Peanut Growth Control Plating System. Surgical Technique

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Transcription:

Peanut Growth Control Plating System Surgical Technique

1 Peanut Growth Control Plating System Table of Contents System Design Features... 2 Instrument Tray... 5 Implant Caddy... 6 Surgical Technique... 7 Post-Operative Care... 12 Removal... 12 Ordering Information... 14 Indications and Contraindications... 15 This technique is presented to demonstrate surgical techniques of Charles Price, M.D., Kenneth Noonan, M.D., and Jack Flynn, M.D. Biomet Trauma, as the manufacturer and distributor of this system, does not practice medicine. The surgeon who performs any surgical procedure is responsible for determining and utilizing the appropriate devices and techniques for implanting all products in each patient.

2 Peanut Growth Control Plating System System Design Features Plate Holding Forceps integrate a split K-Wire channel for a 1.6 mm guide wire. Offset design allows for easy passage of instruments into the plate and facilitates unobstructed fluoroscopic views P/N 24400 Plate design incorporates proximal and distal K-wire holes, providing the option of centering the plate without invading the physis P/N 24472 P/N 24436 P/N 24425 P/N 24474 Variable Drill Sleeves limit extreme drilling trajectories which can cause poor screw seating Non-locking, Fixed, and Variable 2.7 mm Drill Sleeves accommodate the Wire Sleeve Inserts for efficient stepwise screw insertion preparation and soft tissue protection P/N 24470 Working Cannula can be used to protect against soft tissue damage and can also serve as an inserter when used with locking drill sleeves

3 Peanut Growth Control Plating System P/N 24420 Plate Inserter/Extractor is cannulated to pass over a central guide wire Plate removal is simple. The Inserter/Extractor s tip threads into the plate s center hole to allow for captured removal as screws are disengaged P/N 24412 3.5 mm Cannulated Hex Driver with Ratcheting AO Handle Stepped tip securely holds hex slot to protect against screw loss P/N 22880 P/N 24485 In the event that a screw head becomes damaged during insertion or removal, the surgeon may utilize the 3.5 mm Hex Screw Extractor as a means of retrieval The Extractor tip is designed with cutting flutes that will engage any 3.5 mm hex P/N 24480 Overwire Depth Gauge for screw sizing

4 Peanut Growth Control Plating System System Design Features (cont.) Low profile pre-contoured plate geometry conforms to patient anatomy for optimized fit and functionality. Two plate styles Arched and Stepped for plate-to-bone interface Built in washer and elevated plate design for reduced contact with growth plate and periosteum Color coded for easy discernment Threaded screw holes are designed to hold drill sleeves securely within the plate during screw hole preparation Recessed screw holes allow for low profile seating of screws Screw Material: Titanium alloy Reverse buttress threads designed to resist pull out Both plates available in 16 mm and 12 mm sizes to accommodate varying patient anatomies Stepped Arched

5 Peanut Growth Control Plating System Instrument Tray Catalog No. Description Qty 22880 Ratcheting AO Handle 1 24400 Plate Holding Forcep 1 24412 3.5 mm Cannulated Hex Driver 2 24420 Plate Inserter / Extractor 1 24425 Variable Drill Sleeve 2.7 mm 2 24436 Fixed Drill Sleeve 2.7 mm 2 24440 2.7 mm Solid AO Drill 2 24445 2.7 mm Cannulated AO Drill 2 24470 Working Cannula 1 24472 Non-Locking Drill Sleeve 2 24474 Wire Sleeve Insert 3 24480 Overwire Depth Gauge 1 24485 3.5 mm Hex Screw Extractor 2 595402 Instrument Tray 1

6 Peanut Growth Control Plating System Implant Caddy Catalog No. Description Qty 24612 12 mm Stepped Peanut Plate 4 24616 16 mm Stepped Peanut Plate 4 24632 12 mm Arched Peanut Plate 4 24636 16 mm Arched Peanut Plate 4 24516 4.5 mm x 16 mm Cannulated Screw 8 24524 4.5 mm x 24 mm Cannulated Screw 8 24532 4.5 mm x 32 mm Cannulated Screw 16 24540 4.5 mm x 40 mm Cannulated Screw 8 24716 4.5 mm x 16 mm Solid Screw 8 24724 4.5 mm x 24 mm Solid Screw 8 24732 4.5 mm x 32 mm Solid Screw 16 24740 4.5 mm x 40 mm Solid Screw 8 456469 Screw Holding Forceps 1 24415 8 in Guide Wire, Threaded Tip 8

