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Cited by 352

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

An overview of drug-induced acute kidney injury

Pannu, Neesh, Nadim, Mitra K.·2008·Critical Care Medicine

Abstract

The complex nature of critical illness often necessitates the use of multiple therapeutic agents, many of which may individually or in combination have the potential to cause renal injury. The use of nephrotoxic drugs has been implicated as a causative factor in up to 25% of all cases of severe acute renal failure in critically ill patients. Acute tubular necrosis is the most common form of renal injury from nephrotoxin exposure, although other types of renal failure may be seen. Given that this is a preventable cause of a potentially devastating complication, a comprehensive strategy should be used to avoid nephrotoxicity in critically ill patients including: accurate estimation of pre-existing renal function using serum creatinine-based glomerular filtration rates, avoidance of nephrotoxins if possible, ongoing monitoring of renal function, and immediate discontinuation of suspected nephrotoxins in the event of renal dysfunction.

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Metadata

Authors
Pannu, N., & Nadim, M. K.
Venue
Critical Care Medicine
Published
2008-04
Volume
36
Issue
Suppl
Pages
S216-S223
ISSN
0090-3493 (ISSN-L)
OpenAlex
W2138745304
Cited by
352
References
1
FWCI
16.08
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: An overview of drug-induced acute kidney injury. https://app.cochat.ai/papers/10.1097/ccm.0b013e318168e375
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Pannu, N., & Nadim, M. K. (2008). An overview of drug-induced acute kidney injury. Critical Care Medicine. https://doi.org/10.1097/ccm.0b013e318168e375

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.