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Dentomaxillofacial Radiology logoLink to Dentomaxillofacial Radiology
. 2017 Sep 25;46(7):20170030. doi: 10.1259/dmfr.20170030

Head and neck effective dose and quantitative assessment of image quality: a study to compare cone beam CT and multislice spiral CT

Cosimo Nardi 1,, Cinzia Talamonti 2, Stefania Pallotta 2, Paola Saletti 3, Linda Calistri 1, Cesare Cordopatri 1, Stefano Colagrande 1
PMCID: PMC5988185  PMID: 28511564

Abstract

Objectives:

To evaluate the effective dose and image quality of horizontal CBCT in comparison with multislice spiral CT (MSCT) in scans of the head, cervical spine, ear and dental arches.

Methods:

A head and neck Alderson-Rando® phantom (The Phantom Laboratory, Salem, NY) equipped with 74 thermoluminescence dosemeters was exposed according to 5 different scans in CBCT and 4 different scans in MSCT. Spatial and contrast resolutions, in terms of modulation transfer function and contrast-to-noise ratio (CNR), were measured to obtain a quantitative assessment of image quality.

Results:

The CBCT effective dose was 248, 249, 361, 565 and 688 µSv in the cervical spine, head, ear, dental arches with small field of view and dental arches with medium field of view, respectively. The MSCT effective dose was 3409, 1892, 660 and 812 µSv in the cervical spine, head, ear and dental arches, respectively. The modulation transfer function was 0.895 vs 0.347, 0.895 vs 0.275, 0.875 vs 0.342 and 0.961 vs 0.352 for CBCT vs MSCT in the cervical spine, head, ear and dental arches, respectively. Head and cervical spine MSCT showed greater CNR than CBCT, whereas CNR of the ear and dental arches showed comparable values.

Conclusions:

CBCT was preferable to MSCT for the ear and dental arches volumetric imaging due to its lower radiation dose and significantly higher spatial resolution. In the case of cervical spine and head imaging, MSCT should be generally recommended if a high contrast resolution is required, despite the greater radiation exposure.

Keywords: CBCT, radiation exposure, effective dose, spatial/contrast resolution, image quality

Introduction

In recent years, employment of diagnostic radiography has increased progressively, and at the same time, the cancer risk induced by multislice spiral CT (MSCT) scans seems to have increased.1 CBCT is a relatively new imaging technique that has recently emerged in the field of radiodiagnostics. It utilizes a conic/pyramidal X-ray beam which hits a two-dimensional detector (image intensifier or flat panel) during a lengthy single rotation (5.4–40 s).2 The reduced presence of metal artefacts and the high spatial resolution (0.075–0.4 mm isotropic voxel) have made CBCT a technique widely used not only in dentomaxillofacial radiology3 but also for cervical spine and middle ear imaging.4

Many studies investigated head/dental CBCT effective dose and dosimetric differences between MSCT and CBCT.59 They proved that the CBCT effective dose is undoubtedly lower than the MSCT dose, regardless of the broad variability in CBCT dose resulting from the appliance and the protocol employed.

However, only few studies concerning the head and neck area tried to establish a relationship between effective dose and quantitative measurement of image quality.6,1012 Moreover, there are only three works on ear dose,10,13,14 and no article exists regarding spine dose.

The aim of this study was to evaluate the effective dose and image quality of horizontal CBCT in comparison with MSCT in the scans of the head, cervical spine, ear and dental arches (concurrently the upper and lower jaws).

Methods and materials

Devices and protocols

Scans were carried out via SOMATOM® Sensation 64 MSCT (Siemens, Erlangen, Germany) and NewTom5G CBCT (QR srl, Verona, Italy). The latter was equipped with a pulsed pyramidal X-ray beam (360° of rotation), a very small focal spot (0.3 mm) and an amorphous silicon flat-panel detector (20 × 25 cm). In addition, it embedded the SafeBeam. This technology features the use of intermittent bursts of radiation (ms) and automatically adjusts the radiation dosage by modifying the tube current (mA) according to pre-set dose levels determined by the patient's size as measured on the scout images.

All technical/geometrical parameters were the same as those used in the clinical practice (Table 1). Since even small modifications in the size and position of field of view (FOV) heavily influenced the effective dose, an accurate positioning of FOV was mandatory (Figure 1).

Table 1.

