Parenteral nutrition compatibility and stability: Practical considerations

Author:

Boullata Joseph I.1,Salman Genene2,Mirtallo Jay M.3,Canada Todd W.4ORCID,Monczka Jessica5,Gura Kathleen M.6ORCID,Kiritsy Paul7

Affiliation:

1. JBoullata, PharmD Consulting Services Troy Pennsylvania USA

2. Department of Pharmacy Practice, College of Pharmacy Marshall B. Ketchum University Fullerton California USA

3. The American Society for Parenteral and Enteral Nutrition Silver Spring Maryland USA

4. University of Texas MD Anderson Cancer Center Houston Texas USA

5. Option Care Health Bannockburn Illinois USA

6. Division of Gastroenterology, Hepatology and Nutrition, Department of Pharmacy Boston Children's Hospital and Harvard Medical School Boston Massachusetts USA

7. Department of Pharmacy Practice Massachusetts College of Pharmacy and Health Sciences Boston Massachusetts USA

Abstract

AbstractParenteral nutrition (PN) is a complex preparation that contains multiple component products with the associated risk for incompatibilities and diminished stabilities when combined together as an admixture. Significant patient harm can result from prescribing, preparing, and administering PN without confirming compatibility and stability. Incompatibility or instability is rarely obvious to the unaided eye, so safe PN admixture relies on incorporating physicochemical properties of the included components into compatibility and stability decisions. Practices include applying active ingredient concentration limits to reduce risk for incompatibilities and instabilities. The purpose of the current article is to distill the wide‐ranging information on PN compatibility and stability into a feasible blueprint that individual healthcare organizations can then use to design and implement practical initiatives. Compatibility and stability considerations can be incorporated into the routine tasks of PN prescribing, order reviewing, preparing, and administering. The focus of this review is on identifying potential physicochemical interactions that can be addressed at each step in the PN use process. Organizations should incorporate compatibility and stability considerations into the routine procedures and practices of all clinicians involved with PN therapy. Those clinicians in healthcare organizations and caregivers in the home should then be in a position to safely provide the appropriate PN admixtures in terms of compatibility and stability.

Publisher

Wiley

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