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Special Design Considerations for Cardiac CT
Spatial Resolution
Spatial resolution is the product of multiple variables including detector characteristics and collimation, sam­pling rate, and reconstruction methods. State of the art scanners use thin 0.5–0.625 mm collimation. This reduces volume averaging thus increasing image detail of small objects, and allows reconstruction of isotropic datasets, thereby preserving z-axis resolution and permitting multi­planar reformatting necessary for analysis of cardiac anatomy.
GE Healthcare has focused their system development on spatial resolution, developing a new detector scintilla­tion material with a fast decay time (30 ns), minimal afterglow (one-quarter that of conventional Gd
2
O 2 S crys­tals), and increased efficiency. This new detector is one element of a multi-pronged approach to increasing image resolution, which also includes new electronics that per­mit increased sampling, and a new iterative reconstruc­tion algorithm [ 1 ] (Fig. 2.1 ). These innovations increase spatial resolution by 3–4.5 line pairs per cm (lp/cm), which is substantial given that current resolution of sys­tems is approximately 12–15 lp/cm. The enhanced resolu­tion is particularly useful for imaging stented and/or calcified coronary arteries, while lowering radiation requirements.
Temporal Resolution
In order to reconstruct an axial image, attenuation data from multiple view angles that encompass half a rotation around the patient are required. The amount of time needed to obtain this data is the nominal, heart-rate independent temporal resolution of the scanner. Hence, a gantry that requires 330 ms to make one complete rotation has a baseline tempo­ral resolution of 165 ms. This is analogous to shutter speed: just as shutter speed must be suffi ciently fast to capture motion-free images of a moving subject, temporal resolution must be suffi ciently fast to capture the data needed for image reconstruction within the relatively brief period of cardiac diastasis. If temporal resolution is insuffi cient, motion arti­fact occurs (Fig. 2.2 ). A temporal resolution of 165 ms is relatively slow for cardiac imaging, so systems overcome this by various means: faster gantry rotation, multi-cycle reconstruction, and a second x-ray tube.
Multi-cycle reconstruction combines data from multiple contiguous heart beats to complete the half-scan of views (Fig. 2.3 ). This technique is heart-rate dependent: it can only be used within certain ranges of heart rates, since the cardiac cycle and gantry rotation must be asynchronous.
An approach adopted by Siemens in 2006 uses two x-ray tubes mounted on the gantry at 90° angles; therefore, only a quarter turn of the gantry is required to collect the 180° of attenuation data. Hence, a most recent dual-source system with a gantry rotation time of 250 ms has a baseline central temporal resolution of approximately 66 ms. This obviates
Fig. 2.1 Increased sampling improves image quality. Axial images of line-pair phantom demonstrate improved spatial resolution using increased sampling density (on the right ) compared to standard sam- pling frequency (on the left ). Note the improved edge detail and
resolution of the line pairs of the image derived from the high den­sity sampling dataset (Reproduced with permission from Chandra [ 2 ] )
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the need for multi-cycle reconstruction, making the system less susceptible to variation in heart rate, and providing high heart rate independent temporal resolution. Several reports demonstrated very good image quality [ 4 , 5 ] and, in a com- parison of 64 MDCT and DSCT scans, the dual-source sys­tem produced better image quality at higher heart rates [ 6 ]. Image quality is still improved, however, by reducing heart rate before scanning. The improvement of temporal resolu­tion is not the only way to solve the issue for motion artifact. As a post image processor, GE currently provides the motion­correction algorithm (Snapshot Freeze; GE Healthcare) which improves image quality using coronary motion arti­fact and supplements interpretability for diagnostic problems of CAD [ 7 ].
