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Benefits of Polymerase Chain Reaction Combined With Culture for the Diagnosis of Bone and Joint Infections: A Prospective Test Performance Study.
Jacquier, Hervé; Fihman, Vincent; Amarsy, Rishma; Vicaut, Eric; Bousson, Valérie; Cambau, Emmanuelle; Crémieux, Anne-Claude; Delcey, Véronique; Hannouche, Didier; Kaci, Rachid; Laredo, Jean-Denis; Meunier, Fabienne; Nizard, Rémy; Ottaviani, Sébastien; Parlier, Caroline; Richette, Pascal; Sellier, Pierre; Zadegan, Fréderic; Lioté, Fréderic; Berçot, Béatrice.
Affiliation
  • Jacquier H; Laboratory of Bacteriology, Infectious Agents Department, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.
  • Fihman V; IAME UMR 1137, INSERM and Université de Paris, Paris, France.
  • Amarsy R; Bacteriology and Infection Control Unit, Department of Microbiology, University Hospital Henri Mondor, APHP, Creteil, France.
  • Vicaut E; EA Dynamyc, Université Paris Est Créteil-Ecole Vétérinaire de Maison Alfort, Créteil, France.
  • Bousson V; Infection Control Department, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Cambau E; Unit of Clinical Research, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Crémieux AC; Unit of Radiology, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Delcey V; Laboratory of Bacteriology, Infectious Agents Department, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.
  • Hannouche D; IAME UMR 1137, INSERM and Université de Paris, Paris, France.
  • Kaci R; Department of Infectious Diseases, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Laredo JD; Department of Medecine, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Meunier F; Department of Orthopaedic Surgery, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Nizard R; Department of Pathological Anatomy and Cytology, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Ottaviani S; Unit of Radiology, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Parlier C; Laboratory of Bacteriology, Infectious Agents Department, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.
  • Richette P; Department of Orthopaedic Surgery, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Sellier P; Federation of Rheumatology, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Zadegan F; Unit of Clinical Research, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Lioté F; Department of Pathological Anatomy and Cytology, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
  • Berçot B; Department of Medecine, Saint Louis-Lariboisiere-Fernand Widal Hospital Group, APHP, Paris, France.
Open Forum Infect Dis ; 6(12): ofz511, 2019 Dec.
Article in En | MEDLINE | ID: mdl-31909081
ABSTRACT

BACKGROUND:

The microbiological diagnosis of bone and joint infections (BJI) currently relies on cultures, and the relevance of molecular methods is still debated. The aim of this study was to determine whether polymerase chain reaction (PCR) could improve the etiological diagnosis of BJI.

METHODS:

A prospective study was conducted during a 4-year period at Lariboisiere University Hospital (Paris, France), including patients with suspicion of infectious spondylodiscitis, septic arthritis, prosthetic joint infections, and respective noninfected groups. Clinical and radiological data were collected at inclusion and during follow-up. All samples were analyzed by conventional cultures and 16S ribosomal deoxyribonucleic acid (rDNA) gene (16S-PCR). Specific cultures and PCR targeting Mycobacterium tuberculosis were also performed for spondylodiscitis samples. Case records were subsequently analyzed by an independent expert committee to confirm or invalidate the suspicion of infection and definitively classify the patients in a case or control group. The sensitivity of the combination of culture and PCR was compared with culture alone.

RESULTS:

After expert committee analysis, 105 cases of BJI cases and 111 control patients were analyzed. The most common pathogens of BJI were staphylococci (30%), M tuberculosis (19%), and streptococci (14%). Adding PCR enhanced the sensitivity compared with culture alone (1) for the diagnosis of M tuberculosis spondylodiscitis (64.4% vs 42.2%; P < .01) and (2) for nonstaphylococci BJI (81.6% vs 71.3%; P < .01). It is interesting to note that 16S-PCR could detect BJI due to uncommon bacteria such as Mycoplasma and fastidious bacteria.

CONCLUSIONS:

Our study showed the benefit of 16S-PCR and PCR targeting M tuberculosis as add-on tests in cases of suspected BJI.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Observational_studies Language: En Journal: Open Forum Infect Dis Year: 2019 Document type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Observational_studies Language: En Journal: Open Forum Infect Dis Year: 2019 Document type: Article Affiliation country: France