Evidence map›Paper›PMID 32778543›Full record

ArticleAntimicrobial agents and chemotherapy2020

Population Pharmacokinetic Study of Ceftriaxone in Elderly Patients, Using Cystatin C-Based Estimates of Renal Function To Account for Frailty.

Shu Jin Tan, Matthew Cockcroft, Madhu Page-Sharp, Glenn Arendts, Timothy M E Davis, Brioni R Moore, Kevin T Batty, Sam Salman, Laurens Manning

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 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

9 authors at 3 institutions in 1 country.

Shu Jin Tan *Department of Infectious Diseases, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.
Matthew Cockcroft *Faculty of Medicine and Health Sciences, University of Western Australia, Perth, Western Australia, Australia.
Madhu Page-SharpSchool of Pharmacy and Biomedical Sciences, Curtin University, Perth, Western Australia, Australia.
Glenn ArendtsFaculty of Medicine and Health Sciences, University of Western Australia, Perth, Western Australia, Australia.
Timothy M E DavisFaculty of Medicine and Health Sciences, University of Western Australia, Perth, Western Australia, Australia.ORCID 0000-0003-0749-7411
Brioni R MooreFaculty of Medicine and Health Sciences, University of Western Australia, Perth, Western Australia, Australia.
Kevin T BattySchool of Pharmacy and Biomedical Sciences, Curtin University, Perth, Western Australia, Australia.
Sam Salman *Faculty of Medicine and Health Sciences, University of Western Australia, Perth, Western Australia, Australia.ORCID 0000-0002-8276-6784
Laurens Manning *Department of Infectious Diseases, Fiona Stanley Hospital, Murdoch, Western Australia, Australia laurens.manning@uwa.edu.au.
The University of Western Australia · AUCurtin University · AURoyal Perth Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ceftriaxone is widely used for respiratory and urinary infections in elderly and frail patients, but there are few pharmacokinetic studies. A prospective population pharmacokinetic study of ceftriaxone in adults over 65 years old was undertaken. Dried blood spots collected at baseline (predose) and 0.5, 1, 4, 8, and 24 h after administration of 1 g of ceftriaxone were assayed using a validated liquid chromatography-mass spectroscopy analytical method. Frailty was classified using the Edmonton frailty scale and grip strength via a hand dynamometer. Estimates of glomerular filtration rate were determined using creatinine-based and cystatin C-based equations. Of 26 patients recruited, 23 (88%) were vulnerable or very frail. Estimates of drug clearance improved significantly with a cystatin C-based estimate of renal function that accounted for frailty. Simulations indicate that the combined effects of ranges of size and renal function resulted in a 6-fold range in peak ceftriaxone concentrations and 9-fold range in total exposure (area under the concentration-time curve [AUC]). For elderly patients with moderate or severe renal impairment, 48-h dosing results in greater trough concentrations and total exposure than the trough concentrations and total exposure in patients with normal renal function receiving 24-h dosing. Cystatin C-based measures of renal function improved predictions of ceftriaxone clearance in elderly patients.

Indexed as

CeftriaxoneFrailtyAdultAgedCreatinineCystatin CGlomerular Filtration RateHumansProspective StudiesCeftriaxoneCreatinineCystatin Cceftriaxonefrailtypopulation pharmacokinetics

Identifiers

PMID32778543
PMCPMC7508575
OpenAlexW3048191565

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.