eMedicine Specialties > Emergency Medicine > Cardiovascular

Shock, Cardiogenic: Treatment & Medication

Author: Ethan S Brandler, MD, MPH, Clinical Assistant Professor, Attending Physician, Departments of Emergency Medicine and Internal Medicine, University Hospital of Brooklyn, Kings County Hospital
Coauthor(s): Richard H Sinert, DO, Associate Professor of Emergency Medicine, Clinical Assistant Professor of Medicine, Research Director, State University of New York College of Medicine; Consulting Staff, Department of Emergency Medicine, Kings County Hospital Center
Contributor Information and Disclosures

Updated: Oct 30, 2009

Treatment

Prehospital Care

Prehospital care is aimed at minimizing any further ischemia and shock.

  • All patients require intravenous access, high-flow oxygen administered by mask, and cardiac monitoring.
  • Twelve-lead electrocardiography performed in the field by appropriately trained paramedics may be useful in decreasing door to PCI times and/or thrombolytics because acute ST-segment elevation myocardial infarctions can be identified earlier. The ED, can thus be alerted, and may mobilize the appropriate resources.
  • Inotropic medications should be considered in systems with appropriately trained paramedical personnel.
  • When clinically necessary, positive pressure ventilation and endotracheal intubation should be performed.
  • Continuous positive airway pressure (CPAP) or bilevel positive airway pressure (BiPAP) support can be considered in appropriately equipped systems.

Emergency Department Care

ED care of cardiogenic shock is aimed at making the diagnosis, preventing further ischemia, and treating the underlying cause. Treatment of the underlying cause is directed in the case of acute myocardial infarction (AMI) at coronary artery reperfusion. This is best accomplished with rapid transfer of the patient to a cardiac catheterization laboratory. 

Clinicians should be alert to the fact that the SHOCK trial demonstrated that percutaneous coronary intervention (PCI) or coronary artery bypass are the treatments of choice and that they have been shown to markedly decrease mortality rates at 1 year. PCI should be initiated within 90 minutes of presentation; however, it remains helpful, as an acute intervention, within 12 hours of presentation. If such a facility is not immediately available, thrombolytics should be considered. However, this treatment is second best. An increased mortality is seen in situations where thrombolytics are used instead of PCI. This is due to the relative ineffectiveness of the thrombolytic medications to lyse clots in low blood pressure situations.10,5

Treatment begins with assessment and management of the ABCs.

