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eMedicine Journal
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Emergency Medicine
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Cardiovascular
Multifocal Atrial Tachycardia Synonyms, Key Words, and Related Terms: MAT, irregular cardiac rhythm, supraventricular rhythm, multifocal atrial tachycardia, atrial activity, congestive heart failure, sepsis, methylxanthine toxicity, chronic lung disease, heart conduction system, respiratory failure, theophylline toxicity |
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| AUTHOR INFORMATION | Section 1 of 11 |
Authored by Robin R Hemphill, MD, MPH, Associate Professor, Director, Disaster Preparedness, Department of Emergency Medicine, Vanderbilt University Medical Center
Coauthored by Michael A Huott, MD, Consulting Staff, Department of Emergency Medicine, Southwest Texas Methodist Hospital
Robin R Hemphill, MD, MPH, is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and Society for Academic Emergency Medicine
Edited by Edmond Hooker, MD, Assistant Clinical Professor, Department of Emergency Medicine, University of Louisville, Wright State University; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Paul Blackburn, DO, Program Director, Department of Emergency Medicine, Maricopa Medical Center; Assistant Professor, Department of Surgery, University of Arizona; John Halamka, MD, Chief Information Officer, CareGroup Healthcare System, Assistant Professor of Medicine, Department of Emergency Medicine, Beth Israel Deaconess Medical Center; Assistant Professor of Medicine, Harvard Medical School; and Craig Feied, MD, FACEP, FAAEM, FACPh, Professor of Emergency Medicine, Georgetown University, Director, National Institute for Medical Informatics, Director, Federal Project ER One, Director, National Center for Emergency Medicine Informatics
| Author's Email: | Robin R Hemphill, MD, MPH | |
|---|---|---|
| Editor's Email: | Edmond Hooker, MD |
eMedicine Journal, March 7 2006, VOLUME 7,
Number 3
| INTRODUCTION | Section 2 of 11 |
Background: Multifocal atrial tachycardia (MAT) is an irregular cardiac rhythm caused by at least 2 different sites of competing atrial activity.
Pathophysiology: MAT most often is found in the elderly patient with decompensated chronic lung disease and should be thought of as a hypoxic complication of underlying heart conduction pathology. However, other underlying causes may be present, such as congestive heart failure, sepsis, or methylxanthine toxicity. The effect of MAT on the heart conduction system may or may not lead to hemodynamic instability.
Frequency:
Mortality/Morbidity:
Age: This is predominately a condition of the elderly patient with multiple medical problems.
| CLINICAL | Section 3 of 11 |
History:
Physical:
Causes:
| DIFFERENTIALS | Section 4 of 11 |
Atrial Fibrillation
Atrial Flutter
Other Problems to be Considered:
Narrow-complex tachyarrhythmias
Sinus tachycardia
Wide-complex tachyarrhythmias
| WORKUP | Section 5 of 11 |
Lab Studies:
Imaging Studies:
Other Tests:
| TREATMENT | Section 6 of 11 |
Prehospital Care:
Emergency Department Care:
Consultations: A cardiologist may be of assistance with ECG interpretation and may be available for consultation if antiarrhythmic therapy is being considered.
| MEDICATION | Section 7 of 11 |
Although specific drug therapy historically has not demonstrated great efficacy in treating MAT, several small reports describe effectiveness with the use of magnesium sulfate (with concomitant correction of hypokalemia), verapamil, and some beta-blockers.
Drug Category: Antiarrhythmics -- In conjunction with the correction of the underlying medical process, these agents may provide conversion to NSR or control of the ventricular rate.
| Drug Name | Magnesium sulfate -- Considered by some the DOC. Maximum dose not well defined. Patient's deep tendon reflexes should be evaluated serially, as loss of reflexes is a signal to slow or halt the infusion of the drug. |
|---|---|
| Adult Dose | 2 g IV over 60 s, followed by 1-2 g/h |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; heart block; Addison disease; myocardial damage; severe hepatitis |
| Interactions | Concurrent use with nifedipine may cause hypotension and neuromuscular blockade; may increase neuromuscular blockade observed with aminoglycosides and potentiate neuromuscular blockade produced by tubocurarine, vecuronium, and succinylcholine; may increase CNS effects and toxicity of CNS depressants, betamethasone, and cardiotoxicity of ritodrine |
| Pregnancy | A - Safe in pregnancy |
| Precautions | Magnesium may alter cardiac conduction leading to heart block in digitalized patients; monitor respiratory rate, deep tendon reflex, and renal function when administered parenterally; may produce significant hypertension or asystole; correct serum potassium to > 4 mEq/L |
| Drug Name | Verapamil (Calan, Covera-HS) -- During depolarization, inhibits calcium ion from entering slow channels or voltage-sensitive areas of vascular smooth muscle and myocardium. |
|---|---|
| Adult Dose | 5-10 mg IV followed by a second dose 15-30 min later if the patient does not satisfactorily respond to the initial dose |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; severe CHF; sick sinus syndrome or second-degree or third-degree AV block; hypotension (<90 mm Hg systolic) |
