Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19365
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dc.contributor.authorCarr, Anitra-
dc.contributor.authorWohlrab, Christina-
dc.contributor.authorYoung, Paul-
dc.contributor.authorBellomo, Rinaldo-
dc.date.accessioned2018-09-17T01:47:02Z-
dc.date.available2018-09-17T01:47:02Z-
dc.date.issued2018-09-
dc.identifier.citationCritical Care and Resuscitation 2018; 20(3): 180-181-
dc.identifier.issn1441-2772-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19365-
dc.description.abstractThere has recently been a surge of interest in intravenous (IV) vitamin C as a potential therapy in intensive care unit (ICU) patients, particularly in those with septic shock. Establishing the safety and efficacy of IV vitamin C therapy through rigorously conducted randomised controlled trials is a priority. A key logistical issue for such trials is to establish the stability of IV vitamin C solutions prepared for infusion ahead of time. Accordingly, we aimed to assess the stability of IV vitamin C solutions over time using doses of vitamin C from previous pilot trials. We used spectrophotometry to measure the concentration of vitamin C remaining in solutions of 1.5 g per 50 mL of 0.9% saline and 2.5 g per 50 mL of dextrose 5% in water (D5W) at 0, 1, 3, 6, 9, 24, 48, 72 and 96 hours after preparation. The concentration of vitamin C in these solutions over time was assessed at 4°C in the dark and at ambient temperature and light. The concentration of vitamin C in diluted solutions was essentially unchanged over a period of 24 hours, and decreased less than 10% by 96 hours both at 4°C in the dark and at ambient temperature and light. Our findings suggest that vitamin C solutions of 1.5 g per 50 mL of 0.9% saline and 2.5 g per 50 mL of D5W remain stable for up to 96 hours and do not need to be protected from light.-
dc.language.isoeng-
dc.titleStability of intravenous vitamin C solutions: a technical report.-
dc.typeJournal Article-
dc.identifier.journaltitleCritical Care and Resuscitation-
dc.identifier.affiliationDepartment of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand-
dc.identifier.affiliationDepartment of Intensive Care, Wellington Regional Hospital, Wellington, New Zealand-
dc.identifier.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.orcid0000-0002-1650-8939-
dc.identifier.pubmedid30153779-
dc.type.austinJournal Article-
local.name.researcherBellomo, Rinaldo
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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