The prognosis of streptococcal prosthetic bone and joint infections depends on surgical management-A multicenter retrospective study.


Journal

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
ISSN: 1878-3511
Titre abrégé: Int J Infect Dis
Pays: Canada
ID NLM: 9610933

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 18 05 2019
revised: 11 06 2019
accepted: 12 06 2019
pubmed: 19 6 2019
medline: 28 10 2019
entrez: 19 6 2019
Statut: ppublish

Résumé

The optimal treatment of streptococcal prosthetic joint infections (PJIs) is unclear. A cohort of streptococcal PJIs was reviewed retrospectively in seven reference centers for the management of complex bone and joint infections, covering the period January 1, 2010 to December 31, 2012. Seventy patients with monomicrobial infections were included: 47 had infections of total hip arthroplasty and 23 had infections of total knee arthroplasty. The median age was 77 years (interquartile range (IQR) 69-83 years), the median Charlson comorbidity score was 4 (IQR 3-6), and 15.6% (n=11) had diabetes. The most commonly identified streptococcal species were Streptococcus agalactiae and Streptococcus dysgalactiae (38.6% (n=27) and 17.1% (n=12), respectively). Debridement, antibiotics and implant retention (DAIR) was performed after a median time of 7 days (IQR 3-8 days), with polyethylene exchange (PE) in 21% of cases. After a minimum follow-up of 2 years, 27% of patients had relapsed, corresponding to 51.4% of DAIR treatment cases and 0% of one-stage (n=15) or two-stage (n=17) exchange strategy cases. Rifampicin or levofloxacin in combination therapy was not associated with a better outcome (adjusted p= 0.99). S. agalactiae species and DAIR treatment were associated with a higher risk of failure. On multivariate analysis, only DAIR treatment and S. agalactiae were independent factors of relapse. Compared to DAIR without PE, DAIR with PE was only associated with a trend towards a benefit (odds ratio 0.33, 95% confidence interval 0.06-1.96; adjusted p= 0.44). Streptococcal PJIs managed with DAIR have a poor prognosis and S. agalactiae seems to be an independent factor of treatment failure.

Sections du résumé

BACKGROUND BACKGROUND
The optimal treatment of streptococcal prosthetic joint infections (PJIs) is unclear.
METHODS METHODS
A cohort of streptococcal PJIs was reviewed retrospectively in seven reference centers for the management of complex bone and joint infections, covering the period January 1, 2010 to December 31, 2012.
RESULTS RESULTS
Seventy patients with monomicrobial infections were included: 47 had infections of total hip arthroplasty and 23 had infections of total knee arthroplasty. The median age was 77 years (interquartile range (IQR) 69-83 years), the median Charlson comorbidity score was 4 (IQR 3-6), and 15.6% (n=11) had diabetes. The most commonly identified streptococcal species were Streptococcus agalactiae and Streptococcus dysgalactiae (38.6% (n=27) and 17.1% (n=12), respectively). Debridement, antibiotics and implant retention (DAIR) was performed after a median time of 7 days (IQR 3-8 days), with polyethylene exchange (PE) in 21% of cases. After a minimum follow-up of 2 years, 27% of patients had relapsed, corresponding to 51.4% of DAIR treatment cases and 0% of one-stage (n=15) or two-stage (n=17) exchange strategy cases. Rifampicin or levofloxacin in combination therapy was not associated with a better outcome (adjusted p= 0.99). S. agalactiae species and DAIR treatment were associated with a higher risk of failure. On multivariate analysis, only DAIR treatment and S. agalactiae were independent factors of relapse. Compared to DAIR without PE, DAIR with PE was only associated with a trend towards a benefit (odds ratio 0.33, 95% confidence interval 0.06-1.96; adjusted p= 0.44).
CONCLUSIONS CONCLUSIONS
Streptococcal PJIs managed with DAIR have a poor prognosis and S. agalactiae seems to be an independent factor of treatment failure.

Identifiants

pubmed: 31212103
pii: S1201-9712(19)30257-7
doi: 10.1016/j.ijid.2019.06.012
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Levofloxacin 6GNT3Y5LMF
Rifampin VJT6J7R4TR

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

175-181

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Rafael Mahieu (R)

Service de Maladies Infectieuses et Tropicales, CHU Angers, 49933 Angers, France; CRCINA, Inserm, Université de Nantes, Université d'Angers, Angers, France; Equipe ATIP AVENIR, CRCINA, Inserm, Université de Nantes, Université d'Angers, Angers, France. Electronic address: rafael.mahieu@chu-angers.fr.

Vincent Dubée (V)

Service de Maladies Infectieuses et Tropicales, CHU Angers, 49933 Angers, France; CRCINA, Inserm, Université de Nantes, Université d'Angers, Angers, France; Equipe ATIP AVENIR, CRCINA, Inserm, Université de Nantes, Université d'Angers, Angers, France. Electronic address: Vincent.Dubee@chu-angers.fr.

Valérie Seegers (V)

Institut de Cancérologie de l'Ouest, Biometry Department, Angers, France. Electronic address: Valerie.Seegers@ico.unicancer.fr.

Carole Lemarié (C)

Laboratory of Bacteriology, CHU Angers, Angers, France. Electronic address: CaLemarie@chu-angers.fr.

Séverine Ansart (S)

Department of Infectious Diseases, Hôpital Universitaire La Cavale Blanche, Brest, France. Electronic address: severine.ansart@chu-brest.fr.

Louis Bernard (L)

CHRU de Tours, Hôpital Bretonneau, Service de Médecine Interne et Maladies Infectieuses, 37044 Tours CEDEX 9, France. Electronic address: L.bernard@chu-tours.fr.

Gwenaël Le Moal (G)

Service de Maladies Infectieuses et Tropicales, CHU Poitiers, 86000, Poitiers, France. Electronic address: Gwenael.LE-MOAL@chu-poitiers.fr.

Nathalie Asseray (N)

Department of Infectious Diseases, Nantes University Hôpital, and CIC 1413, INSERM, Nantes, France. Electronic address: nathalie.asseray@chu-nantes.fr.

Cédric Arvieux (C)

Service des Maladies Infectieuses, Rennes University Hospital, 2 rue Henri Le Guilloux, 35043 Rennes, France. Electronic address: cedric.arvieux@chu-rennes.fr.

Céline Ramanantsoa (C)

Laboratoire de Microbiologie, Centre Hospitalier, Le Mans, France. Electronic address: cramanantsoa@ch-lemans.fr.

Hélène Cormier (H)

Service de Maladies Infectieuses et Tropicales, CHU Angers, 49933 Angers, France. Electronic address: Helene.Cormier@chu-angers.fr.

Erick Legrand (E)

Service de Rhumatologie, CHU Angers, Angers, France. Electronic address: ErLegrand@chu-angers.fr.

Pierre Abgueguen (P)

Service de Maladies Infectieuses et Tropicales, CHU Angers, 49933 Angers, France. Electronic address: PiAbgueguen@chu-angers.fr.

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Classifications MeSH