STEMI

Dr.Mehelina Hossain
MD,Phase A
Critical Care Medicine
Dhaka Medical College Hospital
 Universal definition of myocardial
infarction
 A combination of criteria is required to meet the diagnosis of acute
MI, namely the detection of an increase and/or decrease of a cardiac
biomarker, preferably high-sensitivity cardiac troponin, with at least
one value above the 99th percentile of the upper reference limit and
at least one of the following:
(1) Symptoms of ischaemia.
(2) New or presumed new significant ST-T wave changes or left
bundle branch block on 12-lead ECG.
(3) Development of pathological Q waves on ECG.
(4) Imaging evidence of new or presumed new loss of viable myocardium or regional
wall motion abnormality.
(5) Intracoronary thrombus detected on angiography or autopsy .
 Types
 Type 1 MI
Type 1 MI is characterized by atherosclerotic plaque rupture, ulceration, fissure,
erosion or dissection with resulting intraluminal thrombus in one or more
coronary arteries leading to decreased myocardial blood flow and/or distal
embolization and subsequent myocardial necrosis.

Type 2 MI

Type 2 MI is myocardial necrosis in which a condition other than coronary plaque

instability contributes to an imbalance between myocardial oxygen supply and
demand. Mechanisms include coronary artery spasm, coronary endothelial
dysfunction, tachyarrhythmias, bradyarrhythmias, anaemia, respiratory failure,
hypotension and severe hypertension, injurious effects of pharmacological agents
and toxins.
 Continue……
 Type 3
sudden cardiac death with symptoms of ischaemia,new ST elevation or
LBBB or coronay thrombus

 Type 4a MI associated with PCI

 Type 4b MI associated with stent thrombosis
 Type 5 MI associated witH CABG
 DEFINITION

 STEMI is a clinical syndrome defined by

characteristic symptoms of myocardial
ischemia in association with persistent
electrocardiographic (ECG) ST elevation
and subsequent release of biomarkers of
myocardial necrosis.
 SIGNS
 Signs of sympathetic activation : Pallor,Sweating,Tachycardia
 Signs of vagal activation : Vomiting,Bradycardia
 Signs of impaired myocardial function :
Hypotension,oliguria,cold periphery.
Narrow pulse pressure
Raised JVP
Third heart sound
Lung Crepitation
 Sign of tissue damage : Fever
 Complications : Murmur
Pericardial rub
 DIAGNOSIS

 It is based on :
Clinical Findings
Classical ECG Changes
Rising Titre of Cardiac Enzymes

 The classic ECG findings:

ST segment elevation, followed by T wave
inversion and Q waves.
 ECG

 Diagnostic ST elevation in the absence of left

ventricular (LV) hypertrophy or left bundle-
branch block (LBBB) is defined as:

New ST elevation at the J point 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 (0.1 mV) in other contiguous chest
leads or the limb leads.
The majority of patients will evolve ECG
evidence of Q-wave infarction.

New LBBB at presentation interfere with ST-

elevation analysis, and not a diagnostic
criteria of AMI in isolation.
 LOCALISATION
Category Anatomy of Occlusion ECG Findings
Proximal LAD Proximal to first septal ST V1-V6, I, aVL
perforator Fascicular or Bundle
Branch Block
Mid LAD Proximal to Large ST V1-V6, I, aVL
Diagonal but Distal to
First Septal Perforator
Distal LAD or Diagonal Distal to Large Diagonal ST ↑ V1–V4, or I, aVL,
or Diagonal Itself V5, V6
Moderate to Large Proximal RCA or Left ST ↑ II, III, aVF, and any
Inferior Circumflex of the following:
(Posterior, Lateral, Right (a) V1, V3R, V4R
Ventricular) (b) V5, V6
(c) R > S in V1, V2
Small Inferior Distal RCA or Left ST ↑ II, III, aVF only
Circumflex Branch
ECG???
ASTEMI(EXT ANT)
ASTEMI(Inf)
POST. ECG
ASTEMI(Inf)with Post.Ext
Differentials for ST-Segment
Elevation Myocardial Infarction
Comorbid ischemia ST elevation but no Chest pain but no
ischemia ischemia
Aortic dissection Early repolarization Aortic dissection
Systemic arterial Left ventricular Myopericarditis
embolism hypertrophy
Hypertensive crisis Left bundle branch block Pleuritis
Aortic stenosis Hyperkalemia Pulmonary embolism
Cocaine use Brugada syndrome Costochondritis
Arteritis Gastrointestinal disorders
The Laboratory Diagnosis of STEMI is
done by :