Detector Coverage and Scan Speed
The several novel multi-slice CTs have achieved wider z-axis coverage. The scan length is 16 cm, which is mostly enough to scan the whole heart in a single heart beat, avoiding breathing or misalignment artifact. In addition,
by increasing coverage or faster temporal resolution, scan times have been recently reduced to just < 1 s, resulting in the minimization of the radiation exposure. The Toshiba’s Aquilion One scanner (Aquilion One Dynamic Volume CT; Toshiba Medical System, Tochigi-ken, Japan) has 320 rows of detectors, with 0.5 mm collimation, 16 cm of cov­erage, and can perform an axial 1-beat acquisition of the entire heart when the rate is well controlled. The GE revo­lution also demonstrated a wider coverage of 16 cm and
0.23 mm collimation, with gantry rotation 280 mm. The Philips iQon (Philips Healthcare, Cleveland, OH), is a 256­row scanner, which allows axial acquisition of the entire heart in 2 beats.
Radiation Exposure
Traditional cardiac CT uses a helical scan mode and very low pitch to perform retrospective ECG-gated reconstructions. This delivers an undesirably high radiation exposure, so vari­ous methods have been designed to reduce radiation exposure.
Fig. 2.2 Better temporal resolution improves image quality of moving structures. 3D volume reconstructions of the right coronary artery in 3 CT scans representing 3 generations of CT scanner (4-, 16-, and 64-slice, from left to right , respectively), possessing temporal resolution of 400, 250, and 180 ms from left to right , respectively. Note that the vessel appears distorted and disjointed, due to motion
artifact, when temporal resolution is insuffi cient ( far left ), while motion artifact is minimally present, and small anatomic details are clearly imaged when temporal resolution is improved ( far right ) (Reproduced with the kind permission of Springer Science + Business Media from Hurlock et al. [ 3 ] )
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One of the fi rst was ECG-based tube current modulation, which fl uctuates tube current in sync with the heart rate, maintaining high tube current during diastasis and providing the best image quality in that phase, then lowering tube cur­rent during other phases when high-resolution detail is not required (Fig. 2.4 ). This results in a dose savings of approximately 40 %.
A great advance in dose reduction was made with the advent of prospective, ECG-triggered, axial cardiac CT (Fig. 2.5 ). By keeping the x-ray tube off during most of the scan, and only turning it on during diastasis, as triggered by the ECG, radiation exposure is dramatically reduced. GE fi rst published results using this method [ 9 ] with good clini- cal results and radiation doses of 1–2 mSv [ 10 ], and this
approach is now offered by all manufacturers. Using a 64-slice system, the entire heart can be covered in 3–4 acquisitions; however this leaves the system vulnerable to fl uctuations in heart rate and rhythm during the scan. Larger coverage mitigates this vulnerability by reducing the number of beats required for data acquisition. However, larger cover­age lends to higher radiation doses, as the detectors are less effi cient when having to expose a wider detector array. Hence, Philips’ 128-row iCT system can cover the entire heart in 2 beats, with a reported radiation exposure of 3–5 mSv. Toshiba’s 320-row Aquilion One scanner can cover the entire heart in one beat, with a reported radiation exposure of approximately 6 mSv. However, lower radiation doses and dependable coronary scanning using 1-beat acquisition requires heart rate reduction. At higher heart rates (>65 bpm), optimal image quality requires a 2- or 3-beat acquisition (and use of multi-cycle recon) which increases radiation exposure to approximately 13 (2-beat) to 19 (3-beat) mSv [ 11 , 12 ]. Acquiring with a wide exposure window (“padding”) can ensure the capture of motion-free data, but increases radiation exposure (Fig. 2.6 ). A narrower exposure window can be used with preservation of image quality if heart rate is controlled and reduces radiation exposure.
