Kao B, Stewart de Ramirez S A, Belfort M B, Hansen A
Division of Newborn Medicine, Department of Medicine, Children's Hospital Boston, Boston, MA, USA.
J Perinatol. 2008 Mar;28(3):205-10. doi: 10.1038/sj.jp.7211917. Epub 2008 Jan 17.
Infants with transient tachypnea of the newborn (TTN) have relatively low levels of epinephrine, which is known to mediate fetal lung fluid absorption. Providing exogenous epinephrine could be a valuable diagnostic and therapeutic intervention for this common condition. Our primary objective was to determine if inhaled racemic epinephrine is safe for the treatment of TTN. Our secondary objective was to determine its efficacy.
We conducted a randomized, blinded, placebo-controlled pilot trial. Inhaled racemic epinephrine or placebo was administered to 20 newborns with TTN. Physiologic variables of cardiopulmonary function were measured during and after treatment.
No infant in either the treatment or control arm experienced an adverse event, including tachycardia or hypertension. We did not detect a difference between the two groups regarding rate of resolution of tachypnea.
We did not observe any adverse effects of inhaled racemic epinephrine when administered for the treatment of TTN. Larger studies are necessary to determine efficacy.
新生儿暂时性呼吸急促(TTN)婴儿的肾上腺素水平相对较低,而肾上腺素已知可介导胎儿肺液吸收。提供外源性肾上腺素可能是针对这种常见病症的一种有价值的诊断和治疗干预措施。我们的主要目的是确定吸入消旋肾上腺素治疗TTN是否安全。我们的次要目的是确定其疗效。
我们进行了一项随机、双盲、安慰剂对照的试点试验。对20例TTN新生儿给予吸入消旋肾上腺素或安慰剂。在治疗期间和治疗后测量心肺功能的生理变量。
治疗组或对照组中均无婴儿出现不良事件,包括心动过速或高血压。我们未检测到两组在呼吸急促缓解率方面存在差异。
我们在使用吸入消旋肾上腺素治疗TTN时未观察到任何不良反应。需要进行更大规模的研究来确定疗效。