Bone and Joint Prosthetic Infections
Conditions
Keywords
Staphylococci, Streptococci, P acnes and Gram-negative bacteria
Brief summary
A national, prospective, open-label, non-interventional, multicentre, controlled study designed to evaluate a diagnostic method in patients undergoing hip, knee or shoulder prosthetic removal regardless of whether or not infection is suspected. Serological test results will have no impact on the therapeutic approach. Study objective: To evaluate the diagnostic performance of an antibody detection kit for the serological diagnosis of bone and joint prosthetic device infections cause by Staphylococci, Streptococci, Propionibacterium acnes (P. acnes) and Gram-negative bacteria versus the reference method: the bacterial culture of deep intraoperative samples.
Interventions
None listed
Sponsors
Diaxonhit
Study design
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Male or female patients 2. Patients 18 years of age or older 3. Patient with a bone and joint prosthetic device: total hip prosthesis (THP) or total knee prosthesis (TKP) or total shoulder prosthesis (TSP) 4. Patients with a revision of a failed prosthesis, regardless of the cause and whether septic or not 5. Patients who have not expressed their opposition to the use of their personal medical data and blood samples
Exclusion criteria
1. Patients already enrolled or clinically reviewed following a relapse 2. Patients with several prostheses requiring at least two revisions during the same surgical procedure 3. Patients for whom the microbiologist and/or doctor responsible for the care refuses that these patients participate in the study 4. HIV+ patients 5. Patients undergoing chemotherapy for a blood disease or solid tumour 6. Patients under guardianship or trusteeship 7. Patients who are expected to be difficult to monitor (life expectancy less than 1 year, or homeless people, foreigner in transit)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Sensitivity and specificity of test BJI 2 | 2 years | The diagnostic performance of the test during unique titration. * Sensitivity: estimated from the proportion of septic group patients with an antibody level above the defined threshold antibody concentration. * Specificity: estimated from the proportion of non-septic-group patients with an antibody level less than or equal to the defined threshold antibody concentration. * Positive likelihood ratio. * Negative likelihood ratio. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Interest of test BJI 2 | 2 years | * To evaluate the diagnostic interest of the BJI Inoplex 2 test in conjunction with the clinical and laboratory data collected: diagnostic strategy and score combining several criteria. * To evaluate the potential medical and economic benefits of using the test: number and cost of joint aspirations or hospital stays that would have been avoided, delayed diagnosis. * To describe the serological outcome after surgery in septic patients. |
Countries
France
Outcome results
None listed