High Pitch Helical Scanning
Radiation exposure is inversely proportional to pitch in ECG-gated helical CT. Thus, increasing the pitch could dramatically lower radiation requirements in cardiac CT. In 2009, Siemens introduced an innovative scanning method using a high pitch helical mode which takes advan­tage of the dual-source design [ 13 , 14 ] (Fig. 2.7 ). The high pitch (3.2–3.4) would normally produce gaps in the attenu­ation data using a single-source system, but, in a dual­source system, these gaps are compensated for by gathering data from the second detector. Scan time is less than one second, with radiation exposures now reported less than 1 mSv. Initial studies performed on the fi rst-generation dual-source system proved the feasibility of the method, though the authors noted that these fi rst-generation sys­tems are not suitable for this high pitch technique. High pitch scanning with their new scanner, with faster gantry rotation (250 ms) and larger coverage (96 rows), has been reported to produce very good coronary image quality with radiation exposure of <1 mSv [ 4 , 15 , 16 ], or even lower, with <0.1 mSv [ 17 ]. Of note, in this initial investigational phase, low heart rates (<60 bpm) are absolutely required, as the entire data collection takes place within a 250– 270 ms acquisition window of one heart beat; hence
z
z
t
t
180°
45°
45°
45°
45°
Fig. 2.3 Multi-cycle reconstruction. Single cycle recon ( a ): The dura- tion of the acquisition window ( gray bar ) is approximately equivalent to one-half the gantry rotation time, since this is the time required to obtain 180° of attenuation data. Multi-cycle recon ( b ): When multiple detector rows are present, the axial slice position in the z-position can be imaged at multiple different times, using multiple, shorter, acquisi­tion windows distributed across multiple contiguous beats. This data can then be combined to provide 180° of attenuation data and used to reconstruct the axial image. Temporal resolution of the image is improved because the duration of the each acquisition window is shorter (Reproduced with permission of Wolters Kluwer from Vembar et al. [ 8 ] )
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diastasis must be at least this long to provide motion free data acquisition.
The GE Revolution can now utilize the new detector and reconstruction system, along with a fast pitch algo­rithm, to lower radiation exposure by preserving image quality while scanning with less radiation (<1 mSv), because images are of higher resolution and lower noise than would otherwise be achievable with a low-exposure scan.
Future Directions
Future scanner designs are closely guarded industry secrets, but some concepts have been openly discussed. Flat-panel volume CT systems replace detector rows with a large area detector, and provide coverage of the entire heart in one axial acquisition and extremely high spatial resolution of up to 26 lp/cm, comparable to invasive angiography [ 19 ]. However, the contrast resolution is inferior to that of multi­detector CT, a high radiation exposure is needed to achieve a suffi cient contrast-to-noise ratio, scintillation times are slow and temporal resolution is insuffi cient for cardiac imaging.
Dual energy scanning is being developed by all vendors by various means, including rapid fl uctuation of tube energy, stacked detectors, or the dual-tube design in which each tube
100 %
20 %
Time
Tube output
Fig. 2.4 ECG-based tube current modulation reduces radiation exposure. Once the desired acquisition phase is determined, based on heart rate, in this case 75 % phase, scanning proceeds with maintenance of 100 % tube output during that phase, while tube current is reduced outside of that phase. This can reduce effective radiation dose by 40 % or more; however, note that images reconstructed from the low tube output phases ( left image ) will be excessively noisy, and are usually considered unusable for coronary interpretation (Reproduced with permission of Wolters Kluwer from Vembar et al. [
8 ] )
Table move
75 % 75 %
Fig. 2.5 Prospective ECG-triggered acquisition method. Cardiac rhythm is monitored while table remains stationary. When cardiac cycle reaches pre-determined acquisition phase (in this case 75 %, diastolic, phase), x-ray source is briefl y turned on (<1 s, blue bars ) and acquires attenuation data of a length equivalent to the craniocaudal coverage of the detector array, and is then turned off. The table is advanced almost the length of craniocaudal coverage (minus a small amount of overlap), and the process repeats again. Depending on the craniocaudal coverage of the scanner, the entire heart can be scanned in 1–4 acquisitions (Reproduced with the kind permission of Springer Science + Business Media from Weigold et al. [ 18 ] )
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emits photons of different energy levels. Dual energy CT could take the fi eld to a new level of diagnostic power if it can be used for refi ned tissue characterization, such as dif­ferentiating plaque characteristics. This is diffi cult to do in the coronary arteries, and initial studies have not yielded any
breakthroughs, but at the least it has the potential to enhance coronary lumen visualization in heavily calcifi ed vessels by differentiating calcium and iodine [ 20 , 21 ] (Fig. 2.8 ). Dual- energy CT may also yield new applications for non-coronary imaging, such as imaging of myocardial perfusion [ 22 ].
