Radiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published online before print June 28, 2002, 10.1148/radiol.2242011581
This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2242011581v1
224/2/487    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Winer-Muram, H. T.
Right arrow Articles by Lombardo, G. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Winer-Muram, H. T.
Right arrow Articles by Lombardo, G. T.
(Radiology 2002;224:487-492.)
© RSNA, 2002


Medical Physics

Pulmonary Embolism in Pregnant Patients: Fetal Radiation Dose with Helical CT1

Helen T. Winer-Muram, MD, John M. Boone, PhD, Haywood L. Brown, MD, S. Gregory Jennings, MD, William C. Mabie, MD and Gerard T. Lombardo, MD

1 From the Department of Radiology, Indiana University School of Medicine, 550 N University Blvd, Indianapolis, IN 46202 (H.T.W.M., S.G.J.); Department of Radiology, University of California-Davis Medical Center, Sacramento (J.M.B.); Department of Obstetrics and Gynecology, St Vincent’s Medical Center, Indianapolis, Ind (H.L.B.); Department of Obstetrics and Gynecology, University of Tennessee College of Medicine, Memphis (W.C.M.); and Division of Pulmonary Medicine and Critical Care, New York Methodist Hospital, Brooklyn, NY (G.T.L.). Received September 24, 2001; revision requested November 27; revision received December 17; accepted January 22, 2002. Address correspondence to H.T.W.M. (e-mail: hwinermu@iupui.edu).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
PURPOSE: To calculate mean fetal radiation dose from helical chest computed tomography (CT) by using maternal-fetal geometries obtained from healthy pregnant women and to compare the calculated CT doses with the fetal doses reported with scintigraphy.

MATERIALS AND METHODS: Maternal-fetal geometries were determined in 23 pregnant women with varying body mass index and fetal gestational age. Monte Carlo techniques were used to estimate the dose that would be received by each fetus from CT scanning performed with the following parameters: 120 kVp; 100 mA; scanning time, 1 second per section; collimation, 2.5 mm; pitch of 1. Craniocaudal extent of the scan was 11 cm, with the most caudal section edge being 5 mm inferior to the xiphoid process.

RESULTS: For helical CT, estimated mean fetal doses in micrograys at varying gestational ages were as follows: 3.3–20.2 µGy, first trimester; 7.9–76.7 µGy, second trimester; and 51.3–130.8 µGy, third trimester. These values were all less than mean fetal doses reported with scintigraphy, with 37-74 MBq of macroaggregates of human serum albumin labeled with technetium 99m. If 200 mAs (pitch of 1.8) was used, the mean fetal doses were still less than those with scintigraphy.

CONCLUSION: The average fetal radiation dose with helical CT is less than that with ventilation-perfusion lung scanning during all trimesters.

© RSNA, 2002

Index terms: Embolism, pulmonary, 60.72 • Pregnancy, 85.131, 85.47 • Radiations, exposure to patients and personnel • Thorax, CT, 60.1211, 60.12115


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Venous thromboembolism is a leading cause of maternal mortality and has been reported to occur in 0.5–3.0 of 1,000 pregnancies (1,2). Pregnancy increases the risk of venous thromboembolism by a factor of five over that of a nonpregnant woman of similar age (3). Increased venous stasis is the most important factor, but prolonged bed rest, pregnancy-related hypercoagulability, decreased fibrinolysis, and familial predisposition are also implicated (4). While the risk of thrombosis has usually been considered greatest during the third trimester and immediately postpartum, there is evidence that venous thromboembolism may occur with almost equal frequency in all three trimesters (4).

The incidence of pulmonary embolism (PE) depends on whether deep venous thrombosis (DVT) has been treated adequately. Up to 24% of patients with untreated DVT develop PE, with a mortality rate of approximately 15% (5). Because venous thromboembolism is potentially preventable and treatable, early and accurate diagnosis and treatment are mandatory (6).

Several studies have provided guidelines for investigating PEs in pregnant patients who are suspected of having them. These guidelines attempt to balance diagnostic efficacy and minimization of fetal exposure to ionizing radiation (68). Ventilation-perfusion (V-P) lung scanning is still considered to be the primary diagnostic tool for PE in pregnant women (9,10). By using 37–74 MBq of macroaggregates of human serum albumin labeled with technetium 99m, the fetal dose from lung scanning is approximately 100–370 µGy, a relatively low exposure for the fetus (7,8).