 Cardiac Troponin
The most sensitive and specific marker of
myocardial necrosis.
 CK-MB
 Myoglobin
Causes of Serum Troponin T and I Elevations,
Including Both ACS, Non Coronary Events and Non
Cardiac Events
 Acute Myocardial Infarction
 Shock of any form (Cardiogenic, Obstructive, Distributive)
 Myocarditis and Myopericarditis
 Cardiomyopathies
 Acute Congestive Failure (Pulmonary Edema)
 Sepsis
 Pulmonary Embolism
 Renal Failure
 Burns
 Acute CNS Event
 Rhabdomyolysis
 Cardiiac Neoplasm, Inflammatory Syndromes, Infiltrative Diseases
 Sympathomimetic Ingestions
 Congenital Coronary Anomalies
 Extreme Physical Exertion
Other Investigation

 Cardiac Imaging :
Echocardiography : Wall motion Defect
LV Impairment
 Chest X Ray : Pulmonary edema
Cardiomegaly
Widened mediastinum
 Routine Blood Tests: U&E
Lipid Profile
RBS
Risk Stratification

Five simple baseline parameters have been reported to

account for > 90% of the prognostic information for 30-day
mortality. These characteristics are given in descending order
of importance:

 Age
 Systolic blood pressure
 Killip classification
 Heart rate
 Location of MI

In addition, various risk models have been created to improve

risk prediction.
TIMI Risk Model for Prediction of Short-Term
Mortality in ST-Segment Elevation Myocardial
Infarction Patients
 Management

 Early and Emergency Medical Management :

 Cardiac Monitoring
 Oxygen
 IV Access and Blood for U&E, Glucose, CBC, Cardiac Enzyme
 Brief History and Clinical Assessment
 Loading Dose of Aspirin and Clopidogrel
 Analgesia if Continuing Pain
 Antiemetic and Anxiolytic if required
 Reperfusion Therapy / Thrombolytic Therapy
STEMI Management Outline
 Reperfusion at a PCI-Capable Hospital

1. Primary PCI in STEMI: Recommendations

 CLASS I
Primary PCI should be performed in patients with
1.STEMI and ischemic symptoms of less than 12 hours’ duration
2.STEMI and ischemic symptoms of less than 12 hours’ duration who
have contraindications to fibrinolytic therapy, irrespective of the
time delay from FMC
3. STEMI and cardiogenic shock or acute severe HF, irrespective of time
delay from MI onset. (Level of Evidence: B)
 Contd..

 CLASS IIa
1. Primary PCI is reasonable in patients with STEMI
if there is clinical and/or ECG evidence of
ongoing ischemia between12 and 24 hours
after symptom onset (94,95). (Level of Evidence:
B)

 CLASS IIb
1. PCI may be performed in a noninfarct artery at the
time of primary PCI in patients with STEMI who
are hemodynamically stable .
Adjunctive Antiplatelet
Therapy
 Class I

1. Aspirin 162 to 325 mg should be given before primary PCI. (LOE: B)

2. After PCI, aspirin should be continued indefinitely.(81 to 325 mg
daily maintenance dose) (LOE: A)
3. A loading dose of a P2Y12 receptor inhibitor should
be given as early as possible or at time of primary
PCI to patients with STEMI. Options include:
a. Clopidogrel 600 mg (LOE: B); or
b. Prasugrel 60 mg(LOE: B); or
c. Ticagrelor 180 mg. (LOE: B)
Continue….
4. P2Y12 inhibitor therapy should be given for 1
year to patients with STEMI who receive a stent
(BMS or DES) during primary PCI using the
following maintenance doses:
a. Clopidogrel 75 mg daily (LOE: B);or
b. Prasugrel 10 mg daily (LOE: B); or
c. Ticagrelor 90 mg twice a day. (LOE: B)

 Class III: Harm

Prasugrel should not be administered to patients with a history of
prior stroke or transient ischemic attack. (LOE: B)
Adjunctive Anticoagulant Therapy :
 Class I

