Describe Ketamine in detail.
Pharmacology & ‘dissociative’ Anaesthesia
Ketamine is unique among the IV agents: it acts mainly by antagonising the NMDA (glutamate) receptor and produces ‘dissociative anaesthesia’ — a trance-like, cataleptic state with profound analgesia and amnesia in which the eyes may remain open. It can be given intravenously (1–2 mg/kg) or intramuscularly (useful where IV access is difficult, e.g. Children, field/disaster settings).
Distinctive Effects
Unlike other IV agents, ketamine is sympathomimetic — it tends to maintain or raise blood pressure and heart rate and to bronchodilate — and it relatively preserves airway reflexes and respiration. This makes it valuable in the shocked/hypovolaemic or asthmatic patient, in trauma and burns (dressings), and in paediatric and resource-poor settings. It provides potent analgesia even at sub-anaesthetic doses.
Adverse Effects
The main drawbacks are emergence phenomena — vivid dreams, hallucinations, delirium on waking (reduced by benzodiazepines and a quiet recovery) — increased secretions (an antisialagogue helps), and rises in intracranial and intra-ocular pressure and in heart rate/blood pressure, which limit its use in some patients. It can cause hypertension and tachycardia.
DANGER / REMEMBER
Ketamine raises intracranial pressure, intra-ocular pressure and blood pressure, so it is used cautiously (or avoided) in raised ICP, penetrating eye injury, and severe hypertension/ischaemic heart disease. Conversely, its cardiovascular stability makes it valuable in the shocked patient.
CLINICAL PEARL
Ketamine is the anaesthetist’s friend in the shocked, asthmatic or field patient: it provides analgesia, maintains blood pressure and airway, and bronchodilates. Its price is emergence phenomena (cover with a benzodiazepine) and rises in ICP/IOP.
Practical Use & Combinations
Ketamine’s unusual profile makes it useful in situations that defeat other agents: it can be given intramuscularly when no vein is available, it provides analgesia and anaesthesia while largely maintaining ventilation and airway reflexes, and its bronchodilating, blood-pressure-supporting properties suit the asthmatic and the shocked trauma patient. In practice its unwanted effects are managed by co-administering a benzodiazepine to reduce emergence phenomena and an antisialagogue to control the increased secretions, and by recovering the patient in a calm, quiet environment; at low, sub-anaesthetic doses it is increasingly used purely for its analgesic and opioid-sparing effects.
Contraindications & the Balance of Effects
The decision to use ketamine is a balance between its valuable cardiovascular stability and analgesia and its unwanted rises in intracranial pressure, intra-ocular pressure, heart rate and blood pressure. It is therefore used cautiously or avoided in patients with a raised intracranial pressure, a penetrating eye injury, severe systemic or pulmonary hypertension, or significant ischaemic heart disease, in whom the sympathetic stimulation could be harmful, while it is positively indicated in the hypovolaemic, shocked, asthmatic or trauma patient in whom its blood-pressure-supporting, bronchodilating and airway-preserving effects are exactly what is wanted — a striking example of the same drug being contraindicated in one patient and ideal in another.
CLINICAL PEARL
Ketamine is the drug that breaks the usual rules: an NMDA antagonist rather than a GABA drug, it supports rather than depresses the circulation and airway, provides analgesia, and can be given intramuscularly — at the cost of emergence phenomena and rises in intracranial and intra-ocular pressure.
DANGER / REMEMBER
The same sympathomimetic effect that makes ketamine so valuable in shock makes it hazardous elsewhere: its rises in intracranial and intra-ocular pressure and in heart rate and blood pressure argue against its use in raised ICP, penetrating eye injury and severe cardiac or hypertensive disease, so the patient, not the drug’s reputation, decides whether it is the right choice.
Preserves airway reflexes and cardiovascular stability — useful in shock.
| Effect | Detail |
|---|---|
| Mechanism | NMDA receptor antagonist |
| State produced | Dissociative anaesthesia with analgesia |
| Cardiovascular | BP and heart rate rise — useful in shock |
| Respiratory | Airway reflexes preserved; bronchodilator |
| Adverse | Emergence delirium, ↑ secretions, ↑ ICP and IOP |
| Uses | Trauma, burns dressing, asthma, field anaesthesia |
KEY POINT
Key points TO remember
- Ketamine: NMDA antagonist → ‘dissociative’ anaesthesia with profound analgesia & amnesia; IV or IM.
- Sympathomimetic: maintains BP/HR, bronchodilates, preserves airway/respiration.
- Ideal in shock/hypovolaemia, asthma, trauma/burns, paediatric & field settings.
- Adverse: emergence phenomena (cover with benzodiazepine), secretions, ↑ICP/↑IOP, tachycardia/hypertension.
- Cautious/avoid in raised ICP, penetrating eye injury, severe hypertension/IHD.
EXAM TIP
Sources: Morgan & Mikhail’s Clinical Anesthesiology; Miller’s Anesthesia; Ajay Yadav’s Short Textbook of Anaesthesia.
All questions in Intravenous Anaesthetic Agents
- Q1Describe Intravenous Induction Agents — Overview in detail. ★
- Q2Describe Propofol in detail. ★
- Q3Describe Thiopentone in detail. ★
- Q4Describe Ketamine in detail. ★
- Q5Total Intravenous Anaesthesia ★
- SN1Write a short note on Etomidate. ★
- SN2Write a short note on Intra-arterial Injection of Thiopentone. ★
- SN3Describe Midazolam in detail.
- SN4Describe Propofol Infusion Syndrome in detail.
- SN5Describe Context-Sensitive Half-Time in detail.
- SN6Write a short note on Fentanyl. ★
- SN7Describe Naloxone in detail.