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dc.contributor.authorKiguli, Sarah
dc.contributor.authorAkech, Samuel O
dc.contributor.authorMtove, George
dc.contributor.authorOpoka, Robert O
dc.contributor.authorEngoru, Charles
dc.contributor.authorOlupot-Olupot, Peter
dc.contributor.authorNyeko, Richard
dc.contributor.authorEvans, Jennifer
dc.contributor.authorCrawley, Jane
dc.contributor.authorPrevatt, Natalie
dc.contributor.authorReyburn, Hugh
dc.contributor.authorLevin, Michael
dc.contributor.authorGeorge, Elizabeth C
dc.contributor.authorSouth, Annabelle
dc.contributor.authorBabiker, Abdel G
dc.contributor.authorGibb, Diana M
dc.contributor.authorMaitland, Kathryn
dc.date.accessioned2021-07-29T06:27:08Z
dc.date.available2021-07-29T06:27:08Z
dc.date.issued2014
dc.identifier.citationKiguli, S... et al (2014). Authors’ reply to Southall. Bmj, 348.en_US
dc.identifier.other348:g1619
dc.identifier.urihttps://hdl.handle.net/123456789/302
dc.description.abstractSouthall made several points about our recent article.1 2 He suggests that “lethal hyperchloraemia” secondary to use of normal saline in FEAST (for boluses or maintenance) resulted in excess mortality. However, he did not comment on the key finding of the trial—that the increased 48 hour mortality was identical in both normal saline bolus (10.6%) and albumin bolus (10.6%) arms compared with the no bolus control group (7.3%).3 Harm was shown for every age group, in every condition, at each of the six hospitals, regardless of degree of acidosis,4 and for all definitions of shock.5 Despite differences in physical properties of albumin and saline, the timing of excess mortality after administration was identical (Kaplan-Meier mortality curves),3 making his hypothesis improbable.en_US
dc.language.isoenen_US
dc.publisherBMJ Publishing Group Ltden_US
dc.relation.ispartofseries;348:g1619
dc.subjectFluid resuscitationen_US
dc.subjectChildrenen_US
dc.titleWHO guidelines on fluid resuscitation in children : Authors’ reply to Southallen_US
dc.title.alternativeen_US


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