CBCT (standard-regular protocol) and multislice spiral CT (MSCT) exposure parameters about the head, cervical spine, ear and dental arches

Device Anatomical area Tube voltage (kV) CTDIvola (mGy) DLP (mGy cm) DAP (mGy cm2) Air kerma (mGy) Current × exposure time (mAs) Rotation timeb (s) Scan diameter (cm) Scan length (cm) Reconstruction FOV (AP, LL × CC) (cm cm) Reconstruction kernel Voxel side (mm) Pixel sizec (mm) Slice thickness (mm) Pitch (mm)
CBCT Head 110 2.49 39.87 794.87 3.75 10.23 18 18 16 18 × 16 0.30
Cervical spine 110 2.84 45.39 904.85 4.27 13.08 18 18 16 18 × 16 0.30
Ear 110 20.57 128.57 1835.18 29.10 141.92 36 15 5 15 × 5 0.15
Dental arches 110 10.53 94.80 1502.40 17.41 77.60 36 12 8 12 × 8 0.15
Dental arches 110 7.44 66.98 1006.42 14.85 63.80 36 8 8 8 × 8 0.15
MSCT Head 120 23.24 553.00 150 22 24 × 22 H40s medium 0.34 4.80
Cervical spine 120 13.49 314.33 200 1 18 12 × 18 B40s medium 0.39 2.00 0.90
Ear 120 36.94 317.69 120 1 6 15 × 6 U90u ultra sharp 0.41 2.00 0.85
Dental arches 120 12.53 173.53 80 1 10 15 × 10 H60s sharp 0.39 0.60 0.90

AP, anteroposterior diameters; CC, craniocaudal diameters; CTDI, CT dose index; DAP, dose–area product; DLP, dose–length product; FOV, field of view; LL, laterolateral diameters.

Size of AP and LL was equal.

The protocols were optimized in such a way as to simulate the routine clinical practice. Since the acquisition was performed in a sequential manner, no rotation time and pitch value have been indicated for the MSCT head scan.

a

CTDIvol values are referenced to a 16-cm-diameter CTDI phantom.

b

The rotation time was the time for each 360° rotation. In CBCT, the rotation time corresponds to the full scan time.

c

The pixel size was measured in the axial plane.

Figure 1.

Figure 1

Overview of all fields of view (FOVs). The multislice spiral CT FOVs are represented in the middle of the picture. The corresponded FOVs used in CBCT are showed on the edge of the picture.

In CBCT, the FOV of the head was the widest available (18 × 16 cm). It was placed so that the soft tissues of the nose and chin were completely included to fulfil the clinician's requirements for orthognathodontic treatment/surgical planning; the cranial vertex and occipital bone were thus excluded. In MSCT, the FOV of the head included the entire skull since scanning the head for orthognathodontic purposes is not recommended due to the high radiation dose.7,15 The FOV of the cervical spine, ear and dental arches was kept as similar as possible between both devices whilst still trying to maintain the standard settings. CBCT of dental arches was studied with two different FOVs: small (8 × 8 cm) and medium (12 × 8 cm). It is important to remind that an exact dosimetric match between CBCT and MSCT is only achievable when the FOV of CBCT completely includes the scanned object. In MSCT, the diameter of the X-ray beam always covers the entire object, therefore only the scan length is relevant from a dosimetric point of view.

NewTom5G exposure parameters could not be altered by the operator and were automatically set in relation to the FOV, radiographic absorption and available acquisition protocol. The two protocols chosen—named standard-regular and high-resolution (hi-res) enhanced by the producer—lasted 18 and 36 s, and included 360 and 480 basis image frames, respectively. The protocol was chosen accordingly to the diagnostic application. The ear and dental arches were acquired with smaller voxels and greater mA (hi-res-enhanced protocol) than the head and cervical spine (standard-regular protocol) to better depict fine anatomical structures such as ossicular chain in ear study or neurovascular canal in dental extractive/implant planning. Both CBCT and MSCT scans were performed at normal dose settings, except for scans of the dental arches with MSCT, which were conducted at significantly reduced dose settings by decreasing mAs value (low-dose Dentascan).16

Phantom and experimental setup

An adult male Alderson-Rando® anthropomorphic phantom (The Phantom Laboratory, Salem, NY) was used. The phantom consisted of a real human skeleton filled with tissue equivalent material according to The International Commission on Radiation Units and Measurements-44 specification, transected horizontally into 2.5-cm-thick slices from the head vertex to the groin. For the current study, only the upper 12 slices (i.e. head and neck) were used. Each slice had cylindrical drilled holes in default locations that were plugged with two lithium fluoride (LiF:Mg,Ti) thermoluminescence dosemeter (TLD-100 rods; Harshaw Chemical Company, Solon, OH) chips (3.2 × 3.2 × 0.5 mm) to measure radiation exposure. The holes used for the measurements were chosen among those that more accurately represented the anatomical location of the organs of interest (Table 2). The dosimetric response for each hole was calculated as the arithmetic mean of the two thermoluminescence dosemeter (TLD) chip exposures. 37 anatomical sites were considered for both CBCT and MSCT, thereby 74 TLDs were used for each scan. Consequently, a total of 370 and 296 dosemeters were used in the 5 CBCT and 4 MSCT scans, respectively. The TLD response was well above the background dose and also showed low variability in each phantom hole. For this reason, only one exposure was performed for each technique and therefore no scan was repeated.

