The patient did well until 18 months later, when she presented to the Emergency Department with erythema and drainage from a medial malleolar wound. She was again treated with oral cephalexin, and on follow-up, an aspirate was taken from the ankle joint with only bloody return and negative culture results (no growth). Radiographs showed only a possible subtle loosening find more of the tibial component of the prosthesis. Nonetheless, based on clinical suspicion, the patient was admitted for intravenous antibiotics and taken to surgery for explantation of the TAR components with the placement of a vancomycin/gentamicin spacer. Intraoperative

irrigation with methylene blue demonstrated a sinus track from the medial malleolar wound to the joint space. Intraoperative cultures were positive only for methicillin-resistant Staphylococcus Tofacitinib price aureus (MRSA). Explanted specimens are the subject of this report. Tibial and talar components recovered during the implant removal surgery were placed aseptically in sterile specimen bags and placed directly on ice. Additionally, associated reactive

tissue was collected in sterile specimen containers and placed on ice. Two pieces of tissue for RT-PCR were deposited directly into RNase-free tubes containing RNALater® (Ambion) and stored at −20 °C. Postoperatively, the patient was maintained on intravenous vancomycin for 3 weeks, but was changed to daptomycin for a possible antibiotic-induced leucopenia. She subsequently

required re-exploration for persistent wound failure, with replacement of her selleck screening library antibiotic-impregnated cement spacer and treatment with tigecycline. Thereafter, her wound ultimately healed and she is now ambulating as tolerated with the cement spacer in place. We used the Ibis T5000 Universal Biosensor System, which is a multiprimer PCR technique used to rapidly identify bacteria associated with clinical specimens (Ecker et al., 2008). The Ibis T5000 is for research use only (RUO) and is not yet approved for use in diagnostic procedures. First, we extracted DNA from the tissue: approximately 1 mm3 of tissue was transferred to a microcentrifuge tube containing lysis buffer (Qiagen) and 20 μg mL−1 proteinase K (Qiagen). The sample was incubated at 55 °C until visual inspection indicated that lysis was achieved. Zirconia/Silica Beads (0.45 g of 0.1 mm diameter, Biospec, PN: 11079101z) were added to the microcentrifuge tube and the sample was homogenized for 10 min at 25 Hz using a Qiagen Tissuelyser (Model MM300, cat# 85210). Nucleic acid from the lysed sample was extracted using the Qiagen DNeasy Tissue kit. Supernatants (200 μL) containing the extracted nucleic acid were removed and aliquoted into the wells of an Ibis Bacterial Surveillance microtiter plate (Abbott, cat# 03N33-01), which is used for broad identification of bacterial species.