Skip to main content

Impact of furosemide on mortality and the requirement for renal replacement therapy in acute kidney injury: a systematic review and meta-analysis of randomised trials



To 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 sources

PubMed (Medline) and Embase were searched from 1998 to October 2018.

Study selection

We 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 extraction

Two reviewers independently extracted appropriate data. PRISMA guidelines were followed for data preparation and reporting.

Data synthesis

We 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).


Furosemide 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.


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]. Therefore, it is not surprising that AKI develops quite frequently, affecting one in five of all hospitalised patients [2], and more than half of all patients admitted to the ICU [3]. AKI has serious sequelae: progression to chronic renal failure; increased risk and progression of multiple organ failure; increased risk of cardiovascular disease; and, finally, increased in-hospital mortality [4].

Pharmacological and non-pharmacological interventions are made for AKI treatment, including metabolic and haemodynamic stabilisation, growth factor and adenosine receptor antagonist’s administration. Unfortunately, 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. However, this is based on low evidence (II C recommendation). RRT is the only treatment option for severe AKI.

Previously, several investigators were concerned with increased mortality in patients with AKI treated with furosemide [5, 6]. These findings were rejected by many others [7, 8]. Due to the discrepancy mentioned earlier, the impact of furosemide on mortality in AKI patients has become a subject of several systematic reviews and meta-analyses [9,10,11,12,13]. As all of these meta-analyses included papers published over 20 years ago, their results should be cautiously extrapolated to current clinical practice due to evident changes in the treatment of the patients at risk of AKI (e.g. those with cardio-renal syndrome, sepsis, in the perioperative period, in the ICU setting). Therefore, we attempted to verify this interesting relationship taking into account the most recent data. We also sought to investigate the possible impact of furosemide on the requirement for renal replacement therapy (RRT).

Materials and methods

In this systematic review, we conducted a comprehensive literature search for studies published in English from 1998 up to October 2018. We searched the electronic databases PubMed (Medline) and Embase using a pre-specified strategy (Additional file 1: Table S1). The MeSH (Medical Subject Headings) terms and key words were: furosemide, mortality, renal replacement therapy, acute kidney injury, acute renal failure and renal insufficiency. We searched for all related randomised controlled trials (RCTs) that compared prevention or treatment with furosemide, to a placebo, standard of care or RRT in adult patients with AKI, or at risk of AKI (or acute renal failure). Moreover, additional relevant studies were searched manually by checking the reference lists of identified studies or reviews. We excluded unpublished reports and conference abstracts. Two independent investigators (LJK and PFCz) screened the abstracts and/or manuscripts and extracted appropriate data. Short-term mortality was considered a primary outcome while the requirement for RRT was a secondary outcome. If the outcomes (i.e. OR; 95% CI) for individual RCTs were not revealed in the index publications, we calculated them based on raw data. Subgroup analyses defined by intervention strategy (prevention/treatment), AKI origin (cardio-renal syndrome, contrast-induced nephropathy, post-cardiopulmonary bypass, critical illness), control arm comparator (RRT, saline/placebo/standard of care) and furosemide dose (< 160/≥ 160 mg) were also performed. PRISMA guidelines were followed for appropriate data preparation and reporting [14]. A review protocol regarding this study has not been published before. Flow diagram of the study selection process is presented in Fig. 1. The quality of the trials was verified using the RoB 2.0 tool for assessing the risk of bias in randomised trials (Table 1) [15]. No disagreements occurred between the investigators on the quality of data extracted.

Fig. 1
figure 1

Flow diagram of the study selection process

Table 1 Quality assessment of the included studies

Statistical analysis

Statistical analysis was performed using licensed MedCalc Statistical Software version 17.7 (MedCalc Software bvba, Ostend, Belgium;; 2017). We applied random and fixed effect models to verify the association between furosemide treatment and the outcomes. Odds ratios (OR) with 95% confidence intervals (95% CI) were calculated. Forest plots were drawn. We used I2 test to evaluate the magnitude of heterogeneity between studies, with values more than 50% defined as significant heterogeneity. Funnel plots were drawn to visually evaluate the potential publication bias. P < 0.05 was considered significant.