  • The airway should be assessed for patency and breathing evaluated for effectiveness and increased work of breathing. Endotracheal intubation and mechanical ventilation should be considered for patients with excessive work of breathing. Positive pressure ventilation may improve oxygenation but may also compromise venous return, preload, to the heart. In any event, the patient should be treated with high-flow oxygen. Recent studies in patients with acute cardiogenic pulmonary edema have shown noninvasive ventilation to improve hemodynamics and reduce the intubation rate. Mortality is, however, unaffected.
  • Other interventions are directed at supporting myocardial perfusion and maximizing cardiac output. Intravenous fluids should be provided to maintain adequate preload. The administration of such fluids should be guided by central venous pressure, pulmonary capillary wedge pressure monitoring, or sonographic assessment of IVC filling.
  • Anticoagulants and aspirin should be used as in other cases of acute myocardial infarctions. Care should be taken to ensure that the patient does not have myocardial wall rupture that is amenable to surgery before initiating therapy. There is no need to start clopidogrel until after angiography as this may determine a need for urgent coronary bypass.5
  • Intravenous vasopressors provide inotropic support increasing perfusion of the ischemic myocardium and all body tissues. However, extreme heart rates should be avoided because they may increase myocardial oxygen consumption, increase infarct size, and further impair the pumping ability of the heart. No particular vasopressor has been shown to be superior to another. Carefully chosen combinations of pressors may be useful.11,12
    • Dopamine may provide vasopressor support. With higher doses, it has the disadvantage of increasing the heart rate and myocardial oxygen consumption.
    • Dobutamine, inamrinone (formerly amrinone), or milrinone may provide inotropic support. In addition to their positive inotropic effects, inamrinone and milrinone have a beneficial vasodilator effect, which reduces preload and afterload.
    • Norepinephrine infusion can also be considered in refractory cardiogenic shock, though it significantly increases afterload.
  • Nitrates and/or morphine are advised for the management of pain; however, they must be used with caution because these patients are in shock, and excessive use of either of these agents can produce profound hypotension. Neither of these options has been shown to improve outcomes in cardiogenic shock.
  • Other supportive medications to be considered include nesiritide (Natrecor) and levosimendan.
    • Nesiritide (Natrecor) may be considered. Although nesiritide has been shown to increase mortality and renal dysfunction, it continues to be studied as a treatment of acute congestive heart failure and currently retains Food and Drug Administration (FDA) approval. It should be used with caution in the setting of cardiogenic shock because it has been shown to cause hypotension.
    • Levosimendan, though not approved for use in the United States, can be considered in conjunction with vasopressors. It should be used with caution as it can cause hypotension. Used with vasopressors, levosimendan may improve hemodynamics and improve coronary blood flow.13,14
  • Mechanical device supports may be used to support patients in cardiogenic shock.
    • The use of an intra-aortic balloon pump (IABP) is recommended for cardiogenic shock not quickly reversed with pharmacologic therapy. It is also recommended as a stabilizing measure combined with thrombolytic therapy when angiography and revascularization are not readily available. Counterpulsation of the IABP reduces LV afterload and improves coronary artery blood flow. Although this procedure is generally not performed in the ED, planning is essential, and early consultation with a cardiologist regarding this option is recommended. Although complications may occur in up to 30% of patients, extensive retrospective data support its use.15,16
    • Left-ventricular assist devices (LVAD) may be used in selected patients with refractory shock as a bridge to cardiac transplantation. This is still controversial and requires the assistance of cardiologists and cardiac surgeons.17,15 LVADs have not been shown to be superior in terms of outcomes.16

Consultations

Consult a cardiologist at the earliest opportunity because his or her insight and expertise may be invaluable for facilitating echocardiographic support, placement of an IABP, and transfer to more definitive care (eg, cardiac catheterization suite, intensive care unit, operating room). In severe cases, also consider discussing the case with a cardiothoracic surgeon.

Medication

The goals of pharmacotherapy are to reduce morbidity and to prevent complications.

Vasopressors

These drugs augment both coronary and cerebral blood flow present during the low-flow state associated with shock. Sympathomimetic amines with both alpha-adrenergic and beta-adrenergic effects are indicated. Dopamine and dobutamine are the drugs of choice to improve cardiac contractility.


Dopamine (Intropin)

Stimulates both adrenergic and dopaminergic receptors. Hemodynamic effect is dependent on the dose. Lower doses predominantly stimulate dopaminergic receptors that, in turn, produce renal and mesenteric vasodilation. Higher doses cause cardiac stimulation and renal vasodilation.

Adult

5-20 mcg/kg/min IV continuous infusion; increase by 1-4 mcg/kg/min q10-30min to optimal response (>50% of patients have satisfactorily responses with doses <20 mcg/kg/min)

Pediatric

Administer as in adults

Phenytoin, alpha-adrenergic and beta-adrenergic blockers, general anesthetics, and MAOIs increase and prolong effects

Documented hypersensitivity; pheochromocytoma; ventricular fibrillation

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Tachycardia may increase myocardial oxygen consumption; ventricular dysrhythmias may occur; closely monitor urine output, cardiac output, pulmonary wedge pressure, and BP during infusion; prior to infusion, correct hypovolemia with whole blood or plasma, as indicated; central venous pressure or LV filling pressure may help in detecting and treating hypovolemia


Dobutamine (Dobutrex)

Sympathomimetic amine with stronger beta effects than alpha effects. Produces vasodilation and increases inotropic state. Higher doses may increase heart rate, exacerbating myocardial ischemia.

