Straumann® SmartMulti
Straumann® SmartMulti
Step 2
Treatment planning
Straumann® SmartMulti
Surgical procedures
Step 1 | Implant surgery
7 – 10 days
6 – 8 weeks
Prosthetic procedures
Step 1 | Impression-taking
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Straumann® SmartMulti
Contents
Introduction4
Learning objectives 5
3. Radiographic planning 14
3.1 Outline important landmarks 14
3.2 Evaluate and assess 14
3.3 Measure the available vertical bone height and select the
appropriate implant type, diameters and lengths 16
4. Risk assessment 19
Appendix 23
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Straumann® SmartMulti
Introduction
A thorough patient assessment is the basis of any dental treatment
plan. You can finalize the diagnosis and prognosis of the oral situation,
and undertake treatment planning in your office with the information
gathered from the initial visit with the patient.
3. Radiographic planning
4. Risk assessment
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Straumann® SmartMulti
Learning objectives
Be able to use the information gathered from the patient’s history
and examination to:
Prepare the treatment plan, costs and options for discussion with
the patient at the next visit.
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Select the implant diameters, implant type, and positions. Discuss Discuss with your
with your dental technician on how to design the restoration so dental technician about
that the necessary oral hygiene measures can be carried out. the design of the final
restoration.
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Straumann® SmartMulti
To establish the ideal topographical situation, axial orientation, and Ask your dental
choice of implants, we recommend the following to be fabricated by technician to create a
the dental technician: diagnostic wax-up and
ѹѹ A diagnostic wax-up in the edentulous area surgical drill template.
ѹѹ A resin-based surgical drill template to help determine the correct
implant position during implant surgery
2.1 Procedure
Apply the Straumann® Diagnostic T Use calipers and the
and calipers on the study model to Straumann® Diagnostic
obtain an initial measurement of the T on the study model to
interproximal distance of bone, for estimate the space avail-
the choice of which implant shoulder able for the future pros-
diameter and prosthetic reconstruc- thetic reconstruction.
tion to use.
Analyze the implant positions three-dimensionally on the study model. Assess the 3D space for
the implants on the study
2.1.1 Interproximal distance of bone model.
2.1.2 Bucco-lingual (or bucco-palatal) width of bone
2.1.3 Inter-occlusal distance
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Straumann® SmartMulti
For a 3-unit implant-supported fixed dental prosthesis in the poste- For a 3-unit implant-
rior area, additional space for the pontic should be respected in the supported FDP respect
calculations². additional space for the
pontic:
ѹѹ The approximate diameter of a premolar is 7.0 mm. - approx. Ø of a premolar:
ѹѹ The approximate diameter of a molar is 11.0 mm. 7 mm
- approx. Ø of a molar:
11 mm
At least 1.5 mm
at bone level
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Straumann® SmartMulti
The minimum distance from the bone level of the adjacent tooth to Minimum distance from
the implant’s central axis depends on the shoulder or platform of the the bone level of adja-
implant used. These numbers have been rounded up in the calculations. cent tooth to the im-
plant’s central axis:
With Standard Plus (SP) Implants, this distance is approximately: SP Implants:
ѹѹ 4 mm for Regular Neck (RN) Implants with Ø 4.8 mm shoulder - 4 mm for RN platform
diameter. - 5 mm for WN platform
ѹѹ 5 mm for Wide Neck (WN) Implants with Ø 6.5 mm shoulder BLT Implants:
diameter. - 4 mm for RC platform
Pontic
Example of a 3-unit implant-
diameter
supported FDP with SP Implants with
RN ∅ 4.8 mm RN ∅ 4.8 mm Regular Neck (RN) ∅ 4.8 mm shoul-
der diameter.
Pontic
Example of a 3-unit implant-
diameter
supported FDP with BLT Implants
with Regular CrossFit® (RC) Ø 4.1 mm
RC ∅ 4.1 mm RC ∅ 4.1 mm
endosteal and shoulder diameter.
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≥ 3 mm ≥ 3 mm
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≥ 1 mm ≥ 1 mm
For SP Implants, please refer For BLT Implants, please refer Charts for reference
to this chart for the minimum to this chart for the minimum
bucco-lingual or bucco-palatal bucco-lingual or bucco-palatal
width. width.
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Straumann® SmartMulti
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3. Radiographic planning
The vertical bone availability de-
termines the maximum allowable
length of the implant that can be
placed and can be assessed on a ra-
diographic image.