We identified 20 relevant studies (2608 patients: 1330 in the treatment arm and 1278 in the control arm) [7, 8, 16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33] (Table 2, Additional file 2: Table S2). There were 7 studies on AKI prevention and 13 studies describing AKI treatment with furosemide. Eight trials investigated AKI secondary to heart failure (i.e. cardio-renal syndrome), 4 described contrast-induced AKI (i.e. contrast-induced nephropathy), and 4 studies were conducted in the ICU setting (i.e. AKI of heterogeneous origin). Eighteen trials revealed data on mortality, while 8 trials presented data on the need for RRT. The quality of the papers was deemed suboptimal with the risk of bias noticeable across them (Table 1). Nineteen were included in the meta-analysis (i.e. except from the study of Lim [29]). It was possible to calculate the daily furosemide dose in 17 studies (i.e. apart from the studies of Barbanti [18], Hanna [28] and van der Voort [33]), based on mean or median values given by the authors, or based on the infusion rate and body weight of the participants. This ranged from 20 to 2500 mg, with a median value of 160 mg. A detailed description of all reviewed and included trials is presented in Supplemental Digital Content.

Table 2 Systematic review of studies on furosemide and the outcome

Furosemide had no impact on mortality (random effect model OR = 1.051, 95% CI 0.825–1.339, p = 0.4; fixed effect model OR = 1.051, 95% CI 0.827–1.334, p = 0.4) (Fig. 2). Heterogeneity between studies was low (I2 = 0%, 95% CI 0–10.4%, p = 0.9), and publication bias was low (Additional file 3: Figure S1A). Furosemide had no impact on the need for RRT (random effect model OR = 0.947, 95% CI 0.521–1.721, p = 0.2; fixed effect model OR = 0.878, 95% CI 0.602–1.281, p = 0.7) (Fig. 3). Heterogeneity was acceptable (I2 = 28.62%, 95% CI 0–69.29%, p = 0.2), and publication bias was low (Additional file 4: Figure S1B).

Fig. 2
figure 2

Forest plot for furosemide use and mortality

Fig. 3
figure 3

Forest plot for furosemide use and the requirement for renal replacement therapy

The results of additional analyses are shown in Table 3. Irrespective of intervention strategy (prevention/treatment), AKI origin (cardio-renal syndrome, post-cardiopulmonary bypass, critical illness), control arm comparator (RRT, saline/placebo/standard of care) and furosemide dose (< 160/≥ 160 mg), there was no effect of furosemide either on mortality or the need for RRT. However, subjects who received furosemide with matched hydration in the prevention of CIN had a less frequent need for RRT (by 79%, with borderline significance).

Table 3 Subgroup analyses


In this systematic review of 20 RCTs covering over 2600 patients with AKI, or at risk of AKI, we found that furosemide had an impact neither on mortality nor on the requirement for RRT. Furosemide had no effect on the outcomes regardless of intervention strategy, AKI origin, control arm comparator and furosemide dose. Only patients at risk of CIN may benefit from furosemide administration.

These observations are comparable with the available data. In the most recent meta-analysis, Bove et al. [13] revealed no association between furosemide and mortality, the need for RRT, length of hospital stay and worsening of AKI. The authors found significant improvement in survival of patients receiving furosemide as a preventive measure (OR = 0.62; 95% CI 0.41–0.94). It needs to be underlined that they included 8 studies published over 20 years ago and compared intermittent furosemide administration (only) with any comparator (including continuous furosemide infusion) in subjects with or at risk of AKI. In their meta-analysis published in 2006, Ho and Sheridan [9] also found no impact of furosemide, either on mortality or on the need for RRT, regardless of the fact whether it was used to prevent acute deterioration of renal function or treat acute renal failure. However, they included only 9 RCTs describing ARF patients, while only 3 of them investigated the requirement dialysis. Moreover, Bagshaw et al. [10] in 2007 described no effect of furosemide on mortality and renal recovery. In their study, loop diuretics were associated with a shorter duration of RRT (by 1.4 days), a shorter time to spontaneous decline in serum creatinine level (by 2.1 days) and a greater increase in urine output from the baseline (OR = 2.56; 95% CI 1.35–4.85). However, they analysed 5 RCTs only, 4 of which were published over 20 years ago, and all of which were of very low quality. Last but not least, Cheng et al. [34] in their meta-analysis of 7 RCTs, revealed comparable mortality between patients with decompensated heart failure receiving heamofiltration or diuretics (OR = 0.95; 95% CI 0.58–1.55).

