Evidence map›Paper›PMID 33439417›Full record

ArticleInternal and emergency medicine2021

Impact of combining vancomycin with piperacillin/tazobactam or with meropenem on vancomycin-induced nephrotoxicity.

R F Tookhi, N A Kabli, M A Huntul, A K Thabit

Abstract read
PubMed Publisher
In one paragraph

Article in Internal and emergency medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.6field-weighted citation impact, top 31% of its field
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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Nephrotoxicity and antibiotics.Internal and emergency medicine · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

R F TookhiPharmacy Practice Department, Faculty of Pharmacy, King Abdulaziz University, 7024 Abdullah Al-Suliman Rd, Jeddah, 22254-2265, Saudi Arabia.
N A KabliPharmacy Practice Department, Faculty of Pharmacy, King Abdulaziz University, 7024 Abdullah Al-Suliman Rd, Jeddah, 22254-2265, Saudi Arabia.
M A HuntulPharmacy Practice Department, Faculty of Pharmacy, King Abdulaziz University, 7024 Abdullah Al-Suliman Rd, Jeddah, 22254-2265, Saudi Arabia.
A K ThabitPharmacy Practice Department, Faculty of Pharmacy, King Abdulaziz University, 7024 Abdullah Al-Suliman Rd, Jeddah, 22254-2265, Saudi Arabia. akthabit@kau.edu.sa.ORCID http://orcid.org/0000-0002-0369-9094
King Abdulaziz University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vancomycin (VAN) is a broad-spectrum antibiotic against Gram-positive cocci used empirically with other broad-spectrum antibiotics, such as piperacillin/tazobactam (TZP), cefepime, or meropenem (MEM). Conflicting literature on the rates of acute kidney injury (AKI) of VAN with TZP is reported, and studies on AKI rate with MEM are limited. This study aimed to evaluate AKI rates in patients receiving VAN with either TZP or MEM. This was a retrospective cohort study of patients received either VAN-TZP or VAN-MEM for ≥ 72 h. Patients with a baseline serum creatinine (SCr) of ≥ 1.5 mg/dL were excluded. The primary outcome was rate of AKI as defined by the Kidney Disease: Improving Global Outcomes (KDIGO) guidelines. SCr was recorded at baseline and 3-5 days post antibiotics initiation. 158 patients were included, 77 in the VAN-TZP group versus 81 in the VAN-MEM group. While the percentage of patients meeting AKI definition was numerically higher in the VAN-MEM group, the difference was not significant (10.4% vs. 21%; P = 0.07). As such, change in SCr was not significantly different between the two groups (- 7.4 vs. - 6.1%; P = 0.7). In-hospital mortality was higher in the VAN-MEM group (23.4% vs. 39.5%; P = 0.03) possibly because the majority of this group's patients were critically ill. This study showed that combining MEM with VAN did not offer the benefit of a lower rate of AKI compared with a combination with TZP. Therefore, patients with no risk factors for infections resistant to TZP can continue to receive TZP with VAN without risking AKI development.

Indexed as

Acute Kidney InjuryAdultAgedAged, 80 and overAnti-Bacterial AgentsDrug Therapy, CombinationFemaleHumansMaleMeropenemMiddle AgedPiperacillin, Tazobactam Drug CombinationRetrospective StudiesSaudi ArabiaVancomycinAnti-Bacterial AgentsMeropenemPiperacillin, Tazobactam Drug CombinationVancomycinAcute kidney injuryCreatinineMeropenemNephrotoxicityPiperacillin/tazobactamVancomycin

Identifiers

PMID33439417
OpenAlexW3120242683

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.