Table 2.

Tissue weighting factors (WT), fractions irradiated (fi) and dosemeters (number and location) used to calculate the effective dose

Organ WT fi Number of TLD Slice
Lens of eye     1–4 4
 Right lens of eye     1, 2 4
 Left lens of eye     3, 4 4
Ossicles chain     5–8 5
 Right ossicles chain     5, 6 5
 Left ossicles chain     7, 8 5
Thyroid 0.04 1 9–12 9
 Thyroid—right     9, 10 9
 Thyroid—left     11, 12 9
Salivary glands 0.01 1 13–22 7, 8
 Right submandibular gland     13, 14 8
 Left submandibular gland     15, 16 8
 Right parotid     17, 18 7
 Left parotid     19, 20 7
 Centre sublingual gland     21, 22 8
Bone marrow 0.12 0.123 23-28, 33–36, 41-46 2, 3, 6, 7, 8, 9
 Calvaria/skull base   0.076 23-28, 45, 46 2, 3, 6
  Calvarium anterior     23, 24 2
  Calvarium posterior     25, 26 3
  Calvarium right     27, 28 3
  Skull base     45, 46 6
 Mandible   0.008 33–36 8
  Mandible right (trabecular)     33, 34 8
  Mandible left (trabecular)     35, 36 8
 Cervical spine   0.039 41–44 7, 9
  Cervical spine C2 (trabecular)     41, 42 7
  Cervical spine C4 (trabecular)     43, 44 9
Bone surface 0.01 0.133 23-32, 37-40 2, 3, 7, 8, 9
 Calvaria   0.112 23–28 2, 3
  Calvarium anterior     23, 24 2
  Calvarium posterior     25, 26 3
  Calvarium right     27, 28 3
 Mandible   0.011 29–32 8
  Mandible right (cortical)     29, 30 8
  Mandible left (cortical)     31, 32 8
 Cervical spine   0.010 37–40 7, 9
  Cervical spine C2 (cortical)     37, 38 7
  Cervical spine C4 (cortical)     39, 40 9
Brain 0.01 1 47–50 3, 4
 Pituitary gland     47, 48 4
 Mid-brain     49, 50 3
Oesophagus 0.04 0.1 51, 52 9
Skin 0.01 0.05 53–56 6, 7
 Skin—right cheek     53, 54 6
 Skin—back of the neck     55, 56 7
Extrathoracic airway 0.0086 1 57–62 4, 5, 7
 Oropharyngeal airway     57, 58 7
 Right maxillary sinus     59, 60 5
 Left ethmoid     61, 62 4
Oral mucosa 0.0086 1 63, 64 6
Lymph nodes 0.0086 0.05 65–68 9
 Right laterocervical lymph nodes     65, 66 9
 Left laterocervical lymph nodes     67, 68 9
Muscles 0.0086 0.05 69–74 5, 6, 8
 Right cutaneous muscles     69, 70 6
 Left masticatory muscle     71, 72 5
 Back of the neck muscles     73, 74 8

TLD, thermoluminescence dosemeter.

Extrathoracic airways, oral mucosa, lymphatic nodes and muscles form part of the remainder tissues.

The phantom was always positioned with a headrest as if it were a real patient, so that

  • – the occlusal plane was perpendicular to the patient table

  • – the midheight/midsagittal plane was centred on the horizontal/vertical positioning light beam

  • – the midsagittal plane was aligned with the midline of the gantry.

Dosimetric method and effective dose calculation

Dosimetric evaluation17 was performed with TLDs. On irradiated fraction, the collected charge in the TLD was read in a regularly calibrated automatic nitrogen flow Harshaw 5500 reader (Harshaw Chemical Company). The background dose was estimated by using non-irradiated TLDs and subtracted from all the TLD measured values. The following equation was used to calculate the mean equivalent dose or radiation weighted dose HT for all organs or tissues T:

HT=WRifiDTi

where WR is the radiation weighting factor (1 for X-rays), fi is the irradiated fraction of the tissue T in the slice i and DTi is the mean absorbed dose of tissue/organ T in slice i (Table 2).

As described by Golikov and Nikitin,18 each organ in the phantom, except bone, was a homogeneous soft-tissue organ, therefore the mass fraction to volume fraction ratio was 1. The Golikov and Nikitin's method was used by Scalzetti et al19 to determine the mass fraction for the organs at risk.

