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a Cardiac Surgery, Queen Elizabeth Hospital, Queen Elizabeth Medical Centre, Edgbaston, Birmingham, B15 2TH United Kingdom
b The Cardiothoracic Centre, Liverpool NHS Trust, The Research Laboratories, Thomas Dr, Liverpool, L14 3PE United Kingdom
(Email: kardiac_pai{at}rediffmail.com; conant{at}liv.ac.uk).
We read with interest the article by Kulik and colleagues [1] describing supporting evidence for the use of phenoxybenzamine as a topical treatment for radial artery grafts. The original demonstration of phenoxybenzamine's use by Taggart's group in 2000 [2], employed a similar dose to Kulik and colleagues (2 mg/mL) [1]. However, later studies, including those of Taggart's group, demonstrated a complete inhibition of catecholamine-induced vasoconstriction at lower doses [3–5].
Previous studies measured endothelium-mediated vasodilatation immediately after treatment. We were interested in the effects on endothelial viability, which may be slow to develop. Endothelial cells were cultured from sections of radial artery (n=5), obtained excess to surgery with informed patient consent and ethical committee approval. Cells were treated with phenoxybenzamine for 30 minutes and viability assessed immediately or after 24 hours recovery, using a resazurin-based viability assay [6]. Table 1 demonstrates that the true extent of damage is only apparent with time and is significant only at higher doses.
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A. Kulik, F. D. Rubens, and M. Ruel Reply. Ann. Thorac. Surg., July 1, 2008; 86(1): 351 - 352. [Full Text] [PDF] |
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