RÉSUMÉ
In X-ray breast imaging, Digital Mammography (DM) and Digital Breast Tomosynthesis (DBT), are the standard and largely used techniques, both for diagnostic and screening purposes. Other techniques, such as dedicated Breast Computed Tomography (BCT) and Contrast Enhanced Mammography (CEM) have been developed as an alternative or a complementary technique to the established ones. The performance of these imaging techniques is being continuously assessed to improve the image quality and to reduce the radiation dose. These imaging modalities are predominantly used in the diagnostic setting to resolve incomplete or indeterminate findings detected with conventional screening examinations and could potentially be used either as an adjunct or as a primary screening tool in select populations, such as for women with dense breasts. The aim of this review is to describe the radiation dosimetry for these imaging techniques, and to compare the mean glandular dose with standard breast imaging modalities, such as DM and DBT.
Sujet(s)
Tumeurs du sein , Région mammaire , Région mammaire/imagerie diagnostique , Densité mammaire , Tumeurs du sein/imagerie diagnostique , Femelle , Humains , Mammographie/méthodes , Radiométrie/méthodes , Rayons XRÉSUMÉ
According to the World Health Organization (WHO), at the end of 2020, 7.8 million women alive were diagnosed with breast cancer in the past 5 years, making it the world's most prevalent cancer. It is largely recognized and demonstrated that early detection represents the first strategy to follow in the fight against cancer. The effectiveness of mammography screening for early breast cancer detection has been proven in several surveys and studies over the last three decades. The estimation of the Mean Glandular Dose (MGD) is important to understand the radiation-associated risk from breast x-ray imaging exams. It continues to be the subject of numerous studies and debates, since its accuracy is directly related to risk estimation and for optimizing breast cancer screening programs. This manuscript reviews the main dosimetry formalisms used to estimate the MGD in mammography and to understand the continuing efforts to reduce the absorbed dose over the last forty years. The dosimetry protocols were formulated initially for mammography. Digital breast tomosynthesis (DBT) either in conjunction with synthesized digital mammogram (SDM) or with digital mammography (DM), is routinely used in many breast cancer screening programs and consequently the dosimetry protocols were extended for these techniques.
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Tumeurs du sein , Région mammaire/imagerie diagnostique , Tumeurs du sein/imagerie diagnostique , Dépistage précoce du cancer/méthodes , Femelle , Humains , Mammographie/méthodes , Dépistage de masse , Rayons XRÉSUMÉ
BACKGROUND AND PURPOSE: Advancements in medical device and imaging technology as well as accruing clinical evidence have accelerated the growth of the endovascular treatment of cerebrovascular diseases. However, the augmented role of these procedures raises concerns about the radiation dose to patients and operators. We evaluated patient doses from an x-ray imaging platform with radiation dose-reduction technology, which combined image noise reduction, motion correction, and contrast-dependent temporal averaging with optimized x-ray exposure settings. MATERIALS AND METHODS: In this single-center, retrospective study, cumulative dose-area product inclusive of fluoroscopy, angiography, and 3D acquisitions for all neurovascular procedures performed during a 2-year period on the dose-reduction platform were compared with a reference platform. Key study features were the following: The neurointerventional radiologist could select the targeted dose reduction for each patient with the dose-reduction platform, and the statistical analyses included patient characteristics and the neurointerventional radiologist as covariates. The analyzed outcome measures were cumulative dose (kerma)-area product, fluoroscopy duration, and administered contrast volume. RESULTS: A total of 1238 neurointerventional cases were included, of which 914 and 324 were performed on the reference and dose-reduction platforms, respectively. Over all diagnostic and neurointerventional procedures, the cumulative dose-area product was significantly reduced by 53.2% (mean reduction, 160.3 Gy × cm2; P < .0001), fluoroscopy duration was marginally significantly increased (mean increase, 5.2 minutes; P = .0491), and contrast volume was nonsignificantly increased (mean increase, 15.3 mL; P = .1616) with the dose-reduction platform. CONCLUSIONS: A significant reduction in patient radiation dose is achievable during neurovascular procedures by using dose-reduction technology with a minimal impact on workflow.
