2017, Number 4
<< Back Next >>
Rev Hosp Jua Mex 2017; 84 (4)
Comparison of a furosemide stress test and biomarkers for the prediction of acute kidney injury
Pérez-Cruz E, Monroy-Chargoy A, Conde-Mercado JM, Méndez-Calderillo E
Language: Spanish
References: 35
Page: 196-202
PDF size: 204.55 Kb.
ABSTRACT
Background: Currently we have not an early marker to determine the progression of acute kidney injury (AKI) and the requirement for renal replacement therapy. The aim of this study was to compare the sensitivity (S) and specificity (E) of serum biomarkers versus furosemide stress test in patients with AKI.
Material and methods: Prospective, clinical study conducted from December 2016 to March 2017. All patients between 18 and 65 years with diagnosis of AKI AKIN 1 and 2 were included. Serum creatinine was determined (at the beginning and at 72 hours), cystatin C was measured, and a furosemide stress test was made.
Results: The early diagnostic test that had a greater significance with respect to the others for the prediction of the progression of AKI was the stress test with furosemide. Thirty-five patients were included, 71.4% men and 28.6% women, with a median age of 45 ± 12.1 years. The sensitivity and specificity of serum creatinine at 72 hours to predict the progression of AKI was 64.3% and 95.2%, respectively (χ
2 = 0.001); in relation to the prediction of the need for renal replacement therapy, the sensitivity was 75 % and the specificity, 85.2% (χ
2 = 0.001). The furosemide stress test showed a sensitivity of 57% and specificity of 95.2% (χ
2 = 0.001); regarding the prediction to receive renal replacement therapy, it had a sensitivity and specificity of 62.5% and 85.2%, respectively (χ
2 = 0.007).
Conclusion: The determination of serum creatinine at 72 hours showed adequate sensitivity and specificity, as did the furosemide stress test; however, the latter is more useful for predicting early progression of AKI and the requirement of renal replacement therapy.
REFERENCES
Nisula S, Kaukonen KM, Vaara ST, Korhonen AM, Poukkanen M, Karlsson S, et al. Incidence, risk factors and 90-day mortality of patients with acute kidney injury in Finnish intensive care units: the FINNAKI study. Intensive Care Med 2013; 39(3): 420-8.
Bellomo R, Kellum JA, Ronco C. Acute kidney injury. Lancet 2012; 380(9843): 756-66.
Verma SK, Molitoris BA. Renal endothelial injury and microvascular dysfunction in acute kidney injury. Semin Nephrol 2015; 35(1): 96-107.
Godin M, Murray P, Mehta RL. Clinical approach to the patient with AKI and sepsis. Semin Nephrol 2015; 35(1): 12-22.
Zafrani L, Payen D, Azoulay E, Ince C. The microcirculation of the septic kidney. Semin Nephrol 2015; 35(1): 75-84.
Macedo E, Mehta RL. Prerenal failure: from old concepts to new paradigms. Curr Opin Crit Care 2009; 15(6): 467-73.
Feehally J, Floege J, Savill J, Turner AN. Glomerular injury and glomerular response. In: AM Davison (Ed.) Oxford textbook of clinical nephrology. Oxford: Oxford University Press; 2005. pp. 363-87.
Stoegeman CA, Kallenberg CGM. Pathogenesis of angiitis. in: AM Davison (Ed.) Oxford textbook of clinical nephrology. Oxford: Oxford University Press; 2005. pp. 741-52.
Agarwal A, Dong Z, Harris R, Murray P, Parikh SM, Rosner MH, et al. Cellular and molecular mechanisms of AKI. J Am Soc Nephrol 2016; 27 (5): 1288-99.
Mahmoudi M, Willgoss D, Cuttle L, Yang T, Pat B, Winterford C, et al. In vivo and in vitro models demonstrate a role for caveolin-1 in the pathogenesis of ischaemic acute renal failure. J Pathol 2003; 200(3): 396-405.
Kaushal GP, Haun RS, Herzog C, Shah SV. Meprin A metalloproteinase and its role in acute kidney injury. Am J Physiol Renal Physiol 2013; 304(9): F1150-8.
Park F, Mattson DL, Roberts LA, Cowley AW Jr. Evidence for the presence of smooth muscle alpha actin within pericytes of the renal medulla. Am J Physiol 1997; 273(5 Pt 2): R1742-8.
Kennedy-Lydon TM, Crawford C, Wildman SS, Peppiatt-Wildman CM. Renal pericytes: regulators of medullary blood flow. Acta Physiol (Oxf) 2013; 207(2): 212-25.
