Skip to main content
Journal of Radiation Research logoLink to Journal of Radiation Research
. 2019 Jun 14;60(4):466–475. doi: 10.1093/jrr/rrz029

Radiation doses with various body weights of phantoms in brain 128-slice MDCT examination

Hung-Chih Lin 1,2, Te-Jen Lai 1,3, Hsien-Chun Tseng 4,5, Ching-Hsiang Wang 2, Yen-Ling Tseng 2, Chien-Yi Chen 5,6,
PMCID: PMC6640898  PMID: 31197311

Abstract

The effective dose (HE) and organ or tissue equivalent dose (HT) for use in brain computed tomography (CT) examinations with various body weights were evaluated. Thermoluminescent dosimeters (TLD-100H) were inserted into Rando and five anthropomorphic phantoms. These phantoms were made of polymethylmethacrylate (PMMA), according to the specifications of ICRU 48, with masses from 10 to 90 kg. Brain CT examinations were conducted, scanning the maxillae from the external auditory meatus to the parietal bone using a 128-slice multi-detector CT (MDCT) scanner. To reduce errors, three independent trials were conducted. Calculated HE,TLD, based on the weighting factor recommended by ICRP 103, was 1.72 ± 0.28 mSv, which slightly exceeds the HE,DLP of 1.70 mSv, that was calculated from the dose–length product (DLP) of the Rando phantom. This experiment yielded HE,TLD values of ICRP 103 from the highest 1.85 ± 0.28 (90 kg) to the lowest 1.47 ± 0.22 (10 kg) mSv. HE,TLD (mSv) = 5.45×10−3 W(kg) + 1.361, with an R2 of 0.87667. Using the DLP protocol, HE,DLP was estimated from CTDIvol that was recorded directly from the console display of the CT unit and multiplied by the conversion coefficient (k) recommended by the ICRP 103. Finally, the experimental results obtained herein are compared with those in the literature. Physicians should choose and adjust protocols to prevent the exposure of patients to unnecessary radiation, satisfying the as low as reasonably achievable (ALARA) principle. These findings will be valuable to patients, physicians, radiologists and the public.

Keywords: computed tomography, effective dose, thermoluminescent dosimeters, Rando phantom, ICRP 103

INTRODUCTION

According to statistics from the Ministry of Health and Welfare for 2016 [1], the two leading causes of death in Taiwan from 2007 to 2016 were malignant tumor and heart disease. Brain computed tomography (CT) examinations were the most common CT examination, representing 36.8% of all such examinations in Taiwan from 2000 to 2013 [2]. Chen et al. stated that the annual CT examination frequency per 1000 population increased by an average of 8.1% per year from 1997 to 2008 [3]. Hu et al. found that the annual frequency of CT scans increased from 11.1% in 2009 to 17.7% in 2013, and that the frequency increased for all age groups in Taiwan [4]. The number of CT examinations increased rapidly, with an average annual growth rate of 7.6%, and this trend was similar to those in other countries [5]. Patients undergoing CT examinations range from neonates to oversized adults.

The increasing clinical use of pediatric brain CT scans has raised concerns about their potential detrimental effects on the health of children [615]. CT scans are recognized as a higher radiation dose modality than other imaging modalities. Fujii et al. and Feng et al. presented detailed dose data for pediatric CT examinations [9, 11]. The increasing use of CT has raised particular concerns about the possible detrimental effects of this extra radiation, especially on the health of children. CT examinees always ask physicians and radiologists to tell them how high the out-of-field doses to normal tissue or organs are during an examination. Since the introduction of 128-slice brain CT scanners, short CT data acquisition times and high imaging qualities could be achieved. Since a patient is exposed to significant radiation, the extra doses delivered to adjacent normal organs during brain CT examinations using a 128-slice CT scanner following the manufacturer’s instructions for routine clinical imaging should be evaluated.

The effective dose (HE,TLD) and organ or tissue equivalent dose (HT) were calculated herein using a thermoluminescent dosimeter (TLD-100H) approach with Rando (Radiology Support Devices, Long Beach, British Columbia, Canada) and five tissue equivalent phantoms, which served as patient substitutes to assess radiation doses during brain CT examinations. In this work, TLDs were inserted into an organ or tissue of each phantom during an axial brain scan. HT values were estimated from TLD measurements that were positioned inside and on the surface of the phantom.

A simple equation can be used to estimate HE,TLD for brain CT examinations of phantoms with various body weights [16, 17]. HE,DLP values were calculated herein using the computed tomography dose index (CTDIvol) and the dose–length product (DLP), displayed on the console monitor of the 128-slice CT scanner; these values were then multiplied by the conversion coefficient (k) recommended by ICRP 103 [18, 19]. The DLP conversion method is commonly used in clinical practice owing to its simplicity and the ready accessibility of HE,DLP.

The experimental results obtained herein are compared with those in the literature. A suitable protocol is strongly recommended to prevent unnecessarily radiating patients and to satisfy the as low as reasonably achievable (ALARA) principle [2023].

