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1.
Scand J Gastroenterol ; 41(4): 488-92, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16635919

ABSTRACT

OBJECTIVE: Submucosal injection is used to prevent complications, such as perforation, during endoscopic mucosal resection (EMR). Since injection of normal saline produces mucosal elevation of short duration, repeated injection is needed for extensive resection. To overcome this limitation, various submucosal injection solutions have been developed but there are few data comparing their efficacy. This study was therefore conducted to compare the physical and chemical properties and the duration of mucosal elevation of various submucosal injection solutions. MATERIAL AND METHODS: A fresh transverse colon specimen acquired from a mongrel was used. Experiments were repeated four times. To compare the efficacy of mucosal elevation, 1 ml of each solution was injected into the submucosa: 0.9% NaCl, 20% mannitol, 0.1% sodium hyaluronate, 0.3% hydroxypropyl methylcellulose (HPMC), and 2% fibrinogen. Physical and chemical properties such as viscosity and osmolarity were compared. RESULTS: The heights of initial mucosal elevations were 6.52+/-0.26 mm, 6.87+/-0.05 mm, 6.92+/-0.09 mm, 6.90+/-0.08 mm, and 6.90+/-0.08 mm for normal saline, mannitol, sodium hyaluronate, HPMC, and fibrinogen, respectively. Whereas injection of normal saline took about 20 min and mannitol about 30 min for the initial elevation to be reduced to more than half the initial height, it took more than 60 min for all the other agents. A correlation was found between the duration of mucosal elevation and viscosity but not with osmolarity. CONCLUSIONS: The mucosal elevation lasted longer with sodium hyaluronate, HPMC, and fibrinogen than with mannitol or normal saline, and this seems to be due to the viscosity rather than the osmolarity of each solution.


Subject(s)
Colon/surgery , Colonoscopy/methods , Intestinal Mucosa/surgery , Solutions , Animals , Dogs , Fibrinogen/pharmacology , Hyaluronic Acid/pharmacology , Hypromellose Derivatives , In Vitro Techniques , Injections , Intestinal Mucosa/drug effects , Mannitol/pharmacology , Methylcellulose/analogs & derivatives , Methylcellulose/pharmacology , Osmolar Concentration , Postoperative Complications/prevention & control , Sodium Chloride/pharmacology , Viscosity
2.
Korean J Gastroenterol ; 46(4): 297-301, 2005 Oct.
Article in Korean | MEDLINE | ID: mdl-16247274

ABSTRACT

Crohn's disease is a chronic inflammatory bowel disease which affects mainly children and young adults, and its cause remains unknown so far. Infliximab, a monoclonal antibody to the pivotal cytokine tumor necrosis factor-alpha, has been approved as a drug for both induction and maintenance therapy for moderately to severely active, or fistula-complicated Crohn's disease. The authors report a 12-year-old male patient diagnosed as Crohn's disease complicated with a perianal fistula, which was refractory to the conventional therapy. After the 0, 2, and 6 week scheduled intravenous infusion of infliximab, the patient reached to clinical remission in both subjective symptoms and objective manifestations. For children or young adults who develop Crohn's disease in a refractory course, infliximab may serve as a drug which leads to a clinical improvement or even to an extent of remission.


Subject(s)
Antibodies, Monoclonal/administration & dosage , Crohn Disease/drug therapy , Gastrointestinal Agents/administration & dosage , Child , Drug Administration Schedule , Humans , Infliximab , Infusions, Intravenous , Male
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