Sujet(s)
Angiographie de soustraction digitale/méthodes , Angiographie cérébrale/méthodes , Angiopathies intracrâniennes/chirurgie , Procédures endovasculaires/méthodes , Radiographie interventionnelle/méthodes , Sujet âgé , Angiopathies intracrâniennes/imagerie diagnostique , Femelle , Radioscopie/méthodes , Humains , Mâle , Adulte d'âge moyen , Dose de rayonnement , Exposition aux rayonnements , Études rétrospectives , Rayons XRÉSUMÉ
BACKGROUND AND PURPOSE: Flow diverters for the treatment of posterior circulation aneurysms remain controversial. We aimed to identify factors contributing to outcome measures in patients treated with the Surpass flow diverter for aneurysms in this location. MATERIALS AND METHODS: We conducted an observational study of 53 patients who underwent flow-diverter treatment for posterior circulation aneurysms at 15 centers. Key outcome measures were mortality, complete aneurysm occlusion, and modified Rankin Scale score at follow-up. RESULTS: At follow-up (median, 11.3 months; interquartile range, 5.9-12.7 months), 9 patients had died, resulting in an all-cause mortality rate of 17.3% (95% CI, 7%-27.6%); 7 deaths (14%) were directly related to the procedure and none occurred in patients with a baseline mRS score of zero. After adjusting for covariates, a baseline mRS of 3-5 was more significantly (P = .003) associated with a higher hazard ratio for death than a baseline mRS of 0-2 (hazard ratio, 17.11; 95% CI, 2.69-109.02). After adjusting for follow-up duration, a 1-point increase in the baseline mRS was significantly (P < .001) associated with higher values of mRS at follow-up (odds ratio, 2.93; 95% CI, 1.79-4.79). Follow-up angiography in 44 patients (median, 11.3 months; interquartile range, 5.9-12.7 months) showed complete aneurysm occlusion in 29 (66%; 95% CI, 50.1%-79.5%). CONCLUSIONS: Clinical results of flow-diverter treatment of posterior circulation aneurysms depend very much on patient selection. In this study, poorer outcomes were related to the treatment of aneurysms in patients with higher baseline mRS scores. Angiographic results showed a high occlusion rate for this subset of complex aneurysms.
Sujet(s)
Prothèse vasculaire , Anévrysme intracrânien/chirurgie , Artère cérébrale postérieure/chirurgie , Adolescent , Adulte , Sujet âgé , Implantation de prothèses vasculaires/mortalité , Angiographie cérébrale , Embolisation thérapeutique , Femelle , Études de suivi , Humains , Anévrysme intracrânien/imagerie diagnostique , Angiographie par résonance magnétique , Mâle , Adulte d'âge moyen , Artère cérébrale postérieure/imagerie diagnostique , Études rétrospectives , Résultat thérapeutique , Jeune adulteRÉSUMÉ
Advances in image-guided, catheter-based interventions have shown great potential to improve outcomes in patients with venous thromboembolism. Catheter-directed thrombolysis has been shown in one randomized controlled trial to reduce the risk of post-thrombotic syndrome in patients with acute lower extremity deep vein thrombosis; data from a larger national institute of health trial are expected in early 2017. The use of catheter-directed thrombolysis is also being increasingly considered for patients with submassive or massive pulmonary embolism. Preliminary studies suggest that endovascular stent placement and ablative therapies may be used to reduce symptoms and improve quality of life in severely affected patients with established post-thrombotic syndrome. In this article, we summarize the risks and benefits of endovascular venous thromboembolism therapies as currently understood, highlight clinical situations where their benefit may outweigh risks, and describe ongoing and upcoming pivotal research initiatives with multidisciplinary participation.