MATERIALS AND METHODS

128-Slice multi-detector computed tomography

At Lukang Christian Hospital (LKCH), brain CT examinations of patients were conducted using 128-slice multi-detector computed tomography (MDCT) (Brilliance; Philips Healthcare, the Netherlands) following the manufacturer’s standard protocol. Extended Brilliance Workspace v4.0 was used to process and analyze the data. The scan conditions were fixed for routine clinical imaging. Before the CT examination began, a ‘surview’ of the phantom was recorded in the CT to plan the examination scan length. Table 1 presents the detailed technical parameters for patients of various body weights during routine brain CT examinations.

Table 1.

Imaging parameters for six phantoms for routine brain CT examinationsa

Phantom Rando Anthropomorphic
Weight (kg) 70 10 30 50 70 90
Average tube currents (mA) 400 250 300 350 400 400
Rotation arcs (°) 420 360 360 420 420 420
Rotation time (s) 1.0 0.75 1.0 1.0 1.0 1.0
CTDIvol (mGy) 69.2 42.7 51.1 60.1 69.2 69.2
Scan length (cm) 12.5 6.4 9.2 10.8 12 14.4
DLP (mGy cm) 896.8 302.2 517.8 666.3 896.8 996.5

aCurrent tube voltage setting at 120 kVp, collimator 10 mm, beam pitch 1.

Anthropomorphic phantoms

Measurements of HT were made using TLDs that were implanted at tissue and organ positions in Rando and polymethylmethacrylate (PMMA) phantoms. It included (i) 400 mAs, (ii) 1.5 s total rotate time, (iii) 10 mm collimation, (iv) 5 mm thickness and (v) 12.5 cm scanned length. The HE of the 70 kg PMMA phantom was verified with that of the Rando phantom. For patients with various body mass, 10–90 kg PMMA phantoms were preset to simulate patients undergoing brain CT examinations. The exposure doses were greatly affected by the patients’ weight, yet the HE,DLP only roughly estimated the given kVp and mAs of the CT intensity with scanned length. Thus, a comprehensive analysis of HE,TLD on the basis of various weights is essential and critical in reality. The standard anthropomorphic phantom, the Rando phantom, represents an adult and has holes for TLDs. The Rando phantom used herein comprised 35 numbered sections that represented the trunk of a man 170 cm tall with a mass of 70 kg [24]. The phantom comprised a human skeleton that was embedded in the anthropomorphic material. The specified densities of the components of the anthropomorphic phantom were 0.98 g cm−3 for the soft tissue, 2.70 g cm−3 for the skeleton and 0.32 g cm−3 for the lungs [25]. Anthropometrically shaped skeletons, constructed from epoxy-resin and PMMA, were used to simulate humans [26]. The PMMA phantoms were based on a general human design. Each had 31 sections, representing the head, neck, torso and abdomen, but without arms or legs. Each phantom was based on the GSF-Forshungszentrum fur Umwelt und Gesundheit (Germany) mathematical models, and the lung masses were based on the ICRP reference man. The densities of the materials were as follows: that of the lung anthropomorphic was 0.296 g cm−3; that of the skeleton-cortical-bone anthropomorphic was 1.486 g cm−3; and that of the anthropomorphic was 1.105 g cm−3. Figure 1 presents the outer appearance of these phantoms.

Fig. 1.

Fig. 1.

Rando and five anthropomorphic phantoms used as patient substitutes.

Table 2 shows the dimensions and physical properties of the phantoms, and the weight and age that correspond to people living in Taiwan [1, 26].

Table 2.

Dimension and physical properties of Rando, anthropomorphic phantoms and corresponding to age in Taiwana

Phantom Rando Anthropomorphic
Weight (kg)b 70 10 30 50 70 90
Height (cm)b 94.5 50 78 84 93 112
Weight (kg)c 34.5 6.75 19.0 31.5 44.1 57
cm section−1 2.5 1.6 2.3 2.7 3.0 3.6
Age (year) Adult 1 10 15 Adult Adult

aavailable in ref [1].

bOriginal design from ref [26].

cWithout arms and legs.

The phantoms were positioned on a patients’ couch and aligned with the isocenter of the gantry using a laser positioning system. Figure 2a presents the Rando phantom in the 128-slice CT of LKCH, Fig. 2b the surview of the Rando phantom, Fig. 2c details of the TLDs in the third section, which represented the brain, and Fig. 2d a medical image of the third section of the 30 kg PMMA phantom.

Fig. 2.

Fig. 2.

(a) Rando phantom in the 128-slice CT. (b) View of the Rando phantom. (c) Details of the TLDs in the third section, which represented the brain. (d) Medical imaging of the third section of the 30 kg PMMA phantom.

Assessment of HE,TLD using the TLD approach

A well-trained senior radiologist (H C Lin) with 10 years experience performed routine brain CT examinations. The examination is whole-brain area axial scans from the maxillae, including the external auditory meatus, to the parietal bones (Fig. 2b).

In 2007, ICRP assigned weighing factors to 14 organs and a group of remainder organs for the purposes of calculating total HE,TLD. Only the brain, salivary glands and skin were directly exposed during the brain CT herein. Sensitive organs and tissues were located by visually comparing the phantom sections with anatomical cross-sections from CT examination.