Although helical CT is being used more and more to diagnose PE, there are questions about the safety of its use during pregnancy. The purpose of this study was to calculate the mean fetal radiation dose from helical chest CT by using maternal-fetal geometries obtained from healthy pregnant women and to compare the calculated CT doses with the reported fetal doses with scintigraphy.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Clinical Data
Institutional review board approval with waiver of informed consent was obtained. From July 2001 to August 2001, 23 consecutive healthy pregnant patients of one author (H.L.B.) were selected for measurement of maternal-fetal geometry. Maternal age, height, and weight and fetal gestational age (estimated by using ultrasonography [US]) were noted (H.L.B.). For pregnant patients with less than 13 weeks gestation, the uterine dimensions were measured with US that incorporated the entire uterine volume. The length was measured by using transvaginal and transabdominal US to obtain the most accurate uterine, or fetal, dimensions. The measurement was from the top of the fundus of the uterus to the level of the internal os of the cervix.

Transverse dimensions were measured at the widest point of the uterus. The top of the uterus, or fundal height, was marked, and the distance from the xiphoid process to the fundus was measured. Measurements in patients with more than 13 weeks gestation were performed with standard techniques. The top of the fundus of the uterus was again marked by using transabdominal US and measured down to the pubic symphysis and up to the xiphoid process. The widest uterine measurement was obtained by marking the maximum outer width on both sides of the umbilicus by using US and then was measured from mark to mark. Geometric assumptions for the Monte Carlo studies are discussed later.

The following CT protocol was used for calculations: 120 kVp, 100 mAs, 2.5-mm section interval, 11-cm craniocaudal distance, pitch of 1. This distance is generally sufficient to extend from just inferior to the xiphoid process to the aortic arch. With this protocol, the mean fetal doses were calculated by using Monte Carlo techniques in the 23 study patients.

Monte Carlo Calculations
The circumference in each of the 23 women was measured physically, but for the Monte Carlo studies we also needed to obtain an estimate of the relative shape of a patient at the xiphoid process. Assuming an ellipsoidal cross section, we computed the eccentricity from a number of CT scans. CT scans that were acquired as a part of clinical care in 21 consecutive nonpregnant women (mean age, 50.6 years; SD, 17.8) were evaluated. Coronal and sagittal diameters at the level of the xiphoid process were determined by using quantitative measurement software (E-Film; E-Film, Toronto, Ontario, Canada). This analysis of existing patient data was performed with a protocol approved by the institutional review board at University of California-Davis Medical Center, Sacramento, with waiver of informed consent.

An elliptical cross section was assumed, and the eccentricity of each patient at the level of the xiphoid process was calculated on the basis of image-based measurements of the thickness and width of the patient. The mean eccentricity and the median eccentricity were 0.68 and 0.66, respectively (Fig 1). Since the mean age of this group was substantially higher than that of the study group, the eccentricity was evaluated as a function of patient age by using linear regression. Only a slight dependence was found, and, therefore, the mean eccentricity value was used for all 23 pregnant women modeled in the Monte Carlo calculations. Although the eccentricity measurements were obtained in nonpregnant women, the shape of a woman at the level of the thoracic cavity changes only slightly during pregnancy, and, thus, we thought that the eccentricity measurement determined in this group would be reasonably reflective of the pregnant patient.



View larger version (29K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 1. Drawing illustrates the geometry used in the Monte Carlo calculations. The mother was modeled as an ellipse with a mean eccentricity of 0.68. The specific dimensions (a and b) were determined by measuring the circumference of the mother. The fetus was modeled as a right cylinder, where the fetal diameter, fetal height (H), and distance from the top of the fetus to the scanned volume (S) were individually measured by using US.

