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Sodium Valproate Incompatibility with Parenteral Nutrition Admixtures-A Risk to Patient Safety: An In Vitro
Ludwika Piwowarczyk1, Szymon Tomczak1, Patryk Antkowiak1
1Department of Pharmaceutical Chemistry, Poznan University of Medical Sciences, 6 Grunwaldzka, 60-780 Poznań, Poland.
Insights
Sodium valproate (VPA) co-administration with parenteral nutrition admixtures (PNAs) was studied. Compatibility was only met with omega-3-acid-triglyceride-based PNAs, highlighting risks of simultaneous VPA infusion.
Area of Science:
- Pharmacology
- Clinical Pharmacy
- Patient Safety
Background:
- Epilepsy management often requires antiepileptic drugs like sodium valproate (VPA).
- Intensive care units (ICUs) frequently administer VPA and parenteral nutrition admixtures (PNAs) simultaneously.
- Drug-PNA incompatibilities are a significant risk to patient safety, yet VPA-PNA compatibility is unstudied.
Purpose of the Study:
- To investigate the compatibility of sodium valproate (VPA) when co-administered with various parenteral nutrition admixtures (PNAs).
- To assess the impact of PNA composition on VPA stability and safety during simultaneous infusion.
Main Methods:
- Evaluated VPA-PNA compatibility using visual inspection, pH, osmolality, zeta potential, particle size, polydispersity index, and turbidity.
- Tested multiple commercially available PNAs, focusing on those containing omega-3-acid-triglycerides.
Main Results:
- PNA lipid emulsion composition significantly impacts drug-PNA compatibility.
- Acceptance criteria for VPA compatibility were met only by PNAs containing omega-3-acid-triglycerides (Omegaflex special and peri).
- Most tested PNAs exhibited particle fractions >1000 nm, disqualifying simultaneous administration with VPA.
Conclusions:
- Simultaneous administration of sodium valproate (VPA) with most common parenteral nutrition admixtures (PNAs) is not recommended due to incompatibility.
- PNAs containing omega-3-acid-triglycerides demonstrate better compatibility with VPA.
- Further research and clear guidelines are needed to ensure safe co-administration of VPA and PNAs in clinical practice.
Abstract:
Epilepsy is defined as a group of concerning problems related to the nervous system; its defining feature is a predisposition to epileptic seizures. The frequency of seizures in intensive care units (ICU) ranges from 3.3% to 34%, and ICU antiepileptic treatment is routine practice. The administration of drugs through the same infusion line is not recommended but is common clinical practice, especially in ICU. Incompatibilities between parenteral drugs and between drugs and parenteral nutrition admixtures (PNAs) are common medical errors and pose risks to patient safety. The co-administration of drugs must always be confirmed and clearly defined. The simultaneous infusion of sodium valproate (VPA, drug used to treat seizures and epilepsy) with parenteral PNAs has not yet been studied. During the experiment reported in this study, a visual control, pH, osmolality, zeta potential, particle size, polydispersity index, and turbidity were measured. The conducted research shows that the lipid emulsion composition has a significant influence on drug-PN (drug-parenteral nutrition) compatibility. The acceptance criteria were met only for PNs containing omega-3-acid-triglycerides (Omegaflex special and peri). The second fraction of particles above 1000 nm was observed for most of the tested PNAs (Lipoflex special, Lipoflex peri, Kabiven, SmofKabiven, Kabiven Peripheral, and Olimel Peri N4E), which disqualifies their simultaneous administration with VPA.
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