Evidence map›Paper›PMID 42292850›Full record

ArticleFrontiers in pharmacology2026

Disease severity modifies the ceftazidime-avibactam exposure-response relationship in critically ill patients: a retrospective study.

Shiyu Qian, Defang Xu, Yinqiu Xu, Hui Qi, Pei Liang

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 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

5 authors.

Shiyu Qian *Department of Pharmacy, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Defang Xu *Department of Pharmacy, Nanjing Drum Tower Hospital, China Pharmaceutical University, Nanjing, China.
Yinqiu XuDepartment of Pharmacy, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Hui QiDepartment of Critical Care Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Pei LiangDepartment of Pharmacy, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ceftazidime-avibactam (CAZ-AVI) is a key agent for MDR-GNB, but significant pharmacokinetic (PK) variability in critically ill patients poses challenges to achieving optimal dosing. Objectives: To investigate the association and influencing factors between CAZ-AVI serum concentration and clinical efficacy in critically ill patients, and specifically to evaluate the influence of disease severity on this relationship, with the aim of identifying a therapeutic target for critically ill patients with different disease severity. Methods: A retrospective study was conducted of 168 critically ill patients receiving ceftazidime/avibactam between 2021 and 2025. The relationship between plasma drug concentration, clinical efficacy and disease severity was evaluated. Results: 168 patients were included. C Conclusion: This retrospective analysis provides evidence that optimizing CAZ-AVI plasma concentrations is crucial for improving outcomes in critically ill patients, and that this relationship is significantly modulated by disease severity, necessitating a severity-adapted therapeutic drug monitoring (TDM) strategy.

Indexed as

anti-bacterial agentsceftazidime-avibactam (CAZ-AVI)intensive care units (ICU)sequential organ failure assessment scores (SOFA)therapeutic drug monitoring (TDM)

Identifiers

PMID42292850
PMCPMC13258538

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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.