Literature DB >> 23400860

Pathophysiology and management of septic acute kidney injury.

Adam Romanovsky1, Catherine Morgan, Sean M Bagshaw.   

Abstract

Acute kidney injury (AKI) is a commonly encountered complication in critically ill children and portends a worse prognosis. Sepsis-induced AKI (SAKI) is a leading contributor to AKI in children and significantly modifies the risk for less favorable outcome. It has increasingly become clear that SAKI represents a unique and distinct cause of AKI. Studies focused on renal hemodynamics, bioenergetics, and immune-mediated injury have provided further insights into the pathobiology of SAKI; however, many of the nuanced mechanisms remain incompletely understood. Although there have been numerous strategies evaluated for the prevention and management of SAKI, no specific intervention has proven unequivocally efficacious. Currently, the mainstays for managing SAKI focus on alleviating ongoing kidney damage by optimizing systemic and kidney hemodynamic support, avoiding nephrotoxins, and mitigating the anticipated complications of kidney failure. The timely referral for renal support to manage azotemia, metabolic derangements, and fluid accumulation remains critical for this population. The extracorporeal removal of inflammatory mediators has shown some potential benefit in limiting systemic and kidney immune-mediated injury; however, the precise role of these technologies in the management of SAKI has yet to be defined.

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Year:  2013        PMID: 23400860     DOI: 10.1007/s00467-013-2427-6

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  98 in total

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Journal:  Crit Care       Date:  2008-04-10       Impact factor: 9.097

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Authors:  C R Sims; L A MacMillan-Crow; P R Mayeux
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2.  Quantification of Inflammasome Adaptor Protein ASC in Biological Samples by Multiple-Reaction Monitoring Mass Spectrometry.

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Journal:  Crit Care Med       Date:  2015-08       Impact factor: 7.598

Review 4.  Could Biomarkers Direct Therapy for the Septic Patient?

Authors:  Clark R Sims; Trung C Nguyen; Philip R Mayeux
Journal:  J Pharmacol Exp Ther       Date:  2016-02-08       Impact factor: 4.030

Review 5.  Sepsis-associated acute kidney injury.

Authors:  Rashid Alobaidi; Rajit K Basu; Stuart L Goldstein; Sean M Bagshaw
Journal:  Semin Nephrol       Date:  2015-01       Impact factor: 5.299

6.  Alkaline phosphatase protects against renal inflammation through dephosphorylation of lipopolysaccharide and adenosine triphosphate.

Authors:  E Peters; S Geraci; S Heemskerk; M J Wilmer; A Bilos; B Kraenzlin; N Gretz; P Pickkers; R Masereeuw
Journal:  Br J Pharmacol       Date:  2015-09-22       Impact factor: 8.739

7.  GPR120 Ameliorates Apoptosis and Inhibits the Production of Inflammatory Cytokines in Renal Tubular Epithelial Cells.

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8.  Identification of phosphorylated MYL12B as a potential plasma biomarker for septic acute kidney injury using a quantitative proteomic approach.

Authors:  Fan Wu; Xiu-Juan Dong; Yan-Yan Li; Yan Zhao; Qiu-Lin Xu; Lei Su
Journal:  Int J Clin Exp Pathol       Date:  2015-11-01

9.  Protective role of fenofibrate in sepsis-induced acute kidney injury in BALB/c mice.

Authors:  Zuowei Pei; Shuling Deng; Dengmei Xie; Mingyi Lv; Wenyan Guo; Duping Liu; Zhenzhen Zheng; Xiaofeng Long
Journal:  RSC Adv       Date:  2018-08-10       Impact factor: 4.036

10.  Serum and urinary NGAL in septic newborns.

Authors:  Mike Smertka; Jolanta Wroblewska; Anna Suchojad; Malgorzata Majcherczyk; Danuta Jadamus-Niebroj; Teresa Owsianka-Podlesny; Aniceta Brzozowska; Iwona Maruniak-Chudek
Journal:  Biomed Res Int       Date:  2014-01-21       Impact factor: 3.411

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