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J Thorac Cardiovasc Surg 2010;139:453-458
© 2010 The American Association for Thoracic Surgery
Evolving Technology/Basic Science |
a Division of Cardiac Electrophysiology, Virginia Commonwealth University Medical Center, Richmond, Va
b Department Cardiothoracic Surgery, Virginia Commonwealth University Medical Center, Richmond, Va
Received for publication March 23, 2009; revisions received May 18, 2009; accepted for publication June 4, 2009. * Address for reprints: Mark A. Wood, MD, Box 980053, Virginia Commonwealth University Medical Center, Richmond, VA 23298-0053. (Email: mwoodmd{at}pol.net).
Objective: Creation of transmural myocardial lesions with epicardial surgical devices to treat atrial fibrillation is difficult. A new cooled bipolar radiofrequency ablation probe was used to create transmural myocardial lesions under controlled conditions.
Methods: The Coolrail (AtriCure, Inc, West Chester, Ohio) is a handheld probe with 2 parallel 30-mm long radiofrequency conductors. Conductors are cooled by water irrigation. Lesions were delivered to epicardial surface of isolated bovine myocardium sliced 3- to 8-mm thick, with blood flow beneath tissue at 0 or 0.4 m/s. Contact pressure between probe and tissue was either 450 g or 900 g. Tissue temperatures were measured. Tissue was sectioned every 5 mm along lesion long axis to determine lesion dimensions.
Results: For 80 experiments with 450-g contact pressure, epicardial lesion length was 31.3 mm (interquartile range, 30.1–32.8 mm); endocardial lesion length was 14.1 mm (interquartile range, 0.0–22.6 mm). Average lesion depth was 4.2 ± 0.74 mm. Temperature at probe interface was 81°C ± 21°C; that at blood pool interface was 53°C ± 12°C. Lesions were always transmural when tissue thickness was 4.0 mm or less. Endocardial blood flow did not influence lesion depth. With 900-g contact pressure, increased depth was always transmural at 4.8-mm tissue thickness or less.
Conclusions: This irrigated bipolar radiofrequency probe consistently produced transmural lesions in tissue 4 mm or thinner under controlled conditions in vitro. Lesion depth was increased by greater pressure on probe and not affected by blood flow. Endocardial lesions were smaller than epicardial dimensions.
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