The effect of histopathologic analysis and tissue cultures on inpatient management of cellulitis: a randomized control trial.


Journal

Archives of dermatological research
ISSN: 1432-069X
Titre abrégé: Arch Dermatol Res
Pays: Germany
ID NLM: 8000462

Informations de publication

Date de publication:
23 Jul 2024
Historique:
received: 06 06 2024
accepted: 06 07 2024
revised: 01 07 2024
medline: 23 7 2024
pubmed: 23 7 2024
entrez: 23 7 2024
Statut: epublish

Résumé

In the absence of a gold-standard diagnostic modality for cellulitis, sterile inflammatory disorders may be misdiagnosed as cellulitis. To determine the utility of skin biopsy and tissue culture for the diagnosis and management of patients admitted with a diagnosis of presumed cellulitis. Pilot single-blind parallel group randomized controlled clinical trial in 56 patients with a primary diagnosis of presumed cellulitis. In the intervention group only, skin biopsy and tissue culture results were made available to the primary care team to guide diagnosis and management. Length of hospital stay and antibiotic use were evaluated as outcome measures. Length of stay showed the greatest opportunity for further study as a primary outcome (intervention: 4, IQR (2-6) vs. control: 5 IQR (3-8) days; p = 0.124). The COVID-19 pandemic placed limitations on participant enrollment and study duration; in addition, data was collected from a single medical center. This study demonstrates that length of stay and anti-pseudomonal antibiotic de-escalation are endpoints that may be influenced by biopsy and tissue culture results in presumed cellulitis patients; these outcomes warrant further study.

Sections du résumé

BACKGROUND BACKGROUND
In the absence of a gold-standard diagnostic modality for cellulitis, sterile inflammatory disorders may be misdiagnosed as cellulitis.
OBJECTIVE OBJECTIVE
To determine the utility of skin biopsy and tissue culture for the diagnosis and management of patients admitted with a diagnosis of presumed cellulitis.
DESIGN METHODS
Pilot single-blind parallel group randomized controlled clinical trial in 56 patients with a primary diagnosis of presumed cellulitis. In the intervention group only, skin biopsy and tissue culture results were made available to the primary care team to guide diagnosis and management. Length of hospital stay and antibiotic use were evaluated as outcome measures.
RESULTS RESULTS
Length of stay showed the greatest opportunity for further study as a primary outcome (intervention: 4, IQR (2-6) vs. control: 5 IQR (3-8) days; p = 0.124).
LIMITATIONS CONCLUSIONS
The COVID-19 pandemic placed limitations on participant enrollment and study duration; in addition, data was collected from a single medical center.
CONCLUSION CONCLUSIONS
This study demonstrates that length of stay and anti-pseudomonal antibiotic de-escalation are endpoints that may be influenced by biopsy and tissue culture results in presumed cellulitis patients; these outcomes warrant further study.

Identifiants

pubmed: 39042316
doi: 10.1007/s00403-024-03224-5
pii: 10.1007/s00403-024-03224-5
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

482

Subventions

Organisme : The Center for Clinical and Translational Science at The Ohio State University Wexner Medical Center
ID : Patient Safety Advancement Grant

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Michael Lause (M)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Emma Hansen (E)

College of Medicine, The Ohio State University, Columbus, OH, USA.

Karissa Libson (K)

College of Medicine, The Ohio State University, Columbus, OH, USA.

Cory Pettit (C)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Sonia Himed (S)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Kyle P Rismiller (KP)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Sara Huff (S)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Abraham M Korman (AM)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Alecia M Blaszczak (AM)

College of Medicine, The Ohio State University, Columbus, OH, USA.

Willa Hsueh (W)

College of Medicine, The Ohio State University, Columbus, OH, USA.

Nima Milani-Nejad (N)

Department of Dermatology, University of California Los Angeles, Los Angeles, CA, USA.

Leah Kofmehl (L)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Courtney Hebert (C)

Department of Internal Medicine, The Ohio State University, Columbus, OH, USA.
Department of Infectious Disease, The Ohio State University, Columbus, OH, USA.

Jeffrey M Caterino (JM)

Department of Emergency Medicine, The Ohio State University, Columbus, OH, USA.

Henry E Wang (HE)

Department of Emergency Medicine, The Ohio State University, Columbus, OH, USA.

Vedat Yildiz (V)

Department of Biomedical Informatics, The Ohio State University, Columbus, OH, USA.

John C Trinidad (JC)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Catherine G Chung (CG)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Department of Pathology, The Ohio State University, Columbus, OH, USA.

Benjamin H Kaffenberger (BH)

Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA. Benjamin.kaffenberger@osumc.edu.
, 1328 Dublin Road, Suite 100, Columbus, OH, 43215, USA. Benjamin.kaffenberger@osumc.edu.

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