header advert
Results 1 - 3 of 3
Results per page:
Applied filters
Content I can access

Include Proceedings
Dates
Year From

Year To
Orthopaedic Proceedings
Vol. 104-B, Issue SUPP_10 | Pages 6 - 6
1 Oct 2022
Schoenmakers J Boer R Gard L Kampinga GA van Oosten M van Dijl JM Jutte PC Wouthuyzen-Bakker M
Full Access

Aim

Prompt recognition and identification of the causative microorganism in acute septic arthritis of native and prosthetic joints is vital to increase the chances of successful treatment. The aim of this study was to independently assess the diagnostic accuracy of the multiplex BIOFIRE® Joint Infection (JI) Panel (investigational use only) in synovial fluid for rapid diagnosis

Method

Synovial fluid samples were prospectively collected at the University Medical Center Groningen from patients who had a clinical suspicion of a native septic arthritis, early acute (post-operative, within 3 months after arthroplasty) periprosthetic joint infection (PJI) or late acute (hematogenous) PJI. JI Panel results were compared to culture-based methods as reference standard.


Bone & Joint Open
Vol. 2, Issue 10 | Pages 879 - 885
20 Oct 2021
Oliveira e Carmo L van den Merkhof A Olczak J Gordon M Jutte PC Jaarsma RL IJpma FFA Doornberg JN Prijs J

Aims

The number of convolutional neural networks (CNN) available for fracture detection and classification is rapidly increasing. External validation of a CNN on a temporally separate (separated by time) or geographically separate (separated by location) dataset is crucial to assess generalizability of the CNN before application to clinical practice in other institutions. We aimed to answer the following questions: are current CNNs for fracture recognition externally valid?; which methods are applied for external validation (EV)?; and, what are reported performances of the EV sets compared to the internal validation (IV) sets of these CNNs?

Methods

The PubMed and Embase databases were systematically searched from January 2010 to October 2020 according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. The type of EV, characteristics of the external dataset, and diagnostic performance characteristics on the IV and EV datasets were collected and compared. Quality assessment was conducted using a seven-item checklist based on a modified Methodologic Index for NOn-Randomized Studies instrument (MINORS).


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_22 | Pages 15 - 15
1 Dec 2017
Gelderman SJ Jutte PC Boellaard R Kampinga GA Ploegmakers JJ Glaudemans AWJM Wouthuyzen-Bakker M
Full Access

Aim

Diagnosing a prosthetic joint infection (PJI) can be difficult. Several imaging modalities are available, but the choice which technique to use is often based on local expertise, availability and costs. Some centers prefer to use 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) as first imaging modality of choice, but due to a lack of accurate interpretation criteria, FDG-PET is currently not routinely applied for diagnosing PJI. With FDG-PET it is difficult to differentiate between FDG uptake due to reactive inflammation and uptake due to an infection. Since the physiological uptake pattern around a joint prosthesis is not fully elucidated, the aim of this study was to determine: i) the FDG uptake pattern in non-infected total hip prostheses and, ii) to evaluate whether there is a difference in uptake between cemented and non-cemented prostheses.

Method

Patients with a primary total hip arthroplasty (1995–2016) without clinical signs of an infection that underwent a FDG-PET for another indication (mainly suspicion of malignancy) were included and retrospectively analysed. Patients in whom the prosthesis was implanted < 6 months prior to FDG-PET were excluded, to avoid post-surgical effects. Scans were visually and quantitatively analysed. Quantitative analysis was performed by calculating maximum and peak standardized uptake values (SUVmax and SUVpeak) by volume of interests (VOIs) at eight different locations around the prosthesis, from which the mean SUV was calculated. SUV was standardized by the liver SUV that was taken as background.