LOSTINDIAB: Comparison of a Low Dose to a Standard Dose of Insulin in Adult DKA in ICU to Reduce Metabolic Complications
Study Details
Study Description
Brief Summary
Diabetic ketoacidosis (DKA), a frequent complication of diabetes, is the consequence of a profound insulin deficiency responsible for osmotic polyuria and thus major losses of water, glucose, sodium and potassium as well as a metabolic acidosis due to the uncontrolled production of ketonic acids. Management includes fluid replacement, insulin therapy and correction of metabolic disorders (including potassium loss).
Initially described in patients with type 1 diabetes (T1D), it is now often observed in patients with type 2 diabetes (T2D) in whom it is more a matter of insulin resistance than an absolute deficiency. However, international guidelines recommend a similar dose of intravenous insulin (0.10 IU/kg/hour) regardless of the type of diabetes.
During treatment, metabolic complications are frequent and potentially serious, especially in T2D due to cardiovascular comorbidities.
The research hypothesis is that decreasing the insulin dose will reduce metabolic complications without influencing time to resolution in adult patients, regardless of diabetes type.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Diabetic ketoacidosis (DKA), a frequent complication of diabetes, is the consequence of a profound insulin deficiency responsible for osmotic polyuria which leads to major losses of water, sodium and potassium as well as the generation of metabolic acidosis due to the uncontrolled production of ketonic acids. Management includes fluid replacement, insulin therapy and correction of metabolic disorders (including potassium loss and acidosis).
Initially described in patients with type 1 diabetes (T1D), it is now often observed in patients with type 2 diabetes (T2D) in whom it is more insulin resistance than absolute deficiency. However, international guidelines recommend a similar dosage of intravenous insulin (0.10 IU/kg/hour) regardless of the type of diabetes.
During treatment, metabolic complications are frequent and potentially serious, especially in T2D due to cardiovascular comorbidities.
A British study reported 27.6% hypoglycaemia and 55% hypokalemia during the first 24 hours of treatment. Comparable figures were observed by conducting a multicenter retrospective study of 122 patients: hypokalaemia and hypoglycaemia were observed in nearly two thirds of cases.
A pediatric study showed that a lower dose of insulin (0.05 IU/kg/h) reduced the rate of hypoglycaemia (20% vs 4%) and hypokalaemia (48% vs 20%) compared to at the standard dose (0.10 IU/kg/h) without modifying the time to resolution. But the very small number (25 children per arm), the questionable statistical analysis and the pediatric population (T1D only) do not make it possible to anticipate the potential benefit in a much more heterogeneous adult population.
The hypothesis of the research is that decreasing the insulin dose will reduce metabolic complications without influencing time to resolution in adult patients, regardless of diabetes type.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Experimental Reduced dose of rapid-acting insulin of 0.05 IU/kg/h from randomization until resolution of DKA |
Drug: Insulin 0.05 IU/kg/h
In the experimental arm, the patients will be given an insulin dose of 0.05 IU/kg/h.
|
| Other: Control Rapid-acting insulin dose of 0.10 IU/kg/h in accordance with usual recommendations until resolution of DKA |
Drug: Insulin 0.10 IU/kg/h
In the control arm, patients will receive an insulin dose of 0.10 IU/kg/h.
|
Outcome Measures
Primary Outcome Measures
- Reduced metabolic complications [48 hours]
To assess whether a reduced insulin dosage (0.05 IU/kg/h versus 0.10 IU/kg/h) for DKA management in adult patients admitted to a ICU reduces the incidence of metabolic complications (hypokalaemia < 3.5 mmol/L and/or hypoglycaemia < 3.9 mmol/L)
Secondary Outcome Measures
- resolution of DKA [48 hours]
Time in hours between randomisation and resolution of DKA (defined by ph>7.3 and ketonemia < 0.3 mmol/L)
- Episode of hypokalaemia [48 hours]
Proportion of patients with at least one episode of hypokalaemia < 3.5 mmol/L between randomization and resolution of DKA
- Episode of hypoglycemia [48 hours]
Proportion of patients with at least one episode of hypoglycemia < 3.9 mmol/L between randomization and resolution of DKA
- Episode of severe hypoglycemia [48 hours]
Proportion of patients with at least one episode of hypoglycemia < 2.9 mmol/L between randomization and resolution of DKA
- Cardiac arrythmia diagnosed by EKG [48 hours]
Proportion of patients with onset of new cardiac arrhythmia diagnosed by EKG analysis (atrial fibrillation and ventricular arrhythmia) between randomization and resolution of DKA
- Cardiac arrythmia diagnosed by scopic monitoring [48 hours]
Proportion of patients with onset of new cardiac arrhythmia diagnosed by scopic monitoring between randomization and resolution of DKA
- Glucose infusion 1000mL [48 hours]
Proportion of patients who received more than 1000 mL of 10% glucose solution (indicating tendency of hypoglycemia) between randomization and resolution of DKA or 48h after inclusion if DKA is unresolved
- Glucose infusion of 30% glucose solution [48 hours]
Proportion of patients who received one infusion of 30% glucose solution between randomization and resolution of DKA or 48h after inclusion if DKA is unresolved
- Amount of glucose perfused [48 hours]
Amount of glucose infused (in grams) (glucose 5%, 10% and 30%) between randomization and resolution of the DKA or 48 hours after inclusion if the DKA is not resolved
- Potassium infusion [48 hours]
Potassium intake (in grams) orally and intravenously between patient randomization and resolution of DKA or 48 hours after inclusion if DKA is not resolved
