STEMI resident survival guide: Difference between revisions

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{{familytree | | C01 | | | | | C02 | | | C01=<div style="float: left; text-align: center; width: 15em; padding:1em;">'''Yes''' </div>| C02= <div style="float: left; text-align: center; width: 15em; padding:1em;">'''No''' </div> }}
{{familytree | | C01 | | | | | C02 | | | C01=<div style="float: left; text-align: center; width: 15em; padding:1em;">'''Yes''' </div>| C02= <div style="float: left; text-align: center; width: 15em; padding:1em;">'''No''' </div> }}
{{familytree | | |!| | | | | | |!| | }}
{{familytree | | |!| | | | | | |!| | }}
{{familytree | | D01 | | | | | D02 | | |D01=<div style="float: left; text-align: left; width: 20em; padding:1em;">Send to cath lab for primary PCI within 90 minutes of FMC (Class I, level of evidence A)</div>| D02=<div style="float: left; text-align: left; width: 20em; padding:1em;"> Evaluate for <br> ❑ The time from onset of symptoms <br> ❑ The risk of complications related to STEMI <br> ❑ The risk of bleeding with fibrinolysis <br> ❑ The presence of shock or severe HF <br> ❑ The time required for transfer to a [[PCI]]-capable hospital  </div>}}
{{familytree | | D01 | | | | | D02 | | |D01=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''Send to cath lab for primary PCI within 90 minutes''' <br>
❑ Symptoms of [[ischemia]] <12 hours (Class I, level of evidence A) <br>
❑ Symptoms of [[ischemia]] <12 hours and contraindications to fibrinolytics irrespective of time delay (Class I, level of evidence B)<br>
❑ [[Cardiogenic shock]] irrespective of time delay (Class I, level of evidence B)<br>
❑ [[Heart failure]] irrespective of time delay (Class I, level of evidence B) <br>
❑ Ongoing [[ischemia]] 12-24 hours following onset (Class IIa, level of evidence B)<br></div>
| D02=<div style="float: left; text-align: left; width: 20em; padding:1em;"> Evaluate for <br> ❑ The time from onset of symptoms <br> ❑ The risk of complications related to STEMI <br> ❑ The risk of bleeding with fibrinolysis <br> ❑ The presence of shock or severe HF <br> ❑ The time required for transfer to a [[PCI]]-capable hospital  </div>}}
{{familytree | | |!| | | | |,|-|^|-|.| }}
{{familytree | | |!| | | | |,|-|^|-|.| }}
{{familytree | | E01 | | | E02 | | E03 | E01=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''Adjunctive Antithrombotic Therapy to Support Reperfusion With Primary PCI'''</div> | E02=<div style="float: left; text-align: left; width: 15em; padding:1em;">❑ Transfer for primary PCI <br> ❑ FMC to device time as soon as possible and ≤ 120 min (Class I, level of evidence B) </div>| E03=<div style="float: left; text-align: left; width: 15em; padding:1em;"> ❑ Administer [[fibrinolytic therapy|fibrinolytic]] agent within 30 min of arrival when anticipated FMC to device ≥ 120 min (Class I, level of evidence B)</div>}}
{{familytree | | E01 | | | E02 | | E03 | E01=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''Adjunctive Antithrombotic Therapy to Support Reperfusion With Primary PCI'''</div> | E02=<div style="float: left; text-align: left; width: 15em; padding:1em;">❑ Transfer for primary PCI <br> ❑ FMC to device time as soon as possible and ≤ 120 min (Class I, level of evidence B) </div>| E03=<div style="float: left; text-align: left; width: 15em; padding:1em;"> ❑ Administer [[fibrinolytic therapy|fibrinolytic]] agent within 30 min of arrival when anticipated FMC to device ≥ 120 min (Class I, level of evidence B)</div>}}

Revision as of 20:28, 5 March 2014


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Alejandro Lemor, M.D. [2]

Definition

ST elevation myocardial infarction (STEMI) is a syndrome defined by symptoms of myocardial ischemia associated with persistent ST elevation on ECG and elevated cardiac enzymes.

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated. STEMI is a life-threatening condition and must be treated as such irrespective of the causes.

