Cochrane · intervention · CD004151
Interventions for replacing missing teeth: dental implants in zygomatic bone for the rehabilitation of the severely deficient edentulous maxilla
Esposito, M, Worthington, HV · Cochrane Database of Systematic Reviews · 2013 · Cochrane Library
Full textEvery question was extracted from the full review (methods and results), not only its Summary of Findings table.
Questions
7
current version
GRADE rated
0
No studies
7
Included studies
0
as reported
No studies 7 · 100%Ungraded 0 · 0%Very low 0 · 0%Low 0 · 0%Moderate 0 · 0%High 0 · 0%
Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.
Review question
| Element | Planned (methods) | Found (results) |
|---|---|---|
| Population | Participants with an atrophic maxilla who cannot be rehabilitated with conventional dental implants due to lack of bone (including patients subjected to cancer ablation surgery and irradiation therapy); partially or totally edentulous | No eligible studies identified |
| Intervention | Zygomatic implants with or without bone grafts | No eligible studies identified |
| Comparison | Conventional dental implants in augmented maxillae | No eligible studies identified |
| Outcomes | Prosthesis could not be placed or loss of prosthesis secondary to implant failure; Implant failures (mobile implants, removal of stable implants, implant fractures, implants left 'sleeping' due to wrong alignment); Complications; Patient satisfaction and, when possible, preference; Cost-effectiveness | No eligible studies identified |
| Study designs | Randomised controlled trials (RCTs) with a parallel group or split-mouth design | No eligible studies identified |
| Timing | Follow-up of at least one year in function | No eligible studies identified |
Search date: 2013-06. Databases: Cochrane Oral Health Group's Trials Register; Cochrane Central Register of Controlled Trials (CENTRAL); MEDLINE via OVID; EMBASE via OVID
Questions and results
Current version onlyZygomatic implants without bone grafts (as a complete alternative to any bone augmentation procedure) vs Conventional dental implants in augmented maxillae
Population: Participants with an atrophic maxilla who cannot be rehabilitated with conventional dental implants due to lack of bone (including patients subjected to cancer ablation surgery and irradiation therapy); partially or totally edentulous
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Patient satisfaction (and, when possible, preference) At least 1 year in function | Results (Effects of interventions): we could not identify any eligible randomised controlled trials (RCTs). | 0 studies | No studies |
Cost-effectiveness At least 1 year in function | Results (Effects of interventions): we could not identify any eligible randomised controlled trials (RCTs). | 0 studies | No studies |
Complications At least 1 year in function | Results (Effects of interventions): we could not identify any eligible randomised controlled trials (RCTs). | 0 studies | No studies |
Prosthesis failure (prosthesis could not be placed or loss of prosthesis secondary to implant failure) At least 1 year in function | Summary of findings 'Zygomatic implants versus conventional implants'; Prosthesis failure: Assumed risk (conventional) Low risk population 10 per 1000, High risk population 100 per 1000; Corresponding risk (zygomatic)… | 0 studies | No studies |
Implant failure (mobile implants, removal of stable implants due to progressive marginal bone loss or infection, implant fractures) At least 1 year in function | Results (Effects of interventions): we could not identify any eligible randomised controlled trials (RCTs). | 0 studies | No studies |
Zygomatic implants with bone grafts (as a partial alternative to bone augmentation; some augmentation still required in the frontal maxilla) vs Conventional dental implants in augmented maxillae
Population: Patients with a severely atrophic maxilla for whom some bone augmentation is still required in the frontal portion of the maxilla; partially or totally edentulous
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Outcome NR At least 1 year in function | Results (Effects of interventions): we could not identify any eligible randomised controlled trials (RCTs). | 0 studies | No studies |
Zygomatic implants for retaining a maxillary obturator vs Non-implant retained obturators, local and regional flaps, or microvascular free flaps
Population: Patients requiring maxillary reconstruction after partial or total maxillectomy (cancer patients)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Outcome NR At least 1 year in function | Results (Effects of interventions): we could not identify any eligible randomised controlled trials (RCTs). | 0 studies | No studies |
Zygomatic implants without bone grafts (as a complete alternative to any bone augmentation procedure) vs Conventional dental implants in augmented maxillae
Population: Patients with an atrophic maxilla that cannot be rehabilitated with conventional dental implants due to lack of bone (including patients subjected to cancer ablation surgery and irradiation therapy); partially or totally edentulous
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Side effects At least 1 year follow-up | Results (Effects of interventions): no published or ongoing randomised controlled clinical trials or controlled clinical trials were identified. | 0 studies | No studies |
Implant failure (mobile implants, removal of stable implants due to progressive marginal bone loss or infection, implant fractures) At least 1 year follow-up | Results (Effects of interventions): no published or ongoing randomised controlled clinical trials or controlled clinical trials were identified. | 0 studies | No studies |
Patient satisfaction (and, if possible, preference) At least 1 year follow-up | Results (Effects of interventions): no published or ongoing randomised controlled clinical trials or controlled clinical trials were identified. | 0 studies | No studies |
Prosthesis failure (prosthesis could not be placed or loss of prosthesis secondary to implant failure) At least 1 year follow-up | Results (Effects of interventions): no published or ongoing randomised controlled clinical trials or controlled clinical trials were identified. | 0 studies | No studies |
Cost effectiveness At least 1 year follow-up | Results (Effects of interventions): no published or ongoing randomised controlled clinical trials or controlled clinical trials were identified. | 0 studies | No studies |
Zygomatic implants with bone grafts (as a partial alternative to bone augmentation; some augmentation still required in the frontal maxilla) vs Conventional dental implants in augmented maxillae
Population: Patients with a severely atrophic maxilla for whom some bone augmentation is still required in the frontal portion of the maxilla; partially or totally edentulous
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Outcome NR At least 1 year follow-up | Results (Effects of interventions): no published or ongoing randomised controlled clinical trials or controlled clinical trials were identified. | 0 studies | No studies |
Zygomatic implants for retaining a maxillary obturator vs Non-implant retained obturators, local and regional flaps, or microvascular free flaps
Population: Patients requiring maxillary reconstruction after partial or total maxillectomy (cancer patients)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Outcome NR At least 1 year follow-up | Results (Effects of interventions): no published or ongoing randomised controlled clinical trials or controlled clinical trials were identified. | 0 studies | No studies |
Zygomatic implants without bone grafts (as a complete alternative to any bone augmentation procedure) vs Conventional dental implants with bone grafts or other procedures for bone augmentation such as guided bone regeneration (GBR)
Population: Patients with a maxilla that cannot be rehabilitated with conventional dental implants due to lack of bone (including patients subjected to cancer ablation surgery and irradiation therapy); partially or totally edentulous
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Patient satisfaction At least 1 year follow-up | Results (Effects of interventions): no randomised controlled clinical trial was identified. | 0 studies | No studies |
Side effects At least 1 year follow-up | Results (Effects of interventions): no randomised controlled clinical trial was identified. | 0 studies | No studies |
Implant failure (mobile implants, removal of stable implants due to progressive marginal bone loss or infection, implant fractures) At least 1 year follow-up | Results (Effects of interventions): no randomised controlled clinical trial was identified. | 0 studies | No studies |
Cost effectiveness At least 1 year follow-up | Results (Effects of interventions): no randomised controlled clinical trial was identified. | 0 studies | No studies |
Prosthesis failure (prosthesis could not be placed or loss of prosthesis secondary to implant failure) At least 1 year follow-up | Results (Effects of interventions): no randomised controlled clinical trial was identified. | 0 studies | No studies |