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Isoprostane levels in urine of preterm newborns treated with ibuprofen for patent ductus arteriosus closure

机译:布洛芬治疗闭合动脉导管未闭的早产儿尿中异前列腺素水平

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Patent ductus arteriosus (PDA) is the most common cardiovascular abnormality of the preterm infant usually treated with ibuprofen (IBU). PDA is strictly related to oxidative stress (OS) in neonates. This study tests the hypothesis that OS occurs in neonates with PDA and that IBU treatment reduces OS. Forty-three preterm babies with gestational age (GA) <33 weeks were studied prospectively. Three urine samples were collected: at time 0 (before starting treatment), time 1 (after pharmacological PDA closure), and time 2 (7 days after the end of treatment) in all patients. OS was studied by measuring urinary isoprostane (IPs) levels. The results showed significant changes in urinary IP levels from time 0 to time 2 (Kruskal–Wallis, p = 0.047). Time trend showed a significant decrease in IPs from time 0 to time 1 after IBU therapy (p = 0.0067). This decrease was followed by an increase in IPs levels 7 days after treatment. IBU therapy for PDA closure reduced the risk of OS related to free-radical (FR) generation. This antioxidant effect of IBU may be beneficial in preterm babies with PDA who are at high risk for OS.
机译:动脉导管未闭(PDA)是通常用布洛芬(IBU)治疗的早产儿最常见的心血管异常。 PDA与新生儿的氧化应激(OS)密切相关。这项研究检验了在PDA新生儿中发生OS以及IBU治疗降低OS的假设。前瞻性研究了43个胎龄(GA)<33周的早产婴儿。在所有患者中收集了三个尿液样本:时间0(开始治疗前),时间1(药理PDA封闭后)和时间2(治疗结束后7天)。通过测量尿中异丙肾上腺素(IPs)水平来研究OS。结果显示,从时间0到时间2,尿中IP含量发生了显着变化(Kruskal–Wallis,p = 0.047)。时间趋势显示,IBU治疗后从时间0到时间1的IP显着降低(p = 0.0067)。在治疗7天后,IPs水平下降。 PDA封闭的IBU治疗降低了与自由基(FR)产生相关的OS风险。 IBU的这种抗氧化作用可能对患有OS高风险的PDA早产婴儿有益。

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