1. For patients with STEMI undergoing primary PCI,

the following supportive anticoagulant regimens are
recommended:
a. UFH, with additional boluses administered as
needed to maintain therapeutic activated clotting
time levels, taking into account whether a GP
IIb/IIIa receptor antagonist has been administered
(LOE: C); or
b. Bivalirudin with or without prior treatment with
UFH.(LOE: B)
Continue……..
 Class IIa

1. In patients with STEMI undergoing PCI who are at high

risk of bleeding, it is reasonable to use bivalirudin
monotherapy in preference to the combination of UFH
and a GP IIb/IIIa receptor antagonist. (Level of
Evidence: B)

 Class III: Harm

1. Fondaparinux should not be used as the sole

anticoagulant to support primary PCI because of the risk
of catheter thrombosis.304 (Level of Evidence: B)
Reperfusion at a Non–PCI
Capable Hospital

1) Fibrinolytic Therapy When There Is an

Anticipated Delay to Performing Primary
PCI Within 120 Minutes of FMC
Indications for Fibrinolytic Therapy
When There Is a >120-Minute Delay
From FMC to Primary PCI
FibrinoLytics
 Contraindications and Cautions for
Fibrinolytic Therapy in STEMI

Absolute contraindications

 Any prior ICH

 Known structural cerebral vascular lesion (eg, AVM)

 Known malignant intracranial neoplasm (primary or metastatic)

 Ischemic stroke within 3 months

EXCEPT acute ischemic stroke within 4.5 h

 Suspected aortic dissection

 Active bleeding or bleeding diathesis (excluding menses)

 Significant closed-head or facial trauma within 3 mo

 Intracranial or intraspinal surgery within 2 mo

 Severe uncontrolled hypertension (unresponsive to emergency therapy)

 For streptokinase, prior treatment within the previous 6 mo

CONTINUE…..
 Relative contraindications

 History of chronic, severe, poorly controlled hypertension

 Significant hypertension on presentation (SBP 180 mm Hg or DBP
 110 mm Hg)
 History of prior ischemic stroke 3 mo
 Dementia
 Known intracranial pathology not covered in absolute
contraindications
 Traumatic or prolonged (10 min) CPR
 Major surgery (3 wk)
 Recent (within 2 to 4 wk) internal bleeding
 Noncompressible vascular punctures
 Pregnancy
 Active peptic ulcer
 Oral anticoagulant therapy
Adjunctive Antiplatelet
therapy
 Aspirin (162- to 325-mg loading dose) and
clopidogrel (300-mg loading dose) for
patients ≤75 years of age, 75-mg dose for
patients >75 years of age) should be
administered to patients with STEMI who
receive fibrinolytic therapy.(C.O.R : IA)
 Aspirin should be continued indefinitely
(C.O.R: IA)
 Clopidogrel (75 mg daily) for atleast 14 days
(C.O.R. IA)
 And upto 1 year (C.O.R IC)
Adjunctive Anticoagulant
Therapy
 Patients with STEMI undergoing reperfusion with fibrinolytic
therapy should receive anticoagulant therapy for a minimum of
48 hours, and preferably for the duration of the index
hospitalization, up to 8 days or until revascularization if
performed.
 Recommended Regimen :
a. UFH adm. as a weight-adjusted intravenous bolus and infusion
to obtain an aPTT time of 1.5 to 2.0 times control, for 48 hours
or until revascularization.(COR IC)
b. Enoxaparin adm. a/c to age, weight, and creatinine clearance,
given as an i.v bolus, followed in 15 min. by s/c inj. for the
duration of the index hospitalization, up to 8 days or until
revascularization; or
Continue…..
 Fondaparinux administered with initial i.v dose, followed in 24
hrs by daily s/c inj. if the estimated creatinine clearance is greater
than 30 mL/min, for the duration of the index hospitalization, up
to 8 days or until revascularization.

