Evidence map›Paper›PMID 31828686›Full record

ReviewEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2020

Diagnostic and medical needs for therapeutic drug monitoring of antibiotics.

Claude Mabilat, Marie Francoise Gros, David Nicolau, Johan W Mouton, Julien Textoris, Jason A Roberts, Menino O Cotta, Alex van Belkum, Isabelle Caniaux

Abstract readReview
In one paragraph

Review in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  13. Isotope-dilution-LC-MS/MS candidate reference measurement procedure for cefepime in human serum.Journal of mass spectrometry and advances in the clinical lab · 2024
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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.

Claude MabilatMedical Affairs, bioMérieux, Marcy l'Étoile, Lyon, France. claude.mabilat@biomerieux.com.
Marie Francoise GrosMedical Affairs, bioMérieux, Marcy l'Étoile, Lyon, France.
David NicolauCenter for Anti-Infective Research & Development, Hartford Hospital, 80 Seymour Street, Hartford, CT, 06102, USA.
Johan W MoutonDepartment of Medical Microbiology and Infectious Diseases, Erasmus University Medical Centre, Rotterdam, Dr Molewaterplein 40, 3015 GD, Rotterdam, Netherlands.
Julien TextorisMedical Affairs, bioMérieux, Marcy l'Étoile, Lyon, France.
Jason A RobertsCentre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.
Menino O CottaCentre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.
Alex van BelkumData Analytics Department, bioMérieux, La Balme Les Grottes, Grenoble, France.
Isabelle CaniauxMedical Affairs, bioMérieux, Marcy l'Étoile, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic drug monitoring (TDM) of antibiotics has been practiced for more than half a century, but it is still not widely applied for infected patients. It has a traditional focus on limiting toxicity of specific classes of antibiotics such as aminoglycosides and vancomycin. With more patients in critical care with higher levels of sickness severity and immunosuppression as well as an increasingly obese and ageing population, an increasing risk of suboptimal antibiotic exposure continues to escalate. As such, the value of TDM continues to expand, especially for beta-lactams which constitute the most frequently used antibiotic class. To date, the minimum inhibitory concentration (MIC) of infectious microbes rather than classification in terms of susceptible and resistant can be reported. In parallel, increasingly sophisticated TDM technology is becoming available ensuring that TDM is feasible and can deliver personalized antibiotic dosing schemes. There is an obvious need for extensive studies that will quantify the improvements in clinical outcome of individual TDM-guided dosing. We suggest that a broad diagnostic and medical investigation of the TDM arena, including market analyses and analytical technology assessment, is a current priority.

Indexed as

Drug MonitoringAnti-Bacterial AgentsBacteriaClinical Trials as TopicCritical CareDrug Resistance, Multiple, BacterialHumansIntensive Care UnitsMicrobial Sensitivity TestsAnti-Bacterial Agents

Identifiers

PMID31828686
PMCPMC7182631

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.