Evidence map›Paper›PMID 35294951›Full record

ArticleAmerican journal of nephrology2022

Nephrotoxin Exposure in the 3 Years following Hospital Discharge Predicts Development or Worsening of Chronic Kidney Disease among Acute Kidney Injury Survivors.

Diana J Schreier, Andrew D Rule, Kianoush B Kashani, Kristin C Mara, Sandra L Kane-Gill, John C Lieske, Alanna M Chamberlain, Erin F Barreto, ACT Study Team

Abstract read
In one paragraph

Article in American journal of nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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

10 citing papers in PubMed.

  1. Article
  2. Acute Kidney Injury in Care Transitions (ACT): A Randomized Controlled Feasibility Trial.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2025
    Article
  3. Review
  4. Review
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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

9 authors.

Diana J SchreierDepartment of Pharmacy, Mayo Clinic, Rochester, Minnesota, USA.
Andrew D RuleDivision of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
Kianoush B KashaniDivision of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
Kristin C MaraDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota, USA.
Sandra L Kane-GillSchool of Pharmacy, University of Pittsburgh, Rochester, Minnesota, USA.
John C LieskeDivision of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
Alanna M ChamberlainDivision of Epidemiology, Mayo Clinic, Rochester, Minnesota, USA.
Erin F BarretoDepartment of Pharmacy, Mayo Clinic, Rochester, Minnesota, USA.
ACT Study Team

Funding

Rochester Epidemiology ProjectR01AG034676 · NIA · MAYO CLINIC ROCHESTER · PI ROCCA, WALTER A, ST SAUVER, JENNIFER LYNN · 2010 to 2019
$9.5M
Interdisciplinary Infrastructure for Aging Research: Rochester Epidemiology ProjectR33AG058738 · NIA · MAYO CLINIC ROCHESTER · PI LEBRASSEUR, NATHAN K, OLSON, JANET E · 2020 to 2022
$2.4M
Beta-lactam individualization for critically ill patientsK23AI143882 · NIAID · MAYO CLINIC ROCHESTER · PI BARRETO, ERIN FRAZEE · 2020 to 2024
$986k
Enhanced kidney follow-up for AKI survivors in Care Transitions (the ACT Study)R03HS028060 · AHRQ · MAYO CLINIC ROCHESTER · PI BARRETO, ERIN FRAZEE · 2021 to 2022
$100k
AHRQ HHS R03 HS028060NIAID NIH HHS K23 AI143882NIA NIH HHS R01 AG034676NIA NIH HHS R33 AG058738
6 · The paper itself

Abstract

introductionSurvivors of acute kidney injury (AKI) are at high risk of progression to chronic kidney disease (CKD), for which drugs may be a modifiable risk factor.

methodsWe conducted a population-based cohort study of Olmsted County, MN residents who developed AKI while hospitalized between January 1, 2006, and December 31, 2014, using Rochester Epidemiology Project data. Adults with a hospitalization complicated by AKI who survived at least 90 days after AKI development were included. Medical records were queried for prescription of potentially nephrotoxic medications over the 3 years after discharge. The primary outcome was de novo or progressive CKD defined by either a new diagnosis code for CKD or ≥30% decline in estimated glomerular filtration rate from baseline. The composite of CKD, AKI readmission, or death was also evaluated.

resultsAmong 2,461 AKI survivors, 2,140 (87%) received a potentially nephrotoxic medication during the 3 years following discharge. When nephrotoxic medication use was analyzed in a time-dependent fashion, those actively prescribed at least one of these drugs experienced a significantly higher risk of de novo or progressive CKD (HR 1.38: 95% CI: 1.24, 1.54). Similarly, active potentially nephrotoxic medication use predicted a greater risk of the composite endpoint of CKD, AKI readmission, or death within 3 years of discharge (HR 1.41: 95% CI: 1.28, 1.56).

conclusionIn this population-based cohort study, AKI survivors actively prescribed one or more potentially nephrotoxic medications were at significantly greater risk for de novo or progressive CKD. An opportunity exists to reassess nephrotoxin appropriateness following an AKI episode to improve patient outcomes.

Indexed as

Acute Kidney InjuryRenal Insufficiency, ChronicAdultCohort StudiesFemaleHospitalsHumansMalePatient DischargeRetrospective StudiesRisk FactorsSurvivorsAcute kidney injuryAdverse drug eventEpidemiologyLong-term outcomes

Identifiers

PMID35294951
PMCPMC9090945

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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.