Comparison of gonadal radiation doses from CT enterography and small-bowel follow-through in pediatric patients.

OBJECTIVE. CT enterography is superior to small-bowel follow-through (SBFT) for diagnosis of inflammatory bowel disease (IBD). It is widely assumed that the radiation dose from CT enterography is greater than that from SBFT in the pediatric patient. This study was designed to compare gonadal doses from CT enterography and SBFT to verify the best imaging choice for IBD evaluation in children. This study also challenges the assumption that CT enterography imparts a higher radiation dose through comparison of calculated radiation doses from CT enterography and SBFT. MATERIALS AND METHODS. Patients 0-18 years old who underwent either CT enterography or SBFT over a 2-year period were included. The CT enterography group consisted of 39 boys and 51 girls, whereas the SBFT group consisted of 89 boys and 113 girls. CT enterography was performed at 120 kVp and approximately 132 mAs (range, 54-330 mAs) using weight-based protocols. SBFT used automated control of kilovoltage and tube current-exposure time product. Patient demographics and technical parameters were collected for CT enterography and SBFT, data were cross-paired between CT enterography and SBFT, and gonadal dose was calculated. RESULTS. Mean (± SD) CT enterography testis and ovarian doses were 0.93 ± 0.3 cGy (n = 39) and 0.64 ± 0.2 cGy (n = 51), respectively. Mean SBFT testis and ovarian doses were 2.3 ± 1.6 cGy (n = 89) and 1.49 ± 0.3 cGy (n = 113), respectively. Mean fluoroscopy time for SBFT was 2.6 ± 2 minutes. Gonadal dose for CT enterography was significantly lower than that for SBFT in boys and girls (p < 0.001). SBFT dose was lower in girls than boys (p < 0.001), whereas CT enterography dose was higher in boys than girls (p < 0.001). CONCLUSION. Gonadal dose for CT enterography was lower than that for SBFT for boys and girls of all sizes and age. Controlled exposure time made CT enterography dose more consistent, whereas the range of dose for SBFT was highly operator dependent and related to extent of disease. Thus, for IBD, CT enterography is preferred over SBFT for all children.

Optimization of kilovoltage and tube current-exposure time product based on abdominal circumference: an oval phantom study for pediatric abdominal CT.

OBJECTIVE: This CT study evaluates image noise and radiation dose using a modified CT dose index phantom to approximate pediatric abdominal shape. Contrast-to-noise ratio (CNR) and radiation dose were measured. MATERIALS AND METHODS: The oval shape was simulated by fixing 1000-mL saline bags aside cylindric phantoms with variable circumferences. The doses at the center and peripheral holes in the phantom were recorded. Measurements were obtained at 50-400 mAs and 80-140 kVp. Diluted iodine contrast agent filled the center hole, and distilled water filled the peripheral holes. CNR was defined as the difference in CT number between diluted iodine and water divided by the standard deviation (SD) of CT number of water. RESULTS: Dose increased linearly with increases in tube current-exposure time product and by a power function (proportional to kVp(n), where n = 2.64-3.09) for increases in kilovoltage. A range of scanning parameters was established for each circumference from which technique optimization curves were created to determine the best tube current-time product and kilovoltage pairs when noise was less than 20 HU and dose was less than 2.5 cGy. CNR increased by 40% as kilovoltage was reduced from 140 to 80 kVp. A dose reduction of 70% was observed for 140 versus 80 kVp for the same CNR. CONCLUSION: Because pediatric patients of the same age and weight come in all shapes and sizes, abdominal circumference is a useful clinical parameter on which to base CT scan techniques controlling radiation output--namely kilovoltage and tube current-time product. Low-kilovoltage techniques for patients with small circumference show better iodine CNR.

Comparison of indirect radiation dose estimates with directly measured radiation dose for patients and operators during complex endovascular procedures.