When the absorbed dose in the tissue or organ (DT) was measured at several points at a fixed distance from the CT scanning center using TLDs, those values obtained for a particular organ were averaged to obtain a representative dose for that organ (Table 3). The TLDs were also placed at the lens of the eye and at the thyroid to evaluate tissue reactions. Numerous TLDs were placed in each section of each large organ, such as the brain, and the mean estimated absorbed dose was taken as Dbrain. For smaller organs, such as the lens, absorbed doses were obtained by averaging three TLDs in one bag. DT was obtained from these three TLDs that were inserted into the centroid of the organ. Muscles were excluded from the remainder since they extended throughout the body, making Hmuscles difficult to measure.

Table 3.

Weighting factor (WT) of organ or tissue recommended by ICRP 103 as well as number of TLD-100Hs inserted into the phantom

Organ/Tissue Measured points WT Number of TLDs
Breast Breast 0.12 3
Bone marrow 0.12
C-spine 0.06 6
Thighbone femur 0.06 3
Colon Colon 0.12 3
Lung Lung 0.12 3
Stomach Stomach 0.12 3
Gonads Gonads 0.08 3
Bladder Bladder 0.04 3
Esophagus Esophagus 0.04 3
Liver Liver 0.04 3
Thyroid Thyroid 0.04 6
Bone surface 0.01 3
Brain Brain 0.01 39
Salivary gland Salivary gland 0.01 6
Skin Skin 0.01 93
Remainder 0.12
Heart 0.03 3
Pancreas 0.03 3
Kidney 0.03 3
Small intestine 0.03 3
Lens 6
Total 1.000 207

The calculation of HE,TLD values for a large number of organs and tissues is recommended by ICRP 103. To determine the organ- or tissue-equivalent dose, HT, the following equation is used.

HT=DT×WR (1)

where WR is the radiation weighting factor (WR = 1 Sv/Gy for X-rays).

To calculate the effective dose, HE,TLD, the products of HT and WT are summed.

HE,TLD=ΣTHT×WT (2)

Some organs and tissues are explicitly listed in Table 3; others are classified as ‘remainder tissues’. To make dosimetry evaluations for the remainder tissues, organs/tissues which were within or close to the radiation field were selected. For these tissues, HE,TLD was calculated from the product of WT for the remainder tissues and HT, divided by the total number of remainder organs. The WT values have been demonstrated to be broadly applicable to both adults and children, although the best method for evaluating the risk associated with a brain CT examination requires knowledge of HT and age-specific organ risk factors [18].

The locations of the organs from the head to the gonads, including the remainder organs, were used in evaluating HT. A total of 207 TLDs were used. To minimize the errors coming from scattering and absorption in/at TLDs, three TLDs were placed in each bag to obtain DT at a particular location [16, 24]. For brain CT imaging, in vivo measurements were made inserting TLDs into the brain, while other TLDs were exposed to extra scattered radiation. Fifty-one TLDs were located in the head of the patients. Nine TLDs were used to measure the background radiation in a low background laboratory. The total errors were effectively suppressed by performing three independent trials that involved 31 bags of TLDs that were attached to the surface of the phantom. Table 3 shows the attachment points on organs or tissues that are recommended by ICRP 103, along with the corresponding values of WT [18].

Accuracy and calibration of TLDs

To calibrate the photon dose and the linearity of the TLDs as well as to reduce experimental errors, the TLDs were pre-calibrated using X-ray beams to those used in the 120 kV, 30 mA on the 128-slice Brilliance CT at LKCH. TLDs were irradiated at doses of 0.5–15 mGy, which includes the prescribed daily fraction dose, at a depth of 5 cm in solid water (CIRS, Norfolk, VA, USA). Solid water was used rather than water to make experimental uncertainty negligible. A Farmer-type ionization chamber of type NE 2571 (Nuclear Enterprises, UK) with a volume of 0.6 ml was positioned in the solid water. The TLD-100H was used owing to its small dimensions and the lower dependence of its response on photon energy, dose rate and the direction of incidence of radiation. Radiation doses were read out from a glow curve of a Harshaw 3500 analyzer (Harshaw, Cleveland, OH, USA) after 24 h of exposure. TLDs were preheated to 70°C at a rate of 10°C s–1 by applying 780 V and further heated to a maximum temperature of 300°C. Moreover, after responding adequately to the annealing process, the TLDs could be recycled.

Evaluation of HE,DLP from measured CTDIvol values

To estimate HE,DLP, the DLP protocol was used. The CTDIvol value at 120 kV was obtained from dosimetry data during the routine quality assurance program at LKCH and is presented in Table 1. CTDIvol was particularly marked for the brain CT, as the most radiosensitive organ, and the CTDIvol value was increasingly far from the X-ray beam as the size of the phantom increased. The DLP was obtained from measurements that were made on the specific dosimetry phantom with an adult head diameter of 16 cm and an adult body diameter of 32 cm [27]. Some values of HE,DLP for variously sized patients or phantoms have been published [12]. HE,DLP is an indicator of effective dose, but takes no account of the variations in organ sensitivities.

The CTDIvol value that was directly recorded on the console display of the 128-slice CT during the scan was multiplied by the scan length to yield the DLP.