Pallone TL, Silldorff EP. Pericyte regulation of renal medullary blood flow. Exp Nephrol. 2001; 9(3): 165-70.
Crawford C, Kennedy-Lydon TM, Callaghan H, Sprott C, Simmons RL, Sawbridge L, et al. Extracellular nucleotides affect pericyte-mediated regulation of rat in situ vasa recta diameter. Acta Physiol (Oxf) 2011; 202(3): 241-51.
Crawford C, Kennedy-Lydon T, Sprott C, Desai T, Sawbridge L, Munday J, et al. An intact kidney slice model to investigate vasa recta properties and function in situ. Nephron Physiol 2012; 120(3): 17-31.
Eglen RM, Reddy H, Watson N, Challiss RA. Muscarinic acetylcholine receptor subtypes in smooth muscle. Trends Pharmacol Sci 1994; 15(4): 114-9.
Macedo E, Malhotra R, Claure-Del Granado R, Fedullo P, Mehta RL. Defining urine output criterion for acute kidney injury in critically ill patients. Nephrol Dial Transplant 2011; 26(2): 509-15.
Bagshaw SM, Gibney RT. Acute kidney injury: clinical value of urine microscopy in acute kidney injury. Nat Rev Nephrol 2009; 5(4): 185-6.
Bagshaw SM, Bellomo R. Urine abnormalities in acute kidney injury and sepsis. Contrib Nephrol 2010; 165: 274-83.
Murray PT, Palevsky PM. Acute kidney injury and critical care nephrology. NephSAP 2007; 6(5): 286-90.
Van Biesen W, Vanholder R, Lamiere N. Defining acute renal failure: RIFLE and beyond. Clin J Am Soc Nephrol 2006; 1(6): 1314-9.
Bonventre JV, Basile D, Liu KD, McKay D, Molitoris BA, Nath KA, et al. AKI: a path forward. Clin J Am Soc Nephrol 2013; 8(9): 1606-08.
Jo SK, Rosner MH, Okusa MD. Pharmacologic treatment of acute kidney injury. Why drugs haven’t and what is on the horizon. Clin J Am Soc Nephrol 2007; 2(2): 356-65.
Brzin J, Popovic T, Turk V, Borchart U, Machleidt W. Human cystatin, a new protein inhibitor of cysteine proteinases. Biochem Biophys Res Commun 1984; 118(1): 103-9.
Kaseda R, Iino N, Hosojima M, Takeda T, Hosaka K, Kobayashi A, et al. Megalin-mediated endocytosis of cystatin C in proximal tubule cells. Biochem Biophys Res Commun 2007; 357(4): 1130-34.
Nejat M, Hill JV, Pickering JW, Edelstein CL, Devarajan P, Endre ZH. Albuminuria increases cystatin C excretion: implications for urinary biomarkers. Nephrol Dial Transplant 2012; 27 Suppl 3: iii96-103.
Togashi Y, Sakaguchi Y, Miyamoto M, Miyamoto Y. Urinary cystatin C as a biomarker for acute kidney injury and its immunohistochemical localization in kidney in the CDDP-treated rats. Exp Toxicol Pathol. 2012; 64 (7-8): 797-805.
Sasaki D, Yamada A, Umeno H, Kurihara H, Nakatsuji S, Fujihira S, et al. Comparison of the course of biomarker changes and kidney injury in a rat model of drug-induced acute kidney injury. Biomarkers 2011; 16(7): 553-66.
Hasannejad H, Takeda M, Taki K, Shin HJ, Babu E, Jutabha P, et al. Interactions of human organic anion transporters with diuretics. J Pharmacol Exp Ther 2004; 308(3): 1021-9.
Bowman RH. Renal secretion of furosemide and depression by albumin binding. Am J Physiol 1975; 229(1): 93-8.
Charlton JR, Portilla D, Okusa MD. A basic science view of acute kidney injury biomarkers. Nephrol Dial Transplant 2014; 29(7): 1301-11.
Koyner JL, Davison DL, Brasha-Mitchell E, Chalikonda DM, Arthur JM, Shaw AD, et al. Furosemide stress test and biomarkers for the prediction of AKI severity. J Am Soc Nephrol 2015; 26(8): 2023-31.
Parikh CR, Moledina DG, Coca SG, Thiessen-Philbrook HR, Garg AX. Application of new acute kidney injury biomarkers in human randomized controlled trials. Kidney Int 2016; 89(6): 1372-9.
Uchino S. Creatinine. Curr Opin Crit Care. 2010; 16(6): 562-7.