BACKGROUND: A great deal of attention has been directed at the necessity and potential for deleterious outcomes as a result of radiation exposure during diagnostic evaluations and interventional procedures. We embarked on this study in an attempt to accurately determine the amount of radiation exposure given to patients undergoing complex endovascular aortic repair. These measured doses were then correlated with radiation dose estimates provided by the imaging equipment manufacturers that are typically used for documentation and analysis of radiation-induced risk. METHODS: Consecutive patients undergoing endovascular thoracoabdominal aneurysm (eTAAA) repair were prospectively studied with respect to radiation dose. Indirect parameters as cumulative air kerma (CAK), kerma area product (KAP), and fluoroscopy time (FT) were recorded concurrently with direct measurements of dose (peak skin dose [PSD]) and radiation exposure patterns using radiochromatic film placed in the back of the patient during the procedure. Simultaneously, operator exposure was determined using high-sensitivity electronic dosimeters. Correlation between the indirect and direct parameters was calculated. The observed radiation exposure pattern was reproduced in phantoms with over 200 dosimeters located in mock organs, and effective dose has been calculated in an in vitro study. Scatter plots were used to evaluate the relationship between continuous variables and Pearson coefficients. RESULTS: eTAAA repair was performed in 54 patients over 5 months, of which 47 had the repair limited to the thoracoabdominal segment. Clinical follow-up was complete in 98% of the patients. No patients had evidence of radiation-induced skin injury. CAK exceeded 15 Gy in 3 patients (the Joint Commission on Accreditation of Healthcare Organizations [JCAHO] threshold for sentinel events); however, the direct measurements were well below 15 Gy in all patients. PSD was measured by quantifying the exposure of the radiochromatic film. PSD correlated weakly with FT but better with CAK and KAP (r = 0.55, 0.80, and 0.76, respectively). The following formula provides the best estimate of actual PSD = 0.677 + 0.257 CAK. The average effective dose was 119.68 mSv (for type II or III eTAAA) and 76.46 mSv (type IV eTAAA). The operator effective dose averaged 0.17 mSv/case and correlated best with the KAP (r = 0.82, P < .0001). CONCLUSION: FT cannot be used to estimate PSD, and CAK and KAP represent poor surrogate markers for JCAHO-defined sentinel events. Even when directly measured PSDs were used, there was a poor correlation with clinical event (no skin injuries with an average PSD >2 Gy). The effective radiation dose of an eTAAA is equivalent to two preoperative computed tomography scans. The maximal operator exposure is 50 mSv/year, thus, a single operator could perform up to 294 eTAAA procedures annually before reaching the recommended maximum operator dose.

Optimization of kVp and mAs for pediatric low-dose simulated abdominal CT: is it best to base parameter selection on object circumference?

OBJECTIVE: The objective of our study was to determine the effect of mAs and kVp reduction on pediatric phantoms based on patient circumference to optimize dose reduction and maintain image quality for abdominal CT. SUBJECTS AND METHODS: Three polymethylmethacrylate right cylindric CT dose index (CTDI) phantoms with diameters of 10, 16, and 32 cm simulated the abdomen of an infant, child, and adolescent, respectively. Using a National Institute of Standards & Technology ion chamber and Victoreen 660 electrometer, doses at centerline were recorded on a 16-MDCT scanner. Measurements were obtained in incremental steps from 50 to 400 mAs and from 80 to 140 kVp. Noise was calibrated to clinical images through a calibration factor. RESULTS: For phantoms of all circumferences, doses increased linearly with an increase in mAs and by the power function of kVp(n) for increases in kVp. There was an associated decrease in noise for all circumferences and a sharp decrease at lower doses with a plateau at higher doses. Using a noise threshold of 20 HU and a dose threshold of 2.5 cGy, a range of imaging parameters was established for each circumference from which technique optimization curves were created to determine optimal mAs and kVp pairs. The mean measured dose was 2.435 ± 0.019 cGy. The mean measured noise was 29.35 ± 1.45 HU. CONCLUSION: For pediatric CT, the most accurate way to strike the balance between image quality and radiation dose is to adjust dose to abdominal circumference, not body weight or age. Our data support the use of technique optimization curves to optimize kVp and mAs.