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Ablation par cathéter , Procédures endovasculaires , Fibrinolytiques/administration et posologie , Embolie pulmonaire/thérapie , Traitement thrombolytique , Thromboembolisme veineux/thérapie , Thrombose veineuse/thérapie , Ablation par cathéter/effets indésirables , Cathétérisme périphérique , Procédures endovasculaires/effets indésirables , Procédures endovasculaires/instrumentation , Fibrinolytiques/effets indésirables , Humains , Sélection de patients , Syndrome post-thrombotique/diagnostic , Syndrome post-thrombotique/thérapie , Embolie pulmonaire/diagnostic , Appréciation des risques , Facteurs de risque , Endoprothèses , Traitement thrombolytique/effets indésirables , Résultat thérapeutique , Thromboembolisme veineux/diagnostic , Thrombose veineuse/diagnosticRÉSUMÉ
BACKGROUND AND PURPOSE: Developments in flat panel angiographic C-arm systems have enabled visualization of both the neurovascular stents and host arteries in great detail, providing complementary spatial information in addition to conventional DSA. However, the visibility of these structures may be impeded by artifacts generated by adjacent radio-attenuating objects. We report on the use of a metal artifact reduction algorithm for high-resolution contrast-enhanced conebeam CT for follow-up imaging of stent-assisted coil embolization. MATERIALS AND METHODS: Contrast-enhanced conebeam CT data were acquired in 25 patients who underwent stent-assisted coiling. Reconstructions were generated with and without metal artifact reduction and were reviewed by 3 experienced neuroradiologists by use of a 3-point scale. RESULTS: With metal artifact reduction, the observers agreed that the visibility had improved by at least 1 point on the scoring scale in >40% of the cases (κ = 0.6) and that the streak artifact was not obscuring surrounding structures in 64% of all cases (κ = 0.6). Metal artifact reduction improved the image quality, which allowed for visibility sufficient for evaluation in 65% of the cases, and was preferred over no metal artifact reduction in 92% (κ = 0.9). Significantly higher scores were given with metal artifact reduction (P < .0001). CONCLUSIONS: Although metal artifact reduction is not capable of fully removing artifacts caused by implants with high x-ray absorption, we have shown that the image quality of contrast-enhanced conebeam CT data are improved drastically. The impact of the artifacts on the visibility varied between cases, and yet the overall visibility of the contrast-enhanced conebeam CT with metal artifact reduction improved in most the cases.
Sujet(s)
Artéfacts , Tomodensitométrie à faisceau conique/instrumentation , Tomodensitométrie à faisceau conique/méthodes , Anévrysme intracrânien/imagerie diagnostique , Anévrysme intracrânien/chirurgie , Endoprothèses , Écrans renforçateurs de rayons X , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Prothèse vasculaire , Humains , Adulte d'âge moyen , Amélioration d'image radiographique/instrumentation , Amélioration d'image radiographique/méthodes , Reproductibilité des résultats , Études rétrospectives , Sensibilité et spécificitéRÉSUMÉ
PURPOSE: Phase contrast breast imaging has the potential to improve visualization of anatomic structures. While the physics is well-understood, there are several choices for implementation. In order to evaluate these choices, it is essential to design a phantom for phase contrast imaging with appropriate breast-equivalent materials. METHODS: Phantoms for mammography use materials that mimic the x-ray attenuation properties of breast tissue. Hence, the refractive index decrement (delta) was determined for breast tissues of varying glandular fraction [Hammerstein, Radiology 130(2):485-91, 1979] for the energy range (5-100 KeV) relevant to mammography and breast CT using XOP software (Version 2.3, ESRF, France) and compared to that of commonly used phantom materials. Delta for 50% and 70% glandular breast-equivalent material (CIRS Inc., Norfolk, VA), solid water, BR-12, polymethyl methacrylate (PMMA), beeswax (C46H92O2, density: 0.97 g/cm3 ) and paraffin wax (C25H52, density: 0.95 g/cm3 ) were determined. Microcalcifications in vivo are either of oxalate or phosphate composition. Delta of