Our findings are also in line with the results of Putzu et al. [35] who evaluated whether the administration of furosemide with matched hydration using the RenalGuard System might have reduced the incidence of CIN. Based on 4 trials, they found the beneficial impact of furosemide use on CIN occurrence (OR = 0.31; 95% CI 0.19–0.50), as well as the need for RRT (OR = 0.19; 95% CI 0.05–0.79).

From a clinical point of view, our observations are of particular importance to practitioners as, based on experimental data, furosemide may have some detrimental effects in patients with or at risk of AKI [5, 6, 36]. This observation plays also a key role in determining the necessity of early initiation of RRT in critically ill subjects with deterioration of renal function and/or fluid overload. This is in line with the above-mentioned observations of Cheng et al. [34].

Fluid overload is frequently found in AKI patients in the ICU setting. Fluid excess of at least 10% is associated with increased mortality and morbidity, including pulmonary oedema, cardiac failure, delayed wound healing, tissue breakdown and impaired bowel function [37, 38]. Although there are several methods of evaluating fluid status, most of them are fairly inaccurate [39, 40]. Moreover, the optimisation and management of fluid therapy remains difficult [41,42,43]. Diuretics are considered a reasonable first-line treatment but only in responsive subjects [1]. When selecting a diuretic, clinicians should consider evidence-based indications, possible adverse effects, compatibility, pharmacokinetics and other issues of particular diuretics [36]. Diuretics are not recommended to treat AKI per se but are suggested to treat volume overload [37]. According to current data, it is still difficult to predict which patients will respond to diuretics and which patients will benefit from early initiation of RRT.

The severity of AKI alters both the pharmacokinetics and pharmacodynamics of furosemide [40], making appropriate dosing of this agent difficult. The requirement for increased dosing of loop diuretics is associated with worse AKI prognosis in patients with congestive heart failure [44] and in other groups of critically ill subjects [45]. The use of high-dose furosemide to convert oliguric to non-oliguric AKI may exacerbate injury to the kidneys (increased markers of oxidative stress), especially in hypovolaemic patients with reduced renal perfusion [46].

Based on our results, implementation of RRT should be considered at an early stage of critical illness in patients with fluid overload, as well as those with AKI and concomitant indications for immediate extracorporeal treatment [47]. The effect of RRT modality seems to be of lower importance [48, 49].

Study limitations

Firstly, we focused on trials published only in the last 20 years. All previous meta-analyses took into account data published before 1998. Although this subjective decision may cause publication bias, one ought to remember that clinical practice has improved markedly: currently we do not use such high doses of furosemide due to its side effects, while the pharmacological and non-pharmacological treatment of many co-existing acute conditions in critically ill patients has changed (acute heart failure treatment, antimicrobial treatment, perioperative care, fluid therapy, etc.). In addition, an understanding of the role of RRT in critical illness has led to its earlier implementation. Secondly, almost all data from the ICU setting compared furosemide with alternative pharmacological treatment (usually a placebo). So far, no single randomised trial has reported a comparison between furosemide and any modality of RRT in this heterogeneous group of critically ill patients. We can only extrapolate data from patients with isolated AKI due to acute decompensated heart failure to current ICU practice. Thirdly, as there are newer intravenous diuretics available on the market, including torasemide and aldactone, further research is needed to investigate their effect (on its own or in combination with furosemide) on mortality in AKI. Finally, our observations need further investigations. In the era of numerous non-renal indications for RRT, which are usually considered in the mixed population of ICU subjects, our results may be inadequate. Moreover, the quality of previously published RCTs remains suboptimal, while the heterogeneity of the populations recruited in earlier trials constitutes an important limitation in generalising results.


Based on our meta-analysis of RCTs, furosemide administration has no impact either on mortality or on the requirement for RRT, regardless of intervention strategy, AKI origin, control arm comparator and furosemide dose. However, patients at risk of CIN may benefit from furosemide treatment, if proper hydration is guaranteed beforehand. Further well-designed RCTs are needed in order to verify these findings.

Availability of data and materials

All data generated or analysed during this study are included in this published article [and its supplementary information files].


  1. Kidney Disease: Improving Global Outcomes (KDIGO) Acute Kidney Injury Work Group. KDIGO clinical practice guideline for acute kidney injury. Kidney Int Suppl. 2012;2:1–138.

