医学
支气管肺发育不良
早产儿视网膜病变
重症监护医学
坏死性小肠结肠炎
堆积红细胞
小肠结肠炎
输血
儿科
胎龄
怀孕
外科
内科学
遗传学
生物
作者
Luise Bellach,Michael Eigenschink,Abtin Hassanein,Danylo Savran,Ulrich Salzer,Ernst W. Müllner,Andreas Repa,Katrin Klebermaß-Schrehof,Lukas Wisgrill,Vito Giordano,Angelika Berger
标识
DOI:10.1016/s2352-3026(22)00207-1
摘要
Premature infants commonly receive adult packed red blood cells (pRBCs) during their hospital stay. As adult erythrocytes differ substantially from those of preterm infants, transfusion of adult pRBCs into preterm infants can be considered inappropriate for the physiology of a preterm infant. An absence of standardisation of transfusion protocols makes it difficult to compare and interpret pertinent clinical data, as reflected by unclear associations between pRBC transfusion and complications related to prematurity, such as bronchopulmonary dysplasia, neurodevelopmental impairment, retinopathy of prematurity, or necrotising enterocolitis. The difficulty in interpreting clinical data is further increased by differences in study designs that either overestimate pRBC-associated complications of prematurity or have not yet been designed to directly link pRBC transfusions to their respective complications. Thus, neonatal transfusion practice has become an ongoing difficulty, in which differences in transfusion guidelines hinder the ability to generate comparable clinical data, and heterogeneity in clinical data prevents the implementation of standardised transfusion protocols. To overcome these issues, novel approaches with biochemical-clinical translational designs could enable clinicians to gather causal evidence instead of circumstantial correlation.
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