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Comparative Study
. 2014 Jan;164(1):167-72.
doi: 10.1016/j.jpeds.2013.08.037. Epub 2013 Oct 3.

Primary hemostasis in neonates with thrombocytopenia

Affiliations
Comparative Study

Primary hemostasis in neonates with thrombocytopenia

Emoke Deschmann et al. J Pediatr. 2014 Jan.

Abstract

Objective: To evaluate the relationship between platelet counts and the platelet function analyzer-100 closure times (CTs) in neonates with thrombocytopenia, and to determine what other factors significantly affect CTs.

Study design: In a single institution prospective cross-sectional study, blood samples from neonates with platelet counts <150 × 10(9)/L were tested on the platelet function analyzer-100 with CT-collagen/epinephrine (CT-Epi) and CT-collagen/adenosine diphosphate (CT-ADP) cartridges.

Results: The mean platelet count was 95 ± 28 × 10(9)/L for 48 infants with a mean gestational age 30.9 ± 5.3 weeks and median postnatal age of 5 (3-18) days. No association was evident between CT-Epi and platelet count. However, the CT-ADP was prolonged in many (but not all) infants with platelet counts <90 × 10(9)/L. Among infants <32 weeks gestational age, we found a moderate negative correlation between CT-ADP and platelet count (r = -0.54, P = .0045). The negative correlation was strongest in infants <32 weeks and <10 days old (r = -0.8, P = .0017). Other variables examined (hematocrit, infection, Score of Neonatal Acute Physiology II) did not have a significant effect on CT-ADP in a linear regression model.

Conclusions: Platelet counts <90 × 10(9)/L are associated with prolonged CT-ADP times in some but not all infants. Gestational and postnatal age-related differences in platelet function account for some of this variability. The predictive value of CT-ADP on neonatal bleeding risk remains to be studied.

Keywords: CT; CT-ADP; CT-Epi; Closure time; Closure time-collagen/adenosine diphosphate; Closure time-collagen/epinephrine; NICU; Neonatal intensive care unit; PFA-100; Platelet function analyzer-100; SNAP II; Score of Neonatal Acute Physiology, Version II.

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