Acute kidney injury e-alerts in pregnancy: rates, recognition and recovery

Author:

Gama Rouvick M1,Clark Katherine2,Bhaduri Mahua3,Clery Amanda4,Wright Kelly1,Smith Priscilla1,Martin Hayley3,Vincent Royce P5,Jayawardene Satish1,Bramham Kate12

Affiliation:

1. King’s Kidney Care, King’s College Hospital NHS Trust, London, UK

2. Department of Women and Children’s Health, School of Life Course Sciences, King’s College London, London, UK

3. Department of Obstetrics and Gynaecology, King’s College Hospital NHS Foundation Trust, London, UK

4. School of Population Health and Environmental Sciences, King’s College London, London, UK

5. Department of Biochemistry (Viapath), King’s College Hospital NHS Foundation Trust, London, UK

Abstract

Abstract Background Acute kidney injury (AKI) in pregnancy (Pr-AKI) is associated with substantial maternal morbidity and mortality. E-alerts are routinely used for detection of AKI in non-pregnant patients but their role in maternity care has not been explored. Methods All pregnant or postpartum women with AKI e-alerts for AKI Stages 1–3 (Kidney Disease Improving Global Outcomes (KDIGO) criteria) were identified at a tertiary centre >2 years. Two women matched by delivery date for each case were selected as controls. AKI stage, recognition of AKI, pregnancy outcomes, renal recovery, AKI aetiology and risk factors were extracted from electronic patient records. Results 288 of 11 922 (2.4%) women had AKI e-alerts, of which only 118 (41%) were recognized by the obstetric team. Common Pr-AKI causes included infection (48%), pre-eclampsia (26%) and haemorrhage (25%), but no cause was identified in 15% of women. Renal function recovered in 213 (74%) women, but in 47 (17%) repeat testing was not undertaken and 28 (10%) did not recover function. Hypertensive disorders of pregnancy and Caesarean section were associated with increased incidence of Pr-AKI compared with controls. Conclusions Pr-AKI e-alerts were identified in ∼1 in 40 pregnancies. However, a cause for Pr-AKI was not identified in many cases and e-alerts may have been triggered by gestational change in serum creatinine. Pregnancy-specific e-alert algorithms may be required. However, 1 in 10 women with Pr-AKI had not recovered kidney function on repeat testing. Better understanding of long-term impacts of Pr-AKI on pregnancy and renal outcomes is needed to inform relevant Pr-AKI e-alert thresholds.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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