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Tarek M. Aziz
Jonathan Forty
Colin J. Hilton
Asif Hasan
John H. Dark
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Ann Thorac Surg 2003;75:990-995
© 2003 The Society of Thoracic Surgeons


Original article: general thoracic

Perfadex for clinical lung procurement: is it an advance?

Tarek M. Aziz, FRCS*a, Thaseegaran M. Pillay, FRCSa, Paul A. Corris, FRCPa, Jonathan Forty, FRCSa, Colin J. Hilton, FRCSa, Asif Hasan, FRCSa, John H. Dark, FRCSa

a Transplant Unit, Freeman Hospital, Newcastle upon-Tyne, United Kingdom

Accepted for publication September 16, 2002.

* Address reprint requests to Dr Aziz, Division of Cardiothoracic Surgery, Morriston Hospital, Morriston, Swansea, West Glamorgan, Wales SW6 6NL2, United Kingdom
e-mail: tarekaziz55{at}hotmail.com

BACKGROUND: Extensive laboratory experience suggested that low potassium dextran lung preservation solution (Perfadex; Medisan, Uppsala, Sweden) is superior to Euro-Collins (EC; Frusen, Hamburg, Germany), the clinical standard. The purpose of this study was to evaluate Perfadex in clinical lung transplantation.

METHODS: A retrospective analysis of the outcome of 69 consecutive lung allografts retrieved and used for transplantation was made. Donor lungs were flushed with EC in 37 patients and Perfadex in 32 patients. The evaluation measurements were quantitative chest roentgenogram score (grade 0 to 4), graft oxygenation, duration of mechanical ventilation, length of intensive care treatment, and survival.

RESULTS: The mean chest roentgenogram score was 1.55 and 1.81 for the EC group compared with 1.18 and 2.09 for the Perfadex group at 1 and 48 hours, respectively (p = 0.1 and 0.8, respectively). Arterial alveolar oxygen tension ratio was similar at 12 and 24 hours (0.61 vs 0.67; p = 0.8; and 0.64 vs 0.53; p = 0.3, respectively). The mean ventilation time was 71.2 ± 32.3 hours versus 81.9 ± 43.6 hours for the EC and Perfadex groups, respectively (p = 0.4). The mean ITU stay was 3.1 ± 2.6 days for the EC group compared with 4.1 ± 3.9 days for the Perfadex group (p = 0.4). Death caused by primary organ failure was 5.1% for the EC group compared with 3.1% for the Perfadex group (p = 0.8).

CONCLUSIONS: There was no difference between Perfadex and EC in clinical lung preservation. This may reflect the difference between controlled laboratory environment and the real world of brain death lung injury. Further studies are required to investigate the impact of Perfadex in the long-term outcome of lung transplantation.




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