Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Colitis coliti

M. Nitta, I. Hirata, K. Toshina, M. Murano, K. Maemura, N. Hashimoto, S. Sasaki, H. Yamauchi, K. Katsu, Expression of the EP4 prostaglandin E2 receptor subtype with rat dextran sodium sulphate colitis Colitis suppression by a selective agonist, ONO-AE1-329, Scand. J. Immunol. 56 (2002) 66. [Pg.656]

E. histolytica and G. lamblia are waterborne infectious diseases that cause colitis and liver abscess, and enteritis, respectively. [Pg.180]

E. histolytica colonization of the large intestine is eradicated using a luminal agent such as diloxanid furoate or paromomycin. Invasive amoebiasis (colitis,... [Pg.180]

Hematologic diseases autoimmune hemolytic anemia, idiopathic thrombocytopenic purpura, pernicous anemia Kidney disease Goodpasture syndrom, lipoid nephroses, minimal change glomerulonephritis Diseases of the gastrointestinal tract autoimmune chronic active hepatitis, autoimmune atrophic gastritis, Crohn s disease, ulcerative colitis... [Pg.241]

Important members of this toxin family are Clostridium difficile toxins A and B, which are implicated in antibiotics-associated diarrhea and pseudomembranous colitis. The large clostridial cytotoxins are single-chain toxins with molecular masses of 250-308 kDa. The enzyme domain is located at the N terminus. The toxins are taken up from an acidic endosomal compartment. They glucosylate RhoA at Thr37 also, Rac and Cdc42 are substrates. Other members of this toxin family such as Clostridium sordellii lethal toxin possess a different substrate specificity and modify Rac but not Rho. In addition, Ras subfamily proteins (e.g., Ras, Ral, and Rap) are modified. As for C3, they are widely used as tools to study Rho functions [2] [4]. [Pg.247]

OA were aborted in 2003 due to the development of mild to moderate liver fibrosis in dogs treated for 9 months with high doses of pralnacasan. This was in spite of recent evidence demonstrating the effectiveness of pralnacasan treatment in the acute dextran sulfate sodium (DSS)-induced colitis model, which resembles Crohn s disease (CD) characteristics, and in transient ischemia induced brain damage. [Pg.333]

Colon inflammation 1. AEA levels are elevated in the colon of DNBS-treated mice and in the colon submucosa of TNBS-treated rats, two animal models of inflammatory bowel diseases, and in the biopsies of patients with ulcerative colitis, to control inflammation 1. Inhibitors of degradation (both FAAH and cellular re-uptake)... [Pg.467]

Entamoeba histolytica is an anaerobic rhizopod that occurs in tropical and subtropical areas. It can cause intestinal and extraintestinal manifestations. It is transmitted orally by ingestion of cysts that develop into trophozoites in the large intestine. Amebic trophozoites release several cytolytic factors, e.g. amoe-bapore, which enable the parasite to invade tissue. In intestinal amoebiasis, E. histolyticatrophozoites invade the intestinal mucosa, causing a form of ulcerative colitis with bloody and mucous diarrhoea. Extraintestinal manifestation of amebiasis results in abscess formation, usually in the liver but sometimes in the brain. [Pg.477]

In the pathogenesis of many chronic inflammatory diseases (e.g., rheumatoid arthritis, glomerulonephritis, colitis ulcerosa, Morbus Crohn, atopic dermatitis, psoriasis) autoimmune processes play an important role, too. Although first of all nonsteroidal antiinflammatory agents or glucocorticoids should be applied, immunosuppressive agents may also be indicated. [Pg.622]

As with all drugs, the specific side effects of the quinolones must be considered when they are chosen for treatment of bacterial infections [5]. Reactions of the gastrointestinal tract and the central neivous system are the most often observed adverse effects during therapy with quinolones. It should be underlined, however, that compared with many other antimicrobials, diarrhea is less frequently observed during quinolone treatment. Antibiotic-associated colitis has been observed rarely during quinolone therapy. Similarly, hypersensitivity reactions, as observed during therapy with penicillins and other (3-lactams, is less frequently caused by quinolones. Some other risks of quinolone therapy have been defined and must be considered if a drug from this class is chosen for treatment of bacterial infections. [Pg.1057]

Polycystic kidney disease (Polycyst in-1 activates canonical Wnt signaling pathway) Injury-induced renal fibrosis Heart failure Ulcerative colitis Osteoporosis-Pseudoglioma Syndrome (genetic syndrome of defective bone formation) Ulcerative colitis Familial Alzheimer s disease (through interaction with Presenilin-1) Familial Alzheimer s disease (through interaction with Presenilin-1)... [Pg.1321]

The ongoing assessment for patients receiving sulfasalazine for ulcerative colitis includes observation for evidence of Hie relief or intensification of the symptoms of the disease. The nurse inspects all stool samples and records Hieir number and appearance... [Pg.62]

Promoting an Optimal Response to Therapy The patient receiving a sulfonamide drug almost always lias an active infection. Some patients may be receiving one of Hiese drugs to prevent an infection (prophylaxis) or as part of Hie management of a disease such as ulcerative colitis. [Pg.62]

Discuss hypersensitivity reactions and pseudomembranous colitis as they relate to antibiotic therapy. [Pg.65]

Pseudomembranous colitis may occur after 4 to 9 days of treatment with penicillin or as long as 6 weeks after the drug is discontinued. [Pg.70]

