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. 2022 Jul;17(7):949-956.
doi: 10.2215/CJN.15231121. Epub 2022 Jun 28.

Urine Output Monitoring for the Diagnosis of Early-Onset Acute Kidney Injury in Very Preterm Infants

Affiliations

Urine Output Monitoring for the Diagnosis of Early-Onset Acute Kidney Injury in Very Preterm Infants

Aurélie De Mul et al. Clin J Am Soc Nephrol. 2022 Jul.

Abstract

Background and objectives: The current threshold used for oliguria in the definition of neonatal AKI has been empirically defined as 1 ml/kg per hour. Urine output criteria are generally poorly documented, resulting in uncertainty in the most accurate threshold to identify AKI in very preterm infants with known tubular immaturity.

Design, setting, participants, & measurements: We conducted a bicentric study including 473 very preterm infants (240/7-296/7 weeks of gestation) born between January 2014 and December 2018 with urine output measurements every 3 hours during the first 7 days of life and two serum creatinine measurements during the first 10 days of life. AKI was defined using the neonatal Kidney Disease Improving Global Outcomes (KDIGO) definition. We tested whether higher urine output thresholds (1.5 or 2 ml/kg per hour) in modified AKI definitions may better discriminate neonatal mortality compared with the current definition.

Results: Early-onset AKI was developed by 101 of 473 (21%) very preterm infants. AKI was diagnosed on the basis of urine output criteria alone (no rise in creatinine) for 27 of 101 (27%) participants. Early-onset AKI was associated with higher risk of death before discharge (adjusted odds ratio, 3.9; 95% confidence interval, 1.9 to 7.8), and the AKI neonatal KDIGO score showed good discriminative performance for neonatal mortality, with an area under the receiver operating characteristic (ROC) curve of 0.68 (95% confidence interval, 0.61 to 0.75). Modified AKI definitions that included higher urine output thresholds showed significantly improved discriminative performance, with areas under the ROC curve of 0.73 (95% confidence interval, 0.66 to 0.80) for the 1.5-ml/kg per hour threshold and 0.75 (95% confidence interval, 0.68 to 0.81) for the 2-ml/kg per hour threshold.

Conclusions: Early-onset AKI was diagnosed on the basis of urine output exclusively for a quarter of the cases. Furthermore, modified AKI definitions that included higher urine output improved the discriminative performance for predicting mortality.

Keywords: acute kidney injury; early diagnosis; infant; mortality; neonatal KDIGO; preterm; tubular immaturity; urine output; very preterm.

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Figures

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Graphical abstract
Figure 1.
Figure 1.
Study cohort flow chart.
Figure 2.
Figure 2.
Urine output and creatinine distribution among 473 very preterm infants and AKI incidence using different definitions: neonatal Kidney Disease Improving Global Outcomes (NKDIGO) versus very preterm AKI 1.5 versus very preterm AKI 2. Italic green numbers indicate patients diagnosed with the NKDIGO AKI definition. Bold red numbers indicate patients newly diagnosed with AKI using the modified definition: very preterm AKI 1.5 and 2. Stages 2 and 3 are not modified; 101 of 473 (21%) very preterm infants developed AKI according the NKDIGO definition. By raising the oliguria threshold for stage 1, 150 of 473 infants (32%) developed AKI using the very preterm AKI 1.5 definition, and 217 of 473 infants (46%) developed AKI using the very preterm AKI 2 definition. *The blue number indicates patients without AKI even using the modified definition.

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