Adult

5-20 mcg/kg/min IV continuous infusion

Pediatric

Administer as in adults

Beta-adrenergic blockers antagonize effects; general anesthetics may increase toxicity

Documented hypersensitivity; idiopathic hypertrophic subaortic stenosis; atrial fibrillation or flutter

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Extreme caution in myocardial infarction; correct hypovolemic state before use

Phosphodiesterase enzyme inhibitors

These agents improve cardiac output in refractory hypotension and shock. Milrinone and inamrinone (formerly amrinone) may be used.


Milrinone (Primacor)

Bipyridine with positive inotropic and vasodilator effects; little chronotropic activity; mode of action differs from that of digitalis glycosides and catecholamines.

Adult

Loading dose: 50 mcg/kg IV over 10 min
Continuous infusion: 0.375-0.75 mcg/kg/min IV

Pediatric

Administer as in adults; DOC in many pediatric intensive care units, but safety and efficacy are not well established

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Monitor fluids, electrolytes, renal function, BP, heart rate, and clinical symptoms during therapy; excessive diuresis may increase potassium loss and predispose patients taking digitalis to arrhythmias; correct hypokalemia with potassium supplementation prior to treatment; stop or slow infusion rates with excessive decreases in BP; vigorous diuretic therapy may cause significant decreases in cardiac filling pressure


Inamrinone - formerly amrinone (Inocor)

Phosphodiesterase inhibitor with positive inotropic and vasodilator activity. Produces vasodilation and increases inotropic state. More likely than dobutamine to cause tachycardia; may exacerbate myocardial ischemia.

Adult

Initial bolus: 0.75 mg/kg IV slowly over 2-3 min
Maintenance infusion: 5-10 mcg/kg/min IV; not to exceed 10 mg/kg; adjust dose according to response

Pediatric

Administer as in adults

Coadministration with diuretics may cause hypovolemia and decrease filling pressure; cardiac glycosides have additive effects

Documented hypersensitivity; cardiac outlet obstruction (eg, aortic stenosis, pulmonary stenosis, idiopathic hypertrophic subaortic stenosis and/or hypertrophic cardiomyopathy)

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Discontinue therapy with symptoms or liver toxicity; correct hypokalemic states before therapy; causes thrombocytopenia in 2-3% of patients; hypotension may occur following loading dose; requires adequate preload; ventricular dysrhythmias may occur (but may be related to the underlying condition)

Adrenergic Agonist Agent


Norepinephrine

Naturally occurring catecholamine with potent alpha-receptor and mild beta-receptor activity. Stimulates beta1- and alpha-adrenergic receptors, resulting in increased cardiac muscle contractility, heart rate, and vasoconstriction. Increases blood pressure and afterload. Increased afterload may result in decreased cardiac output, increased myocardial oxygen demand, and cardiac ischemia. Generally reserved for use in patients with severe hypotension (eg, systolic blood pressure <70 mm Hg) or hypotension unresponsive to other medication.

Adult

0.5-1 mcg/min IV infusion initially, titrated to effect; not to exceed 30 mcg/min

Pediatric

Not established

Effects increase when administered concurrently with tricyclic antidepressants, MAO inhibitors, antihistamines, guanethidine, methyldopa, ergot alkaloids; atropine may block reflex tachycardia caused by norepinephrine and enhances pressor response

Documented hypersensitivity; peripheral or mesenteric vascular thrombosis because ischemia may be increased and the area of the infarct extended

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Correct blood-volume depletion, if possible, before giving norepinephrine therapy; extravasation may cause severe tissue necrosis and, thus, should be administered into a large vein; caution in occlusive vascular disease

Analgesic, Salicylate


Aspirin

Odorless white powdery substance available in 81 mg, 325 mg, and 500 mg for oral use. When exposed to moisture, aspirin hydrolyzes into salicylic acid and acetic acids.

Stronger inhibitor of both prostaglandin synthesis and platelet aggregation than other salicylic acid derivatives. Acetyl group is responsible for inactivation of cyclooxygenase via acetylation. Aspirin is hydrolyzed rapidly in plasma, and elimination follows zero order pharmacokinetics.

