Furosemide as a functional marker of acute kidney injury in ICU patients: a new role for an old drug

2019 ◽  
Vol 32 (6) ◽  
pp. 883-893 ◽  
Author(s):  
Filippo Mariano ◽  
Alberto Mella ◽  
Marco Vincenti ◽  
Luigi Biancone
CHEST Journal ◽  
2014 ◽  
Vol 146 (4) ◽  
pp. 223A ◽  
Author(s):  
Syed Amin ◽  
Reejis Stephen ◽  
David Morris ◽  
David Kaufman

2019 ◽  
Vol 41 (4) ◽  
pp. 462-471 ◽  
Author(s):  
Kellen Hyde Elias Pinheiro ◽  
Franciana Aguiar Azêdo ◽  
Kelsy Catherina Nema Areco ◽  
Sandra Maria Rodrigues Laranja

Abstract Acute kidney injury (AKI) has an incidence rate of 5-6% among intensive care unit (ICU) patients and sepsis is the most frequent etiology. Aims: To assess patients in the ICU that developed AKI, AKI on chronic kidney disease (CKD), and/or sepsis, and identify the risk factors and outcomes of these diseases. Methods: A prospective observational cohort quantitative study that included patients who stayed in the ICU > 48 hours and had not been on dialysis previously was carried out. Results: 302 patients were included and divided into: no sepsis and no AKI (nsnAKI), sepsis alone (S), septic AKI (sAKI), non-septic AKI (nsAKI), septic AKI on CKD (sAKI/CKD), and non-septic AKI on CKD (nsAKI/CKD). It was observed that 94% of the patients developed some degree of AKI. Kidney Disease Improving Global Outcomes (KDIGO) stage 3 was predominant in the septic groups (p = 0.018). Nephrologist follow-up in the non-septic patients was only 23% vs. 54% in the septic groups (p < 0.001). Dialysis was performed in 8% of the non-septic and 37% of the septic groups (p < 0.001). Mechanical ventilation (MV) requirement was higher in the septic groups (p < 0.001). Mortality was 38 and 39% in the sAKI and sAKI/CKD groups vs 16% and 0% in the nsAKI and nsAKI/CKD groups, respectively (p < 0.001). Conclusions: Patients with sAKI and sAKI/CKD had worse prognosis than those with nsAKI and nsAKI/CKD. The nephrologist was not contacted in a large number of AKI cases, except for KDIGO stage 3, which directly influenced mortality rates. The urine output was considerably impaired, ICU stay was longer, use of MV and mortality were higher when kidney injury was combined with sepsis.


2019 ◽  
Vol 85 (7) ◽  
pp. 725-729 ◽  
Author(s):  
Joshua Parreco ◽  
Hahn Soe-Lin ◽  
Jonathan J. Parks ◽  
Saskya Byerly ◽  
Matthew Chatoor ◽  
...  

Prior studies have used vital signs and laboratory measurements with conventional modeling techniques to predict acute kidney injury (AKI). The purpose of this study was to use the trend in vital signs and laboratory measurements with machine learning algorithms for predicting AKI in ICU patients. The eICU Collaborative Research Database was queried for five consecutive days of laboratory measurements per patient. Patients with AKI were identified and trends in vital signs and laboratory values were determined by calculating the slope of the least-squares-fit linear equation using three days for each value. Different machine learning classifiers (gradient boosted trees [GBT], logistic regression, and deep learning) were trained to predict AKI using the laboratory values, vital signs, and slopes. There were 151,098 ICU stays identified and the rate of AKI was 5.6 per cent. The best performing algorithm was GBT with an AUC of 0.834 ± 0.006 and an F-measure of 42.96 per cent ± 1.26 per cent. Logistic regression performed with an AUC of 0.827 ± 0.004 and an F-measure of 28.29 per cent ± 1.01 per cent. Deep learning performed with an AUC of 0.817 ± 0.005 and an F-measure of 42.89 per cent ± 0.91 per cent. The most important variable for GBT was the slope of the minimum creatinine (30.32%). This study identifies the best performing machine learning algorithms for predicting AKI using trends in laboratory values in ICU patients. Early identification of these patients using readily available data indicates that incorporating machine learning predictive models into electronic medical record systems is an inevitable requisite for improving patient outcomes.


2018 ◽  
Vol 50 (11) ◽  
pp. 2111-2112
Author(s):  
Liu-Jia-Zi Shao ◽  
Fu-Shan Xue ◽  
Rui-Juan Guo ◽  
Li Zheng

Author(s):  
Martin Beed ◽  
Richard Sherman ◽  
Ravi Mahajan

Fluid balance disordersAcute kidney injuryRhabdomyolysis/crush syndromeFluid balance disorders include hypovolaemia (oligaemia), dehydration/acute fluid depletion, and hypervolaemia/fluid overload. Careful attention to fluid balance is essential in ICU. Patients are likely to require ‘maintenance’ fluids in addition to any fluid resuscitation.Hypovolaemia (see also Shock, ...


2018 ◽  
Vol 33 (suppl_1) ◽  
pp. i262-i263
Author(s):  
Robin Lohse ◽  
Michael Ibsen ◽  
Jørgen Wiis ◽  
Anders Perner ◽  
Theis Lange ◽  
...  

2019 ◽  
Vol 156 (6) ◽  
pp. S-1351
Author(s):  
Ahmed M. Agameya ◽  
Lolwa Al Obaid ◽  
Ainul Wahajia ◽  
Ahmed Abdelfattah ◽  
Yuxiu Lei ◽  
...  

Nephron ◽  
2015 ◽  
Vol 131 (1) ◽  
pp. 23-33 ◽  
Author(s):  
Jorge Ruiz-Criado ◽  
Maria-Angeles Ramos-Barron ◽  
Gema Fernandez-Fresnedo ◽  
Emilio Rodrigo ◽  
Angel-Luis Martin De Francisco ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Caren Cristina Grabulosa ◽  
Marcelo Costa Batista ◽  
Miguel Cendoroglo ◽  
Beata Marie Redublo Quinto ◽  
Roberto Narciso ◽  
...  

Genetic variations in TGF-βand IFN-γmay interfere with proinflammatory cytokine production and, consequently, may be involved with inflammatory diseases, as acute kidney injury (AKI). We considered that genetic polymorphisms of these cytokines may have a crucial role in the outcome of critically ill patients. To investigate whether the genetic polymorphisms of rs1800470 (codon 10 T/C), rs1800471 (codon 25 C/G) from the TGF-β, and rs2430561 (+874 T/A) from IFN-γmay be a risk factor for ICU patients to the development of AKI and/or death. In a prospective nested case-control study, were included 139 ICU patients who developed AKI, 164 ICU patients without AKI, and 244 healthy individuals. We observed a higher frequency to T/A genotype for IFN-γ(intermediate producer phenotype) and higher frequency of TT GG and TC GG genotype (high producer) for TGF-βpolymorphism in overall population. However, these polymorphisms have not been shown as a predictor of risk for AKI and death. We found an increased prevalence of high and intermediate producer phenotypes from TGF-βand IFN-γ, respectively, in patients in ICU setting. However, the studied genetic polymorphism of the TGF-βand IFN-γwas not associated as a risk factor for AKI or death in our population.


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