Critical Care Medicine-Neurologic Disorders>>>>>Arrhythmias and Pacemaker
Question 3#

A 51-year-old male underwent an uncomplicated triple-vessel coronary artery bypass grafting 4 weeks ago and now presents to the emergency department with chest pain, a friction rub on auscultation, and diffuse ST-segment elevations on ECG. While blood samples are drawn for analysis, the patient states that he “feels lightheaded”. A noninvasive blood pressure obtained is recorded to be 62/36 mm Hg. An ECG reveals a heart rate of 33/min with narrow complex QRS complexes. The patient is quickly given three boluses of 1 mg atropine IV with no response in heart rate.

While you are waiting for the transcutaneous pacing (TCP) equipment to arrive, which of the following interventions is MOST appropriate?

A. Administer more atropine
B. Administer norepinephrine
C. Administer dopamine
D. Administer dobutamine
E. Administer isoproterenol

Correct Answer is C

Comment:

Correct Answer: C

Atropine is an anticholinergic, which is a muscarinic acetylcholine receptor antagonist. The Advanced Cardiovascular Life Support guidelines suggest a maximum dose of up to 3 milligram in the setting of symptomatic sinus bradycardia. If atropine does not yield a sufficient heart rate increase, TCP is recommended. Should TCP not be available or require time to be obtained, it is reasonable to start either an epinephrine or dopamine infusion. Norepinephrine has a nonlinear effect on heart rate; at lower doses, norepinephrine may cause reflex bradycardia, whereas at higher doses, it causes an increase in heart rate. Dobutamine and isoproterenol are strong chronotropes. Because of their isolated beta activities, their administration is associated with hypotension due to vasodilation, which would be deleterious in this patient. Dopamine and epinephrine are the preferred chronotropes should atropine fail and TCP not be immediately available. Although isoproterenol is a possible third alternative chronotrope, the known hypotensive effects are of particular concern in this patient. 

References:

  1. Rigaud M, Boschat J, Rocha P, et al. Comparative haemodynamic effects of dobutamine and isoproterenol in man. Intensive Care Med. 1977;3:57- 62.
  2. Tuttle RR, Mills J. Dobutamine: development of a new catecholamine to selectively increase cardiac contractility. Circ Res. 1975;36:185-196.
  3. Neumar RW, Shuster M, Callaway CW, et al. Part 1: executive summary: 2015 American Heart Association guidelines update for cardiopulmonary resuscitation and emergency cardiovascular care. Circulation. 2015;132:S315-S367.
  4. Goldstein DS, Zimlichman R, Stull R, et al. Plasma catecholamine and hemodynamic responses during isoproterenol infusions in humans. Clin Pharmacol Ther. 1986;40:233-238.
  5. VanValkinburgh D, McGuigan JJ. Inotropes and Vasopressors. Treasure Island, FL: StatPearls; 2018.
  6. Kusumoto FM, Schoenfeld MH, Barrett C, et al. 2018 ACC/AHA/HRS guideline on the evaluation and management of patients with bradycardia and cardiac conduction delay: a report of the American College of Cardiology/American Heart Association task force on clinical practice guidelines and the Heart Rhythm Society. Heart Rhythm. 2018,doi:10.1016/j.hrthm.2018.10.037.