 
Monte Carlo techniques were used to compute the radiation doses that the fetuses would have received if the patients had undergone chest CT with the parameters previously described. The initial CT section (section 1) was positioned with the inferior edge of the scan 5 mm below the xiphoid process, and the dose computations included the contribution of an additional 43 (for a total of 44) 2.5-mm-thick, contiguous, transverse (nonhelical) sections. The dose distribution as modeled was virtually identical to that of a helical CT study with a pitch of 1, with the same scanning volume. This geometry is equivalent to the acquisition of CT sections along a craniocaudal axis of 11 cm, regardless of the combination of section thickness or image numbers. For example, the dose associated with 44 2.5-mm sections is equivalent to that associated with 37 3-mm, 22 5-mm, or 11 10-mm sections, as long as the scanned volume (in relative position to the fetus) and other CT parameters remain the same.

Previously validated simple investigational environment for radiology research applications, or SIERRA, Monte Carlo techniques were used for this study (11,12), and additional validation efforts were also performed. The Monte Carlo code propagated 22 million x-ray photons per patient. Photoelectric, Compton, and Rayleigh scattering interactions were modeled with the energy range of 1–150 keV. Energy deposition was determined in water-equivalent ellipsoid (mathematic) phantoms by using the geometries of each of the 23 study patients. The same eccentricity (mean, 0.68) was assumed for each patient.

The x-ray output data of a commercially available CT scanner (CT/i; GE Medical Systems, Milwaukee, Wis) were used to relate milliampere seconds to photon fluence. The normalized output (milliroentgens per milliampere seconds at isocenter versus kilovolt peak) of a scanner was measured by using an exposure meter (MDH 1015; Radcal, Monrovia, Calif) and a 3-cm3 CT pencil chamber. By using a physical scale drawing of an actual beam-shaping filter. The projection thickness of an actual beam-shaping filter was measured on a scale drawing with a ruler and protractor as a function of fan angle, and the thickness was computer fit as a function of angle. The filter composition was synthetic resin (Teflon) (C2F4), with a density of 2.2 g/cm3. The x-ray attenuation of the beam-shaping filter was used to modify the photon distribution in the plane of the fan angle. A source-to-isocenter distance of 63 cm was used. The x-ray spectrum was generated by using a spectral model (13), and a half-value layer of 8.2 mm of aluminum was achieved by filtering the native spectrum with 8.0 mm of aluminum. This half-value layer matched that measured with a clinical scanner at 120 kVp at University of California-Davis Medical Center.

A Monte Carlo simulation was performed in each patient by using the measurements for each maternal-fetal geometry. The axial diameter and craniocaudal length were used to simulate the fetus as a right cylinder at the center of the ellipse that was used to define the mother’s geometry (Fig 1). The energy deposited in this cylindric simulated fetus of water-equivalent unit-density material was used for calculating the dose. The assumption of a cylindric shape for the fetus facilitates the Monte Carlo computation of dose to this region.

Differences in shape between a cylinder and the actual fetus have only a small effect on the fetal dose calculation, as long as the cylinder dimensions simulate the bounds of the fetus. The US-based anatomic measurements were performed to accurately determine these distances. In each woman, the measured circumference at the xiphoid process was used to determine the dimensions of each elliptic semiaxis (values a and b in Fig 1). In addition to calculation of the mean fetal dose, determination of the maximum fetal dose was performed in a separate series of Monte Carlo experiments. The maximum fetal dose was estimated by means of calculating the dose to the uppermost 1 cm of the fetus (the portion closest to the scanned volume).


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Monte Carlo Comparisons
Results were reported for the 120-kVp spectrum, in which the output was measured as 19.70 mR/mAs (air kerma, 0.172 mGy/mAs) at the isocenter of the scanner. Figure 2 illustrates SIERRA Monte Carlo results compared with the reported data of Caon et al (14) and shows both their physically measured and Monte Carlo–derived results that are based on the EGS4 code. Results were calculated both with (Fig 2, A) and without (Fig 2, B) a beam-shaping filter. Figure 3 illustrates the CT dose index calculated by using the SIERRA code with the same conditions as those reported by Huda et al (15).



View larger version (29K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2. Graphs show a comparison of the results of this study ({circ}) with the physically measured results ({diamondsuit}) and the results derived by means of the EGS4 Monte Carlo calculations ({bullet}) as reported by Caon et al (14). The x axis refers to the location along a diameter within a cylindric phantom, with the position of x = 0 cm being at the center. A, Moderate agreement is seen with no bow tie filter. B, Excellent agreement between the SIERRA-derived results and the measured data of Caon et al (14) is seen with the bow tie filter in place. The bow tie filter was used in the development of the pediatric dose values in this study.

