STEP-BY-STEP INSTRUCTIONS ON THE PROSTHETIC PROCEDURES. Straumann Anatomic IPS e.max Abutment
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1 STEP-BY-STEP INSTRUCTIONS ON THE PROSTHETIC PROCEDURES Straumann Anatomic IPS e.max Abutment
2 The ITI (International Team for Implantology) is academic partner of Institut Straumann in the areas of research and education.
3 CONTENT Straumann Anatomic IPS e.max 1 Abutment 2 1. Cement-retained crowns and bridges Straumann Anatomic IPS e.max 1 Abutment Lab procedure Straumann Anatomic IPS e.max 1 Abutment Prosthetic procedure Straumann Anatomic IPS e.max 1 Abutment Chairside procedure for temporary restorations 8 2. Screw-retained crowns, directly veneered Straumann Anatomic IPS e.max 1 Abutment Lab procedure Straumann Anatomic IPS e.max 1 Abutment Prosthetic procedure Screw-retained crowns using the press-on technique Straumann Anatomic IPS e.max 1 Abutment Lab procedure Straumann Anatomic IPS e.max 1 Abutment Prosthetic procedure 26 Important guidelines 27
4 STRAUMANN ANATOMIC IPS e.max 1 ABUTMENT Intended use p Cement-retained crowns and bridges via mesostructure Conventional procedure Temporary restoration chairside p Screw-retained crowns Direct veneering (with IPS e.max Ceram 1 ) Press-on technique (with IPS e.max ZirPress 1 ) Material p Zirconium dioxide Characteristics Simple p Processing of a highly esthetic ceramic abutment in different colors with conventional lab methods p Less grinding necessary due to prepared mucosa margins p Adaptation to natural soft tissue contour due to prepared mucosa margins in different heights p Oval shape resembles emergence profile of a natural tooth Reliable p Biocompatible and low thermal conductivity p High-performance all-ceramics thanks to a high strength and high fracture toughness p Reduced risk of margins shining through the soft tissue even with thin mucosa biotype p CrossFit Connection p Precise fit Only use an original Straumann basal screw for ceramic abutment for the final insertion of the Straumann Anatomic IPS e.max 1 Abutment. The Straumann Anatomic IPS e.max 1 Abutment is available in the following shades: MO 0 and MO 1 (MO = Medium Opacity). Recommendations regarding the sterilization procedure can be found in the instructions for use. 2 Straumann Anatomic IPS e.max Abutment
5 1. CEMENT-RETAINED CROWNS AND BRIDGES Cement-retained restorations need to fulfill the following criteria (see 2c): p Individualized abutments must have cusp and marginal ridge support. p The maximum thickness of the veneering material on top of the coping must not exceed a maximum of 2.0 mm in all directions. p Avoid any sharp edges. 1.1 Straumann Anatomic IPS e.max 1 Abutment Lab procedure The following case describes the fabrication of a cement-retained crown by using the Straumann Anatomic IPS e.max 1 Abutment. 1a Step 1 Fabricating the master cast and wax-up p Fabricate the master cast including a gingival mask with the corresponding implant analog (see instructions in chapter 5 in brochure Art. No ). 1b p For optimal esthetic planning, design a full anatomical wax-up. 1c p Make a silicone key over the full wax-up in order to define the optimal shape of the modified abutment. 1. Cement-retained crowns and bridges 3
6 2a Step 2 Preparing the Straumann Anatomic IPS e.max 1 Abutment p Place the abutment on the polishing aid / analog and hand tighten the screw using the SCS screwdriver. 2b p For the individualization of the Straumann Anatomic IPS e.max 1 Abutment, it is recommended to work with a water-cooled turbine and abrasive instruments that are appropriate for grinding sintered ZrO 2 material. Work with a low grinding pressure and avoid any spark formation. The Ivoclar Vivadent grinding instrument recommendations for IPS e.max 1 must be followed. 2c 0.75 mm 0.5 mm RC GH min. 4 mm 1.3 mm 0.75 mm 0.5 mm 3.5 mm RC GH 3.5 mm min. 4 mm In order to keep sufficient stability of the abutment, do not deviate from the dimensions shown in the following graphics (2c). The height of the abutment must achieve at least 65 % of the complete restoration. 16 mm RC 16 mm RC NC GH NC GH 3.5 mm 0.5 mm 0.3 mm min. 4 mm 3.5 mm 1.3 mm 16 mm NC 16 mm NC min. 4 mm p The final geometry of the abutment has to meet the requirements of the material of the final restoration for cementretained crowns and bridges. Cemented 4 1. Cement-retained crowns and bridges
