PPIs and antiplatelet drugs can be used together after careful consideration of risks and benefits

The potential benefits of antiplatelet therapy for patients with atherosclerotic CV disease have been amply demonstrated, especially among patients at higher risk of CV events. However, use of antiplatelet drugs increases the risk of upper GI bleeding from pre-existing ulcers, lesions and other tissue breaks in the GI tract. Those at highest risk for GI bleeding are patients with a history of previous GI bleeding, as well as patients with multiple risk factors for upper GI bleeding, including: a history of peptic ulcer disease; advanced age; use of anticoagulants, steroids, or NSAIDs; and H. pylori infection.

"PPIs are prescribed together with antiplatelet drugs for one reason ─ to reduce the increased risk of GI complications caused by antiplatelet drugs," according to the new expert consensus document. PPIs suppress gastric acid production, which helps heal the pre-existing lesions and aspirin-related ulcers.

"Our goal was to carefully evaluate recent studies that suggested a potential dangerous interaction between PPIs and thienopyridines, in order to provide clinicians with a pragmatic evidence-based approach for safer prescribing of antiplatelet drugs, especially among patients in whom the risk-benefit ratio requires a careful assessement," said Neena S. Abraham, M.D., MSCE, FACG, a gastroenterologist at the Michael E. DeBakey VAMC and Baylor College of Medicine, the chair of the document's writing committee. "The document summarizes the best evidence and incorporates the expert clinical viewpoints of both cardiologists and gastroenterologists, who face this dilemma on a daily basis."

Conflicting Data Clouded Clinical Picture for PPIs and Antiplatelet Drugs

Following the publication of the organizations' 2008 document recommending simultaneous prescription of a PPI in high-risk patients, new research suggested an adverse interaction between the two drugs that may lessen the antiplatelet effects of thienopyridines and thereby place patients at an increased risk of CV events. Experts from the ACCF, ACG and AHA observe that it has been difficult for physicians to assimilate this flood of information and to develop optimal treatment strategies for managing patients who might benefit from antiplatelet therapy, yet who might suffer from GI bleeding.

"The flurry of conflicting data published following the 2008 Expert Consensus Document left many practitioners confused," Abraham commented. "However, much of the published data used results of platelet function tests as surrogate markers of cardiovascular risk. The differences in drug levels and in platelet function studies caused concern about an adverse drug interaction, but the clinical significance of these laboratory test results has not been substantiated when held to the higher scientific standard of large patient studies with clinically relevant endpoints, such as heart attacks or strokes."

Moreover, the recent publication of a randomized trial (COGENT) of 3761 patients with cardiovascular disease demonstrated a substantial decrease (56 percent) in GI bleeding, with no significant difference in cardiac events, among the patients randomized to concomitant use of clopidogrel and a PPI compared with patients randomized to clopidogrel alone. "This study is of particular importance as it is the only published randomized controlled trial specifically designed to assess the clinical occurrence of GI bleeding, heart attacks and strokes associated with the prescription of clopidogrel alone versus clopidogrel with a PPI," noted Dr. Abraham.

New Recommendations Clarify Appropriate Therapy by Weighing Risk-Benefit

The new recommendations include:

The use of PPIs is recommended for patients with a history of upper GI bleeding or for those with multiple risk factors for upper GI bleeding, including a history of peptic ulcer disease; advanced age; use of anticoagulants, steroids, or NSAIDs; and H. pylori infection.

PPIs are not recommended to reduce upper GI bleeding in patients who have a lower risk of upper GI bleeding, and who have much less potential to benefit from prophylactic therapy.

Future studies are required to assess the impact of concomitant PPI and antiplatelet use among the small subset of high-risk cardiac patients with an impaired ability to metabolize antiplatelet drugs.

"Use of PPIs and antiplatelet drugs must be individualized, not done as a matter of routine," said Mark A. Hlatky, M.D., FACC, a cardiologist at Stanford University School of Medicine and vice-chair of the writing group. "The risk of GI bleeding varies among individuals, as does the risk of cardiac events. In patients at high risk of GI bleeding who require antiplatelet therapy for heart disease, the balance of risk and benefit favor use of PPIs together with antiplatelet drugs. In patients at low risk of GI bleeding, however, the balance of risk and benefit tips away from using PPIs together with antiplatelet drugs. We need additional research to determine whether genetic testing or platelet function testing are useful in individualizing treatment with antiplatelet drugs."

INFORMATION: Full text of this report will be published in the Journal of the American College of Cardiology, The American Journal of Gastroenterology, and Circulation: Journal of the American Heart Association. It will also be available on the ACC (www.cardiosource.org), AHA (www.heart.org), and ACG (www.acg.gi.org) web sites.

The work of the writing committee was supported exclusively by the ACCF without any commercial support. Dr. Abraham and Dr. Hlatky report no conflicts of interest.

The American College of Cardiology is transforming cardiovascular care and improving heart health through continuous quality improvement, patient-centered care, payment innovation and professionalism. The College is a 39,000-member nonprofit medical society comprised of physicians, surgeons, nurses, physician assistants, pharmacists and practice managers, and bestows credentials upon cardiovascular specialists who meet its stringent qualifications. The College is a leader in the formulation of health policy, standards and guidelines, and is a staunch supporter of cardiovascular research. The ACC provides professional education and operates national registries for the measurement and improvement of quality care. More information about the association is available online at http://www.cardiosource.org/ACC.

The American Heart Association, founded in 1924, is the nation's oldest and largest voluntary health organization dedicated to building healthier lives, free of heart disease and stroke. To help prevent, treat and defeat these diseases — America's No. 1 and No. 3 killers — we fund cutting-edge research, conduct lifesaving public and professional educational programs, and advocate to protect public health. To learn more or join us in helping all Americans, call 1-800-AHA-USA1 or visit www.heart.org.

Founded in 1932, the American College of Gastroenterology (ACG) is an organization with an international membership of more than 12,000 individuals from 80 countries. The College is committed to serving the clinically oriented digestive disease specialist through its emphasis on scholarly practice, teaching and research. The mission of the College is to serve the evolving needs of physicians in the delivery of high quality, scientifically sound, humanistic, ethical, and cost-effective health care to gastroenterology patients. www.acg.gi.org