Evidence map›Paper›PMID 33743171›Full record

Trial reportEuropean journal of drug metabolism and pharmacokinetics2021

Pharmacokinetics and Pharmacodynamics of High-Dose Piperacillin-Tazobactam in Obese Patients.

John J Veillette, S Alexander Winans, Victoria K Maskiewicz, James Truong, Ronald N Jones, Steven C Forland

Registry-linked trialOpen access · hybridAbstract readClinical Trial
In one paragraph

Trial report in European journal of drug metabolism and pharmacokinetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01923363 (Pharmacokinetics and Pharmacodynamics of High-Dose Piperacillin/Tazobactam in Obese Patients), which is not on this map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 26% 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.

NCT01923363 nacompletednot on this map

Pharmacokinetics and Pharmacodynamics of High-Dose Piperacillin/Tazobactam in Obese Patients

TypeinterventionalSponsorLoma Linda UniversityRan2014 to 2016Enrolled29ConditionsObesityArmsPiperacillin/Tazobactam Standard Dose to High Dose
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Updated antimicrobial dosing recommendations for obese patients.Antimicrobial agents and chemotherapy · 2024
    Pooled it
  2. Review
  3. Article
  4. Article
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 at 3 institutions in 1 country.

John J VeilletteDepartment of Pharmacy Practice, Loma Linda University School of Pharmacy, Loma Linda, CA, USA. john.veillette@gmail.com.
S Alexander WinansDepartment of Pharmacy Practice, Loma Linda University School of Pharmacy, Loma Linda, CA, USA.
Victoria K MaskiewiczDepartment of Pharmaceutical and Administrative Sciences, Loma Linda University School of Pharmacy, Loma Linda, CA, USA.
James TruongDepartment of Pharmacy Practice, Loma Linda University School of Pharmacy, Loma Linda, CA, USA.
Ronald N JonesJMI Laboratories, North Liberty, IA, USA.
Steven C ForlandDepartment of Pharmacy Practice, Loma Linda University School of Pharmacy, Loma Linda, CA, USA.
Loma Linda University · USJMI Laboratories · USLoma Linda University Medical Center · US

Funding

Loma Linda University 360031
6 · The paper itself

Abstract

BACKGROUND AND

objectiveStandard piperacillin-tazobactam (P-T) dosing may be suboptimal in obesity, but high-dose regimens have not been studied. We prospectively evaluated the pharmacokinetics and pharmacodynamics of standard- and high-dose P-T in obese adult inpatients.

methodsThose receiving standard-dose P-T with BMI ≥ 30 kg/m

resultsPiperacillin and tazobactam half-lives ranged from 0.5-10.6 to 0.9-15.0 h, while volumes of distribution ranged from 13.6-54.8 to 11.5-60.1 L, respectively. Predicted dose requirements for target attainment ranged from 2.25 g every 6 h in hemodialysis patients to a 27 g/24-h continuous infusion in a patient with a short P-T half-life. An amount of 4.5 g every 6 h would have met the target for only 1/12 (8%) patients with creatinine clearance ≥ 80 mL/min and 13/28 (46%) for all enrolled patients. One patient (3%) experienced an adverse event deemed probably related to high-dose P-T.

conclusionSome patients required high P-T doses for target attainment, but dosing requirements were highly variable. Doses up to 6.75 g or 9 g every 6 h may be tolerable; however, studies are needed to see if high dosing, prolonged infusions, or real-time therapeutic drug monitoring improves outcomes in obese patients. CLINICAL TRIAL REGISTRATION (CLINICALTRIALS.GOV): NCT01923363.

Indexed as

Models, BiologicalAdultAgedAnti-Bacterial AgentsCreatinineDose-Response Relationship, DrugFemaleHalf-LifeHumansMiddle AgedObesityPiperacillin, Tazobactam Drug CombinationProspective StudiesRenal DialysisTissue DistributionYoung AdultAnti-Bacterial AgentsCreatininePiperacillin, Tazobactam Drug Combination

Identifiers

PMID33743171
PMCPMC8093170
OpenAlexW3135923252

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

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.