MOA antagonis reseptor dopamine
- mengganggu transmisi serotonin, NE, GABA
- tranquilizer, antiemetic
- blok α-adrenergik
STRUCTURE mirip haloperidol
FK
A IM/IV
D rapid distribution phase, but sedative effect delayed by HIGH MOLECULAR WEIGHT & EXTENSIVE PROTEIN BINDING
B Liver
E Urine
Effect
CV
CV
- blok α-adrenergik :
- turunkan aBP karena periferal vasodilatation, jangan pada pasien hipovolemik
- antiaritmia efek
- QT interval memanjang, Torsaded de pointes
- Katekolamin release : jangan digunakan pada pasien feokromositoma
RESP
- TIDAK mendepresi pernapasan
- stimulasi hipoxic ventilatory drive
CEREBRAL
- turunkan CBF, ICP : serebral vasoconstriction
- TIDAK MENURUNKAN CMRO2
- poten antiemetic
- may presipitasi EPSE
- AVOID : Parkinson, restless leg syndrome, movement disorder
- dysphoria
- tdk ANALGETIK, tdk amnesia / unconsious pada dosis biasa
- kombinasi fentanil dengan droperidol (Innovar) -> analgesia, immobility, variable amnesia (neuroleptanalgesia)
- + NO2 or hipnotik agent -> unconscious & general anesthesia similar dissosiatif state induce by ketamine
DRUG INTERACTION (DI)
- Antagonis efek levodopa : presipitasi parkinson, renal effect of dopamine are encountered by droperidol
- antagonis sentral α-adrenergik action of clonidine & precipitate rebound hypertension
- turunkan kardio efek dari ketamine
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