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[Is it necessary to suspend betablockers in decompensated heart failure with low output?]
Marcelo Villaça Lima1, Juliano Novaes Cardoso, Marcelo Eidi Ochiai
1Instituto do Coração, Faculdade de Medicina, USP, São Paulo, SP, Brasil. villacalima@cardiol.br
Insights
Maintaining beta-blockers (BB) with dobutamine in heart failure patients did not worsen outcomes or increase hospital stay. Patients not suspending BB were discharged on higher BB doses, suggesting continued benefit.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Beta-blockers (BB) suspension in decompensated heart failure may increase mortality.
- Dobutamine (dobuta), a common inotrope, has antagonist actions to BB at the same receptor, potentially hindering compensation during concurrent use.
Purpose of the Study:
- To evaluate if maintaining BB alongside dobutamine complicates cardiac compensation in heart failure patients.
Main Methods:
- A study of 44 heart failure patients (LVEF < 45%) requiring inotropics.
- Patients were divided into three groups: no BB, BB suspended for dobutamine, and BB concomitant with dobutamine.
- Statistical tests (Student t, Fisher exact, chi-square) were used for comparison (p < 0.05 significant).
Main Results:
- Mean LVEF was 23.8 ± 6.6%.
- Dobutamine use was similar across groups (p = 0.35).
- Concomitant dobutamine and BB did not increase length of stay (20.36 ± 11.04 days vs 28.37 ± 12.76 days, p = NS).
- Patients not suspending BB received higher doses (35.8 ± 16.8 mg/day vs 23.0 ± 16.7 mg/day, p = 0.004).
Conclusions:
- Maintaining BB with dobutamine did not worsen outcomes or prolong hospitalization.
- Patients who continued BB were discharged on higher BB doses, indicating continued therapeutic benefit.
Background:
there is evidence that the suspension of betablockers (BB) in decompensated heart failure may increase mortality. Dobutamine (dobuta) is the most commonly used inotrope in decompensation, however, BB and dobuta act with the same receptor with antagonist actions, and concurrent use of both drugs could hinder compensation.
Objective:
to evaluate whether the maintenance of BB associated with dobuta difficults cardiac compensation.
Methods:
we studied 44 patients with LVEF < 45% and the need for inotropics. Divided into three groups according to the use of BB. Group A (n=8): those who were not using BB at baseline; Group B (n=25): those who used BB, but was suspended to start dobuta; Group C (n = 11): those who used BB concomitant to dobuta. To compare groups, we used the Student t, Fisher exact and chi-square tests. Considered significant if p < 0.05.
Results:
mean LVEF 23.8 ± 6.6%. The average use of dobuta use was similar in all groups (p = 0.35), and concomitant use of dobutamine with BB did not increase the length of stay (BB 20.36 ± 11.04 days vs without BB 28.37 ± 12.76 days, p = NS). In the high dose, BB was higher in patients whose medication was not suspended (35.8 ± 16.8 mg/day vs 23.0 ± 16.7 mg/day, p = 0.004).
Conclusion:
maintaining BB associated with dobutamine did not increase the length of hospitalization and was not associated with the worst outcome. Patients who did not suspend BB were discharged with higher doses of the drug.
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