Edentulous Alveolar Ridge
Conditions
Brief summary
To investigate clinical outcomes of transcrestal maxillary sinus floor elevation performed with an injectable xenograft in gel form, analyzing variables possibly influencing the results. Patients needing unilateral sinus floor elevation (residual crestal height \<5 mm) for the placement of a single implant were enrolled. Xenograft in gel form was injected through a crestal antrostomy in order to elevate sinus membrane and fill the sub-antral space. Simultaneous implant placement was performed when adequate primary stability was achievable. Graft height was measured immediately after surgery (T0) and after six months of healing (T1). Univariate and multivariate regression models were built to assess associations between clinical variables with implant survival and graft height at T1.
Detailed description
Purpose: To investigate clinical outcomes of transcrestal maxillary sinus floor elevation performed with an injectable xenograft in gel form, analyzing variables possibly influencing the results. Methods: Patients needing unilateral sinus floor elevation (residual crestal height \<5 mm) for the placement of a single implant were enrolled. Xenograft in gel form was injected through a crestal antrostomy in order to elevate sinus membrane and fill the sub-antral space. Simultaneous implant placement was performed when adequate primary stability was achievable. Graft height was measured immediately after surgery (T0) and after six months of healing (T1). Univariate and multivariate regression models were built to assess associations between clinical variables with implant survival and graft height at T1.
Interventions
PROCEDUREtranscrestal sinus floor elevation
Under local anesthesia (articaine 4% with epinephrine 1:100.000), a minimally invasive full-thickness flap was elevated to expose the alveolar crest. Clinicians were left free to choose their preferred transcrestal antrostomy technique. After checking sinus membrane integrity with visual inspection and Valsalva maneuver, pre-heated (40°C) xenogeneic porcine bone substitute in gel form (Gel 40, Tecnoss, Giaveno, Italy) was injected through the crestal antrostomy in order to elevate the membrane and fill the sub-antral space. Duration of graft injection (in seconds) was recorded using a digital chronometer. Periapical intraoperative radiographs were taken to confirm membrane elevation of at least 10 mm.
PROCEDUREImplant placement
Simultaneous implant placement was performed when it was possible to achieve adequate primary stability in the residual crestal bone, otherwise crestal antrostomy was sealed by collagen sponges (Hemocollagene, Septodont, Saint-Maur-des-Fossés, France) and implant insertion was postponed. Flaps were sutured with Sentineri technique and single stitches using synthetic monofilament
Sponsors
Teresa Lombardi DDS private practice
Fabio Bernardello MD, DDS private practice
Luca Lamazza DDS, PhD private practice
Grzegorz Zietek DDS private practice
Giuseppe Troiano DDS, PhD private practice
International Piezosurgery Academy
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* residual bone crest height \<5 mm and width ≥6 mm in the planned implant site; * healed bone crest (at least 6 months elapsed from tooth loss/extraction); * age \>18 years; * written informed consent given
Exclusion criteria
absolute medical contraindications to implant surgery; * uncontrolled diabetes (HBA1c \> 7.5%); * treated or under treatment with antiresorptives; * irradiated in the head and neck area in the last five years; * pregnant or breastfeeding; * substance abusers; * psychiatric problems or unrealistic expectations; * patient not fully able to comply with the study protocol. * large sinus cavity (distance \>12 mm between buccal and palatal walls at 10-mm level, comprising the residual alveolar crest); * maxillary sinus conditions contraindicating sinus floor elevation; * poor oral hygiene and motivation (Full Mouth Plaque Score \>20% and or Full Mouth Bleeding Score \>10%)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| implant survival | 12 months | implant survival rate after one year of prosthetic loading |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| vertical bone gain | six months | vertical bone gain (measured in mm on x-ray) six months after sinus augmentation |
| percentual graft shrinkage | six months | % graft shrinkage during 6-month healing period |
| occurrence of complications | 12 months | occurrence of any complication or adverse event |
Countries
Italy
Outcome results
None listed