DLP(mGycm)=CTDIvol(mGy)×scanned length(cm) (3)

The DLP denotes the total energy absorbed during (and therefore the potential biological effect attributable to) the complete scan [18, 19].

HE,DLP(mSv)k×DLP (4)

where k (mSv mGy−1 cm−1) is the conversion factor of HE,DLP/DLP for the CT scan.

ICRP 103 states that, using this methodology, HE,DLP can be estimated from DLP, which is obtained by most CT systems; k values for the Rando and various body weight phantoms are Rando, 0.0019; 10 kg, 0.0053; 30 kg, 0.0027; 50 kg, 0.0019; 70 kg, 0.0019; and 90 kg, 0.0019 mSv mGy−1 cm−1 [18, 19, 28]. In addition, the protocol of HE,DLP calculation is most commonly used in a clinical setting.

RESULTS AND DISCUSSION

Brain CT examinations irradiate multiple organs or tissues with various radiation sensitivities. HE values take into account how much radiation is received by an individual tissue as well as the tissue’s relative sensitivity to radiation.

In this investigation, HE,TLD values for brain CT examinations were calculated using the TLD-100H approach. However, radiation doses in brain CTs vary widely with the type of CT scanner and the scan parameters that are set by the medical facility [6]. The HE,DLP protocol was conversion factor (k) multiplied the total energy absorbed during the complete brain CT scan. DLP can be calculated from the CTDIvol value, directly recorded on the console display of the CT unit after the imaging of patients, multiplied by the scan length. It is simply and easily obtained by most CT systems from a clinical viewpoint. In contrast, equivalent doses of organs or tissues (DT) are essential to measure the specific exposure doses. Thus, in reality, the HE,TLD protocol is the most suitable technique. The HE,TLD protocol is better than HE,DLP and is not used in clinical investigations.

TLD calibration and uncertainty

The TLD-100H responded linearly to radiation doses from 0.5 to 15 mSv. The conversion factor for the TLD-100H, obtained using the EXCEL linear regression function, was Y(mSv) = −0.768 + 9.978 × TLD (nC), and the square of the correlation coefficient (R2) was 0.9877 [25].

The precision and accuracy of the dose estimations using TLD-100H are specified by several parameters. The total errors in this study were obtained mostly from (i) TLD-100H counting statistical errors (Δcounting) from 3% for measurements within or close to the direct beam to over 10% for measurements well outside the beam, where the measurements are close to the background; (ii) the systematic uncertainties of the 3500 reader (Δreader) have been demonstrated to be <10% (ranging from 5% to 8%); (iii) the uncertainty in WTWT) was set to 5% because the WT was normalized [18]; (iv) the linear calibration (Δcalibration) of the X-ray of 128-slice CT was from 3% to 10%; (v) the uncertainty of the locations (Δlocation) of the TLDs in an organ was 5%; (vi) the uncertainty that arose from non-tissue equivalence effects (Δnon-tissue) for the anthropomorphic phantom was set to 5%, because PMMA phantoms are entirely based on ICRU 48 [26]; and (vii) the variations in power fluctuations (Δ128-MDCT) coming from 128-MDCT were <2% during monthly clinical quality assurance at LKCH. The total uncertainty (Δtotal) was derived as the square root of the sum of squares of the individual errors from (i) to (vii). Symbolically, this can be represented as equation 5:

Δtotal=Δcounting2+Δreader2+ΔwT2+Δcalibration2+Δlocation2+Δnontissue2+Δ128MDCT2 (5)

The total uncertainties ranged from 11.0% to 18.5%. Other phenomena affecting the total uncertainties such as uncertainty in the DLP arose mainly from the calibration of the ion chamber that was used to measure the weighted CTDI (CTDIW) and was calculated to be <2%.

Equivalent doses delivered to organs or tissues (HT) of examinees with various body weights

Figure 3 plots the measured HT values that were delivered to the phantom. High HT values were recorded in the brain, lens, skin, salivary gland, bone marrow and bone surface. Parts of the skin and salivary gland were scanned. All these organs had relatively low tissue weighting factors (WT) in Table 3. Doses delivered to the red bone marrow (RBM) and bone surface were evaluated from the doses that were measured in various bone tissues. HE,TLD values were calculated as recommended by ICRP 103 [18].

Fig. 3.

Fig. 3.

Equivalent doses (mSv) delivered to critical organs in six phantoms during brain CT examination. HT was measured by placing various TLDs in each organ/tissue. Average values and spread over TLDs are shown (bars).

Entrance surface air kerma or skin dose

Based on 31 measurements (Table 3), estimates reflected the entrance surface air kerma (ESAK) or skin dose at any point in phantoms with various body weights. ESAK at the entrance and the exit of the CT scanner were measured using 93 TLDs that were attached to the surface of each phantom. Most X-rays originated in the target of the 128-slice CT and scanned the first to fifth sections of the PMMA phantom. Figure 4a–f plots ESAK values as a function of measurements over three trials, based on the distance from the scanning edge of the phantom. ESAK at the periphery of the scan volume can have significant variations because of extra irradiation.

Fig. 4.

Fig. 4.

