Sola-Visner Martha, Bercovitz Rachel S
Division of Newborn Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA.
Medical Sciences Institute, BloodCenter of Wisconsin, Milwaukee, WI.
Transfus Med Rev. 2016 Oct;30(4):183-8. doi: 10.1016/j.tmrv.2016.05.009. Epub 2016 May 27.
Thrombocytopenia affects approximately one fourth of neonates admitted to neonatal intensive care units, and prophylactic platelet transfusions are commonly administered to reduce bleeding risk. However, there are few evidence-based guidelines to inform clinicians' decision-making process. Developmental differences in hemostasis and differences in underlying disease processes make it difficult to apply platelet transfusion practices from other patient populations to neonates. Thrombocytopenia is a risk factor for common preterm complications such as intraventricular hemorrhage; however, a causal link has not been established, and platelet transfusions have not been shown to reduce risk of developing intraventricular hemorrhage. Platelet count frequently drives the decision of whether to transfuse platelets, although there is little evidence to demonstrate what a safe platelet nadir is in preterm neonates. Current clinical assays of platelet function often require large sample volumes and are not valid in the setting of thrombocytopenia; however, evaluation of platelet function and/or global hemostasis may aid in the identification of neonates who are at the highest risk of bleeding. Although platelets' primary role is in establishing hemostasis, platelets also carry pro- and antiangiogenic factors in their granules. Aberrant angiogenesis underpins common complications of prematurity including intraventricular hemorrhage and retinopathy of prematurity. In addition, platelets play an important role in host immune defenses. Infectious and inflammatory conditions such as sepsis and necrotizing enterocolitis are commonly associated with late-onset thrombocytopenia in neonates. Severity of thrombocytopenia is correlated with mortality risk. The nature of this association is unclear, but preclinical data suggest that thrombocytopenia contributes to mortality rather than simply being a proxy for disease severity. Neonates are a distinct patient population in whom thrombocytopenia is common. Their unique physiology and associated complications make the risks and benefits of platelet transfusions difficult to understand. The goal of this review was to highlight research areas that need to be addressed to better understand the risks and benefits of platelet transfusions in neonates. Specifically, it will be important to identify neonates at risk of bleeding who would benefit from a platelet transfusion and to determine whether platelet transfusions either abrogate or exacerbate common neonatal complications such as sepsis, chronic lung disease, necrotizing enterocolitis, and retinopathy of prematurity.
血小板减少症影响了约四分之一入住新生儿重症监护病房的新生儿,预防性血小板输注通常用于降低出血风险。然而,几乎没有基于证据的指南来指导临床医生的决策过程。止血方面的发育差异以及潜在疾病过程的差异使得将其他患者群体的血小板输注方法应用于新生儿变得困难。血小板减少症是常见早产并发症(如脑室内出血)的一个危险因素;然而,尚未确立因果关系,且血小板输注尚未显示能降低发生脑室内出血的风险。血小板计数常常驱动是否输注血小板的决策,尽管几乎没有证据表明早产新生儿安全的血小板最低点是多少。目前血小板功能的临床检测通常需要大量样本量,在血小板减少的情况下无效;然而,评估血小板功能和/或整体止血情况可能有助于识别出血风险最高的新生儿。尽管血小板的主要作用是建立止血,但血小板在其颗粒中还携带促血管生成和抗血管生成因子。异常血管生成是早产常见并发症(包括脑室内出血和早产儿视网膜病变)的基础。此外,血小板在宿主免疫防御中起重要作用。感染性和炎症性疾病(如败血症和坏死性小肠结肠炎)通常与新生儿晚期血小板减少症相关。血小板减少症的严重程度与死亡风险相关。这种关联的性质尚不清楚,但临床前数据表明血小板减少症导致死亡,而不仅仅是疾病严重程度的一个指标。新生儿是血小板减少症常见的独特患者群体。他们独特的生理机能和相关并发症使得血小板输注的风险和益处难以理解。本综述的目的是突出需要解决的研究领域,以便更好地理解新生儿血小板输注的风险和益处。具体而言,识别有出血风险且能从血小板输注中获益的新生儿,并确定血小板输注是否能消除或加剧败血症、慢性肺病、坏死性小肠结肠炎和早产儿视网膜病变等常见新生儿并发症,将是很重要的。