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- W3042220379 abstract "Background: Neonatal alloimmune thrombocytopenia (NAIT) is defined as an uncommon platelet disorder caused by maternal alloimmunization to human-specific antigens (HPAs) that are paternally inherited, resulting in low fetal/neonatal platelet levels and debilitating effects on the newborn. The incidence of NAIT is 1 in every 1000 live births within the United States; it is the most common cause of severe thrombocytopenia (<30 × 10 9 /L) and intracranial hemorrhage in term newborns. Purpose: The purpose of this article is to discuss the pathophysiology, clinical manifestations, diagnosis, and treatment of NAIT and its implications upon the lifespan of the neonate. Methods: A literature review was conducted using PubMed, CINAHL, and Google Scholar (2014-2019). Search terms included NAIT, neonatal/fetal alloimmune thrombocytopenia, newborn platelets, and intracranial bleeding and NAIT. Results: NAIT can affect first pregnancies and often goes undiagnosed until delivery. Universal screening tools with a focus on HPA-1a typing via noninvasive testing have been successfully trialed and have yielded promising results indicating a 75% reduction in risks associated with NAIT; however, none have been incorporated into practice and prophylactic treatment remains unavailable. Implications for Research: Adopting a universal screening tool and prophylaxis for NAIT would allow for early diagnosis and treatment in utero. Implications for Practice: Many healthcare providers are not familiar with NAIT often focusing on other causes of thrombocytopenia as a potential diagnosis." @default.
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- W3042220379 date "2020-07-07" @default.
- W3042220379 modified "2023-10-17" @default.
- W3042220379 title "Neonatal Alloimmune Thrombocytopenia" @default.
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- W3042220379 doi "https://doi.org/10.1097/anc.0000000000000775" @default.
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