Generalized Anesthesia Flashcards
1
Q
Inhaled Anesthetics (6)
A
- Isoflurane
- Desflurane
- Sevoflurane
- Halothane
- Nitrous Oxide
NEW: Halogenation increases potency and is non-flammable
OLD NOTES: All but Nitrous Oxide are halogenated, which adds stability, increases solubility and potency [TQ]
(DISH N)
2
Q
IV Anesthetics (6)
A
- Benzodiazepines (Midazolam)
- Opioids
- Ketamine
- Propofol
- Etomidate
- Dexmedetomidine
(BOP-KED)
3
Q
Sedatives (5)
A
- Benzodiazepines (Anxiolytics and Hypnotics)
- Propofol
- Dexmedetomidine
4
Q
Isoflurane (6)
A
- Flourine + Chlorine
- Lowest MAC at 1.15%
- (most potent, good)
- Highest Blood:Gas Partition Coefficient
- (lower affinity of blood or anesthetic, bad)
5
Q
Desflurane
A
- Flourine
- Highest halogenated MAC (6.3%)
- Lowest Blood:Gas Partition Coefficient
- Good!
- Lower Blood Solubility
- More rapid anesthetic effect and recovery
- Not used for induction (high pungency, high RI)
6
Q
Sevoflurane
A
- Flourine
- Between Desflurane and Isoflurane for both MAC and Blood:Gas Partition Coefficient
- Causes seizures and agitation
- Used for induction, low pungency and low RI
- OLD: Useful in patients with myocardial ischemia [TQ]
7
Q
Nitrous Oxide
A
- Produces anesthesia without decreasing BP or CO
- Can cause myocardial depression, offset by gas-associated sympathetic stimulation
- Amnestic and analgesic properties
- Decreases requirements of inhaled and IV anesthetics
- 25-40%: CNS depression (safely used clinically)
- 25%: produces maximum analgesic effects
- Unconscious at inspired levels of 60-80%
8
Q
Benzodiazepines: as IV anesthetics
A
- Midazolam
- Bind close to GABAa receptor and trigger opening of Cl channel, Cl ion influx (hyperpolarization) inhibits AP formation
- Preferred agent for balanced anesthesia
- Active metabolie – accumulation (caution with multiple doses)
- Uses: sedation, hypnotic (high doses), anticonvulsant, muscle relaxant, anxiolytic, anterograde amnesia [TQ], preserves hemodynamic stability
- Antidote: Flumazenil
- ADRs: respiratory depression
9
Q
Midazolam
A
- Preferred agent for balanced anesthesia
- Synergistic other agents (propofol), opioids:
- decreased dose requirements
- potentiation with opioids
- respiratory depression is enhanced though
- Rapid onset (30-60 sec), peak 60 min
- ADRs: dose-dependent respiratory depression, active metabolite accumulation
10
Q
Flumazenil (4)
A
- Antidote for Benzo overdose
- Binds to same receptor without enhancing GABA binding
- Onset (1-2 min), peak (10 min), dose-dependent DOA
- High safety margin
11
Q
Opioids
A
- Interact at Mu receptors in CNS and GI tract
- Uses: analgesia and sedation (no amnesia)
- ADRs: respiratory depression, post-operative nausea/vomiting, bradycardia, hypotension
- Risk factors: co-administration with sedatives, old people, high doses
12
Q
Remifentanil
A
- First Mu-opioid receptor agonist
- No histamine release
- Rapid onset and recovery
- Uses: ED, ICU, procedures in SDS or endoscopy, combo therapy for induction
- Disadvantages: sudden onset of pain or withdrawal
13
Q
Naloxone
A
- Competitive opioid antagonist, strong mu affinity
- No analgesic effects
- Narcotic reversal in 1-3 min (IV)
- Ventilation can be restored without losing pain benefit of narcotic
14
Q
Ketamine
A
- PCP analog, slow onset
- Enhanced response to glutamate at NMDA receptor
- Interacts with CNS opiate receptors for pain relief
- Low dose: analgesia/anxiolysis for debridement/dressing changes
- Moderate dose: analgesia/anxiolysis plus sedation and amnesia
- High dose: used in prolonged surgical procedures (impairs airway reflexes)
- ADRs: dissociative anesthesia [TQ] (patient appears awake but unconscious and doesn’t feel pain)
- give with benzos to alleviate side effects
15
Q
Propofol: as IV anesthetic
A
- GABA mechanism
- Rapid onset (90 seconds), DOA (5-10 min), very apid recovery, hepatic elimination, easily titrated
- High lipid concentration, careful for bacterial growth
- Uses: long or short procedures, good for induction in ambulatory procedures, sedative hypnotic
- No analgesia and no amnesia
- ADRs: nausea/vomiting, residual drowsiness, pain on injection (give with lido), apnea, hypotension, respiratory depression, allergic reactions (egg whites)
16
Q
Etomidate (6)
A
- Depresses RAS and mimics effects of GABA
- Onset (30-60 seconds), DOA (3-5 min)
- Uses: IV induction, procedural sedation
- Advantage: hemodynamic stability
- ADRs: adrenal suppression [TQ]