Abstract
Objective
To determine the diagnostic accuracy of panoramic radiography (PR) in detecting calcified carotid artery atheroma (CCAA) compared with Doppler ultrasonography or angiography (the reference standard).
Sources
Cochrane, LILACS, PubMed, Scopus, Web of Science, Google Scholar, Open Grey, and ProQuest were searched. The reference lists of the included studies were also screened.
Data
Observational studies.
Methods
Only studies comparing the diagnostic accuracy of PR in detecting CCAA to Doppler ultrasonography or angiography (the reference standard) were included. The primary outcome measures were sensitivity and specificity. The secondary outcomes were negative predictive values, positive predictive values, diagnostic odds ratios, likelihood ratios (positive and negative), receiver operating characteristic curves, accuracy, and Youden’s index. Two reviewers independently participated in the study selection, data extraction, and risk of bias assessment without language restriction. Risk of bias was assessed thought QUADAS-2, and the level of evidence was assessed through GRADE.
Results
A total of 773 citations were identified after duplicates were removed, and 12 studies including 1002 patients were included in the final study. The sensitivity and specificity of the different selected studies varied substantially, with sensitivity ranging from 0.31 to 0.95 and specificity from 0.19 to 0.99.
Conclusions
Most studies reported excellent sensitivity and good specificity. The diagnostic accuracy of PR was good or excellent in 50% of the studies.
Clinical significance
The identification of CCAA by PR can be a risk predictor for stroke when used as a secondary screening tool.
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Appendices
Appendix 1 Search
Appendix 2
Appendix 3 Pooled Results
Summary sensitivity
Study | Sen | (95% conf. interval) | TP/(TP + FN) | TN/(TN + FP) |
---|---|---|---|---|
Abecasis, P.V., Kust | 0.778 | 0.577–0.914 | 21/27 | 23/27 |
Alman, A.C. et al. | 0.771 | 0.599–0.896 | 27/35 | 72/86 |
Bastos, J.S. et al. | 0.739 | 0.516–0.898 | 17/23 | 7/19 |
Damakos, S. et al. | 0.609 | 0.454–0.749 | 28/46 | 16/34 |
Ertas, E.T., Sisman | 0.798 | 0.708–0.870 | 83/104 | 86/106 |
Khambete, N. et al. | 0.760 | 0.549–0.906 | 19/25 | 74/75 |
Imanimoghaddam, M. et al. | 0.875 | 0.617–0.984 | 14/16 | 3/14 |
Madden, R.P. et al. | 0.308 | 0.199–0.434 | 20/65 | 34/39 |
Khosropanah, S.H. et al. | 0.500 | 0.211–0.789 | 6/12 | 23/32 |
Romano-Sousa, C.M. et al. | 0.950 | 0.751–0.999 | 19/20 | 9/12 |
Pornprasertsuk-Damro | 0.864 | 0.651–0.971 | 19/22 | 31/63 |
Yeluri, G. et al. | 0.937 | 0.858–0.979 | 74/79 | 4/21 |
Pooled Sen | 0.732 | 0.690–0.771 |
Summary specificity
Study | Spe | (95% conf. interval) | TP/(TP + FN) | TN/(TN + FP) |
---|---|---|---|---|
Abecasis, P.V., Kust | 0.852 | 0.663–0.958 | 21/27 | 23/27 |
Alman, A.C. et al. | 0.837 | 0.742–0.908 | 27/35 | 72/86 |
Bastos, J.S. et al. | 0.368 | 0.163–0.616 | 17/23 | 7/19 |
Damakos, S. et al. | 0.471 | 0.298–0.649 | 28/46 | 16/34 |
Ertas, E.T., Sisman | 0.811 | 0.724–0.881 | 83/104 | 86/106 |
Khambete, N. et al. | 0.987 | 0.928–1000 | 19/25 | 74/75 |
Imanimoghaddam, M. et al. | 0.214 | 0.047–0.508 | 14/16 | 3/14 |
Madden, R.P. et al. | 0.872 | 0.726–0.957 | 20/65 | 34/39 |
Khosropanah, S.H. et al. | 0.719 | 0.533–0.863 | 6/12 | 23/32 |
Romano-Sousa, C.M. et al. | 0.750 | 0.428–0.945 | 19/20 | 9/12 |
Pornprasertsuk-Damro | 0.492 | 0.364–0.621 | 19/22 | 31/63 |
Yeluri, G. et al. | 0.190 | 0.054–0.419 | 74/79 | 4/21 |
Pooled Spe | 0.723 | 0.683–0.761 |
Summary positive likelihood ratio (random effects model)
Study | LR+ | (95% conf. interval) | % weight |
---|---|---|---|
Abecasis, P.V., Kust | 5.250 | 2.078–13.262 | 7.12 |
Alman, A.C. et al. | 4.739 | 2.840–7.908 | 9.11 |
Bastos, J.S. et al. | 1.170 | 0.768–1.782 | 9.49 |
Damakos, S. et al. | 1.150 | 0.776–1.703 | 9.59 |
Ertas, E.T., Sisman | 4.230 | 2.817–6.351 | 9.54 |
Khambete, N. et al. | 57.000 | 8.035–404.37 | 3.40 |
Imanimoghaddam, M. et al. | 1.114 | 0.800–1.550 | 9.81 |
Madden, R.P. et al. | 2.400 | 0.980–5.879 | 7.27 |
Khosropanah, S.H. et al. | 1.778 | 0.805–3.924 | 7.78 |
Romano-Sousa, C.M. et al. | 3.800 | 1.419–10.177 | 6.84 |
Pornprasertsuk-Damro | 1.700 | 1.267–2.282 | 9.92 |
Yeluri, G.et al. | 1.157 | 0.933–1.435 | 10.13 |
(REM) pooled LR+ | 2.319 | 1.492–3.603 |
Summary negative likelihood ratio (random effects model)
Study | LR− | (95% conf. interval) | % weight |
---|---|---|---|
Abecasis, P.V., Kust | 0.261 | 0.127–0.538 | 9.05 |
