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Masanori Nakamura
Ignacio G. Duarte
Russell S. Ronson
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Robert A. Guyton
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Ann Thorac Surg 1998;66:1216-1223
© 1998 The Society of Thoracic Surgeons


Original articles: cardiovascular

Recombinant human megakaryocyte growth and development factor attenuates postbypass thrombocytopenia

Masanori Nakamura, MDa, Christopher F. Toombs, PhDa, Ignacio G. Duarte, MDa, Russell S. Ronson, MDa, L. Susan Schmarkey, BSa, Sara L. Katzmark, BSa, Jill Robinson, BSa, Dirck L. Dillehay, PhDb, Jakob Vinten-Johansen, PhDa, Robert A. Guyton, MDa

a Section of Cardiothoracic Surgery, Department of Surgery, Carlyle Fraser Heart Center of Emory University, Cardiothoracic Research Laboratory, Atlanta, Georgia, USA
b Division of Animal Resources, Department of Pathology, Emory University, Atlanta, Georgia, USA

Address reprint requests to Dr Vinten-Johansen, Cardiothoracic Research Laboratory, 550 Peachtree St, NE, Atlanta, GA 30365-2225

Presented at the Poster Session of the Thirty-fourth Annual Meeting of The Society of Thoracic Surgeons, New Orleans, LA, Jan 26–28, 1998.

Background. Cardiopulmonary bypass contributes to platelet loss and dysfunction by exposure to shear stresses, foreign surfaces, and hypothermia. This study tested the hypothesis that pegylated recombinant human megakaryocyte growth and development factor (PEG-rHuMGDF) accelerates recovery of the platelet population after hypothermic extracorporeal circulation (HEC).

Methods. In a blinded study, subcutaneous injections of drug or placebo were given to dogs daily for 3 days preoperatively (day 0, 1, and 2) with no drug on day 3. On day 4, the animal was prepared for arteriovenous HEC. After heparinization, HEC was initiated at 30 to 40 mL · kg-1 · min-1. Hypothermic extracorporeal circulation (25°C) was continued for 90 minutes.

Results. Preoperative platelet count (x103 platelets/µL) did not differ from predrug count in placebo (256 ± 27 versus 255 ± 20) or PEG-rHuMGDF (271 ± 30 versus 291 ± 38). During 60 minutes of HEC, the platelet count decreased to ~10% of baseline in placebo (29 ± 5) and PEG-rHuMGDF (46 ± 8), and recovered to ~70% of baseline after rewarming (90 minutes of HEC: placebo, 185 ± 17, versus PEG-rHuMGDF, 169 ± 22). After HEC, platelet count was greater in PEG-rHuMGDF–treated animals (p < 0.05) without altering function (aggregation responses). Within the first 6 hours after HEC, platelet count in PEG-rHuMGDF–treated animals was rising and increased to 260 ± 29 (p < 0.01), but was unchanged in placebo animals (186 ± 21). Thereafter, platelet count in placebo animals declined to a nadir of 124 ± 15 (72 hours after HEC), whereas platelet count in PEG-rHuMGDF animals approximated the preoperative value (>200) at all times.

Conclusions. Appropriately timed presurgical administration of PEG-rHuMGDF counteracts post-HEC relative thrombocytopenia without increasing platelet population and enhancing aggregation preoperatively or during extracorporeal circulation.




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