Literature DB >> 12924104

[Mucosa protective therapy with long-term nonsteroidal antirheumatic drugs].

Wolfgang Cozzarini1, Johannes Rath, Andreas Bauer, Ina Györög, Manfred Györög, Markus Prenner, Theodorus Trianto, Hermann Maderbacher, Erik Höller, Bernhard Grusch, Christian Sebesta.   

Abstract

Due to the extraordinary high prevalence of peptic lesions in the upper gastrointestine in the long-term treatment with nonsteroidal anti-inflammatory drugs, a prophylaxis in patients belonging to high-risk groups is essential. Misoprostol, proton pump inhibitors and histamine 2-receptor antagonists have been evaluated in prospective studies. The efficacy of Misoprostol is well documented, though its use in prevention is frequently limited due to side effects. Proton pump inhibitors are also well established, especially in the therapy of nonsteroidal anti-inflammatory drugs associated peptic ulcers and in consecutive secondary prevention. The histamine 2-receptor antagonist Famotidine in a high oral dosage is able to reduce the frequency of peptic lesions too, but not to the same degree as Misoprostol and proton pump inhibitors. It is very likely that helicobacter pylori eradication without any further mucosaprotective therapy will only decrease the incidence of upper gastrointestinal bleeding in low dose Aspirin application. In spite of controversial studies this eradication seems to be a useful additional therapy for ulcer prophylaxis in high risk groups. Selective Cyclooxygenase-2 inhibitors may become a promising alternative, from a pathophysiological perspective. However, to date there has been a lack of clear comparative studies with common nonsteroidal anti-inflammatory drugs plus mucosaprotecting agents. Daily therapy costs are higher with a Cyclooxygenase-2 inhibitor than using the traditional nonsteroidal anti-inflammatory drugs together with either proton pump inhibitors, histamine 2-receptor antagonists or Misoprostol--a fact that should be considered in primary therapeutic decisions. In the following review we will present the most important results of the different prophylactic and therapeutic modalities. On the basis of placebo-controlled, prospective studies on the one hand and the recommendations of the scientific societies on the other, a guideline for daily clinical practice will be suggested.

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Year:  2003        PMID: 12924104     DOI: 10.1046/j.1563-258x.2003.03035.x

Source DB:  PubMed          Journal:  Wien Med Wochenschr        ISSN: 0043-5341


  67 in total

1.  A double-blind comparison of the gastroduodenal safety and efficacy of diclofenac and a fixed dose combination of diclofenac and misoprostol in the treatment of rheumatoid arthritis.

Authors:  W Verdickt; C Moran; H Hantzschel; A M Fraga; H Stead; G S Geis
Journal:  Scand J Rheumatol       Date:  1992       Impact factor: 3.641

2.  Use of microbleeding and an ultrathin endoscope to assess gastric mucosal protection by famotidine.

Authors:  T K Daneshmend; P J Prichard; N K Bhaskar; P J Millns; C J Hawkey
Journal:  Gastroenterology       Date:  1989-10       Impact factor: 22.682

Review 3.  Are there differences among nonsteroidal antiinflammatory drugs? Comparing acetylated salicylates, nonacetylated salicylates, and nonacetylated nonsteroidal antiinflammatory drugs.

Authors:  D E Furst
Journal:  Arthritis Rheum       Date:  1994-01

4.  Risk of upper gastrointestinal bleeding and perforation associated with individual non-steroidal anti-inflammatory drugs.

Authors:  L A García Rodríguez; H Jick
Journal:  Lancet       Date:  1994-03-26       Impact factor: 79.321

5.  Prevention of nonsteroidal anti-inflammatory drug-induced gastrointestinal mucosal injury. A meta-analysis of randomized controlled clinical trials.

Authors:  M Koch; A Dezi; F Ferrario; I Capurso
Journal:  Arch Intern Med       Date:  1996-11-11

6.  Dose effects of aspirin on gastric prostaglandins and stomach mucosal injury.

Authors:  M Lee; B Cryer; M Feldman
Journal:  Ann Intern Med       Date:  1994-02-01       Impact factor: 25.391

7.  Non-steroidal anti-inflammatory drugs and life threatening complications of peptic ulceration.

Authors:  C P Armstrong; A L Blower
Journal:  Gut       Date:  1987-05       Impact factor: 23.059

8.  Prostaglandin synthase 2 gene disruption causes severe renal pathology in the mouse.

Authors:  S G Morham; R Langenbach; C D Loftin; H F Tiano; N Vouloumanos; J C Jennette; J F Mahler; K D Kluckman; A Ledford; C A Lee; O Smithies
Journal:  Cell       Date:  1995-11-03       Impact factor: 41.582

9.  Gastrointestinal tract complications of nonsteroidal anti-inflammatory drug treatment in rheumatoid arthritis. A prospective observational cohort study.

Authors:  G Singh; D R Ramey; D Morfeld; H Shi; H T Hatoum; J F Fries
Journal:  Arch Intern Med       Date:  1996-07-22

10.  Misoprostol dosage in the prevention of nonsteroidal anti-inflammatory drug-induced gastric and duodenal ulcers: a comparison of three regimens.

Authors:  J B Raskin; R H White; J E Jackson; A L Weaver; E A Tindall; R B Lies; D S Stanton
Journal:  Ann Intern Med       Date:  1995-09-01       Impact factor: 25.391

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