Ozkan Hasan, Duman Nuray, Tuzun Funda, Narter Fatma, Akyildiz Can, Altuncu Emel, Satar Mehmet, Ozdemir Mustafa, Kurt Abdullah, Tugcu Ali U, Konak Murat, Uygun Saime Sundus, Yilmaz Semerci Seda, Dikmen Rahime T, Baysal Bora, Zeybek Cemile K, Kostekci Yasemin Ezgi, Sahin Suzan, Tutal Merve, Anik Ayse, Buyuktiryaki Mehmet, Karagol Belma S, Tunç Gaffari, Colak Derya, Cetin Hasan, Orman Aysen, Olukman Ozgur, Deveci Mehmet Fatih, Sarici Dilek, Cakir Salih C, Keskinoglu Pembe
Faculty of Medicine, Dokuz Eylül University, Izmir, Türkiye.
Istanbul Kartal Dr.Lutfi Kirdar Education and Research Hospital, Istanbul, Türkiye.
Front Nutr. 2024 Sep 19;11:1410571. doi: 10.3389/fnut.2024.1410571. eCollection 2024.
The objective of this study was to evaluate the efficacy and safety of isotonic and hypotonic intravenous fluids in maintenance fluid therapy for term infants.
This was a multi-centre, prospective, observational study conducted in 21 participating centres from December 30, 2020, to June 30, 2023. The study included term newborns requiring parenteral fluid therapy for maintenance (NCT04781361). The fluid treatment was divided into two groups based on the concentration of sodium in the parenteral fluid, designated as hypotonic (NaCl <130 mmol/L) and isotonic (NaCl = 130-154 mmol/L). The primary outcomes were the change in mean plasma sodium (pNa) levels per hour (∆pNa mmol/L/h), the incidence of hyponatremia (pNa <135 mmol/L) and hypernatremia (pNa >145 mmol/L), and the occurrence of clinically significant changes in sodium levels (∆pNa >0.5 mmol/L/h).
A total of 420 patients from 21 centers were included. The ∆pNa was negative in the hypotonic fluid group and positive in the isotonic fluid group, with a significant difference between the groups [respectively -0.07 ± 0.03 (95% CI: -0.13 to -0.02); 0.04 ± 0.03 (95%CI: -0.02 to 0.09), = 0.04]. There was no difference between the groups in terms of the development of hypernatremia or a clinically meaningful pNa increase. The hypotonic fluid group had a higher incidence of hyponatremia and a clinically meaningful sodium decrease compared to the isotonic fluid group [7.9% vs. 1.2% (OR:6.5, p:0.03)] and [12.2% vs.4.2% (OR:2.9, = 0.03)].
Contrary to current understanding, this large-scale study is the first to demonstrate that the use of hypotonic fluids in maintenance fluid therapy for newborns poses a risk of hyponatremia development, whereas isotonic fluid therapy appears safe.
本研究的目的是评估等渗和低渗静脉输液在足月儿维持性液体治疗中的疗效和安全性。
这是一项多中心、前瞻性观察性研究,于2020年12月30日至2023年6月30日在21个参与中心进行。该研究纳入了需要肠外液体治疗以维持的足月儿(NCT04781361)。根据肠外液体中钠的浓度将液体治疗分为两组,分别为低渗组(氯化钠<130 mmol/L)和等渗组(氯化钠=130-154 mmol/L)。主要结局指标为每小时平均血浆钠(pNa)水平的变化(∆pNa mmol/L/h)、低钠血症(pNa<135 mmol/L)和高钠血症(pNa>145 mmol/L)的发生率,以及钠水平临床显著变化(∆pNa>0.5 mmol/L/h)的发生情况。
共纳入了来自21个中心的420例患者。低渗液组的∆pNa为负值,等渗液组为正值,两组间差异有统计学意义[分别为-0.07± 0.03(95%CI:-0.13至-0.02);0.04± 0.03(95%CI:-0.02至0.09),P=0.04]。两组在高钠血症的发生或临床上有意义的pNa升高方面无差异。与等渗液组相比,低渗液组低钠血症的发生率更高,且钠水平有临床意义的降低[7.9%对1.2%(OR:6.5,P:0.03)]以及[12.2%对4.2%(OR:2.9,P=0.03)]。
与目前的认识相反,这项大规模研究首次表明,在新生儿维持性液体治疗中使用低渗液有发生低钠血症的风险,而等渗液治疗似乎是安全的。