| Literature DB >> 35076562 |
Rodolfo Reda1, Alessio Zanza1, Andrea Cicconetti1, Shilpa Bhandi2, Renzo Guarnieri1, Luca Testarelli1, Dario Di Nardo1.
Abstract
BACKGROUND: The most used types of retention of implant-supported prostheses are screw-retained or cement-retained restorations. The advantages and disadvantages of both have been identified by various authors over the years. However, cement-retained implant crowns and fixed partial dentures are among the most used types of restorations in implant prostheses, due to their aesthetic and clinical advantages. When cemented prostheses are made on implants, the problem of cement residues is important and often associated with biological implant pathologies. The objective of this research was to establish to what extent the techniques to reduce excess cement really affect the volume of cement residues.Entities:
Keywords: cement excess; cementation technique; chamfer; peri-implantitis; shoulder
Year: 2022 PMID: 35076562 PMCID: PMC8788496 DOI: 10.3390/mps5010009
Source DB: PubMed Journal: Methods Protoc ISSN: 2409-9279
Search algorithm used.
| Search Algorithm | Database | Results |
|---|---|---|
| ((((cementation) OR (cementing)) AND ((technique) OR (method))) AND ((cement) OR (luting agent))) AND (excess). | Scopus | 758 |
| ((((cementation) OR (cementing)) AND ((technique) OR (method))) AND ((cement) OR (luting agent))) AND (excess). | Cochrane Library | 92 |
| ((((cementation) OR (cementing)) AND ((technique) OR (method))) AND ((cement) OR (luting agent))) AND (excess). | Pubmed | 704 |
Figure 1PRISMA search flow results.
Main characteristics of the articles included in the study.
| Studies | Year | Sample Size | Sample Characteristics (and Follow-Up) | Implant Type | Implant | Type of Prostheses | Type of Cementation | Type of Cement | Type of Cement Remotion | Cement Remnants Analysis |
|---|---|---|---|---|---|---|---|---|---|---|
| Kiran et al. | 2017 | 12 patients | Bilateral-single tooth gap (extraction no later than 6 months before), presence of M-D teeth, | Locking taper connection | 1 mm subgingival | Metal ceramic crown | Extraoral (abutment with locking taper connection) | Zinc Polycarboxylate | Not Described | X-ray periapical radiograph |
| Canullo et al. | 2015 | 46 patients | 2 adjacent implants posterior maxilla | Screwed Abutment 8–12° of convergence | 1.5 mm subgingival (abutment with shoulder or with feath er edge) | Metal ceramic crown (with occlusal opening closed with composite resin) | Extraoral | Eugenol free Zinc Oxide cement | Stainless steel explorer + ultrasonic plastic tip + superfloss | Optical light microscope analysis of the occupied surface by cement remnants |
| Frisch et al. | 2015 | 68 patients | Variable anatomical distribution, single crown | Screwed abutment | 1.5 mm subgingival (abutment with shoulder preparation) | Metal ceramic crown | Extraoral | Zinc oxide cement | Extraoral | X-ray periapical radiographs |
Risk of bias of the included studies according to Cochrane risk of bias for randomized, controlled trials.
| Studies | Random Sequence Generation | Allocation Concealment | Blinding of Participants and Personnel | Blinding of Outcome Assessment | Incomplete Outcome Data | Selective Reporting |
|---|---|---|---|---|---|---|
| Kiran et al. 2017 | Low | Low | High | High | Low | Low |
| Canullo et al. 2015 | Low | Low | High | High | Low | Low |
| Frisch et al. 2015 | Unclear | High | High | High | Low | High |
Newcastle–Ottawa risk-of-bias assessment.
| Study | Selection (***) | Comparability (**) | Outcome (**) | Total | |||
|---|---|---|---|---|---|---|---|
| Representativeness | Selection of non | Ascertainment of exposure | Assessment of outcome (*) | Adequacy of follow-up (*) | |||
| Kiran et al. 2017 | * | * | * | 3 | |||
| Canullo et al. 2015 | * | * | * | ** | * | 6 | |
| Frisch et al. 2015 | * | * | * | * | * | 5 | |
Follow-up period for each study.
| Study | Type of the Study | Follow-Up |
|---|---|---|
| Kiran et al. 2017 | Prospective clinical study | 6 months |
| Canullo et al. 2015 | Randomized controlled prospective clinical study | 3 months |
| Frisch et al. 2015 | Prospective clinical study | 12 months |