NSTEMI & Unstable Angina Management
NSTEMI or EKG
changes suggest ischemia with high risk:
¡ Aspirin
¡ Beta blocker
¡ Nitrates
¡ Heparin (UFH or
LMWH)
¡ ACE-I/ARB
¡ Statin
¡ Consider GP
IIb/IIIa inhibitor and clopidogrel
EKG normal or
non-specific changes with intermediate or low risk:
¡ Rule out ACS
with 3 sets of troponin, EKG
¡ Consider
pre-discharge stress test
Early
Treatment
q MONA
•
Morphine- for analgesia
•
Oxygen- sPO2 >94%
•
Sublingual nitroglycerin
•
Aspirin, 160 to 325 mg
•
Clopidogrel
•
Adjunct therapy
Acute
MI: Outcome
•
Outcome after acute myocardial infarction is a
function of vessel patency rate and time from occlusion to reperfusion
•
Benefits of Rapid Reperfusion
–
Decreased mortality
–
Decreased morbidity
–
Increased myocardial salvage
–
Increased left ventricular function
•
Preferred therapy if performed in a timely fashion by
skilled individuals in high-volume centers
•
Reperfusion strategy in patients with risk of bleeding
contraindications to thrombolytic therapy
Acute
MI: Thrombolysis
•
Benefit greatest if therapy initiated early
•
Highly significant reduction in mortality
•
Benefits patients irrespective of age, gender, and
comorbid conditions
•
Slightly increased risk of intracerebral hemorrhage
•
Candidates
Ø Time to therapy
12 hours or less
Ø Acute ST-segment
elevation
Ø Symptoms
consistent with acute MI and presence of Left Bundle Branch Block
Ø Patients without
ST-segment elevation should not receive thrombolytic therapy
Thrombolytic
Therapy
Contraindications
•
Active bleeding
•
Recent major trauma/surgery in 3 weeks
•
Recent GI bleed in 1 month
•
Ischemic stroke within 6 months
•
Haemorrhagic stroke at any time
•
Markedly elevated blood pressure
•
Significant bleeding diathesis
•
Pregnancy or post partum
Thrombolytic
Agents
•
Nonspecific agents deplete coagulation factors
A.
Streptokinase
B.
Anistreplase
C.
Urokinase
•
Specific agents do not deplete coagulation factors
A.
Alteplase (tPA)
B.
Reteplase
Thrombolytic
Agents:
Comparative Pharmacologic Features
Feature SK APSAC UK
SCUPA rtPA
Half-Life
(min) 18 90 20 7 5
Fibrin-Selective + + ++ ++++ +++
Duration
of
Infusion 60 min 2-5 m 5-15 m
Hours Hours
Antigenicity Yes Yes No No? No?
Incidence
of
Reperfusion (%) 60-70 60-70 60-70 60-70 60-70
Frequency
of
Reocclusion (%) 15 10 10 NA 20
Fibrinogenolysis ++++ ++++ +++ ++ ++
Platelet
Activation +++ +++ 0 ? ++++
Acute MI
Adjunct Drug Therapy
Aspirin
•
Inhibition of Thromboxane A2 formation
•
Blockage of platelet aggregation and thrombus
propagation
•
Prevention of coronary re-occlusion after successful
thrombolysis
•
Potential Benefits
Ø Mortality
decreased 23%
Ø Non-fatal MI
decreased 44%
Ø Non-fatal stroke
decreased 46%
Ø 42% reduction in
mortality when added to Streptokinase
Heparin
•
Post thrombolytic therapy, heparin administration
based more on current practice than on evidence
•
Intravenously in patients receiving
alteplase/retaplase
•
Subcutaneously in all patients not treated with
thrombolytic therapy
•
Should be used in large AWMI or in patients with LV
mural thrombus to reduce risk of stroke
•
Potential Benefits
Ø Prevention of
venous thrombosis
Ø Decrease left
ventricular mural thrombus
Ø Decrease
arterial embolization
Ø Decrease
re-infarction or extension of infarct
Beta
Blockers
•
Patients without contraindications should receive
intravenous beta blockers when acute infarction is suspected, followed by oral
agents when they are hemodynamically stable
•
All patients within 12 hours of myocardial infarction
•
Continuing or recurrent ischemic pain
•
Tachyarrhythmias
•
Potential Benefits
Ø 13% reduction in
mortality in the pre-thrombolytic trials
Ø Reduce chest
pain
Ø Reduce
myocardial-wall stress
Ø Reduce infarct
size
Contraindications
•
Bradycardia
•
Second- or third-degree AV block
•
Hypotension
•
Clinical evidence of congestive heart failure
•
Cardiogenic shock
•
Active bronchospasm
Nitrates
•
Intravenously for first 24 to 48 hours
A.
Acute MI and CHF
B.
Large anterior infarction
C.
Persistent ischemia
D.
Hypertension
•
Beyond 48 hours in patients with recurrent angina or
persistent pulmonary congestion
•
Potential Benefits
Ø Primary action
is vasodilation
Ø May increase
myocardial perfusion
Ø May increase
peri-infarct ischemia
Ø Systemic
arterial vasodilation decreases blood pressure and decreases myocardial oxygen
demand
Ø Increased venous
capacitance decreases preload
ACE
Inhibitors
•
Potential Benefits
Ø Mortality
benefit when administered within 24 hours of MI
Ø Systemic and
coronary vasodilation may:
Ø A.
Reduce peri-infarct ischemia
Ø B.
Limit infarct expansion
Ø C.
Prevent early remodeling
Ø May have some
antithrombotic properties
Calcium
Channel Blockers
•
Reduce angina
•
Reduce blood pressure
•
Reduce coronary spasm
•
No reduction in mortality
•
Short-acting nifedipine may increase mortality (TRENT,
SPRINT II)
Ø Not recommended
as standard first-line therapy
Ø May be used for
significant hypertension or refractory ischemia
Rhythm
Disturbances
Atrial Fibrillation
•
Electrical cardioversion for unstable patients
(ischemic chest pain, hypotension, congestive heart failure)
•
Slow the ventricular response:
A.
IV Digitalis
B.
IV Beta Blockers
C.
IV Diltiazem or Verapamil
Post
discharge Care
A –
Antiplatelets & Antianginals
B – Beta
blocker, Blood pressure control
C –
Cholesterol lowering, Cigarettes cessation
D – Diabetes
control, Diet
E –
Education & Exercise
Thrombolytic
drugs
•
Depletion of fibrinogen, reduction in factor II, V,
and VIII levels, impairment of platelet aggregation, and the appearance of
fibrin split products.
•
If surgery is required for persistent ischemia after
failed thrombolytic therapy, it should be delayed by at least 12–24 hours.
•
If it is required emergently, plasma and
cryoprecipitate will probably be necessary to correct the anticipated
coagulopathy.


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