Evidence map›Paper›PMID 23539228›Full record

Observational studyClinical journal of the American Society of Nephrology : CJASN2013

Adverse drug events during AKI and its recovery.

Zachary L Cox, Allison B McCoy, Michael E Matheny, Gautam Bhave, Neeraja B Peterson, Edward D Siew, Julia Lewis, Ioana Danciu, Aihua Bian, Ayumi Shintani and 3 more

Abstract readObservational Study
In one paragraph

Observational study in Clinical journal of the American Society of Nephrology : CJASN, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Zachary L CoxDepartment of Pharmacy, Vanderbilt University Medical Center, Nashville, Tennessee, USA. zachary.l.cox@vanderbilt.edu
Allison B McCoy
Michael E Matheny
Gautam Bhave
Neeraja B Peterson
Edward D Siew
Julia Lewis
Ioana Danciu
Aihua Bian
Ayumi Shintani
T Alp Ikizler
Erin B Neal
Josh F Peterson

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
Vanderbilt Biomedical Informatics Training ProgramT15LM007450 · NLM · VANDERBILT UNIVERSITY · PI Jessica S. Ancker, Bradley A. Malin · 2002 to 2026
$19.7M
Vanderbilt Multidisciplinary Clinical Research CenterP60AR056116 · NIAMS · VANDERBILT UNIVERSITY · PI GRIFFIN, MARIE R. · 2008 to 2012
$6.2M
The Vanderbilt Institute for Clinical and Translational Research (VICTR) KL2KL2RR024977 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$3.0M
Information Systems for Detecting and Managing Acute Kidney InjuryR01LM009965 · NLM · VANDERBILT UNIVERSITY · PI PETERSON, JOSEPH F. · 2008 to 2010
$998k
NCRR NIH HHS 5KL2 RR024977NCRR NIH HHS KL2 RR024977NCRR NIH HHS UL1 RR024975NIAMS NIH HHS P60 AR056116NLM NIH HHS R01 LM009965NLM NIH HHS T15 LM007450
6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe impact of AKI on adverse drug events and therapeutic failures and the medication errors leading to these events have not been well described. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: A single-center observational study of 396 hospitalized patients with a minimum 0.5 mg/dl change in serum creatinine who were prescribed a nephrotoxic or renally eliminated medication was conducted. The population was stratified into two groups by the direction of their initial serum creatinine change: AKI and AKI recovery. Adverse drug events, potential adverse drug events, therapeutic failures, and potential therapeutic failures for 148 drugs and 46 outcomes were retrospectively measured. Events were classified for preventability and severity by expert adjudication. Multivariable analysis identified medication classes predisposing AKI patients to adverse drug events.

resultsForty-three percent of patients experienced a potential adverse drug event, adverse drug event, therapeutic failure, or potential therapeutic failure; 66% of study events were preventable. Failure to adjust for kidney function (63%) and use of nephrotoxic medications during AKI (28%) were the most common potential adverse drug events. Worsening AKI and hypotension were the most common preventable adverse drug events. Most adverse drug events were considered serious (63%) or life-threatening (31%), with one fatal adverse drug event. Among AKI patients, administration of angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, antibiotics, and antithrombotics was most strongly associated with the development of an adverse drug event or potential adverse drug event.

conclusionsAdverse drug events and potential therapeutic failures are common and frequently severe in patients with AKI exposed to nephrotoxic or renally eliminated medications.

Indexed as

Medication ErrorsAcute Kidney InjuryAdultAgedBiomarkersCreatinineDrug Dosage CalculationsDrug-Related Side Effects and Adverse ReactionsFemaleGlomerular Filtration RateHospitalizationHumansHypotensionInappropriate PrescribingKidneyLinear ModelsBiomarkersCreatinine

Identifiers

PMID23539228
PMCPMC3700703

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.