Abstract
Non-steroidal anti-inflammatory drugs (NSAIDs) are well recognised as causing peptic ulceration and ulcer complications. However, several critical issues, including the amount of both gastrointestinal and non-gastrointestinal disease affected by NSAIDs, their interaction with ancillary risk factors, and how to optimise management in subgroups, remain poorly understood. In this article, strategies for subgroups that take account of non-specific gastrointestinal risks, minimisation of residual risk, and the importance of non-gastrointestinal toxicity are suggested, and areas for research identified.
MeSH terms
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Anti-Inflammatory Agents, Non-Steroidal / adverse effects*
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Anti-Ulcer Agents / therapeutic use
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Cyclooxygenase 2
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Cyclooxygenase 2 Inhibitors
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Cyclooxygenase Inhibitors / adverse effects*
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Drug Interactions
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Gastrointestinal Diseases / chemically induced*
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Gastrointestinal Diseases / epidemiology
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Gastrointestinal Diseases / prevention & control
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Humans
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Isoenzymes / metabolism
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Membrane Proteins
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Peptic Ulcer / chemically induced
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Prostaglandin-Endoperoxide Synthases / metabolism
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Proton Pump Inhibitors*
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Risk Factors
Substances
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Anti-Inflammatory Agents, Non-Steroidal
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Anti-Ulcer Agents
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Cyclooxygenase 2 Inhibitors
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Cyclooxygenase Inhibitors
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Isoenzymes
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Membrane Proteins
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Proton Pump Inhibitors
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Cyclooxygenase 2
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PTGS2 protein, human
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Prostaglandin-Endoperoxide Synthases