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首页> 外文期刊>Frontiers in Pediatrics >Renal Precision Medicine in Neonates and Acute Kidney Injury: How to Convert a Cloud of Creatinine Observations to Support Clinical Decisions
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Renal Precision Medicine in Neonates and Acute Kidney Injury: How to Convert a Cloud of Creatinine Observations to Support Clinical Decisions

机译:肾脏精密药物在新生儿和急性肾损伤:如何转化肌酐观测云以支持临床决策

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Renal precision medicine in neonates is useful to support decision making on pharmacotherapy, signal detection of adverse (drug) events, and individual prediction of short- and long-term prognosis. To estimate kidney function or glomerular filtration rate (GFR), the most commonly measured and readily accessible biomarker is serum creatinine (S cr ). However, there is extensive variability in S cr observations and GFR estimates within the neonatal population, because of developmental physiology and superimposed pathology. Furthermore, assay related differences still matter for S cr , but also exist for Cystatin C. Observations in extreme low birth weight (ELBW) and term asphyxiated neonates will illustrate how renal precision medicine contributes to neonatal precision medicine. When the Kidney Disease Improving Global Outcome (KDIGO) definition of acute kidney injury (AKI) is used, this results in an incidence up to 50% in ELBW neonates, associated with increased mortality and morbidity. However, urine output criteria needed adaptations to broader time intervals or weight trends, while S cr and its trends do not provide sufficient detail on kidney function between ELBW neonates. Instead, we suggest to use assay-specific centile S cr values to better describe postnatal trends and have illustrated its relevance by quantifying an adverse drug event (ibuprofen) and by explaining individual amikacin clearance. Term asphyxiated neonates also commonly display AKI. While oliguria is a specific AKI indicator, the majority of term asphyxiated cases are non-oliguric. Asphyxia results in a clinical significant—commonly transient—mean GFR decrease (?50%) with a lower renal drug elimination. But there is still major (unexplained) inter-individual variability in GFR and subsequent renal drug elimination between these asphyxiated neonates. Recently, the Baby-NINJA (nephrotoxic injury negated by just-in-time action) study provided evidence on the concept that a focus on nephrotoxic injury negation has a significant impact on AKI incidence and severity. It is hereby important to realize that follow-up should not be discontinued at discharge, as there are concerns about long-term renal outcome. These illustrations suggest that integration of renal (patho)physiology into neonatal precision medicine are an important tool to improve contemporary neonatal care, not only for the short-term but also with a positive health impact throughout life.
机译:新生儿的肾脏精密药物可用于支持药物治疗的决策,信号检测不利(药物)事件,以及对短期和长期预后的个人预测。为了估算肾功能或肾小球过滤速率(GFR),最常见的测量和易于接近的生物标志物是血清肌酐(SC)。然而,由于发育生理学和叠加病理学,在新生儿群体中的SCR观测结果和GFR估算中存在广泛的变化。此外,SC的测定相关差异仍然重要,但也存在于胱抑素C.在极端低出生体重(ELBW)和术语中的观察结果将说明肾精密药如何有助于新生儿精密药物。当使用改善全球结果(KDIGO)对急性肾脏损伤(AKI)的肾病的定义时,这导致ELBW新生儿的发病率高达50%,与增加的死亡率和发病率增加。然而,尿液输出标准需要适应更广泛的时间间隔或体重趋势,而SCR及其趋势则不会在ELBW新生儿之间提供足够的细节肾功能。相反,我们建议使用特定于特定的Celile S CR值来更好地描述产后趋势,并通过量化不良药物事件(布洛芬)并通过解释单独的Amikacin清除来说明其相关性。术语窒息的新生儿也通常显示AKI。虽然寡核桃是一种特定的AKI指标,但大多数术语窒息病例是非寡糖。窒息导致临床显着的临床瞬态平均GFR减少(?50%),肾脏药物较低。但仍有主要(未解释的)GFR间间的个性变异性和这些窒息新生儿之间的随后肾脏药物消除。最近,婴儿忍者(即时行动否定的肾毒性损伤)研究提供了关于肾毒性损伤否定对症症发病率和严重程度影响的概念的证据。因此,重要的是意识到在放电时不应停止随访,因为关于长期肾果糖的担忧。这些插图表明,肾(Patho)生理到新生儿精密药物的整合是改善当代新生儿护理的重要工具,不仅是短期,而且在整个生命中产生积极的健康影响。

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