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1.
Rev Hosp Clin Fac Med Sao Paulo ; 55(6): 201-6, 2000.
Article in English | MEDLINE | ID: mdl-11313659

ABSTRACT

A low frequency of Helicobacter pylori in the gastric mucosa of patients with alkaline gastritis has been reported. At the same time, it can be noted that the growth of bacteria can be inhibited by bile acids. We studied 40 patients with chronic gastritis related to Helicobacter pylori in order to determine the effect of ursodeoxycholic acid on this infection. Diagnoses of the infection and the inflammatory process were obtained by histologic study of gastric biopsies collected during endoscopy. Two groups were studied: group I received ursodeoxycholic acid - 300 mg/day, and group II received the placebo, twice a day, both for 28 days. The colonization by Helicobacter pylori and the intensity of the mononuclear and polymorphonuclear inflammatory infiltrate were determined before (time 1) and after (time 2) treatment. Ursodeoxycholic acid had no effect on the Helicobacter pylori infection. A significant reduction in the intensity of the mononuclear inflammatory infiltrate of the gastric antrum mucosa was observed in patients from group I, when we compared not only times 1 and 2 but also groups I and II. However, this was not the case with the body mucosa. We concluded that ursodeoxycholic acid had no action on the colonization by Helicobacter pylori or on the polymorphonuclear inflammatory infiltrate, but it caused a significant reduction in the intensity of the mononuclear inflammatory infiltrate of the gastric antrum.


Subject(s)
Cholagogues and Choleretics/pharmacology , Gastric Mucosa/microbiology , Gastritis/microbiology , Helicobacter pylori/drug effects , Ursodeoxycholic Acid/pharmacology , Adult , Cholagogues and Choleretics/therapeutic use , Female , Gastric Mucosa/drug effects , Gastritis/drug therapy , Helicobacter pylori/growth & development , Humans , Male , Pyloric Antrum/drug effects , Pyloric Antrum/microbiology , Ursodeoxycholic Acid/therapeutic use
3.
J Thorac Cardiovasc Surg ; 70(3): 499-508, 1975 Sep.
Article in English | MEDLINE | ID: mdl-126336

ABSTRACT

We studied eight homologous dura mater valves removed 1 to 35 months after implantation. Five dura mater valves were placed in the mitral position and three in the aortic position. Two of the valves were obtained after deaths not related to the valve itself and six after reoperations due to immediate or late incompetence. In 2 cases the dura mater valves were entirely normal, both macroscopically and microscopically. In 2 other cases the leaflets were caught by stitches related to the struts, a technical error that caused laceration of the leaflets. Not withstanding this fact, the dura mater was normal on histologic examination. In 3 cases, and probably in 1 other, one or two leaflets were detached partially from the suture line, probably because of a technical error in the manufacture of the valve. These studies demonstrated satisfactory evolution of the homologous dura mater valves until 35 months after implantation. No signs of rejection or degeneration of the dura mater were observed in the present series.


Subject(s)
Aortic Valve/surgery , Dura Mater/transplantation , Heart Valve Prosthesis , Mitral Valve/surgery , Adolescent , Adult , Aortic Valve/pathology , Autopsy , Collagen , Evaluation Studies as Topic , Female , Fibrin , Fibroblasts , Humans , Male , Mitral Valve/pathology , Polyethylene Terephthalates , Polytetrafluoroethylene , Prosthesis Design/standards , Sutures/adverse effects , Transplantation, Homologous
4.
J Thorac Cardiovasc Surg ; 69(5): 722-8, 1975 May.
Article in English | MEDLINE | ID: mdl-123977

ABSTRACT

A group of 533 patients had cardiac valves replaced with homologous dura mater valves. The dura mater was preserved in a solution of 98 per cent glycerol and antibiotics for a period of 12 days before used. The leaflets were mounted in a stainless steel ring covered by Dacron velour. Two hundred forty-five patients had mitral valve replacement; 205 patients, aortic valve replacement; 17 patients, tricuspid valve replacement; and 2 patients, pulmonary valve replacement. Sixty-four patients were subjected to multivalvular replacements. The patients were followed for a period of 1 to 40 months after surgery with satisfactory clinical and hemodynamic results. Because 2 patients developed endocarditis produced by fungii, fungicidal drugs were added to the preservative solution. No bacterial endocarditis has been observed. No pressure gradient through the valve has been noted at rest. Anticoagulant drugs have not been used in the postoperative period.


Subject(s)
Dura Mater/transplantation , Heart Valve Prosthesis , Adolescent , Adult , Aged , Aortic Valve/surgery , Child , Child, Preschool , Evaluation Studies as Topic , Female , Follow-Up Studies , Heart Murmurs , Heart Valve Prosthesis/methods , Humans , Male , Middle Aged , Mitral Valve/surgery , Polyethylene Terephthalates , Postoperative Complications , Pulmonary Valve/surgery , Stainless Steel , Transplantation, Homologous , Tricuspid Valve/surgery
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