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dc.contributor.authorSeidler, Anna Lene
dc.contributor.authorAskie, Lisa
dc.contributor.authorRay, Joel G.
dc.date.accessioned2021-03-24T02:52:08Z
dc.date.available2021-03-24T02:52:08Z
dc.date.issued2018en_AU
dc.identifier.urihttps://hdl.handle.net/2123/24722
dc.description.abstractAspirin prophylaxis is recommended for women at higher risk of preeclampsia; yet, there is no consensus about the optimal dose., Moreover, in North America, aspirin is routinely only available in 81 mg and 325 mg tablets. While a recent metaanalysis suggested a dose-response effect, limitations therein included the inability to control for trial effects and maternal risk factors and a susceptibility to publication bias. Metaanalyses that use aggregate data pooled from different randomized controlled trials (RCTs) are also more likely to overestimate aspirin’s efficacy compared with those metaanalyses that use individual participant data (IPD). In response, we evaluated the efficacy of aspirin at different doses, using IPD from a large metaanalysis of preeclampsia prevention1 and then compared those findings to that of the recent Aspirin for Evidence-based Preeclampsia Prevention trial (ASPRE).en_AU
dc.language.isoenen_AU
dc.publisherAmerican Journal of Obstetrics & Gynecologyen_AU
dc.relation.ispartofAmerican Journal of Obstetrics & Gynecologyen_AU
dc.rightsCopyright All Rights Reserveden_AU
dc.titleOptimal aspirin dosing for preeclampsia preventionen_AU
dc.typeArticleen_AU
dc.subject.asrc11 Medical and Health Sciencesen_AU
dc.identifier.doi10.1016/j.ajog.2018.03.018
dc.rights.other© This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/en_AU
usyd.facultySeS faculties schools::Faculty of Medicine and Health::NHMRC Clinical Trials Centreen_AU
usyd.citation.volume219en_AU
usyd.citation.issue1en_AU
usyd.citation.spage117en_AU
usyd.citation.epage118en_AU
workflow.metadata.onlyNoen_AU


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