7 Peanut Growth Control Plating System Surgical Technique Patient Positioning Position patient in the supine position on the appropriately sized fracture table. Abduct the leg for fluoroscopic unit access and drape in the customary fashion. Step 1 Fluoroscopically locate the growth plate and hold the Peanut Plate in position using the Plate Holding Forceps (PN 24400). Mark a 2-3 cm incision on the skin. Incise and carefully divide skin and fascia, avoiding disturbance of the periosteum. For provisional fixation of the plate, insert a 1.6 mm K-Wire (PN 24415) into the growth plate as shown. Select the appropriate sized plate to best match the patient s anatomy (12 mm/16 mm plates available in both Arched and Stepped designs). The Stepped plates are designed primarily for usage on the proximal tibia, but either plate can be used according to surgeon preference. Technique Note: If you elect to avoid wire placement in the growth plate, alternative K-Wire holes have been incorporated into the plate s design to provide the option of placing wires proximally and distally to the physeal line.

8 Peanut Growth Control Plating System Shown: 16 mm Stepped Plate (PN 24616) Top screw hole with Variable Drill Sleeve/Wire Sleeve Insert, bottom screw hole with Fixed Drill Sleeve/Wire Sleeve Insert Step 2 The appropriate drill sleeves are selected and threaded into the screw holes. Wire Sleeve Inserts (PN 24474) are threaded into the drill sleeves. The surgeon has the option of using Fixed (PN 24436) or Variable (PN 24425) 2.7 mm Drill Sleeves. Once the insertion apparatus is assembled, the plate is passed over the guide wire through the central hole of the plate, centering the plate over the physis. Confirm position with the fluoroscope.

9 Peanut Growth Control Plating System Step 3 The epiphyseal guide wire is placed through the Wire Sleeve. Insert followed by the metaphyseal guide wire. Once both wires are placed, the epiphyseal Wire Sleeve Insert is removed in preparation for drilling. With two or more K-Wires in place, two points of fixation are achieved allowing the Plate Holding Forceps and central guide wire to be removed. Technique Note: To allow for maximum screw angulation prior to becoming fixed, place wire/ screws as parallel as possible.

10 Peanut Growth Control Plating System Step 4 After removing the Wire Sleeve Insert, the epiphyseal screw hole is prepared using the 2.7 mm Cannulated A/O Drill (P/N 24445). Bicortical drilling is not necessary. Step 5 An appropriate sized screw (16, 24, 32, or 40 mm) is selected and passed over the guide wire. Provisionally tighten the screw to allow for any later adjustments required when the second screw is introduced. Drill bits are calibrated to read off the top of the Drill Sleeves.

11 Peanut Growth Control Plating System Step 6 Metaphyseal screw preparation ensues in the same fashion as the epiphyseal screw using the 2.7 mm Cannulated Drill. Step 7 The metaphyseal screw can now be inserted over the guide wire. Lastly, both screws are definitively tightened and fully seated into the plate. Technique Note: Avoid over-tightening of screws. Doing so can create excessive pressure between the periosteum and plate. Confirm fluoroscopically that screws are not violating the growth plate or joint space and close the wound in the customary fashion.

12 Peanut Growth Control Plating System Post-Operative Care Patients are typically discharged from the hospital the same or next day. It is recommended that guided growth progress visits take place every 2-3 months, or per surgeon preference, to limit over correction as well as to monitor implant condition. Removal Plate removal is imperative to limit over correction and will usually occur within a window of 6 to 18 months following introduction. It is important to bear in mind that the time of removal is contingent upon the amount of correction needed to fully correct the deformity. Once the implant is removed, patients should also be monitored until skeletal maturity to protect against recurrent deformities. Before disengaging the screws, the Plate Inserter/ Extractor (PN 24420) is threaded into the central hole of the plate to allow for captured removal.