DIARRHEA Diarrhea may be an indication of a super-infection of the gastrointestinal tract or pseudomembranous colitis. The nurse inspects all stools and notifies the primary health care provider if diarrhea occurs because it may be necessary to stop the drug. If diarrhea does occur and there appears to be blood and mucus in the stool, it is important to save a sample of the stool and test for occult blood using a test such as Hemoccult. If the stool tests positive for blood, the nurse saves the sample for possible further laboratory analysis. [Pg.72]

Therapy with cephalosporins may result in a bacterial or fungal superinfection. Diarrhea may be an indication of pseudomembranous colitis, which is one type of bacterial superinfection. See Chapter 7 for a discussion of bacterial and fungal superinfections and pseudomembranous colitis. [Pg.77]

DIARRHEA. Frequent liquid stools may be an indication of a superinfection or pseudomembranous colitis. If pseudomembranous colitis occurs, it is usually seen 4 to 10 days after treatment is started. [Pg.79]

The nurse inspects each bowel movement and immediately reports to the primary health care provider the occurrence of diarrhea or loose stools containing blood and mucus because it may be necessary to discontinue the drug use and institute treatment for diarrhea, a superinfection, or pseudomembranous colitis. [Pg.80]

Abdominal pain, esophagitis, nausea, vomiting, diarrhea, skin rash, and blood dyscrasias may be seen with the use of the lincosamides. These drag s also can cause pseudomembranous colitis, which may range from mild to very severe Discontinuing the drag may relieve mild symptoms of pseudomembranous colitis. [Pg.86]

Bacterial or fungal superinfections and pseudomembranous colitis (see Chap. 7) may occur with the use of both of these drugs. The administration of any drug may result in a hypersensitivity reaction, which can... [Pg.91]


See other pages where Colitis coliti is mentioned: [Pg.1035]    [Pg.181]    [Pg.830]    [Pg.42]    [Pg.194]    [Pg.7]    [Pg.171]    [Pg.200]    [Pg.240]    [Pg.242]    [Pg.466]    [Pg.630]    [Pg.854]    [Pg.1021]    [Pg.1181]    [Pg.60]    [Pg.64]    [Pg.65]    [Pg.70]    [Pg.70]    [Pg.76]    [Pg.76]    [Pg.84]    [Pg.84]    [Pg.84]    [Pg.84]    [Pg.85]    [Pg.86]   
See also in sourсe #XX -- [ Pg.994 ]

See also in sourсe #XX -- [ Pg.994 ]




SEARCH



Antibiotic-associated pseudomembranous colitis

Antibiotic-associated pseudomembranous colitis, Clostridium

Antibiotic-associated pseudomembranous colitis, Clostridium difficile

Antibiotics ulcerative colitis

Antimicrobial drugs colitis

Azathioprine ulcerative colitis

Balsalazide ulcerative colitis

Campylobacter colitis

Carcinoma Ulcerative colitis

Chronic colitis

Ciclosporin ulcerative colitis

Clostridium Pseudomembranous colitis

Clostridium difficile colitis

Clostridium difficile pseudomembranous colitis

Colitis

Colitis

Colitis antibiotic-associated

Colitis causing

Colitis drugs

Colitis experimental/model

Colitis hemorrhagic

Colitis microscopic

Colitis model

Colitis mucous

Colitis ulcerosa

Colitis, allergic

Colitis, parenteral nutrition

Colitis, risk factor

Collagenous colitis

Corticosteroids ulcerative colitis

Cyclosporin ulcerative colitis

Dextran sodium sulfate-induced colitis

Dextran sulfate sodium colitis

Dextran sulfate sodium induced colitis model

Enemas ulcerative colitis

Gastrointestinal disease ulcerative colitis

Hydrocortisone ulcerative colitis

Immunosuppressant drugs ulcerative colitis

Immunosuppressants ulcerative colitis

Inflammatory bowel disease colitis

Inflammatory bowel disease ulcerative colitis

Ischaemic colitis

Ischemic colitis

Ischemic colitis therapy

Lansoprazole colitis

Lymphocytic colitis

Methotrexate ulcerative colitis

Mucus colitis

Neutropenic colitis

Nicotine ulcerative colitis

Olsalazine ulcerative colitis

Prednisolone ulcerative colitis

Pseudo-membranous colitis

Pseudomembraneous colitis

Pseudomembraneous colitis cephalosporins

Pseudomembraneous colitis clindamycin

Pseudomembraneous colitis lincomycin

Pseudomembranous colitis

Pseudomembranous colitis from

Pseudomembranous colitis superinfection

Pseudomembranous colitis treatment

Pseudomembranous colitis vancomycin therapy

Sulfasalazine ulcerative colitis

Sulfonamides ulcerative colitis

Tacrolimus colitis

Thiopurines ulcerative colitis

Ulcerative colitis

Ulcerative colitis clinical presentation

Ulcerative colitis complications

Ulcerative colitis diagnosis

Ulcerative colitis disease

Ulcerative colitis drug therapy

Ulcerative colitis epidemiology

Ulcerative colitis etiology

Ulcerative colitis hepatobiliary complications

Ulcerative colitis moderate

Ulcerative colitis pathogenesis

Ulcerative colitis pathophysiology

Ulcerative colitis remission therapy

Ulcerative colitis risk factors

Ulcerative colitis severe

Ulcerative colitis severe management

Ulcerative colitis severe or intractable disease

Ulcerative colitis surgery

Ulcerative colitis treatment

Ulcers ulcerative colitis

© 2024 chempedia.info