Irreversibly inhibits platelet aggregation by inhibiting platelet cyclooxygenase. This, in turn, inhibits conversion of arachidonic acid to PGI2 (potent vasodilator and inhibitor of platelet activation) and thromboxane A2 (potent vasoconstrictor and platelet aggregate). Platelet-inhibition lasts for life of cell (approximately 10 d). May be used in low dose to inhibit platelet aggregation and improve complications of venous stases and thrombosis. Reduces likelihood of myocardial infarction. Also very effective in reducing risk of stroke. Early administration of aspirin in patients with AMI may reduce cardiac mortality in first mo.

Adult

160-324 mg PO or chewed; suppository if patient is unable to take PO medications

Pediatric

Not established

Effects may decrease with antacids and urinary alkalinizers; corticosteroids decrease salicylate serum levels; additive hypoprothrombinemic effects and increased bleeding time may occur with coadministration of anticoagulants; may antagonize uricosuric effects of probenecid and increase toxicity of phenytoin and valproic acid; doses >2 g/d may potentiate glucose-lowering effect of sulfonylurea drugs; simultaneous administration of other NSAIDs may decrease the cardioprotective and stroke preventive effects

Documented hypersensitivity; liver damage, hypoprothrombinemia, vitamin K deficiency, bleeding disorders, asthma; because of association of aspirin with Reye syndrome, do not use in children (<16 y) with viral infections

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

May cause transient decrease in renal function and aggravate chronic kidney disease; avoid use in patients with severe anemia, with history of blood coagulation defects, or taking anticoagulants

Vasodilators

Smooth-muscle relaxers and vasodilators that can reduce systemic vascular resistance, allowing more forward flow and improving cardiac output.


Nitroglycerin (Nitro-Bid)

Relaxes vascular smooth muscle by stimulating intracellular cyclic guanosine monophosphate production to decrease BP.

Adult

10-20 mcg/min IV infusion

Pediatric

0.1-1 mcg/kg/min IV infusion

Aspirin may increase nitrate serum concentrations; marked symptomatic orthostatic hypotension may occur with coadministration of calcium-channel blockers (may need to adjust doses of either agent)

Documented hypersensitivity; severe anemia; shock; postural hypotension; head trauma; closed-angle glaucoma; cerebral hemorrhage

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in coronary artery disease and low systolic BP

Analgesics

Pain control is essential to quality patient care. It ensures patient comfort and promotes pulmonary toilet.


Morphine sulfate (Duramorph, MS Contin)

DOC for analgesia because of reliable and predictable effects, safety profile, and ease of reversibility with naloxone.

Adult

Starting dose: 0.1 mg/kg IV/IM/SC
Maintenance dose: 5-20 mg/70 kg IV/IM/SC q4h; titrate to desired effect
In relatively hypovolemic patients: Start with 2 mg IV/IM/SC; reassess hemodynamic effects

Pediatric

Infants and children: 0.05-0.2 mg/kg dose IV/IM/SC q2-4h prn; not to exceed 15 mg/dose

Phenothiazines may antagonize analgesic effects; tricyclic antidepressants, MAOIs, and other CNS depressants may potentiate adverse effects

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in hypotension, respiratory depression, nausea, emesis, constipation, urinary retention, atrial flutter and other supraventricular tachycardias; potentially compromised airway where establishing rapid airway control may be difficult; has vagolytic action and may increase ventricular response rate

Diuretics

These drugs cause diuresis to decrease plasma volume and edema and thereby decrease cardiac output BP. The initial decrease in cardiac output causes a compensatory increase in peripheral vascular resistance. With continuing diuretic therapy, extracellular fluid and plasma volumes almost return to pretreatment levels. Peripheral vascular resistance decreases below that of pretreatment baseline.


Furosemide (Lasix)

Inhibits reabsorption of sodium and chloride in the ascending loop of Henle and distal renal tubule; this inhibition interferes with the chloride-binding cotransport system, causing increased excretion of water, sodium, chloride, magnesium, and calcium.