The salivary glands, thyroid gland, brain, extrathoracic airways and oral mucosa were entirely within the head and neck area (100% irradiated fraction), whereas the oesophagus, skin, lymphatic nodes, muscles, bone marrow and bone surface were only partially included. The extrathoracic airways, oral mucosa, lymphatic nodes and muscles formed part of the remainder tissues. The head and neck area included 10% of the oesophagus and 5% of the skin, muscles and lymphatic nodes with respect to the total body amount of these organs.5 In the case of a 40-year-old patient, 7.6%, 0.8% and 3.9% of the whole body's active bone marrow resides in the cranium, mandible and cervical spine, respectively.20

The bone surface was calculated as the percentage of fresh skull, mandible and cervical spine over the total fresh skeletal mass21 (the mass of cervical vertebrae was estimated as being 7/34 of total vertebral mass). The trabecular component percentage was then subtracted from the total skeletal mass to obtain the cortical portion.22

The effective dose was determined by the equation:

E=iWTHT

where Σ represents the sum of the products of the tissue weighting factors (WT)—established by the International Commission on Radiological Protection23—and the absorbed dose within that tissue HT. For instance, the contribution of the oesophagus to the effective dose, as well as for the other organs, was calculated by multiplying its absorbed dose by the oesophageal irradiated fraction (0.1); the resulting value was multiplied by the weight factor of the oesophagus (0.04).

Image quality

Quantitative assessment of image quality was implemented by measuring spatial and contrast resolution, represented by modulation transfer function (MTF) and contrast-to-noise ratio (CNR, contrast resolution), respectively.24 CNR and MTF were considered together when interpreting the image quality.

Spatial resolution was measured with a CATPHAN® 504 phantom (The Phantom Laboratory), a cylindrical phantom consisting of five modules enclosed in a 20-cm plastic housing that is employed for quality assurance of CT scanners (http://www.phantomlab.com). A hi-res module containing a point source was scanned for all MSCT and CBCT protocols. All data sets were exported in digital imaging and communications in medicine format and assessed with a customized version of MATLAB® (MathWorks®, Natick, MA; https://www.mathworks.com/products/matlab.html) to calculate the MTF. The MTF is given by the Fourier transform of the point spread function, a delta function which describes the imaging system response to a point input. The ideal MTF is independent from the spatial frequency and corresponds to the point spread function. A broader point spread function corresponds to a narrower MTF and a greater loss of high spatial frequency information. In the present study, the MTF was evaluated at 50% frequency cut-off, since MTF evaluation at 10% frequency cut-off was unachievable in some acquisitions.

Owing to the limited size of the FOV, the CNR evaluation in CBCT required the use of a special phantom obtained by assembling five tissue substitute plugs of different certified materials (Gammex RMI®, Middelton, WI) with electron density relative to water ranging from 1.018 to 1.82 g cm−3. The phantom was scanned for every CBCT and MSCT protocol, and the images were processed using ImageJ25 (a public domain, Java-based open architecture source code developed at the National Institutes of Health, https://imagej.nih.gov/ij). The mean values and standard deviations for the regions of interest set on each insert were calculated to evaluate the CNR, according to the following definition:

CNRi=IiIweσi2+σwe2

where Ii, σi and Iwe, σwe represent the mean values and standard deviations for the insert i and for the water equivalent one, respectively. The latter had the lowest contrast with the background.

Results

Dose

The organ dose and effective dose for each anatomical area are illustrated in Tables 3 and 4.

Table 3.

Absorbed dose, effective dose and the contribution (WTHT) of the dose of each organ/tissue to the cervical spine and head effective doses

Tissue/organ Cervical spine
Head          
Absorbed dose (mGy)
WTHT (µSv, %)
Absorbed dose (mGy)
WTHT (µSv, %)      
MS CB MS CB CB/MS MS CB MS CB CB/MS
Lens of eye
27.3 1.1       30.8
4.2  
   
Ossicles chain
19.1 0.1       28.1
3.1  
   
Thyroid gland
49.0 4.4 1960 (57.5%) 178 (71.8%) 9.1% 10.0
2.3 400 (21.1%)
92 (36.7%) 23.0%
Salivary glands
32.0 2.5 320 (9.4%) 26 (10.5%) 8.1% 30.7
3.6 307 (16.2%)
36 (14.5%) 11.7%
Bone marrow
4.0 0.2 488 (14.3%) 29 (11.7%) 5.9% 3.4
0.3 409 (21.6%)
41 (16.5%) 10.0%
Bone surface
3.4 0.2 34 (1.0%) 3 (1.2%) 8.8% 2.8
0.3 28 (1.5%)
3 (1.2%) 10.7%
Brain
9.0 0.1 90 (2.6%) 1 (0.4%) 1.1% 22.7
1.2 228 (12.0%)
13 (5.2%) 5.7%
Oesophagus
2.9 0.1 116 (3.4%) 3 (1.2%) 2.6% 2.3
0.2 93 (4.9%)
11 (4.4%) 11.8%
Skin
1.3 0.1 13 (0.4%) 1 (0.4%) 7.6% 1.2
0.1 13 (0.7%)
2 (0.8%) 12.0%
RT EA 22.3 0.4 192 (5.7%) 3 (1.2%) 1.5% 20.5
3.1 177 (9.4%)
27 (10.8%) 15.3%
Oral mucosa 20.0 0.2 172 (5.1%) 2 (0.8%) 1.1% 24.5
2.4 211 (11.2%)
21 (8.4%) 9.9%
Lymph nodes 1.4 0.1 12 (0.3%) 1 (0.4%) 8.3% 1.6
0.2 14 (0.7%)
2 (0.8%) 14.2%
Muscles 1.4 0.1 12 (0.3%) 1 (0.4%) 8.3% 1.4
0.2 12 (0.6%)
1 (0.4%) 8.3%
Total 45.1 0.8 388 (11.4%) 7 (2.8%) 1.8% 48.0
5.9 414 (21.9%)
51 (20.5%) 12.3%
Effective dose [µSv] 3409 (100%) 248 (100%) 7.2% 1892 (100%) 249 (100%) 13.1%  

