์ด๋ฏธํ๋ผ๋ฏผ
์ด๋ฏธํ๋ผ๋ฏผ์ ์์ํ์์ ํ๊ฐ ์ธ(off-label)๋ก ์ฌ์ฉ๋๋ **์ผํ๊ณ ํญ์ฐ์ธ์ (TCA)**์ ๋๋ค. ์ฃผ๋ก ๋ถ๋ฆฌ ๋ถ์๊ณผ ๊ฐ์ ํ๋ ๋ฌธ์ ์ ์ฌ์ฉ๋๋ ๊ฒ์ผ๋ก ์๋ ค์ ธ ์์ง๋ง, ๋ ํนํ ์์ฉ์ฒด ํ๋กํ์ผ ๋๋ถ์ ํ์ฉ๋๊ฐ ๋งค์ฐ ๋์ต๋๋ค. * **๊ฐ์ ๊ณ ์์ด**์์๋ **์์ค๊ธ**๊ณผ **ํ๋ ฅ๋ฐ์(cataplexy)** ์น๋ฃ์ ์์ฃผ ์ฌ์ฉ๋ฉ๋๋ค. * **๋ง**์์๋ **๊ธฐ๋ฉด์ฆ(narcolepsy)** ๊ด๋ฆฌ ๋ฐ ์ฝ๋ฌผ ์ ๋ ์ฌ์ ์ ์ฌ์ฉ๋ฉ๋๋ค. > **์์ ํ:** ์ด๋ฏธํ๋ผ๋ฏผ์ 3๊ธ ์๋ฏผ TCA๋ก, ๊ฐ์์ ํ์ฑ 2๊ธ ์๋ฏผ ๋์ฌ์ฐ๋ฌผ์ธ **๋ฐ์ํ๋ผ๋ฏผ(desipramine)**์ผ๋ก ๋น ๋ฅด๊ฒ ๋์ฌ๋ฉ๋๋ค. ์ด๋ฌํ ์ด์ค ์์ฉ์ ์ธ๋กํ ๋๊ณผ ๋ ธ๋ฅด์ํผ๋คํ๋ฆฐ ๊ฒฝ๋ก ๋ชจ๋์ ์ํฅ์ ๋ฏธ์ณ ์ฝ๋ฆฌํ์ ์์ฉ ๋ฒ์๋ฅผ ๋ํ์ค๋๋ค.
์์ฉ ๊ธฐ์ : Imipramine and its active metabolite, desipramine, exert their effects through a complex, multi-receptor pharmacologic profile: * **Monoamine Reuptake Inhibition**: Blocks the presynaptic amine pump, preventing the reuptake of **serotonin (5-HT)** and **norepinephrine (NE)** โ increases neurotransmitter concentrations in the synaptic cleft โ modulates mood, arousal, and pain pathways. * **Anticholinergic Activity**: Antagonizes **muscarinic receptors** centrally and peripherally. This mechanism is primarily responsible for its efficacy in treating urinary incontinence (facilitating urine storage by relaxing the detrusor muscle) and its common side effects (dry mouth, tachycardia). * **Alpha-Adrenergic Agonism/Antagonism**: Exhibits complex interactions at alpha receptors, which may contribute to increasing internal urethral sphincter tone. * **Antihistaminic (H1) Activity**: Contributes to its significant **sedative** properties.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Urethral incompetence ยท 2.5-5 mg (total dose) ยท PO ยท q12h
- Adjunctive cancer pain treatment ยท 2.5-5 mg (total dose) ยท PO ยท q12h
- Anxiety, inappropriate urination ยท 0.5-1 mg/kg ยท PO ยท q12-24h
- Pharmacologic induced ejaculation ยท 2 mg/kg ยท IV ยท once ยท If imipramine alone does not induce erection and ejaculation in 10-15 minutes, give xylazine 0.2-0.3 mg/kg IV. (Note: ARCI UCGFS Class 2 Drug)
- Narcolepsy/cataplexy ยท 0.55 mg/kg IV or 250-750 mg (total dose) orally ยท IV, PO ยท once ยท PO administration produces inconsistent results.