    Article  Google Scholar 

  2. Uchino S, Bellomo R, Goldsmith D, et al. An assessment of the RIFLE criteria for acute renal failure in hospitalized patients. Crit Care Med. 2006;34:1913–7.

    Article  PubMed  Google Scholar 

  3. Hoste EA, Clermont G, Kersten A, et al. RIFLE criteria for acute kidney injury are associated with hospital mortality in critically ill patients: a cohort analysis. Crit Care. 2006;10:R73.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Hoste EA, Kellum JA. Acute renal failure in the critically ill: impact on morbidity and mortality. Contrib Nephrol. 2004;144:1–11.

    Article  PubMed  Google Scholar 

  5. Minuth AN, Terrell JB Jr, Suki WN. Acute renal failure: a study of the course and prognosis of 104 patients and of the role of furosemide. Am J Med Sci. 1976;271(3):317–24.

    Article  CAS  PubMed  Google Scholar 

  6. Mehta RL, Pascual MT, Soroko S, et al. Diuretics, mortality, and nonrecovery of renal function in acute renal failure. JAMA. 2002;288(20):2547–53.

    Article  CAS  PubMed  Google Scholar 

  7. Lassnigg A, Donner E, Grubhofer G, et al. Lack of renoprotective effects of dopamine and furosemide during cardiac surgery. J Am Soc Nephrol. 2000;11(1):97–104.

    CAS  PubMed  Google Scholar 

  8. Cantarovich F, Rangoonwala B, Lorenz H, et al. High-dose furosemide for established ARF: a prospective, randomized, double-blind, placebo-controlled, multicenter trial. Am J Kidney Dis. 2004;44(3):402–9.

    Article  CAS  PubMed  Google Scholar 

  9. Ho KM, Sheridan DJ. Meta-analysis of frusemide to prevent or treat acute renal failure. BMJ. 2006;333:420–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Bagshaw SM, Delaney A, Haase M, et al. Loop diuretics in the management of acute renal failure: a systematic review and meta-analysis. Crit Care Resusc. 2007;9:60–8.

    PubMed  Google Scholar 

  11. Karajala V, Mansour W, Kellum JA. Diuretics in acute kidney injury. Minerva Anestesiol. 2009;75(5):251–7.

    CAS  PubMed  Google Scholar 

  12. Landoni G, Bove T, Székely A, et al. Reducing mortality in acute kidney injury patients: systematic review and international web-based survey. J Cardiothorac Vasc Anesth. 2013;27(6):1384–98.

    Article  PubMed  Google Scholar 

  13. Bove T, Belletti A, Putzu A, et al. Intermittent furosemide administration in patients with or at risk for acute kidney injury: meta-analysis of randomized trials. PLoS One. 2018;13(4):1–18.

    Article  Google Scholar 

  14. PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines.

  15. Higgins JP, Altman DG, Gøtzsche PC, et al. The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ. 2011;343:d5928.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Badawy SI, Fahmy A. Efficacy and cardiovascular tolerability of continuous veno-venous hemodiafiltration in acute decompensated heart failure: a randomized comparative study. J Crit Care. 2012;27(1):7–13.

    Article  Google Scholar 

  17. Bagshaw SM, Gibney RTN, Kruger P, et al. The effect of low-dose furosemide in critically ill patients with early acute kidney injury: a pilot randomized blinded controlled trial (the SPARK study). J Crit Care. 2017;42:138–46.

    Article  CAS  PubMed  Google Scholar 

  18. Barbanti M, Gulino S, Capranzano P, et al. Acute kidney injury with the RenalGuard System in patients undergoing transcatheter aortic valve replacement: the PROTECT-TAVI Trial (PROphylactic effecT of furosEmide-induCed diuresis with matched isotonic intravenous hydraTion in Transcatheter Aortic Valve Implantation). JACC Cardiovasc Interv. 2015;8(12):1595–604.

    Article  PubMed  Google Scholar 

  19. Bart BA, Boyle A, Bank AJ, et al. Ultrafiltration versus usual care for hospitalized patients with heart failure: the Relief for Acutely Fluid-Overloaded Patients With Decompensated Congestive Heart Failure (RAPID-CHF) trial. J Am Coll Cardiol. 2005;46(11):2043–6.

