Open reduction and internal fixation (ORIF) with trans-articular screws or dorsal plating is the standard surgical technique for displaced Lisfranc injuries. This aim of this study is to compare the clinical outcomes of percutaneous reduction and internal fixation (PRIF) of low energy Lisfranc injuries with a matched, control group of patients treated with ORIF. Over a seven-year period (2012–2019), 16 consecutive patients with a low energy Myerson B2-type injury were treated with PRIF. Patient demographics were recorded within a prospectively maintained database at the institution. This study sample was matched for age, sex and mechanism of injury to a control group of 16 patients with similar Myerson B2-type injuries treated with ORIF. Clinical outcome was compared using the American Orthopaedic Foot and Ankle Society (AOFAS) midfoot score and Manchester Oxford Foot Questionnaire (MOXFQ). At a mean follow up of 43.0 months (95% CI 35.6 – 50.4), both the AOFAS and MOXFQ scores were significantly higher in the PRIF group compared to the control ORIF group (AOFAS 89.1vs 76.4, p=0.03; MOXFQ 10.0 vs 27.6, p=0.03). There were no immediate postoperative complications in either group. At final follow up, there was no radiological evidence of midfoot osteoarthritis in any patient in the PRIF group. Three patients in the ORIF group developed midfoot osteoarthritis, one of whom required midfoot fusion. PRIF is a technically simple, less invasive method of operative stabilisation of low energy Lisfranc injures which also appears to be associated with better mid-term clinical outcomes compared to ORIF.
This study aims to define the epidemiology of trauma presenting to a single centre providing all orthopaedic trauma care for a population of ∼ 900,000 over the first 40 days of the COVID-19 pandemic compared to that presenting over the same period one year earlier. The secondary aim was to compare this with population mobility data obtained from Google. A cross-sectional study of consecutive adult (> 13 years) patients with musculoskeletal trauma referred as either in-patients or out-patients over a 40-day period beginning on 5 March 2020, the date of the first reported UK COVID-19 death, was performed. This time period encompassed social distancing measures. This group was compared to a group of patients referred over the same calendar period in 2019 and to publicly available mobility data from Google.Aims
Methods
During open orthopaedic surgery, joints may be exposed to air, potentially leading to cartilage drying and chondrocyte death, however, the long-term effects of joint drying The patellar groove of anaesthetised rats was exposed (sham-operated), or exposed and then subjected to laminar airflow (0.25m/s; 60 minutes) before wounds were sutured and animals recovered. Animals were monitored for up to eight weeks and then sacrificed. Cartilage and chondrocyte properties were studied by histology and confocal microscopy, respectively.Objectives
Methods
Articular cartilage is attached to subchondral bone but it is not clear whether the tissues interact and influence in situ (within the matrix) chondrocyte survival. The aim of this study was to determine whether subchondral bone influences in situ chondrocyte survival. Articular cartilage explants harvested from the meta-carpophalangeal joints (N=6) of three-year old cows were placed into three groups:
subchondral bone excised from articular cartilage (Group A) subchondral bone left attached to articular cartilage (Group B) subchondral bone excised, but co-cultured with articular cartilage (Group C). Explants were cultured in serum-free media over 7 days. Using confocal laser scanning microscopy, fluorescent probes and biochemical assays, in situ chondrocyte viability and biophysical parameters (cartilage thickness, cell density, culture medium composition) were quantified over time (2.5 hours vs. 7 days) for Groups A, B and C. With excision of subchondral bone from articular cartilage (Group A), there was a marked increase in chondrocyte death over 7 days primarily within the superficial zone (p<
0.05). There was no significant increase in chondrocyte death within the superficial zone over the same time period for Groups B and C (p>
0.05). There was no significant difference in cartilage thickness or cell density between Groups A, B and C (p>
0.05). Corresponding increases in the protein content of the culture media for Groups B and C but not for Group A, suggested that the release of soluble factors from subchondral bone may have influenced chondrocyte survival. Subchondral bone significantly influences chondrocyte survival in articular cartilage in vitro. These data support the concept of a functional bone-cartilage system in vivo.