| Literature DB >> 32340384 |
Marco Cicciù1, Luca Fiorillo1, Cesare D'Amico1, Dario Gambino1, Emanuele Mario Amantia1, Luigi Laino2, Salvatore Crimi3, Paola Campagna3, Alberto Bianchi3, Alan Scott Herford4, Gabriele Cervino1.
Abstract
The advent of new technologies in the field of medicine and dentistry is giving improvements that lead the clinicians to have materials and procedures able to improve patients' quality of life. In dentistry, the last digital techniques offer a fully digital computerized workflow that does not include the standard multiple traditional phases. The purpose of this study is to evaluate all clinical trials and clinical randomized trials related to the digital or dental impression technique in prosthetic dentistry trying to give the readers global information about advantages and disadvantages of each procedure. Data collection was conducted in the main scientific search engines, including articles from the last 10 years, in order to obtain results that do not concern obsolete impression techniques. Elsevier, Pubmed and Embase have been screened as sources for performing the research. The results data demonstrated how the working time appears to be improved with digital workflow, but without a significant result (P = 0.72596). The papers have been selected following the Population Intervention Comparison Outcome (PICO) question, which is related to the progress on dental impression materials and technique. The comparison between dentists or practitioners with respect to classic impression procedures, and students open to new device and digital techniques seem to be the key factor on the final impression technique choice. Surely, digital techniques will end up supplanting the analogical ones altogether, improving the quality of oral rehabilitations, the economics of dental practice and also the perception by our patients.Entities:
Keywords: dental; dental impression materials; dental impression technique; diagnosis; digital workflow; oral; prosthodontics; technology
Year: 2020 PMID: 32340384 PMCID: PMC7215909 DOI: 10.3390/ma13081982
Source DB: PubMed Journal: Materials (Basel) ISSN: 1996-1944 Impact factor: 3.623
Individual Risk of Bias Table.
| Author and Year | Risk of Bias | |||
|---|---|---|---|---|
| Unclear | Low | Moderate | High | |
| Zitzmann et al. 2017 [ | x | |||
| Zeltner et al. 2017 [ | x | |||
| Sailer et al. 2019 [ | x | |||
| Capparè et al. 2019 [ | x | |||
| Sakornwimon et al. 2017 [ | x | |||
| Joda et al. 2017 [ | x | |||
| Joda et al. 2016 [ | x | |||
| Gherlone et al. 2016 [ | x | |||
| Benic et al. 2016 [ | x | |||
| Boeddinghaus et al. 2015 [ | x | |||
| Gjelvold et al. 2016 [ | x | |||
| Yuzbasioglu et al. 2014 [ | x | |||
Risk of bias according to Cochrane reviews.
| Author and Year | Entry | Risk of Bias | Support for Judgement |
|---|---|---|---|
| Zitzmann et al. 2017 [ | Random Sequence Generation (selection bias) | High risk. | “Fifty undergraduate dental students with no clinical experience at the School of Dental Medicine, University of Basel, Switzerland were included in the study.” |
| Allocation Concealment (selection bias) | Low risk. | “Randomly divided” | |
| Blinding of participant and personnel (performance bias) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (Mortality) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | (outcomes by all participants) | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | (outcomes by all participants) | |
| Selective reporting (reporting bias) | Low risk | Statistics has been performed on all outcomes | |
| Zeltner et al. 2017 [ | Random Sequence Generation (selection bias) | Low risk | Random selection of participants |
| Allocation Concealment (selection bias) | Low risk | “The sequence of the crown assessment was randomly allocated according to a computer-generated list.” | |
| Blinding of participant and personnel (performance bias) | Low risk | “To eliminate operator bias, the investigators generated and evaluated the replicas without being able to distinguish among the crowns under investigation.” | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | Not applicable | |
| Blinding of outcome assessment (detection bias) (Mortality) | Low risk | Blinded outcome assessment | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data | |
| Sailer et al. 2019 [ | Random Sequence Generation (selection bias) | Low risk | 10 participants in need of a tooth supported 3-unit fixed denture included |
| Allocation Concealment (selection bias) | Low risk. | “Software ( | |
| Blinding of participant and personnel (performance bias) | High risk | “The same clinician carried out all the scanning and impression making on the assigned participants.” | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | Not specified (maybe no blinding) | |
| Blinding of outcome assessment (detection bias) (Mortality) | High risk. | Not specified (maybe no blinding) | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | No selective reporting | |
| Capparè et al. 2019 [ | Random Sequence Generation (selection bias) | Low risk | “patients were randomly selected for this clinical study” |
