Evidence map›Paper›PMID 42212968›Full record

ArticleAntimicrobial agents and chemotherapy2026

Cefazolin surgical prophylaxis in obesity: a body composition-driven population pharmacokinetic approach.

Andrew Wassef, Katarzyna Kosicka-Noworzyń, Hyunmoon Back, Anna Siemiątkowska, Christine Yohn, Ragui Sadek, Leonid Kagan, Luigi Brunetti

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Andrew WassefDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.ORCID 0009-0005-0655-8480
Katarzyna Kosicka-NoworzyńDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.ORCID 0000-0003-3551-4784
Hyunmoon BackDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
Anna SiemiątkowskaDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.ORCID 0000-0003-3568-4716
Christine YohnDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
Ragui SadekAdvanced Surgical and Bariatrics of New Jersey, Somerset, New Jersey, USA.
Leonid KaganDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
Luigi BrunettiDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.ORCID 0000-0003-0565-6167

Funding

Mechanisms of obesity-induced changes in drug pharmacokineticsR01GM124046 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI KAGAN, LEONID · 2018 to 2022
$2.6M
NIH HHS R01GM124046
6 · The paper itself

Abstract

Cefazolin serves as the antibiotic choice for surgical prophylaxis to prevent surgical site infection, yet consensus on dosing guidelines for patients with obesity is not well defined. To quantify cefazolin exposure in plasma and subcutaneous adipose tissue during abdominal surgery, and to build a popPK model comparing standard anthropometrics, calculated body-composition metrics, and directly measured body-composition values as predictors of interindividual variability. A single center prospective study was conducted at Robert Wood Johnson Barnabas University Hospital, NJ, USA. Institutional standard for dosing was 2 g < 120 kg, or 3 g of cefazolin for subjects ≥ 120 kg for 101 adult subjects. Serial blood samples and subcutaneous adipose tissue samples were collected for the assessment of cefazolin concentration. All subjects received body composition assessments. Cefazolin concentrations in plasma remained within the therapeutic range in all stratification groups, yet subcutaneous adipose tissue concentrations failed to meet therapeutic cut offs, with 2- to 8.5-fold decrease in target attainment in subjects with increasing body fat percentages and BMI. A three-compartment biophase model best characterized our data and served as our base popPK model. Stepwise covariate modeling of measured body composition metrics outperformed both calculated body composition metrics and standard anthropomorphic values. The results support the claim that existing weight-based dosing methods fall short at the site of action, while simultaneously providing a proof of concept for the first in-human body composition informed popPK model. Measured body composition metrics can enhance characterization of cefazolin prophylactic exposure for subjects with obesity receiving abdominal surgery.

Indexed as

Anti-Bacterial AgentsAntibiotic ProphylaxisCefazolinObesitySurgical Wound InfectionAdultAgedBody CompositionBody Mass IndexFemaleFirst Generation CephalosporinsHumansMaleMiddle AgedProspective StudiesSubcutaneous FatAnti-Bacterial AgentsCefazolinFirst Generation Cephalosporinsantibioticsbody compositioncefazolinobesitypharmacokineticspopulation pharmacokinetic modelingsurgical prophylaxis

Identifiers

PMID42212968
PMCPMC13321816

What OpenQuestion holds

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Registered trials

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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.