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ERK 2–3 diagnostic threshold<br />

AUC (SE) CI opt.<br />

sens.<br />

opt.<br />

spec.<br />

ICDAS<br />

cut-off<br />

0.84 (0.04) 0.76–0.93 0.84 0.75 2–3<br />

0.84 (0.05) 0.75–0.93 0.80 0.79 2–3<br />

0.86 (0.04) 0.78–0.94 0.64 0.90 2–3<br />

0.84 (0.04) 0.76–0.92 0.88 0.68 2–3<br />

study [Ekstrand et al., 1997] using comparable visual<br />

criteria. Interexaminer kappa values between the reference<br />

examiner and 3 trained examiners were also acceptable<br />

( table 3 ).<br />

Histological validation of caries and in particular occlusal<br />

caries is notoriously difficult as preparing thin sections<br />

entails tooth tissue loss. Simply hemisecting a tooth<br />

through the lesion may not pass through the deepest aspect<br />

of the lesion in question. Taking a single section<br />

through an investigation site is also problematic if only<br />

one side of the section is examined as the depth of a lesion<br />

will vary from one side of a section to another [Ricketts<br />

et al., 1998]. Whilst only one side of the section was viewed<br />

in this study because of the mounting technique used, the<br />

sections were serial and the side viewed on one section<br />

corresponded to the side not viewed on the preceding<br />

section. These problems arise because of the three-dimensional<br />

nature of the spread of caries dictated by the<br />

complex anatomy of the occlusal surface. A lesion may<br />

originate at one site on the surface of the tooth but spread<br />

obliquely and non-symmetrically beneath the tooth surface.<br />

To overcome this problem and to record the deepest<br />

aspect of the lesion from where it originated at the investigation<br />

site, 1–4 sections were used depending on the<br />

severity of the lesion. The use of the coordinate system<br />

ensured accurate location of each section and thus that<br />

the lesion on the section originated from the investigation<br />

site in question. Because of the mode of spread alluded<br />

to above, it could be argued that the appearance at<br />

one site may influence the decision at another. For example,<br />

if one site was obviously carious, the likelihood of<br />

an adjacent site also being carious and recorded as such<br />

is much higher. The data collected at multiple sites cannot<br />

therefore be regarded as independent. To overcome this<br />

problem one investigation site per tooth was randomly<br />

selected for analysis.<br />

In previous studies comparing both visual classification<br />

systems and histological classification systems of increasing<br />

lesion severity, the relationships between the<br />

two variables have been strong, with Spearman correlation<br />

coefficients of 0.87 for an eight-point visual scale<br />

[Ekstrand et al., 1995] and 0.87–0.93 for a five-point visual<br />

scale [Ekstrand et al., 1997]. In this study the relationship<br />

between the ICDAS-II visual classification system<br />

and either histological classification system was not<br />

as strong (r s = 0.48–0.72 using Downer histology and<br />

0.43–0.68 for ERK histology).<br />

For comparison with other studies using similar visual<br />

classification systems or different novel technologies,<br />

the Downer histology was used in the ROC analyses<br />

for each examiner at the D1 and D3 diagnostic threshold<br />

and the ERK histology was used similarly at the 2–3<br />

threshold. For all examiners the ICDAS-II system produced<br />

areas under the ROC curves in excess of 0.7.<br />

At the D1 diagnostic threshold the mean sensitivity<br />

and specificity of the ICDAS-II were 0.69 and 0.82, respectively<br />

( table 6 ). The sensitivity was found to be higher<br />

than that reported in a previous study using a different<br />

eight-point visual scale and three groups of examiners<br />

[Fyffe et al., 2000b] where sensitivity ranged between 0.46<br />

and 0.5. The specificity in this study was similar to that<br />

reported by Fyffe et al. [2000b], who found specificities<br />

of 0.66–0.86. However, in this study optimum sensitivity<br />

and specificity were achieved at the ICDAS-II cut-off 1–2<br />

and not 0–1, which would have been consistent with the<br />

D1 diagnostic threshold. When the 0–1 cut-off was used,<br />

sensitivity was high (mean = 0.89), but specificity was low<br />

(mean = 0.52). This means that a large number of sound<br />

sites were incorrectly scored as carious and this may have<br />

been due to stained sites, areas of fluorosis or developmental<br />

defects being incorrectly scored as caries. It is important<br />

to question what impact this would have clinically.<br />

From table 4 it can be seen that the sound sites<br />

that were incorrectly scored as carious were given a low<br />

ICDAS-II score which would not require operative treatment.<br />

The worse clinical outcome would therefore be giving<br />

prevention to a sound site, which in a high-risk patient<br />

would be of benefit.<br />

In this study, at the D3 diagnostic threshold mean sensitivity<br />

was 0.70 and specificity was 0.89 using ICDAS-II<br />

scores 2–3 to differentiate sound sites from those with<br />

dentine caries ( table 6 ). These are similar to those reported<br />

by Downer [1989], who in a review of the literature<br />

found that trained and experienced examiners using a<br />

Reproducibility/Accuracy of a Method for<br />

Caries Detection<br />

Caries Res 2008;42:79–87 85

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