 


View larger version (32K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 3. Graphs show a comparison of CT dose index (CTDI) data determined in this study and of the values reported by Huda et al (15). The values determined at the center of the plastic (polymethylmethacrylate) phantom are shown in A, and the values determined at the edge of the phantom are illustrated in B. The head phantom is a 16-cm-diameter plastic cylinder, and the body phantom is a 32-cm-diameter plastic cylinder.

 
The CT dose index data are compared at the center of the cylindric plastic phantom (Fig 3, A) and at its edge (Fig 3, B) for both the head phantom (16 cm diameter) and the body phantom (32 cm diameter). For purposes of comparison with other CT dose index values, the scanner that was simulated in this investigation produced a CT dose index multiple scan average dose of 4.50 mGy per 100 mAs at the center of a 32-cm-diameter plastic phantom and a CT dose index MSAD of 5.93 mGy per 100 mAs at the edge of the phantom. Because penumbra cutoff effects were not included in this simulation, the CT dose index values from real multisection CT scanners should be slightly higher than these values.

Fetal Dose Assessment
Maternal and fetal measurements are presented in Table 1. Eight patients were in the first trimester, nine were in the second trimester, and six were in the third trimester. Mean maternal age was 31 years (SD, 6.7).


View this table:
[in this window]
[in a new window]

 
TABLE 1. Characteristics of Study Population

 
The mean fetal dose was calculated for each patient for 44 individual 2.5-mm-thick CT scans (Fig 4). These exposure conditions are identical to those associated with 37 3-mm, 22 5-mm, or 11 10-mm-thick CT sections. An equation that corresponds to the best-fit line is shown in Figure 4. The equation was determined for 100 mAs and transverse scans; for different milliampere second values and helical acquisition with pitches other than 1.0, the values generated by the equation should be adjusted. The actual fetal dose varies linearly with the milliampere second values; for example, if 200 mAs is used, the fetal dose is multiplied by 200 divided by 100. For helical acquisition, the dose is additionally multiplied by the factor 1/pitch. Mean fetal doses were compared with reported (8) doses delivered with scintigraphy (Table 2).



View larger version (51K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 4. Graph shows the mean fetal dose for each of 23 patients. These data were determined by summing the dose contribution from each of the 44 CT sections in the study.

 

View this table:
[in this window]
[in a new window]

 
TABLE 2. Theoretic CT Doses

 
With cranial-to-caudal progression, the dose to the fetus decreases exponentially. Near the caudal end of the fetus, very small doses are received, and these small doses substantially lower the mean fetal dose. Because of this bias, the maximum fetal dose was also computed (Fig 5) (Table 2). The maximum fetal dose is experienced by the uppermost 1 cm of the fetus, or that portion closest to the scanned volume.



View larger version (52K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 5. Graph shows the maximum dose per individual CT section for a 2.5-mm-thick, nonhelical, 120-kVp, 100-mAs scan. The data points correspond to the dose computed for the single highest-dose CT section in each of the 23 patients. In all cases, the highest dose was delivered to the CT section closest to the fetus.

 

    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
In all three trimesters, the mean fetal dose delivered with helical CT (120 kVp, 100 mAs, pitch of 1) is less than that delivered with V-P scanning. In 20 of our 23 study patients, the mean fetal dose was less than 60 µGy, the mean fetal dose described by Sharp et al (16). For different CT parameters or scanning volumes, with a specific maternal-fetal geometry, the maximum fetal dose can be calculated as demonstrated in Figure 5. The doses in Table 2 do not include additional exposure from a scanogram. Because the helical CT scan begins near an anatomic landmark (the xiphoid process), we believe that a scanogram is not necessary (17).

Numerous studies have been published in which the researchers describe the value of helical CT for PE diagnosis, and findings in most show that helical CT is an accurate tool for diagnosis of PE in main, lobar, and segmental pulmonary arteries. For emboli in these sites, helical CT is approximately 90% sensitive (range, 60%–100%) and 90% specific (range, 80%–100%) (18). Helical CT also has been reported (19) to demonstrate excellent interobserver agreement. However, helical CT is less accurate for imaging peripheral emboli in subsegmental vessels.

