Paper Details
- Takafumi Nakano (Department of Pharmacy, Fukuoka University Hospital / Department of Oncology and Infectious Disease Pharmacy, Faculty of Pharmaceutical Sciences, Fukuoka University / naka0625@fukuoka-u.ac.jp)
1) Department of Pharmacy, Fukuoka University Hospital , 2) Department of Oncology and Infectious Disease Pharmacy, Faculty of Pharmaceutical Sciences, Fukuoka University
In Western countries, magnesium sulfate (MgSO4) for threatened preterm labor is recommended as short-term tocolysis (4 tocolysis on maternal renal function. This retrospective observational study included pregnant women hospitalized for threatened preterm labor who received MgSO4 therapy at Fukuoka University Hospital between January and December 2021. Eligible patients were ≥18 years old, ≥22 weeks of gestation, and treated with MgSO4 for ≥24 h. A total of 66 patients were classified into short-term (n = 26) and long-term (≥48 h) group (n = 40). The primary outcome was the incidence of acute kidney injury (AKI). Secondary outcomes included changes in serum creatinine level (ΔCr; peak – baseline) and correlations between ΔCr and Mg exposure (duration, daily dose, serum Mg concentration). Neonatal laboratory values at birth were also assessed. AKI occurred in 0% and 2.5% (1/40) of the short- and long-term groups, respectively; the affected case met creatinine-based AKI criteria but impairment was not clinically significant. ΔCr showed a weak positive correlation with treatment duration (ρ = 0.321, P = 0.009), while daily Mg dose and serum Mg levels were not correlated. Long-term group neonates showed higher serum Mg (P = 0.038) and lower Ca (P = 0.045). Long-term MgSO4 tocolysis may cause mild renal burden but appears unlikely to induce clinically significant maternal renal dysfunction under careful monitoring. Maternal and neonatal electrolyte monitoring is advisable during prolonged MgSO4 therapy.

