| Literature DB >> 33924167 |
Serena Vi1, Damon Pham1, Yu Yian Marina Du1, Himanshu Arora2, Santosh Kumar Tadakamadla1,3.
Abstract
PURPOSE: Mini-dental implants (MDIs) have been used to support and retain overdentures, providing patients with a less invasive placement procedure. Although lucrative, the use of MDIs to retain a maxillary overdenture is still not an established treatment modality. This systematic review aims to answer the question: Do mini-implant-retained maxillary overdentures provide a satisfactory treatment outcome for complete edentulism?Entities:
Keywords: maxilla; osseointegration; patient satisfaction; survival rate
Mesh:
Year: 2021 PMID: 33924167 PMCID: PMC8074399 DOI: 10.3390/ijerph18084377
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Search strategy in PubMed.
| # | Search Term |
|---|---|
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| Maxilla [MeSH term] OR Maxilla [All Fields] |
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| Maxillary [All Fields] |
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| (#1 OR #2) |
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| Mini dental implant* [All Fields] |
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| Narrow dental implant * [All Fields] |
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| Mini implant* [All Fields] |
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| Narrow implant* [All Fields] |
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| Mini implant overdenture* [All Fields] |
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| Narrow implant overdenture* [All Fields] |
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| Mini implant supported overdenture* [All Fields] |
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| Narrow implant supported overdenture* [All Fields] |
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| Mini implant supported denture* [All Fields] |
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| Narrow implant supported denture [All Fields] |
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| Mini implant overlay denture* [All Fields] |
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| Narrow implant overlay denture* [All Fields] |
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| Mini implant supported overlay denture* [All Fields] |
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| Narrow implant supported overlay denture* [All Fields] |
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| Full mouth rehabilitation [All Fields] |
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| (#4 OR #5 OR #6 OR #7 OR #8 OR #9 OR #10 OR #11 OR #12 OR #13 OR #14 OR #15 OR #16 OR #17 OR #18) |
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| #3 AND #19 |
Inclusion and exclusion criteria.
| Selection Criteria | Inclusion Criteria | Exclusion Criteria |
|---|---|---|
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| English | Non-English |
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| Empirical studies including randomised controlled trials, nonrandomised clinical trials, cohort studies, case series | Review studies including narrative reviews, systematic reviews, literature reviews |
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| Flapless placement of implants | Adjunct surgical procedures used for implant placement |
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| At least one of the following parameters: | Studies focusing on participants pre-treatment characteristics |
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| Publications from 2010 to present | Publications prior to 2010 |
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| Human studies (all ages) | In vitro studies |
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| Inclusion Criteria | Exclusion Criteria |
Figure 1PRISMA flowchart.
Study design of the included studies.
| Author | Design | Study Setting | Sample Size and Dropout Rates | Mean Age and Gender (M:F) | Opposing Dentition | Implant System | Number of Implants Placed Per Patient in Maxilla | Denture Design | Loading Period | Number of Follow-Ups | Length of Follow-Up |
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| Fonteyne (2019) | Prospective cohort study | University Clinic Ghent and General Hospital AZ ZENO Knokke-Blankenberge, Belgium | 25; 21.9% | 62.6; 17:13 | Natural teeth and combination of natural teeth and partial prosthesis | ILZ Southern Implant Inc. | 5 to 6 | Complete denture with partial palatal coverage | 6 months | Two: | 6 months |
| Elsyad | Prospective cohort study | Mansoura University, Mansoura, Egypt | 19; 0.0% | 63.8; 11:8 | All patients were given new mandibular dentures | MAX Thread, Sendaxs MDI, IMTECT | 6 | Group I—Full palatal coverage | Immediate- same day | Three: | 24 months |
| Van Doorne (2020) | Prospective cohort study | University Clinic Ghent and General Hospital AZ ZENO Knokke-Blankenberge, Belgium | 31; 6.5% | 62.3; 17:14 | Natural teeth and combination of natural teeth and partial prosthesis | ILZ Southern Implants Inc. | 6 | Complete denture with horseshoe design | 6 months | Six: | 24 months |
| Mundt | Retrospective study | Nine private practices in Germany | 54; 26.9% | 71.2; 54:79 | Not specified | 3M ESPE | 4, 5, 6, 7, 8, or 10 | Complete dentures with complete and partial palatal coverage | Immediate or delayed with 3 to 4 months | Not specified | 27.1 ± 12.8 months |
| Preoteasa | Prospective cohort study | University of Medicine and Pharmacy, Bucharest, Romania | 23; 4.2% | 62.0; 10:13 | Natural teeth or fixed prosthetic restoration | IMTEC/3M ESPE | 5 or 6 | Complete denture with complete palatal coverage | Not specified | Six: | 36 months |
| Tomasi | Prospective cohort study | University of Gothenburg, Gothenburg and private practice, Mjolby, Sweden | 21; 8.7% | 71.0; 9:12 | Not specified | Dentatus Atlas | 2 and 4 | All complete dentures with full palatal coverage | Not specified | One: | 12 months |
Risk of bias within studies.