calcium oxalate monohydrate (COM) and calcium hydroxyapatite (CH) were determined and compared with that of calcium carbonate, gold and aluminum. RESULTS: In terms of delta, paraffin wax (4% higher) and beeswax (4% higher) best simulated 50% and 100% glandular breast, respectively. Delta of other commonly used phantom materials such as 50% and 70% glandular breast-equivalent material, solid water, and BR-12 were two orders of magnitude higher, and that of PMMA was 28% higher, than 50% glandular breast tissue. For microcalcifications, delta of gold was 4.6 to 6.5 times higher than that of COM and CH, respectively. Delta of aluminum and calcium carbonate were found to straddle that of COM and CH. CONCLUSIONS: For phase contrast imaging, a phantom comprising paraffin wax to simulate 50% glandular background tissue, beeswax to simulate a mass equivalent to 100% glandular tissue, and calcium carbonate or aluminum to simulate microcalcifications is appropriate. Supported in part by the National Institutes of Health (NIH) grants R01 CA128906 and R21 CA134129. The contents are solely the responsibility of the authors and do not represent the official views of the NIH or NCI.
RÉSUMÉ
PURPOSE: To test the hypothesis that the mean skin thickness determined using cone-beam dedicated breast CT varied between breasts with malignant, hyperplasia and benign pathology, and to determine the appropriate skin thickness for Monte Carlo based estimation of normalized glandular dose coefficients. METHODS: Breast skin thickness was estimated in 137 women scheduled for biopsy (BI-RADS 4 or 5), who underwent unilateral cone-beam dedicated CT of the breast to be biopsied, after providing written informed consent and in adherence to an IRB-approved protocol. Pathology results were available for 132 women and there were 38 malignancies. A previously reported method [Huang et al., Med Phys 35(4): 1199-206, 2008] was applied to coronal (transverse) images reconstructed to 0.273 mm voxel size. The accuracy of the method was determined by imaging two phantoms of differing wall thickness and shape. For each breast, the mean, intra-breast standard deviation (SD) and the median skin thickness were computed. The mean skin thickness and associated confidence intervals (CI) in our study population were obtained from the mean skin thickness of each breast. RESULTS: The estimated mean wall thicknesses for both phantoms were within +/-1% of the measured thickness. At the 0.05 level (ANOVA), the skin thickness means did not vary significantly with pathology (p=0.61). For each breast, the median, mean and intra-breast SD, in mm, were in the range [0.87,2.23], [0.87,2.34], and [0.22,0.85], respectively. From all 137 women, the mean +/- inter-breast SD and 95% CI were 1.44+/-0.25 and [1.40,1.48], respectively. CONCLUSIONS: The skin thickness means were not different between breasts with malignant and non-malignant pathology. Our estimate of mean skin thickness is in agreement with a previous report. Skin thickness of approximately 1.45 mm, rather than the standard 4 mm [Wu et al., Radiology 193:83-9, 1994], is appropriate for Monte Carlo based determination of normalized glandular dose coefficients. Supported in part by the National Institutes of Health (NIH) grants R01 CA128906 and R21 CA134129. The contents are solely the responsibility of the authors and do not represent the official views of the NIH or NCI.
RÉSUMÉ
SUMMARY: The post-thrombotic syndrome (PTS) is increasingly recognized to be a common and important complication of deep venous thrombosis (DVT). Because there is no 'gold standard' objective test to establish its presence, PTS is diagnosed primarily on the basis of the presence of typical symptoms and clinical signs in a limb that was affected by DVT. As a wide variety of definitions of PTS have been used by researchers, it is difficult to compare data across studies and to formally combine data in meta-analyses. In a step towards standardization of the measurement of PTS in clinical studies, available scales and evidence to support their utility to diagnose PTS and to classify its severity were reviewed and discussed at the Control of Anticoagulation Subcommittee of the International Society on Thrombosis and Haemostasis (Vienna, July 2008).
