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J Thorac Cardiovasc Surg 2003;125:1451-1460
© 2003 The American Association for Thoracic Surgery


Cardiopulmonary Support and Physiology

Embolic material generated by multiple aortic crossclamping: A perfusion model with human cadaveric aorta

Patrik Boivie, BSa, Magnus Hansson, MD, PhDb, Karl Gunnar Engström, MD, PhD, FRCSa

From the Departments of Surgical and Perioperative Science,a and Integrative Medical Biology,b Section for Anatomy and Department of Medical Biosciences, Section for Pathology, Umeå University Hospital, Umeå, Sweden.

This work was supported by Swedish Society for Medical Research and funds of the Medical Faculty, Umeå University Hospital, Swedish Medical Research Council (12X-11204), Swedish Heart and Lung Foundation, and the Heart Foundation of North Sweden.

Received for publication May 10, 2002. Revisions requested July 22, 2002; revisions received Aug 27, 2002. Accepted for publication Sept 11, 2002. Address for reprints: Patrik Boivie, Cardiothoracic Division, Department of Surgical and Perioperative Science, Umeå University Hospital, S-901 85 Umeå, Sweden (E-mail: patrik_boivie{at}hotmail.com).

Background: Atherosclerosis of the ascending aorta and use of aortic crossclamping are risk factors for neurologic injury during cardiac surgery.
Objectives: Repeated aortic manipulation is part of the surgical approach to most cardiac operations. The aim of this study was to assess the amount and size of particulate matter that is dislodged from the aortic wall as a function of repeated aortic crossclamping.
Methods: In 10 subjects undergoing autopsy the aorta was dissected and mounted in a perfusion model. The ascending aorta was crossclamped and washed out 10 times, with the perfusate collected in aliquots (1 to 10). The aliquots were examined by computerized image processing, both macroscopically and under the microscope for calcified and cellular material.
Results: Aortic crossclamping produced substantial output of particulate matter. After repeated aortic crossclamping the number of particles decreased (P = .012) and approached the baseline for aliquots 6 to 10. The average particle diameter was 0.63 ± 0.03 mm, with a maximum of 4.74 mm. Similar variability in particle outputs were recorded microscopically, with findings of both calcified and cellular material. Nine of 10 aortas had calcifications seen during simple visual inspection.
Conclusions: The washouts of dislodge material at aortic crossclamping had embolic potential. During the initial aortic crossclamping procedures the amount of particles was substantial, both macroscopically and microscopically. On the microscopic scale noncalcified cellular debris represents a significant pool of embolic material. Repeated aortic crossclamping reduced the amount of particles. These findings question surgical techniques associated with repeated aortic crossclamping.


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