Key result
In patients with baseline gastric erosions, PA32540 (enteric-coated aspirin plus omeprazole) significantly reduced the development of endoscopic gastric ulcers compared to aspirin alone (4.2% vs 13.0%; P=0.001).
Why the study?
Does the addition of immediate-release omeprazole to enteric-coated aspirin prevent the development of endoscopic gastric ulcers in gastrointestinal-risk patients on secondary cardiovascular prevention?
RCT
double-blind
randomized
Does the addition of immediate-release omeprazole to enteric-coated aspirin prevent the development of endoscopic gastric ulcers in gastrointestinal-risk patients on secondary cardiovascular prevention?
Absolute Event Rate: 4.2% vs 13%
p-value: p=0.001
In patients at gastrointestinal risk taking aspirin for secondary cardiovascular prevention, baseline gastric erosions predispose to ulcer development, which is significantly reduced by the addition of immediate-release omeprazole.
May support omeprazole addition for ulcer prevention in erosions; leaves open need for outcome trials in secondary prevention.
Aspirin for secondary cardiovascular disease prevention is well established, but treatment discontinuation, often because of gastrointestinal mucosal injury or symptoms, can lead to increased risk for cardiovascular events. Proton pump inhibitor therapy is recommended for aspirin-treated patients at gastrointestinal risk. PA32540 [enteric-coated aspirin (EC-ASA) 325 mg + immediate-release omeprazole 40 mg] was compared with EC-ASA 325 mg alone once daily for 6 months in 2 duplicate, randomized double-blind trials in gastrointestinal-risk patients taking aspirin for ≥3 months for secondary prevention. In this post hoc analysis, we determined the prevalence of endoscopic upper gastrointestinal ulcers at screening and whether baseline endoscopic gastric erosions impacted subsequent ulcer development. At the screening endoscopy, 6% of subjects had upper gastrointestinal ulcers (not eligible for randomization) and 40% had gastric erosions. Conditional logistic regression modeling showed that baseline gastric erosions are significantly associated with endoscopic gastric ulcer development (OR = 2.12, 95% confidence interval, 1.26-3.57). In subjects with baseline gastric erosion, 4.2% of PA32540-treated versus 13.0% of EC-ASA-treated subjects (P = 0.001) subsequently developed endoscopic gastric ulcers. These data suggest that gastric injury predisposes to gastric ulcer development when taking EC-ASA, and exposure to immediate-release omeprazole in the presence of aspirin therapy significantly reduces the likelihood of progressing to gastric ulcers.
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Goldstein et al. (2016) conducted an RCT in Secondary cardiovascular disease prevention in gastrointestinal-risk patients. PA32540 (enteric-coated aspirin + immediate-release omeprazole) vs. EC-ASA 325 mg alone once daily was evaluated on Endoscopic gastric ulcer development in subjects with baseline gastric erosion (p=0.001). In patients with baseline gastric erosions, PA32540 (enteric-coated aspirin plus omeprazole) significantly reduced the development of endoscopic gastric ulcers compared to aspirin alone (4.2% vs 13.0%; P=0.001).
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