Low heart rate
75 % 75 %
High heart rate
Table move
Table move
40 % 40 %
a
b
Fig. 2.6 Prospective CCTA phase selection and padding. Acquisition phase and padding depend on heart rate: For low heart rates ( a ), target late diastole (75 % phase) for prospective acquisition, but if heart rate is high ( b ) (>75 bpm), target end-systole (40 % phase) which is more likely to produce motion-free images. By restricting acquisition to the minimum exposure window ( dark gray ), radiation dose is minimized,
but ability to reconstruct adjacent cardiac phases is obliterated. Widening the acquisition window (“padding,” light gray shading) allows reconstruction of a small number of additional phases, which can help interpretation of motion artifact, but increases the radiation dose (Reproduced with the kind permission of Springer Science + Business Media from Weigold et al. [ 18 ] )
83 ms
Fig. 2.7 Method of high-pitch coronary CCTA. Single source helical CT requires a pitch 1.5; a faster pitch results in gaps in the data ( left panel ). A dual-source system can scan at a higher pitch (up to 3.2), using the second x-ray source-detector system to fi ll in what would oth­erwise be gaps in the data. Since the table speed is so high, the entire heart can be imaged in a fraction of a second, from data derived from a
single heartbeat ( right panel ). If the image acquisition is triggered appropriately to synchronize acquisition with diastasis, and the heart rate is suffi ciently low, motion-free images can be obtained with a very low radiation dose (Reproduced with permission of Elsevier from Achenbach et al. [ 14 ] )
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Conclusions
Since the turn of the twenty-fi rst century, there has been an explosion in technological development of cardiac CT systems, with concomitant gain in reliability and accu­racy, especially of coronary imaging. The theme has been one of progressively improved spatial and temporal reso­lution, reduced scan time, and, most recently, a focus on driving down radiation exposure. In appropriately selected patients, using careful technique, it is easily achievable to perform a cardiac CT using less radiation exposure than that of a standard chest CT or an invasive coronary angio­gram. The goal of future systems will be to make this more widely achievable in a larger group of patients with­out requiring patient selection or stringent patient prep. Given the history of rapid technological advancement, we can expect to see this goal achieved in the near future.
References
1. Thibault JB, Sauer KD, Bouman CA, Hsieh J. A three-dimensional
statistical approach to improved image quality for multislice helical CT. Med Phys. 2007;34:4526–44.
2. Reproduced with permission from Chandra N. CT sampling tech-
nology [white paper]. Waukesha: GE Healthcare; 2008.
3. Hurlock GS, Higashino H, Mochizuki T. History of cardiac com-
puted tomography: single to 320-detector row multislice computed tomography [Review]. Int J Cardiovasc Imaging. 2009;25:31–42.
4. Hell MM, Bittner D, Schuhbaeck A, et al. Prospectively ECG-
triggered high-pitch coronary angiography with third-generation dual-source CT at 70 kVp tube voltage: feasibility, image quality, radiation dose, and effect of iterative reconstruction. J Cardiovasc Comput Tomogr. 2014;8:418–25.
