针对早产婴儿的动脉管的重复药理疗程的有效性
Carlo Dani1, Giovanni Sassudelli2, Carlotta Milocchi2
1Department of Neuroscience, Psychology, Drug Research and Child Health, Careggi University Hospital of Florence, Largo Brambilla 3, 50134 Firenze, Italy; Division of Neonatology, Careggi University Hospital of Florence, Largo Brambilla 3, 50134 Firenze, Italy.
Early human development
|December 1, 2024
概括
在早产婴儿中,针对血液动力学上显著的专利动脉管 (hsPDA) 进行重复的布洛芬或青疗程显示出失败率的增加. 进一步的药物疗程可能会增加非常早产婴儿的不良影响.
科学领域:
- 新生儿科学 新生儿科学
- 儿童心脏病学 儿童心脏病学
- 药理学 药理学是指药理学的学科.
背景情况:
- 血液动力学显著的专利动脉管 (hsPDA) 在早产婴儿中很常见.
- 有限的数据存在于hsPDA关闭的重复药物疗程的有效性.
- 这项研究研究了在怀孕29周以下的婴儿中对hsPDA进行重复的布洛芬和/或青治疗.
研究的目的:
- 评估第二或第三疗程的伊布罗芬和/或帕拉西他摩尔对hsPDA在早产婴儿的有效性.
- 评估hsPDA连续药理治疗的失败率.
主要方法:
- 包括107名早产婴儿 (<29周) 患有心声诊断hsPDA.
- 婴儿接受了布洛芬,,或组合治疗.
- 在每次治疗后都进行了心声扫描.
主要成果:
- 第一个,第二个和第三个药物课程的失败率分别为38%,76%和92%.
- 在那些未能接受初始治疗的人中,有些人以>3个疗程完成关闭,有些人需要手术,有些人死亡.
- 没有确定第二/第三课程失败的独立风险因素.
结论:
- 对hsPDA的第二和第三药物疗程的失败率比以前报告的要高.
- 额外课程的高失败率可能导致长期暴露hsPDA不良影响.
- 建议小心考虑进一步的药理治疗,对于非常早产的婴儿hsPDA.
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