| Allocation Concealment (selection bias) | Low risk | Patients have been scheduled randomly into control (conventional impression group, CIG) and test (digital impression group, DIG) groups respectively for a fully conventional workflow and a fully digital workflow. | |
| Blinding of participant and personnel (performance bias) | Low risk | “Randomization processes occurred by lots in closed envelopes and were performed by a blinded operator” | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (Mortality) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Follow up to 24 months | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Follow up to 24 months | |
| Selective reporting (reporting bias) | Low risk | No selective reporting | |
| Sakornwimon et al. 2017 [ | Random Sequence Generation (selection bias) | High risk | Not random selection |
| Allocation Concealment (selection bias) | Unclear risk | Not specified, maybe not | |
| Blinding of participant and personnel (performance bias) | Low risk | Blinded operator | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | Unclear risk | No patient reported outcomes | |
| Blinding of outcome assessment (detection bias) (Mortality) | Low risk | Blinded | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data | |
| Joda et al. 2017 [ | Random Sequence Generation (selection bias) | Low risk | Randomly selected |
| Allocation Concealment (selection bias) | Unclear risk | Not specified | |
| Blinding of participant and personnel (performance bias) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | No blinding | |
| Blinding of outcome assessment (detection bias) (Mortality) | High risk | No blinding | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data | |
| Joda et al. 2016 [ | Random Sequence Generation (selection bias) | Low risk | Random selection |
| Allocation Concealment (selection bias) | Low risk | “Random allocation” | |
| Blinding of participant and personnel (performance bias) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (Mortality) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data | |
| Gjelvold et al. 2016 [ | Random Sequence Generation (selection bias) | Low risk | Randomly selection |
| Allocation Concealment (selection bias) | Low risk | Randomly allocation | |
| Blinding of participant and personnel (performance bias) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | Unclear risk | Not applied | |
| Blinding of outcome assessment (detection bias) (Mortality) | Low risk | “This dentist was not present at the dental office when the impressions were taken” | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data | |
| Gherlone et al. 2016 [ | Random Sequence Generation (selection bias) | Low risk | Randomly selected |
| Allocation Concealment (selection bias) | Low risk | Randomly allocated | |
| Blinding of participant and personnel (performance bias) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | Not performed | |
| Blinding of outcome assessment (detection bias) (Mortality) | High risk | Not performed | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data | |
| Benic et al. 2016 [ | Random Sequence Generation (selection bias) | Low risk | Randomly selected |
| Allocation Concealment (selection bias) | Low risk | Randomly allocated | |
| Blinding of participant and personnel (performance bias) | Low risk | Blinded personnel | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | Not applicable | |
| Blinding of outcome assessment (detection bias) (Mortality) | Low risk | “The impression sequences were concealed by means of sealed envelopes until the time of the clinical procedure that required the tooth impression.” | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data | |
| Boeddinghaus et al. 2015 [ | Random Sequence Generation (selection bias) | High risk | Not highlighted |
| Allocation Concealment (selection bias) | Unclear risk | Not specified | |
| Blinding of participant and personnel (performance bias) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | High risk | |
| Blinding of outcome assessment (detection bias) (Mortality) | High risk | Random application only of digital technique | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data | |
| Yuzbasioglu et al. 2014 [ | Random Sequence Generation (selection bias) | Unclear risk | Not specified |
| Allocation Concealment (selection bias) | Unclear risk | Not specified | |
| Blinding of participant and personnel (performance bias) | High risk | (cannot be conducted on digital vs. conventional impression techniques) | |
| Blinding of outcome assessment (detection bias) (patient-reported outcomes) | High risk | Not specified | |
| Blinding of outcome assessment (detection bias) (Mortality) | High risk | Not specified | |
| Incomplete outcome data addressed (attrition bias) (Short-term outcomes (2–6 weeks)) | Low risk | Complete data | |
| Incomplete outcome data addressed (attrition bias) (Longer-term outcomes (>6 weeks)) | Low risk | Complete data | |
| Selective reporting (reporting bias) | Low risk | Complete data |
Outcomes by the results.