5. Achenbach S, Ropers D, Kuettner A, et al. Contrast-enhanced
coronary artery visualization by dual-source computed tomogra­phy – initial experience. Eur J Radiol. 2006;57:331–5.
aa
cd
Fig. 2.8 Dual energy CT. Dual energy CT can be used to characterize tissue: Vessel cross sectional images derived from high- (140 keV) and low-energy (90 keV) attenuation profi les ( a and b , respectively) demon- strate the infl uence of photon energy on photoattenuation. The contrast­fi lled lumen ( arrow ) exerts greater photoattenuation on low- energy photons, and hence appears brighter in ( b ), while calcifi cation ( aster-
isk ) appears high-density in both images. In the subtracted image ( c ), dense calcifi cation has been “removed.” By adding in the low- energy (90 keV) attenuation data to this subtracted image, depiction of the lumen edge is enhanced (because of reduced contrast blooming), and visualization of a small side branch ( arrowhead ) is improved ( d ) (Reproduced with permission of Wolters Kluwer from Boll et al. [ 23 ] )
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6. Achenbach S, Ropers U, Kuettner A, et al. Randomized compari­son of 64-slice single- and dual-source computed tomography coronary angiography for the detection of coronary artery disease. JACC Cardiovasc Imaging. 2008;1:177–86.
7. Leipsic J, Labounty TM, Hague CJ, et al. Effect of a novel vendor­specifi c motion-correction algorithm on image quality and diag­nostic accuracy in persons undergoing coronary CT angiography without rate-control medications. J Cardiovasc Comput Tomogr. 2012;6:164–71.
8. Vembar M, Walker MJ, Johnson PC. Cardiac imaging using multislice computed tomography scanners: technical consider­ations. Coron Artery Dis. 2006;17:115–23.
9. Hsieh J, Londt J, Vass M, Li J, Tang X, Okerlund D. Step-and-shoot data acquisition and reconstruction for cardiac x-ray computed tomography. Med Phys. 2006;33:4236–48.
10. Earls JP, Berman EL, Urban BA, et al. Prospectively gated trans­verse coronary CT angiography versus retrospectively gated helical technique: improved image quality and reduced radiation dose. Radiology. 2008;246:742–53.
11. Hoe J, Toh KH. First experience with 320-row multidetector CT coronary angiography scanning with prospective electrocardiogram gating to reduce radiation dose. J Cardiovasc Comput Tomogr. 2009;3:257–61.
12. Steigner ML, Otero HJ, Cai T, et al. Narrowing the phase window width in prospectively ECG-gated single heart beat 320-detector row coronary CT angiography. Int J Cardiovasc Imaging. 2009;25:85–90.
13. Hausleiter J, Bischoff B, Hein F, et al. Feasibility of dual-source cardiac CT angiography with high-pitch scan protocols. J Cardiovasc Comput Tomogr. 2009;3:236–42.
14. Achenbach S, Marwan M, Schepis T, et al. High-pitch spiral acqui­sition: a new scan mode for coronary CT angiography. J Cardiovasc Comput Tomogr. 2009;3:117–21.
15. Gordic S, Desbiolles L, Sedlmair M, et al. Optimizing radiation dose by using advanced modelled iterative reconstruction in high- pitch coronary CT angiography. Eur Radiol. 2016;26(2):459–68.
16. Layritz C, Schmid J, Achenbach S, et al. Accuracy of pro­spectively ECG-triggered very low-dose coronary dual-source CT angiography using iterative reconstruction for the detec­tion of coronary artery stenosis: comparison with invasive catheterization. Eur Heart J Cardiovasc Imaging. 2014;15: 1238–45.
17. Schuhbaeck A, Achenbach S, Layritz C, et al. Image quality of ultra-low radiation exposure coronary CT angiography with an effective dose <0.1 mSv using high-pitch spiral acquisition and raw data-based iterative reconstruction. Eur Radiol. 2013;23: 597–606.
18. Weigold W, Olszewski M, Walker MJ. Low-dose prospectively gated 256-slice coronary computed tomographic angiography. Int J Cardiovasc Imaging. 2009;25 Suppl 2:217–30.
19. Gupta R, Cheung AC, Bartling SH, et al. Flat-panel volume CT: fundamental principles, technology, and applications. Radiographics. 2008;28:2009–22.
20. Andreini D, Pontone G, Mushtaq S, et al. Diagnostic accuracy of rapid kilovolt peak-switching dual-energy CT coronary angiogra­phy in patients with a high calcium score. JACC Cardiovasc Imaging. 2015;8:746–8.
