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- W3136759132 abstract "Concerns have been raised by Klang and Gura,1 about study results reported by myself and colleagues on the compatibility of medications with intravenous lipid emulsions. The first concern raised is that our methodology did not evaluate the impact of parenteral nutrition (PN) on the compatibilities reported. That was a noted limitation of the study. We appreciate the authors’ concern that the results may be interpreted incorrectly; however, this is an inherent risk of any publication. When applying this information to clinical practice, the onus is on practitioners to review the literature and ensure they are confident in their recommendation. We could argue this is true of compatibility databases on a broader scope. When assessing compatibility, it is tempting to look at the compatibility summary, but on further investigation the compatibility doesn’t apply to the clinical situation due to limitations such as differences in formulation (eg, a 3:1 total nutrient admixture vs a 2:1 total parenteral nutrition [TPN]:lipid admixture), and poor methodology, to name a few." @default.
- W3136759132 created "2021-03-29" @default.
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- W3136759132 date "2021-03-26" @default.
- W3136759132 modified "2023-09-26" @default.
- W3136759132 title "Validity of methods used in medication Y-site mixing study" @default.
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- W3136759132 doi "https://doi.org/10.1093/ajhp/zxab126" @default.
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