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11.

5  Volumetric Measurements for Evaluation of Oral Soft Tissue Changes 11

11.5 Volumetric Measurements 11.5.2 Clinical Measurements


Clinical intraoral linear measurements for the
for Evaluation of Oral Soft
quantification of, e.g., gingival recessions, papilla
Tissue Changes height or the width of the alveolar ridge, can be
performed with periodontal probes or calipers
David Schneider and (Covani et al., 2004; Chen et al., 2008; Grunder,
Sven Mühlemann 2011; Grunder, 2000). The use of tooth supported
stents guiding these instruments at a defined pos-
ition and direction allows standardized measure-
11.5.1 Introduction ments at different time points and by different
Quantitative volumetric analyses focusing on examiners (Perez et al., 2005). Stents and probes
alterations of tissue dimensions are of great inter- can also be used for the mapping of the surface
est in various fields of preclinical and clinical topography. Endodontic files can be used for soft
research. Different methods have been used for tissue thickness measurements and assessment of
the measurement of changes of hard and soft tis- the bony contour by ridge mapping (Östlund,
sue dimensions following various therapeutic 1958); (Studer et al., 1997) (Fig 11.5-2). Soft tis-
interventions. In particular, such analyses have sue thickness has also been measured by ultra-
been performed in connection with bone aug- sonic devices (Cardaropoli et al., 2006; Eger et al.,
mentation and soft tissue grafting procedures 1996; Tsiolis et al., 2003).
(Friedmann et al., 2011; Proussaefs et al., 2002; It is of great importance that the measurements
Schneider et al., 2011) for implant site develop- are always performed in a reproducible manner,
ment or at pontic areas, comparison of ridge pres- i.e., using the same, stable reference points, in the
ervation techniques following tooth extraction same direction using the same tools, etc. A cali-
(Covani et al., 2011; Fickl et al., 2008), for the bration of the method and examiner(s) is manda-
determination of tooth wear (Kramer et al., 2006; tory.
Mehl et al., 1997; Petersilka et al., 2003), to Direct intraoral measurements have several
measure the effects of orthodontic treatment advantages. They are relatively fast, simple and
(Marini et al., 2007), and for analyses of long- inexpensive and the results are available immedi-
term tissue stability, e.g., around dental implants ately. No secondary data processing is necessary
(Cardaropoli et al., 2006; Jemt and Lekholm, and therefore possible errors from additional work
2005; Schneider et al., 2011). In general, the steps are excluded. However, the measurements
analysis is based on the comparison of tissue can be falsified by reading or rounding errors, lim-
dimensions within a defined area of interest at ited accessibility or non-standardized measure-
two or more time points. The dimensions of the ment technique. Moreover, more clinical time is
tissues are either assessed by the measurement of usually needed for data collection than in the case
the actual tissue volume, which is then compared, of post-clinical bench top measurements. In addi-
or by comparison of a tissue surface to a reference tion, measurements cannot be verified or repeated
surface. at a later time point. Depending on the invasive-
The measurements can be performed either ness of the method, patient discomfort can arise.
clinically by obtaining the measured value This is particularly true for the evaluation of bone
intraorally or post-clinically by capturing the clin- dimensions that usually require surgical re-open-
ical situation (photograph, conventional impres- ing of the site for direct access to the site. Even
sion, intraoral optical scan, radiographs, etc.) and after flap elevation, some of the areas may not be
secondary data processing (Fig 11.5-1). accessible for measurements and, therefore, may
require radiographic evaluation.

183
Analytical Methods

Clinical chairside Post-clinical


approach labside approach

Clinical chairside Capturing of clinical situation


Clinical
measurement (photograph, impression,
appointment
(probe, caliper,…) optical scan,…)
- Timepoint 1

Value 1 Data Set 1

Processing of data (fabrication/


sectioning of models, digitization,
Laboratory transformation of file format,…)

Data Set 1.1

Clinical chairside Capturing of clinical situation


Clinical
measurement (photograph, impression,
appointment
(probe, caliper,…) optical scan,…)
- Timepoint 2

Value 2 Data Set 2

Processing of data (fabrication/


sectioning of models, digitization,
Laboratory transformation of file format,…)

Data Set 2.1

Matching of data sets;


Measurements in data sets
Laboratory

Values

Comparison and analysis


Analysis of values obtained from
of obtained values from
post-clinical lab side measurement
Data analysis measurement 1 and 2

Results Results

Fig 11.5-1 Workflow of clinical and bench top based volumetric evaluation.