CB, CBCT; EA, extrathoracic airways; HT, equivalent dose; MS, multislice CT; RT, remainder tissues; WT, tissue weighting factor.

The value of absorbed dose of each organ is already multiplied by its irradiated fraction. All values of the effective dose are approximate.

Table 4.

Absorbed dose, effective dose and the contribution (WTHT) of the dose of each organ/tissue to the ear and dental arches effective doses

Tissue/organ Ear
Dental Arches          
Absorbed dose (mGy)
WTHT (µSv, %)
Absorbed dose (mGy)
(WTHT) (µSv, %)      
MS CB MS CB CB/MS MS CBm CBs MS CBm CBm/MS CBs CBs/MS
Lens of eye
42.3 5.1       9.1
6.7 3.9  
       
Ossicles chain
37.7 19.0       9.4
7.0 4.1  
       
Thyroid gland
2.2 0.8 86 (13.0%) 31 (8.6%) 36.0% 5.6
5.4 4.2 226 (27.8%)
216 (31.4%) 95.5% 170 (30.1%) 75.2%
Salivary glands
13.4 9.8 134 (20.3%) 98 (27.1%) 73.1% 14.6
12.0 10.7 146 (18.0%)
120 (17.4%) 82.2% 107 (18.9%) 73.2%
Bone marrow
1.5 0.8 187 (28.3%) 96 (26.6%) 51.3% 1.2
1.0 0.6 142 (17.5%)
117 (17.0%) 82.3% 70 (12.4%) 49.3%
Bone surface
0.7 0.3 8 (1.2%) 3 (0.8%) 37.5% 1.2
1.0 0.7 12 (1.5%)
10 (1.5%) 83.3% 7 (1.2%) 58.3%
Brain
10.4 3.1 104 (15.8%) 31 (8.6%) 29.8% 3.6
0.4 0.5 36 (4.4%)
4 (0.6%) 11.1% 5 (0.9%) 13.8%
Oesophagus
0.4 0.4 16 (2.4%) 12 (3.3%) 75.0% 1.4
0.8 0.7 55 (6.8%)
30 (4.4%) 54.5% 26 (4.6%) 47.2%
Skin
0.5 0.6 5 (0.8%) 6 (1.7%) 120.0% 0.6
0.6 0.5 6 (10.7%)
5 (0.7%) 83.3% 5 (0.9%) 83.3%
RT EA 11.2 8.2 96 (14.6%) 70 (19.4%) 72.9% 9.5
9.5 9.8 81 (10.0%)
81 (11.8%) 100.0% 84 (14.9%) 103.7%
Oral mucosa 1.3 0.8 11 (1.6%) 7 (1.9%) 63.6% 11.8
11.3 10.0 101 (12.4%)
97 (14.1%) 96.0% 86 (15.2%) 85.1%
Lymph nodes 0.1 0.1 1 (0.2%) 0.3 (0.1%) 30.0% 0.4
0.6 0.3 3 (0,4%)
5 (0.7%) 166.6% 3 (0.5%) 100.0%
Muscles 1.4 0.8 12 (1.8%) 7 (1.9%) 58.3% 0.5
0.3 0.3 4 (0.5%)
3 (0.5%) 75.0% 2 (0.3%) 50.0%
Total 14.0 9.9 120 (18.2%) 84 (23.3%) 70.0% 22.2
21.7 20.4 191 (23.5%)
187 (27.1%) 97.9% 175 (30.9%) 91.6%
Effective dose [µSv] - - 660 (100%) 361 (100%) 54.7% - - - 812 (100%) 688 (100%) 84.7% 565 (100%) 69.5%  

CB, CBCT (high-resolution-enhanced protocol); CBm, CBCT with medium FOV (12 × 8 cm); CBs, CBCT with small FOV (8 × 8 cm); EA, extrathoracic airways; FOV, field of view; HT, equivalent dose; MS, multislice CT; RT, remainder tissues; WT, tissue weighting factor.

