Abstract

ObjectiveTo examine the impact of furosemide on mortality and the need for renal replacement therapy (RRT) in adult patients with acute kidney injury (AKI) based on current evidence.Data sourcesPubMed (Medline) and Embase were searched from 1998 to October 2018.Study selectionWe retrieved data from randomised controlled trials comparing prevention/treatment with furosemide at any stage of AKI with alternative treatment/standard of care/placebo. The outcome was short-term mortality and the requirement for RRT, when applicable.Data extractionTwo reviewers independently extracted appropriate data. PRISMA guidelines were followed for data preparation and reporting.Data synthesisWe identified 20 relevant studies (2608 patients: 1330 in the treatment arm and 1278 in the control arm). Heterogeneity between studies was deemed acceptable, and the publication bias was low. Furosemide had neither an impact on mortality (OR = 1.015; 95% CI 0.825–1.339) nor the need for RRT (OR = 0.947; 95% CI 0.521–1.721). Furosemide had also no effect on the outcomes in strata defined by intervention strategy (prevention/treatment), AKI origin (cardio-renal syndrome, post-cardiopulmonary bypass, critical illness), control arm comparator (RRT, saline/placebo/standard of care) and its dose (< 160/≥ 160 mg) (p > 0.05 for all). Subjects who received furosemide with matched hydration in prevention of contrast-induced nephropathy (CIN) had a less frequent need for RRT (OR = 0.218; 95% CI 0.05–1.04; p = 0.055).ConclusionsFurosemide administration has neither an impact on mortality nor the requirement for RRT. Patients at risk of CIN may benefit from furosemide administration. Further well-designed RCTs are needed to verify these findings.

Highlights

  • Acute kidney injury (AKI) constitutes a serious clinical hazard in critically ill patients

  • Patients at risk of contrast-induced nephropathy (CIN) may benefit from furosemide administration

  • Eight trials investigated AKI secondary to heart failure, 4 described contrast-induced AKI, and 4 studies were conducted in the intensive care unit (ICU) setting (i.e. AKI of heterogeneous origin)

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Summary

Introduction

Acute kidney injury (AKI) constitutes a serious clinical hazard in critically ill patients. There are multiple acknowledged risk factors for AKI which can be found in the intensive care unit (ICU) setting, including sepsis, circulatory shock, trauma, and use of nephrotoxic drugs [1]. Pharmacological and non-pharmacological interventions are made for AKI treatment, including metabolic and haemodynamic stabilisation, growth factor and adenosine receptor antagonist’s administration. Some of these were found to have unsatisfactory results. According to KDIGO guidelines [1], diuretics should not be used for the treatment of AKI, except for fluid overload. This is based on low evidence (II C recommendation).

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