13 Peanut Growth Control Plating System Damaged Screw Removal In the event that the hex head of the screw becomes damaged during insertion or removal, the surgeon may utilize the 3.5 mm Hex Screw Extractor (PN 24485) as a means of retrieval. The Extractor tip is designed with cutting flutes to engage any 3.5 mm hex slot.

14 Peanut Growth Control Plating System Ordering Information Plates Catalog No. Description Qty 24612 24616 24632 24636 12 mm Stepped Peanut Plate 16 mm Stepped Peanut Plate 12 mm Arched Peanut Plate 16 mm Arched Peanut Plate 4 4 4 4 Screws Catalog No. Description Qty 24516 24524 24532 24540 24716 24724 24732 24740 4.5 mm x 16 mm Cannulated Peanut Screw 4.5 mm x 24 mm Cannulated Peanut Screw 4.5 mm x 32 mm Cannulated Peanut Screw 4.5 mm x 40 mm Cannulated Peanut Screw 4.5 mm x 16 mm Solid Peanut Screw 4.5 mm x 24 mm Solid Peanut Screw 4.5 mm x 32 mm Solid Peanut Screw 4.5 mm x 40 mm Solid Peanut Screw 8 8 16 8 8 8 16 8 Instruments Catalog No. Description Qty 22880 24400 24412 24420 24425 24436 24470 24472 24474 24480 24485 456469 595402 Ratcheting AO Handle Plate Holding Forcep 3.5 mm Cannulated Hex Driver Plate Inserter / Extractor Variable Drill Sleeve 2.7 mm Fixed Drill Sleeve 2.7 mm Working Cannula Non-Locking Drill Sleeve Wire Sleeve Insert Overwire Depth Gage 3.5 mm Hex Screw Extractor Screw Holding Forceps Instrument Tray 1 1 2 1 2 2 1 2 3 1 2 1 1 Disposables Catalog No. Description Qty 24445 24440 24415 2.7 mm Cannulated AO Drill 2.7 mm Solid AO Drill 8 inch Guide Wire, Threaded Tip 2 2 8

15 Peanut Growth Control Plating System Indications and Contraindications INDICATIONS The Peanut Growth Control Plating System is designed for redirecting the angle of growth of long bone(s) in pediatric patients (patients who have not had physeal closure/reached skeletal maturity). This is useful for gradually correcting angular deformities in pediatric patients with an open physis. Specific conditions/diseases for which the device will be indicated include valgus, varus or flexion extension deformities of the knee (femur and/or tibia); valgus, varus or plantar flexion deformities of the ankle, valgus or varus deformities of the elbow, as well as radial or ulnar deviation, flexion or extension deformities of the wrist (radius). CONTRAINDICATIONS 1. Physeal closure/skeletal maturity. 2. Active infection. 3. Patient conditions including blood supply limitations, and insufficient quantity or quality of bone. 4. Patients with mental or neurologic conditions who are unwilling or incapable of following postoperative care instructions or materials. 5. Foreign body sensitivity. Where material sensitivity is suspected, testing is to be completed prior to implantation of the device.

16 Peanut Growth Control Plating System Notes

This material is intended for health care professionals and the Zimmer Biomet sales force only. Distribution to any other recipient is prohibited. All content herein is protected by copyright, trademarks and other intellectual property rights owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated. This material must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet. Check for country product clearances and reference product specific instructions for use. For complete product information, including indications, contraindications, warnings, precautions, and potential adverse effects, see the package insert, zimmerbiomet.com, or contact your local Zimmer Biomet representative. Not for distribution in France. 2016 Zimmer Biomet Authorized Representative Biomet UK Ltd. Waterton Industrial Estate Bridgend, South Wales CF31 3XA UK BMET0341.0-GBL REV0316 Legal Manufacturer Biomet Trauma P.O. Box 587 56 E. Bell Drive Warsaw, Indiana 46581 USA www.zimmerbiomet.com 0086 CE mark on a surgical technique is not valid unless there is a CE mark on the product label.