Adult

40-80 mg/d IV/IM

Pediatric

1 mg/kg IV/IM slowly under close supervision; not to exceed 6 mg/kg

Metformin decreases concentrations; interferes with hypoglycemic effect of antidiabetic agents and antagonizes muscle-relaxing effect of tubocurarine; auditory toxicity may increase with coadministration of aminoglycosides; hearing loss may occur; anticoagulant activity of warfarin may be enhanced when taken concurrently; increased plasma lithium levels and toxicity are possible when taken concurrently

Documented hypersensitivity; hepatic coma; anuria; severe electrolyte depletion

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Frequently determine serum electrolyte, CO2, glucose, creatinine, uric acid, calcium, and BUN levels during first few months of therapy and periodically thereafter; observe for blood dyscrasias, liver or kidney damage, or idiosyncratic reactions

Natriuretic peptide

These drugs cause arterial and venous dilation by binding to cyclic GMP receptor on vascular smooth muscle causing smooth muscle relaxation. This medication produces dose-dependent decreases in pulmonary capillary wedge pressure and systemic arterial pressure.


Nesiritide (Natrecor)

Recombinant DNA form of human B-type natriuretic peptides (hBNP), which dilate veins and arteries.
Human BNP binds to particulate guanylate cyclase receptor of vascular smooth muscle and endothelial cells. Binding to receptor causes increase in cyclic GMP, which serves as second messenger to dilate veins and arteries. Reduces pulmonary capillary wedge pressure and improves dyspnea in patients with acutely decompensated congestive heart failure.

Adult

Initial 2 mcg/kg IV bolus over 30 min followed by continuous infusion at 0.01 mcg/kg/min

Pediatric

Not established

Cannot be administered in same IV line as furosemide, enalaprilat, heparin, insulin; may cause profound hypotension when given in concert with ACE inhibitors or loop diuretics

Documented hypersensitivity; hypotension; renal insufficiency

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Must be used with extreme caution in patients with renal insufficiency, has been shown to have severe negative effects on renal function; has also been shown to increase mortality; in case of hypotension, infusion should be interrupted

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References
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References

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Further Reading

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Keywords

cardiogenic shock, cardiac shock, shock, global hypoperfuse, acute myocardial infarction, AMI, decreased pumping of the heart, decreased urine output, altered mentation, hypotension, jugular venous distension, cardiac gallop, pulmonary edema, acute cardiac ischemia

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Contributor Information and Disclosures

Author

Ethan S Brandler, MD, MPH, Clinical Assistant Professor, Attending Physician, Departments of Emergency Medicine and Internal Medicine, University Hospital of Brooklyn, Kings County Hospital
Ethan S Brandler, MD, MPH is a member of the following medical societies: American College of Emergency Physicians and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Coauthor(s)

Richard H Sinert, DO, Associate Professor of Emergency Medicine, Clinical Assistant Professor of Medicine, Research Director, State University of New York College of Medicine; Consulting Staff, Department of Emergency Medicine, Kings County Hospital Center
Richard H Sinert, DO is a member of the following medical societies: American College of Physicians and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Medical Editor

Daniel J Dire, MD, FACEP, FAAP, FAAEM, Clinical Professor, Department of Emergency Medicine, University of Texas-Houston; Clinical Professor, Department of Pediatrics, University of Texas Health Sciences Center, San Antonio, Texas
Daniel J Dire, MD, FACEP, FAAP, FAAEM is a member of the following medical societies: American Academy of Clinical Toxicology, American Academy of Emergency Medicine, American Academy of Pediatrics, American College of Emergency Physicians, and Association of Military Surgeons of the US
Disclosure: Talecris Biotherapeutics Honoraria Speaking and teaching

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

A Antoine Kazzi, MD, Chair and Medical Director, Department of Emergency Medicine, American University of Beirut, Lebanon
A Antoine Kazzi, MD is a member of the following medical societies: American Academy of Emergency Medicine
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

 
 
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