Effect of altering automatic exposure control settings and quality reference mAs on radiation dose, image quality, and diagnostic efficacy in MDCT enterography of active inflammatory Crohn's disease.

OBJECTIVE: The purpose of our study was to determine whether the MDCT enterography dose can be reduced by changing automatic exposure control (AEC) setting and quality reference milliampere-seconds (mAs) without altering subjective image quality or efficacy in active inflammatory Crohn's disease. SUBJECTS AND METHODS: This is a prospective study of 2,310 MDCT enterography procedures performed using 16- and 64-MDCT in three cohorts (original, intermediate, and final dose levels). For 16-MDCT, the original and intermediate dose level quality reference mAs was 200, and weight-based (1 pound [0.45 kg] = 1 mAs) for the final dose level. For 64-MDCT, the original dose level quality reference mAs was 260; the mAs was 220 for intermediate and weight-based for the final dose level. For the intermediate and final dose levels, AEC was changed from strong to weak increase for obese and weak to strong decrease for slim patients. Demographic data and volume CT dose index (CTDI(vol)) were analyzed. Three readers evaluated the cases for image quality and efficacy differentiating normal from active inflammatory Crohn's disease. RESULTS: For 16-MDCT, CTDI(vol) decreased from 12.82 to 10.14 mGy and 10.14 to 8.7 mGy between original to intermediate and intermediate to final dose levels. For 64-MDCT, the CTDI(vol) decreased from 15.72 to 11.42 mGy and 11.42 to 9.25 mGy between original to intermediate and intermediate to final dose levels. Images were rated suboptimal or nondiagnostic more often in the intermediate dose level (p < 0.05) but not in the final. There was no reduction in diagnostic efficacy as measured by area under the ROC curve (p > 0.1443 except for one comparison with one reader). CONCLUSION: Substantial dose reduction can be achieved using weight-based quality reference mAs and altering AEC settings without affecting diagnostic efficacy in active inflammatory Crohn's disease of the terminal ileum. However, subjective image quality can be compromised at these dose settings, depending on radiologist preference.

CT arthrography: in vitro evaluation of single and dual energy for optimization of technique.

The purpose of this study was to optimize CT arthrography technique and determine if dual energy CT (DECT) can provide any benefit over single energy CT (SECT). Iodinated contrast attenuation at different concentrations was measured using DECT and SECT at different beam energies (140, 120, and 80 kVp). Dose and noise were measured on phantoms at different tube currents. Three bovine femoral condyles with artificially created cartilage defects were scanned with dose-equivalent protocols. Contrast-to-noise ratio (CNR) between cartilage and iodine was measured, and the appearance of cartilage defects was graded by two readers. DECT scans were post-processed for iodine quantification. The beam energy 80 kVp had the highest iodine signal, 50% greater than DECT, 75% greater than 120 kVp, and 100% greater than 140 kVp. Noise was nearly identical for all techniques when dose was matched. The 80 kVp level had the highest CNR, 25% higher than 120 kVp and DECT, and 33% greater than 140 kVp. The 80 kVp technique was also preferred by both readers. DECT iodine quantification was significantly limited by the post-processing application, noise, and beam hardening. In this in-vitro study, the SECT 80 kVp CT arthrography technique was superior to currently performed 120 and 140 kVP SECT techniques and DECT.

Rheumatoid arthritis: evaluation with contrast-enhanced CT with digital bone masking.

