Division of Neonatology, Department of Pediatrics, University of Utah Health, Salt Lake City, UT; Obstetric and Neonatal Operations, Intermountain Health, Murray, UT.
Division of Neonatology, Department of Pediatrics, University of Utah Health, Salt Lake City, UT; Obstetric and Neonatal Operations, Intermountain Health, Murray, UT.
J Pediatr. 2023 Dec;263:113666. doi: 10.1016/j.jpeds.2023.113666. Epub 2023 Aug 11.
To understand better those factors relevant to the increment of rise in platelet count following a platelet transfusion among thrombocytopenic neonates.
We reviewed all platelet transfusions over 6 years in our multi-neonatal intensive care unit system. For every platelet transfusion in 8 neonatal centers we recorded: (1) platelet count before and after transfusion; (2) time between completing the transfusion and follow-up count; (3) transfusion volume (mL/kg); (4) platelet storage time; (5) sex and age of platelet donor; (6) gestational age at birth and postnatal age at transfusion; and magnitude of rise as related to (7) pre-transfusion platelet count, (8) method of enhancing transfusion safety (irradiation vs pathogen reduction), (9) cause of thrombocytopenia, and (10) donor/recipient ABO group.
We evaluated 1797 platelet transfusions administered to 605 neonates (median one/recipient, mean 3, and range 1-52). The increment was not associated with gestational age at birth, postnatal age at transfusion, or donor sex or age. The rise was marginally lower: (1) with consumptive vs hypoproductive thrombocytopenia (P < .001); (2) after pathogen reduction (P < .01); (3) after transfusing platelets with a longer storage time (P < .001); and (4) among group O neonates receiving platelets from non-group O donors (P < .001). Eighty-seven neonates had severe thrombocytopenia (<20 000/μL). Among these infants, poor increments and death were associated with the cause of the thrombocytopenia.
The magnitude of post-transfusion rise was unaffected by most variables we studied. However, the increment was lower in neonates with consumptive thrombocytopenia, after pathogen reduction, with longer platelet storage times, and when not ABO matched.
更好地了解与血小板输注后血小板计数升高相关的因素,这些因素与血小板减少症新生儿有关。
我们回顾了我们多新生儿重症监护病房系统 6 年来的所有血小板输注。在 8 个新生儿中心的每一次血小板输注中,我们记录了:(1)输注前后的血小板计数;(2)完成输注与随访计数之间的时间;(3)输注量(mL/kg);(4)血小板储存时间;(5)血小板供体的性别和年龄;(6)出生时的胎龄和输注时的新生儿年龄;以及与(7)输注前血小板计数、(8)增强输注安全性的方法(照射与病原体减少)、(9)血小板减少症的原因以及(10)供体/受者 ABO 组相关的升高幅度。
我们评估了 1797 次血小板输注给 605 名新生儿(中位数为每个受者,平均 3 次,范围为 1-52 次)。增量与出生时的胎龄、输注时的新生儿年龄或供体的性别或年龄无关。消耗性与产生产性血小板减少症(P <.001)、(2)病原体减少后(P <.01)、(3)储存时间较长的血小板输注后(P <.001)和(4)O 组新生儿接受非 O 组供体血小板时(P <.001),升高幅度较低。87 名新生儿有严重血小板减少症(<20 000/μL)。在这些婴儿中,血小板减少症的原因与较差的增量和死亡有关。
我们研究的大多数变量对输注后升高的幅度没有影响。然而,在消耗性血小板减少症、病原体减少后、血小板储存时间较长以及 ABO 不匹配的情况下,增量较低。