Evidence map›Paper›PMID 40995023›Full record

ArticleJAC-antimicrobial resistance2025

Evaluation of clindamycin use in bone and joint infections: is monotherapy a safe option? A monocentric observational study 2014-19.

Simon Jamard, Marie-Frédérique Lartigue, Louis-Romée Le Nail, Vianney Tuloup, Marion Lacasse, Adrien Lemaignen, CRIOGO local group

Abstract read
In one paragraph

Article in JAC-antimicrobial resistance, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Simon JamardService de Maladies Infectieuses et Tropicales, Hôpital Bretonneau, CHRU de Tours, Tours 37044, France.
Marie-Frédérique LartigueUMR1282, Infectiologie et Santé Publique, BRMF, Université de Tours, INRAE, Tours, France.ORCID https://orcid.org/0000-0003-4948-7959
Louis-Romée Le NailService de Chirurgie Orthopédique, Hôpital Trousseau, CHRU de Tours, Tours 37044, France.
Vianney TuloupPharmacie à Usage Intérieur, Hôpital Trousseau, CHRU de Tours, Tours 37044, France.
Marion LacasseService de Maladies Infectieuses et Tropicales, Hôpital Bretonneau, CHRU de Tours, Tours 37044, France.
Adrien LemaignenService de Maladies Infectieuses et Tropicales, Hôpital Bretonneau, CHRU de Tours, Tours 37044, France.
CRIOGO local group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Selecting an optimal antibiotic regimen for bone and joint infections (BJIs) is challenging due to limited high-quality evidence. Although clindamycin is widely used as an alternative treatment for susceptible microorganisms in combination therapy, its use as monotherapy is increasing. This study aimed to evaluate the efficacy and safety of clindamycin monotherapy for BJI treatment. Methods: A monocentric observational study was conducted using data from the Reference Centre for complex BJI at our tertiary university hospital between 2014 and 2019. All adult patients with microbiologically confirmed BJI receiving clindamycin after a multidisciplinary meeting were included. Patients infected with clindamycin non-susceptible strains were excluded. Treatment failure was defined as relapse, treatment change or death from any cause within 1 year. Associations between monotherapy and treatment failure were assessed using multivariate logistic regression and inverse probability of treatment weighting (IPTW) analysis to adjust for the propensity to receive monotherapy. Results: A total of 137 patients were included, of whom 88 received clindamycin monotherapy. Overall, 41/137 treatment failures were observed (16/88 in the monotherapy group, 25/49 in the combination group). Monotherapy was associated with fewer failures in both multivariate (OR = 0.18; 95% CI, 0.07-0.46; Conclusions: Clindamycin monotherapy appears to be a reliable and safe therapeutic option for selected patients with less severe BJI.

Identifiers

PMID40995023
PMCPMC12455409

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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.