All authors: Department of Neonatology and Pediatric Intensive Care Medicine, University Children's Hospital Bonn, Bonn, Germany.
Pediatr Crit Care Med. 2021 Jul 1;22(7):e382-e390. doi: 10.1097/PCC.0000000000002665.
Infants with congenital diaphragmatic hernia frequently suffer from cardiac dysfunction and pulmonary hypertension during the postnatal course. With the use of the inodilator levosimendan, a therapeutic approach is available in situations with catecholamine-refractory low-cardiac-output failure and severe pulmonary hypertension.
Retrospective single-center cohort study.
University-based, tertiary-care children's hospital neonatal ICU.
Cohort of 24 infants with congenital diaphragmatic hernia and levosimendan therapy, without underlying major cardiac defect, treated at the University Children´s Hospital Bonn, Germany, between January 2017 and December 2018.
None.
Twenty-four infants with congenital diaphragmatic hernia were treated with levosimendan (41% of hospitalized congenital diaphragmatic hernia infants in the study period). In 88%, the congenital diaphragmatic hernia was left-sided. The median observed-to-expected lung-to-head ratio was 36%. About 60% of the infants were supported with venovenous extracorporeal membrane oxygenation and the mortality was 38% (9/24 infants). Levosimendan administration was associated with improvement of pulmonary hypertension severity (p = 0.013 and p = 0.000) and right ventricular dysfunction (p = 0.011 and p = 0.000) at 24 hours and 7 days after treatment. Similarly, the prevalence of left ventricular dysfunction decreased from 50% at baseline to 10% after 7 days (p = 0.026). A significant reduction in the peak inspiratory pressure was observed after drug application (p = 0.038) and a significant decrease of the Vasoactive-Inotropic Score was apparent (p = 0.022). A relevant arterial hypotension as a drug-related adverse event occurred in one patient.
This is the first study exploring clinical and hemodynamic changes after levosimendan treatment in a cohort of infants with congenital diaphragmatic hernia. An association of levosimendan application and an improvement in pulmonary hypertension, right ventricular, and left ventricular dysfunction were observed within 7 days after drug infusion. However, due to the retrospective design of this study, the results should be interpreted carefully.
患有先天性膈疝的婴儿在出生后常伴有心功能障碍和肺动脉高压。在儿茶酚胺抵抗性低心输出量衰竭和严重肺动脉高压的情况下,使用正性肌力药物米力农可以提供一种治疗方法。
回顾性单中心队列研究。
德国波恩大学附属的三级儿童医院新生儿重症监护病房。
2017 年 1 月至 2018 年 12 月期间,在德国波恩大学儿童医院接受米力农治疗且无主要心脏缺陷的 24 例先天性膈疝婴儿组成的队列。
无。
24 例先天性膈疝婴儿接受米力农治疗(研究期间住院先天性膈疝婴儿的 41%)。88%的膈疝为左侧,观察到的与预期的肺与头的比值中位数为 36%。约 60%的婴儿接受静脉-静脉体外膜肺氧合支持,死亡率为 38%(9/24 例婴儿)。米力农治疗后 24 小时和 7 天,肺动脉高压严重程度(p = 0.013 和 p = 0.000)和右心室功能障碍(p = 0.011 和 p = 0.000)得到改善。同样,左心室功能障碍的患病率从基线时的 50%降至 7 天后的 10%(p = 0.026)。药物应用后,吸气峰压显著降低(p = 0.038),血管活性-正性肌力评分显著下降(p = 0.022)。1 例患者出现与药物相关的显著动脉低血压不良事件。
这是第一项研究,探讨了米力农治疗先天性膈疝婴儿队列的临床和血液动力学变化。在药物输注后 7 天内观察到米力农应用与肺动脉高压、右心室和左心室功能障碍的改善有关。然而,由于这项研究的回顾性设计,结果应谨慎解释。