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Urine phenobarbital drug screening: Potential use for compliance assessment in neonates

机译:尿苯巴比妥药物筛查:新生儿顺应性评估的潜在用途

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This study was done to determine if urine phenobarbital measurements provide a reliable indicator of presence of the drug in neonates. Urine was collected from neonates treated with phenobarbital for clinical indications within 4 to 6 hours of clinically indicated collection of serum phenobarbital levels. Urine samples were also collected from control neonates not treated with phenobarbital. One aliquot was assayed fresh, another frozen at -30°C and assayed 1 to 3 months later. Phenobarbital was assayed using the ONLINE TDM Roche/Hitachi automated clinical chemistry analyzer. Serum and urine concentrations were compared as were fresh and frozen urine measurements. Serum phenobarbital ranged from 5.6 to 52.7 μg/mL. Matched urine samples were 56.6 ± 12.5% of the serum level. Frozen samples were 98.3 ± 8.0% of the fresh samples. Urine phenobarbital concentrations, either fresh or frozen, can be used in neonates as a noninvasive estimate of drug levels.
机译:进行这项研究是为了确定尿液苯巴比妥测量是否可以提供新生儿中药物存在的可靠指标。在临床指示的血清苯巴比妥水平收集后的4至6个小时内,从接受苯巴比妥治疗的新生儿中收集尿液用于临床指征。还从未经苯巴比妥治疗的对照新生儿中收集尿液样品。将一份等分试样新鲜测定,将另一份等分试样在-30°C冷冻,并在1-3个月后测定。使用ONLINE TDM Roche / Hitachi自动化临床化学分析仪测定苯巴比妥。比较血清和尿液浓度,以及新鲜和冷冻尿液的测量值。血清苯巴比妥范围为5.6至52.7μg/ mL。匹配的尿液样本为血清水平的56.6±12.5%。冷冻样品占新鲜样品的98.3±8.0%。尿中苯巴比妥的浓度新鲜或冷冻均可用于新生儿,作为药物水平的非侵入性评估。

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