The purpose of this HIPAA-compliant study was to prospectively evaluate the feasibility of contrast material-enhanced computed tomography (CT) with digital bone masking for the evaluation of synovitis and tenosynovitis in patients with rheumatoid arthritis. Four patients with rheumatoid arthritis and findings at magnetic resonance (MR) imaging were evaluated after informed consent for this institutional review board-approved study was obtained. To improve the conspicuity of synovial enhancement, postcontrast CT was performed with a relatively low kilovoltage and high iodine concentration and precontrast images were used as a subtraction mask to eliminate high-attenuation cortical bone contours. Moderate to high agreement between CT and MR imaging findings for synovitis and tenosynovitis was demonstrated, which suggests that this technique may be an acceptable alternative to MR imaging in the evaluation of rheumatoid arthritis.

Imaging characteristics of zinc sulfide shell, cadmium telluride core quantum dots.

AIMS: Quantum dots are optical nanocrystals whose in vitro and in vivo use in molecular imaging is expanding rapidly. In comparison with organic fluorophores, quantum dots exhibit desirable properties, such as multiwavelength fluorescence emission, excellent brightness and resistance to photobleaching. Their electron-dense, metallic cores suggest utility in other clinical imaging modalities. METHODS: Core-shell zinc sulfide-cadmium telluride quantum dots were studied by magnetic resonance and computed tomography phantoms. Quantum dots were also injected into rat brain, as well as intravenously, using convection-enhanced delivery, prior to animal imaging. RESULTS: Computed tomography studies suggest that current formulations of quantum dots might be imaged in vivo in animals. CONCLUSIONS: Used in conjunction with optical imaging techniques, quantum dots have the potential to function as multimodal imaging platforms in vivo. The ability to detect an optical nanoparticle preoperatively with clinical imaging modality offers a distinct advantage to clinicians engaged in image-guided surgical applications.

Radiation exposure to the surgeon and the patient during kyphoplasty.

STUDY DESIGN: Prospective study of patients who underwent single or multilevel kyphoplasty for vertebral fractures. OBJECTIVE: To quantify the radiation exposure to the surgeon and to the patient during kyphoplasty, and also to provide a procedural algorithm that effectively minimizes the radiation exposure to the surgeon during any fluoroscopic-guided procedure. SUMMARY OF BACKGROUND DATA: Spine surgeons who perform minimally invasive procedures often employ fluoroscopy for intraoperative navigation. METHODS: Twenty-seven patients were enrolled. Two fluoroscopes (1 anterior/posterior and 1 lateral) were used for localization, navigation, and monitoring cement flow. All surgeons wore thyroid shields and lead aprons. The dose of radiation exposure was measured by dosimeter badges. One badge was attached to each patient. The surgeons wore 3 badges: under the thyroid shield (protected), under the lead apron over the left chest (protected), and outside the lead apron over the left chest (unprotected). A thermoluminescent ring dosimeter was worn on the right hand for 18 cases, and on the left hand for 9 cases. RESULTS: The exposure time was 5.7+/-2.0 minutes/vertebra for a single level (n=10), 3.9+/-0.8 minutes/vertebra for a 2 level (n=9), 2.9+/-1.2 minutes/vertebra for a 3 level kypholasty (n=8). The exposure time of single level kyphoplasy was significantly different from that of multilevel kyphoplasy (2 level, P=0.040; 3 level, P=0.002). Surgeon exposure as measured by the protected dosimeter was less than the minimum reportable dose (<0.010 mSv). Exposure as measured by the unprotected dosimeter, which is equivalent to deep whole body exposure was 0.248+/-0.170 mSv/vertebra. The eye exposure was 0.271+/-0.200 mSv/vertebra, and the shallow exposure (hand/skin) was 0.273+/-0.200 mSv/vertebra. The hand exposure was 1.744+/-1.173 mSv/vertebra. CONCLUSIONS: Without eye or hand protection, the total radiation exposure dose to these areas would exceed the occupational exposure limit after 300 cases per year. Surgeons should wear lead lined glasses and keep their hands out of the radiation beam.

Sealing of type III endoleaks with ethylene vinyl alcohol copolymer in a canine model.