ESAK (%) vs lateral distance (cm) from the CT target center during brain CT examination. (a) 10 kg. (b) 30 kg. (c) 50 kg. (d) Rando. (e) 70 kg. (f) 90 kg phantoms.

ESAK values ranged from 7.13 ± 1.14 mSv (10 kg) to 8.89 ± 1.60 mSv (70 kg). They were normalized independently to 100% of the background CT field for each phantom. Out-of-field doses revealed a gradual reduction in ESAK with increasing distance from the scanning edge in brain CT, as expected. The ESAK values outside the CT volume varied significantly, and decreased as the distance from the CT field increased. ESAK values depended on whether the skin was in or out of the direct beam.

The highest average equivalent doses are the brain, Hbrain, in the brain CT examinations. The Hbrain value of the Rando phantom, 59.7 ± 10.1 mSv, was ~0.92 times lower than that of the 70 kg phantom, which was 64.6 ± 10.7 mSv. The error bars represent uncertainties in the Hbrain values. The difference between the Rando and 70 kg phantoms was 7.59%. The large deviation was caused mainly by the skeleton-cortical-bone anthropomorphic density (1.486 g cm−3) in the head of the PMMA phantom [24].The density effect is related to the soft tissues, rib or spine inside the PMMA phantoms. The Hbrain values are much lower than the threshold (~500–2000 mSv) dose for cataractogenesis [18].

Despite angling the gantry to reduce the dose, the lens doses (Hlens) received by the eyes of the six phantoms during brain CT ranged from 56.6 ± 9.6 mSv (10 kg) to 92.1 ± 15.6 mSv (90 kg). These values are higher than those of Mettler et al. of 30–50 mGy [29], but they were still well below the threshold of ~1.5 Gy for cataractogenesis [18].

The thyroid is located in section 10 of the PMMA phantom. It is a radiosensitive organ and, being located on the border edge of the CT scan section, received the highest, 2.86 ± 0.49 mSv (90 kg), to the lowest, 1.42 ± 0.24 mSv (Rando), doses of any organ in the six phantoms. Lungs, breast, colon and gonad thus received relatively low HT in this examination. No significant differences were observed between the estimated Hheart and Hgonad. From the brain CT examinations, organs or tissues that did not lie close to the vicinity of the CT field received approximately the background radiation.

Effective doses (HE,TLD)

Figure 5 indicates that the estimated effective doses (HE,TLD) increased with body weight. In addition, the HE,TLD that was evaluated accoding to ICRP 103 varied from the highest value of 1.85 ± 0.28 mSv (90 kg) to the lowest value of 1.47 ± 0.22 mSv (10 kg). The regression equation between HE,TLD and the body weight of the examinee, HE,TLD (mSv) = 5.45×10–3 W (kg)+1.361, has an R2 of 0.87667. Because the R2 in linear regression is high, it reveals that TLD is a good approach for evaluating the HE,TLD of PMMA phantoms during brain CT examinations [25, 30]. The HE,TLD value of the Rando phantom was 1.72 ± 0.28 mSv, which was lower than that of the 70 kg phantom, 1.80 ± 0.24 mSv. HE,TLD values in this study were obtained mostly from the doses of RBM owing primarily to the fact that it had the largest tissue WT of 0.12.

Fig. 5.

Fig. 5.

Estimate of HE,TLD as a regression function of various body weights of the phantom compared with others, the coefficient of which was calculated to be R2 = 0.87667. Error bars represent counting errors.

Effective dose (HE,DLP) estimated by ICRP 103

CTDIvol and DLP have been proposed as the most effective doses for establishing diagnostic reference levels. In the DLP protocol, one of the main reasons for the discrepancies is that the relative radioactive sensitivity of an anatomical region does not vary with patient size, as recommended by ICRP 103 [18]. HE,DLP was estimated from CTDIvol that was recorded directly from the console display of the CTDIvol of the 128-slice CT scanner during the quality assurance program at LKCH. HE,DLP values were multiplied by specific normalized conversion factors (k), which were obtained from ICRP 103 [12, 18]. Those considerable differences are mainly attributable to differences between the designs of Rando and PMMA phantoms that are used to generate the DLP conversion factors. This indicates that the values of HE,TLD, and HE,DLP for the Rando phantom that were calculated using TLD and DLP protocols were 1.72 ± 0.28 mSv and 1.70 mSv, respectively. The slight discrepancy can be explained by the difference between (i) the densities of the Rando and 70 kg PMMA phantoms and (ii) the scanning ranges used. However, the literature from 1998 to 2017 includes no exact scanning ranges [5, 9, 11, 14].

Limitations

This investigation has many limitations, including the following: (i) inherent variation among TLD-100H dosimeters, TLD chip positioning and directionality error; (ii) a lack of published data on conversion factors (k) of the new generation of CT scanners (128-slice CT scanners) for adult and pediatric use; (iii) lack of verification of results in clinical practice as TLDs cannot be used in patients for ethical reasons; (iv) limited evaluation of image noise in the quantitative image quality assessment; (v) effect of scanning range on HE,DLP values as a result of allowing a wider beam width in scanning acquisitions [6]; and (vi) inherent uncertainties in the definition of HE,TLD that arise from the use of an approximate WT, averaged over a population. Despite their limitations, TLDs remain the most practically useful devices for obtaining DT and HT values for medical procedures [25].

