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991.
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993.
Jean-Pierre Bayley Henricus PM Kunst Alberto Cascon Maria Lourdes Sampietro José Gaal Esther Korpershoek Adolfo Hinojar-Gutierrez Henri JLM Timmers Lies H Hoefsloot Mario A Hermsen Carlos Suárez A Karim Hussain Annette HJT Vriends Frederik J Hes Jeroen C Jansen Carli M Tops Eleonora P Corssmit Peter de Knijff Jacques WM Lenders Cor WRJ Cremers Mercedes Robledo 《The lancet oncology》2010,11(4):366-372
994.
Elisabetta Pagani MPhil Jochen G. Hirsch PhD Petra J.W. Pouwels PhD Mark A. Horsfield PhD Elisabetta Perego MD Achim Gass MD Stefan D. Roosendaal MD Frederik Barkhof MD Federica Agosta MD Marco Rovaris MD Domenico Caputo MD Antonio Giorgio MD Jacqueline Palace MD Silvia Marino MD Nicola De Stefano MD Stefan Ropele PhD Franz Fazekas MD Massimo Filippi MD 《Journal of magnetic resonance imaging : JMRI》2010,31(6):1458-1468
Purpose:
To assess the effect on diffusion tensor (DT) magnetic resonance imaging (MRI) of acquiring data with different scanners.Materials and Methods:
Forty‐four healthy controls and 36 multiple sclerosis patients with low disability were studied using eight MR scanners with acquisition protocols that were as close to a standard protocol as possible. Between 7 and 13 subjects were studied in each center. Region‐of‐interest (ROI) and histogram‐based analyses of fractional anisotropy (FA), axial (Dax), radial (Drad), and mean diffusivity (MD) were performed. The influence of variables such as the acquisition center and the control/patient group was determined with an analysis of variance (ANOVA) test.Results:
The patient/control group explained ≈25% of data variability of FA and Drad from midsagittal corpus callosum (CC) ROIs. Global FA, MD, and Drad in the white matter differentiated patients from controls, but with lower discriminatory power than for the CC. In the gray matter, MD discriminated patients from controls (30% of variability explained by group vs. 17% by center).Conclusion:
Significant variability of DT‐MRI data can be attributed to the acquisition center, even when a standardized protocol is used. The use of appropriate segmentation methods and statistical models allows DT‐derived metrics to differentiate patients from healthy controls. J. Magn. Reson. Imaging 2010;31:1458–1468. © 2010 Wiley‐Liss, Inc. 相似文献995.
Frederik Anton Verburg Marcel P. M. Stokkel Christian Düren Robbert B. T. Verkooijen Uwe Mäder Johannes W. van Isselt Robert J. Marlowe Johannes W. Smit Christoph Reiners Markus Luster 《European journal of nuclear medicine and molecular imaging》2010,37(2):276-283
Purpose
To compare disease-specific survival and recurrence-free survival (RFS) after successful 131I ablation in patients with differentiated thyroid carcinoma (DTC) between those defined before ablation as low-risk and those defined as high-risk according to the European Thyroid Association 2006 consensus statement.Methods
Retrospective data from three university hospitals were pooled. Of 2009 consecutive patients receiving ablation, 509 were identified as successfully ablated based on both undetectable stimulated serum thyroglobulin in the absence of antithyroglobulin antibodies and a negative diagnostic whole-body scan in a follow-up examination conducted 8.1±4.6 months after ablation. Of these 509 patients, 169 were defined as high-risk.Results
After a mean follow-up of 81±64 months (range 4–306 months), only three patients had died of DTC, rendering assessment of disease-specific survival differences impossible. Of the 509 patients, 12 (2.4%) developed a recurrence a mean 35 months (range 12–59 months) after ablation. RFS for the duration of follow-up was 96.6% according to the Kaplan-Meier method. RFS did not differ between high-risk and low-risk patients (p=0.68). RFS differed slightly but significantly between those with papillary and those with follicular thyroid carcinoma (p=0.03) and between those aged ≤45 years those aged >45 years at diagnosis (p=0.018).Conclusion
After (near) total thyroidectomy and successful 131I ablation, RFS does not differ between patients classified as high-risk and those classified as low-risk based on TNM stage at diagnosis. Consequently, the follow-up protocol should be determined on the basis of the result of initial treatment rather than on the initial tumour classification. 相似文献996.