The value of absorbed dose of each organ is already multiplied by its irradiated fraction. All values of effective dose are approximate.

Multislice spiral CT vs CBCT

The effective dose measured for CBCT was 7.2%, 13.1%, 54.7%, 69.5% and 84.7% of the effective dose of MSCT in the cervical spine, head, ear, dental arches with small FOV and dental arches with medium FOV, respectively. In CBCT standard-regular protocol for cervical spine and head scans, the most significant difference between the two CT technologies was observed in the thyroid gland. The CBCT thyroid effective dose was 9.1% and 23.0% of MSCT thyroid effective dose for the cervical spine and head scans, respectively. On the contrary, in CBCT hi-res-enhanced protocols (scans of the ear and dental arches), some organs showed the same or almost identical effective dose with respect to MSCT. This is the case for the skin in scans of the ear and for the remainder tissue in scans of the dental arches.

In CBCT, the highest organ doses were those of the ossicular chain (19.0 mGy) and salivary glands (12.0 mGy) in scans of the ear and dental arches, respectively. In MSCT, the highest organ dose affected the thyroid gland (49.0 mGy) in the cervical spine scan, followed by the eye lens (42.3 mGy) and ossicular chain (37.7 mGy) in ear scan.

Cervical spine scan

The thyroid gland contributed the most to the effective dose (57.5% in MSCT and 71.8% in CBCT).

Head scan

In MSCT, the thyroid gland, bone marrow and remainder tissues provided around 21.5% of the effective dose, each. In CBCT, the thyroid gland contributed the most to the effective dose with 36.7%, followed by the remainder tissues and bone marrow with 20.5% and 16.5%, respectively.

Ear scan

The dominant contributions to the effective dose originated from the bone marrow, salivary glands and remainder tissues. They were 28.3%, 20.3% and 18.2% in MSCT; 26.6%, 27.1% and 23.3% in CBCT, respectively.

In addition, the contributing percentage of the brain to the effective dose in ear and head MSCT scans was around twice that of CBCT (15.8% vs 8.6% and 12.0% vs 5.2%, respectively).

Dental arches scan

The most significant contributions to the effective dose derived from the thyroid gland and remainder tissues (around 25% in MSCT and 30% in CBCT), followed by the bone marrow and salivary glands (17.5% in both MSCT and CBCT).

Image quality

The MTF of CBCT was 0.895, 0.895, 0.875 and 0.961 in the cervical spine, head, ear and dental arches, respectively. The MTF of MSCT was 0.347, 0.275, 0.342 and 0.352 in the cervical spine, head, ear and dental arches, respectively. In Figure 2, 50% cut-offs of the MTFs were reported. The 50% MTF ratios between CBCT and MSCT were 2.6 (cervical spine and ear), 2.7 (dental arches) and 3.3 (head). This demonstrated that CBCT images had better spatial resolution than MSCT for all protocols.

Figure 2.

Figure 2

Multislice spiral CT (MSCT) and CBCT values in correspondence of the modulation transfer function (MTF) 50% cut-off for each anatomical area.

The CNR values, as function of the plugs density, were reported in Figures 3 and 4. At densities around 1 g cm−3 (solid water and brain), the CNR showed similar values in MSCT and CBCT whilst at higher densities—i.e. between 1 and 2 (inner and cortical bone)—head and cervical spine MSCT showed progressively greater CNR than CBCT. The CNR values were comparable in all the other protocols, even though CBCT showed slightly better values than MSCT.

Figure 3.

Figure 3

Multislice spiral CT (MSCT) contrast-to-noise (CNR) values as a function of the plugs density for each anatomical area.

Figure 4.

Figure 4

CBCT contrast-to-noise (CNR) values as a function of the plugs density for each anatomical area.

When MTF and CNR values were considered together, CBCT image quality was higher than MSCT for scans of the ear and dental arches, whereas for head and cervical spine scans, a definite judgment on which CT-technologies had the highest image quality was not possible.

Discussion

In scans of the dental arches, CBCT showed effective dose somewhat below (around three-quarters) and image quality greater for its obvious higher spatial resolution than low-dose Dentascan-MSCT. The same considerations can be applied to the ear study in which the effective dose of CBCT was about half that of MSCT, but the image quality of CBCT was greater thanks to its superior spatial resolution with similar contrast resolution.

In head and cervical spine scans, the effective dose of CBCT was evidently lower (around one-tenth) than MSCT. CBCT showed superior spatial resolution (MTF) but inferior CNR than MSCT. It is not possible to assess the individual contribution of MTF and CNR to the overall image quality, therefore which CT technology has the highest image quality remains unclear in this case. Since the current article focused on the technical quality of the image, it is also worth emphasising that technical and clinical image quality do not always correlate.

