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Solar® Total Shoulder System Upper Extremity Surgical Protocol (2)
Continued by :
【史赛克 Solar 全肩置换系统(一)】

http://www.gkqcw.cn/gkwinclude/show.asp?id=201

Fig 16. In cases where residual glenoid cartilage is present, a curette is used to remove the cartilage, then the spherical reamer is used to prepare the glenoid face (not fossa).

Fig 17. After glenoid sizing is completed with the surface trials, the superior/inferior and anterior/posterior axis is marked.

Fig 18. The superior drill hole is prepared first, using the universal drill/driver.

Fig 19. Each of the peg holes is checked to make certain that there is no break in the cortical shell.

Fig 20. A single batch of polymethylmethacrylate is mixed, the Gelfoam™ is removed and each of the holes is pressurized using a cement delivery
system. The implant is then placed and held by using the glenoid pusher
or thumb until completion of polymerization.

Fig 21. In cases where residual glenoid cartilage or a non-uniform glenoid surface is present, a spherical reamer is used to prepare the glenoid fossa and provide a uniform surface for instrumentation and implant placement.
The glenoid fossa is sized using surface templates.

Fig 22. When the appropriate coverage and size has been determined, a
matching spherical reamer is then used to prepare the surface.

Fig 23. The appropriate sized keeled glenoid guide is located on the glenoid fossa and the preparation is then marked using methylene blue or electrocautery.

Fig 24. The appropriate sized keeled glenoid trial is then introduced in the preparation and a trial reduction is performed to make certain there is a uniform seating of the component and that the keel is not bottoming out.

Fig 25. A single batch of polymethylmethacrylate is mixed, the Gelfoam™
is removed and the preparation is pressurized using a cement delivery system.

Fig 26. The implant is then placed and held until polymerization is complete.

Fig 27. If a long stem prosthesis is indicated, reaming depth is to the circumferential groove positioned at the top of the reamer shaft.

Fig 28. The broach should be seated to the circumferential groove around the proximal section. Do not seat the broach beyond this line.

Fig 29. The last broach used for reaming can be left in place and modular head trials can be tested.

Fig 30. The sizing of the modular head is important for success of this procedure. The previously resected head is compared with the modular trial head to determine both width and height.When a glenoid is used, this lateralizes the joint line so the humeral head height will be 4mm less than the resected head.

Fig 31. Only one fin cutter needs to be introduced; which should match the last size of broach and reamer used.

Fig 32. Continue to introduce until final placement is achieved. Be sure to remove any excess cement.

Fig 33. Final seating of the implant is achieved using the stem impactor as mentioned above.

Fig 34.Several sharp mallet blows are used to seat the head. Be sure the angle of the driver is in line with the axis of the trunnion (90° to collar face).
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    史赛克公司是全球最大的骨科及医疗科技公司之一,总部设于美国密西根州的克拉马苏市,在全球有14个生产研发及销售分部,员工超过一万六千多人。产品涉及关节置换、创伤、颅面、脊柱、手术设备、神经外科、耳鼻喉、介入性疼痛管理、微创手术、导航手术、智能化手术室及网络通讯、生物科技、医用床、急救推床等。由于业绩良好,史赛克公司分别被美国著名的《财富》杂志及《Business Week》 评为财富500强公司及全美50大医疗公司之一。在2005年更被评为在医疗业界中最受景仰的公司。美国史赛克公司在纽约股票交易所上市。
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