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Parenteral Protein Decision Support System Improves Protein Delivery in Preterm Infants: A Randomized Clinical Trial
Mhd Wael Alrifai1, David P Mulherin2, Stuart T Weinberg1,3
1Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Insights
The Parenteral Protein Calculator (PPC) improved protein dosing accuracy for preterm infants receiving parenteral nutrition (PN). This clinical decision support system helps optimize protein intake for vulnerable newborns.
Area of Science:
- Neonatology
- Clinical Nutrition
- Medical Informatics
Background:
- Accurate parenteral protein delivery is critical but complex for preterm infants.
- Daily adjustments are needed based on infant's age, weight, and enteral intake.
- Existing methods present challenges in precise protein dosing.
Purpose of the Study:
- To develop and assess the Parenteral Protein Calculator (PPC).
- To evaluate the PPC as a clinical decision support system for parenteral nutrition (PN) in preterm infants.
- To enhance the accuracy of protein administration in this vulnerable population.
Main Methods:
- A randomized controlled trial compared the PPC to routine care.
- The PPC was integrated into a computerized provider order entry system.
- Infants under 3 days old with birth weight ≤1500g were eligible.
Main Results:
- The PPC group showed significantly more accurate protein dosing (OR=5.8).
- Absolute deviation from the protein target was reduced by 0.41 g/kg in the PPC group.
- The study involved 42 infants across 432 total PN days.
Conclusions:
- The PPC effectively improved protein dosing accuracy for preterm infants on PN.
- Further research is warranted to assess the impact of such systems on growth and uremia.
- Replication in other PN nutrient management is suggested.
Background:
Management of neonatal parenteral protein intake for preterm infants is challenging and requires daily modifications of the dose to account for the infant's postnatal age, birth weight, current weight, and the volume and protein concentration of concurrent enteral nutrition. The objective of this study was to create and evaluate the Parenteral Protein Calculator (PPC), a clinical decision support system to improve the accuracy of protein intake for preterm infants who require parenteral nutrition (PN).
Materials And Methods:
We integrated the PPC into the computerized provider order entry system and tested it in a randomized controlled trial (routine or PPC). Infants were eligible if they were ≤3 days old, had a birth weight ≤1500 g, and had no inborn error of metabolism. The primary outcome was the appropriate total protein intake, defined as target protein dose ±0.5 g/kg.
Results:
We randomly allocated 42 infants for 221 PN days in the control group and 211 in the PPC group. Total protein intake in the PPC group was more accurate as compared with the control group (appropriate protein dosing: odds ratio = 5.8; 95% CI, 2.7-12.4). Absolute deviation from protein target was 0.41 g/kg (0.24-0.58) lower in the PPC group.
Conclusion:
The PPC improved appropriate protein dosing for premature infants receiving PN. Further studies are needed to test whether clinical decision support systems will reduce uremia and improve growth and to replicate similar findings in the cases of other PN nutrients.
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