Haemodynamic effects of aliskiren in decompensated severe heart failure

J Renin Angiotensin Aldosterone Syst. 2012 Mar;13(1):128-32. doi: 10.1177/1470320311423281. Epub 2011 Oct 10.

Abstract

Aim: The renin-angiotensin-aldosterone system (RAAS) has dual pathways to angiotensin II production; therefore, multiple blockages may be useful in heart failure. In this study, we evaluated the short-term haemodynamic effects of aliskiren, a direct renin inhibitor, in patients with decompensated severe heart failure who were also taking angiotensin-converting enzyme (ACE) inhibitors.

Materials and methods: A total of 16 patients (14 men, two women, mean age: 60.3 years) were enrolled in the study. The inclusion criteria included hospitalisation due to decompensated heart failure, ACE inhibitor use, and an ejection fraction < 40% (mean: 21.9 ± 6.7%). The exclusion criteria were: creatinine > 2.0 mg/dl, cardiac pacemaker, serum K(+) > 5.5 mEq/l, and systolic blood pressure < 70 mmHg. Patients either received 150 mg/d aliskiren for 7 days (aliskiren group, n = 10) or did not receive aliskiren (control group, n = 6). Primary end points were systemic vascular resistance and cardiac index values. Repeated-measures analysis of variance (ANOVA) was used to assess variables before and after intervention. A two-sided p-value < 0.05 was considered statistically significant.

Results: Compared to pre-intervention levels, systemic vascular resistance was reduced by 20.4% in aliskiren patients, but it increased by 2.9% in control patients (p = 0.038). The cardiac index was not significantly increased by 19.0% in aliskiren patients, but decreased by 8.4% in control patients (p = 0.127). No differences in the pulmonary capillary or systolic blood pressure values were observed between the groups.

Conclusion: Aliskiren use reduced systemic vascular resistance in patients with decompensated heart failure taking ACE inhibitors.

Publication types

  • Controlled Clinical Trial

MeSH terms

  • Amides / pharmacology*
  • Amides / therapeutic use*
  • Antihypertensive Agents / pharmacology*
  • Antihypertensive Agents / therapeutic use*
  • Female
  • Fumarates / pharmacology*
  • Fumarates / therapeutic use*
  • Heart Failure / drug therapy*
  • Heart Failure / physiopathology*
  • Hemodynamics / drug effects*
  • Humans
  • Male
  • Middle Aged
  • Vascular Resistance / drug effects

Substances

  • Amides
  • Antihypertensive Agents
  • Fumarates
  • aliskiren