Alman, A.C. et al. | 0.273 | 0.147–0.505 | 9.63 |
Bastos, J.S. et al. | 0.708 | 0.286–1751 | 8.06 |
Damakos, S. et al. | 0.832 | 0.501–1381 | 10.18 |
Ertas, E.T., Sisman | 0.249 | 0.168–0.369 | 10.69 |
Khambete, N. et al. | 0.243 | 0.121–0.489 | 9.19 |
Imanimoghaddam, M. et al. | 0.583 | 0.113–3005 | 4.76 |
Madden, R.P. et al. | 0.794 | 0.649–0.972 | 11.33 |
Khosropanah, S.H. et al. | 0.696 | 0.380–1275 | 9.68 |
Romano-Sousa, C.M. et al. | 0.067 | 0.010–0.463 | 3.86 |
Pornprasertsuk-Damro | 0.277 | 0.094–0.817 | 7.13 |
Yeluri, G. et al. | 0.332 | 0.098–1130 | 6.44 |
(REM) pooled LR− | 0.396 | 0.249–0.632 |
Summary diagnostic odds ratio (random effects model)
Study | DOR | (95% conf. interval) | % weight |
---|---|---|---|
Abecasis, P.V., Kust | 20.125 | 4.980–81.336 | 8.35 |
Alman, A.C. et al. | 17.357 | 6.548 –46.007 | 9.74 |
Bastos, J.S. et al. | 1.653 | 0.443–6170 | 8.61 |
Damakos, S. et al. | 1.383 | 0.564–3390 | 9.98 |
Ertas, E.T., Sisman | 16.995 | 8.588–33.634 | 10.59 |
Khambete, N. et al. | 234.33 | 26.590–2065.1 | 5.98 |
Imanimoghaddam, M. et al. | 1.909 | 0.270–13.495 | 6.59 |
Madden, R.P. et al. | 3.022 | 1.030–8.868 | 9.41 |
Khosropanah, S.H. et al. | 2.556 | 0.650–10.048 | 8.44 |
Romano-Sousa, C.M. et al. | 57.000 | 5.181–627.14 | 5.42 |
Pornprasertsuk-Damro | 6.135 | 1.649–22.830 | 8.62 |
Yeluri, G.et al. | 3.482 | 0.845–14.357 | 8.28 |
(REM) pooled DOR | 6.923 | 3.220–14.884 |
Analysis of diagnostic threshold
Spearman correlation coefficient: 0.364 p value = 0.245 | ||||
---|---|---|---|---|
(Logit(TPR) vs Logit(FPR) | ||||
Moses’ model (D = a + bS) Weighted regression (inverse variance) | ||||
Var | Coeff. | Std. error | T | p value |
a | 2.042 | 0.406 | 5033 | 0.0005 |
b(1) | − 0.261 | 0.196 | 1332 | 0.2126 |
Appendix 4 Test indicators
Test indicators | Data analysis | References |
---|---|---|
Accuracy | Accuracy (effectiveness) is affected by the disease prevalence. This percentage of correctly classified subjects should always be weighed considering other measures of diagnostic accuracy, especially predictive values. | Simundic [56] |
DOR | The value of a DOR ranges from 0 to infinity, with higher values indicating better discriminatory test performance. A value of 1 means that a test does not discriminate between patients with the disorder and those without it. Values lower than 1 point to improper test interpretation (more negative tests among the diseased). | Glas et al. [57] |
LR | LR tells us how many times more likely particular test result is in subjects with the disease than in those without disease. LR+ > 3 and an LR− < 0.3—acceptable diagnostic test accuracy (DTA) LR+ > 10 and LR− < 0.1—excellent DTA. | Simundic [56] |
Predictive values | PPV and NPV are largely dependent on disease prevalence in examined population, therefore, predictive values from on study should not be transferred to some other setting with a different prevalence of the disease in the population. | Simundic [56] |
ROC curve | The shape of a ROC curve and the area under the curve (AUC) helps us estimate how high is the discriminative power of a test. The closer the curve is located to upper-left hand corner and the larger the area under the curve, the better the test is at discriminating between diseased and nondiseased. The area under the curve can have any value between 0 and 1 and it is a good indicator of the goodness of the test. A perfect diagnostic test has an AUC 1.0. whereas a nondiscriminating test has an area 0.5. | Simundic [56] |
Sensitivity | Sensitivity > 80% excellent, 70–80% good, 60–69% fair, < 60% poor, no consensus in this regard exists in the literature. | No consensus in this regard exists in the literature. |
Specificity | Specificity > 90% excellent, 80–90% good, 70–79% fair, < 70% poor, no consensus in this regard exists in the literature. | No consensus in this regard exists in the literature. |
Youden’s index | Youden’s index values close to 1 indicate high accuracy; a value of zero is equivalent to uninformed guessing and indicates that a test has no diagnostic value. | Deeks et al. [58] |
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Schroder, A.G.D., de Araujo, C.M., Guariza-Filho, O. et al. Diagnostic accuracy of panoramic radiography in the detection of calcified carotid artery atheroma: a meta-analysis. Clin Oral Invest 23, 2021–2040 (2019). https://doi.org/10.1007/s00784-019-02880-6
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DOI: https://doi.org/10.1007/s00784-019-02880-6