| Literature DB >> 30358024 |
Nils Gustafsson1, Jan Ahlqvist1, Eva Levring Jäghagen1.
Abstract
PURPOSE: To study general dental practitioners (GDPs) ability to detect calcified carotid artery atheromas (CCAAs) in panoramic radiographs (PRs) and if their diagnostic accuracy in long term is improved after a short training programme.Entities:
Keywords: calcified carotid artery atheroma; carotid artery calcification; education; panoramic radiography; radiology
Mesh:
Year: 2018 PMID: 30358024 PMCID: PMC7328722 DOI: 10.1111/eje.12402
Source DB: PubMed Journal: Eur J Dent Educ ISSN: 1396-5883 Impact factor: 2.355
Figure 1A panoramic radiograph depicting calcified carotid artery atheromas on the left and right sides
Figure 2Flow chart of education programme and participant dropout
Mean values for each variable describing diagnostic accuracy with standard deviation (SD) and minimum (min) and maximum (max) values before and after training
| Variables | Baseline | Two weeks follow‐up | ANOVA | ||||||
|---|---|---|---|---|---|---|---|---|---|
| Mean (min‐max) | CI 95% | SD | Mean (min‐max) | CI 95% | SD |
|
|
| |
| Kappa | 0.66 (0.51‐0.75) | 0.62‐0.70 | 0.07 | 0.71 (0.60‐0.77) | 0.67‐0.75 | 0.05 | 0.08 | 0.04 | 0.05 |
| Sensitivity | 41.8% (8.8%‐63.8%) | 32.1%‐51.5% | 18.2% | 55.7% (33.8%‐71.3%) | 46.0%‐65.4% | 10.9% | 0.05 | 0.02 | 0.05 |
| Specificity | 87.2% (65.0%‐99.2%) | 82.5%‐91.9% | 7.8% | 86.7% (70.0%‐96.7%) | 82.0%‐91.4% | 8.8% | 0.88 | 0.87 | 0.91 |
| PPV | 67.6% (25.9%‐94.7%) | 59.3%‐75.8% | 17.9% | 75.8% (58.1%‐91.3%) | 67.6%‐84.1% | 10.2% | 0.16 | 0.17 | 0.16 |
| NPV | 69.9% (57.8%‐78.2%) | 66.2%‐73.5% | 6.0% | 74.9% (67.1%‐80.0%) | 71.3%‐78.5% | 3.5% | 0.05 | 0.01 | 0.04 |
| +LR | 5.16 (0.53‐23.0) | 1.97‐8.35 | 5.52 | 6.05 (2.08‐15.75) | 3.85‐8.25 | 3.81 | 0.65 | 0.66 | 0.54 |
| −LR | 0.67 (0.41‐1.10) | 0.54‐0.78 | 0.21 | 0.51 (0.38‐0.74) | 0.45‐0.56 | 0.09 | 0.02 | 0.01 | 0.02 |
+LR, positive likelihood ratio; −LR, negative likelihood ratio; NPV, negative predictive value; PPV, positive predictive value.
P‐values calculated using LSD post‐hoc comparing follow‐up session to baseline. P < 0.05 is considered significant.
P‐values calculated using paired t test between the 2 wk follow‐up to baseline. P < 0.05 is considered significant.
Mean values for each variable describing diagnostic accuracy with standard deviation (SD) and minimum (min) and maximum (max) values before and after training
| Variables | Baseline | One year follow‐up | ANOVA | ||||||
|---|---|---|---|---|---|---|---|---|---|
| Mean (min‐max) | CI 95% | SD | Mean (min‐max) | CI 95% | SD |
|
|
| |
| Kappa | 0.66 (0.51‐0.75) | 0.62‐0.70 | 0.07 | 0.74 (0.64‐0.99) | 0.68‐0.79 | 0.10 | 0.01 | 0.26 | 0.05 |
| Sensitivity | 41.8% (8.8%‐63.8%) | 32.1%‐51.5% | 18.2% | 57.8% (30.0%‐98.7%) | 46.9%‐73.2% | 19.2% | 0.04 | 0.78 | 0.05 |
| Specificity | 87.2% (65.0%‐99.2%) | 82.5%‐91.9% | 7.8% | 90.1% (69.2%‐100%) | 82.0%‐94.8% | 8.7% | 0.44 | 0.36 | 0.91 |
| PPV | 67.6% (25.9%‐94.7%) | 59.3%‐75.8% | 17.9% | 80.8% (61.5%‐100%) | 68.6%‐90.9% | 11.2% | 0.05 | 0.44 | 0.16 |
| NPV | 69.9% (57.8%‐78.2%) | 66.2%‐73.5% | 6.0% | 77.1% (67.5%‐99.2%) | 72.5%‐82.3% | 8.8% | 0.02 | 0.44 | 0.04 |
| +LR | 5.16 (0.53‐23.0) | 1.97‐8.35 | 5.52 | 7.72 (2.39‐22.50) | 2.25‐13.20 | 6.54 | 0.27 | 0.47 | 0.54 |
| −LR | 0.67 (0.41‐1.10) | 0.54‐0.78 | 0.21 | 0.46 (0.01‐0.76) | 0.31‐0.62 | 0.20 | 0.01 | 0.61 | 0.02 |
+LR, positive likelihood ratio; −LR, negative likelihood ratio; NPV, negative predictive value; PPV, positive predictive value.
P‐values calculated using LSD post‐hoc comparing follow‐up session to baseline. P < 0.05 is considered significant.
P‐values calculated using LSD post‐hoc comparing the two follow‐up sessions. P < 0.05 is considered significant.
Figure 3Comparison of participants’ diagnostic accuracy at baseline (light grey), the 2‐week follow‐up (medium grey) and the 1‐year follow‐up (dark grey) regarding sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy. The line in the box marks the median and × marks the mean. P‐values in the graph are for comparison of changes in means between follow‐up sessions and baseline, and P‐values on x‐axis are from the ANOVA comparing all three sessions