Abstract
A newin vitro bleeding time (BT) device was applied to various surgical patients. After setting the optimal assay condition, the normalin vitro bleeding time (T2) and volume (V2) were obtained from healthy volunteers, being 114.7 secs±25.8 (SD) and 272.2 μl±69.1 (SD), respectively. When the T2 was below 210 secs, the platelet count was inversely proportional to the T2 and V2 of thein vitro BT with p<0.01. The value of thein vitro BT was not affected by heparin. Agents, which modify platelet functions, such as PGI2, DN9693 (an inhibitor of phosphodiesterase) and aspirin, prolonged thein vitro BT (T2, V2) dose-dependently. Administration of aspirin (660 mg) to volunteers prolonged the T2 from 108 to over 300 secs and the V2 from 253 to over 600 μl but ticlopidine (500 mg/day for 3 days) had no effect. In 8 patients with liver cirrhosis who underwent hepatectomy, one patient with a prolonged T2 (260 secs) and a normal skin BT bled postoperatively, however, 3 patients with a prolonged skin BT (>15 min) and a normal T2 had no hemorrhagic complications. From these observations it was concluded thatin vitro BT is a convenient and useful tool to examine primary hemostasis or platelet function.
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Brinkhons KM. WW Duke and his bleeding test, a commentary on platelet function. JAMA 1983; 250: 1210–1214.
Kratzer MAA, Born GVR. Simulation of primary haemostasisin vitro. Haemostasis 1985; 15: 357–362.
Kratzer MAA, Bellucci S, Caen JP. Detection of abnormal platelet functions with anin vitro model of primary haemostasis. Haemostasis 1985; 15: 363–370.
Kumar R, Ansell JE, Canoso RT, Deykin D. Clinical trial of a new bleeding time device. Am J Clin Pathol 1978; 70: 642–645.
Toomey KC, Kim HC, Kosmin M, Kosmin M, Saidi P. Clinical trial of a new disposable bleeding-time device. Am J Clin Pathol 1986; 85: 610–613.
Kratzer MAA, Knedel M. Evaluation and standardization of the “in vitro” bleeding time technique. Thromb Haemost 1987; 58: 389.
Mielke CH, Kaneshiro MM, Maher IA, Weiner JM, Rapaport SI. The standardized normal ivy bleeding time and its prolongation by aspirin. Blood 1969: 34: 204–215.
Arfors KE, Bergqvist D, Bygdeman S, McKenzie FN, Svensjö E. The effect of inhibition of the platelet release reaction on platelet behaviourin vitro andin vivo. Scand J Haematol 1972; 9: 322–332.
Minno GD, Cerbone AM, Mattioli PL, Turco S, Iovine C, Mancini M, Functionally thrombasthenic state in normal platelets following the administration of ticlopidine. J Clin Invest 1985; 75: 328–338.
Bellucci S, Cambau E, Candalot B, Caen JP. Pharmacological studies of platelet antiaggregants using anin vitro model of primary hemostasis. Thromb Haemost 1987; 58: 173.
Ballard HS, Marcus AJ. Platelet aggregation in portal cirrhosis. Arch Intern Med 1976; 136: 316–319.
Mannucci PM, Vicente V, Vianello L, Cattaneo M, Alberca I, Coccato MP, Faioni E, Mari D. Controlled trial of desmopressin in liver cirrhosis and other conditions associated with a prolonged bleeding time. Blood 1986; 67: 1148–1153.
Burns ER, Billett HH, Frater RWM, Sisto DA. The preoperative bleeding time as a predictor of postoperative hemorrhage after cardiopulmonary bypass. J Thorac Cardiovasc Surg 1986; 92: 310–312.
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Tsujinaka, T., Itoh, T., Uemura, Y. et al. Clinical application of a newin vitro bleeding time device on surgical patients. The Japanese Journal of Surgery 18, 430–437 (1988). https://doi.org/10.1007/BF02471469
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DOI: https://doi.org/10.1007/BF02471469