Mucosal loss as a critical factor in esophageal stricture formation after mucosal resection: a pilot experiment in a porcine model

2019 ◽  
Vol 34 (2) ◽  
pp. 551-556
Author(s):  
Bing-Rong Liu ◽  
Dan Liu ◽  
Wenyi Yang ◽  
Saif Ullah ◽  
Zhen Cao ◽  
...  
2012 ◽  
Vol 26 (12) ◽  
pp. 3500-3508 ◽  
Author(s):  
Eric M. Pauli ◽  
Steve J. Schomisch ◽  
Joseph P. Furlan ◽  
Andrea S. Marks ◽  
Amitabh Chak ◽  
...  

2014 ◽  
Vol 47 (2) ◽  
pp. 155 ◽  
Author(s):  
Bashar Qumseya ◽  
Abraham M. Panossian ◽  
Cynthia Rizk ◽  
David Cangemi ◽  
Christianne Wolfsen ◽  
...  

2011 ◽  
Vol 74 (4) ◽  
pp. 753-760 ◽  
Author(s):  
Jason J. Lewis ◽  
Joel H. Rubenstein ◽  
Amit G. Singal ◽  
B. Joseph Elmunzer ◽  
Richard S. Kwon ◽  
...  

2010 ◽  
Vol 12 (4) ◽  
pp. 286-290 ◽  
Author(s):  
Alexander D. Bennett ◽  
Catriona M. MacPhail ◽  
Debra S. Gibbons ◽  
Michael R. Lappin

Retention of tablets or capsules in the feline esophagus can be associated with esophagitis and esophageal stricture formation. The objective of this study was to evaluate the esophageal passage of tablets and capsules when administered with either a one-step pill gun with flavored liquid (FlavoRx pill glide) or a pill delivery treat (Pill Pockets). Four different medication administrations were evaluated on different days in eight normal cats: tablets with FlavoRx pill glide (T-FG), tablets with pill delivery treats (T-PP), capsules with FlavoRx pill glide (C-FG) and capsules with pill delivery treats (C-PP). The estimated average transit time was 36 s for T-FG, 60 s for T-PP, 16 s for C-FG, and 24 s for C-PP. The results of this study suggest that either pill delivery method is acceptable for successful passage of tablets or capsules into the stomach of cats using a single replicate.


2014 ◽  
Vol 52 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Murat Dereli ◽  
Bartlomiej E. Krazinski ◽  
Suleyman Ayvaz ◽  
Burhan Aksu ◽  
Mehmet Kanter ◽  
...  

Author(s):  
Min Tae Kim ◽  
Kun Yung Kim

Corrosive burns lead to progressive esophageal stricture and dysphagia. There are many trials to prevent Esophageal stricture formation after corrosive burn. This study aimed to access the effects of EW-7197 on prevention for esophageal stricture formation after corrosive esophageal burn. animal study were classified divided into three groups: a healthy group, a control group (corrosive burn without EW-7197), and a treatment group (corrosive burn with EW-7197). Corrosive esophageal burns were produced using 30% NaOH on the lower esophagus. For 3 weeks, the control group received vehicle and the treatment group received 20 mg/kg/day EW-7197. Treatment efficacy was assessed by measuring the stenosis ratio by esophagogram with contrast media on day 21. histologic staining was performed to evaluate the fibrosis area ratio, and western blotting was performed to evaluate fibrotic markers. Among 20 rats that underwent surgery, 14 survived. Three in the treatment group died because of esophageal perforation, and three in the control group died due to their debilitating status. The esophageal stenosis ratio was significantly lower in the treatment group than in the control group (12.1 ± 9.5% and 42.2 ± 8.3%, respectively; p = 0.001). The histologic fibrosis area ratio was also significantly lower in the treatment group (12.5 ± 3.0% and 21.6 ± 2.1%, respectively; p = 0.001). The treatment group showed lower expressions of profibrogenic proteins such as TGF-β1, pSmad3, and α-SMA. EW-7197 may be a good alternative for the prevention esophageal stricture formation after corrosive burn.


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