Please confirm topic selection

Are you sure you want to trigger topic in your Anconeus AI algorithm?

Please confirm action

You are done for today with this topic.

Would you like to start learning session with this topic items scheduled for future?

Review Question - QID 100847

In scope icon M 3 D
QID 100847 (Type "100847" in App Search)
A 62-year-old male is rushed to the emergency department (ED) for what he believes is his second myocardial infarction (MI). His medical history is significant for severe chronic obstructive pulmonary disease (COPD) and a prior MI at the age of 58. After receiving aspirin, morphine, and face mask oxygen in the field, the patient arrives to the ED tachycardic (105 bpm), diaphoretic, and normotensive (126/86). A 12 lead electrocardiogram shows ST-elevation in I, aVL, and V5-V6. The attending physician suspects a lateral wall infarction. Which of following beta-blockers should be given to this patient and why?

Propranolol, because it is a non-selective ß-blocker

18%

52/295

Metoprolol, because it is a selective ß1 > ß2 blocker

64%

189/295

Atenolol, because it is a selective ß2 > ß1 blocker

5%

16/295

Labetalol, because it is a selective ß1 > ß2 blocker

5%

15/295

Nadolol, because it is a selective ß1 > ß2 blocker

1%

2/295

Select Answer to see Preferred Response

bookmode logo Review TC In New Tab

Because the patient has a history of COPD, he should be treated with a selective ß1 blocker such as metoprolol or atenolol.

When using a ß-blocker to treat a patient with hypertension, tachycardia, acute MI, history of MI, or arrhythmia, it is important to tailor pharmacotherapy to the patient's comorbidities based on the drugs' selectivity. Non-selective ß1 and ß2 antagonists (propanolol, nadolol, and timolol) should be avoided in patients with asthma and COPD because of the risk of bronchoconstriction caused by ß2 blockade. Selective ß1 blockers (metoprolol, atenolol, betaxolol, and esmolol) decrease heart rate and contractility by their ß1 effect without causing marked bronchoconstriction secondary to ß2 cross-reactivity. Nonselective a- and ß-antagonists (labetalol and carvedilol) are primarily used in heart failure and have similar risks for patients with COPD and asthma as non-selective ß-blockers.

In a summary of the American College of Cardiology and American Heart Association guidelines for the management of acute MI, Campbell-Scherer and Green review the role of ß-blockers in improving mortality. In the review the authors list absolute contraindications to ß-blocker therapy for acute MI: evidence of low output state; increased risk of cardiogenic shock; and signs of heart failure because ß-blocker therapy increases mortality in these patients.

In an editorial, Rutten and Groenwold review the benefits of ß-blocker therapy for acute and subacute myocardial infarction. They emphasize that even for patients with COPD, ß-blocker therapy is associated with a 0.59 mortality hazard ratio.

Illustration A shows the mechanism of adrenergic blockade.

Incorrect Answers:
Answers 1 and 5: Propranolol and nadolol are non-selective ß-blockers, which could theoretically exacerbate COPD in this patient; a selective ß1 is a better choice in this patient.

Answer 3: Atenolol is a selective ß1 > ß2 blocker.

Answer 4: Labetalol is a non-selective adrenergic blocker with the affinity to ß1 = ß2 = a1 > a2.

ILLUSTRATIONS:
REFERENCES (2)
Authors
Rating
Please Rate Question Quality

4.2

  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon

(9)

Attach Treatment Poll
Treatment poll is required to gain more useful feedback from members.
Please enter Question Text
Please enter at least 2 unique options
Please enter at least 2 unique options
Please enter at least 2 unique options