21. Barreto M, Schoenhagen P, Nair A, et al. Potential of dual-energy computed tomography to characterize atherosclerotic plaque: ex vivo assessment of human coronary arteries in comparison to histology. J Cardiovasc Comput Tomogr. 2008;2:234–42.
22. Ruzsics B, Schwarz F, Schoepf UJ, et al. Comparison of dual­energy computed tomography of the heart with single photon emis­sion computed tomography for assessment of coronary artery stenosis and of the myocardial blood supply. Am J Cardiol. 2009;104:318–26.
23. Boll DT, Hoffmann MH, Huber N, Bossert AS, Aschoff AJ, Fleiter TR. Spectral coronary multidetector computed tomography angiog­raphy: dual benefi t by facilitating plaque characterization and enhancing lumen depiction. J Comput Assist Tomogr. 2006;30(5): 804–11.
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© Springer International Publishing 2016 M.J. Budoff, J.S. Shinbane (eds.), Cardiac CT Imaging: Diagnosis of Cardiovascular Disease, DOI 10.1007/978-3-319-28219-0_3
Radiation Dosimetry and CT Dose
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Reduction Techniques
Kai H. Lee
Abstract
Increasing radiation exposure to the population from widespread use of multi-row detector CT necessitates efforts to limit the x-rays applied in CT procedures. Options are available on CT scanners to modulate the patient dose. This chapter describes the metrics of radiation dose, and the influence of various technical parameters in the scan and dose modulation options on patient dose and image quality. With that information, practitioners of CT will be better prepared to optimize the scan protocols to reduce the patient dose without sacrific­ing the image quality necessary for interpretation.
Keywords
CT radiation metrics • Dose modulation • Scanning parameters
3
Introduction
The ability of modern multi-detector CT scanners with sub- millimeter resolution, sub-second rotation time, and large volume imaging has resulted in widespread use of CT. However, the widespread use of CT has also raised con­cerns about the risks of radiation to patients. The National Council on Radiation Protection, NCRP Report No. 160, in 2006 [1] reported that radiation exposure to the United States population due to medical sources increased more than seven times in the 20 years between 1986 and 2006. According to the NCRP report, CT constituted about 10 % of the diagnostic examinations that utilize x-rays in 2006, it contributed to nearly 50 % of the population dose. The use of CT continued to rise since publication of NCRP Report 160. Reports in sci-
K.H. Lee, PhD
Associate Professor of Clinical Radiology,
Department of Radiology, Keck School of Medicine, University of Southern California, 1200 North State Street, Los Angeles, CA 90033, USA
e-mail: kailee@usc.edu
entific and lay journals found fewer than three million CT examinations done in 1980, which rose to 62 million in 2007, and to 80 million at the end of 2014 [24]. Based on our current knowledge of radiation biology, the deleterious effects of radiation are cumulative and medical radiation is increas­ingly a significant contributor to the amount of radiation accu­mulated in a person’s lifetime [5, 6]. The risk of cancer from radiation exposure is especially worrisome to children and young women who received multiple CT examinations early in their life. For example, studies found that one CT examina­tion of the female chest gives as much radiation as 10 mam­mograms to each breast [7]. In addition to radiation from CT, cardiac patients may be exposed to radiation from nuclear medicine perfusion studies and coronary angiography. Therefore, the practitioners of CT must be constantly aware of the risks of radiation, and strive toward applying the lowest dose to the patient consistent with the clinical study.
One of the difficulties confronting the clinicians when evaluating the radiation safety of a CT procedure is the pleth­ora of terms used to quantify the amount of radiation given to the patient. Thus, this chapter sets out on two aims. The first aim is to explain the fundamental concepts of radiation dosimetry associated with CT scans. The second aim is to describe the scanning techniques and available technologies to reduce radiation dose to patients.
33
34
11
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-
W.
