Literature DB >> 8804228

Management of acute renal failure: new perspectives.

A M Alkhunaizi1, R W Schrier.   

Abstract

Despite major developments in medicine, surgery, and intensive care, acute renal failure (ARF) still remains a common problem affecting approximately 5% of all general hospital patients. Mortality of all forms of ARF continues to be greater than 50%, and this percentage has not decreased significantly over the last 30 years. There are multiple factors, which may explain the persistence of such high mortality; the most important of these is probably the evolution of the disease spectrum underlying the development of ARF. At present, ARF is more often observed in older or more complex patients frequently in association with multiorgan system failure. The annual cost of managing ARF is staggering. This article reviews several of the new strategies and approaches that have been developed to aid in the management and prevention of ARF. For example, the use of biocompatible membranes has been proven to positively influence the course of ARF, which necessitates renal replacement therapy. Although continuous renal replacement therapy has a theoretical advantage compared with intermittent hemodialysis in critically ill and hemodynamically unstable patients, there are no well-controlled clinical studies to support a beneficial effect on mortality. There is, however, good evidence that calcium channel blockers play a positive role in the management of ARF, especially that associated with cadaveric kidney transplantation. Vasoactive agents, such as dopamine, may have the advantage of increasing the urine output in patients with oliguric ARF; however, their efficacy in otherwise altering the course of ARF is not well substantiated. Finally, growth factors and atrial natriuretic peptide appear to have the potential for accelerating renal recovery and decreasing morbidity and mortality from this commonly encountered medical problem. Prospective randomized clinical studies are the key to many of the dilemmas encountered with ARF.

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Year:  1996        PMID: 8804228     DOI: 10.1016/s0272-6386(96)90487-4

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  6 in total

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Authors:  P W Perdue; J R Balser; P A Lipsett; M J Breslow
Journal:  Ann Surg       Date:  1998-04       Impact factor: 12.969

2.  Lipopolysaccharide pretreatment protects from renal ischemia/reperfusion injury : possible connection to an interleukin-6-dependent pathway.

Authors:  U Heemann; A Szabo; P Hamar; V Müller; O Witzke; J Lutz; T Philipp
Journal:  Am J Pathol       Date:  2000-01       Impact factor: 4.307

3.  Evaluation of applying drug dose adjustment by physicians in patients with renal impairment.

Authors:  Abdulrahman M Alahdal; Ahmed A Elberry
Journal:  Saudi Pharm J       Date:  2011-12-24       Impact factor: 4.330

4.  Hemofiltration in sepsis: where do we go from here?

Authors:  J A Kellum; R Bellomo
Journal:  Crit Care       Date:  2000-02-16       Impact factor: 9.097

5.  Human Alpha-1-Antitrypsin (hAAT) therapy reduces renal dysfunction and acute tubular necrosis in a murine model of bilateral kidney ischemia-reperfusion injury.

Authors:  Nuria Maicas; Johan van der Vlag; Janin Bublitz; Sandrine Florquin; Marinka Bakker-van Bebber; Charles A Dinarello; Vivienne Verweij; Roos Masereeuw; Leo A Joosten; Luuk B Hilbrands
Journal:  PLoS One       Date:  2017-02-24       Impact factor: 3.240

6.  Clinical Decision Support System with Renal Dose Adjustment Did Not Improve Subsequent Renal and Hepatic Function among Inpatients: The Japan Adverse Drug Event Study.

Authors:  Ryuhei Wada; Jiro Takeuchi; Tsukasa Nakamura; Tomohiro Sonoyama; Shinji Kosaka; Chisa Matsumoto; Mio Sakuma; Yoshinori Ohta; Takeshi Morimoto
Journal:  Appl Clin Inform       Date:  2020-12-23       Impact factor: 2.342

  6 in total

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