Comparison of results with those in other studies

HE,TLD and HE,DLP measurements of phantoms and patients who are undergoing brain and head CT examinations fall in a rather wide range, HE from 0.7 to 2.8 mSv. Fujii et al. stated that a comparison of results must consider the particular phantoms and scanning ranges that are used [9]. Overall, the HE,TLD and HE,DLP values in this investigation agree closely with those in Fig. 5 and Table 4, except for the value of 2.8 mSv for a 3.5 kg newborn phantom and 0.7 mSv for a 5-year-old 19 kg phantom [11, 20].

Table 4.

Comparisons made for the HE,TLD and HE,DLP per scan among Germany, Greece, Italy, Malaysia, Taiwan and the UK

CT HE,TLD (mSv) HE,DLP (mSv) Weight (kg) Age (years) Method, phantom, CT examination Reference
Philips 128 1.72 ± 0.28 1.70 70 Adult TLD, Rando, brain This study
Philips 128 1.47 ± 0.22 1.60 10 1 TLD, PMMA phantom, brain This study
Philips 128 1.47 ± 0.26 1.40 30 9 TLD, PMMA phantom, brain This study
Philips 128 1.58 ± 0.25 1.27 50 13 TLD, PMMA phantom, brain This study
Philips 128 1.80 ± 0.24 1.70 70 Adult TLD, PMMA phantom, brain This study
Philips 128 1.85 ± 0.28 1.84 90 Adult TLD, PMMA phantom, brain This study
4 hospitals 1.9 ± 0.4 55.7–71.7 Adult Patients, brain, Malaysia, 2016 6
Hospital 1.9 Adult Patients, brain, Malaysia, 2009 6
Hospital 1.5 Adult Patients, brain, UK, 2003 6
Hospital 2.8 Adult Patients, brain, Germany, 2002 6
Hospital 1.8 Patients, brain, Germany, 1998 6
30 hospitals 1.80 ± 0.5 Adult 1754 Patients, head, Taiwan, 2016 2
Sensation 16 1.2 10 1 DLP, ATOM phantom, head 28
Sensation 16 1.0 19 5 DLP, ATOM phantom, head 28
Sensation 16 1.3 32 10 DLP, ATOM phantom, head 28
Sensation 16 1.9 70 Adult DLP, Rando, head 28
Toshiba 64 2.8 3.5 0 DLP, CIRS newborns phantom, head 20
Toshiba 64 1.5 20 6 DLP, CIRS phantom, head 20
Toshiba 64 1.5 60 Adult DLP, Japanese male phantom, head 20
Siemens 16 1.4 1.7 32 10 TLD, CIRS phantom, brain 5
Aquilion 64 2.4 10 1 DLP, CIRS infant phantom, head 9
Discovery 750 2.3 10 1 DLP, CIRS infant phantom, head 9
16-slice CT 1.6 63–78 Adult 167 Patients, head, Sudan 30
GE 64 0.7 19 5 DLP, CIRS phantom, head 11
CT in Taiwan 1.8 All age Patients, head, Taiwan, 2008 3
CT in Taiwan 1.6 146 Patients, head, Taiwan, 2007 13
14 CT scanners 2.1
0.7–3.7
70 Adult Patients, head, Greece, 2003 14
32 CT scanners 1.6 70 Adult Patients, head, Italy, 2003 14
Siemen Somoton 2.27 9.36 1 TLD, Cristy phantom, head 21
Siemen Somoton 1.46 19.1 5 TLD, Cristy phantom, head 21
Siemen Somoton 1.67 32.1 10 TLD, Cristy phantom, head 21

Here, HE,DLP is derived from the DLP conversion method and HE,TLD is derived from the TLD approach.

Karim et al. reported on 376 brain CT examinations that were performed in many hospitals in Malaysia. The HE,DLP values for patients with weights from 55.7 to 71.7 kg ranged from 1.6 ± 0.7 to 2.1 ± 0.6 mSv [6].

Yeh et al. collected brain CT data from 4467 patients in Taiwan from 2000 to 2013, and obtained an HE,DLP value of 1.8 ± 0.5 mSv for head CT examinations (39.8% of 1754 patients) [2]. Chen et al. presented estimates of HE,DLP for head CT examinations with different medical modalities in 2008. The averaged HE,DLP value during 3.60×105 head CT examinations was 1.8 mSv [3]. The published HE,DLP values for adults in Taiwan in 2008 and 2007 are 1.8 and 1.6 mSv, respectively, and 1.80 ± 0.5 mSv for adults in Germany in 1998. The Rando phantom dose that was evaluated in this investigation was similar to those reported in Taiwan in 2016, 2008 and 2007, and in Germany in 1998 [2, 3, 6].

Sugimoto et al. stated that detailed evaluations of HT and HE,DLP for patients from infants to adults who are undergoing head CT examinations are very important in assessing their risk of cancer. They obtained HE,DLP values for newborn (3.5 kg) and 6-year-old children (20 kg) and for a standard Japanese adult phantom (60 kg) under a non-helical head CT examination using the planner silicon pin-photodiodes approach; the values were 2.8, 1.5 and 1.5 mSv, respectively [20]. The HE,DLP of the newborn phantom, 2.8 mSv, is 1.79 times higher than that obtained from our regression curve in Fig. 5.