Sujet(s)
Jambe/anatomopathologie , Thrombose veineuse/complications , Humains , Incidence , Syndrome , Thrombose veineuse/physiopathologieRÉSUMÉ
OBJECTIVES: Understand the potential consequences of deep vein thrombosis (DVT) in patients undergoing superficial venous interventions, the proper way to assess DVT risk in patients with superficial venous disease and the appropriate management of patients stratified by risk level. METHODS: Review of published literature RESULTS: Because DVT can have major long-term consequences, DVT risk should be assessed as a routine part of the preprocedure evaluation of venous disease. Chronic venous disease may have multiple contributing factors amenable to treatment in both the superficial and deep venous systems. CONCLUSION: Superficial venous interventions should be deferred in patients at particularly high risk for DVT, but may be performed with appropriate countermeasures for DVT prophylaxis in patients at moderate risk.
Sujet(s)
Varices/thérapie , Procédures de chirurgie vasculaire/effets indésirables , Thrombose veineuse/étiologie , Humains , Appréciation des risques , Thrombose veineuse/prévention et contrôleRÉSUMÉ
Spatially coherent fiberoptic plates are important components of some charge-coupled device (CCD)-based x-ray imaging systems. These plates efficiently transmit scintillations from the phosphor, and also filter out x-rays not absorbed by the phosphor, thus protecting the CCD from direct x-ray interaction. The thickness of the fiberoptic plate and the CCD package present a significant challenge in the design of a digital x-ray cassette capable of insertion into the existing film-screen cassette holders of digital mammography systems. This study was performed with an aim to optimize fiberoptic plate thickness. Attenuation measurements were performed on nine fiberoptic plates varying in material composition that exhibit desirable optical characteristics such as good coupling efficiency. Mammographic spectra from a clinical mammographic system and an Americium-241 (Am-241) source (59.54 KeV) were used. The spectra were recorded with a high-resolution cadmium zinc telluride (CZT)-based spectrometer and corrected for dead time and pile-up. The linear attenuation coefficients varied by a factor of 3 in the set of tested fiberoptic plates at both mammographic energies and 59.54 keV. Our results suggest that a 3-mm thick high-absorption plate might provide adequate for shielding at mammographic energies. A thickness of 2-mm is feasible for mammographic applications with further optimization of the fiberoptic plate composition by incorporating non-scintillating, high-atomic number material. This would allow more space for cooling components of the cassette and for a more compact device, which is critical for clinical implementation of the technology.
RÉSUMÉ
RATIONALE AND OBJECTIVES: The purpose of this study was to comparatively evaluate digital planar mammography and both linear and nonlinear tomosynthetic reconstruction methods. MATERIALS AND METHODS: A "disk" (ie, target) identification study was conducted to compare planar and reconstruction methods. Projective data using a composite phantom with circular disks were acquired in both planar and tomographic modes by using a full-field, digital mammographic system. Two-dimensional projections were reconstructed with both linear (ie, backprojection) and nonlinear (ie, maximization and minimization) tuned-aperture computed tomographic (TACT) methods to produce three-dimensional data sets. Four board-certified radiologists and one 4th-year radiology resident participated as observers. All images were compared by these observers in terms of the number of disks identified. RESULTS: Significant differences (P < .05, Bonferroni adjusted) were observed between all reconstruction and planar methods. No significant difference, however, was observed between the planar methods, and only a marginally significant difference (P < .054, Bonferroni adjusted) was observed between TACT-backprojection and TACT-minimization. CONCLUSION: A combination of linear and nonlinear reconstruction schemes may have potential implications in terms of enhancing image visualization to provide radiologists with valuable diagnostic information.