    Article  PubMed  Google Scholar 

  20. Bart BA, Goldsmith SR, Lee KL, et al. Ultrafiltration in decompensated heart failure with cardiorenal syndrome. N Engl J Med. 2012;367(24):2296–304.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Berthelsen RE, Perner A, Jensen AK, et al. Forced fluid removal in intensive care patients with acute kidney injury: the randomised FFAKI feasibility trial. Acta Anaesthesiol Scand. 2018;62(7):936–44.

    Article  CAS  PubMed  Google Scholar 

  22. Briguori C, Visconti G, Focaccio A, et al. Renal Insufficiency After Contrast Media Administration Trial II (REMEDIAL II): renalGuard System in high-risk patients for contrast-induced acute kidney injury. Circulation. 2011;124(11):1260–9.

    Article  CAS  PubMed  Google Scholar 

  23. Costanzo MR, Johannes RS, Pine M, et al. The safety of intravenous diuretics alone versus diuretics plus parenteral vasoactive therapies in hospitalized patients with acutely decompensated heart failure: a propensity score and instrumental variable analysis using the Acutely Decompensated Heart Failure National Registry (ADHERE) database. Am Heart J. 2007;154(2):267–77.

    Article  CAS  PubMed  Google Scholar 

  24. Costanzo MR, Saltzberg MT, Jessup M, et al. Ultrafiltration is associated with fewer rehospitalizations than continuous diuretic infusion in patients with decompensated heart failure: results from UNLOAD. J Card Fail. 2010;16(4):277–84.

    Article  PubMed  Google Scholar 

  25. Costanzo MR, Negoianu D, Jaski BE, et al. Aquapheresis versus intravenous diuretics and hospitalizations for heart failure. JACC Heart Fail. 2016;4(2):95–105.

    Article  PubMed  Google Scholar 

  26. Dussol B, Morange S, Loundoun A, et al. A randomized trial of saline hydration to prevent contrast nephropathy in chronic renal failure patients. Nephrol Dial Transplant. 2006;21(8):2120–6.

    Article  CAS  PubMed  Google Scholar 

  27. Grams ME, Estrella MM, Coresh J, et al. Fluid balance, diuretic use, and mortality in acute kidney injury. Clin J Am Soc Nephrol. 2011;6(5):966–73.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Hanna MA, Tang WH, Teo BW, et al. Extracorporeal ultrafiltration vs. conventional diuretic therapy in advanced decompensated heart failure. Congest Heart Fail. 2012;18(1):54–63.

    Article  CAS  PubMed  Google Scholar 

  29. Lim E, Ali ZA, Attaran R, et al. Evaluating routine diuretics after coronary surgery: a prospective randomized controlled trial. Ann Thorac Surg. 2002;73(1):153–5.

    Article  PubMed  Google Scholar 

  30. Mahesh B, Yim B, Robson D, et al. Does furosemide prevent renal dysfunction in high-risk cardiac surgical patients? Results of a double-blinded prospective randomised trial. Eur J Cardiothorac Surg. 2008;33(3):370–6.

    Article  PubMed  Google Scholar 

  31. Marenzi G, Ferrari C, Marana I, et al. Prevention of contrast nephropathy by furosemide with matched hydration: the MYTHOS (induced diuresis with matched hydration compared to standard hydration for contrast induced nephropathy prevention) trial. JACC Cardiovasc Interv. 2012;5(1):90–7.

    Article  PubMed  Google Scholar 

  32. Marenzi G, Muratori M, Cosentino ER, et al. Continuous ultrafiltration for congestive heart failure: the CUORE trial. J Card Fail. 2014;20(5):1–9.

    Google Scholar 

  33. van der Voort PH, Boerma EC, Koopmans M, et al. Furosemide does not improve renal recovery after hemofiltration for acute renal failure in critically ill patients: a double blind randomized controlled trial. Crit Care Med. 2009;37(2):533–8.

    Article  PubMed  Google Scholar 

  34. Cheng Z, Wang L, Hu S. Efficacy and safety of ultrafiltration in decompensated heart failure patients with renal insufficiency. Int Heart J. 2015;56:319–23.

    Article  PubMed  Google Scholar 

  35. Putzu A, Boscolo Berto M, Belletti A, et al. Prevention of contrast-induced acute kidney injury by furosemide with matched hydration in patients undergoing interventional procedures: a systematic review and meta-analysis of randomized trials. JACC Cardiovasc Interv. 2017;10(4):355–63.

