Material & methods: A clinical and radiographic study of implants (5)
Prosthodontic treatment
Forty-nine days (range: 27–113 days) after placement of the healing abutment, the abutment was removed and the implant position was registered by an impression coping on the implant.
The final implant-supported restoration was fabricated by using an individually designed angulated screw channel (ASC) zirconium abutment (Nobel Biocare®, Zürich, Switzerland) and veneering porcelain. The metal adaptor (Nobel Biocare®, Zürich, Switzerland), ASC abutment (Nobel Biocare®, Zürich, Switzerland) and porcelain crown were screw-retained with a torque of 35 Ncm. All materials and clinical procedures were handled according to the manufacturer’s instructions.
Follow-up regimen
All patients were recalled after a mean follow-up period of 24 months from crown placement (range: 14–32 months) by JH.
Outcome measures
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Implant survival: Implant failure was defined as implant mobility or removal of a stable implant due to progressive peri-implant marginal bone loss or infection.
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Implant crown survival: Failure of the implant crown was defined as a loss of a mounted crown irrespective of the cause.
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Clinical parameters (probing depth, bleeding on probing, presence of plaque, keratinised peri-implant tissue, recession of peri-implant soft tissue)
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Radiographic peri-implant marginal bone change
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Radiographic marginal bone change of the adjacent tooth surfaces
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Biological and technical complication
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Patient-related outcome measures (PROMs)
Probing depth (PD) and bleeding on probing (BOP) were measured using a light probing force (approximately 25 g) to the nearest millimeter with a conventional periodontal probe at six sites per implant (mesiobuccal, buccal, distobuccal, distooral, lingual and mesiooral). Plaque was registered using a plaque control record (PCR; presence of plaque yes/no) [34]. Recession of peri-implant tissue (REC; six sites) and the width of the keratinised peri-implant tissue (KT; 1 buccal aspect of the implant) were measured to the nearest millimeter with the above-mentioned periodontal probe.
Serial posts:
- A clinical and radiographic study of implants placed in autogenous bone grafts
- Background: A clinical and radiographic study of implants (1)
- Background: A clinical and radiographic study of implants (2)
- Material & methods: A clinical and radiographic study of implants (1)
- Material & methods: A clinical and radiographic study of implants (2)
- Material & methods: A clinical and radiographic study of implants (3)
- Material & methods: A clinical and radiographic study of implants (4)
- Material & methods: A clinical and radiographic study of implants (5)
- Material & methods: A clinical and radiographic study of implants (6)
- Results: A clinical and radiographic study of implants (1)
- Results: A clinical and radiographic study of implants (2)
- Results: A clinical and radiographic study of implants (3)
- Results: A clinical and radiographic study of implants (4)
- Discussion: A clinical and radiographic study of implants (1)
- Discussion: A clinical and radiographic study of implants (2)
- Discussion: A clinical and radiographic study of implants (3)
- Abbreviations & References: A clinical and radiographic study of implants
- Table 1 Demographics and survival rates of implants and implant crowns
- Table 2 Radiographic peri-implant marginal bone level in mm
- Table 3 Radiographic marginal bone level and clinical recession on neighbouring tooth surface
- Table 4 Patient-related outcome measures at baseline and at the final follow-up
- Figure 1. Intraoperative photos illustrating bone harvesting
- Figure 2. Box plot of the radiographic peri-implant marginal bone level
- Figure 3. Data from the VAS of patient-related outcome measures at the time of mounting of the implant-supported crown and at the final follow-up of the PRF and control group