In general terms, CBCT has greater spatial resolution than MSCT because it uses flat-panel detectors with thinner scintillator layers and smaller pixels than those of MSCT. Unlike MSCT, in CBCT there is no post-patient collimation. As a result, the image is obtained with fewer photons being wasted, although its quality is degraded by scattered radiation. Both these techniques use the same image reconstruction principle, termed back-projection, with the addition of Feldkamp's algorithm in CBCT.26 MSCT is characterized by greater mA and wider dynamic range. For all the above reasons, MSCT has greater contrast and temporal resolution than CBCT.27

Additional differences shall be taken into account for a fair comparison between CBCT and MSCT. The latter is widespread in all developed countries and so more easily accessible, allows a better image quality for soft tissue visualization and can also be used for contrast-enhanced examinations. Conversely, CBCT is typically used for any type of dental and jaw disorders, except for neoplastic lesions where the administration of contrast agents and the assessment of the soft tissues are mandatory. The same observations can be applied to the ear and cervical studies, where MSCT is undoubtedly preferable to CBCT if a malignant lesion involving the skull base or the vertebral canal is suspected. When the head scan is carried out for orthognathodontic purposes, CBCT is recommended, but in the case of trauma and/or inflammation/neoplastic lesions, MSCT is mandatory.15

CBCT comes at lower mean technical and operating costs per procedure, approximately €60 and €150 for CBCT and unenhanced MSCT, respectively.28,29 A disadvantage of CBCT is represented by its long scan time. This facilitates the presence of motion artefacts30 and can negatively affect both the technical and clinical quality of the image compared with MSCT.

With two efficient CT techniques available for head and neck imaging, clinicians and radiologists must carefully evaluate—depending on the clinical query and anatomical structures under examination—whether to favour the reduction of radiation dose at the detriment of image quality, or better image quality at the cost of higher radiation dose. Finding a balance between benefit and potential harm to the patient is a critical point in the field of radiology.

The concept of irradiated fraction has long been debated. In our study, it does not represent the portion of a certain organ included in a specific FOV, but the percentage of the organ included in the head and neck area with respect to the total body amount of that same organ. Consequently, the irradiated fraction was 100% for salivary glands, thyroid gland, brain, extrathoracic airways and oral mucosa, whereas it was 13.3% for bone surface, 12.3% for bone marrow, 10% for oesophagus and 5% for skin, muscles and lymphatic nodes.5,2022 In case a different approach is used, the various organ irradiated fractions may vary, therefore the relative dosimetric values will not be comparable.

Organs and tissues receiving the highest organ dose were those located inside the primary beam and studied with high tube current–exposure time products. They were the thyroid gland in cervical spine scan and the eye lens, ossicular chain and muscles in ear scan.

In head scans, the dose to the thyroid gland—in comparison to the overall effective dose—showed a percentage value clearly higher in CBCT than MSCT (36.7% vs 21.1%). This is because in CBCT, the head scan is performed for orthodontic purposes, and all the soft tissues of the face must be included within the FOV. Therefore in CBCT, at least part of the thyroid gland is directly exposed to the primary beam, whereas in MSCT, it completely sits below the field of direct exposure. Consequently, the caudal positioning of the FOV becomes a critical point. Slight downward movement or rotation of the Frankfort plane31,32 can lead to a significant increase of the dose to the thyroid, with an obvious increase of the effective dose. To reduce the patient's radiation dose in the case of CBCT with large FOV, the head should be slightly extended as to avoid the thyroid gland being affected by the primary beam. This does not jeopardize the correct execution of the examination since CBCT uses isotropic voxels, thus the volumetric data set can be oriented at any plane desired during the reconstruction process.33

In head and ear scans performed with MSCT, the dose percentage to the brain was twice that of CBCT. That was because in the MSCT head scan, the cranial positioning of the FOV affected the entire head, whereas it just barely included the frontal sinus in CBCT. In the ear scan, it was because the FOV of the MSCT was cranially 1 cm larger than the FOV of CBCT (6 vs 5 cm), including the pituitary gland in the radiation field. In the current study, bone marrow, salivary glands and remainder tissues were predominantly responsible for the effective dose in CBCT and MSCT ear scans. Zou et al14 reported lower dose values for the salivary glands and remainder tissues in CBCT ear scan due to the use of a different CBCT unit with a smaller FOV (6 × 6 cm) that included mainly the brain in the primary beam, as well as the bone marrow.

In cervical scans, the thyroid gland was responsible for most of the effective dose (57.5% in MSCT and 71.8% in CBCT) because it was the only one highly radiation-sensitive organ (weight factor 0.04) with high irradiated fraction (100%) included in the primary beam. The lower thyroid dose percentage in MSCT depended on the bigger craniocaudal diameter of the FOV (18 vs 16 cm), producing higher dose to the brain, oesophagus and extrathoracic airway.

