4.6 Article

Co-administration of drugs with parenteral nutrition in the neonatal intensive care unit-physical compatibility between three components

Journal

EUROPEAN JOURNAL OF PEDIATRICS
Volume 181, Issue 7, Pages 2685-2693

Publisher

SPRINGER
DOI: 10.1007/s00431-022-04466-z

Keywords

Numeta G13E; Morphine; Dopamine; Cefotaxime; Precipitation; Oil-droplet growth

Categories

Funding

  1. University of Oslo
  2. South-Eastern Norway Regional Health Authority [2018096]
  3. Hospital Pharmacy Enterprise South-Eastern Norway
  4. Oslo University Hospital

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This study provides compatibility data for intravenous therapy in neonatal intensive care unit (NICU) patients. By assessing particle formation and emulsion destabilisation, the study concludes that the drugs dopamine, morphine, and cefotaxime are compatible with the 3-in-1 parenteral nutrition Numeta G13E, ensuring safe co-administration in NICU patients.
There is a lack of compatibility data for intravenous therapy to neonatal intensive care unit (NICU) patients, and the purpose of this study was to contribute with documented physical compatibility data to ensure safe co-administration. We selected Numeta G13E, the 3-in-1 parenteral nutrition (PN) used at our NICU, together with the frequently used drugs morphine, dopamine and cefotaxime in two- but also three-component combinations. Incompatibility may lead to particle formation (precipitation) and oil-droplet growth (emulsion destabilisation), both which are undesirable and pose a safety risk to already unstable patients. We assessed potential particle formation of three mixing ratios for each combination (always including 1 + 1 ratio) using light obscuration, turbidity and pH measurements combined with visual inspection by focused Tyndall beam. Potential droplet-growth and emulsion destabilisation was assessed by estimating PFAT5 from droplet size measurements and counts, mean droplet diameter and polydispersity index from dynamic light scattering, and pH measurements. Mixed samples were always compared to unmixed controls to capture changes as a result of mixing and samples were analysed directly after mixing and after 4 h to simulate long contact time. None of the samples showed any sign of precipitation, neither in the drug-drug nor in the two- or three-component mixture with PN. Neither did we detect any form of emulsion destabilisation. Conclusion: Dopamine, morphine and cefotaxime were found to be compatible with NumetaG13E, and it is safe to coadminister these drugs together with this PN in NICU patients.

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