 Enoxaparin:
 ● If age 75 y: 30-mg IV bolus, followed in 15 min by 1 mg/kg
subcutaneously every 12 h (maximum 100 mg for the first 2
doses)
 ● If age> 75 y: no bolus, 0.75 mg/kg subcutaneously every 12 h
(maximum 75 mg for the first 2 doses)
 ● Regardless of age, if CrCl 30 mL/min: 1 mg/kg subcutaneously
every 24 h
 ● Duration: For the index hospitalization, up to 8 d or until
revascularization
Routine Medical Therapies
DELAYED INVASIVE
MANAGEMENT
Indications for Coronary Angiography in Patients Who Were Managed
With Fibrinolytic Therapy or Who Did Not Receive Reperfusion Therapy
Complications
EARLY COMPLICATION (<1 WEEK)

 Acute Cardiac Failure

 Cardiogenic Shock

 Arrythmias : Supraventricular Arrythmia :

Sinus Tachycardia or Bradycardia
Atrial Ectopic Beats
Atrial Fibrillation / Flutter

Ventricular Arrythmia :
Ventriculat Ectopic Beats
Accelerated Idioventricular Rhythm
VT
Contd…

 AV Block and Intraventricular Block

 Mitral Regurgitation
 Rupture of Interventricular septum
 Cardiac Temponade
 Post-Infarct Angina
 Pericarditis
 Mural Thrombus
 Contd..

 Late Complications(>1 Week Post-MI)

 Post MI(Dressler’s) Syndrome

 LV Aneurysm
 Chronic Cardiac Failure
CARDIAC REHABILITATION
 A. Cardiac Rehabilitation Programme
1. Formal rehabilitation programs which use exercise and patient
education to help patients modify their lifestyles
2. Home programme and family care.

 B. Lifestyle Modification :
1. Optimal control of hypertension and diabetes
2. Weight reduction
3. Resumption of daily activities

 C.Secondary Prevention
Thank you All
 SYMPTOMS
 THE CLASSIC SYMPTOMS INCLUDE
Severe crushing substernal chest pain at rest > 20 minutes
Not relieved by sublingual nitrates or rest
Radiation to the neck, jaw, back, shoulder, right arm and epigastrium.
 ASSOCIATED SYMPTOMS :
Diaphoresis, Dyspnea, Fatigue, light-headedness, palpitations, acute confusion,
indigestion, nausea, or vomiting. Gastrointestinal symptoms are especially
common with inferior infarction.

Myocardial ischemic pain localized to the epigastrium is often misdiagnosed

as indigestion.

 Acute MI can occur without chest pain, especially among postoperative

patients, the elderly, and those with diabetes mellitus.
Residual Risk and Use of Oral
Anticoagulants
 Patients with ACS remain at a significant risk of recurrent
ischemic events after initial revascularization despite optimal
medical therapy and aggressive risk factor modification.
 1 in 10 patients experiences a significant atheroembolic event
(cardiac death, myocardial infarction or stroke) within a year of
the first ACS episode.
 This is felt to be secondary to a persistent thrombogenic state
that extends well beyond the initial ACS event.
 New oral anticoagulants have emerged in the last decade with
the potential to minimize residual risk ie. Rivaroxaban
Electrographic Criteria For The
Diagnosis of AMI In The Presence of
LBBB
Criteria Score
ST-segment elevation > 1 mm concordant with QRS 5
ST-segment depression > 1 mm in leads V1, V2 or V3 3
ST-segment elevation > 5 mm discordant with QRS 2

Point scores for each criteria met are added. Total Point Score of # yields
>90% specificity and 88% positive predictive value.
 Advantages
CK-MB Myoglobin Troponin
1. Rapid, cost-efficient, 1. High sensitivity 1. Greater sensitivity and
accurate assays specificity than CK-MB

2. Ability to detect early 2. Useful in early 2. Detection of recent MI

reinfarction detection of MI up to 2 weeks after onset

3.Detection of 32. Detection of recent

reperfusion MI up to 2 weeks after
onset

4.Most useful in ruling 4. Detection of

out MI reperfusion
 Disadvantages

CK-MB Myoglobin Troponins

1. Lack of specificity with 1. Very low specificity with 1. Low sensitivity in
skeletal muscle disease/injury skeletal muscle injury or early phase of MI (<6
disease h after symptom
2. Low sensitivity during early onset)
MI (<6 h) or late (>36 h) after 2. Rapid return to normal
symptom onset and for minor 2. Limited ability to
myocardial damage detect late minor re-
infarction
The Global Registry of Acute
Coronary Events (GRACE) score
 STEMI

 ST segment elevations
 T wave changes
 Q wave development
 Enzyme elevations
 Reciprocals