Sujet(s)
Mammographie/méthodes , Amélioration d'image radiographique , Tumeurs du sein/imagerie diagnostique , Femelle , Humains , Fantômes en imagerie , Sensibilité et spécificitéRÉSUMÉ
RATIONALE AND OBJECTIVES: The authors performed this study to investigate the potential applicability of tomosynthesis to digital mammography. Four methods of tomosynthesis-tuned aperture computed tomography (TACT)-backprojection, TACT-iterative restoration, iterative reconstruction with expectation maximization, and Bayesian smoothing-were compared to planar mammography and analyzed in terms of their contrast-detail characteristics. Specific comparisons between the tomosynthesis methods were not attempted in this study. MATERIALS AND METHODS: A full-field, amorphous, silicon-based, flat-panel digital mammographic system was used to obtain planar and tomosynthesis projection images. A composite tomosynthesis phantom with a centrally located contrast-detail insert was used as the object of interest. The total exposure for multiple views with tomosynthesis was always equal to or less than that for the planar technique. Algorithms were used to reconstruct the object from the acquired projections. RESULTS: Threshold contrast characteristics with all tomosynthesis reconstruction methods were significantly better than those with planar mammography, even when planar mammography was performed at more than twice the exposure level. Reduction of out-of-plane structural components was observed in all the tomosynthesis methods analyzed. CONCLUSION: The contrast-detail trends of all the tomosynthesis methods analyzed in this study were better than those of planar mammography. Further optimization of the algorithms could lead to better image reconstruction, which would improve visualization of valuable diagnostic information.
Sujet(s)
Mammographie/méthodes , Amélioration d'image radiographique , Traitement du signal assisté par ordinateur , Tomodensitométrie , Tumeurs du sein/imagerie diagnostique , Fantômes en imagerieRÉSUMÉ
An amorphous silicon-based full-breast imager for digital mammography was evaluated for detector stability over a period of 1 year. This imager uses a structured CsI:TI scintillator coupled to an amorphous silicon layer with a 100-micron pixel pitch and read out by special purpose electronics. The stability of the system was characterized using the following quantifiable metrics: conversion factor (mean number of electrons generated per incident x-ray), presampling modulation transfer function (MTF), detector linearity and sensitivity, detector signal-to-noise ratio (SNR), and American College of Radiology (ACR) accreditation phantom scores. Qualitative metrics such as flat field uniformity, geometric distortion, and Society of Motion Picture and Television Engineers (SMPTE) test pattern image quality were also used to study the stability of the system. Observations made over this 1-year period indicated that the maximum variation from the average of the measurements were less than 0.5% for conversion factor, 3% for presampling MTF over all spatial frequencies, 5% for signal response, linearity and sensitivity, 12% for SNR over seven locations for all 3 target-filter combinations, and 0% for ACR accreditation phantom scores. ACR mammographic accreditation phantom images indicated the ability to resolve 5 fibers, 4 speck groups, and 5 masses at a mean glandular dose of 1.23 mGy. The SMPTE pattern image quality test for the display monitors used for image viewing indicated ability to discern all contrast steps and ability to distinguish line-pair images at the center and corners of the image. No bleeding effects were observed in the image. Flat field uniformity for all 3 target-filter combinations displayed no artifacts such as gridlines, bad detector rows or columns, horizontal or vertical streaks, or bad pixels. Wire mesh screen images indicated uniform resolution and no geometric distortion.
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Mammographie/instrumentation , Fantômes en imagerie , Amélioration d'image radiographique/méthodes , Silicium , Femelle , Humains , Mammographie/méthodes , Phénomènes physiques , PhysiqueRÉSUMÉ
The physical characteristics of a clinical charge coupled device (CCD)-based imager (Senovision, GE Medical Systems, Milwaukee, WI) for small-field digital mammography have been investigated. The imager employs a MinR 2000 (Eastman Kodak Company, Rochester, NY) scintillator coupled by a 1:1 optical fiber to a front-illuminated 61 x 61 mm CCD operating at a pixel pitch of 30 microns. Objective criteria such as modulation transfer function (MTF), noise power spectrum (NPS), detective quantum efficiency (DQE), and noise equivalent quanta (NEQ) were employed for this evaluation. The results demonstrated a limiting spatial resolution (10% MTF) of 10 cy/mm. The measured DQE of the current prototype utilizing a 28 kVp, Mo-Mo spectrum beam hardened with 4.5 cm Lucite is approximately 40% at close to zero spatial frequency at an exposure of 8.2 mR, and decreases to approximately 28% at a low exposure of 1.1 mR. Detector element nonuniformity and electronic gain variations were not significant after appropriate calibration and software corrections. The response of the imager was linear and did not exhibit signal saturation under tested exposure conditions.