7 2d p Following the Ivoclar Vivadent grinding instrument recommendations for IPS e.max 1 a regeneration firing for cement-retained crowns and bridges is not required. The regeneration firing has to be conducted if the Ivoclar Vivadent grinding instrument recommendations for IPS e.max 1 are not followed or if a further thermal processing is necessary. The regeneration firing parameter are: 65 C (117 F) per minute heating up to 1050 C (1922 F) / 15 minute holding time and long-term cooling down with 25 C (45 F) per minute to 750 C (1382 F). 3a Step 3 Fabricating the superstructure p Use a standard procedure to fabricate the ceramic coping with the Straumann CARES Scan CS2 scanner and the Straumann CARES Visual software. 3b p Veneer the coping with conventional veneering material synchronized to the thermal expansion coefficient of the ceramic coping. p Coefficient of thermal expansion 2 (CTE) ( C ) ± K -1 p For veneering follow the recommendations of the ceramic material manufacturer. 1. Cement-retained crowns and bridges 5
8 3c 3d In case of adhesive bonding, sandblast the portions of the abutment surface which will be covered with cement with Al 2 O 3 (type 100 microns) at bar (15 30 psi). While sandblasting, the implant configuration must be protected with the polishing aid Cement-retained crowns and bridges
9 1.2 Straumann Anatomic IPS e.max 1 Abutment Prosthetic procedure The final restoration is delivered to the doctor s office on the master cast. Step 1 Preparation p Remove the healing cap or temporary restoration. p Remove the superstructure from the master cast and unscrew the abutment from the analog. p Clean and dry the interior of the implant and the abutment thoroughly. p Prepare the surface of the abutment corresponding to the cementation material which will be used (e.g. in case of adhesive bonding apply primer). p Condition the inner surface of the superstructure according to the instructions for use given by the according manufacturer (e.g. in case of adhesive bonding apply primer). 2a Step 2 Final insertion p Position the cleaned abutment in the implant. Tighten the screw to 35 Ncm using the SCS screwdriver along with the ratchet and the torque control device (see instructions in chapter 7.5 in brochure Art. No ). 2b p Close the SCS screw channel with cotton and sealing compound (i.e. gutta-percha). This allows for later removal of the modified abutment in the event a restoration replacement is required. p Cement the superstructure onto the abutment. p Remove any excess cement. Only use an original Straumann basal screw for ceramic abutment for the final insertion of the Straumann Anatomic IPS e.max 1 Abutment. 1. Cement-retained crowns and bridges 7
10 1.3 Straumann Anatomic IPS e.max 1 Abutment Chairside procedure for temporary restorations The following case describes the usage of the Straumann Anatomic IPS e.max 1 Abutment chairside. 1a Step 1 Preparing the Straumann Anatomic IPS e.max 1 Abutment p For the individualization of the Straumann Anatomic IPS e.max 1 Abutment, it is recommended to work with a watercooled turbine and abrasive instruments that are appropriate for grinding sintered ZrO 2 material. Work with a low grinding pressure and avoid any spark formation. The Ivoclar Vivadent grinding instrument recommendations for IPS e.max 1 must be followed. 1b 0.75 mm 0.5 mm RC GH min. 4 mm 1.3 mm 0.75 mm 0.5 mm 3.5 mm RC GH 3.5 mm min. 4 mm In order to keep sufficient stability of the abutment, do not deviate from the dimensions shown in the following graphics (1b). The height of the abutment must achieve at least 65 % of the complete restoration. 16 mm RC 16 mm RC NC GH NC GH 3.5 mm 0.5 mm 0.3 mm min. 4 mm 3.5 mm 1.3 mm 16 mm NC 16 mm NC min. 4 mm p The final geometry of the abutment has to meet the requirements of the material of the final restoration for cementretained crowns and bridges. Cemented 8 1. Cement-retained crowns and bridges
