Evaluation of the Safety of Rapid Parenteral Nutrition Titration
Autor: | Amanda Giancarelli, Donald C. Vickers, Dominick Curry |
---|---|
Rok vydání: | 2018 |
Předmět: |
Adult
medicine.medical_specialty Parenteral Nutrition 030309 nutrition & dietetics Critical Illness Medicine (miscellaneous) Refeeding syndrome Gastroenterology Hypomagnesemia 03 medical and health sciences 0302 clinical medicine Internal medicine medicine Humans In patient Retrospective Studies 0303 health sciences Nutrition and Dietetics business.industry Incidence (epidemiology) Retrospective cohort study medicine.disease Hypokalemia Parenteral nutrition Hyperglycemia 030211 gastroenterology & hepatology Parenteral Nutrition Total medicine.symptom business Hypophosphatemia |
Zdroj: | JPEN. Journal of parenteral and enteral nutritionReferences. 44(3) |
ISSN: | 1941-2444 |
Popis: | Initiation of parenteral nutrition (PN) can cause complications including hyperglycemia (HGL), electrolyte abnormalities, and refeeding syndrome (RFS). These concerns lead many to titrate over several days, but our practice is to titrate PN to goal within 8 hours. The aim of this study was to evaluate the safety of titrating PN to goal within 8 hours.This was a single-center, retrospective study of adult patients initiated on continuous PN with titration to goal rate in8 hours. The primary composite outcome included the incidence of HGL, hypomagnesemia, hypophosphatemia, or hypokalemia within 24 hours of PN initiation. Secondary outcomes included analyses of patients with risk factors for HGL and RFS, critically ill patients, and individual components of the composite outcome.Three hundred forty-two patients were included, with a primary outcome incidence of 24.6% (HGL 17.4%; hypokalemia 1.8%; hypomagnesemia 0.6%; hypophosphatemia 8.5%). The primary outcome was more common in the HGL group (34.3% vs 14.7%, P0.01) and in the ICU group (40.9% vs 20.7%, P0.01). Mean 24-hour blood glucose180 mg/dL occurred more in the HGL group (27.9% vs 7.6%, P0.01) and in the ICU group (34.8% vs 13.8%, P0.01). In patients with no risk factors, the primary outcome was 11.9%.Rapid PN titration was likely safe in patients without risk factors for HGL or RFS. Further evaluation of protocolized HGL management is needed to determine the risk of HGL in patients with HGL risk factors. |
Databáze: | OpenAIRE |
Externí odkaz: |