| Literature DB >> 30057608 |
Gabriella Balli1, Andreas Ioannou1, Charles A Powell2, Nikola Angelov1, Georgios E Romanos3,4, Nikolaos Soldatos1.
Abstract
BACKGROUND: The purpose of this systematic review was to accurately assess the procedural success of ridge preservation technique through the application of strict inclusion and exclusion criteria. DATA SOURCES: A methodical search of PubMed of the US National Library of Medicine and the Cochrane Central Register of Controlled Trials was conducted for applicable articles. Only randomized controlled trials comparing ridge preservation treatment with a nongrafting control, ten-subject minimum sample size, and three or more months of follow-up were included in our study. TYPES OF STUDIES REVIEWED: In a screening between January 1980 and September 2017, articles meeting predetermined criteria were further examined in a qualitative data analysis. A thorough search of the databases provided 1876 articles. Of these records, 174 were assessed for eligibility through the systematic employment of inclusion and exclusion criteria.Entities:
Year: 2018 PMID: 30057608 PMCID: PMC6051091 DOI: 10.1155/2018/8546568
Source DB: PubMed Journal: Int J Dent ISSN: 1687-8728
Figure 1The PRISMA flow diagram.
The studies included in the final review.
| Study | Pang et al. [ | Temmerman et al. [ |
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| Methods | Randomized controlled clinical trial | Randomized controlled clinical split mouth trial |
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| Participants | 60 patients | 22 patients |
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| Surgical considerations | Extraction with two vertical releasing incisions (mesial/distal) plus collagen membrane with DBB collagen sponge | Extraction plus 2-3 PRF |
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| Intervention |
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| Measurement method | CBCT/ISQ | CBCT |
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| Follow-up | 6 months postoperatively | 3 months postoperatively |
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| Outcome |
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| (i) Level A ( | −0.7 ± 0.8 mm (control group) | |
| (ii) Level A ( | −0.3 ± 1.2 mm (L-PRF group) | |
| (iii) Level B ( |
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| (iv) Level B ( | −1.6 ± 1.2 mm (control group) | |
| −0.1 ± 1.6 mm (L-PRF group) | ||
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| (i) Level A ( |
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| (ii) Level A ( | HW-1 mm: −2.0 ± 2.6 mm | |
| (iii) Level B ( | HW-3 mm: −0.2 ± 0.3 mm | |
| (iv) Level B ( | HW-5 mm: −0.1 ± 0.3 mm | |
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| HW-1 mm: −0.3 ± 1.9 mm | ||
| HW-3 mm: −0.1 ± 0.3 mm | ||
| HW-5 mm: −0.0 ± 0.1 mm | ||
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| Immediately after implant placement: 62.33–63.40 |
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| 1 month postoperatively: 60 | HW-1 mm: −3.3 ± 2.6 mm | |
| 3 months postoperatively: 72 | HW-3 mm: −1.0 ± 1.1 mm | |
| HW-5 mm: −0.5 ± 0.7 mm | ||
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| 1 month postoperatively:– | HW-1 mm: −1.2 ± 2.6 mm | |
| 3 months postoperatively: 70 | HW-3 mm: −0.8 ± 0.9 mm | |
| HW-5 mm: −0.5 ± 0.6 mm | ||
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| Secondary outcome | Level B (control group): implants could not be placed in 3 patients | L-PRF group: 94.7% socket fill |
| Control group: 63.3% socket fill | ||
The risk of bias for both studies.
| Study | Pang et al. [ | Temmerman et al. [ |
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| Random sequence generation | High risk | Low risk |
| Allocation concealment | High risk | Low risk |
| Blinding of participants | High risk | Low risk |
| Blinding of personnel/care providers | High risk | High risk |
| Detection bias | High risk | High risk |
| Incomplete outcome data | Low risk | Low risk |
| Selective reporting | Low risk | Low risk |
| Group similarity at the baseline | High risk | High risk |
| Cointerventions | Low risk | Low risk |
| Compliance | Low risk | Low risk |
| Intention-to-treat analysis | Low risk | Low risk |
| Timing of outcome assessments | Low risk | Low risk |
| Other biases | High risk | High risk |