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Bone
height
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0 0 0
2 2 2
4 4 4
0 0
2 2
4 4
6
8 6
∅ 4.8 mm ∅ 4.1 mm 10
∅ 3.3 mm 8
∅ 4.8 mm ∅ 4.1 mm ∅ 3.3 mm
Example:
12 10
14 12
16 14
18
16
18
0
2
Scale 1.2 : 1 = R
eference Sphere
1.1 : 1 (049.076V4) = ∅ 5.5 mm (049.076V4) = ∅ 6.5 mm 1.3 : 1
4
Straumann® Bone Level Tapered Implant Straumann® Bone Level Tapered Implant
∅ 6.0 mm
4 4
10
6
6
8
10 8
12 10
14
16
18
12
14
12
16
14
025.0003/B/00 01/16
18
8
16
0.4 mm 18
∅ 4.8 mm
of the edentulous ridge to the anatomical landmarks that limit the
∅ 4.1 mm ∅ 3.3 mm
0
∅ 4.8 mm ∅ 4.1 mm ∅ 3.3 mm
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* Taking into consideration all implant-related anatomic structures (e.g. mandibular canal, sinus max-
illaris, etc.)
The effective bone availability would be 10.8 mm, therefore you would
choose an implant length of 10 mm.
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Straumann® SmartMulti
The Bone Level Tapered Implant is best placed with the outer rim
of the small 45° sloping edge (chamfer) at bone level.
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Straumann® SmartMulti
4. Risk assessment
After collecting all relevant information of the patient history and af-
ter performing a comprehensive clinical and radiographic examination
and study model analysis, assess the complexity and risks associated
with placing an implant in your patient’s mouth.
The SAC classification system developed by the ITI (International Team Use the SAC classification
for Implantology) differentiates between straightforward, advanced tool to determine if the
and complex cases. The assessment for the surgical and restorative case is straightforward.
part of implant placement takes into consideration the patient, the
site of implantation and the processes involved.
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Straumann® SmartMulti
ѹѹ Multiple tooth gaps (including free-end situations) in the posterior Ensure that the prerequi-
non-esthetic zone sites of a straightforward
ѹѹ Healthy patient (ASA³-1: a normal healthy patient; or ASA³-2, a pa- implant case are fulfilled.
tient with mild systemic disease) with undisturbed wound healing
capability
ѹѹ Good patient motivation and compliance, preferably a non-smoker
ѹѹ No active periodontitis or occlusal parafunction
ѹѹ Healed ridge (≥ 5 months post-extraction) with sufficient bone vol-
ume
ѹѹ Conventional loading protocol (≥ 3 months after implant place-
ment)
ѹѹ Sufficient mesio-distal width of bone for the regular neck platform
(RN or RC) implants or wide neck platform (WN) implants
ѹѹ Sufficient bucco-lingual or bucco-palatal bone width and height for
placing implants without the need for bone augmentation
ѹѹ Sufficient inter-occlusal distance for the prosthetic restoration
ѹѹ Minimum vertical oral opening space of 30 mm to allow access with
surgical instruments
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Straumann® SmartMulti
5.1 Establish a diagnosis and prognosis of the remaining Prepare a diagnosis and
dentition to discuss with the patient treatment plan for the
discussion with your
patient.
5.2 Elaborate a treatment plan and calculate the amount
of chairside time per visit and total number of visits
Include chairside time
required by the patient
and total number of
ѹѹ All diseases in the oral cavity (hard and soft tissue) have to be patient visits in the
treated before implant placement starts. treatment plan.
ѹѹ In case of insufficient oral hygiene or active periodontal disease,
additional dental treatment may be needed before starting with
the implant procedure, and should be calculated into the cost pro-
posal. Consider this when:
‒‒ the patient presents with poor oral hygiene
‒‒ there is active periodontal disease, requiring professional plaque
removal along with scaling and root planing
‒‒ there are teeth with hopeless prognosis which have to be
extracted
‒‒ there is active caries
‒‒ there are failing endodontically treated teeth
‒‒ there are stomatological lesions
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Straumann® SmartMulti
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Assuming min. width of pontic is 7.0 mm for premolar and 11.0 mm for molar, calculations have been rounded up to nearest 0.5 mm.
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Assuming min. width of pontic is 7.0 mm for premolar and 11.0 mm for molar, calculations have been rounded up to nearest 0.5 mm.
