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Gastrointestinal bleeding after percutaneous coronary intervention
Tetsuya Tanigawa1, Toshio Watanabe, Yuji Nadatani
1Department of Gastroenterology, Osaka City University Graduate School of Medicine, Abeno-ku, Osaka City, Japan. ttanigawa@med.osaka-cu.ac.jp
Insights
Dual antiplatelet therapy after percutaneous coronary intervention (PCI) increases gastrointestinal (GI) bleeding risk by approximately 2%. Identifying and mitigating risk factors is crucial for patient outcomes following PCI procedures.
Area of Science:
- Cardiology
- Gastroenterology
- Pharmacology
Background:
- Percutaneous coronary intervention (PCI) is a common procedure for coronary artery disease.
- Dual antiplatelet therapy (DAPT) with aspirin and thienopyridine is standard post-PCI care.
- Gastrointestinal (GI) bleeding is a serious complication of DAPT.
Purpose of the Study:
- To review published studies on GI bleeding in patients undergoing PCI.
- To identify the prevalence, risk factors, and consequences of GI bleeding after PCI.
- To evaluate current prophylactic strategies and the need for further research.
Main Methods:
- Systematic review of published literature on GI bleeding post-PCI.
- Analysis of prevalence, associated risk factors, and clinical outcomes.
- Assessment of proposed prophylactic measures.
Main Results:
- GI bleeding occurs in approximately 2% of patients on DAPT post-PCI.
- Major risk factors include advanced age, history of peptic ulcers, NSAID/anticoagulant use, and stress.
- GI bleeding increases morbidity, mortality, hospitalization duration, and costs.
Conclusions:
- DAPT following PCI significantly increases GI bleeding risk.
- Several risk factors are identified, necessitating careful patient selection and monitoring.
- Further randomized controlled trials are needed to establish optimal prophylactic strategies against GI bleeding post-PCI.
Abstract:
Percutaneous coronary intervention (PCI) is now performed in a wide range of patients with coronary artery disease. Complications of PCI include in-stent re-stenosis and in-stent thrombosis. According to the recent 2005 guidelines of the American College of Cardiology/American Heart Association/Society for Cardiovascular Angiography and Interventions, dual antiplatelet therapy with low-dose aspirin and thienopyridine derivatives such as ticlopidine and clopidogrel should be used in patients who have undergone PCI. A serious complication of dual antiplatelet therapy is bleeding, most of which arise from the gastrointestinal (GI) tract. In this article we review published studies about GI bleeding in patients who have undergone PCI. The prevalence of GI bleeding in patients who are administered dual antiplatelet therapy following PCI is approximately 2%, and GI bleeding after PCI is associated with increased morbidity, mortality, duration of hospitalization and cost. Advanced age, a history of peptic ulcer disease, co-administration of non-steroidal anti-inflammatory drugs, co-administration of anticoagulants, and physiological stress are considered to be the major risk factors for GI bleeding in patients undergoing antiplatelet therapy following PCI. Recent clinical and experimental studies indicate that administration of low-dose aspirin may also increase the risk of adverse events in the small intestine. Although some prophylactic strategies such as proton-pump inhibitor, H₂ receptor antagonist and eradication of Helicobacter pylori are proposed, there are few randomized controlled trials assessing the best strategy for the prevention of GI bleeding after PCI. Further extensive studies are required to ascertain the beneficial effect of prophylactic agents for dual antiplatelet therapy following PCI.
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