Evidence map›Paper›PMID 41756381›Full record

ArticleFrontiers in medicine2026

Therapeutic drug monitoring of daptomycin in a critically ill patient cohort.

Rubi Stephani Hellwege, Mattia Müller, Rolf Erlebach, Onur Sazpinar, Alix Buhlmann, Reto A Schuepbach, Sascha David, Daniel A Hofmaenner

Abstract read
In one paragraph

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

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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

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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.

Rubi Stephani HellwegeInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Mattia MüllerInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Rolf ErlebachInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Onur SazpinarInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Alix BuhlmannInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Reto A SchuepbachInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Sascha DavidInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Daniel A HofmaennerInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pharmacokinetics of antimicrobial agents are altered in critically ill patients. Therefore, therapeutic drug monitoring (TDM) has gained much attention in recent years. Specifically, the role of TDM for daptomycin, its potential influence on dose adaptations and subsequent daptomycin levels, as well as daptomycin-related side effects is so far unclear in the critical care setting. Methods: This was a retrospective study including critically ill, adult patients from January 2010 to July 2023. No criteria for TDM were predefined and the decision to perform TDM was left to the discretion of the treating physician. The primary outcome was the evaluation of baseline daptomycin trough levels in patients undergoing TDM, and how subsequent levels were affected by potential dose adaptations. Further outcomes included daptomycin-free days alive over 14 days and the occurrence of side effects between patients with and without daptomycin TDM. Results: Two hundred seventy patients were included. The patient group was heterogeneous regarding elective or emergency admissions and had surgical and medical underlying conditions. Over the ICU stay, median daptomycin trough levels were 9 mg/L (IQR 5.8-16.4 mg/L) and median peak levels were 29. 8 mg/L (IQR 14.8 - 46 mg/L). The first measured daptomycin trough level was too low (<10 mg/L) in 62 patients (54.4%) with TDM. Despite dosage increases in 14 patients (22.6%), median subsequent levels did not increase and were only 7.0 mg/L (IQR 4.8-13.6 mg/L). Patients who underwent TDM experienced significantly more frequent daptomycin dose increases than those who did not (28.8% vs. 13.1%, Conclusion: Daptomycin levels might be commonly low in critically ill patients and often appear not to increase after dose adjustments. TDM was associated with more frequent dose escalations and fewer daptomycin-free days, but did not significantly reduce the incidence of adverse events in a large cohort of critically ill patients.

Indexed as

antibioticsdaptomycinintensive care unitside effectstrough level

Identifiers

PMID41756381
PMCPMC12932621

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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.