When all pulmonary vessels are included, the sensitivity and specificity of helical CT for the diagnosis of PE range from 53%–100% and 75%–100%, respectively (18). Poor contrast opacification, motion artifacts, or technical factors may cause 5%–10% of CT scans to be nondiagnostic (18). In addition, for diagnosis of PE, administration of intravenous contrast material is necessary. Although intravenous administration of nonionic contrast material during pregnancy is performed with other imaging studies (eg, head CT), and studies in pregnant animals have shown no evidence of harm to the fetus caused by nonionic contrast media (20), to our knowledge, no adequate and well-controlled studies have been performed in pregnant women.

Scintigraphy is the primary screening study in the assessment of PE in pregnant patients (9). However, V-P scans are usually not definitive in the diagnosis of acute PE; the presence or absence of PE is inconclusive in up to 80% of these scans (21). Most radiologists categorize abnormal lung scans into three classes according to the probability—low, intermediate, or high—that the finding is a PE. Even for a scan with a high probability, the sensitivity is only 41% (21). Thus, most patients with PE will have scans with intermediate or low probability. Moreover, prior episodes of PE may cause a false-positive result (21).

Magnetic resonance (MR) imaging is an alternative to V-P scanning and helical CT because the fetus is not exposed to ionizing radiation or intravenous contrast material. Moreover, the sensitivity (90%) and specificity (77%) of MR are similar to those of helical CT for the diagnosis of PE (22). However, for this application, long acquisition times are needed, as well as respiratory and cardiac gating, and even then spatial resolution is relatively poor. Availability of this MR protocol is limited as well.

Because clinicians are reluctant to order additional imaging tests in pregnant women following an inconclusive V-P scan, we believe that it is important for them to recognize that helical CT is not only safe during pregnancy but also accurate for the diagnosis of PE in main, lobar, and segmental pulmonary arteries. Accurate diagnosis is critical, because there is substantial risk of morbidity to both mother and fetus from treatment. The recommended therapy for DVT and PE during pregnancy is intravenously administered heparin for 5–10 days, followed by subcutaneously administered heparin for the remainder of the pregnancy (4).

Postpartum therapy includes combined administration of heparin and warfarin initially, followed by administration of warfarin alone for 6 weeks or until at least 3 months of anticoagulation therapy have been completed (4). DVT prophylaxis must be considered during subsequent pregnancies, as the incidence of recurrent PE during each subsequent pregnancy is 4%–15% (23). Furthermore, a history of PE may preclude the future use of oral contraceptives or hormonal replacement therapy (24).

Although it is desirable to limit fetal radiation exposure, a review of the literature suggests that in utero exposure of up to 50,000 µGy results in a negligible increase in the risk of childhood cancer (4,7). With careful use of available procedures, a diagnosis of PE can be made with exposures of less than 5,000 µGy. For example, even the combination of chest radiography (10 µGy), V-P scanning (370 µGy), helical CT scanning (131 µGy), and pulmonary angiography with a brachial approach (500 µGy) exposes the fetus to approximately 1,000 µGy. This dose is less than that received by the fetus from background radiation (eg, cosmic rays, radon, potassium 40) during the 9 months of pregnancy (1,150–2,550 µGy) (25). By comparison, an exposure of at least 100,000 µGy is necessary before pregnancy termination is considered (26).

In summary, findings in this study show that the average fetal radiation dose with helical CT is less than that with V-P lung scanning during all trimesters. Pregnancy should not preclude use of helical CT for the diagnosis of PE.


    FOOTNOTES
 
Abbreviations: DVT = deep venous thrombosis, PE = pulmonary embolism, V-P = ventilation-perfusion