Risk Factors

Management

Diagnostic Approach

Shown below is an algorithm summarizing the diagnostic approach to STEMI based on the 2013 ACCF/AHA Guideline for the Management of ST-Elevation Myocardial Infarction[1]


 
 
 
 
 
Characterize the symptoms:

Chest pain

❑ Sudden onset
❑ Sensation of tightness, pressure, or squeezing
❑ Absence of physical exertion
❑ Duration> 20 minutes
❑ Radiation to the jaw or left arm
❑ No relief with medications
❑ No relief with rest
❑ Worse with time

Dyspnea
Nausea
Vomiting

Sweating
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Obtain a detailed history:

❑ Age
❑ Previous MI
❑ Previous PCI or CABG
❑ Cardiac risk factors:

Hypertension
Diabetes
Hypercholesterolemia
Smoking
Obesity
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:

❑ Measure the blood pressure
❑ Measure the heart rate
❑ Auscultate the heart searching for murmurs
❑ Search for signs of CHF

❑ Decreased air entry in the lungs
❑ Edema in the extremities
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Rule out life threatening alternative diagnoses:

Aortic dissection
Pulmonary embolism
Cardiac tamponade
Tension pneumothorax

Esophageal rupture
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order labs and tests:

EKG
❑ Biomarkers

❑ Troponin I
❑ CK-MB

Creatinine
Glucose

Hemoglobin
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Confirm STEMI by the presence of the following:

❑ EKG changes

❑ ST elevation in at least 2 contiguous leads of 2 mm (0.2 mV) in men or 1.5 mm (0.15 mV) in women in leads V2–V3 and/or of 1 mm (0.1mV) in other contiguous chest leads or the limb leads
❑ ST depression in at least two precordial leads V1-V4 (suggestive of posterior myocardial infarction)
❑ ST depression in several leads plus ST elevation in lead aVR (suggestive of occlusion of the left main or proximal LAD artery)
❑ New LBBB

❑ Increase in troponin

 
 
 
 
 

Therapeutic Apporach

Shown below is an algorithm depicting the therapeutic approach to STEMI based on the 2013 ACCF/AHA Guideline for the Management of ST-Elevation Myocardial Infarction.[1]

 
 
 
 
Initial Treatment
❑ Administer 162 - 325 mg of aspirin[2]

❑ Administer oxygen when Sat <90%[3]
❑ Administer beta-blockers (unless contraindicated)[4] [5]
❑ Administer sublingual nitroglycerin (0.4 mg) every 5 minutes for a total of 3 doses[6]
❑ Monitor with a 12-lead EKG all the time

❑ Administer morphine IV (initial dose 2-4 mg with increments of 2-8 mg every 5 to 15 minutes)[6]
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Is PCI available?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
 
 
 
No
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Send to cath lab for primary PCI within 90 minutes

❑ Symptoms of ischemia <12 hours (Class I, level of evidence A)
❑ Symptoms of ischemia <12 hours and contraindications to fibrinolytics irrespective of time delay (Class I, level of evidence B)
Cardiogenic shock irrespective of time delay (Class I, level of evidence B)
Heart failure irrespective of time delay (Class I, level of evidence B)

❑ Ongoing ischemia 12-24 hours following onset (Class IIa, level of evidence B)
 
 
 
 
Evaluate for
❑ The time from onset of symptoms
❑ The risk of complications related to STEMI
❑ The risk of bleeding with fibrinolysis
❑ The presence of shock or severe HF
❑ The time required for transfer to a PCI-capable hospital
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Adjunctive Antithrombotic Therapy to Support Reperfusion With Primary PCI
 
 
❑ Transfer for primary PCI
❑ FMC to device time as soon as possible and ≤ 120 min (Class I, level of evidence B)
 
❑ Administer fibrinolytic agent within 30 min of arrival when anticipated FMC to device ≥ 120 min (Class I, level of evidence B)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Antiplatelet Therapy

P2Y12 receptor inhibitors

Clopidogrel (600 mg), or
Ticagrelor (180 mg), or

❑ IV GP IIb/IIIa inhibitors

Abciximab
❑ Loading dose 0.25 mg/kg IV bolus
❑ Maintenance dose 0.125 mg/kg/min, or
Eptifibatide
❑ Loading dose 180 mcg/kg IV bolus followed by another bolus after 10 minutes
❑ Maintenance dose 2 mcg/kg/min, or
Tirofiban
❑ Loading dose 25 mcg/kg
❑ Maintenance dose 0.15 mcg/kg/min
 
Anticoagulant Therapy

UFH

❑ With GP IIb/IIIa receptor antagonist planned: 50- to 70-U/kg IV bolus to achieve therapeutic ACT of 200-250 s.
❑ With no GP IIb/IIIa receptor antagonist planned: 70- to 100-U/kg bolus to achieve therapeutic ACT of 250-300 s.
Bivalirudin: 0.75-mg/kg IV bolus, then 1.75–mg/kg/h infusion with or without prior treatment with UFH. An additional bolus of 0.3 mg/kg may be given if needed.
 