PURPOSE: To test ethylene vinyl alcohol copolymer (EVOH) as a sealing agent for persistent abdominal aortic aneurysm (AAA) endograft leaks. MATERIALS AND METHODS: Twelve dogs underwent creation of AAAs with a Palmaz P4014 stent. A 10-mm x 5-cm Wallgraft endoprosthesis with a 4-mm-diameter hole cut into its side was deployed within the AAA. One week later, computed tomography (CT) and angiography were performed and the aneurysm sac was catheterized through the 4-mm hole. Then, EVOH was injected into the sac and lumbar arteries. Four weeks thereafter, all surviving animals underwent repeat CT scanning and angiography and were then euthanized. The AAA underwent gross and microscopic study. RESULTS: Three dogs died from aortic rupture within 24 hours of AAA creation and the remaining nine dogs survived to receive EVOH. All nine dogs had persistent flow into the sac and lumbar arteries at the time of EVOH delivery. Seven dogs survived to the end of the experiment, and all aneurysm sacs and lumbar arteries remained occluded on angiography and CT. Histologic examination revealed EVOH and thrombus admixed, with thrombus in varying stages of organization filling the aneurysm sac and lumbar arteries. CONCLUSIONS: Embolization of type III endoleaks with EVOH proved to be feasible in a canine model. Further work is warranted to determine its therapeutic utility.

Diagnostic imaging: radiation dose and patients' concerns.

Exposure to ionizing radiation during diagnostic radiologic procedures carries small but real risks, and children, young adults, and pregnant women are especially vulnerable. Exposure of patients to diagnostic energy levels of ionizing radiation should be kept to the minimum necessary to provide useful clinical information and allay patients' concerns about radiation-related risks.

Selective retention of bone marrow-derived cells to enhance spinal fusion.

Connective tissue progenitors can be concentrated rapidly from fresh bone marrow aspirates using some porous matrices as a surface for cell attachment and selective retention, and for creating a cellular graft that is enriched with respect to the number of progenitor cells. We evaluated the potential value of this method using demineralized cortical bone powder as the matrix. Matrix alone, matrix plus marrow, and matrix enriched with marrow cells were compared in an established canine spinal fusion model. Fusions were compared based on union score, fusion mass, fusion volume, and by mechanical testing. Enriched matrix grafts delivered a mean of 2.3 times more cells and approximately 5.6 times more progenitors than matrix mixed with bone marrow. The union score with enriched matrix was superior to matrix alone and matrix plus marrow. Fusion volume and fusion area also were greater with the enriched matrix. These data suggest that the strategy of selective retention provides a rapid, simple, and effective method for concentration and delivery of marrow-derived cells and connective tissue progenitors that may improve the outcome of bone grafting procedures in various clinical settings.

Spine fusion using cell matrix composites enriched in bone marrow-derived cells.

Bone marrow-derived cells including osteoblastic progenitors can be concentrated rapidly from bone marrow aspirates using the surface of selected implantable matrices for selective cell attachment. Concentration of cells in this way to produce an enriched cellular composite graft improves graft efficacy. The current study was designed to test the hypothesis that the biologic milieu of a bone marrow clot will significantly improve the efficacy of such a graft. An established posterior spinal fusion model and cancellous bone matrix was used to compare an enriched cellular composite bone graft alone, bone matrix plus bone marrow clot, and an enriched bone matrix composite graft plus bone marrow clot. Union score, quantitative computed tomography, and mechanical testing were used to define outcome. The union score for the enriched bone matrix plus bone marrow clot composite was superior to the enriched bone matrix alone and the bone matrix plus bone marrow clot. The enriched bone matrix plus bone marrow clot composite also was superior to the enriched bone matrix alone in fusion volume and in fusion area. These data confirm that the addition of a bone marrow clot to an enriched cell-matrix composite graft results in significant improvement in graft performance. Enriched composite grafts prepared using this strategy provide a rapid, simple, safe, and inexpensive method for intraoperative concentration and delivery of bone marrow-derived cells and connective tissue progenitors that may improve the outcome of bone grafting.