11 1c p Following the Ivoclar Vivadent grinding instrument recommendations for IPS e.max 1 a regeneration firing for cement-retained crowns and bridges is not required. The regeneration firing has to be conducted if the Ivoclar Vivadent grinding instrument recommendations for IPS e.max 1 are not followed or if a further thermal processing is necessary. The regeneration firing parameter are: 65 C (117 F) per minute heating up to 1050 C (1922 F) / 15 minute holding time and long-term cooling down with 25 C (45 F) per minute to 750 C (1382 F). 2a Step 2 Placing the modified Straumann Anatomic IPS e.max 1 Abutment p Place the abutment on the implant and tighten the screw with a torque between 15 Ncm and 35 Ncm using the SCS screwdriver along with the ratchet and the torque control device (see instructions in chapter 7.5 in brochure Art. No ). 2b Before taking the abutment level impression the abutment needs to be torqued with 35 Ncm. p Cover the screw head with absorbent cotton or gutta-percha and seal the screw channel temporarily (e.g. with absorbent cotton). 1. Cement-retained crowns and bridges 9
12 2c p Take an impression with an individualized impression tray and order the final restoration. 3 Step 3 Fabricating the cement-retained temporary single crown Use a standard procedure to fabricate the cement-retained single crown (e.g. grind out a prefabricated plastic tooth). 4 Step 4 Cementing the temporary single crown p Coat the internal configuration of the crown with temporary cement and cement it onto the Straumann Anatomic IPS e.max 1 Abutment. p Remove any excess cement Cement-retained crowns and bridges
13 5a Step 5 Insertion of the final restoration p Remove the temporary restoration. p Clean and dry the interior of the abutment thoroughly. 5b p Close the SCS screw channel with cotton and sealing compound (i.e. gutta-percha). This allows for later removal of the modified abutment in the event a restoration replacement is required. p Cement the superstructure onto the abutment. p Remove any excess cement. 1. Cement-retained crowns and bridges 11
14 2. SCREW-RETAINED CROWNS, DIRECTLY VENEERED Screw-retained restorations need to fulfill the following criteria (see 2c): p In the anterior region, screw hole access must be located in the palatal/lingual area of the restoration. p The screw hole position in the incisal or labial area is contraindicated. p In the posterior area, screw hole position must be located in the center of the occlusal area of the restoration. p Before veneering or press-on procedure the individualized abutment must have a reduced anatomically supporting design (cusp and marginal support). p The maximum thickness of the veneering material on top of the individualized abutments (layering ceramic and/or press-on ceramic) must not exceed a maximum of 2.0 mm in all directions of the screw retained restoration. 2.1 Straumann Anatomic IPS e.max 1 Abutment Lab procedure The following case describes the fabrication of screw-retained crowns directly veneered, when using the Straumann Anatomic IPS e.max 1 Abutment and IPS e.max Ceram 1. 1a Step 1 Fabricating the master cast and wax-up p Fabricate the master cast including a gingival mask with the corresponding implant analog (see instructions in chapter 5 in brochure Art. No ). 1b p For optimal esthetic planning, design a full anatomical wax-up. 1c p Make a silicone key over the full wax-up in order to define the optimal shape of the modified abutment Screw-retained crowns, directly veneered
15 2a Step 2 Preparing the Straumann Anatomic IPS e.max 1 Abutment p Place the abutment on the polishing aid / analog and hand tighten the screw using the SCS screwdriver. 2b p For the individualization of the Straumann Anatomic IPS e.max 1 Abutment, it is recommended to work with a water-cooled turbine and abrasive instruments that are appropriate for grinding sintered ZrO 2 material. Work with a low grinding pressure and avoid any spark formation. The Ivoclar Vivadent grinding instrument recommendations for IPS e.max 1 must be followed. 2. Screw-retained crowns, directly veneered 13
16 2c 0.75 mm 0.5 mm RC GH min. 4 mm 1.3 mm 0.75 mm 0.5 mm 3.5 mm RC GH 3.5 mm min. 4 mm In order to keep sufficient stability of the abutment, do not deviate from the dimensions shown in the following graphics (2c). The height of the abutment must achieve at least 65 % of the complete restoration. 16 mm RC 16 mm RC NC GH NC GH 3.5 mm 0.5 mm 0.3 mm min. 4 mm 3.5 mm 1.3 mm 16 mm NC 16 mm NC min. 4 mm max. p The final geometry of the abutment has to meet the requirements of the veneering material. max. max. max. max. max. max. Directly veneered 2d p After grinding and/or polishing the abutment a regeneration firing has to be conducted in a firing furnace: 65 C (117 F) per minute heating up to 1050 C (1922 F) / 15 minutes holding time and long-term cooling down with 25 C (45 F) per minute to 750 C (1382 F) Screw-retained crowns, directly veneered