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Straumann® SmartMulti
Endosteal Shoulder
diameter (mm) diameter (mm)
Bucco-lingual or
Implant type Shoulder bucco-palatal Recommended use for
(endosteal diameter) diameter (mm) width of bone Straumann® SmartMulti cases
(mm)
For narrow interdental spaces and narrow partially or
fully edentulous bone ridges.
Caution/Precaution:
Small-diameter implants are not recommended for
the posterior region.
SP ∅ 4.8 mm RN 4.8 7
SP ∅ 4.8 mm WN 6.5 7
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Straumann® SmartMulti
Endosteal Shoulder
diameter (mm) diameter (mm)
Bucco-lingual or
Implant type Shoulder bucco-palatal Recommended use for
(endosteal diameter) diameter (mm) width of bone Straumann® SmartMulti cases
(mm)
For narrow interdental spaces and narrow partially or
fully edentulous bone ridges.
BLT ∅ 3.3 mm NC 3.3 5.5 Caution/Precaution:
Small-diameter implants are not recommended for
the posterior region.
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Straumann® SmartMulti
REFERENCES
1 Buser D, von Arx T, ten Bruggenkate C, Weingart D. Basic surgical principles with ITI implants. Clin
Oral Impl Res 2000: 11 (Suppl.): 59–68. C Munksgaard 2000.
2 Major M. Ash, Stanley Nelson. Wheeler’s Dental Anatomy, Physiology and Occlusion. 10th Edition,
2010 Saunders/Elsevier.
3 American Society of Anesthesiologists® Physical Status Classification System, [Link]
org/resources/clinical-information/asa-physical-status-classification-system.
4 Vogel R, Smith-Palmer J, Valentine W. Evaluating the Health Economic Implications and Cost-
Effectiveness of Dental Implants: A Literature Review. Int J Oral Maxillofac Implants 2013;28:343–
356. doi: 10.11607/jomi.2921.
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Straumann® SmartMulti
DISCLAIMER
Straumann® Smart is a blended training and education program focused on the education of general
dentists who want to become surgically active in the field of dental implantology. The program is
limited to information pertaining to straightforward implant cases and focuses on a reduced portfolio
of products that are suitable for the treatment of such cases.
All clinical Straumann® Smart content – such as texts, medical record forms, pictures and videos –
was created in collaboration with Prof. Dr. Christoph Hämmerle, Prof. Dr. Ronald Jung, Dr. Francine
Brandenberg-Lustenberger and Dr. Alain Fontolliet from the University of Zürich, Clinic for Fixed and
Removable Prosthodontics and Dental Material Science, Switzerland.
Straumann does not give any guarantee that Straumann® Smart provides sufficient knowledge or
instruction for the dental professional to become surgically active in the field of implantology. It is
the dental professional’s sole responsibility to ensure that he/she has the appropriate knowledge and
instruction before placing dental implants.
Straumann® Smart does not replace a careful and thorough analysis of each individual patient by a
dental professional. Further, it does not imply any guarantee or warranty with regard to complete-
ness of the information provided to the patient. It does not replace the dental professional’s duty
to inform the patient about the treatment, the products and the risks involved and to receive the
patient’s informed consent. The dental professional is solely responsible for determining whether or
not a treatment or product is suitable for a particular patient and circumstances. Knowledge of dental
implantology and instruction in the handling of the relevant products is always necessary and the
sole responsibility of the dental professional. The dental professional must always comply with the
individual product’s Instructions For Use as well as all laws and regulations.
STRAUMANN DISCLAIMS, TO THE EXTENT POSSIBLE BY LAW, ANY LIABILITY, EXPRESS OR IMPLIED,
AND BEARS NO RESPONSIBILITY FOR ANY DIRECT, INDIRECT, PUNITIVE, CONSEQUENTIAL OR OTHER
DAMAGES, ARISING OUT OF OR IN CONNECTION WITH ANY INFORMATION PROVIDED TO PATIENTS,
ERRORS IN PROFESSIONAL JUDGMENT, IN PRODUCT CHOICES OR PRACTICE IN THE USE OR INSTALLA-
TION OF STRAUMANN PRODUCTS.
All clinical content as well as clinical and radiographic images are provided by courtesy of Prof. Dr. Chris-
toph Hämmerle, Prof. Dr. Ronald Jung, Dr. Francine Brandenberg-Lustenberger and Dr. Alain Fontolliet
from the University of Zürich, Clinic for Fixed and Removable Prosthodontics and Dental Material
Science, Switzerland.
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