Though healthy newborn infants do not bleed despite low levels of blood coagulation factor activities, hemorrhage or thrombosis is found in 40% of neonatal deaths and is associated with prematurity, hypoxemia, acidosis, blood loss, and hypotension. There is little information on the development of hemostasis in the fetus. The chronically catheterized fetal lamb model will also serial study of normal hemostasis throughout the third trimester of gestation. It is a model for study of the effects of individual and combined stresses such as acidosis, hypothension, blood loss, and hypoxia on this developing system. It can also be used or adopted for examining the effects of hormonal changes such as cortisol, thyroxin, and insulin. Measurement of coagulation factors, fibrinolytic activities, and vascular endothelial release of important mediaters are necessary to evaluate hemostasis. This project proposed such measures in chronically catheterized fetal lambs. The fetuses will be exposed to common physiologic stresses such as hypotension with and without acidosis, blood loss, and hyperinsulinemia. The studies will complement our previous experiments on the effects of hypoxemia, acidosis, glucocorticoids, and thyroxin on fetal hemostasis. Having defined the responses of fetal hemostatis to the physiologic stresses and hormonal changes commonly experienced in premature infants, studies of prematurely delivered fetuses will be conducted. These studies will determine which stresses are important in the development of hemostatic disorders found in premature infants, and indicate therapeutic modalities to be tested for their effectiveness in preventing these hemorrhagic and thrombotic complications. The studies will provide needed information on the development of hemostasis in the fetus, the causes of disorders of hemostasis in the neonate, and lead to improved therapeutic measures to prevent hemorrhage and thrombosis.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD012574-08
Application #
3311924
Study Section
Human Embryology and Development Subcommittee 2 (HED)
Project Start
1978-12-01
Project End
1988-08-31
Budget Start
1986-09-01
Budget End
1987-08-31
Support Year
8
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Kisker, C T; Manco-Johnson, M (1995) Effect of hyperinsulinemia on the development of blood coagulation in the lamb fetus. Pediatr Res 38:169-72
Kisker, C T; Bohlken, D; Clarke, W R (1993) Thyroxine and fetal blood coagulation: a fetal lamb study. J Dev Physiol 19:57-9
Kisker, C T; Perlman, S; Bohlken, D et al. (1988) Measurement of prothrombin mRNA during gestation and early neonatal development. J Lab Clin Med 112:407-12
Kisker, C T (1987) The animal models for hemorrhage and thrombosis in the neonate. Thromb Haemost 57:118-22
Younoszai, M K; Kisker, T; Robillard, J et al. (1986) Effect of acidosis and hypoxia on intestinal blood flow of sheep fetus. Biol Neonate 49:29-35
Kisker, C T; Bohlken, D P; Clarke, W R (1985) Effects of acidosis on fetal and maternal blood coagulation: a fetal lamb model. Pediatr Res 19:78-82