    Article  PubMed  Google Scholar 

  36. Krzych Ł, Czempik P. Loop diuretics and mortality in patients with acute kidney injury. In: Landoni G, Pisano A, Zangrillo A, Bellomo R, editors. Reducing mortality in acute kidney injury. Bern: Springer; 2016. p. 175–84.

    Chapter  Google Scholar 

  37. Joannidis M, Druml W, Forni LG, et al. Prevention of acute kidney injury and protection of renal function in the intensive care unit: update 2017: expert opinion of the Working Group on Prevention, AKI section, European Society of Intensive Care Medicine. Intensive Care Med. 2017;43(6):730–49.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Malbrain ML, Marik PE, Witters I, et al. Fluid overload, de-resuscitation, and outcomes in critically ill or injured patients: a systematic review with suggestions for clinical practice. Anaesthesiol Intensive Ther. 2014;46(5):361–80.

    Article  PubMed  Google Scholar 

  39. Claure-Del Granado R, Mehta RL. Fluid overload in the ICU: evaluation and management. BMC Nephrol. 2016;17(1):109.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Silbert BI, Ho KM, Lipman J, et al. Determinants of urinary output response to IV furosemide in acute kidney injury: a pharmacokinetic/pharmacodynamic study. Crit Care Med. 2016;44(10):923–9.

    Article  Google Scholar 

  41. Malbrain ML, Van Regenmortel N, Owczuk R. The debate on fluid management and haemodynamic monitoring continues: between Scylla and Charybdis, or faith and evidence. Anaesthesiol Intensive Ther. 2014;46(5):313–8.

    Article  PubMed  Google Scholar 

  42. Hahn RG, He R, Li Y. Central venous pressure as an adjunct to flow-guided volume optimisation after induction of general anaesthesia. Anaesthesiol Intensive Ther. 2016;48(2):110–5.

    Article  PubMed  Google Scholar 

  43. van der Mullen J, Wise R, Vermeulen G, et al. Assessment of hypovolaemia in the critically ill. Anaesthesiol Intensive Ther. 2018;50(2):141–9.

    Article  PubMed  Google Scholar 

  44. Ricci F, Ramírez T, Marmorato R, et al. Predisposing factors for acute kidney injury in Hispanic patients treated with diuretics for decompensated heart failure. P R Health Sci J. 2013;32(2):63–7.

    PubMed  Google Scholar 

  45. de Louw EJ, Sun PO, Lee J, et al. Increased incidence of diuretic use in critically ill obese patients. J Crit Care. 2015;30(3):619–23.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Silbert BI, Ho KM, Lipman J, et al. Does furosemide increase oxidative stress in acute kidney injury? Antioxid Redox Signal. 2017;26(5):221–6.

    Article  CAS  PubMed  Google Scholar 

  47. Shiao CC, Huang TM, Spapen HD, et al. Optimal timing of renal replacement therapy initiation in acute kidney injury: the elephant felt by the blindmen? Crit Care. 2017;21(1):146.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Czempik P, Cieśla D, Knapik P, et al. Outcomes of patients with acute kidney injury with regard to time of initiation and modality of renal replacement therapy—first data from the Silesian Registry of Intensive Care Units. Kardiochir Torakochirurgia Pol. 2016;13(2):122–9.

    PubMed  PubMed Central  Google Scholar 

  49. Nash DM, Przech S, Wald R, et al. Systematic review and meta-analysis of renal replacement therapy modalities for acute kidney injury in the intensive care unit. J Crit Care. 2017;41:138–44.

    Article  PubMed  Google Scholar 

Download references


Not applicable.


Not applicable.

Author information

Authors and Affiliations



LJK and PFCz screened the abstracts and/or manuscripts and extracted appropriate data. LJK performed statistical analysis. LJK and PFCz read and approved the final manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Piotr F. Czempik.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Additional files

Additional file 1: Table S1.

Search strategy.

Additional file 2: Table S2.

Detailed characteristics of included studies.

Additional file 3: Figure S1A.

Funnel plot for studies on mortality.

Additional file 4: Figure S1B.

Funnel plot for studies on the requirement for renal replacement therapy.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Krzych, Ł.J., Czempik, P.F. Impact of furosemide on mortality and the requirement for renal replacement therapy in acute kidney injury: a systematic review and meta-analysis of randomised trials. Ann. Intensive Care 9, 85 (2019).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: