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Risk Threshold for Starting Low Dose Aspirin in Pregnancy to Prevent Preeclampsia: An Opportunity at a Low Cost
Author(s) -
Emily Bartsch,
Alison L. Park,
John‏ Kingdom,
Joel G. Ray
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0116296
Subject(s) - medicine , preeclampsia , warrant , absolute risk reduction , aspirin , pregnancy , clinical trial , intensive care medicine , randomized controlled trial , risk assessment , relative risk , obstetrics , confidence interval , genetics , financial economics , economics , biology , computer security , computer science
Background Preeclampsia (PE) increases maternal and perinatal morbidity and mortality. Based on a multitude of data from randomized clinical trials, clinical practice guidelines endorse using ASA to prevent PE in women who are “at risk.” However, data are lacking about the level of absolute risk to warrant starting ASA prophylaxis. Methods and Findings We present two approaches for objectively determining the minimum absolute risk for PE at which ASA prophylaxis is justified. The first is a new approach—the minimum control event rate (CER min ). The second approach uses a pre-existing concept—the minimum event rate for treatment (MERT). Here we show how the CER min is derived, and then use the CER min and the MERT to guide us to a reasonable risk threshold for starting a woman on ASA prophylaxis against PE based on clinical risk assessment. We suggest that eligible women need not be at “high risk” for preeclampsia to warrant ASA, but rather at some modestly elevated absolute risk of 6–10%. Conclusions Given its very low cost, its widespread availability, ease of administration and its safety profile, ASA is a highly attractive agent for the prevention of maternal and perinatal morbidity worldwide.

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