997.
Katharina P. Aschenbrenner Christian V. Guthier Yulia Lyatskaya Judit Boda-Heggemann Frederik Wenz Jürgen W. Hesser 《Zeitschrift für medizinische Physik》2017,27(3):243-254
Purpose
In stereotactic body radiation therapy of lung tumors, reliable position estimation of the tumor is necessary in order to minimize normal tissue complication rate. While kV X-ray imaging is frequently used, continuous application during radiotherapy sessions is often not possible due to concerns about the additional dose. Thus, ultra low-dose (ULD) kV X-ray imaging based on a single photon counting detector is suggested. This paper addresses the lower limit of photons to locate the tumor reliably with an accuracy in the range of state-of-the-art methods, i.e. a few millimeters.Method
18 patient cases with four dimensional CT (4D-CT), which serves as a-priori information, are included in the study. ULD cone beam projections are simulated from the 4D-CTs including Poisson noise. The projections from the breathing phases which correspond to different tumor positions are compared to the ULD projection by means of Poisson log-likelihood (PML) and correlation coefficient (CC), and template matching under these metrics.Results
The results indicate that in full thorax imaging five photons per pixel suffice for a standard deviation in tumor positions of less than half a breathing phase. Around 50 photons per pixel are needed to achieve this accuracy with the field of view restricted to the tumor region. Compared to CC, PML tends to perform better for low photon counts and shifts in patient setup. Template matching only improves the position estimation in high photon counts. The quality of the reconstruction is independent of the projection angle.Conclusions
The accuracy of the proposed ULD single photon counting system is in the range of a few millimeters and therefore comparable to state-of-the-art tumor tracking methods. At the same time, a reduction in photons per pixel by three to four orders of magnitude relative to commercial systems with flatpanel detectors can be achieved. This enables continuous kV image-based position estimation during all fractions since the additional dose to the patient is negligible. 相似文献998.
Frederik Voss Lars Eckardt Sonia Busch Heidi L. Estner Daniel Steven Philipp Sommer Christian von Bary Hans-Ruprecht Neuberger 《Herzschrittmachertherapie & Elektrophysiologie》2016,27(4):381-389
The AV-reentrant tachycardia (AVRT) is a supraventricular tachycardia with an incidence of 1–3/1000. The pathophysiological basis is an accessory atrioventricular pathway (AP). Patients with AVRT typically present with palpitations, an on–off characteristic, anxiety, dyspnea, and polyuria. This type of tachycardia may often be terminated by vagal maneuvers. Although the clinical presentation of AVRT is quite similar to AV-nodal reentrant tachycardias, the correct diagnosis is often facilitated by analyzing a standard 12-lead ECG at normal heart rate showing ventricular preexcitation. Curative catheter ablation of the AP represents the therapy of choice in symptomatic patients. This article is the fourth part of a series written to improve the professional education of young electrophysiologists. It explains pathophysiology, symptoms, and electrophysiological findings of an invasive EP study. It focusses on mapping and ablation of accessory pathways. 相似文献
999.
1000.
Trinh XB Peeters F Tjalma WA 《European journal of obstetrics, gynecology, and reproductive biology》2006,124(2):250-253
There is not only a need for scientific data regarding the risk of recurrence of breast cancer by starting hormone replacement therapy (HRT) but also regarding the patients' needs for HRT. OBJECTIVES: To examine the severity of climacteric complaints in breast cancer patients and to examine if they are willing to take HRT. METHODS: In November 2003, a questionnaire was sent to 469 breast cancer survivors. The survey examined on a scale base the severity of climacteric complaints and the patient's opinion on starting HRT. RESULTS: More than 76% of the patients complained that they experience or had experienced hot flushes or night sweating. More than half (53%) of this group found the inconvenience severe to extreme, affecting the patient's quality of life. A majority (80.5%) patients who had already taken HRT, found that it improved their quality of life substantially. When the results of observational studies were explained regarding HRT in breast cancer survivors, a majority said they would take or would consider taking HRT (57.9%). CONCLUSION: While physicians are more reserved in prescribing HRT in breast cancer survivors, a combination of severe symptomatic climacteric complaints and the willingness of the patient to be treated should at least result in a "consideration" of prescribing HRT. 相似文献