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Please use this identifier to cite or link to this item: https://hdl.handle.net/11055/767
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dc.contributor.authorDennis ATen_US
dc.contributor.authorMulligan Sen_US
dc.date.accessioned2018-10-17T23:00:11Z-
dc.date.available2018-10-17T23:00:11Z-
dc.date.issued2016-
dc.identifier.citation35(4):520-528en_US
dc.identifier.urihttp://hdl.handle.net/11055/767-
dc.description.abstractOBJECTIVE: We determined pain experience and analgesic usage in women with preeclampsia (PE) after caesarean section (CS). METHOD: We conducted a one-year retrospective case (PE), control (healthy pregnancy HP) study in women undergoing CS. RESULTS: Sixty-two women were included. Cases received more intrathecal bupivacaine (mean difference 0.4 mg) and in the first six hours postoperatively received (mean ± SD, % or median (interquartile range, IQR)), less oxycodone (11.5 ± 3.9 mg versus 14.3 ± 5.1 mg, p < 0.031), less often received parecoxib (43% versus 100%, p < 0.001), and reported less maximum pain scores (0 (0,5) versus 4 (3,6), p < 0.005). CONCLUSION: Women with PE received less analgesia and experienced less pain compared to controls.en_US
dc.subjectPregnancyen_US
dc.subjectpre-eclampsiaen_US
dc.subjectanalgesicsen_US
dc.subjectPain Managementen_US
dc.subjectanalgesiaen_US
dc.subjectcesarean sectionen_US
dc.titleAnalgesic requirements and pain experience after caesarean section under neuraxial anaesthesia in women with preeclampsiaen_US
dc.typeJournal Articleen_US
dc.type.contentTexten_US
dc.identifier.journaltitleHypertension in Pregnancyen_US
dc.identifier.doihttps://doi.org/10.1080/10641955.2016.1192643en_US
dc.type.studyortrialCase Control Studiesen_US
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
Appears in Collections:Scholarly and Clinical
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