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European Heart Journal Advance Access originally published online on March 26, 2009
European Heart Journal 2009 30(14):1771-1780; doi:10.1093/eurheartj/ehp086
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Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2009. For permissions please email: journals.permissions@oxfordjournals.org

The haemodynamic effects of adjunctive hormone therapy in potential heart donors: a prospective randomized double-blind factorially designed controlled trial

Rajamiyer V. Venkateswaran1, Richard P. Steeds2, David W. Quinn1, Peter Nightingale1, Ian C. Wilson1, Jorge G. Mascaro1, Richard D. Thompson3, Jonathan N. Townend2 and Robert S. Bonser1,*

1 Department of Cardiothoracic Surgery, University Hospital Birmingham NHS foundation Trust, Birmingham and University of Birmingham, Edgbaston, Birmingham B15 2TH, UK
2 Department of Cardiology, University Hospital Birmingham NHS foundation Trust, Birmingham and University of Birmingham, Birmingham, UK
3 Department of Medicine, University Hospital Birmingham NHS foundation Trust, Birmingham and University of Birmingham, Birmingham, UK

Received 27 June 2008; revised 28 January 2009; accepted 18 February 2009; online publish-ahead-of-print 26 March 2009.

* Corresponding author. Tel: +44 121 627 2543, Fax: +44 121 627 2542, Email: robert.bonser{at}uhb.nhs.uk

See page 1690 for the editorial comment on this article (doi:10.1093/eurheartj/ehp215)

Aims: The aim of this study was to assess the haemodynamic effects of tri-iodothyronine (T3) and methylprednisolone in potential heart donors.

Methods and results: In a prospective randomized double-blind trial, 80 potential cardiac donors were allocated to receive T3 (0.8 µg kg–1 bolus; 0.113 µg kg–1 h–1 infusion) (n = 20), methylprednisolone (1000 mg bolus) (n = 19), both drugs (n = 20), or placebo (n = 21) following initial haemodynamic assessment. After hormone or placebo administration, cardiac output-guided optimization was initiated, using vasopressin as a pressor and weaning norepinephrine and inotropes. Treatment was administered for 5.9 ± 1.3 h until retrieval or end-assessment. Cardiac index increased significantly (P < 0.001) but administration of T3 and methylprednisolone alone or in combination did not affect this change or the heart retrieval rate. Thirty-five per cent (14/40) of initially marginal or dysfunctional hearts were suitable for transplant at end-assessment. At end-assessment, 50% of donor hearts fulfilled criteria for transplant suitability.

Conclusion: Cardiac output-directed donor optimization improves donor circulatory status and has potential to increase the retrieval rate of donor hearts. Tri-iodothyronine and methylprednisolone therapy do not appear to acutely affect cardiovascular function or yield.

Key Words: Heart transplantation • Hormone replacement therapy • Donor management


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