 
 
Indications for PCI in patients who were managed with fibrinolytic therapy

❑ Cardiogenic shock or acute severe HF
❑ Intermediate- or high-risk findings on predischarge noninvasive ischemia testing

❑Spontaneous or easily provoked myocardial ischemia

FMC: First medical contact; UFH: Unfractionated Heparin; ACT: Activated clothing time

Discharge Medication[7]

 
 
 
 
 
 
 
Post-PCI Patient
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
For all patients
 
 
 
For patients with LVEF< 40%
 
For patients with AF or Flutter
 
For patients that where already on
ACE inhibitors and Beta-blockers and
have LVEF<40% or Diabetes or HF
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
❑ Give aspirin
❑ 165-325 mg/d for 1 month for BMS: for 3 months for sirolimus-eluting stent; 6 months for paclitaxel-eluting stent
❑ 75-162 mg/d indefinitely

❑ Give clopidogrel

❑ 75 mg/d for at least 12 months for DES
❑ 75 mg/d minimum 1 month up to 12 months for BMS
❑ Give beta-blockers
 
 
 
❑ AddACE inhibitor
❑ Give ARBs if intolerant to ACE inhibitor
 
❑ Give warfarin to achieve INR of 2.0-3.0
❑ In patients requiring warfarin, clopidogrel, and aspirin therapy, an INR of 2.0 to 2.5 is recommended with low dose aspirin (75 mg to 81 mg) and a 75 mg dose of clopidogrel.
❑ Monitor closely for bleeding
 
❑ Use aldosterone blockade
 

Do's

  • Administer reperfusion therapy for all patients presenting with STEMI within 12 hours of the beginning of the symptoms (Class I, level of evidence A).
  • Administer a loading dose followed by a maintenance dose of clopidogrel, ticagrelor or prasugrel (if PCI is planned) as initial treatment instead of aspirin among patients with gastrointestinal intolerance or hypersensitivity reaction to aspirin.
  • Administer sublingual nitroglycerin in patients with ischemic chest pain; however, administer IV nitroglycerin among patients with persistent chest pain after three sublingual nitroglycerins.[8]
  • Discontinue non-steroidal anti-inflamatory drugs immediately. [9] [10]
  • Initiate therapeutic hypothermia among comatose patients with STEMI (Class I, level of evidence B).

Don'ts

  • Do not administer IV beta-blockers among hemodynamically unstable patients.
  • Do not administer IV GP IIb/IIIa inhibitors to patients with low risk of ischemic events or at high risk of bleeding and who are already on aspirin and P2Y12 receptor inhibitors therapy.
  • Do not administer nitroglycerine to patients with systolic BP < 90 mm Hg or ≥ to 30 mm Hg below baseline, severe bradycardia (< 50 bpm), tachycardia (> 100 bpm), or suspected RV infarction.
  • Do not delay the time for reperfusion.
  • Do not administer prasugrel among patients with prior history of strokes o TIAs.
  • Do not administer abciximab for patients nor scheduled for PCI. [12]

