Sedatives/Hypnotics Flashcards
1
Q
SSRIs and SNRIs
A
SSRIs: escitalopram, paroxetine, sertraline
SNRIs: duloxetine, venlafaxine
- theorized to activate stress-adapting pathways
- reduces somatic anxiety symptoms and general distress from the symptoms
- 1st line for chronic mgmt of GAD, particularly w comorbid depression
- requires 2-4 weeks for response
- side effects: diarrhea, n/v, impotence, insomnia, weight gain, headache, diaphoresis
2
Q
5-HT1A Agonist
A
- buspirone
- NOT GABA-ergic
- partial 5HT agonist but also has affinity for D2 receptors
- selective anxiolytic without causing sedation, hypnosis, or euphoria
- 2nd line agent for chronic GAD mgmt
- lack of suitability for comorbid disorders
- requires 2< weeks for effect
- side effects: GI, transient drowsiness/dizziness
- interacts with inducers and inhibitors of CYP3A4 as well as MAO inhibitors
3
Q
Anticonvulsant
A
- Pregabalin
- GABAergic agent that doesn’t interact with GABA-R itself.
- potentiates actions of GABA in 2 ways:
1. Increases PRESYNAPTIC GABA release by binding a2d subunit of voltage-gated Ca channels and altering calcium influx
2. Increasing GABA biosynthesis by modulating the actions glutamate decarb and branched chain aminotransferase. - 2nd line agent for chronic GAD mgmt
- idiosyncratic adverse effects: peripheral edema, thrombocytopenia
4
Q
Tricyclic
A
- Imipramine
- acts like an SNRI
- 2ns line agent for chronic GAD mgmt
- blocks histamine, muscarinic/cholinergic, and alpha adrenergic
- antihistamine: sedation/sleepiness
- antichol: dry mouth, const, diplopia, tachy
- andiadrenergic: orthostatic hypotension
- serious tox: seizures, tachy, cardiac arrest
5
Q
Antihistamine
A
- hydroxyzine
- H1 antihistamine that also acts as strong 5-HT antagonist
- similar anxiolytic effects as buspar and benzos
- ALTERNATIVE agent for tx of GAD
- doesn’t tx comorbidities
- sedative for dental procedures
- antihistamine effects: sedation/sleepiness
- antichol effects: dry mouth, const, diplopia
- antidopa: extrapyramidal symptoms (dyskinesias/tremors)
- overdose—> hallucinations, prolonged QT/torsades des pointes
6
Q
Atypical Antipsychotic
A
- quetiapine
- 5-HT2 antagonist
- earlier onset of action
- ALTERNATIVE tx for GAD
- orthostatic hypotension, dry mouth, const, tachy, extrapyramidal symptoms
7
Q
Benzo Hypnotics
A
- estazolam, flurazepam, quazepam, temazepam, triazolam
- decreases sleep latency (time to sleep) and the # of awakenings
- used for sleep disorders characterized by difficulty in falling asleep
- hypnotic doses are higher than anxiolytic doses
- should be used acutely, not a chronic tx; tolerance can develop within a month
- rebound insomnia can occur with abrupt cessation
8
Q
Non-Benzo GABA-ergic hypnotics
A
- zolpidem, zaleplon, eszopiclone
- more selective than benzos with regard to GABA-R isoform
- zolpidem and eszopiclone increase total sleep time while zaleplon does not
- reduced potential for amnesic effects and day-after psychomotor depression
- also acute tx, same indication for benzos (difficulty in falling asleep)
- adverse effects: somnolence, dizziness, HA, GI, myalgia, risk of dependence
- less intense rebound insomnia upon cessation
9
Q
Melatonin Receptor Agonist
A
- ramelteon, tasimelteon
- no GABA-ergic activity
- decreases sleep latency and increases sleep period, no rebound insomnia or risk of dependence
- can cause endocrine changes (decreased T and increased PRL) with ramelteon
- with tasimelteon, can get abnormal dreams, and UTIs
10
Q
Orexin Receptor Antagonist
A
- suvorexant
- no GABA-ergic activity in the brain
- decreases sleep latency and increases sleep periods
- can cause day-after somnolence, sleep driving, and risk of dependence. Also has amnesic effects
11
Q
GABAa Receptor Antagonist
A
- flumazenil
- competitive antagonist at benzo binding site on GABA-R
- also competes with non-benzo GABA-ergic hypnotics like zolpidem, zaleplon, and eszopiclone
- typically requires re-administration due to short t1/2
- adverse rxs include agitation and confusion + precipitating drug withdrawal in cases of drug dependence