The safety and efficacy of intranasal ketamine delivery for sedation of children in the emergency department. Is a needle-free approach to the care of children in the emergency department, practical and attainable?
Ketamine Intranasal Delivery in the Emergency Room: A multicentre randomised controlled trial of Intranasal(IN) versus Intravenous(IV)/Intramuscular(IV) ketamine for paediatric sedation in the Emergency Department. Is a totally needle-free approach feasible?
The Townsville Hospital and Health Service
652 participants
Aug 1, 2016
Interventional
Conditions
Summary
Sedation of children in the Emergency Department (ED) for either urgent therapeutic procedures that may be painful or which require a still and cooperative child (such as wound closure, abscess drainage, foreign body removal, lumbar puncture or fracture reduction) or to obtain critical diagnostic information (for example via medical imaging) is an important aspect of emergency medical practice for which a considerable and evolving body of evidence has developed over several decades. Sedation and analgesia for painful procedures is certainly considered a standard of care that should be offered to all children undergoing painful procedures where possible. While there are some published guidelines there is considerable variation in practice both locally and internationally in terms of choice of sedative agent and conduct of the procedure of sedation. Most of the literature relates to parenteral routes of administration of sedative drugs, typically intravenous (IV) or intramuscular (IM) routes, due to the ability to titrate the dose and the reliability of drug effects when administered via these routes. Study aims 1. Investigate the feasibility of a novel needle-free approach to paediatric sedation in the emergency department 2. Investigate the scientific merit of IN ketamine sedation of children in the emergency department 3. Investigate the practical merit of IN ketamine sedation of children in the emergency department 4. Improve emergency paediatric sedation practices consistent with humane processes of paediatric emergency care 5. Establish a greater evidence base for the intranasal route of sedative drug administration in the emergency department Study hypotheses 1. That IN ketamine sedation will not require significant rates of IV cannulation to safely complete the procedure where an IV cannula is not already considered essential for a patient’s ongoing care 2. That IN ketamine (10mg/kg) will provide non-inferior sedation compared with IV ketamine (1.0-2.0mg/kg) and IM ketamine (4-5mg/kg) 3. That IN ketamine would be associated with higher parental/caregiver satisfaction with the overall procedure and general care in the emergency department 4. That IN ketamine would be associated with greater physician satisfaction with the overall performance of the sedation and the process required to ready the patient for sedation 5. That IN ketamine sedation will lead to earlier readiness for performance of the procedure or diagnostic intervention and hence earlier procedural completion 6. That IN ketamine sedation will not be associated with an overall increase in ED length of stay 7. That IN ketamine sedation will not be associated with an increased rate of emesis, unpleasant psychomimetic effects or other adverse events
Eligibility
Inclusion Criteria3
- Child of aged between greater than or equal to 12 months and less than or equal to 11 years
- Weight between greater than or equal to 10kg and less than or equal to 40kg; corresponding to 100-400mg IN ketamine
- Considered by appropriately qualified senior treating clinician (FACEM or SMO) to have an indication for emergency department sedation
Exclusion Criteria9
- IV cannula already in situ at time of consideration for recruitment; or required for non-sedation indications prior to initiation of the sedation
- Any previous adverse reaction or allergy to ketamine or other components of Ketalar (registered trade name)
- Past history of significant cardiac disease, especially pulmonary hypertension
- American Society of Anaesthesiology Classification > 1
- Predicted difficult bag-mask ventilation or laryngoscopy
- Critical illness
- Severe trauma
- Procedure better managed in operating theatre
- Disease of the nose, significant coryza or nasal discharge, nasal obstruction or other condition preventing effective administration by the IN route
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Interventions
This is a comparative study of intranasal (spray inhaled through the nose) to intramuscular/intravenous (injection into the muscle or vein) delivery of ketamine to children for procedural sedation. Intranasal (N) IN ketamine 10mg/kg, should be given in a staged and titrated fashion as outlined below. Doses inconsistent with this protocol will be considered protocol violations. 1. 10 minutes before ready to initiate procedure: 2.5mg/kg (0.025mL/kg Ketalar (registered trade name of ketamine) right/left nostril via Mucosal atomising device (MAD) AND 2.5mg/kg (0.025mL/kg Ketalar other nostril via MAD Total initial dose = 5mg/kg 2. Assess level of sedation after 2 minutes from initial dose (8 minutes before procedure expected to begin) 3. If initial 5mg/kg dose of sedation is considered insufficient to initiate procedure at this point, further IN doses can be titrated up to total initial load of 10mg/kg to achieve adequate dissociation/sedation to initiate procedure. Do this by alternating further doses of 2.5mg/kg between nostrils: 2.5mg/kg (0.025mL/kg Ketalar right/left nostril via MAD AND/OR 2.5mg/kg (0.025mL/kg Ketalar other nostril via MAD If 10mg/kg is reached and sedation is still insufficient to allow initiation of procedure 15 minutes after the first intranasal dose was administered, this shall be considered failed IN sedation and an IV cannula should be placed to allow titrated 0.25-0.5mg/kg doses of IV ketamine to achieve adequate sedation. The incidence with which this occurs shall impact the needle-free outcome. For a prolonged procedure after successful initiation, repeated IN doses of 2.5mg/kg can be given to alternating nostrils 5 to 10 minutely. The participants level of sedation will be deterined using the FLACC scale (face,legs,acitvity,cry and consolibilty scale), and discussed between the treating doctor and the senior consultant over-viewing the procedure. It should be emphasised that while it may take longer to titrate the dose via the IN route compared with the IV route, this can be performed by the sedationist while the proceduralist finalises readiness for the procedure. It is anticipated that this longer titration period, if it occurs, shall be offset by the time saved by obviating IV. The observation Nurse will be recording all data during the procedure, including baseline observations, indication for procedure, pain scores, fasting status, medication dosing, and 5minutely FLACC scores post initial medication administration.
Locations(4)
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ACTRN12616000399493