Author contributions: Guarantor of integrity of entire study, H.T.W.M.; study concepts, G.T.L.; study design, H.T.W.M., J.M.B.; literature research, H.T.W.M., J.M.B.; clinical studies, H.L.B.; experimental studies, J.M.B.; data acquisition, H.L.B., J.M.B.; data analysis/interpretation, H.T.W.M., J.M.B., S.G.J.; statistical analysis, J.M.B.; manuscript preparation, S.G.J., H.T.W.M.; manuscript definition of intellectual content, H.T.W.M., J.M.B.; manuscript editing, J.M.B., H.T.W.M., S.G.J.; manuscript revision/ review, S.G.J., H.T.W.M., W.C.M.; manuscript final version approval, H.T.W.M.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Atrash HK, Rowley D, Hogue CJR. Maternal and perinatal mortality. Curr Opin Obstet Gynecol 1992; 4:61-71.[Medline]
  2. Barbour LA, Pickard J. Controversies in thromboembolic disease during pregnancy: a critical review. Obstet Gynecol 1995; 86:621-633.[Medline]
  3. NIH Consensus Development. Prevention of venous thrombosis and pulmonary embolism. JAMA 1986; 256:744-749.[Abstract/Free Full Text]
  4. Toglia MR, Weg JG. Venous thromboembolism during pregnancy. N Engl J Med 1996; 335:108-114.[Free Full Text]
  5. Wessler S. Medical management of venous thrombosis. Ann Rev Med 1976; 27:313-319.[CrossRef][Medline]
  6. Demers C, Ginsberg JS. Deep venous thrombosis and pulmonary embolism in pregnancy. Clin Chest Med 1992; 13:645-656.[Medline]
  7. Ginsberg JS, Hirsh J, Rainbow AJ, et al. Risks to the fetus of radiologic procedures used in the diagnosis of maternal venous thromboembolic disease. Thromb Haemost 1989; 61:189-196.[Medline]
  8. Russell JR, Stabin MG, Sparks RB, et al. Radiation absorbed dose to the embryo/fetus from radiopharmaceuticals. Health Phys 1997; 73:756-769.[Medline]
  9. Boiselle PM, Reddy SS, Villas PA, et al. Pulmonary embolus in pregnant patients: survey of ventilation-perfusion imaging policies and practices. Radiology 1998; 207:201-206.[Abstract/Free Full Text]
  10. Balan KK, Critchley M, Vedavathy KK, et al. The value of ventilation-perfusion imaging in pregnancy. Br J Radiol 1997; 70:338-340.[Abstract]
  11. Boone JM, Buonocore MH, Cooper VN. Monte Carlo validation in diagnostic radiological imaging. Med Phys 2000; 27:1294-1304.[CrossRef][Medline]
  12. Boone JM, Cooper VN, Nemzek WR, McGahan JP, Seibert JA. Monte Carlo assessment of computed tomography dose to tissue adjacent to the scanned volume. Med Phys 2000; 27:2393-2407.[CrossRef][Medline]
  13. Boone JM, Seibert JA. An accurate method for computer-generating tungsten anode x-ray spectra from 30 kV to 140 kV. Med Phys 1997; 24:1661-1670.[CrossRef][Medline]
  14. Caon M, Bibbo G, Pattison J. A comparison of radiation dose measured in CT dosimetry phantoms with calculations using EGS4 and voxel-based computational models. Phys Med Biol 1997; 42:219- 229.[CrossRef][Medline]
  15. Huda W, Atherton JV, Ware DE, et al. An approach for the estimation of effective radiation dose at CT in pediatric patients. Radiology 1997; 203:417-422.[Abstract/Free Full Text]
  16. Sharp C, Shrimpton JA, Bury RF. Diagnostic medical exposures: advice on exposure to ionizing radiation during pregnancy Chilton Didcot, Oxon, United Kingdom: National Radiological Protection Board, 1998.
  17. Shrimpton PC, Jones DG, Hillier MC, Wall BF, Le Heron JC, Faulkner K. Survey of CT practice in the UK 2. Dosimetric aspects—National Radiological Protection Board report 249. London, England: HMSO, 1991.
  18. Ryu JH, Swensen SJ, Olson EJ, et al. Diagnosis of pulmonary embolism with use of computed tomographic angiography. Mayo Clin Proc 2001; 76:59-65.[Abstract]
  19. Blachere H, Latrabe V, Montaudon M, et al. Pulmonary embolism reveal on helical CT angiography: comparison with ventilation-perfusion radionuclide lung scanning. AJR Am J Roentgenol 2000; 174:1041-1047.[Abstract/Free Full Text]
  20. Morisetti A, Tirone P, Luzzani F, et al. Toxicological safety assessment of iomeprol, a new x-ray contrast agent. Eur J Radiol 1994; 18(suppl 1):S21-S31.
  21. (PIOPED)—the PIOPED investigators. Value of the ventilation/perfusion scan in acute pulmonary embolism: results of the prospective investigation of pulmonary embolism diagnosis. JAMA 1990; 263:2753-2759.[Abstract/Free Full Text]
  22. Erdman WA, Clarke GD. Magnetic resonance imaging of pulmonary embolism. Semin Ultrasound CT MR 1997; 18:338-348.[CrossRef][Medline]
  23. Tengborn L, Bergqvist D, Matzsch T, et al. Recurrent thromboembolism in pregnancy and puerperium: is there a need for thromboprophylaxis? Am J Obstet Gynecol 1989; 160:90-94.[Medline]
  24. Speroff L, Glass RH, Kase NG. Oral contraception In: Clinical gynecologic endocrinology and infertility. 5th ed. Baltimore, Md: Williams & Wilkins, 1994; 715-763.
  25. National Council on Radiation Protection. Exposure of the population in the United States and Canada from natural background radiation. Report 94 Bethesda, Md: National Council on Radiation Protection, 1987.
  26. Pregnancy and medical radiation: International Commission on Radiological Protection. Ann ICRP 2000; 30:1-43.



