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Hemostasis in the Very Young
Gili Kenet1,2, Assaf Arie Barg1,2, Ulrike Nowak-Göttl3
1National Hemophilia Center, Institute of Thrombosis and Hemostasis and the Amalia Biron Research Institute, Sheba Medical Center, Tel-Hashomer, Israel.
Insights
Developmental hemostasis describes how the blood clotting system changes from infancy to adulthood. This review explores how these age-related changes impact bleeding and clotting risks in neonates.
Area of Science:
- Hematology
- Neonatology
- Pediatric Coagulation
Background:
- Hemostasis, the process of blood clotting, significantly differs between neonates and adults.
- These age-related physiological changes are termed "developmental hemostasis."
- Neonates possess a unique hemostatic profile with implications for health and disease.
Purpose of the Study:
- To review the concept and clinical manifestations of developmental hemostasis.
- To discuss bleeding and thrombotic complications in neonates, particularly preterm infants.
- To explore age-specific phenotypes and treatment strategies for neonatal hemostatic disorders.
Main Methods:
- Literature review of developmental hemostasis.
- Analysis of hemostatic protein concentrations and function in neonates.
- Examination of clinical disease phenotypes, including hemorrhage and thrombosis.
Main Results:
- Neonates exhibit impaired platelet function and lower levels of certain coagulation factors, affecting clot firmness.
- Increased von Willebrand factor activity and reduced inhibitors can counterbalance these effects.
- Sick and preterm neonates have limited hemostatic reserve, increasing risks of bleeding or clotting.
Conclusions:
- Developmental hemostasis influences the presentation of bleeding and thrombotic disorders in neonates.
- Neonatal intracerebral/pulmonary hemorrhage and arterial ischemic stroke are significant concerns.
- Understanding these age-specific differences is crucial for diagnosis and treatment of neonatal hemostatic disorders.
Abstract:
Hemostasis is a dynamic process that starts in utero. The coagulation system evolves with age, as evidenced by marked physiological differences in the concentration of the majority of hemostatic proteins in early life compared with adulthood. This concept, known as "developmental hemostasis," has important biological and clinical implications. Overall, impaired platelet function, along with physiologically reduced levels of vitamin K-dependent and contact coagulation factors, may cause poorer clot firmness even in healthy neonates. However, increased activity of von Willebrand factor and low levels of coagulation inhibitors that promote hemostasis counterbalance the delicate and immature hemostatic system. Since this hemostatic system has little reserve capacity, preterm neonates or sick infants are extremely vulnerable and predisposed to either hemorrhagic or thrombotic complications. This review will address the concept and manifestations of developmental hemostasis with respect to clinical disease phenotypes. It will discuss bleeding diagnosis in neonates, dealing especially with the devastating complications of intracerebral and pulmonary hemorrhage in preterm infants. Neonates, especially the sickest preterm ones, are also extremely susceptible to thrombotic complications; thus, thrombosis in neonates will be reviewed, with special focus on arterial ischemic perinatal stroke. Based on the concept of developmental hemostasis, the phenotypes of clinically relevant bleeding or thrombotic disorders among neonates may differ from those of older infants and children. Treatment options for these conditions will be suggested and reviewed.
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