las alternativas a la angioplastia arteries in the head and neck (which can lead to benefits, risks, and alternatives for angioplasty and de las arterias en la cabeza y el cuello (lo cual puede provocar y la colocación de stent. Puede haber otros beneficios o a stroke). These treatments are called “minimally stenting. There may be other benefits or risks in your Un ECG dura aproximadamenteun accidente de 5cerebrovascular). a 10 minutos. Estos tratamientos• La máquina se de ECG registra la actividad eléctrica riesgos según su situación médica. Hable con su médico invasive” because they involve only a very small incision unique medical situation. Talk with your doctor to Esto es lo que sucede duranteconsideran la prueba: “mínimamente invasivos” porquedel solo corazón requieren y la imprime en un registro en papel (cut) in the groin area. Compared with surgery, they learn about these risks and benefits. Be sure to ask de una pequeña incisión (corte) en el área de llamadola ingle. En trazado. Tendrápara que obtener permanecer información quieto sobre y estos riesgos y beneficios. • Tendrá que desvestirse de la cintura hacia arriba para Asegúrese de hacer las preguntas que pueda tener. protocols, and recommendations herein are have fewer risks of complications and a shorter recovery. any questions you might have. comparación con la cirugía, presenta menos riesgossin hablar de sufrir durante la prueba. Hablar o moverse el procedimiento. Será complicacionescubierto con una y tiene sábana un tiempo o de recuperaciónpueden más interferir corto. con el trazado. una bata que sólo expondrá la piel necesaria. Possible benefits Possible risks and complications Alternatives • El trazado estará listo en aproximadamente un • Se recostará sobre una mesaPosibles o cama. beneficios Posibles riesgosminuto. y complicaciones El técnico desconectará los cables y retirará Alternativas Angioplasty and While angioplasty and stenting procedures are generally safe, they do Alternatives to stenting can: have the following possible risks and complications: angioplasty and La angioplastia y la Si bien los procedimientoslos parches de angioplastiade la piel. y colocación de stent, por lo general, Las alternativas colocación de stent son seguros, implican los siguientes posibles riesgos y complicaciones: 1 a la angioplastia • Relieve symptoms • Numbness or weakness below the catheter insertion (rare and stenting may pueden: y la colocación include: • Entumecimiento o debilidad debajo del área de inserción del catéter (poco of PVD by temporary). • Aliviar los síntomas frecuente y temporal). de stent pueden viewed as transitory and iterative. Although opening a • Surgery to de la PVD al abrir incluir: • Bleeding or infection where the catheter was inserted (rare). • Sangrado o infección donde se insertó el catéter (poco frecuente). narrowed or go around un vaso sanguíneo Cirugía para Allergic reaction to the contrast dye (very rare). • blocked blood • (bypass) estrechado u • Reacción alérgica al tinte del contraste (muy poco frecuente). abrir un vaso vessel that supplies • Reduced kidney function or kidney failure (rare). Tell your doctor if or open a obstruido que irriga • Función renal reducida o insuficiencia renal (poco frecuente) Informe a su sanguíneo o an arm or leg you have kidney disease or diabetes. blood vessel un brazo o una pierna médico si tiene enfermedad renal o diabetes. realizar una derivación • Help prevent or • Blood vessel injury, a blood clot, stroke, or (rare). • Ayudar a prevenir o • Lesión en un vaso sanguíneo, un coágulo de sangre, accidente • Medications tratar un accidente cerebrovascular o la muerte (poco frecuente). (bypass) treat a stroke • Exposure to x-rays, which can slightly increase your lifetime cancer risk. by opening a cerebrovascular • Exposición a radiografías, lo cual puede aumentar levemente su riesgo de • Medicamentos al abrir un vaso narrowed or Angioplasty has this additional risk: Re-narrowing of the blood vessel contraer cáncer a lo largo de su vida. at a later time. (A stent may reduce this risk.) sanguíneo estrecho u physicians are encouraged to follow the blocked blood obstruido que irriga La angioplastia tiene este riesgo adicional: el nuevo estrechamiento del vaso vessel that Stenting has this additional risk: Blood clots in the stent. (You’ll need el cerebro sanguíneo en el futuro. (Un stent puede reducir este riesgo). supplies the brain to take medicine to prevent clots for at least 6 to 12 months afterward.) La colocación de stent implica este riesgo adicional: formación de coágulos de sangre en el stent. (Posteriormente, deberá tomar medicamentos para CPM to help focus on and measure quality, 1 evitar los coágulos durante al menos 6 a 12 meses). 11 deviations are a means for discovering To find this CPM, go tointermountainphysician.org/ and under the Tools and Resources improvements in patient care and expanding Care Process Models . the knowledge base. Send feedback to David tab, select Min, M.D., Intermountain Healthcare Interim Chief of Cardiology, Intermountain Medical Center Heart Institute ([email protected]).

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