This article has been cited by other articles:


Home page
RadioGraphicsHome page
J. K. Pahade, D. Litmanovich, I. Pedrosa, J. Romero, A. A. Bankier, and P. M. Boiselle
Quality Initiatives: Imaging Pregnant Patients with Suspected Pulmonary Embolism: What the Radiologist Needs to Know
RadioGraphics, May 1, 2009; 29(3): 639 - 654.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
L. Larson, M. Miller, N. Mehta, S. Dholakia, N. de Mendonca, M. Hayes, G. Bourjeily, K. Rosene-Montella, N. Hoftman, P. E. Marik, et al.
Venous Thromboembolic Disease and Pregnancy
N. Engl. J. Med., February 5, 2009; 360(6): 638 - 640.
[Full Text] [PDF]


Home page
NEJMHome page
P. E. Marik and L. A. Plante
Venous Thromboembolic Disease and Pregnancy
N. Engl. J. Med., November 6, 2008; 359(19): 2025 - 2033.
[Full Text] [PDF]


Home page
Eur Heart JHome page
Authors/Task Force Members, A. Torbicki, A. Perrier, S. Konstantinides, G. Agnelli, N. Galie, P. Pruszczyk, F. Bengel, A. J.B. Brady, D. Ferreira, et al.
Guidelines on the diagnosis and management of acute pulmonary embolism: The Task Force for the Diagnosis and Management of Acute Pulmonary Embolism of the European Society of Cardiology (ESC)
Eur. Heart J., September 2, 2008; 29(18): 2276 - 2315.
[Full Text] [PDF]


Home page
Br. J. Radiol.Home page
S K DOSHI, I S NEGUS, and J M ODUKO
Fetal radiation dose from CT pulmonary angiography in late pregnancy: a phantom study
Br. J. Radiol., August 1, 2008; 81(968): 653 - 658.
[Abstract] [Full Text] [PDF]


Home page
JAMAHome page
M. D. Siegel
Evaluation of Suspected Pulmonary Embolism During Pregnancy
JAMA, April 9, 2008; 299(14): 1665 - 1665.
[Full Text] [PDF]


Home page
JAMAHome page
J. Glassroth
Evaluation of Suspected Pulmonary Embolism During Pregnancy--Reply
JAMA, April 9, 2008; 299(14): 1665 - 1666.
[Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
T. A. Jaffe, T. T. Yoshizumi, G. I. Toncheva, G. Nguyen, L. M. Hurwitz, and R. C. Nelson
Early First-Trimester Fetal Radiation Dose Estimation in 16-MDCT Without and With Automated Tube Current Modulation
Am. J. Roentgenol., April 1, 2008; 190(4): 860 - 864.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
I. Sechopoulos, S. Suryanarayanan, S. Vedantham, C. J. D'Orsi, and A. Karellas
Radiation Dose to Organs and Tissues from Mammography: Monte Carlo and Phantom Study
Radiology, December 4, 2007; (2007) 2462070256.
[Abstract] [Full Text]


