Handling Technique. Norian CRS Fast Set Putty. Fast hardening bone graft substitute.

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Handling Technique Fast Set Putty. Fast hardening bone graft substitute.

Table of contents Indications 2 Features and basic science 3 Preoperative planning 4 Surgical technique 5 Warning This description is not sufficient for immediate application of the instrumentation. Instruction by a surgeon experienced in handling this instrumentation is highly recommended. 1

Indications Norian Craniofacial Repair System (CRS) Fast Set Putty is a mouldable, biocompatible bone substitute that sets at body temperature. The ingredients for mixing the putty are provided separately. One container contains the sterile powder (calcium phosphate) and a vial contains a sterile aqueous solution (sodium phosphate). Mixing the components produces a mouldable putty, which is suitable for augmentation and restoration of the craniofacial skeleton. When fully cured, Fast Set Putty closely resembles the mineral phase of bone. It gradually remodels to bone via osteoclastic resorption and new bone formation. Indications Fast Set Putty is used for repairing or filling craniofacial defects and craniotomy cuts. It is also indicated for the restoration or augmentation of bony contours of the craniofacial skeleton, including the fronto-orbital, malar and mental areas. Clinical applications include: Cranioplasty Cranial recontouring (e. g. atrophy of temporal bone) Reconstruction of the frontal bone (intraoperative site) Cranial flap augmentation Augmentation genioplasty Skull base defect repair Restrictions Fast Set Putty is not suitable for the restoration of craniofacial continuity defects with a surface area greater than 25 cm 2. Contraindications See package insert. 2

Features and basic science Properties Easily shaped: Highly suitable for implantation into defects and for onlay applications Hardens in a warm, moist environment: There is no need to monitor moisture at the operative site Isothermal hardening prevents thermal injury to surrounding soft tissue Fast setting time (3 6 minutes): Shorter operative times Maximum compressive strength of approximately 30 Mpa (4350 psi) within 24 hours: This is 2 6 times greater than the compressive strength of cancellous bone Gradual remodeling to bone via osteoclastic resorption and new bone formation Basic science Self-setting calcium phosphate bone substitute Hardens isothermally in vivo to form carbonated apatite. This material closely resembles the mineral phase of bone. Fast Set Putty is biocompatible Carbonated apatite (carbonate content 4 6%) comprises 60 70% of the bone dry weight. With a carbonated content of 5%, Fast Set Putty therefore closely resembles the composition of bone. Hydroxylapatite, which is usually regarded as the mineral phase of bone, in contrast has no carbonate content. The properties of bone and Fast Set Putty are compared in Table 1. CNTS/SEC 81 65 49 32 16 0 64 51 38 26 13 0 423 338 254 169 85 0 264 211 158 106 53 0 Bone Sintered Hydroxyapatite 200 111 201 002 102 210 Coral-Derived Hydroxyapatite 2 THETA 211 112 300 202 23 26 29 32 35 Crystallographic analysis by powder x-ray diffraction (XRD) Characteristic Bone 1 Fast Set Putty Carbonate content 4.0 6.0 % ~5.0 % Ca/P molar ratio 1.33 1.73 1.67 Crystal order Low Low Perfect crystal size ~200 Å ~200 Å Chemical make-up Inorganic/organic Inorganic Table 1 Properties of Fast Set Putty vs. bone 1 Constantz B, Ison IC, Fulmer MT, Poser RD, Smith ST, VanWagoner M, Ross J, Goldstein SA, Jupiter JB, Rosenthal DI (1995) Skeletal repair by in situ formation of the mineral phase of bone. Science 267: 1796 1799 3

Preoperative planning Estimating cement volume* Burr hole filling 3 cc Cranial defect 10 25 cc Temporal bone augmentation 25 cc Suboccipital cranioplasty 5 10 cc Genioplasty 5 cc Orbital rim 5 cc * volumes are approximate Timing sequence The flow chart represents the changes in the material over time and the related surgical procedure. Timing sequence Mixing phase Working phase Hardening/Setting phase 45 90 seconds depending on vol. 2 minutes 3 6 minutes Temperature 18 23 C 37 C 37 C CRS properties Beginning of the chemical reaction Body temperature triggers curing Material starts curing, cristalline structure starts to develop Remains mouldable and contourable Surgical procedure Mix until both of the components are fully integrated to produce a homegeneous putty Apply CRS into surgical site Contour CRS Do not manipulate the material after 2 minutes of contact with body to prevent disruption of the crystallisation process Keep the material moist 4

