Hawkins Caitlin, Hemmann Brianna, Hemmelgarn Trina
Department of Pharmacy (CH*), Nationwide Children's Hospital, Columbus, OH; *CH was a student at the time of this study.
Division of Pharmacy (BH, TH), Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
J Pediatr Pharmacol Ther. 2024 Aug;29(4):385-390. doi: 10.5863/1551-6776-29.4.385. Epub 2024 Aug 13.
Vasopressin has systemic vasoconstrictive yet pulmonary vasodilatory effects, making it an ideal agent for hypotension management in infants with congenital diaphragmatic hernia (CDH)-associated pulmonary hypertension. The side effects of vasopressin in this population, such as hyponatremia, are understudied. This study aims to characterize the effect of vasopressin on sodium concentrations in infants with and without CDH.
This was a retrospective review of patients who received vasopressin while admitted to a level IV neonatal intensive care unit. The primary outcome was the incidence of hyponatremia (blood sodium <135 mmol/L) during vasopressin therapy. Secondary outcomes included time to hyponatremia, dose and duration of vasopressin, incidence of severe hyponatremia (blood sodium <125 mmol/L), and hypertonic saline use. Both blood serum and blood gas sample sodium concentrations were used to compare CDH vs non-CDH patients.
The average difference between baseline and lowest blood sodium was significant for both CDH and non-CDH patients for all samples (p < 0.001). There was no significant difference in the primary outcome, nor in the secondary outcomes of time to hyponatremia or duration of vasopressin infusion. The average dose of vasopressin was higher in the CDH vs non-CDH group (p = 0.018). The incidences of severe hyponatremia and hypertonic saline use were greater in the CDH vs non-CDH group for patients who had blood serum sodium samples collected (p = 0.049 and p = 0.033, respectively).
This study showed that severe hyponatremia occurred more frequently in CDH vs non-CDH patients. Extreme caution is necessary when managing total body sodium in patients with CDH.
血管加压素具有全身血管收缩作用,但对肺血管有扩张作用,这使其成为治疗先天性膈疝(CDH)相关肺动脉高压婴儿低血压的理想药物。血管加压素在该人群中的副作用,如低钠血症,尚未得到充分研究。本研究旨在描述血管加压素对患有和未患有CDH的婴儿钠浓度的影响。
这是一项对入住四级新生儿重症监护病房期间接受血管加压素治疗的患者的回顾性研究。主要结局是血管加压素治疗期间低钠血症(血钠<135 mmol/L)的发生率。次要结局包括发生低钠血症的时间、血管加压素的剂量和持续时间、严重低钠血症(血钠<125 mmol/L)的发生率以及高渗盐水的使用情况。血清和血气样本中的钠浓度均用于比较CDH患者与非CDH患者。
所有样本中,CDH患者和非CDH患者的基线血钠与最低血钠之间的平均差异均具有统计学意义(p<0.001)。主要结局以及低钠血症发生时间和血管加压素输注持续时间等次要结局均无显著差异。CDH组血管加压素的平均剂量高于非CDH组(p = 0.018)。对于采集了血清钠样本的患者,CDH组严重低钠血症和高渗盐水的使用发生率高于非CDH组(分别为p = 0.049和p = 0.033)。
本研究表明,CDH患者中严重低钠血症的发生频率高于非CDH患者。在管理CDH患者的总体钠水平时必须格外谨慎。