RecruitingPhase 4NCT04012138

Insulin Dextrose Infusion vs Nebulized Salbutamol vs Combination of Salbutamol and Insulin Dextrose in Acute Hyperkalemia

InSaKa Trial: Insulin Dextrose Infusion Versus Nebulized Salbutamol Versus Combination of Salbutamol and Insulin Dextrose in Acute Hyperkalemia: a Randomized Clinical Trial


Sponsor

Nantes University Hospital

Enrollment

525 participants

Start Date

Dec 20, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

Hyperkalemia is a common electrolyte disorder, especially among patients with chronic kidney disease, diabetes mellitus, or heart failure. Globally, the reported incidence of hyperkalemia varies from 1.1 to 10 per 100 hospitalizations, depending on the patient cohort and comorbidities. Hyperkalemia is a potentially life-threatening electrolyte disturbance that can be fatal if left untreated. Several studies have established the association between hyperkalemia and all-cause mortality. Because of the deleterious cardiac effects of hyperkalemia, its management is an emergency intervention. However, robust evidence is lacking to guide the emergency management of patients with hyperkalemia. Emergency treatment approaches are largely based on small studies, anecdotal experience, and traditionally accepted practice patterns within institutions. Therefore, a rigorous evaluation of the first-line treatments of hyperkalemia in emergency departments is needed and a large scale randomized clinical trial is warranted before robust recommendations for clinical practice can be made. Our clinical trial will improve the safety of patients with acute hyperkalemia and will help clinicians in their day by day practice to choose the treatment that significantly reduces morbidity and mortality during acute hyperkalemia management. Our results will be delivered in a timely fashion, owing to the high prevalence of hyperkalemia in the emergency department setting and to the commitment of the INI-CRCT network of Excellence, along with ED specialists used to work jointly. the primary objective of our trial is to compare insulin/dextrose intravenous infusion, nebulized salbutamol or combination of nebulized salbutamol and insulin/dextrose intravenous infusion to reduce serum potassium concentration at 60 minutes, as first-line treatment, in emergency departments.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Patient older than 18 years old
  • Patient admitted to the emergency department,
  • Patient with local laboratory serum potassium level superior or equal to 5,5 mmol/l,
  • Patient who provide written informed consent prior to participation in the study

Exclusion Criteria11

  • Hemolysis or thrombocytosis > 106/mm3 or hyperleukocytosis > 105/mm3 on the first blood sample suspecting a pseudohyperkalemia,
  • Diabetic ketoacidosis or hyperosmolar hyperglycemic syndrome,
  • Pregnant or lactating woman, women with childbearing potential who didn't have effective contraception*,
  • Patient expected to require emergency intubation and ventilation,
  • Patient expected to require dialysis, diuretics or bicarbonate within the first 60 minutes,
  • Patient with heart rhythm disorders or high grade atrioventricular bloc who require urgent medication as soon as admission or serum potassium level result,
  • Hypersensitivity to the tested active substance or excipients,
  • Acute coronary syndrome,
  • Patient not affiliated to a health insurance plan,
  • Patient under guardianship, curatorship or safeguard of justice.
  • The contraceptives considered as highly effective and acceptable by CTFG recommendations will be considered effective under this protocol. The list of contraceptives considered as highly effective and acceptable by CTFG recommendations is detailed in Appendix 7

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Interventions

DRUGSalbutamol

10 mg of salbutamol nebulized in 30 minutes (with oxygen 8 liters per minute or with air) 10 units of regular insulin (rapid-acting, insuline asparte, intravenous injection) as an intravenous bolus with 500 ml of 10% dextrose in water administered over a 30-minute period.

DRUGInsulin Aspart

Patients in the experimental group will receive either: 1. 10 mg of salbutamol nebulized in 30 minutes (with oxygen 8 liters per minute or with air); OR 2. 10 units of regular insulin (rapid-acting, insuline asparte, intravenous injection) as an intravenous bolus with 500 ml of 10% dextrose in water administered over a 30-minute period plus 10 mg of salbutamol nebulized in 30 minutes (with oxygen 8 liters per minute or with air). The nurse will start by giving the 10 units of insulin and the dextrose, and then, immediately, she will start the nebulization of salbutamol.


Locations(16)

Agen Hospital

Agen, France

Angers University Hospital

Angers, France

Avicenne University Hospital

Bobigny, France

University Hospital, Clermont-Ferrand

Clermont-Ferrand, France

Louis Mourier Hospital

Colombes, France

University Hospital, Grenoble

Grenoble, France

Nancy University Hospital

Nancy, France

Nantes University Hospital

Nantes, France

Nice University Hospital

Nice, France

La Pitié Salpêtrière University Hospital

Paris, France

Lariboisiere Hospital

Paris, France

Saint Antoine University Hospital

Paris, France

Poitiers University Hospital

Poitiers, France

Rennes University Hospital

Rennes, France

Strasbourg University Hospital

Strasbourg, France

Tours University Hospital

Tours, France

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NCT04012138


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