Provision of anesthesia is one of the cornerstones of critical care practice. The ideal induction agent has a rapid onset of action, minimal side effects, and is cleared quickly so that recovery is rapid. No induction agent is ideal for all patients and all medications have side effects. This anesthesia guideline is design around the three phases for intubation: induction, maintenance, and emergence. These phases can be further divided into the four A’s of anesthesia planning: anesthesia, analgesia, autonomic stability, and areflexia. The sequencing of medications and the procedure performed is based on the individual patient’s needs and risk factors.
Cautions:
Cautions should be based around a risk stratification. The complexity of risk stratification revolves around whether airway control is emergent, urgent, or elective. Elements to consider when evaluating an individual patient's risks include:
Amnesia
Induction and maintenance of amnesia is incredibly important to the long-term psychological outcomes of patients who undergo ETI. It can be achieved with the use of:
Analgesia
Effective analgesia not only makes the patient more comfortable, but also decreases the amount of post-intubation sedation required to maintain the desired clinical state through pharmacological synergy. Agents used in maintaining analgesia include:
Autonomic Stability
Most patients will require some form of hemodynamic resuscitation in the peri-intubation phase. Hypotension is associated with an increased morbidity and mortality, which is especially true in patients with traumatic brain injuries or right heart syndromes. Use of tools such as the shock index, in conjunction with clinical judgement, can identify patients at risk of hypotension in the context of endotracheal intubation. Autonomic stability can be achieved through the use of:
Areflexia
Areflexia produces the best laryngoscopic views possible, however it is also fraught with complications and potentially dire consequences. It also lowers the required dose of sedation. Deep sedation does not result in areflexia, but rather suppresses any response to stimulus. Consider the use of:
Adult doses are shown in the table below. See individual drug monographs for pediatric and expanded dosing strategies.
Goal |
Options |
Induction (Phase I) |
Maintenance (Phase II) |
Emergence (Phase III) |
Analgesia |
Morphine (2-10mg)
Fentanyl (25-100mcg)
Ketamine (0.25-0.5 mg/kg)
Hydromorphone (0.2-1mg) |
Morphine (1-10mg/hr)
Fentanyl (25-200mcg/hr)
Ketamine (0.05-1 mg/kg/hr)
Hydromorphone (0.5-3mg/hr) |
See procedural analgesia if required |
|
Amnesia |
Midazolam (0.1-0.3 mg/kg) Ketamine (0.5-2 mg/kg) Propofol (1-3 mg/kg) Etomidate (0.3 mg/kg) Dexmedetomidine |
Midazolam (0.01-0.1mg/kg/hr) Ketamine (0.2-0.5 mg/kg/hr) Propofol (50-200mcg/kg/min) Dexmedetomidine (0.1-0.8 mcg/kg/hour) |
See procedural sedation if required |
|
Autonomic Stability |
IV Fluids |
IV Fluids (10-20ml/kg)
Epinephrine (50-100 mcg)
NORepinephrine (5-10 mcg) |
IV Fluids (2-4ml/kg/hr)
Epinephrine (0.01-0.5 mcg/kg/min)
NORepinephrine (5-60 mcg/min)
Dopamine (2-20mcg/min) |
IV Fluids (2-4ml/kg/hr) |
Areflexia |
Cisatracurium |
Rocuronium (0.6-1.2 mg/kg)
Succinylcholine (0.6-1.1 mg/kg)
Cisatracurium (0.15-0.2 mg/kg) |
Rocuronium (0.6-1 mg/kg)
Cisatracurium (1-2 mcg/kg/min) |
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