| Outcomes |
|---|
| Visual Analog Scales (VAS), Student preference, Time, Occlusal gap, Marginal gap, Discrepancy Shoulder, framework/implant connection (Radiographic evaluation), voids at the bar/implant, bone level, operator preference, discomfort, accuracy, Patients’ perceptions (VAS), Operator difficulty (VAS). |
Study characteristics.
| Author and Year | Outcomes |
|---|---|
| Zitzmann et al. 2017 [ | Visual Analog Scales (VAS), Student preference, Time. |
| Zeltner et al. 2017 [ | Marginal gap, Discrepancy Shoulder, Chairside vs. Centralized techniques, Occlusal gap |
| Sailer et al. 2019 [ | Time, Occlusal registration, VAS |
| Cappare et al. 2019 [ | Time, framework/implant connection (Radiographic evaluation), voids at the bar/implant, bone level. |
| Sakornwimon et al. 2017 [ | Marginal fit, patient’s preferences (VAS) |
| Joda et al. 2017 [ | Time, difficulty, operator preference |
| Joda et al. 2016 [ | Patients’ satisfaction (VAS), Time |
| Gjelvold et al. 2016 [ | Time; difficulty; discomfort; occlusal gap. |
| Gherlone et al. 2016 [ | Time, Accuracy |
| Benic et al. 2017 [ | Time, Patients’ perceptions (VAS), Operator difficulty (VAS). |
| Boeddinghaus et al. 2015 [ | Crown fit and marginal gap |
| Yuzbasioglu et al. 2014 [ | Time, Patient’s satisfaction |
Figure 1PRISMA flow chart.
Figure 2Analysis of Variance between digital and conventional impression techniques. Vertical axis: time in seconds; Horizontal axis: groups.
Study characteristics.
| Author and Year | Outcomes |
|---|---|
| Zitzmann et al. 2017 [ | Visual Analog Scales (VAS), Student preference, Time. |
| Zeltner et al. 2017 [ | Marginal gap, Discrepancy Shoulder, Chairside vs. Centralized techniques, Occlusal gap |
| Sailer et al. 2019 [ | Time, Occlusal registration, VAS |
| Cappare et al. 2019 [ | Time, framework/implant connection (Radiographic evaluation), voids at the bar/implant, bone level. |
| Sakornwimon et al. 2017 [ | Marginal fit, patient’s preferences (VAS) |
| Joda et al. 2017 [ | Time, difficulty, operator preference |
| Joda et al. 2016 [ | Patients’ satisfaction (VAS), Time |
| Gjelvold et al. 2016 [ | Time; difficulty; discomfort; occlusal gap. |
| Gherlone et al. 2016 [ | Time, Accuracy |
| Benic et al. 2017 [ | Time, Patients’ perceptions (VAS), Operator difficulty (VAS). |
| Boeddinghaus et al. 2015 [ | Crown fit and marginal gap |
| Yuzbasioglu et al. 2014 [ | Time, Patient’s satisfaction |
Analysis of Variance.
| Data Summary about Time | ||||
|---|---|---|---|---|
| Groups | Number of Measures | Mean | Standard Deviation | Standard Error |
| Digital | 6 | 689.15 | 428.5407 | 174.951 |
| Conventional | 6 | 770.2833 | 346.7292 | 141.5516 |
Figure 3Risk of Bias according to Cochrane reviews.
Figure 4Sample of computers planning and realization of prosthodontics structure before starting the treatment over patients.
Figure 5Sample of new devices like 3D printing for having dental threedimensional model.