For HTO patients, bi-plane medial-based opening-wedge osteotomy was performed. The method of Miniaci was used to preoperatively define the amount of correction needed, and TomoFix medial high tibial plates and screws (DePuy Synthes, Switzerland) or a Synthes locking compression plate (LCP) system (DePuy Synthes, Switzerland) were used for fixation [26 (link)]. After surgery, partial weight-bearing (maximum 20 kg) was allowed for six weeks, after which full weight-bearing was started gradually. Prophylactic anticoagulant was used for six weeks. At 18 months after surgery, the metal plate and screws were removed, to allow imaging at two years.
Tomofix medial high tibial plates and screws
The TomoFix medial high tibial plates and screws are an orthopedic implant system designed to provide fixation for high tibial osteotomies. The plates and screws are made of titanium alloy and are intended to stabilize the bone during the healing process after the osteotomy procedure.
Lab products found in correlation
2 protocols using tomofix medial high tibial plates and screws
Distraction Surgery and High Tibial Osteotomy Protocols
For HTO patients, bi-plane medial-based opening-wedge osteotomy was performed. The method of Miniaci was used to preoperatively define the amount of correction needed, and TomoFix medial high tibial plates and screws (DePuy Synthes, Switzerland) or a Synthes locking compression plate (LCP) system (DePuy Synthes, Switzerland) were used for fixation [26 (link)]. After surgery, partial weight-bearing (maximum 20 kg) was allowed for six weeks, after which full weight-bearing was started gradually. Prophylactic anticoagulant was used for six weeks. At 18 months after surgery, the metal plate and screws were removed, to allow imaging at two years.
Distraction Osteogenesis for Knee Osteoarthritis
Nephew, Warsaw, IN) with fixation using GentaPalacos cement (Heraeus, Hanau,
Germany). For HTO treatment, biplane medial-based opening-wedge osteotomy was
performed. TomoFix medial high tibial plates and screws (DePuy Synthes,
Switzerland) or Synthes locking compression plate system (DePuy Synthes,
Switzerland) were used for fixation. The method of Miniaci15 (link) was used to preoperatively define the size of the opening. After both TKA
and HTO, routine rehabilitation and thromboembolism prophylaxis was provided
after surgery. Distraction surgery was performed with a proof-of-concept device
consisting of 2 dynamic monotubes (Triax, Stryker, 45 kg spring with 3 mm
displacement) bridging the knee joint medially and laterally. Each monotube was
fixed to 2 bone-pins on each end (tibia and femur). The tubes were distracted by
2 mm during surgery and by 1 mm every day postsurgery, until a total distraction
of 5 mm was reached, confirmed on radiographs. Afterward, patients were
discharged, with heparin prescribed for 9 weeks, and allowed full weightbearing
of the distracted knee, supported by crutches if needed. At 3 to 4 weeks after
surgery, radiographic evaluation of distraction and clinical evaluation of pin
tracts was performed in the outpatient clinic. After 6 to 7 weeks the frame and
pins were surgically removed.
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