Brady obtained an HE,TLD value for a brain CT examination of a 32 kg phantom of 1.4 mSv using the TLD approach and an HE,DLP value of 1.7 mSv using the DLP protocol recommended by ICRP 103. These results were generally lower than those obtained herein [5]. Fujii et al. reported that the HE,DLP for a head CT examination of a 1-year-old infant (10 kg) was 2.4 mSv and the Hbrain values ranged from 28 to 32 mSv [9].

A better agreement of ~10% was found between the HE,DLP that was obtained using the DLP conversion protocol and the HE,TLD that was obtained using the TLD approach, for a Rando during brain CT, as depicted in Fig. 5. The values of HE,TLD herein are close to published data, but higher than 1.6 mSv obtained for 167 adult patients in Sudan with body weights from 63 to 78 kg. An HE value of 2.1 mSv for routine head CT examinations has been obtained in Tanzania [30].

Feng et al. used the TLD approach to obtain HE,DLP from brain CT examinations of a 19 kg phantom (5-year-old child). The HE,TLD was 0.7 mSv, which is much lower than that obtained from the regression curve in our study, as depicted in Fig. 5 [11]. Papadimitriou et al. evaluated HE,DLP for brain CT examinations of children of various ages using k values. Mean HE,DLP values for the Rando phantom of 2.1 mSv in Greece and 1.6 mSv in Italy have been obtained as recommended by ICRP 103 [14]. HE,TLD and HT values for children of various ages under each CT protocol were compared, as reported in a previous study. Chapple et al. reported the HE,DLP mean doses in head CT examinations for 1 year olds (9.36 kg) and 5 year olds (19.1 kg). Cristy mathematical phantoms were 2.27 mSv and 1.46 mSv, respectively. Chapple et al. demonstrated that during brain CT examination of any particular type, HE,DLP varies greatly with the scan length [21].

CONCLUSION

This study is the first to measure the HE,TLD and HE,DLP values of patients with various body weights during brain 128-slice MDCT examinations. The variations of CT is <2%. Brain CT examinations were conducted, scanning the maxillae from the external auditory meatus to the parietal bone. The equivalent doses to the brain, lens and skin were extremely high and differed significantly from those to other organs. The HE varied with the type of CT scanner and the scan parameters that were used at the medical facility. These results indicate that the TLD-100H approach is highly sensitive. Effective doses that were calculated using the TLD approach ranged from 1.47 ± 0.22 mSv to 1.85 ± 0.28 mSv. These can be compared with the natural background radiation of >2 mSv. The quantitative dose information herein indicates the relationship between brain CT examinations and radiation dose, and provides practical guidance for optimizing clinical practice in conducting brain CT examinations. Future work should continue to improve brain CT imaging using sensitivity analysis, Taguchi analysis (method) with an indigenous line-paired flat phantom.

ACKNOWLEDGEMENTS

The authors would like to thank the staff of Lukang Christian Hospital for their efficient support. Financial assistance was partly provided by the Ministry of Science and Technology of the Republic of China under contract no. MOST 105-2314-B-040-010.

CONLICT OF INTEREST

The authors have no conflict of interest directly relevant to this article.