- Urethral incompetence ยท 5-15 mg (total dose) ยท PO ยท q12h
- Urinary incontinence when other agents fail ยท 5-20 mg (total dose) ยท PO ยท q12h
- Cataplexy ยท 0.5-1 mg/kg ยท PO ยท q8h ยท Titrate dose based on clinical effect
- Adjunctive treatment of separation anxiety or other tricyclic antidepressant-responsive behavior disorders ยท 2.2-4.4 mg/kg ยท PO ยท once to twice daily
- Adjunctive cancer pain treatment ยท 0.5-1 mg/kg ยท PO ยท q8h
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Prior sensitivity to any tricyclic antidepressant
- Concomitant use with monoamine oxidase inhibitors (MAOIs) within 14 days
- Glaucoma
- History of seizures
- Urinary retention
- Severe liver disease
- Hypersensitivity to tricyclic antidepressants
์ด์๋ฐ์
- Sedation
- Dry mouth
- Constipation
- Tachycardia
- Hyperexcitability
- Tremors
- Seizures (CNS stimulation)
- Bone marrow suppression
- Diarrhea
- Vomiting
- Diarrhoea
- Excitability
- Arrhythmias
- Hypotension
- Syncope
- Increased appetite
์ฝ๋ฌผ ์ํธ์์ฉ
- Anticholinergic agents ยท Additive anticholinergic effects; use cautiously
- Cimetidine ยท May inhibit tricyclic antidepressant metabolism and increase the risk of toxicity ยท major
- CNS Depressants ยท Additive CNS depressant effects; use cautiously
- Levodopa ยท Imipramine may decrease levodopa oral absorption
- Phenobarbital ยท May decrease tricyclic levels
- Quinidine ยท Increased risk for QTc interval prolongation and tricyclic adverse effects
- Rifampin ยท May decrease tricyclic blood levels
- SSRIs (e.g., fluoxetine, paroxetine, sertraline) ยท Increased risk for serotonin syndrome
- Sympathomimetic agents ยท May increase the risk of cardiac effects (arrhythmias, hypertension, hyperpyrexia)
- Monoamine Oxidase Inhibitors (including amitraz, selegiline) ยท Concomitant use (within 14 days) is generally contraindicated due to risk of serotonin syndrome
- Thyroid agents ยท May increase risk for cardiac arrhythmias
- Cisapride ยท Increased risk for prolonged QT interval
- Clonidine ยท Tricyclics may increase blood pressure
๋ชจ๋ํฐ๋ง
- Clinical efficacy
- Adverse effects
- ECG (Tricyclics can widen QRS complexes, prolong PR intervals, and invert or flatten T-waves)
- Blood Glucose (Tricyclics may increase or decrease blood glucose levels)
- Heart rate and rhythm (ECG) in susceptible patients
- Signs of serotonin syndrome (agitation, tremors, hyperthermia, tachycardia) if used with other serotonergic drugs
- Liver function tests (baseline and periodic)
๊ณผ์ฉ๋
Overdosage with tricyclics can be **life-threatening**, leading to severe arrhythmias and cardiorespiratory collapse. Because the toxicities and therapies for treatment are complicated and controversial, it is highly recommended to **contact a poison control center** for further information in any potential overdose situation.
VetSheet ์ฝ๋ฌผ ๋ ํผ๋ฐ์ค๋ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์์ฌ๊ฒฐ์ ๋ณด์กฐ ๋๊ตฌ์ด๋ฉฐ, ์ ๋ฌธ์ ํ๋จ์ด๋ ์ ์กฐ์ฌ์ ์ต์ ๋ผ๋ฒจ์ ๋์ ํ์ง ์์ต๋๋ค.