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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
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
dc.language.isoenen
dc.publisherAmerican Journal of Obstetrics & Gynecologyen
dc.relation.ispartofAmerican Journal of Obstetrics & Gynecologyen
dc.rightsCopyright All Rights Reserveden
dc.titleOptimal aspirin dosing for preeclampsia preventionen
dc.typeArticleen
dc.subject.asrc11 Medical and Health Sciencesen
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
usyd.facultySeS faculties schools::Faculty of Medicine and Health::NHMRC Clinical Trials Centreen
usyd.citation.volume219en
usyd.citation.issue1en
usyd.citation.spage117en
usyd.citation.epage118en
workflow.metadata.onlyNoen


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