()=()
()
=
()
×
11
K.H. Lee
https://t.me/medicina_free
Fundamentals of Radiation Dosimetry
Absorbed Dose
The damaging health effects of radiation are commonly called radiation effects. Our current knowledge of radiation effects was derived from animal studies, atom bomb survivors, and victims of radiation accidents [6]. There were many contributing factors to the observed radiation effects, but the outcomes ultimately depended on the amount of radiation received. The radiation dose, or dose in short, is the amount of energy deposited by the ionizing radiation per unit mass of tissue. Radiation dosimetry is the field of study which measures and quantifies the radiation dose. Of the bewildering number of terms to quantify radiation dose, there are three related terms fundamental to radiation protection. The three terms are the absorbed dose, the equivalent dose, and the effective dose.
The International System (SI units) of radiation dose
measurements is the Gray [8]. One Gray (Gy) of radiation is defined as 1 J of energy deposited in 1 kg of tissue, i.e.,
joule
Dose Gy
()
1
=
kg tissue.
1
The Gray is a large dose of radiation. When evaluating radiation dose from CT examinations, a sub-unit of the Gray is used. The Gray sub-unit commonly used to quantify radiation dose from CT examinations is the milli-Gray
(mGy). One mGy is one thousandth of a Gray. That is,
3
mG
0
y.=
Equivalent Dose
The severity of biological damage depends not only on the dose of radiation absorbed in tissue, but also on the type of radiation absorbed. For example, 1 mGy of neutron radia­tion produces far greater tissue damages than 1 mGy of x-rays. We therefore need a unit of measurement that accounts for both the quantity of radiation absorbed in the tissues and the effectiveness of the absorbed radiation in producing biological damages. The equivalent dose was devised to incorporate both the physical factors and the effectiveness of the absorbed radiation in producing bio­logical damage. The equivalent dose is a biological scale for measuring the deleterious health effects of radiation. The same biological damage is expected for the same equivalent dose regardless of the type of radiation absorbed in tissue.
The equivalent dose (H) is measured in Sievert (Sv).
A sub-unit of Sievert is the milli-Sievert (mSv). One
Table 3.1 Biological damage weighting factors
Type of radiation Weighting factor
X- and gamma rays, electrons, positrons 1
Protons 2
Neutrons 10
Alpha particles 20
milli-Sievert equals to one thousandth of a Sievert. The equivalent dose in mSv is calculated by multiplying the radiation absorbed dose D in mGy by a quality factor Q, also
called the biological damage weighting factor Wr [9], for the type of radiation absorbed in tissue, i.e.,
HmSv DmGy
´
r
The biological damage weighting factors for four types of radiation are given in Table 3.1.
The values of Wr are proportional to the density of ioniza­tion created by the incident radiation along its path of travel in tissue. For x-rays, gamma rays, beta particles, and elec­trons from radioactive materials, the density of ionization created in tissue is relatively low. The weighting factor Wr equals 1. Thus, when working with x-rays from CT, the equivalent dose and absorbed dose are numerically equal,
i.e., 1 mSv =1 mGy. For neutrons, the weighting factor
Wr= 10. The equivalent dose for 1 mGy of neutron absorbed dose equals
HmSv mGy
mSv.
=
10
0
The above example shows that neutrons are ten times more damaging to the human body than x-rays for the same absorbed dose.
In summary, the absorbed dose in mGy is the quantity of radiation energy deposited per unit mass of tissue. The
equivalent dose in mSv is a measure of biological damage
equal to the absorbed dose modified by a weighting factor according the relative effectiveness of the absorbed radiation to produce biological damage.
Given this metric to quantify radiation, Table 3.2 lists the average equivalent dose received annually to the total body by workers in various occupations [1013]. The table also gives the natural background radiation and the regulatory limits on radiation exposure for ref­erence. It is interesting to note that the transcontinental flight crews who are not classified as occupational radi­ation workers receive an annual equivalent dose from the cosmic rays higher than the nuclear medicine tech­nologists who routinely handle radioactive materials on the job.
