[Prophylaxis and therapy of gastropathy caused by non-steroidal anti-inflammatory drugs]

Orv Hetil. 2002 Jul 7;143(27):1643-8.
[Article in Hungarian]

Abstract

Introduction: The main disadvantage of the nonsteroidal anti-inflammatory drugs (NSAID) is their toxic effect on the gastroduodenal mucosa, which can cause life-threatening complications.

Aims: We discuss the possibilities to prevent the harmful effect of the NSAIDs: the use of safer NSAIDs, and the co-therapy with protective mechanisms.

Methods: Among the safer NSAIDs we discuss the preferentially selective, and the highly selective COX-2 inhibitors, and the new, nitric-oxide releasing NSAIDs. We consider the role of the mucosa-protecting mechanisms: antacids, sucralfate, H2 receptor antagonists, proton-pump inhibitors, and misoprostol.

Conclusions: The most effective opportunities to protect the gastroduodenal mucosa--which is highly recommended for the high risk group of patients--are the usage of highly selective NSAIDs, or the concomitant therapy with proton-pump inhibitors or misoprostol. The value of the letter is diminished by it's side effects.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Antacids / therapeutic use
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects*
  • Anti-Ulcer Agents / therapeutic use*
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / adverse effects
  • Gastric Mucosa / drug effects*
  • Gastric Mucosa / metabolism
  • Histamine H2 Antagonists / therapeutic use
  • Humans
  • Isoenzymes / antagonists & inhibitors
  • Membrane Proteins
  • Peptic Ulcer / chemically induced
  • Peptic Ulcer / drug therapy*
  • Peptic Ulcer / metabolism
  • Peptic Ulcer / prevention & control*
  • Prostaglandin-Endoperoxide Synthases
  • Prostaglandins, Synthetic / therapeutic use
  • Proton Pump Inhibitors
  • Sucralfate / therapeutic use

Substances

  • Antacids
  • Anti-Inflammatory Agents, Non-Steroidal
  • Anti-Ulcer Agents
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Histamine H2 Antagonists
  • Isoenzymes
  • Membrane Proteins
  • Prostaglandins, Synthetic
  • Proton Pump Inhibitors
  • Sucralfate
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases