Novel Intrauterine Brachytherapy Device Allows Precise Targeting of Tissues at Risk While Simultaneously Minimizing Normal Tissue Dose

Brachytherapy ◽  
2011 ◽  
Vol 10 ◽  
pp. S100-S101
Author(s):  
Daniel J. Scanderbeg ◽  
Cheryl C. Saenz ◽  
Steven C. Plaxe ◽  
Edwin A. Alvarez ◽  
Michael T. McHale ◽  
...  
Keyword(s):  
At Risk ◽  
2004 ◽  
Vol 18 (1) ◽  
pp. 131-160 ◽  
Author(s):  
Maria Werner-Wasik ◽  
Xiaoli Yu ◽  
Lawrence B Marks ◽  
Timothy E Schultheiss

2018 ◽  
Vol 30 (7) ◽  
pp. 455 ◽  
Author(s):  
Q. Ghafoor ◽  
B. Allos ◽  
R. Stevenson ◽  
S. Watkins ◽  
S. Yahya ◽  
...  

2019 ◽  
Vol 64 (13) ◽  
pp. 13NT02 ◽  
Author(s):  
Keith T Griffin ◽  
Matthew M Mille ◽  
Christopher Pelletier ◽  
Mahesh Gopalakrishnan ◽  
Jae Won Jung ◽  
...  

2015 ◽  
Vol 33 (3) ◽  
pp. 226 ◽  
Author(s):  
Nuri Hyun Jung ◽  
Youngseob Shin ◽  
In-Hye Jung ◽  
Jungwon Kwak

2018 ◽  
Vol 127 ◽  
pp. S500-S501
Author(s):  
W. Van Elmpt ◽  
T. Lustberg ◽  
J. Van Soest ◽  
M. Gooding ◽  
A. Dekker

2013 ◽  
Vol 40 (6Part21) ◽  
pp. 362-362
Author(s):  
H Liu ◽  
D Andrews ◽  
M Werner-Wasik ◽  
Y Xiao ◽  
Y Yu ◽  
...  

2015 ◽  
Vol 36 (2) ◽  
pp. 283-291 ◽  
Author(s):  
Qiang Shen ◽  
Shiliang Huang ◽  
Timothy Q Duong

T2*-weighted MRI of transient oxygen challenge (OC) showed exaggerated OC percent changes in the ischemic tissue at risk compared to normal tissue. One ambiguity is that regions with high vascular density also showed exaggerated OC percent changes. This study explored time-to-peak (TTP) of the OC percent changes to improve the utility of T2*-weighted OC MRI. Experiments were performed longitudinally at 30 min, 150 min and 24 h after transient (60-min) stroke in rats. Ischemic core, normal, and mismatch tissue were classified pixel-by-pixel based on apparent diffusion coefficient and cerebral blood flow. Major findings were: (i) Delayed OC TTP was localized to and corresponded well with the perfusion-diffusion mismatch. (ii) By contrast, the exaggerated OC percent changes were less localized, with changes not only in the at-risk tissue but also in some areas of the contralesional hemisphere with venous vessel origins. (iii) The OC time-course of the mismatch tissue was biphasic, with a faster initial increase followed by a slower increase. (iv) At-risk tissue with delayed TTP and exaggerated OC was normal after reperfusion and the at-risk tissue was mostly (83 ± 18%) rescued by reperfusion as indicated by normal 24-h T2. OC TTP offers unique information toward better characterization of at-risk tissue in ischemic stroke.


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