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首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Posttransfusion platelet increments after different platelet products in neonates: A retrospective cohort study
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Posttransfusion platelet increments after different platelet products in neonates: A retrospective cohort study

机译:新生儿不同血小板产物后输血后血小板的增加:一项回顾性队列研究

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Background In the Netherlands different platelet (PLT) products are used for neonatal transfusions: volume-reduced PLTs, PLT additive solution (PAS) II PLTs, and plasma PLTs. These are standard products at three different neonatal intensive care units where local transfusion guidelines apply. Here we assess the posttransfusion count increments with these products. Study Design and Methods We performed a retrospective cohort study of neonates who received, in the first month after birth, between January 1, 2007, and December 31, 2008, at least one PLT transfusion. Seventy-four neonates who received 197 volume-reduced PLTs transfusions, 68 neonates who received 105 PASII PLT transfusions, and eight neonates who received eight plasma PLT transfusions were analyzed. Early (within 8 hr after transfusion) and follow-up count increments (16-24 hr after transfusion) were evaluated for 191 and 81 volume-reduced PLTs, 77 and 56 PASII PLTs, and six and five plasma PLT transfusions, respectively, using a random-effects model. Results Volume-reduced PLTs were transfused at twice the dose in one-fifth the volume of PASII and plasma PLTs. The early posttransfusion count increment was higher for volume-reduced PLTs at 111 × 10 9/L (95% confidence interval [CI], 86-135) compared to PASII PLTs at 62 × 109/L (95% CI, 40-84; p = 0.000) and plasma PLTs at 47 × 109/L (95% CI, 14-79). The follow-up count increment was also higher for volume-reduced PLTs at 60 × 109/L (95% CI, 19-100) compared to PASII PLTs at 38 × 109/L (95% CI, -0.2 to 77; p = 0.082) and plasma PLTs at 4 × 109/L (95% CI, -38 to 46). Conclusion Neonates who received twice the PLT dose by volume-reduced PLTs had twice as high early and follow-up count increment showing similar efficacy of products.
机译:背景技术在荷兰,不同的血小板(PLT)产品用于新生儿输血:体积减小的PLT,PLT添加剂溶液(PAS)II PLT和血浆PLT。这些是适用于当地输血指南的三个不同的新生儿重症监护病房的标准产品。在这里,我们评估这些产品的输血后计数增量。研究设计和方法我们对2007年1月1日至2008年12月31日出生的第一个月接受至少一次PLT输血的新生儿进行了一项回顾性队列研究。分析了74例减少197例PLT输血的新生儿,68例105例PASII PLT输血的新生儿和8例血浆PLT输血的8例新生儿。分别使用191和81个体积减小的PLT,77个和56个PASII PLT以及六个和五个血浆PLT输血,分别评估了早期(输血后8小时内)和随访计数的增加(输血后16-24小时)。随机效应模型。结果体积减小的PLT以两倍于PASII和血浆PLT体积五分之一的剂量输注。体积减少的PLT在111×10 9 / L(95%置信区间[CI],86-135)时的早期输血后计数增量高于PASII PLT在62×109 / L(95%CI,40-84) ; p = 0.000)和血浆PLTs为47×109 / L(95%CI,14-79)。体积减少的PLT在60×109 / L(95%CI,19-100)时的随访计数增幅也高于PASII PLT在38×109 / L(95%CI,-0.2至77; p = 0.082)和血浆PLT为4×109 / L(95%CI,-38至46)。结论体积减小的PLT接受两倍PLT剂量的新生儿早期和随访计数增加率高一倍,显示该产品的功效相似。

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