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11.5  Volumetric Measurements for Evaluation of Oral Soft Tissue Changes 11

11.5.3 Lab side Measurements


In the case of post-clinical laboratory analysis, the
clinical situation is recorded in a first step, and
data processing and measurements are performed
in a second step. For this purpose, different tech-
niques have been developed, including analysis of
photographs, cast models, optical scan data and
radiographs (Alpiste-Illueca, 2004; Arasawa et al.,
2012; Ender and Mehl, 2011; Friedmann et al.,
2011; Henriksson and Jemt, 2004; Januario et al.,
2008; Jemt and Lekholm, 2003; 2005; Oberoi et
al., 2009; Oz et al., 2011; Ricci, 2007; Rodrigues
et al., 2012; Schneider et al., 2011; Shirota et al., Fig 11.5-2  Clinical application of stent-guided soft-tissue
2010; Strebel et al., 2009; van Brakel et al., 2011; thickness measurement using an endodontic file.
Weinlander et al., 2009; Windisch et al., 2007).
Usually, data obtained at different time points
during treatment are compared. This implies that image quality or the use of high magnification. A
adequate reference points for measurements are larger variety of measuring tools can be applied
defined and can properly be identified in all data than for intraoral application. For digital data
sets. These reference points must be present in all processing, a broad variety of software programs
data sets, identical in their position and dimension is available and offers almost unlimited options
and also remain stable during the follow-up period for analyses (Figs 11.5-3 to 11.5-7).
to ensure proper matching and superimposition of Disadvantages of the indirect method arise
the data sets. The data analysis can again be per- from possible errors during data acquisition and
formed using analogue techniques, similar to processing (impression taking, cast production,
direct clinical measurements, such as calipers, rul- non-standardized photographs/radiographs,
ers, etc. or by digitalization and analysis in a soft- optical scanning, data digitization, defective dig-
ware program. For the latter, different file formats ital data, radiographic artifacts, etc.). The use of
are considered as a standard, which is important digital techniques is associated with infrastruc-
to ensure data compatibility. Current file formats tural investments and operating expenses and
include JPEG (Joint Photographic Experts Group / requires appropriate training. Moreover, many of
.jpg) and TIFF (Tagged Image File Format / .tiff) the evaluation protocols lack adequate valida-
for image files, STL (Surface Tesselation Language tion. One major challenge is the identification of
/ .stl) for surface files and DICOM (Digital Imag- stable reference points for measurements or ref-
ing and Communications in Medicine /.dcm) for erence surfaces for data superimposition of mul-
radiographic files. tiple data sets. This must be considered during
With the indirect method, clinical data are col- the development of the research protocol and
lected at a given time point and can be processed respected during clinical data collection.
any time after the patient appointment. It can be
analyzed in different ways and several times, if 11.5.4 Considerations for Data Collection
necessary, and by different examiners. Also, stor- and Analysis
age over a long period and additional evaluation Although “volumetric” implies a three-dimen-
at a later time point are possible. The interpreta- sional (3D) analysis, the analyses are primarily
tion of the acquired data can be potentially facil- performed in a 2D way. The distance between
itated, e.g., by enhancement of the original two points on two surfaces is measured in a given

185
Analytical Methods

Fig 11.5-3  Digitalized model of preoperative Fig 11.5-4  Digitalized model of postoperative
situation. situation.

Fig 11.5-5  Superimposed models (yellow-semitrans- Fig 11.5-6  Visualization of volume changes between
parent = preoperative, green = postoperative). models from incisal view (green = postoperative,
Qualitative and quantitative analysis of volume turquoise = projection of preoperative surface in area of
changes in the area of interest. interest).

Fig 11.5-7 Cross-sectional
views of surfaces (yellow =
preoperative, green =
postoperative, gray = area
of interest). Lower left: axial
section, lower right:
bucco-oral section, upper
right: tangential section.

direction (Fickl et al., 2008; Januario et al., 2008; few linear measurements in the most relevant area
Kirmeier et al., 2011). Depending on the size of (e.g., midcrestally).
the area of interest, the absolute volume can be Another way to calculate the volume in digital
calculated from the sum of the linear measure- data sets is the addition of voxels or pixels in differ-
ments. To simplify the procedure and the data ent sections within the area of interest. This analysis
analysis, the measurements are often limited to a is independent of the axis or direction of vectors

186
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