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Evaluation of high-dose insulin/euglycemia therapy for suspected ß-blocker or calcium channel blocker overdose following guideline implementation.
Schult, Rachel F; Nacca, Nicholas; Grannell, Tori L; Jorgensen, Rachel M; Acquisto, Nicole M.
Affiliation
  • Schult RF; Department of Pharmacy, University of Rochester Medical Center, Rochester, NY, USA.
  • Nacca N; Department of Emergency Medicine, University of Rochester Medical Center, Rochester, NY, USA.
  • Grannell TL; Department of Emergency Medicine, University of Rochester Medical Center, Rochester, NY, USA.
  • Jorgensen RM; Department of Pharmacy, University of Rochester Medical Center, Rochester, NY, USA.
  • Acquisto NM; Department of Pharmacy, University of Rochester Medical Center, Rochester, NY, USA.
Am J Health Syst Pharm ; 79(7): 547-555, 2022 03 21.
Article in En | MEDLINE | ID: mdl-34957477
ABSTRACT

PURPOSE:

High-dose insulin/euglycemia (HDIE) is targeted therapy for ß-blocker and calcium channel blocker overdose. A guideline using concentrated insulin infusions (20 units/mL), aggressive monitoring, and supportive recommendations was implemented. We sought to evaluate safety before and after HDIE guideline implementation and describe the patient population, insulin doses, supplemental dextrose, vasopressor use, hospital and intensive care unit (ICU) lengths of stay, and mortality.

METHODS:

Retrospective review was performed of patients receiving HDIE before and after guideline implementation at an academic medical center and community hospital from March 2011 through December 2019. Information on patient and overdose demographics, ingestion data, vital signs, interventions, adverse events, and disposition was collected. Data are presented descriptively with comparisons using Mann-Whitney U analysis and Fisher's exact tests.

RESULTS:

During the study period, 27 patients were treated with HDIE, 10 before guideline implementation (37%; mean [SD] initial insulin dose, 0.49 [0.35] units/kg/h; mean [SD] maximum insulin dose, 2.25 [3.29] units/kg/h; median [interquartile range] duration, 10 [5.5-18.75] hours) and 17 after guideline implementation (63%; mean [SD] initial insulin dose, 1.01 [0.34] units/kg/h; mean [SD] maximum insulin dose, 2.99 [5.05] unit/kg/h; median [interquartile range] duration, 16 [11.5-37] hours). Hypoglycemia, hypokalemia, and volume overload occurred in 80% vs 29% (P = 0.018), 40% vs 53% (P = 0.69), and 50% vs 65% (P = 0.69) of patients in the preguideline vs postguideline group, respectively. Most patients received an initial insulin bolus (85%; mean [SD], 70.3 [21.8] units, 0.9 [0.26] units/kg) and vasopressor infusion (85%). More postguideline patients received a dextrose infusion with a concentration of 20% or higher (93% vs 50%, P = 0.015). There were no differences in cardiac arrest, in-hospital mortality, or hospital or ICU length of stay between the groups.

CONCLUSION:

Hypoglycemia was reduced using an HDIE guideline and concentrated insulin.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperinsulinism / Hypoglycemia Type of study: Evaluation_studies / Guideline Limits: Humans Language: En Journal: Am J Health Syst Pharm Journal subject: FARMACIA / HOSPITAIS Year: 2022 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperinsulinism / Hypoglycemia Type of study: Evaluation_studies / Guideline Limits: Humans Language: En Journal: Am J Health Syst Pharm Journal subject: FARMACIA / HOSPITAIS Year: 2022 Document type: Article Affiliation country: Estados Unidos
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