17 3a Step 3 Veneering p For the veneering of the Straumann Anatomic IPS e.max 1 Abutment, use conventional veneering material synchronized to the thermal expansion coefficient of the abutment. p Coefficient of thermal expansion 2 (CTE) ( C ) ± K -1 p In this case IPS e.max Ceram 1 has been used. For further details please consult the brochure Instructions for use IPS e.max Ceram 1 ( p Steam clean the abutment and apply the IPS e.max Ceram ZirLiner 1 only where IPS e.max Ceram 1 will be applied later on. 3b p The implant configuration must be protected with the polishing aid while applying the IPS e.max Ceram ZirLiner 1. Do not sandblast the abutment before applying the IPS e.max Ceram Liner 1. Avoid any application of IPS e.max Ceram ZirLiner 1 into the screw channel. 3c Do not apply IPS e.max Ceram ZirLiner 1 on the inner configuration. In case of an adaptation of the emergence profile it is recommended to place the abutment upside down on the firing tray to prevent the ZirLiner 1 from flowing towards the inner configuration during firing. 2. Screw-retained crowns, directly veneered 15
18 3d p Particular attention must be given to an even layer thickness of the porcelain veneered on the abutment. Observe the maximum thickness of the layering ceramic material (max. ). 3e 3f p Final restoration Screw-retained crowns, directly veneered
19 2.2 Straumann Anatomic IPS e.max 1 Abutment Prosthetic procedure The final restoration is delivered to the doctor s office on the master cast. Step 1 Preparation p Remove the healing cap or temporary restoration. p Remove the veneered abutment from the master cast. p Clean and dry the interior of the implant and the abutment thoroughly. 2a Step 2 Final insertion p Position the cleaned and veneered abutment in the implant. Tighten the screw to 35 Ncm using the SCS screwdriver along with the ratchet and the torque control device (see instruction in chapter 7.5, in brochure Art. No ). 2b p Close the SCS screw channel with cotton and sealing compound (i.e. gutta-percha, composite). This allows for later removal of the modified abutment in the event a restoration replacement is required. Only use an original Straumann basal screw for ceramic abutment for the final insertion of the Straumann Anatomic IPS e.max 1 Abutment. 2. Screw-retained crowns, directly veneered 17
20 3. SCREW-RETAINED CROWNS USING THE PRESS-ON TECHNIQUE Screw-retained restorations need to fulfill the following criteria (see 2c): p In the anterior region, screw hole access must be located in the palatal/lingual area of the restoration. p The screw hole position in the incisal or labial area is contraindicated. p In the posterior area, screw hole position must be located in the center of the occlusal area of the restoration. p Before veneering or press-on procedure the individualized abutment must have a reduced anatomically supporting design (cusp and marginal support). p The maximum thickness of the veneering material on top of the individualized abutments (layering ceramic and/or press-on ceramic) must not exceed a maximum of 2.0 mm in all directions of the screw retained restoration. 3.1 Straumann Anatomic IPS e.max 1 Abutment Lab procedure The following case describes the fabrication of a screw-retained crown when using the Straumann Anatomic IPS e.max 1 Abutment in combination with the press-on technique. In this case IPS e.max ZirPress 1 has been used. 1a Step 1 Fabricating the master cast and wax-up p Fabricate the master cast including a gingival mask with the corresponding implant analog (see instructions in chapter 5 in brochure Art. No ). 1b p For optimal esthetic planning, design a full anatomical wax-up. 1c p Make a silicone key over the full wax-up in order to define the optimal shape of the modified abutment Screw-retained crowns using the press-on technique