REFERENCES

  • 1.Statistics of General Health Welfare of 2019, Ministry of Health and Welfare, 2019. (https://dep.mohw.gov.tw/DOS/mp-113.html)
  • 2. Yeh DM, Tsai HY, Tyan YS et al. . The population effective dose of medical computed tomography examinations in Taiwan for 2013. PLoS One 2016;11:e0165526. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Chen TR, Tyan YS, Teng PS et al. . Population dose from medical exposure in Taiwan for 2008. Med Phys 2011;38:3139–48. [DOI] [PubMed] [Google Scholar]
  • 4. Hu SY, Hsieh MS, Lin MY et al. . Trends of CT utilisation in an emergency department in Taiwan: a 5-year retrospective study. BMJ Open 2016;6:e010973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Brady Z, Cain TM, Johnston PN. Differences in using the International Commission on Radiological Protection’s publications 60 and 103 for determining effective dose in pediatric CT examinations. Radiat Meas 2011;46:2031–4. [Google Scholar]
  • 6. Karim MKA, Hashim S, Bradley DA et al. . Radiation doses from computed tomography practice in Johor Bahru, Malaysia. Radiat Phys Chem 2016;121:69–74. [Google Scholar]
  • 7. Akhlaghi P, Miri-Hakimabad H, Rafat-Motavalli L. Dose estimations for Iranian 11-year-old pediatric phantoms undergoing computed tomography examinations. J Radiat Res 2015; 56: 646–55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Sulieman A, Alzimami K, Elhag B et al. . Evaluation of radiation dose to pediatric patients during certain special procedures. Radiat Phys Chem 2014;104:267–71. [Google Scholar]
  • 9. Fujii K, Akahane K, Miyazaki O et al. . Evaluation of organ doses in CT examinations with an infant anthropomorphic phantom. Radiat Prot Dosim 2011;147:151–5. [DOI] [PubMed] [Google Scholar]
  • 10. Chen W, Chang MH. New growth charts for Taiwanese children and adolescents based on World Health Organization standards and health-related physical fitness. Pediatr Neonatol 2010;51:69–79. [DOI] [PubMed] [Google Scholar]
  • 11. Feng ST, Law MW, Huang B et al. . Radiation dose and cancer risk from pediatric CT examinations on 64-slice CT: a phantom study. Eur J Radiol 2010;76:e19–e23. [DOI] [PubMed] [Google Scholar]
  • 12. Deak PD, Smal Y, Kalender WA. Multisection CT protocols: sex- and age-specific conversion factors used to determine effective dose from dose–length product. Radiology 2010;257:158–66. [DOI] [PubMed] [Google Scholar]
  • 13. Tsai HY, Tung CJ, Yu CC et al. . Survey of computed tomography scanners in Taiwan: dose descriptors, dose guidance levels, and effective doses. Med Phys 2007;34:1234–43. [DOI] [PubMed] [Google Scholar]
  • 14. Papadimitriou D, Perris A, Manetou A et al. . A survey of 14 computed tomography scanners in Greece and 32 scanners in Italy: examination frequencies, dose reference values, effective dose and doses to organs. Radiat Prot Dosimetry 2003;104:47–53. [DOI] [PubMed] [Google Scholar]
  • 15. Ideguchi R, Yoshida K, Ohtsuru A et al. . The present state of radiation exposure from pediatric CT examinations in Japan—what do we have to do? J Radiat Res 2018;59(suppl_2): ii130–ii6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Tseng HC, Liu WS, Tsai HH et al. . Radiation dose for normal organs by helical tomotherapy for lung cancer. Appl Radiat Isot 2015;102:35–41. [DOI] [PubMed] [Google Scholar]
  • 17. Tsai SY, Chen CY, Lee JS et al. . Evaluation of effective dose using TLDs with different weighted PMMA phantoms undergoing coronary artery calcium computed tomography examination. IEEE Trans Nucl Sci 2013;60:2147–54. [Google Scholar]
  • 18. ICRP (International Commission on Radiological Protection) The 2007 Recommendations of the International Commission on Radiological Protection. ICRP Publication 103. Oxford: Pergamon; 2007, 1–328. [Google Scholar]
  • 19. Tsujiguchi T, Obara H, Ono S et al. . Consideration of the usefulness of a size-specific dose estimate in pediatric CT examination. J Radiat Res 2018;59:430–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Sugimoto N, Aoyama T, Koyama S et al. . Comparison of radiation doses between newborns and 6-y-old children undergoing head, chest and abdominal CT examinations—a phantom study. Radiat Prot Dosimetry 2013;153:85–91. [DOI] [PubMed] [Google Scholar]
  • 21. Chapple CL, Willis S, Frame J. Effective dose in pediatric computed tomography. Phys Med Biol 2002;47:107–15. [DOI] [PubMed] [Google Scholar]
  • 22. International Commission on Radiological Protection (ICRP). 1995 Basic anatomical & physiological data for use in in radiological protection: the skeleton (ICRP Publication 70). Ann. ICRP vol 25 Oxford: Pergamon. [PubMed] [Google Scholar]
  • 23. Yasuda H. Estimation of the cumulative cancer risk of female children attributable to radiocaesium in soil in an evacuation zone, prior to their return. J Radiol Prot 2018;59(suppl_2):ii137–ii41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Tsai CJ, Lee JJS, Chen LK et al. . Evaluation of radiation dose of triple rule-out coronary angiography protocols with different scan length using 256-slice CT. Nucl Instrum Methods Phys Res A 2011;652:771–4. [Google Scholar]
  • 25. Fu HJ, Li CW, Tsai WT et al. . Skin dose for head and neck cancer patients treated with intensity modulated radiation therapy (IMRT). Radiat Phys Chem 2017;140:435–41. [Google Scholar]
  • 26.International Commission on Radiation Unit and Measurements (ICRU) 1992 Photon, electron, proton and neutron interaction data for body tissues ICRU Report 46 (Bethesda, MD: ICRU)
  • 27. Shrimpton PC, Hillier MC, Lewis MA et al. . National survey of doses from CT in the UK: 2003. Br J Radiol 2006;79:968–80. [DOI] [PubMed] [Google Scholar]
  • 28. Papadakis AE, Perisinakis K, Raissaki M et al. . Effect of x-ray tube parameters and iodine concentration on image quality and radiation dose in cerebral pediatric and adult CT angiography: a phantom study. Invest Radiol 2013;48:192–9. [DOI] [PubMed] [Google Scholar]
  • 29. Mettler FA Jr, Huda W, Yoshizumi TT et al. . Effective doses in radiology and diagnostic nuclear medicine: a catalog. Radiology 2008;248:254–63. [DOI] [PubMed] [Google Scholar]
  • 30. Suliman II, Abdalla SE, Ahmed NA et al. . Survey of computed tomography technique and radiation dose in Sudanese hospitals. Eur J Radiol 2011;80:e544–e51. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Radiation Research are provided here courtesy of Oxford University Press

RESOURCES