Evidence map›Paper›PMID 28807922›Full record

ArticleAntimicrobial agents and chemotherapy2017

Using Population Pharmacokinetic Modeling and Monte Carlo Simulations To Determine whether Standard Doses of Piperacillin in Piperacillin-Tazobactam Regimens Are Adequate for the Management of Febrile Neutropenia.

Fekade Bruck Sime, Uwe Hahn, Morgyn S Warner, Ing Soo Tiong, Michael S Roberts, Jeffrey Lipman, Sandra L Peake, Jason A Roberts

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

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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

8 authors at 5 institutions in 1 country.

Fekade Bruck SimeCentre for Translational Anti-infective Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, Australia f.sime@uq.edu.au.
Uwe HahnDepartment of Haematology/Oncology, The Queen Elizabeth Hospital, Adelaide, Australia.
Morgyn S WarnerSA Pathology and the University of Adelaide, Adelaide, Australia.
Ing Soo TiongDepartment of Haematology/Oncology, The Queen Elizabeth Hospital, Adelaide, Australia.
Michael S RobertsTherapeutics Research Centre, School of Pharmacy, The University of South Australia, Adelaide, Australia.
Jeffrey LipmanBurns, Trauma, and Critical Care Research Centre, University of Queensland, Herston, Brisbane, Queensland.
Sandra L PeakeDepartment of Intensive Care Medicine, The Queen Elizabeth Hospital, Adelaide, Australia.
Jason A RobertsCentre for Translational Anti-infective Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, Australia.
Queen Elizabeth Hospital · AUUniversity of South Australia · AURoyal Brisbane and Women's Hospital · AUUniversity of Adelaide · AUUniversity of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Changes in the pharmacokinetics of piperacillin in febrile neutropenic patients have been reported to result in suboptimal exposures. This study aimed to develop a population pharmacokinetic model for piperacillin and perform dosing simulation to describe optimal dosing regimens for hematological malignancy patients with febrile neutropenia. Concentration-time data were obtained from previous prospective observational pharmacokinetic and interventional therapeutic drug monitoring studies. Nonparametric population pharmacokinetic analysis and Monte Carlo dosing simulations were performed with the Pmetrics package for R. A two-compartment model, with between-subject variability for clearance (CL), adequately described the data from 37 patients (21 males, age of 59 ± 12 years [means ± standard deviations] and weight of 77 ± 16 kg). Parameter estimates were CL of 18.0 ± 4.8 liters/h, volume of distribution of the central compartment of 14.3 ± 7.3 liters, rate constant for piperacillin distribution from the central to peripheral compartment of 1.40 ± 1.35 h

Indexed as

AgedAnti-Bacterial AgentsBacterial InfectionsCreatinineFebrile NeutropeniaFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedMonte Carlo MethodPenicillanic AcidPiperacillinPiperacillin, Tazobactam Drug CombinationAnti-Bacterial AgentsCreatininePenicillanic AcidPiperacillinPiperacillin, Tazobactam Drug Combinationfebrile neutropeniapiperacillinpopulation pharmacokinetics

Identifiers

PMID28807922
PMCPMC5655099
OpenAlexW2745792124

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.