Effect of Losartan on Right Ventricular Dysfunction Results From the Double-Blind, Randomized REDEFINE Trial (Right Ventricular Dysfunction in Tetralogy of Fallot: Inhibition of the Renin-Angiotensin-Aldosterone System) in Adults With Repaired Tetralogy of Fallot

Jouke P. Bokma, Michiel M. Winter, Arie P. van Dijk, Hubert W. Vliegen, Joost P. van Melle, Folkert J. Meijboom, Martijn C. Post, Jacqueline K. Berbee, S. Matthijs Boekholdt, Maarten Groenink, Aeilko H. Zwinderman, Barbara J. M. Mulder, Berto J. Bouma*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

BACKGROUND: The effect of angiotensin II receptor blockers on right ventricular (RV) function is still unknown. Angiotensin II receptor blockers are beneficial in patients with acquired left ventricular dysfunction, and recent findings have suggested a favorable effect in symptomatic patients with systemic RV dysfunction. The current study aimed to determine the effect of losartan, an angiotensin II receptor blocker, on subpulmonary RV dysfunction in adults after repaired tetralogy of Fallot.

METHODS: The REDEFINE trial (Right Ventricular Dysfunction in Tetralogy of Fallot: Inhibition of the Renin-Angiotensin-Aldosterone System) is an investigator-initiated, multicenter, prospective, 1:1 randomized, double-blind, placebo-controlled study. Adults with repaired tetralogy of Fallot and RV dysfunction (RV ejection fraction [EF]

RESULTS: Of 95 included patients, 47 patients received 150 mg losartan daily (age, 38.0 +/- 12.4 years; 74% male), and 48 patients received placebo (age, 40.6 +/- 11.4 years; 63% male). Overall, RV EF did not change in patients allocated to losartan (n=42) (44.4 +/- 5.1% to 45.2 +/- 5.0%) and placebo (n=46) (43.2 +/- 6.3% to 43.6 +/- 6.9%). Losartan did not significantly improve RV EF in comparison with placebo (+0.51%; 95% confidence interval, -1.0 to +2.0; P=0.50). No significant treatment effects were found on secondary outcomes: left ventricular EF, peak aerobic exercise capacity, and N-terminal pro-brain natriuretic peptide (P>0.30 for all). In predefined subgroup analyses, losartan did not have a statistically significant impact on RV EF in subgroups with symptoms, restrictive RV, RV EF

CONCLUSIONS: Losartan had no significant effect on RV dysfunction or secondary outcome parameters in repaired tetralogy of Fallot. Future larger studies may determine whether there might be a role for losartan in specific vulnerable subgroups.

Original languageEnglish
Pages (from-to)1463-1471
Number of pages9
JournalCirculation
Volume137
Issue number14
DOIs
Publication statusPublished - 3-Apr-2018

Keywords

  • heart defects, congenital
  • heart failure
  • losartan
  • survival
  • tetralogy of Fallot
  • CONGENITAL HEART-DISEASE
  • PULMONARY VALVE-REPLACEMENT
  • ECHOCARDIOGRAPHIC-ASSESSMENT
  • NEUROHORMONAL ACTIVATION
  • QRS FRAGMENTATION
  • REFERENCE VALUES
  • SURVIVAL
  • MORTALITY
  • FAILURE
  • RECOMMENDATIONS

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