References

  1. 1.0 1.1 O'Gara, Patrick T.; Kushner, Frederick G.; Ascheim, Deborah D.; Casey, Donald E.; Chung, Mina K.; de Lemos, James A.; Ettinger, Steven M.; Fang, James C.; Fesmire, Francis M.; Franklin, Barry A.; Granger, Christopher B.; Krumholz, Harlan M.; Linderbaum, Jane A.; Morrow, David A.; Newby, L. Kristin; Ornato, Joseph P.; Ou, Narith; Radford, Martha J.; Tamis-Holland, Jacqueline E.; Tommaso, Carl L.; Tracy, Cynthia M.; Woo, Y. Joseph; Zhao, David X. (2013). "2013 ACCF/AHA Guideline for the Management of ST-Elevation Myocardial Infarction". Journal of the American College of Cardiology. 61 (4): e78–e140. doi:10.1016/j.jacc.2012.11.019. ISSN 0735-1097.
  2. Nishimura, R. A.; Otto, C. M.; Bonow, R. O.; Carabello, B. A.; Erwin, J. P.; Guyton, R. A.; O'Gara, P. T.; Ruiz, C. E.; Skubas, N. J.; Sorajja, P.; Sundt, T. M.; Thomas, J. D. (2014). "2014 AHA/ACC Guideline for the Management of Patients With Valvular Heart Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines". Circulation. doi:10.1161/CIR.0000000000000029. ISSN 0009-7322.
  3. Shuvy M, Atar D, Gabriel Steg P, Halvorsen S, Jolly S, Yusuf S; et al. (2013). "Oxygen therapy in acute coronary syndrome: are the benefits worth the risk?". Eur Heart J. 34 (22): 1630–5. doi:10.1093/eurheartj/eht110. PMID 23554440.
  4. Rosendorff C, Black HR, Cannon CP, Gersh BJ, Gore J, Izzo JL; et al. (2007). "Treatment of hypertension in the prevention and management of ischemic heart disease: a scientific statement from the American Heart Association Council for High Blood Pressure Research and the Councils on Clinical Cardiology and Epidemiology and Prevention". Circulation. 115 (21): 2761–88. doi:10.1161/CIRCULATIONAHA.107.183885. PMID 17502569.
  5. López-Sendón J, Swedberg K, McMurray J, Tamargo J, Maggioni AP, Dargie H; et al. (2004). "Expert consensus document on beta-adrenergic receptor blockers". Eur Heart J. 25 (15): 1341–62. doi:10.1016/j.ehj.2004.06.002. PMID 15288162.
  6. 6.0 6.1 Antman, Elliott M.; Hand, Mary; Armstrong, Paul W.; Bates, Eric R.; Green, Lee A.; Halasyamani, Lakshmi K.; Hochman, Judith S.; Krumholz, Harlan M.; Lamas, Gervasio A.; Mullany, Charles J.; Pearle, David L.; Sloan, Michael A.; Smith, Sidney C. (2008). "2007 Focused Update of the ACC/AHA 2004 Guidelines for the Management of Patients With ST-Elevation Myocardial Infarction". Journal of the American College of Cardiology. 51 (2): 210–247. doi:10.1016/j.jacc.2007.10.001. ISSN 0735-1097.
  7. Antman EM, Hand M, Armstrong PW; et al. (2008). "2007 Focused Update of the ACC/AHA 2004 Guidelines for the Management of Patients With ST-Elevation Myocardial Infarction: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines: developed in collaboration With the Canadian Cardiovascular Society endorsed by the American Academy of Family Physicians: 2007 Writing Group to Review New Evidence and Update the ACC/AHA 2004 Guidelines for the Management of Patients With ST-Elevation Myocardial Infarction, Writing on Behalf of the 2004 Writing Committee". Circulation. 117 (2): 296–329. doi:10.1161/CIRCULATIONAHA.107.188209. PMID 18071078. Unknown parameter |month= ignored (help)
  8. Kaplan K, Davison R, Parker M, Przybylek J, Teagarden JR, Lesch M (1983). "Intravenous nitroglycerin for the treatment of angina at rest unresponsive to standard nitrate therapy". Am J Cardiol. 51 (5): 694–8. PMID 6402912.
  9. Trelle S, Reichenbach S, Wandel S, Hildebrand P, Tschannen B, Villiger PM; et al. (2011). "Cardiovascular safety of non-steroidal anti-inflammatory drugs: network meta-analysis". BMJ. 342: c7086. doi:10.1136/bmj.c7086. PMC 3019238. PMID 21224324. Review in: Evid Based Med. 2011 Oct;16(5):142-3
  10. Coxib and traditional NSAID Trialists' (CNT) Collaboration. Bhala N, Emberson J, Merhi A, Abramson S, Arber N; et al. (2013). "Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials". Lancet. 382 (9894): 769–79. doi:10.1016/S0140-6736(13)60900-9. PMC 3778977. PMID 23726390. Review in: Ann Intern Med. 2013 Oct 15;159(8):JC12
  11. Anderson HV (1995). "Intravenous thrombolysis in refractory unstable angina pectoris". Lancet. 346 (8983): 1113–4. PMID 7475596.
  12. Jneid H, Anderson JL, Wright RS, Adams CD, Bridges CR, Casey DE; et al. (2012). "2012 ACCF/AHA focused update of the guideline for the management of patients with unstable angina/non-ST-elevation myocardial infarction (updating the 2007 guideline and replacing the 2011 focused update): a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines". J Am Coll Cardiol. 60 (7): 645–81. doi:10.1016/j.jacc.2012.06.004. PMID 22809746.


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