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Mammographie/méthodes , Enregistrement sur magnétoscope , Calibrage , Traitement d'image par ordinateur , Mammographie/instrumentation , Modèles statistiques , Reproductibilité des résultatsRÉSUMÉ
RATIONALE AND OBJECTIVES: To develop collagen stent-grafts impregnated with heparin to improve the biocompatibility of endovascular stents and to design a percutaneous delivery system for graft deployment in a swine model. METHODS: Heparin-impregnated collagen stent-grafts were deployed, and follow-up angiograms were obtained every 15 minutes for 90 minutes to assess acute thromboses and again at 2 and 4 weeks afterward to assess patency. If stenosis or occlusion was detected at the 2-week evaluation, guidewire passage across the lesion was attempted and angioplasty was performed. If stenosis or occlusion was present at the 4-week evaluation, only guidewire passage was attempted; thereafter, the animals were killed and the stent-grafts were harvested and reviewed by a vascular pathologist. RESULTS: Group A represents a feasibility study to optimize the deployment method applied in groups B and C. Fifteen of 17 stent-grafts were successfully deployed using this method. In group B, 89% of grafts were successfully deployed; 12% were patent at 2 weeks and none at 4 weeks. In group C, a 10-minute inflation time was added to the deployment procedure; 88% of grafts were successfully deployed and 28% were patent at 2 weeks and 14% at 4 weeks. Extensive luminal thrombosis and myointimal hyperplasia were present in every case. CONCLUSIONS: A method was developed for percutaneous implantation of collagen stent-grafts into peripheral vessels. The heparin-impregnated grafts did not prevent vessel restenosis. Modification of the graft-processing technique may improve patency.
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Artériosclérose/thérapie , Implantation de prothèses vasculaires , Collagène , Endoprothèses , Animaux , Matériaux biocompatibles , Études de faisabilité , Occlusion du greffon vasculaire/prévention et contrôle , Héparine/administration et posologie , Veines jugulaires/transplantation , SuidaeRÉSUMÉ
The physical characteristics of a clinical prototype amorphous silicon-based flat panel imager for full-breast digital mammography have been investigated. The imager employs a thin thallium doped CsI scintillator on an amorphous silicon matrix of detector elements with a pixel pitch of 100 microm. Objective criteria such as modulation transfer function (MTF), noise power spectrum, detective quantum efficiency (DQE), and noise equivalent quanta were employed for this evaluation. The presampling MTF was found to be 0.73, 0.42, and 0.28 at 2, 4, and 5 cycles/mm, respectively. The measured DQE of the current prototype utilizing a 28 kVp, Mo-Mo spectrum beam hardened with 4.5 cm Lucite is approximately 55% at close to zero spatial frequency at an exposure of 32.8 mR, and decreases to approximately 40% at a low exposure of 1.3 mR. Detector element nonuniformity and electronic gain variations were not significant after appropriate calibration and software corrections. The response of the imager was linear and did not exhibit signal saturation under tested exposure conditions.
