Related Experiment Videos
[The effect of aspirin alone or aspirin plus additional antiplatelets therapy on upper gastrointestinal hemorrhage]
Suh Eun Bae1, Seong-Eun Kim, Sung-Ae Jung
1Department of Internal Medicine, Ewha Medical Research Institute, Ewha Womans University School of Medicine, Seoul, Korea.
Insights
Adding antiplatelet agents to aspirin did not increase upper gastrointestinal hemorrhage rates. However, patients on antiplatelet therapy with GI symptoms require active diagnostic and therapeutic management.
Area of Science:
- Cardiology
- Gastroenterology
- Pharmacology
Background:
- Cardiovascular disease incidence drives antiplatelet agent use.
- Antiplatelet agents increase upper gastrointestinal (GI) hemorrhage risk.
- Understanding hemorrhage in patients on dual/triple antiplatelet therapy is crucial.
Purpose of the Study:
- To examine clinical characteristics of upper GI hemorrhage in patients receiving aspirin alone versus combination antiplatelet therapy.
- To compare hemorrhage rates and clinical outcomes between different antiplatelet regimens.
- To identify risk factors and management strategies for GI bleeding during antiplatelet therapy.
Main Methods:
- Retrospective review of 656 patients undergoing coronary stenting.
- Patients categorized into aspirin alone, aspirin plus clopidogrel, or triple antiplatelet therapy groups.
- Comparison with a control group experiencing GI hemorrhage without antiplatelet use.
Main Results:
- Upper GI hemorrhage occurred in 3.8% of patients; 48.2% had ulcers.
- No significant difference in hemorrhage rates among antiplatelet groups.
- Antiplatelet-related hemorrhage group showed lower H. pylori rates, longer admissions, and higher mortality.
Conclusions:
- Combination antiplatelet therapy with aspirin does not elevate hemorrhage risk compared to aspirin alone.
- Active diagnostic and therapeutic interventions are recommended for GI symptoms in patients on antiplatelet therapy.
- Further research into managing GI complications during antiplatelet treatment is warranted.
Background/Aims:
The increasing incidence of cardiovascular disease has led to an increase in the frequency of upper gastrointestinal (GI) hemorrhage due to the use of antiplatelet agents. This study examined the clinical characteristics of patients with upper GI hemorrhage who were administered aspirin alone or a combination treatment of antiplatelet agents.
Methods:
A 656 patients who underwent drug-eluting coronary stenting at Ewha Mokdong Hospital in 2008 were divided into three groups according to the antiplatetlet agents used after the intervention; groups of aspirin alone, aspirin plus clopidogrel, and aspirin, and clopidogrel plus another antiplatelet agent, respectively. Patients admitted with GI hemorrhage in the same period without a medication history of antiplatelet or nonsteroidal anti-inflammatory drugs were used as the control hemorrhage group. The medical records were reviewed.
Results:
Significant GI symptoms were observed in 21.1% of total patients, of whom 48.2% had ulcers. The upper GI hemorrhage rate was 3.8%. There was no significant difference in the hemorrhage rate between three groups. Compared to the control hemorrhage group, the endoscopic variables of the antiplatelet-related hemorrhage group were not significantly different. However, the Helicobacter pylori infection rate was lower, the admission period was longer, and the mortality rate was higher in the antiplatelet-related hemorrhage group (p<0.05, respectively). There was no direct association between restarting or discontinuance of antiplatelets after the hemorrhage event and mortality.
Conclusions:
Adding other antiplatelet agents to aspirin did not increase the hemorrhage rate. However, active diagnostic and therapeutic efforts are recommended in patients with GI symptoms during antiplatelet therapy.
Related Concept Videos
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Peptic Ulcer Disease IV: Management
The therapeutic approach involves ensuring adequate rest, implementing drug therapy, promoting smoking cessation, making dietary modifications, and emphasizing long-term follow-up care.
Pharmacological management
The prevailing therapy for peptic ulcers involves a combination of managing the patient's current medication...
Drug toxicity: Drug–Drug Interaction
Drugs for Peptic Ulcer Disease: Sucralfate as Mucosal Protective Agents
In this scenario, mucosal protective agents like sucralfate play an essential role. Sucralfate, a complex of sulfated sucrose and aluminum hydroxide, demonstrates its usefulness in acidic conditions,...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...