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  3. The Not-So-Good Prognosis of Streptococcal Periprosthetic Joint Infection Managed by Implant Retention: The Results of a Large Multicenter Study.
 

The Not-So-Good Prognosis of Streptococcal Periprosthetic Joint Infection Managed by Implant Retention: The Results of a Large Multicenter Study.

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BORIS DOI
10.7892/boris.99264
Publisher DOI
10.1093/cid/cix227
PubMed ID
28369296
Description
Background

Streptococci are not an infrequent cause of periprosthetic joint infection (PJI). Management by debridement, antibiotics, and implant retention (DAIR) is thought to produce a good prognosis, but little is known about the real likelihood of success.

Methods

Retrospective, observational, multicenter, international study performed during 2003-2012. Eligible patients had a streptococcal PJI that was managed with DAIR. The primary endpoint was failure, defined as death related to infection, relapse/persistence of infection, or the need for salvage therapy.

Results

Overall, 462 cases were included (median age 72 years, 50% men). The most frequent species was S.agalactiae (34%), and 52% of all cases were hematogenous. Antibiotic treatment was primarily using β-lactams, and 37% of patients received rifampin. Outcomes were evaluable in 444 patients: failure occurred in 187 (42.1%, 95% confidence interval: 37.5%-46.7%) after a median of 62 days from debridement; patients without failure were followed for a median of 802 days. Independent predictors (hazard ratios) of failure were rheumatoid arthritis (2.36), late post-surgical infection (2.20), and bacteremia (1.69). Independent predictors of success were exchange of removable components (0.60), early use of rifampin (0.98 per day of treatment within the first 30 days), and long treatments (≥21 days) with β-lactams, either as monotherapy (0.48) or in combination with rifampin (0.34).

Conclusions

this is the largest series of streptococcal PJI managed by DAIR, showing a worse prognosis than previously reported. The beneficial effects of exchanging the removable components and of β-lactams are confirmed, and maybe also a potential benefit from adding rifampin.
Date of Publication
2017-06-15
Publication Type
article
Subject(s)
600 - Technology::610 - Medicine & health
500 - Science::570 - Life sciences; biology
Keyword(s)
DAIR biofilm bone and joint infection rifampin
Language(s)
en
Contributor(s)
Lora-Tamayo, Jaime
Senneville, Éric
Ribera, Alba
Bernard, Louis
Dupon, Michel
Zeller, Valérie
Li, Ho Kwong
Arvieux, Cédric
Clauss, Martin
Uçkay, Ilker
Vigante, Dace
Ferry, Tristan
Iribarren, José Antonio
Peel, Trisha N
Sendi, Parhamorcid-logo
Universitätsklinik für Infektiologie
Miksic, Nina Gorišek
Rodríguez-Pardo, Dolors
Del Toro, María Dolores
Fernández-Sampedro, Marta
Dapunt, Ulrike
Huotari, Kaisa
Davis, Joshua S
Palomino, Julián
Neut, Danielle
Clark, Benjamin M
Gottlieb, Thomas
Trebše, Rihard
Soriano, Alex
Bahamonde, Alberto
Guío, Laura
Rico, Alicia
Salles, Mauro Jc
Pais, M José G
Benito, Natividad
Riera, Melchor
Gómez, Lucía
Aboltins, Craig A
Esteban, Jaime
Horcajada, Juan Pablo
O'Connell, Karina
Ferrari, Matteo
Skaliczki, Gábor
San Juan, Rafael
Cobo, Javier
Sánchez-Somolinos, Mar
Ramos, Antonio
Giannitsioti, Efthymia
Jover-Sáenz, Alfredo
Baraia-Etxaburu, Josu Mirena
Barbero, José María
Choong, Peter F M
Asseray, Nathalie
Ansart, Séverine
Le Moal, Gwenäel
Zimmerli, Werner
Ariza, Javier
Additional Credits
Universitätsklinik für Infektiologie
Series
Clinical infectious diseases
Publisher
Oxford University Press
ISSN
1058-4838
Access(Rights)
open.access
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