scholarly journals FUNDAMENTAL STUDY OF MRI-GUIDED STEREOTACTIC NEUROSURGERY : THE ACCURACY OF MEASUREMENT OF A TARGET POINT

1991 ◽  
Vol 47 (5) ◽  
pp. 714-720
Author(s):  
KENICHI KASHIKURA ◽  
HAJIME ARAI ◽  
SHIGETOSHI YOSHIDA
2018 ◽  
Vol 3 (3) ◽  
pp. 2515-2522 ◽  
Author(s):  
Ziyan Guo ◽  
Ziyang Dong ◽  
Kit-Hang Lee ◽  
Chim Lee Cheung ◽  
Hing-Choi Fu ◽  
...  

1983 ◽  
Vol 46 (1-4) ◽  
pp. 206-210
Author(s):  
M. Fröder ◽  
D. Seitzer ◽  
G. Büren ◽  
G. Dieckmann

2015 ◽  
Vol 62 (4) ◽  
pp. 1077-1088 ◽  
Author(s):  
Gang Li ◽  
Hao Su ◽  
Gregory A. Cole ◽  
Weijian Shang ◽  
Kevin Harrington ◽  
...  

2017 ◽  
Vol 126 (3) ◽  
pp. 985-996 ◽  
Author(s):  
Georgi Minchev ◽  
Gernot Kronreif ◽  
Mauricio Martínez-Moreno ◽  
Christian Dorfer ◽  
Alexander Micko ◽  
...  

OBJECTIVE Robotic devices have recently been introduced in stereotactic neurosurgery in order to overcome the limitations of frame-based and frameless techniques in terms of accuracy and safety. The aim of this study is to evaluate the feasibility and accuracy of the novel, miniature, iSYS1 robotic guidance device in stereotactic neurosurgery. METHODS A preclinical phantom trial was conducted to compare the accuracy and duration of needle positioning between the robotic and manual technique in 162 cadaver biopsies. Second, 25 consecutive cases of tumor biopsies and intracranial catheter placements were performed with robotic guidance to evaluate the feasibility, accuracy, and duration of system setup and application in a clinical setting. RESULTS The preclinical phantom trial revealed a mean target error of 0.6 mm (range 0.1–0.9 mm) for robotic guidance versus 1.2 mm (range 0.1–2.6 mm) for manual positioning of the biopsy needle (p < 0.001). The mean duration was 2.6 minutes (range 1.3–5.5 minutes) with robotic guidance versus 3.7 minutes (range 2.0–10.5 minutes) with manual positioning (p < 0.001). Clinical application of the iSYS1 robotic guidance device was feasible in all but 1 case. The median real target error was 1.3 mm (range 0.2–2.6 mm) at entry and 0.9 mm (range 0.0–3.1 mm) at the target point. The median setup and instrument positioning times were 11.8 minutes (range 4.2–26.7 minutes) and 4.9 minutes (range 3.1–14.0 minutes), respectively. CONCLUSIONS According to the preclinical data, application of the iSYS1 robot can significantly improve accuracy and reduce instrument positioning time. During clinical application, the robot proved its high accuracy, short setup time, and short instrument positioning time, as well as demonstrating a short learning curve.


Author(s):  
Virgil Peck ◽  
W. L. Carter

Any electron microscopical study of the morphology of bulk polymers has throughout the years been hampered by the lack of any real ability to produce meaningful surface variations for replication. True etching of polymers should show crystalline and amorphous regions in some form of relief. The use of solvents, acids, organic vapors, and inert ion bombardment to etch samples has proved to be useful only in limited applications. Certainly many interpretations of these results are subject to question.The recent use of a radiofrequency (R. F.) plasma of oxygen to degrade and remove organic material with only minor heating has opened a new possibility for etching polymers. However, rigid control of oxygen flow, time, current, and sample position are necessary in order to obtain reproducible results. The action is confined to surface layers; the molecular weight of the polymer residue after heavy etching is the same as the molecular weight of the polymer before attack, within the accuracy of measurement.


2004 ◽  
Vol 171 (4S) ◽  
pp. 223-223
Author(s):  
Jonathan A. Coleman ◽  
Robert C. Susil ◽  
Axel Krieger ◽  
Peter L. Choyke ◽  
Betty Wise ◽  
...  

2020 ◽  
pp. 25-31
Author(s):  
M. L. Mazo ◽  
O. E. Jacobs ◽  
O. S. Puchkova ◽  
M. V. Feldsherov ◽  
E. V. Kondratyev

The rate of detection of breast cancer by MRI, while other methods of radiological diagnosis are not sufficiently informative, ranges from 5.2 to 26.3 per cent. Suspicious breast tumors of category BI-RADS 4, 5 show morphological image-guided biopsy verification, in particular MRI with contrast. Purpose. To show the possibilities and features of carrying out MRI-guided vacuum breast biopsy, including after aesthetic breast augmentation. Material and methods. A comprehensive X-ray, ultrasound and MRI examination of 54 women aged between 28 and 70 years with different breast tumors was conducted. Of these, five were detected only by breast MRI with contrast, and were morphologically verified by MRI-guided vacuum aspiration biopsy. Results. 14 of the 54 patients with breast mass were diagnosed with breast cancer and 26 were diagnosed with benign diseases. The effectiveness of comprehensive examination and low-invasive high-tech MRI-guided procedures in early refined screening for breast cancer, including after aesthetic breast augmentation, has been demonstrated. MRI-guided vacuum-assisted breast biopsy is a fast, safe and accurate diagnostic method of morphological verification of suspicious breast tumors that do not have X-ray and ultrasound.


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