Summary of Recommendation and Evidence
The U.S. Preventive Services Task Force (USPSTF) recommends the use of low-dose aspirin (81 mg per day) as preventive medication after 12 weeks of gestation in women who are at high risk of preeclampsia (Table 1). B recommendation.
|Population||Asymptomatic pregnant women who are at high risk of preeclampsia|
|Recommendation||Prescribe low-dose (81 mg per day) aspirin after 12 weeks of gestation.|
|Risk assessment||Pregnant women are at high risk of preeclampsia if they have one or more of the following risk factors:|
|• History of preeclampsia, especially when accompanied by an adverse outcome|
|• Multifetal gestation|
|• Chronic hypertension|
|• Type 1 or 2 diabetes mellitus|
|• Renal disease|
|• Autoimmune disease (i.e., systemic lupus erythematosus, antiphospholipid syndrome)|
|Preventive medication||Low-dose aspirin (60 to 150 mg per day) initiated between 12 and 28 weeks of gestation reduces the occurrence of preeclampsia, preterm birth, and intrauterine growth restriction in women at increased risk of preeclampsia.|
|The harms of low-dose aspirin in pregnancy are considered to be no greater than small.|
|Balance of benefits and harms||There is a substantial net benefit of daily low-dose aspirin use to reduce the risk of preeclampsia, preterm birth, and intrauterine growth restriction in women at high risk of preeclampsia.|
|Other relevant USPSTF recommendations||The USPSTF recommends that all women planning or capable of pregnancy take a daily supplement containing 0.4 to 0.8 mg (400 to 800 mcg) of folic acid. This recommendation is available at http://www.uspreventiveservicestaskforce.org/.|
See the Clinical Considerations section for additional information about risk factors, timing, and dosage.
Preeclampsia is one of the most serious health problems affecting pregnant women. It is a complication in 2% to 8% of pregnancies worldwide, and contributes to maternal and infant morbidity and mortality. Preeclampsia also accounts for 15% of preterm births in the United States.1 The disorder is defined by the onset of hypertension (blood pressure greater than 140/90 mm Hg) and proteinuria (0.3 g or more of protein in the urine within a 24-hour period) during the second half of pregnancy (after 20 weeks). In the absence of proteinuria, preeclampsia is classified as hypertension with any of the following: thrombocytopenia, impaired liver function, renal insufficiency, pulmonary edema, or cerebral or visual disturbances.2
RECOGNITION OF RISK STATUS
Important risk factors for preeclampsia include history of preeclampsia (including early-onset preeclampsia), intrauterine growth restriction (IUGR), or preterm birth; placental abruption or fetal death; maternal comorbid conditions (including type 1 or 2 pregestational diabetes mellitus, chronic hypertension, renal disease, and autoimmune diseases); and multifetal gestation.1
BENEFITS OF PREVENTIVE MEDICATION
The USPSTF found adequate evidence of a reduction in risk of preeclampsia, preterm birth, and IUGR in women at increased risk of preeclampsia who received low-dose aspirin, thus demonstrating substantial benefit.
Low-dose aspirin (range, 60 to 150 mg per day) reduced the risk of preeclampsia by 24% in clinical trials and reduced the risk of preterm birth by 14% and IUGR by 20%.
HARMS OF PREVENTIVE MEDICATION
The USPSTF found adequate evidence that low-dose aspirin as preventive medication does not increase the risk of placental abruption, postpartum hemorrhage, or fetal intracranial bleeding. In a meta-analysis of randomized controlled trials and observational studies of women at low/average or increased risk of preeclampsia, there was no significantly increased risk of these adverse events. In addition, there was no difference in the risk of placental abruption by aspirin dosage.
The USPSTF also found adequate evidence that low-dose aspirin as preventive medication in women at increased risk of preeclampsia does not increase the risk of perinatal mortality.
Evidence on long-term outcomes in offspring exposed in utero to low-dose aspirin is limited, but no developmental harms were identified by 18 months of age in the one study reviewed.
The USPSTF concludes that the harms of low-dose aspirin in pregnancy are no greater than small.
The USPSTF concludes with moderate certainty that there is a substantial net benefit of daily low-dose aspirin use to reduce the risk of preeclampsia, preterm birth, and IUGR in women at high risk of preeclampsia.
This recommendation applies to asymptomatic pregnant women who are at increased risk of preeclampsia and who have no prior adverse effects with or contraindications to low-dose aspirin.
ASSESSMENT OF RISK FOR PREECLAMPSIA
There are no validated methods of identifying women at high risk of preeclampsia on the basis of biomarkers, clinical diagnostic tests, or medical history. Most clinicians use medical history to identify women at high risk. Risk factors, based on medical history, may help guide clinicians and their patients in the decision to begin aspirin use.
Although clinical risk assessments were not systematically reviewed for this recommendation, a pragmatic approach is described in Table 2.1,5 This approach may help to identify a patient population with an absolute risk of preeclampsia of at least 8%, which is consistent with the lowest preeclampsia incidence observed in control groups in studies reviewed by the USPSTF.1 Women with one or more high-risk factors should receive low-dose aspirin. Women with several moderate-risk factors may also benefit from low-dose aspirin (Table 21 ,5 ), but the evidence is less certain for this approach. Clinicians should use clinical judgment in assessing the risk of preeclampsia and talk with their patients about the benefits and harms of low-dose aspirin use.
|Risk level||Risk factors||Recommendation|
ASSESSMENT OF RISK FOR ADVERSE EFFECTS
Low-dose aspirin use in women at increased risk of preeclampsia has not been shown to increase the occurrence of placental abruption; postpartum hemorrhage; or fetal harms, such as intracranial bleeding and congenital anomalies.
USE OF PREVENTIVE MEDICATION
The dosage and timing of initiation of low-dose aspirin varied across studies. However, the beneficial effects and small harms of low-dose aspirin were consistent across dosages and timing of initiation. It was not possible to determine from the evidence whether a specific dosage or timing of aspirin use conferred greater benefit over other dosages or intervals.
Dosage. Low-dose aspirin at dosages between 60 and 150 mg per day reduced the occurrence of preeclampsia, preterm birth, and IUGR in women at increased risk of preeclampsia in several randomized trials.1 The most commonly used dosage was 100 mg per day, but the two largest trials contributing to the estimates of benefit used 60 mg per day.1,6,7 Although studies did not evaluate a dosage of 81 mg per day, low-dose aspirin is available in the United States as 81-mg tablets, which is a reasonable dosage for prophylaxis in women at high risk of preeclampsia.
Timing. Use of low-dose aspirin was initiated between 12 and 28 weeks of gestation. Evidence did not suggest additional benefit when use of aspirin was started earlier (12 to 16 weeks) rather than later (after 16 weeks) in pregnancy in women at increased risk of preeclampsia.1
This recommendation statement was first published in Ann Intern Med. 2014;161(11):819–826.
The “Other Considerations,” “Discussion,” “Update of Previous USPSTF Recommendation,” and “Recommendations of Others” sections of this recommendation statement are available at http://www.uspreventiveservicestaskforce.org/Page/Topic/recommendation-summary/low-dose-aspirin-use-for-the-prevention-of-morbidity-and-mortality-from-preeclampsia-preventive-medication.
The USPSTF recommendations are independent of the U.S. government. They do not represent the views of the Agency for Healthcare Research and Quality, the U.S. Department of Health and Human Services, or the U.S. Public Health Service.