Home page
RadioGraphicsHome page
S. J. Patel, D. L. Reede, D. S. Katz, R. Subramaniam, and J. K. Amorosa
Imaging the Pregnant Patient for Nonobstetric Conditions: Algorithms and Radiation Dose Considerations
RadioGraphics, November 1, 2007; 27(6): 1705 - 1722.
[Abstract] [Full Text] [PDF]


Home page
RadioGraphicsHome page
C. H. McCollough, B. A. Schueler, T. D. Atwell, N. N. Braun, D. M. Regner, D. L. Brown, and A. J. LeRoy
Radiation Exposure and Pregnancy: When Should We Be Concerned?
RadioGraphics, July 1, 2007; 27(4): 909 - 917.
[Abstract] [Full Text] [PDF]


Home page
BMJHome page
A. F. Scarsbrook and F. V. Gleeson
Investigating suspected pulmonary embolism in pregnancy
BMJ, February 24, 2007; 334(7590): 418 - 419.
[Full Text] [PDF]


Home page
CMAJHome page
A. Mohamed, G. K. Dresser, and S. Mehta
Acute respiratory failure during pregnancy: a case of nitrofurantoin-induced pneumonitis
Can. Med. Assoc. J., January 30, 2007; 176(3): 319 - 320.
[Full Text] [PDF]


Home page
The Obstetrician and GynaecologistHome page
F. Asghar and P. Bowman
A clinical approach to the management of thrombosis in obstetrics. Part 2: diagnosis and treatment of venous thromboembolism
Obstet Gynaecol (Lond), January 1, 2007; 9(1): 3 - 8.
[Abstract] [Full Text] [PDF]


Home page
J Intensive Care MedHome page
J. M. Shapiro
Critical Care of the Obstetric Patient
J Intensive Care Med, September 1, 2006; 21(5): 278 - 286.
[Abstract] [PDF]


Home page
RadiologyHome page
A. M. Groves, S. J. Yates, T. Win, I. Kayani, F. A. Gallagher, R. Syed, J. Bomanji, and P. J. Ell
CT Pulmonary Angiography versus Ventilation-Perfusion Scintigraphy in Pregnancy: Implications from a UK Survey of Doctors' Knowledge of Radiation Exposure
Radiology, September 1, 2006; 240(3): 765 - 770.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
D. K. Yousefzadeh, M. B. Ward, and C. Reft
Internal Barium Shielding to Minimize Fetal Irradiation in Spiral Chest CT: A Phantom Simulation Experiment.
Radiology, June 1, 2006; 239(3): 751 - 758.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Radiol.Home page
S Matthews
Imaging pulmonary embolism in pregnancy: what is the most appropriate imaging protocol?
Br. J. Radiol., May 1, 2006; 79(941): 441 - 444.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
L. M. Hurwitz, T. Yoshizumi, R. E. Reiman, P. C. Goodman, E. K. Paulson, D. P. Frush, G. Toncheva, G. Nguyen, and L. Barnes
Radiation Dose to the Fetus from Body MDCT During Early Gestation.
Am. J. Roentgenol., March 1, 2006; 186(3): 871 - 876.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
S. Patel and E. A. Kazerooni
Helical CT for the Evaluation of Acute Pulmonary Embolism
Am. J. Roentgenol., July 1, 2005; 185(1): 135 - 149.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Radiol.Home page
J H Reid
Multislice CT pulmonary angiography and CT venography
Br. J. Radiol., December 1, 2004; 77(suppl_1): S39 - S45.
[Abstract] [Full Text] [PDF]


Home page
ImagingHome page
C Hill and E J R van Beek
MRI of the chest: present and future
Imaging, October 1, 2004; 16(1): 61 - 70.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
M. E. Schuster, J. E. Fishman, J. F. Copeland, H. Hatabu, and P. M. Boiselle
Pulmonary Embolism in Pregnant Patients: A Survey of Practices and Policies for CT Pulmonary Angiography
Am. J. Roentgenol., December 1, 2003; 181(6): 1495 - 1498.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2242011581v1
224/2/487    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Winer-Muram, H. T.
Right arrow Articles by Lombardo, G. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Winer-Muram, H. T.
Right arrow Articles by Lombardo, G. T.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
RADIOLOGY RADIOGRAPHICS RSNA JOURNALS ONLINE