Avichai Weissbach, Liron Sadovski, Victoria Finkel, Gili Kadmon, Elhanan Nahum, Rotem Davidovich, Gal Benshalom, Eytan Kaplan
In newborns with TGA, PPHN was associated with increased postoperative morbidity. While no statistically significant difference in early mortality was observed, larger multicenter studies are needed to better define the impact of PPHN on mortality risk.
BACKGROUND: Data on metolazone in children with fluid overload and moderate-to-severe acute kidney injury (AKI) inadequately responsive to continuous furosemide infusion are limited. We describe its use and factors associated with kidney replacement therapy (KRT).
METHODS: This retrospective cohort study in a pediatric intensive care unit included patients with KDIGO stage 2/3 AKI, continuous furosemide infusion, metolazone for inadequate urine output, and no chronic dialysis. Urine output was compared between the 6 h before metolazone and predefined 48-h intervals. Multivariable logistic regression and receiver operating characteristic (ROC) analysis evaluated associations with KRT.
RESULTS: Of 196 metolazone-treated children, 62 met inclusion criteria. Median age was 40.5 months (IQR 11-144.5); 61% had stage 3 AKI, 90% were invasively ventilated, and median vasoactive-inotropic score was 10 (IQR 0-26). Median urine output increased from 0.8 mL/kg/h before metolazone to 1.49, 1.37, 2.5, and 2.68 mL/kg/h during 0-6, 6-12, 12-24, and 24-48 h, respectively (all p < 0.01). Children received a median of 3 doses over 48 h. Twenty children (32%) required KRT. Greater 12-24-h urine-output increase was associated with lower KRT odds (odds ratio 0.59, 95% CI 0.36-0.96; p = 0.034). AUC was 0.708 (95% CI 0.568-0.849; p = 0.010), with optimal cutoff ≥ 0.85 mL/kg/h; in 24-h landmark analysis, AUC was 0.683 (95% CI 0.527-0.838; p = 0.021), with the same cutoff.
CONCLUSIONS: Metolazone initiation was followed by increased urine output. Response was associated with lower KRT likelihood. These exploratory findings require prospective validation.