21 2a Step 2 Preparing the Straumann Anatomic IPS e.max 1 Abutment p Place the abutment on the polishing aid / analog and hand tighten the screw using the SCS screwdriver. 2b p For the individualization of the Straumann Anatomic IPS e.max 1 Abutment, it is recommended to work with a water-cooled turbine and abrasive instruments that are appropriate for grinding sintered ZrO 2 material. Work with a low grinding pressure and avoid any spark formation. The Ivoclar Vivadent grinding instrument recommendations for IPS e.max 1 must be followed. 3. Screw-retained crowns using the press-on technique 19
22 2c 0.75 mm 0.5 mm RC GH min. 4 mm 1.3 mm 0.75 mm 0.5 mm 3.5 mm 16 mm RC 16 mm RC GH 3.5 mm RC min. 4 mm In order to keep sufficient stability of the abutment, do not deviate from the dimensions shown in the following graphics (2c). The height of the abutment must achieve at least 65 % of the complete restoration. NC GH NC GH 3.5 mm 0.3 mm 16 mm NC min. 4 mm 1.3 mm 3.5 mm 0.5 mm 16 mm NC min. 4 mm max. p The final geometry of the abutment has to meet the requirements of the framework and veneering material. max. max. max. max. max. max. Directly veneered 2d p After grinding and/or polishing the abutment a regeneration firing has to be conducted in a firing furnace: 65 C (117 F) per minute heating up to 1050 C (1922 F) / 15 minutes holding time and long-term cooling down with 25 C (45 F) per minute to 750 C (1382 F) Screw-retained crowns using the press-on technique
23 3a Step 3 Process of press-on technique p For pressing onto the Straumann Anatomic IPS e.max 1 Abutment, use conventional press-on material synchronized to the thermal expansion coefficient of the abutment. p Coefficient of thermal expansion 2 (CTE) ( C ) ± K -1 p In this case IPS e.max ZirPress 1 has been used. For further details please consult the brochure Instructions for use IPS e.max ZirPress 1 ( p Steam clean the abutment and apply the IPS e.max Ceram ZirLiner 1 only where IPS e.max ZirPress 1 will be applied later on. 3b p The implant configuration must be protected with the polishing aid while applying the IPS e.max Ceram ZirLiner 1. Do not sandblast the abutment before applying the IPS e.max Ceram Liner 1. Avoid any application of IPS e.max Ceram ZirLiner 1 into the screw channel. 3c Do not apply IPS e.max Ceram ZirLiner 1 on the inner configuration. In case of an adaptation of the emergence profile it is recommended to place the abutment upside down on the firing tray to prevent the ZirLiner 1 from flowing towards the inner configuration during firing. 3. Screw-retained crowns using the press-on technique 21
24 3d p Observe the respective material thickness (minimum 0.7 mm up to ) in order to ensure a proper press-on restoration. 3e In order to prevent IPS e.max ZirPress 1 to intrude into the screw channel of the abutment do not cover the screw channel with wax. 3f p Sprueing Screw-retained crowns using the press-on technique
25 3g p Cover the whole abutment with investment material and ensure that the screw channel is also completely filled. 3h p Before pressing, ensure that the pressing furnace is sufficiently preheated. 3i p The implant configuration must be protected with the polishing aid (e. g. sandblasting). 3j 3. Screw-retained crowns using the press-on technique 23
26 3k The long-term success of the prosthetic work depends on the accurate fit of the restoration. Therefore the following recommendations must be observed: 3l p Allow for enough cooling time of the press-on abutment before divestment p Rough divestment is carried out with glass polishing beads at 4 bar (60 psi) pressure p Fine divestment is carried out with glass polishing beads at 2 bar (30 psi) pressure p Do not use Al 2 O 3 for rough or fine divestment p Do not sandblast the conical portion of the abutment and always protect the implant/abutment interface with the polishing aid 3m p Immerse the pressed objects into the IPS e.max Press Invex Liquid 1 ( min. 5 minutes, max. 10 minutes ) and ensure that they are completely covered. p Carefully remove the white reaction layer on the pressed objects with Al 2 O 3 (type 100 microns) at 1 2 bar (15 30 psi) pressure Screw-retained crowns using the press-on technique
27 3n p Veneer, shade and glaze the restoration according to the individual situation. The implant configuration must be protected with the polishing aid while applying the IPS e.max Ceram 1. 3o p Final restoration 3. Screw-retained crowns using the press-on technique 25