Surgical technique 1 Prepare implant site Using lavage and/or suction instruments, remove blood clots and tissue debris while controlling active bleeding. Note: Remove excessive bone wax or collagen prior to implanting Fast Set Putty. 2 Open cup When the site is ready for implantation, prepare materials for mixing. Remove the cup from the tray, tap the cup on a hard surface and slowly peel back the lid to expose the powder. Take care not to spill any powder. 3 Add liquid Remove the vial from the tray and pour the liquid onto the powder. 4 Mix components (45 90 seconds) Using the spatula provided, mix the powder and liquid components together for 45 90 seconds depending on volume. Use a sweeping motion along the sides of the cup to incorporate all powder into the mix. Ensure that the components are fully integrated to produce a homogeneous putty. 5

5 Implant and contour material (within 2 minutes) Immediately apply the Fast Set Putty to the defect site with the spatula or by hand. Contour the putty manually, using a wet gloved finger or a surgical instrument. Complete all contouring within 2 minutes of implantation. Note: If Fast Set Putty is used as an onlay, the perimeter of the defect site should be cut or burred down so that the cement is fully contained. Ridges should also be created on the implant site to improve the mechanical adhesion of the cement to the bone. Skull Original defect Modified defect area for graft containment 6

Surgical technique 6 Allow Fast Set Putty to harden (3 6 minutes) The putty will set within 3 6 minutes at normal body temperature (37 C). Once the putty begins to harden, it must be left undisturbed to set properly. The Fast Set Putty should be kept moist by covering it with the skin flap or by gently drip irrigating the cement with warm saline (approximately 37 C) twice per minute. Note: Once the cement has hardened, an abrasive may be used to modify the contour, taking care not to chip the hardened material. Do not drill into the cement because this could shatter the implant. Fast Set Putty fully cures and reaches its ultimate compressive strength in 24 hours. Important: If more Fast Set Putty is needed to fill the defect, another kit may be mixed and added during the 2-minute implant period. If the 2-minute implant period has elapsed, wait 6 minutes for the putty to completely harden before adding more material. If adding a second layer after the 6-minute set time do not keep the cement moist by covering it with the skin flap, use the drip irrigation method. To increase mechanical bonding between layers, ensure the hardened putty is free of blood. 7

Fast Set Putty. Fast hardening bone graft substitute. Properties Easily shaped: Highly suitable for implantation into defects and for onlay applications Hardens in a warm, moist environment: There is no need to monitor moisture at the operative site Isothermal hardening prevents thermal injury to surrounding soft tissue Fast setting time (3 6 minutes): Shorter operative times Maximum compressive strength of approximately 30 Mpa (4350 psi) within 24 hours: This is 2 6 times greater than the compressive strength of cancellous bone Gradual remodeling to bone via osteoclastic resorption and new bone formation Clinical applications Cranioplasty Cranial recontouring (e.g. atrophy of temporal bone) Cranial flap augmentation Augmentation genioplasty Skull base defect repair Ordering information Fast Set Putty Art. No. FSP-03-01 FSP-05-01 FSP-10-01 FSP-15-01 Volume 3 cc (6 grams), sterile 5 cc (9 grams), sterile 10 cc (17 grams), sterile 15 cc (25 grams), sterile Norian and CRS are registered trademarks of the Norian Corporation. www.synthes.com Manufacturer: Norian Corporation 10260 Bubb Road Cupertino, California 95014-4166 USA A Company of Synthes-Stratec, Inc. Presented by: 0086 036.000.650 SE_0012074 AA Stratec Medical 2005 Printed in Switzerland LAG Subject to modifications.