Evidence map›Paper›PMID 30715208›Full record

SynthesisClinical infectious diseases : an official publication of the Infectious Diseases Society of America2019

Vancomycin Area Under the Curve and Acute Kidney Injury: A Meta-analysis.

Doaa M Aljefri, Sean N Avedissian, Nathaniel J Rhodes, Michael J Postelnick, Kevin Nguyen, Marc H Scheetz

Abstract readMeta-Analysis
In one paragraph

Synthesis in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed, 5 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

100 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. State of Vancomycin Dosing in Neonates: An Overview.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2026
    Article
  19. Article
  20. Article

40 more citing papers are in PubMed but not listed here.

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

6 authors.

Doaa M AljefriDepartment of Pharmacy, Northwestern Memorial Hospital, Chicago, Illinois.
Sean N AvedissianDepartment of Pharmacy, Northwestern Memorial Hospital, Chicago, Illinois.
Nathaniel J RhodesDepartment of Pharmacy, Northwestern Memorial Hospital, Chicago, Illinois.
Michael J PostelnickDepartment of Pharmacy, Northwestern Memorial Hospital, Chicago, Illinois.
Kevin NguyenDepartment of Pharmacy Practice, Midwestern University Chicago College of Pharmacy, Downers Grove, Illinois.
Marc H ScheetzDepartment of Pharmacy, Northwestern Memorial Hospital, Chicago, Illinois.

Funding

Elucidation of an informed drug dosing scheme to minimize kidney injuryR15AI105742 · NIAID · MIDWESTERN UNIVERSITY · PI SCHEETZ, MARC HOWARD · 2014 to 2014
$459k
NIAID NIH HHS R15 AI105742
6 · The paper itself

Abstract

backgroundThis study analyzed the relationship between vancomycin area under the concentration-time curve (AUC) and acute kidney injury (AKI) reported across recent studies.

methodsA systematic review of PubMed, Medline, Scopus, and compiled references was conducted. We included randomized cohort and case-control studies that reported vancomycin AUCs and risk of AKI (from 1990 to 2018). The primary outcome was AKI, defined as an increase in serum creatinine of ≥0.5 mg/L or a 50% increase from baseline on ≥2 consecutive measurements. Odds ratios (ORs) with 95% confidence intervals (CIs) were calculated. Primary analyses compared the impact of AUC cutpoint (greater than ~650 mg × hour/L) and AKI. Additional analysis compared AUC vs trough-guided monitoring on AKI incidence.

resultsEight observational studies met inclusion/exclusion criteria with data for 2491 patients. Five studies reported first-24-hour AUCs (AUC0-24) and AKI, 2 studies reported 24- to 48-hour AUCs (AUC24-48) and AKI, and 2 studies reported AKI associated with AUC- vs trough-guided monitoring. AUC less than approximately 650 mg × hour/L was associated with decreased AKI for AUC0-24 (OR, 0.36 [95% CI, .23-.56]) as well as AUC24-48 (OR, 0.45 [95% CI, .27-.75]). AKI associated with the AUC monitoring strategy was significantly lower than trough-guided monitoring (OR, 0.68 [95% CI, .46-.99]).

conclusionsAUCs measured in the first or second 24 hours and lower than approximately 650 mg × hour/L may result in a decreased risk of AKI. Vancomycin AUC monitoring strategy may result in less vancomycin-associated AKI. Additional investigations are warranted.

Indexed as

Acute Kidney InjuryAnti-Bacterial AgentsHumansMicrobial Sensitivity TestsOdds RatioVancomycinAnti-Bacterial AgentsVancomycinAUCnephrotoxicityvancomycin

Identifiers

PMID30715208
PMCPMC6853683

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.