In dental arches scans, as reported in other studies,5 the salivary glands (especially the parotid) were the organs mostly exposed to radiation because they were directly irradiated by the central X-ray beam. Nevertheless, the organs contributing to the most part of the effective dose were the thyroid glands due to a higher weight factor and irradiated fraction, and the remainder tissues due to the sum of the dose of four organs (extrathoracic airways, oral mucosa, lymphatic nodes, and muscles).

The only previous article estimating the effective dose in the head and neck area with NewTom5G CBCT was published by Dierckx et al.13 They analyzed the ear using identical technical/geometrical CBCT parameters adopted in the current study, nevertheless MSCT delivered an effective dose six times higher than CBCT (and not twice as in our case). This is because of the marked difference in parameters between the two MSCT units, in particular 300 mAs and 140 kV vs 120 mAs and 120 kV in the current study.

When comparing the effective dose of NewTom5G and different CBCT units with similar FOVs,9 NewTom5G fell within the middle range in head scan (249 µSv in the current study vs 46–498 µSv) and over the range in dental scan (565 µSv with small FOV and 688 µSv with medium FOV vs 69–453 µSv) due to different technical/geometrical parameters and hardware between the CBCT units.

Such major differences in patient dose highlight the importance of knowledge and optimization of the parameters during CBCT examinations. This reflects on image resolution because dose reduction leads to reduction in image quality.

The main limit of this study was that no repeated measurements were carried out since the use of a large number of TLDs, although improving the accuracy of dose calculation is a time consuming process. However in our series, the dosimetric values were given by the mean value of two measurements (a couple of dosemeters in each hole) performed during the same session.

Another weakness in our study was the use of CNR metric to compare protocols and scanners with different voxel sizes: smaller voxels do not receive as many photons as larger voxels, resulting in an intrinsic reduction of signal that leads to an increase in noise.

Finally, the effective dose of each anatomical area was compared with the radiation exposure resulting from common everyday occurrences and different diagnostic procedures; it is indeed interesting to notice significant dosimetric differences among the different scans (Tables 3 and 4) and their possible consequences (Table 5).

Table 5.

Effective dose of all anatomical areas compared to different diagnostic procedures and common everyday occurrences

Anatomical area Cervical spine Head Ear Dental arches          
Effective dose (µSv) MS, 3409 CB, 247 MS, 1892 CB, 248 MS, 660 CB, 361 MS, 814 CBm, 689 CBs, 567
Time per capita backgrounda 1 year 1 month 7 months 1 month 2.6 months 1.4 months 3.3 months 2.7 months 2.3 months
Attributable lifetime cancer riskb 41 3 23 3 8 4 1 8 7
Hours of airplane travelc 680 50 380 50 130 70 160 140 110
OPT 54 46 38
OPT + Ceph (2 projections) 90 12
Cervical spine (2 projections) 57 4
Chest (2 projections) 55 4 30 4 9 5 12 9 7

CB, CBCT; CBm, CBCT with medium FOV (12 × 8 cm); CBs, CBCT with small FOV (8 × 8 cm); Ceph, cephalometric radiography; FOV, field of view; MS, multislice CT; OPT, orthopantomography.

The effective dose of OPT, cephalometry (two projections), cervical spine (two projections) and chest (two projections) X-rays are considered 15,34 6,34 6035 and 62 µSv,36 respectively.

a

Time to accumulate comparable natural background dose.37

b

Lifetime attributable risk of cancer per 100,000 patients.36

c

Ionizing radiation in an airplane travel. Cosmic radiation dose is considered 5 µSv h−1 at 12.000 m above sea level.38

In conclusion, even though the current study was carried out on phantoms and thus the results could be slightly different in a clinical setting, it can be stated that:

  • (i) In the ear and dental arches imaging, CBCT was preferable to MSCT due to its lower radiation dose and significantly higher spatial resolution;

  • (ii) In the cervical spine and head imaging, the choice between CBCT and MSCT should depend on the clinical query. MSCT should be recommended when a high contrast resolution is required, despite the greater radiation exposure.

Contributor Information

Cosimo Nardi, Email: cosimo.nardi@unifi.it.

Cinzia Talamonti, Email: cinzia.talamonti@unifi.it.

Stefania Pallotta, Email: stefania.pallotta@unifi.it.

Paola Saletti, Email: salettip@aou-careggi.toscana.it.

Linda Calistri, Email: linda.calistri@unifi.it.

Cesare Cordopatri, Email: cordopatri.cesare@gmail.com.

Stefano Colagrande, Email: stefano.colagrande@unifi.it.

References


Articles from Dentomaxillofacial Radiology are provided here courtesy of Oxford University Press

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