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Published on: December 6, 2016
Carvedilol reduces the severity of central sleep apnea in chronic heart failure
Akira Tamura1, Yoshiyuki Kawano, Junichi Kadota
1Internal Medicine 2, Faculty of Medicine, Oita University, Yufu, Japan. akira@med.oita-u.ac.jp
Insights
Carvedilol treatment improved heart function and reduced central sleep apnea (CSA) severity in chronic heart failure (CHF) patients. However, obstructive sleep apnea events may increase after treatment.
Area of Science:
- Cardiology
- Sleep Medicine
- Pharmacology
Background:
- Central sleep apnea (CSA) is a concern in chronic heart failure (CHF) patients.
- Carvedilol, a beta-blocker, is used for CHF management.
- Potential benefits of carvedilol on CSA severity in CHF patients warrant investigation.
Purpose of the Study:
- To prospectively evaluate the effect of carvedilol on CSA severity in CHF patients.
- To assess changes in polysomnographic findings, left ventricular (LV) function, and brain natriuretic peptide (BNP) levels.
Main Methods:
- 16 CHF patients with CSA (NYHA class II-III, LVEF <50%) received carvedilol for 6 months.
- Polysomnography, LV ejection fraction, and plasma BNP levels were measured pre- and post-treatment.
- Safety and tolerability of carvedilol were assessed.
Main Results:
- Carvedilol treatment improved LV ejection fraction (32% to 45%, P<0.001) and reduced BNP levels (P=0.017).
- Apnea-hypopnea index and central apnea index significantly decreased (P<0.001).
- Obstructive apnea index showed a significant increase (P=0.04).
Conclusions:
- Carvedilol effectively reduces CSA severity in CHF patients.
- Treatment with carvedilol improves cardiac function and reduces CHF biomarkers.
- A potential increase in obstructive sleep apnea events requires further monitoring.
Abstract:
Background Carvedilol may reduce the severity of central sleep apnea (CSA) in patients with chronic heart failure (CHF). Methods and Results This study prospectively examined the effect of carvedilol on the severity of CSA in patients with CHF. Polysomnographic findings, left ventricular (LV) function, and plasma brain natriuretic peptide (BNP) level were evaluated before and 6 months after induction of carvedilol in 16 patients with CHF (New York Heart Association functional class II or III and LV ejection fraction <50%) who had CSA (central apnea index [CAI] >5 with dominant central apneic events). All patients tolerated carvedilol. The 6-month treatment with carvedilol increased the LV ejection fraction (32+/-7.4% to 45+/-9.8%, P<0.001) and decreased the BNP level (159 [69-458] pg/ml to 38 [16-193] pg/ml, P=0.017). The polysomnographic findings showed that the treatment decreased the apnea-hypopnea index (34+/-13 to 14+/-13, P=0.003) and CAI (13+/-11 to 1.9+/-4.3, P<0.001), whereas it increased the obstructive apnea index (1.1+/-1.5 to 3.1+/-3.4, P=0.04). Conclusion This preliminary study shows that treatment with carvedilol reduces the severity of CSA in patients with CHF, but that episodes of obstructive sleep apnea sometimes increase after the treatment.
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