| Were the Two Groups Similar and Recruited from the Same Population? | Were the Exposures Measured Similar to Assign People to both Exposed and Unexposed Groups? | Was the Exposure Measured in a Valid and Reliable Way? | Were Confounding Factors Identified? | Were Strategies to Deal with Confounding Factors Stated? | Were the Groups/Participants Free of the Outcome at the Start of the Study? | Were the Outcomes Measured in a Valid and Reliable Way? | Was the Follow-Up Time Reported and Sufficient to be Long Enough for Outcomes to Occur? | Was the Follow-up Complete, and If Not, Were the Reasons for Loss to Follow-Up Described and Explored? | Were Strategies to Address Incomplete Follow-Up Utilised? | Was Appropriate Statistical Analysis Used? | |
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| Fonteyne, E., et al. (2019) |
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| Elsyad, L., et al. (2013) |
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| Mundt, T., et al. (2013 and 2015) |
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| Preoteasa, E., et al. (2014) |
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| Tomasi, C., et al. (2013) |
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| Van Doorne, L., et al. (2020) |
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—Not applicable; —Yes; —No; —Unclear.
Figure 2Risk of bias across studies.
Study results of the included studies.
| Author | Outcomes Reported | Data Collection Method | Length of Follow-Up | Biological Outcomes | Implant Survival and Success Rates | Patient Satisfaction and Oral Health-Related Quality of Life (OHRQoL) |
|---|---|---|---|---|---|---|
| Fonteyne (2019) | -Articulation | 6 months | Not specified. | Not specified. | Satisfaction with oral health: increased from 67% to 83% | |
| Elsyad | - Peri-implant bone loss around MI | 24 months | Mean vertical bone loss: Group I- 5.38 ± 1.65 mm Group II- 6.29 ± 2.33 mm | Survival rate: | Patient satisfaction with retention: Group I-2.5 ± 0.84; Group II—1.0 ± 0.99 (no significant difference) | |
| Van Doorne (2020) | - Implant stability at surgery | 24 months | Not specified. | Survival rate: 82.3% | Average final patient satisfaction score was 8.6 ± 1.7. | |
| Mundt | - Surgical and prosthetic complications | 27.1 ± 12.8 months | 10.3% MDIs TBL of >2 mm | Survival rate: 94.3% | Significant improvements for all participants in all single questions regarding OHRQoL | |
| Preoteasa | -MDI status | 36 months | 11 MDIs presented with bone loss >1 thread. | MDI health status: 8 failed | Patients generally satisfied with aesthetics, retention, function (mastication and phonation). | |
| Tomasi | - Patient satisfaction | 12 months | Mean plaque score of 20% for maxillary and mandibular MDIs. | Implant failure rate was significantly higher in maxilla than the mandible, 43% and 15%, respectively. | All patients said ‘yes’ when asked if they were satisfied with their denture. |
Figure 3Meta-analysis for MDI survival based on data reported at the final follow-up.