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一名患有心脏异常的新生儿对前列地尔的需求增加以及直肠和口服对乙酰氨基酚的联合使用

Increasing Alprostadil Requirements in a Neonate With Cardiac Anomalies and Co-administration of Rectal and Oral Acetaminophen.

作者信息

Ryder Jennifer M, Bae Esther

机构信息

Department of Pharmacy (JR, EB), Children's Hospital Colorado, Aurora, CO.

Heart Institute (EB), Children's Hospital Colorado, Aurora, CO.

出版信息

J Pediatr Pharmacol Ther. 2022;27(6):573-577. doi: 10.5863/1551-6776-27.6.573. Epub 2022 Aug 19.

Abstract

A patent ductus arteriosus (PDA) results from the failure of the ductus arteriosus to close within 72 hours after birth. In most neonates, a PDA can lead to significant morbidities and often warrants pharmacologic intervention for closure. Common pharmacologic interventions include indomethacin, ibuprofen, and acetaminophen. In cases of ductal-dependent congenital heart defects (CHDs), such as hypoplastic left heart syndrome, it is imperative to keep the ductus arteriosus patent to maintain adequate pulmonary or systemic circulation until surgical intervention can be performed. The only proven pharmacologic agent used for this indication is prostaglandin E1 (PGE1) commonly in the form of intravenous alprostadil. This case report describes a neonate with multiple cardiac and genetic anomalies that required increased alprostadil infusion after exposure to rectal and oral acetaminophen. The patient initially presented with a large PDA on echocardiogram (ECHO); however, after an incidental finding of a small PDA on ECHO, the administration of as needed rectal acetaminophen was discontinued out of concern for its effects on patency. After a few days of increased prostaglandin therapy and 2 reassuring ECHO results, the patient was given oral acetaminophen on an as needed basis. Within 24 hours of restarting the acetaminophen, the repeated ECHO showed a reduction in PDA and flow. In patients with ductal-dependent cardiac lesions, it is important to maintain PDA patency and, therefore, introducing a medication with antiprostaglandin properties should be avoided.

摘要

动脉导管未闭(PDA)是由于动脉导管在出生后72小时内未能闭合所致。在大多数新生儿中,PDA可导致严重疾病,通常需要药物干预以促使其闭合。常见的药物干预包括吲哚美辛、布洛芬和对乙酰氨基酚。在诸如左心发育不全综合征等依赖动脉导管的先天性心脏病(CHD)病例中,在能够进行手术干预之前,必须保持动脉导管开放以维持足够的肺循环或体循环。用于该适应症的唯一经证实的药物是前列腺素E1(PGE1),通常以静脉注射前列地尔的形式使用。本病例报告描述了一名患有多种心脏和遗传异常的新生儿,在接触直肠和口服对乙酰氨基酚后需要增加前列地尔输注量。患者最初经超声心动图(ECHO)检查发现有一个大的PDA;然而,在ECHO偶然发现一个小的PDA后,出于对其对导管通畅性影响的担忧,停止了按需给予直肠对乙酰氨基酚。在增加前列腺素治疗数天且两次ECHO结果令人放心后,患者按需给予口服对乙酰氨基酚。重新开始使用对乙酰氨基酚后24小时内,重复ECHO显示PDA及血流减少。在患有依赖动脉导管的心脏病变的患者中,维持PDA通畅很重要,因此应避免引入具有抗前列腺素特性的药物。

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