28 3.2 Straumann Anatomic IPS e.max 1 Abutment Prosthetic procedure The final restoration is delivered to the doctor s office on the master cast. Step 1 Preparation p Remove the healing cap or temporary restoration. p Remove the overpressed abutment from the master cast. p Clean and dry the interior of the implant and the abutment thoroughly. 2a Step 2 Final insertion p Position the cleaned abutment in the implant. Tighten the screw to 35 Ncm using the SCS screwdriver along with the ratchet and the torque control device (see instructions in chapter 7.5 in brochure Art. No ). 2b p Close the SCS screw channel with cotton and sealing compound (i.e. gutta-percha, composite). This allows a later removal of the modified abutment in the event a restoration replacement is required. Only use an original Straumann basal screw for ceramic abutment for the final insertion of the Straumann Anatomic IPS e.max 1 Abutment Screw-retained crowns using the press-on technique
29 IMPORTANT GUIDELINES Please note Practitioners must have appropriate knowledge and instruction in the handling of the Straumann CADCAM products or other Straumann products ( Straumann Products ) for using the Straumann Products safely and properly in accordance with the instructions for use. Explanation of the symbols on labels and instruction leaflets Batch code Catalogue number The Straumann Product must be used in accordance with the instructions for use provided by the manufacturer. It is the practitioner s responsibility to use the device in accordance with these instructions for use and to determine, if the device fits to the individual patient situation. Sterilized using irradiation Lower limit of temperature The Straumann Products are part of an overall concept and must be used only in conjunction with the corresponding original components and instruments distributed by Institut Straumann AG, its ultimate parent company and all affiliates or subsidiaries of such parent company ( Straumann ), except if stated otherwise in this document or in the instructions for use for the respective Straumann Product. If use of products made by third parties is not recommended by Straumann in this document or in the respective instructions for use, any such use will void any warranty or other obligation, express or implied, of Straumann. min. max. max. Upper limit of temperature Temperature limitation min. Availability Some of the Straumann Products listed in this document may not be available in all countries. Caution In addition to the caution notes in this document, our products must be secured against aspiration when used intraorally. Caution: Federal law restricts this device to sale by or on the order of a dental professional. Validity Upon publication of this document, all previous versions are superseded. Do not re-use Non-sterile Documentation For detailed instructions on the Straumann Products contact your Straumann representative. Caution, consult accompanying documents Copyright and trademarks Straumann documents may not be reprinted or published, in whole or in part, without the written authorization of Straumann. Straumann and/or other trademarks and logos from Straumann mentioned herein are the trademarks or registered trademarks of Straumann Holding AG and/or its affiliates. Use by Keep away from sunlight Straumann Products with the CE mark fulfill the requirements of the Medical Devices Directive 93/42 EEC 0123 Consult instructions for use 27
30 Straumann Anatomic IPS e.max 1 Abutment is avaible in the following shades: MO 0 and MO 1 (MO = Medium Opacity) 1 IPS e.max, IPS e.max Ceram, IPS e.max ZirPress, IPS e.max Ceram ZirLiner, IPS e.max Ceram Liner, IPS e.max Press Invex Liquid are registered trademarks of Ivoclar Vivadent AG, Liechtenstein 2 Ivoclar Vivadent AG, Liechtenstein 28
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32 International Headquarters Institut Straumann AG Peter Merian-Weg 12 CH-4002 Basel, Switzerland Phone +41 (0) Fax +41 (0) Institut Straumann AG, All rights reserved. Straumann and/or other trademarks and logos from Straumann mentioned herein are the trademarks or registered trademarks of Straumann Holding AG and/or its affiliates. All rights reserved. Straumann products are CE marked 10/12 CA /en BG21012
BASIC INFORMATION ON THE STRAUMANN VARIOBASE ABUTMENT. Straumann Variobase Abutment
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