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Mammographie/instrumentation , Amélioration d'image radiographique/méthodes , Silicium , Algorithmes , Conception d'appareillage , Mammographie/méthodes , Diffusion de rayonnements , Sensibilité et spécificité , Rayons XRÉSUMÉ
INTRODUCTION: The authors review their midterm experience with uterine artery embolization for the treatment of uterine fibroids. MATERIALS AND METHODS: Sixty patients were referred for permanent polyvinyl alcohol (PVA) foam particle uterine artery embolization during an 18-month period. Detailed clinical follow-up and ultrasound follow-up were obtained. RESULTS: Bleeding was a presenting symptom in 56 patients and pain was a presenting symptom in 47 patients. All patients underwent a technically successful embolization. One of the patients underwent unilateral embolization. Fifty-nine patients underwent bilateral embolization. Of all patients undergoing bilateral embolization, at last follow-up (mean, 16.3 months), 81% had their uterus and had moderate or better improvement in their symptoms. Ninety-two percent of these patients also had reductions in uterine and dominant fibroid volumes. Overall, the mean uterine and dominant fibroid volume reduction were 42.8% and 48.8%, respectively (mean follow-up, 10.2 months). One infectious complication that necessitated hysterectomy occurred. CONCLUSION: Uterine artery embolization for the treatment of uterine fibroids is a minimally invasive technique with low complication rates and very good clinical efficacy.
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Embolisation thérapeutique/méthodes , Léiomyome/thérapie , Tumeurs de l'utérus/thérapie , Adulte , Sujet âgé , Artères , Loi du khi-deux , Femelle , Humains , Léiomyome/vascularisation , Adulte d'âge moyen , Poly(alcool vinylique)/usage thérapeutique , Résultat thérapeutique , Tumeurs de l'utérus/vascularisation , Utérus/vascularisationSujet(s)
Embolisation thérapeutique , Léiomyome/thérapie , Tumeurs de l'utérus/thérapie , Embolisation thérapeutique/effets indésirables , Femelle , Humains , Équipe soignante , Sélection de patients , Soins postopératoires , Soins préopératoires , Radiologie interventionnelle , Utérus/vascularisationRÉSUMÉ
OBJECTIVE: Recent studies have shown evaluation of the small peripancreatic veins to have potential in improving pancreatic cancer staging. This study was performed to determine the effectiveness of thin-section pancreatic phase helical CT images in visualizing these veins. MATERIALS AND METHODS: Seventy-two patients (30 with pancreatic adenocarcinoma and 42 with no pancreatic disease) underwent dual-phase helical CT with thin-section pancreatic phase acquisition (40-70 sec after i.v. contrast initiation at 3 ml/sec) and hepatic phase acquisition (70-100 sec). Visualization (with diameter measurement) or nonvisualization of the posterior superior pancreaticoduodenal vein (PSPDV), anterior superior pancreaticoduodenal vein (ASPDV), and gastrocolic trunk was recorded for both acquisitions. We also correlated surgical tumor resectability with the status of the small peripancreatic veins. RESULTS: Visualization of peripancreatic veins was significantly better on pancreatic phase images than on hepatic phase images for both healthy individuals (PSPDV, 88% of the veins visualized on the pancreatic phase images versus 50% on the hepatic phase images; ASPDV, 93% on the pancreatic phase images versus 48% on the hepatic phase images; gastrocolic trunk, 98% on the pancreatic phase images versus 76% on the hepatic phase images) and for pancreatic cancer patients (PSPDV, 97% on the pancreatic phase images versus 57% on the hepatic phase images; ASPDV, 77% on the pancreatic phase images versus 43% on the hepatic phase images) (p < .05). The exception was the gastrocolic trunk in cancer patients (83% on the pancreatic phase images versus 77% on the hepatic phase images) (p > .05). In pancreatic cancer patients, 11 dilated peripancreatic veins were identified on the pancreatic phase images compared with six on the hepatic phase images. However, only one of the 11 dilated peripancreatic veins was in a patient with surgically resectable disease. CONCLUSION: In a dual-phase helical CT protocol, thin-section pancreatic phase images provided visualization of the small peripancreatic veins that was superior to hepatic phase images, providing further support for the use of this protocol in pancreatic cancer evaluation.