Use of rifampicin and graft removal are associated with better outcomes in prosthetic vascular graft infection.


Journal

Infection
ISSN: 1439-0973
Titre abrégé: Infection
Pays: Germany
ID NLM: 0365307

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 16 06 2020
accepted: 30 10 2020
pubmed: 4 1 2021
medline: 3 8 2021
entrez: 3 1 2021
Statut: ppublish

Résumé

Prosthetic vascular graft infection (PVGI) is a very severe disease. We aimed to determine the factors associated with treatment failure. Patients admitted to two University Hospitals with PVGI were included in this retrospective study. PVGI was classified as possible, probable or proven according to an original set of diagnostic criteria. We defined treatment failure if one of the following events occurred within the first year after PVGI diagnosis: death and infection recurrence due to the same or another pathogen. One hundred and twelve patients were diagnosed with possible (n = 26), probable (n = 22) and proven (n = 64) PVGI. Bacterial documentation was obtained for 81% of patients. The most frequently identified pathogen was Staphylococcus aureus (n = 39). Surgery was performed in 96 patients (86%). Antibiotics were administered for more than 6 weeks in 41% of patients. Treatment failure occurred in 30 patients (27.5%). The factors associated with a lower probability of treatment failure were total removal of the infected graft (OR = 0.2, 95% CI [0.1-0.6]), rifampicin administration (OR = 0.3 [0.1-0.9]) and possible PVGI according to the GRIP criteria (OR = 0.3 [0.1-0.9]). Treatment failure occurred in 27.5% of patients with PVGI. Total removal of the infected graft and rifampicin administration were associated with better outcomes.

Identifiants

pubmed: 33389709
doi: 10.1007/s15010-020-01551-z
pii: 10.1007/s15010-020-01551-z
doi:

Substances chimiques

Anti-Bacterial Agents 0
Rifampin VJT6J7R4TR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

127-133

Références

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Auteurs

Anne Coste (A)

Service de Médecine Interne, Vasculaire et Pneumologie, Hôpital La Cavale Blanche, CHRU Brest, Brest, France.

Mélanie Poinot (M)

Infectious Diseases and Intensive Care Unit, CHU Rennes, Rennes, France.

Sophie Panaget (S)

Service de Médecine Interne, Vasculaire et Pneumologie, Hôpital La Cavale Blanche, CHRU Brest, Brest, France.

Bénédicte Albert (B)

Service de Chirurgie Cardiaque Thoracique et Vasculaire, CHRU Brest, Brest, France.

Adrien Kaladji (A)

Centre of Cardiovascular and Vascular Surgery, CHU Rennes, Rennes, France.
University of Rennes, Inserm, UMR_1099, Rennes, France.

Hervé Le Bars (H)

Département de Bactériologie-Virologie, Hygiène et Parasitologie-Mycologie, CHRU Brest, Brest, France.

Nasr Bahaa (N)

Service de Chirurgie Cardiaque Thoracique et Vasculaire, CHRU Brest, Brest, France.

Badra Ali (B)

Service de Chirurgie Cardiaque Thoracique et Vasculaire, CHRU Brest, Brest, France.

Caroline Piau (C)

Department of Bacteriology, CHU Rennes, Rennes, France.

Vincent Cattoir (V)

Department of Bacteriology, CHU Rennes, Rennes, France.
University of Rennes, Inserm, BRM (Bacterial Regulatory RNAs and Medicine), UMR_1230, Rennes, France.

Claire de Moreuil (C)

Service de Médecine Interne, Vasculaire et Pneumologie, Hôpital La Cavale Blanche, CHRU Brest, Brest, France.

Matthieu Revest (M)

Infectious Diseases and Intensive Care Unit, CHU Rennes, Rennes, France. matthieu.revest@chu-rennes.fr.
University of Rennes, Inserm, BRM (Bacterial Regulatory RNAs and Medicine), UMR_1230, Rennes, France. matthieu.revest@chu-rennes.fr.
CIC-Inserm 1414, CHU Rennes, Rennes, France. matthieu.revest@chu-rennes.fr.

Rozenn Le Berre (R)

Service de Médecine Interne, Vasculaire et Pneumologie, Hôpital La Cavale Blanche, CHRU Brest, Brest, France. rozenn.leberre@chu-brest.fr.
Brest University, Inserm, UMR_1078, Brest, France. rozenn.leberre@chu-brest.fr.

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