- Length of stay in ICU [48 hours]
Duration of stay (in hours) in ICU
- Time between patient randomization and resolution of DKA in T1D population [48 hours]
Time in hours between patient randomization and resolution of DKA in T1D population
- Time between patient randomization and resolution of DKA in T2D population [48 hours]
Time in hours between patient randomization and resolution of DKA in T2D population
- Time between patient randomization and resolution of DKA in patients suffering from first ketoacidosis episode [48 hours]
Time in hours between patient randomization and resolution of DKA in patients suffering from ketoacidosis
- Episode of hypokalaemia in T1D population [48 hours]
Proportion of patients with at least one episode of hypokalaemia < 3.5 mmol/L between randomisation and resolution of DKA or 48 hours after inclusion if DKA is not resolved within T1D population
- Episode of hypokalaemia in T2D population [48 hours]
Proportion of patients with at least one episode of hypokalaemia < 3.5 mmol/L between randomisation and resolution of DKA or 48 hours after inclusion if DKA is not resolved within T2D population
- Episode of hypokalaemia in patients suffering from first ketoacidosis episode [48 hours]
Proportion of patients with at least one episode of hypokalaemia < 3.5 mmol/L between randomisation and resolution of DKA or 48 hours after inclusion if DKA is not resolved within inaugural ketoacidosis population
- Episode of hypoglycaemia in T1D population [48 hours]
Proportion of patients with at least one episode of hypoglycaemia < 3.9 mmol/L between randomization and resolution of DKA or 48 hours after inclusion if DKA is not resolved within T1D population
- Episode of hypoglycaemia in T2D population [48 hours]
Proportion of patients with at least one episode of hypoglycaemia < 3.9 mmol/L between randomization and resolution of DKA or 48 hours after inclusion if DKA is not resolved within T2D population
- Episode of hypoglycaemia in patients suffering from first ketoacidosis episode [48 hours]
Proportion of patients with at least one episode of hypoglycaemia < 3.9 mmol/L between randomization and resolution of DKA or 48 hours after inclusion if DKA is not resolved within inaugural ketoacidosis population
- Episode of severe hypoglycaemia in T1D population [48 hours]
Proportion of patients with at least one episode of severe hypoglycaemia < 2.9 mmol/L between randomization and resolution of DKA or 48 hours after inclusion if DKA is not resolved within T1D population
- Episode of severe hypoglycaemia in T2D population [48 hours]
Proportion of patients with at least one episode of severe hypoglycaemia < 2.9 mmol/L between randomization and resolution of DKA or 48 hours after inclusion if DKA is not resolved within T2D population
- Episode of severe hypoglycaemia in patients suffering from first ketoacidosis episode [48 hours]
Proportion of patients with at least one episode of severe hypoglycaemia < 2.9 mmol/L between randomization and resolution of DKA or 48 hours after inclusion if DKA is not resolved within inaugural ketoacidosis population
Eligibility Criteria
Criteria
Inclusion Criteria:
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Patient aged 18 years or above
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Admission in Intense/Intermediate Care Unit
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Severe DKA due to all types of diabetes (T1D, T2D and secondary diabetes and inaugural ketoacidosis) defined by association of the following 3 parameters:
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glucose > 11 mmol/L or affirmation of having diabetes
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ketonemia > 3mmol/L or ketonuria ≥ 2
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bicarbonate < 15 mmol/L and/or venous pH < or=7.3
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Randomization possible within 2 hours of insulin initiation
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Informed and written consent. In the absence of parent/ relative/ person of trust, the patient may be included via the emergency procedure and consent will be obtained as soon as possible
Exclusion Criteria:
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Non-diabetic ketoacidosis (fasting or alcoholic)
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Patient weighing less than 30 kg
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Hypokalemia < 3.5 mmol/L at the time of inclusion
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Hyperosmolar hyperglycemic state (defined as efficient plasma osmolarity > 320 mosmol/L)
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Absence of social security coverage
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Pregnant or breastfeeding patient
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Patient under tutelage or curators
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Patient deprived of liberty due to a judicial or administrative decision
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Patient with a renal disease requiring dialysis
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Acute or chronic liver failure with Factor V < 50%
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Patient receiving a high dose of corticosteroids (≥ 0.5 mg/kg) daily
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Patient included in another interventional study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Louis Mourier Hospital | Colombes | France | 92700 |
Sponsors and Collaborators
- Assistance Publique - Hôpitaux de Paris
Investigators
- Principal Investigator: Damien Roux, PhD, Assistance Publique - Hôpitaux de Paris
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- APHP210081