International Journal of Cardiology
Volume 139, Issue 2 , Pages 107-112, 4 March 2010

Effects of perhexiline on myocardial deformation in patients with ischaemic left ventricular dysfunction

  • Manish Bansal

      Affiliations

    • Department of Medicine, University of Queensland, Brisbane, Australia
  • ,
  • Jonathan Chan

      Affiliations

    • Department of Medicine, University of Queensland, Brisbane, Australia
  • ,
  • Rodel Leano

      Affiliations

    • Department of Medicine, University of Queensland, Brisbane, Australia
  • ,
  • Peter Pillans

      Affiliations

    • Department of Medicine, University of Queensland, Brisbane, Australia
  • ,
  • John Horowitz

      Affiliations

    • Department of Medicine, University of Adelaide, Adelaide, Australia
  • ,
  • Thomas H. Marwick

      Affiliations

    • Department of Medicine, University of Queensland, Brisbane, Australia
    • Corresponding Author InformationCorresponding author. Department of Medicine, University of Queensland, Princess Alexandra Hospital, Ipswich Road, Brisbane, Qld 4102, Australia. Tel.: +61 7 3240 5346; fax: +61 7 3240 5399.

Received 7 December 2008; received in revised form 17 April 2009; accepted 11 August 2009. published online 20 October 2009.

Abstract 

Background

Perhexiline improves functional capacity in heart failure, but the mechanisms are undefined. We sought its effects on myocardial deformation in patients with viable myocardium.

Methods

Thirty-six medically-treated patients, stable at least 6 months post-infarction with LV dysfunction and myocardial viability shown by dobutamine echo (DbE) were randomised to receive perhexiline or matching placebo for 1 year. Cardiopulmonary exercise testing and DbE were performed at baseline and follow-up. Peak-systolic strain (S) and strain rate (SR) were measured offline in 111 dysfunctional segments in the placebo and 88 in the treatment group at rest, low-dose (LDD) and peak-dose dobutamine (PDD).

Results

The serum perhexiline level was 0.27±0.7 µg/l. There was no difference in the wall motion response to dobutamine at baseline and follow-up. Resting strain and SR were similar in the two groups at baseline and follow-up. However, SR at LDD and PDD increased in the placebo group and worsened during the same period in the perhexiline group. Patients on perhexiline and placebo had a similar rate-pressure product and exercise duration at baseline (7.9±2.7 vs 8.7±3.3 min, p=NS) and follow-up (9.6±4.6 vs 10.1±3.03 min, p=NS).

Conclusion

Perhexiline does not improve the deformation of abnormal myocardial segments in patients with ischaemic LV dysfunction.

Keywords: Myocardial viability, Heart failure, Coronary artery disease, Myocardial infarction, Strain imaging

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PII: S0167-5273(09)00851-1

doi:10.1016/j.ijcard.2009.08.007

International Journal of Cardiology
Volume 139, Issue 2 , Pages 107-112, 4 March 2010