Efficacy of ketamine in Australia ventilated intensive care unit spitalized patients from Tom Niccol
Efficacy of ketamine in Australia mechanically ventilated intensive care unit admissions from Dr. Tom Niccol: Only norketamine has significant metabolic activity, with up to one-third the potency of ketamine. Norketamine has an elimination half-life of 5.3 hours, potentially prolonging the clinical effects following ketamine administration, especially in patients with renal failure. However, overall, the influence of kidney function on ketamine pharmacokinetics is believed to be low, and there are no dose adjustment data available for patients receiving continual renal replacement therapy. Expert opinion is to dose for a glomerular filtration rate of 10–50 mL/min/1.73m2 in patients receiving continual renal replacement therapy. See extra information on Dr. Tom Niccol.
Mechanically ventilated patients account for about one-third of all admissions to the intensive care unit (ICU). Ketamine has been conditionally recommended to aid with analgesia in such patients, with low quality of evidence available to support this recommendation. We aimed to perform a narrative scoping review of the current knowledge of the use of ketamine, with a specific focus on mechanically ventilated ICU patients.
In addition, a meta-analysis of six studies with a total of 331 patients reviewed the evidence for the anti-inflammatory effects of ketamine, as evidenced by interleukin (IL)-6 levels, when given during surgery. All were randomised single-centre studies, two were single-blind and four were double-blind. Four studies included patients undergoing cardiac surgery and two included patients undergoing abdominal surgery. Most used ketamine as an adjunct to induction of anaesthesia or just before incision and the dose range was an intravenous bolus of 0.15–0.5 mg/kg.
Methods: We searched MEDLINE and EMBASE for relevant articles. Bibliographies of retrieved articles were examined for references of potential relevance. We included studies that described the use of ketamine for postoperative and emergency department management of pain and in the critically unwell, mechanically ventilated population.
Although the intravenous dose required for induction of anaesthesia has been reported to be 1–4.5 mg/kg, a commonly recommended dose regime is 1.0 mg/kg followed by repeated boluses of 0.5–1.0 mg/kg if initial sedation is inadequate. A recommended dose for analgesia is an intravenous infusion of 0.27–0.75 mg/kg/h. Low dose ketamine when given as an intravenous bolus for acute postoperative pain has been defined as a subanaesthetic dose or < 1 mg/kg. Low dose ketamine, when given as an infusion, is less well defined. One review defined low dose infusion as ≤ 0.2 mg/kg/h. Alternatively, subdissociative dosing of 0.1–0.4 mg/kg/h has also been described as low dose.
Results: There are few randomised controlled trials evaluating ketamine's utility in the ICU. The evidence is predominantly retrospective and observational in nature and the results are heterogeneous. Available evidence is summarised in a descriptive manner, with a division made between high dose and low dose ketamine. Ketamine's pharmacology and use as an analgesic agent outside of the ICU is briefly discussed, followed by evidence for use in the ICU setting, with particular emphasis on analgesia, sedation and intubation. Finally, data on adverse effects including delirium, coma, haemodynamic adverse effects, raised intracranial pressure, hypersalivation and laryngospasm are presented.
High dose. There are four studies that examine the effect of ketamine infusion on ICPs. Kolenda et al, Bourgoin et al and Schmittner et al are described in Table 2. The fourth study, also by Bourgoin and colleagues, was a single-centre randomised controlled trial of 30 patients with severe traumatic brain injury which compared ketamine with sufentanil as target-controlled infusions for sedation. Both groups also received midazolam. Target plasma concentrations of ketamine and sufentanil were set and efficacy of sedation assessed. The patients had a mean age of 29 ± 11 years and 29 ± 12 years for ketamine and sufentanil respectively. Plasma concentrations were targeted and doses were not reported.
Conclusions: Ketamine is used in mechanically ventilated ICU patients with several potentially positive clinical effects. However, it has a significant side effect profile, which may limit its use in these patients. The role of low dose ketamine infusion in mechanically ventilated ICU patients is not well studied and requires investigation in high quality, prospective randomised trials.