Low Dose Aspirin Alerts in High-Risk Pregnancies
Preeclampsia, Aspirin, Clinical Decision Support Systems
About this trial
This is an interventional prevention trial for Preeclampsia
Eligibility Criteria
Inclusion Criteria: Receiving prenatal care within Geisinger Initial prenatal visit prior to 28 weeks gestation Determined to be high risk for preeclampsia based on the modified United States Preventive Services Task Force and American College of Obstetrics and Gynecology criteria (at least 1 high risk factor) Exclusion Criteria: Not pregnant No prenatal visit prior to 28 weeks gestation Maternal-Fetal Medicine only visits Not meeting the modified USPSTF high-risk criteria Contraindication to aspirin, including allergy
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Best practice alert (BPA) intervention group
Standard care group
An electronic health record best practice alert (BPA) will alert healthcare providers to recommend low dose aspirin for pregnant patients at high-risk for preeclampsia. This alert also allows the healthcare provider to order an over-the-counter-prescription for low dose aspirin and automatically documents LDA in the patient's medication list.
Healthcare provider's recommendation for aspirin in patients at high-risk for preeclampsia will be based on current practice (no alerts) and the healthcare provider's knowledge.