Department of Pediatrics, Neonatology Division, Faculty of Medicine of the University of São Paulo, Instituto da Criança, Av. Dr. Enéas de Carvalho Aguiar, 647, São Paulo, 05403-000, Brazil.
Department of Pediatric Cardiology, Faculty of Medicine of the University of São Paulo, Instituto do Coração, São Paulo, Brazil.
Eur J Pediatr. 2024 Feb;183(2):543-555. doi: 10.1007/s00431-023-05342-0. Epub 2023 Nov 24.
To evaluate milrinone's impact on pediatric cardiac function, focusing on its specific role as an inotrope and lusitrope, while considering its systemic and pulmonary vasodilatory effects. Search of PubMed, EMBASE, and the Cochrane Library up to August 2023. We included all studies that evaluated milrinone in children under 18 years old in neonatal, pediatric, or cardiac intensive care units. We excluded case reports, studies that did not provide tabular information on milrinone's outcomes, and studies focused on non-intensive care populations. We extracted data on the research design, objectives, study sample, and results of each study, including the impact of milrinone and any associated factors. We screened a total of 9423 abstracts and 41 studies were ultimately included. Milrinone significantly improved left ventricular ejection fraction (WMD 3.41 [95% CI 0.61 - 6.21]), left ventricle shortening fraction (WMD 4.25 [95% CI 3.43 - 5.08]), cardiac index (WMD 0.50 [95% CI 0.32 to 0.68]), left ventricle output (WMD 55.81 [95% CI 4.91 to 106.72]), serum lactate (WMD -0.59 [95% CI -1.15 to -0.02]), and stroke volume index (WMD 2.95 [95% CI 0.09 - 5.82]). However, milrinone was not associated with improvements in ventricular myocardial performance index (WMD -0.01 [95% CI -0.06 to 0.04]) and ventricular longitudinal strain (WMD -2.14 [95% CI -4.56 to 0.28]). Furthermore, milrinone was not associated with isovolumetric relaxation time reduction (WMD -8.87 [95% CI -21.40 to 3.66]).
Our meta-analysis suggests potential clinical benefits of milrinone by improving cardiac function, likely driven by its systemic vasodilatory effects. However, questions arise about its inotropic influence and the presence of a lusitropic effect. Moreover, milrinone's pulmonary vasodilatory effect appears relatively weaker compared to its systemic actions. Further research is needed to elucidate milrinone's precise mechanisms and refine its clinical applications in pediatric practice.
• Milrinone is a phosphodiesterase III inhibitor that has been used to treat a variety of pediatric and neonatal conditions. • Milrinone is believed to exert its therapeutic effects by enhancing cardiac contractility and promoting vascular relaxation.
• Milrinone may not have a significant inotropic effect. • Milrinone's pulmonary vasodilatory effect is less robust than its systemic vasodilatory effect.
评估米力农对儿科心功能的影响,重点关注其作为正性肌力药和变力性药物的特定作用,同时考虑其全身和肺血管扩张作用。
对 PubMed、EMBASE 和 Cochrane 图书馆进行检索,检索时间截至 2023 年 8 月。我们纳入了所有评估 18 岁以下儿童在新生儿、儿科或心脏重症监护病房中米力农的研究。我们排除了病例报告、未提供米力农结局表格信息的研究以及关注非重症监护人群的研究。我们提取了每项研究的研究设计、目标、研究样本和结果的数据,包括米力农的影响和任何相关因素。
我们共筛选了 9423 篇摘要,最终纳入了 41 项研究。米力农显著改善左心室射血分数(WMD 3.41 [95% CI 0.61-6.21])、左心室缩短分数(WMD 4.25 [95% CI 3.43-5.08])、心指数(WMD 0.50 [95% CI 0.32-0.68])、左心室输出量(WMD 55.81 [95% CI 4.91-106.72])、血清乳酸(WMD-0.59 [95% CI-1.15-0.02])和每搏量指数(WMD 2.95 [95% CI 0.09-5.82])。然而,米力农与心室心肌性能指数(WMD-0.01 [95% CI-0.06-0.04])和心室纵向应变(WMD-2.14 [95% CI-4.56-0.28])的改善无关。此外,米力农与等容舒张时间的缩短无关(WMD-8.87 [95% CI-21.40-3.66])。
我们的荟萃分析表明,米力农通过改善心功能可能具有潜在的临床获益,这可能是由其全身血管扩张作用驱动的。然而,关于其正性肌力作用和变力性作用的问题仍存在争议。此外,米力农的肺血管扩张作用似乎比其全身作用相对较弱。需要进一步的研究来阐明米力农的确切作用机制,并细化其在儿科实践中的临床应用。
米力农是一种磷酸二酯酶 III 抑制剂,已被用于治疗各种儿科和新生儿疾病。米力农被认为通过增强心肌收缩力和促进血管松弛来发挥其治疗作用。
米力农可能没有显著的正性肌力作用。米力农的肺血管扩张作用不如全身血管扩张作用强。