EH
=∑
ii
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Table 3.2 Typical annual whole-body radiation dose
mSv
Nuclear medicine technologists 1.7
Airline flight crews between Los Angeles and New York City
Nuclear power plant workers 2.3
Intervention radiologists 18
Cardiologists (catheterization) 16
Natural background radiation at sea level 2.5
Regulatory limit on the occupational workers 50
Regulatory limit on the general public 1
2.2
Radiation Effects to the Patient
The goal of protecting patients undergoing radiological pro­cedures is to prevent the occurrence of deterministic effects, and to minimize the risk of stochastic effects. Deterministic effects are radiation induced somatic injuries. Examples of radiation induced somatic injuries are skin erythema, epila­tion, and cataracts. The FDA has documented severe deter­ministic effects such as hair loss and skin necrosis on patients from CT and prolonged fluoroscopy guided procedures.
Deterministic effects are preventable. There is ample clinical
evidence of threshold doses below which such effects are not seen. Once the threshold dose is reached, severity of the injury increases with the radiation dose.
Stochastic risks are probabilistic occurrences of carcino­genesis and genetic mutations. The current concept of sto­chastic risks assumes no threshold dose for its occurrence. Exposure to any amount of ionizing radiation is harmful. The probability of the occurrence of stochastic effects, rather than its severity, increases in direct proportion to the radia­tion absorbed dose. This is in contrast to deterministic effects in which the severity increases as the dose increases above the threshold. This concept of stochastic risks is called linear no threshold model, and is the basis of radiation protection regulations.
Effective Dose
Our knowledge of stochastic risks is based on data collected from total body exposure to radiation. If we wish to estimate the stochastic risks to a person after a partial body exposure such as a chest CT, we must translate the chest CT dose to an equivalent whole-body dose in order to utilize the database for risk estimates. The effective dose was devised for this purpose. The effective dose is the dose of radiation that when given uniformly to the whole-body will produce the same stochastic risk as the dose of radiation delivered to only a part of the body, such as the chest dose from a cardiac CT study.
Table 3.3
Tissue/organ Weighting factor, Wr
Gonads 0.20
Bone marrow, colon, lung, stomach 0.12
Bladder, breast, liver, esophagus, thyroid 0.05
Skin, bone surface 0.01
Tissue/organ sensitivity
The effective dose translates a partial body exposure to an equivalent uniform dose of radiation delivered to the total body. The purpose for calculating the effective dose is to pro­vide a common denominator for the assessment of stochastic risks using our database of whole-body exposures. Unlike the absorbed dose and the equivalent dose, the effective dose is not a physically measurable quantity. The effective dose is an imaginary total body dose. It is calculated from the absorbed dose given to any region or regions of the body.
If we wish to estimate the stochastic risks from CT of the chest, we must translate the partial body irradiation to an equivalent whole-body dose in order to utilize the database for risk estimates. To do so, a mathematical model is used to compute the doses to other organs resulting from radiation scattered from CT of the chest. These computed organ doses are then multiplied by a risk factor according to the suscepti-
bility of each organ to radiation. Summation of the product
of these computed organ doses and their associated risk weighting factor is called the effective dose. That is, the effective dose E is computed using the equation
w
Where E is the effective dose Hi is the dose equivalent to a given organ wi is the risk weighting factor for that organ.
The effective dose is thus a weighted sum of the com­puted equivalent doses to all organs in the body. Table 3.3 is a partial list of weighting factors for different body organs published in the International Commission on Radiation
Protection Report 103 [14].
One may interpret the effective dose as a calculated equivalent dose of radiation given to the entire body that would be required to produce the same risk of cancer and genetic damage as a dose of radiation delivered to a localized region of the body, such as in a CT examination. In other words, the risk from a part of the body exposed to a given dose of radiation is the same as the total body uniformly receiving the effective dose. The effective dose is an extrapo­lated whole-body dose from a partial body dose. As such, the effective dose is a computed value rather than a physically measurable quantity. The effective dose is calculated to serve as a common denominator for comparing stochastic risks