| Interactions | Verapamil may increase carbamazepine, digoxin, and cyclosporine levels; coadministration with amiodarone can cause bradycardia and a decrease in cardiac output; when administered concurrently with beta-blockers may increase cardiac depression; cimetidine may increase verapamil levels; verapamil may increase theophylline levels |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Hepatocellular injury may occur; transient elevations of transaminases with and without concomitant elevations in alkaline phosphatase and bilirubin have occurred (elevations have been transient and may disappear with continued verapamil treatment); monitor liver function periodically |
| Drug Name | Metoprolol (Lopressor) -- Selective beta1-adrenergic receptor blocker that decreases the automaticity of contractions. During IV administration, carefully monitor blood pressure, heart rate, and ECG. |
|---|---|
| Adult Dose | Initially 5 mg IV q5min; not to exceed 15 mg |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; uncompensated congestive heart failure; bradycardia; asthma or severe COPD; cardiogenic shock; AV conduction abnormalities |
| Interactions | Aluminum salts, barbiturates, NSAIDs, penicillins, calcium salts, cholestyramine, and rifampin may decrease bioavailability and plasma levels of metoprolol, possibly resulting in decreased pharmacologic effects; toxicity of metoprolol may increase with coadministration of sparfloxacin, phenothiazines, astemizole, calcium channel blockers, quinidine, flecainide, and contraceptives; metoprolol may increase toxicity of digoxin, flecainide, clonidine, epinephrine, nifedipine, prazosin, verapamil, and lidocaine |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Beta-adrenergic blockade may reduce signs and symptoms of acute hypoglycemia and may decrease clinical signs of hyperthyroidism; abrupt withdrawal may exacerbate symptoms of hyperthyroidism, including thyroid storm; monitor patient closely and withdraw the drug slowly; during IV administration, carefully monitor blood pressure, heart rate, and ECG |
| FOLLOW-UP | Section 8 of 11 |
Further Inpatient Care:
Further Outpatient Care:
Transfer:
Deterrence/Prevention:
Complications:
Prognosis:
| MISCELLANEOUS | Section 9 of 11 |
Medical/Legal Pitfalls:
| TEST QUESTIONS | Section 10 of 11 |
CME Question 1: Which of the following is not a typical underlying medical condition often associated with multifocal atrial tachycardia (MAT)?
A: Decompensated chronic lung disease
B: Congestive heart failure
C: Digoxin toxicity
D: Methylxanthine toxicity
E: Pulmonary embolism
The correct answer is C: Digoxin toxicity typically leads to atrioventricular blocks, regularization of atrial fibrillation, or ventricular ectopy.
CME Question 2: What is the first line medical therapy for a patient with an ECG that demonstrates multifocal atrial tachycardia (MAT)?
A: IV procainamide
B: IV lidocaine
C: IV beta-blockers
D: Supportive therapy directed at the underlying process
E: IV magnesium
The correct answer is D: In treating MAT, the primary efforts are directed toward correcting the underlying decompensated medical condition, which often correct the MAT.
Pearl Question 1 (T/F): The most common cause of multifocal atrial tachycardia (MAT) is myocardial infarction.
The correct answer is False: The most common cause of MAT is decompensated chronic lung disease. Other causes include pneumonia, congestive heart failure, pulmonary embolism, myocardial infarction, diabetes, hypokalemia, and methylxanthine toxicity.
Pearl Question 2 (T/F): For treatment of multifocal atrial tachycardia (MAT), the recommended dose of IV magnesium is 2 g IV over 60 seconds, then 1-2 g/h.
The correct answer is True: The recommended dose is 2 g IV over 60 seconds, then 1-2 g/h. Patient`s deep tendon reflexes should be evaluated serially, as loss of reflexes is a signal to slow or halt the infusion of the drug.
Pearl Question 3 (T/F): Magnesium sulfate administered with potassium replacement is appropriate therapy for some patients with multifocal atrial tachycardia.
The correct answer is True: Several small reports describe effectiveness with the use of magnesium sulfate (with concomitant correction of hypokalemia), verapamil, and some beta-blockers. Provide potassium replacement to reach a serum potassium level of greater than 4 mEq/L.
Pearl Question 4 (T/F): Cardioversion is often useful in the treatment of multifocal atrial tachycardia (MAT).
The correct answer is False: Cardioversion should be avoided because it is usually ineffective in converting the multiple foci of MAT, and it may lead to rhythm degeneration.
| BIBLIOGRAPHY | Section 11 of 11 |
| NOTE: |
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| Medicine is a constantly changing science and not all therapies are clearly established. New research changes drug and treatment therapies daily. The authors, editors, and publisher of this journal have used their best efforts to provide information that is up-to-date and accurate and is generally accepted within medical standards at the time of publication. However, as medical science is constantly changing and human error is always possible, the authors, editors, and publisher or any other party involved with the publication of this article do not warrant the information in this article is accurate or complete, nor are they responsible for omissions or errors in the article or for the results of using this information. The reader should confirm the information in this article from other sources prior to use. In particular, all drug doses, indications, and contraindications should be confirmed in the package insert. FULL DISCLAIMER |
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