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对乙酰氨基酚在患有严重先天性心脏病的新生儿中用于治疗前列腺素E1诱导的发热的应用

The Utilization of Acetaminophen for Managing PGE1-Induced Fever in Neonates with Critical Congenital Heart Disease.

作者信息

Kaya Başak, Akduman Hasan, Dilli Dilek, Kaya Özkan, Çitli Rumeysa, Zenciroğlu Ayşegül

机构信息

Department of Neonatology, SBU. Dr. Sami Ulus Maternity and Child Research and Training Hospital, Babur St., Number: 36, Altındag 06080, Turkey.

Department of Pediatric Cardiology, SBU. Dr. Sami Ulus Maternity and Child Research and Training Hospital, Babur St., Number: 36, Altındag 06080, Turkey.

出版信息

Children (Basel). 2024 Dec 20;11(12):1547. doi: 10.3390/children11121547.

Abstract

INTRODUCTION

We aimed to retrospectively evaluate the use of acetaminophen, which may be a risk factor for the ductal canal, in the treatment of fever due to prostaglandin E1 (PGE1) infusion in newborns with critical congenital heart disease (CCHD).

METHODS

The study included newborns who were followed-up in our neonatal intensive care unit with the diagnosis of critical congenital heart disease, developed fever due to PGE1 infusion and had acetaminophen administered for antipyretic treatment. The patent ductus arteriosus diameters of the patients were evaluated by echocardiographic imaging before intravenous acetaminophen treatment and at the end of the day of acetaminophen treatment.

RESULTS

PGE1 fever was observed in 10 (6%) of 156 infants with ductus-dependent congenital heart disease. Intravenous acetaminophen treatment administered as an antipyretic in these infants did not cause the narrowing or closure of the ductal canal diameter, which would lead to clinical decompensation if it was closed, and the patients remained hemodynamically stable until surgery.

CONCLUSIONS

It can be considered that controlled and rapidly administered intravenous acetaminophen therapy in the management of fever in neonates with congenital heart disease who develop fever as a side effect of high-dose intravenous PGE1 infusion therapy (≥0.3 mcg/kg/min) may prevent hemodynamic decompensation in these critically ill infants, and as a secondary outcome, it can be speculated that avoiding rapid daily increases in PGE1 maintenance infusion doses may be necessary to limit the number of paracetamol administrations in these infants.

摘要

引言

我们旨在回顾性评估对乙酰氨基酚在患有严重先天性心脏病(CCHD)的新生儿因输注前列腺素E1(PGE1)引起发热的治疗中的使用情况,对乙酰氨基酚可能是动脉导管的一个风险因素。

方法

该研究纳入了在我们新生儿重症监护病房接受随访、诊断为严重先天性心脏病、因输注PGE1而发热且接受对乙酰氨基酚进行退热治疗的新生儿。在静脉注射对乙酰氨基酚治疗前及治疗当天结束时,通过超声心动图成像评估患者的动脉导管直径。

结果

156例依赖动脉导管的先天性心脏病婴儿中有10例(6%)出现PGE1发热。在这些婴儿中作为退热药给予静脉对乙酰氨基酚治疗并未导致动脉导管直径变窄或闭合,如果动脉导管闭合会导致临床失代偿,并且患者在手术前血流动力学保持稳定。

结论

可以认为,对于因高剂量静脉PGE1输注治疗(≥0.3 mcg/kg/min)作为副作用而发热的先天性心脏病新生儿,进行可控且快速的静脉对乙酰氨基酚治疗可能预防这些重症婴儿出现血流动力学失代偿,作为次要结果,可以推测为限制这些婴儿对乙酰氨基酚的给药次数,避免PGE1维持输注剂量每日快速增加可能是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c5/11727204/a72fd41234db/children-11-01547-g001.jpg

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