๋ฒ ๋ผํ๋ฐ
๋ฒ ๋ผํ๋ฐ์ **๋น๋ํ๋๋กํผ๋ฆฌ๋๊ณ ์นผ์ ์ฑ๋ ์ฐจ๋จ์ **์ด์ **์ 4ํ ํญ๋ถ์ ๋งฅ์ **์ ๋๋ค. ์ฃผ๋ก ํ๊ด ํํ๊ทผ์ ์์ฉํ์ฌ ํ๊ด ํ์ฅ์ ์ ๋ฐํ๋ ๋ํ๋๋กํผ๋ฆฌ๋๊ณ ์นผ์ ์ฑ๋ ์ฐจ๋จ์ (์: ์๋ก๋ํ)์ ๋ฌ๋ฆฌ, ๋ฒ ๋ผํ๋ฐ์ ์ฌ์ฅ ์ ๋๊ณ, ํนํ ๋ฐฉ์ค๊ฒฐ์ (AV node)์ ๊น์ ์ํฅ์ ๋ฏธ์นฉ๋๋ค. **์ฃผ์ ์์ ์ฉ๋:** * ์์ํ์์๋ ์ฃผ๋ก ๊ฐ์ ๊ณ ์์ด์ **์์ฌ์ค์ฑ ๋น๋งฅ(SVT)** ๊ด๋ฆฌ์ ์ฌ์ฉ๋ฉ๋๋ค. * ์ฌ๋ฐฉ์กฐ๋ ๋๋ ์ฌ๋ฐฉ์ธ๋์์ ์ฌ์ค ๋ฐ๋์ ์กฐ์ ์ ์ฌ์ฉ๋ ์ ์์ต๋๋ค. * **์์ ์์ :** ๋ฒ ๋ผํ๋ฐ์ ์๋ ค์ง **P-๋น๋จ๋ฐฑ์ง(P-gp)** ์ต์ ์ ์ ๋๋ค. ์ด๋ฌํ ๊ธฐ์ ๋๋ฌธ์ ํญ๊ฒฝ๋ จ์ ๊ฐ ์ค์ถ์ ๊ฒฝ๊ณ์์ ๋ฐฐ์ถ๋๋ ๊ฒ์ ๋ง๊ธฐ ์ํด ์ฝ๋ฌผ ๋์น์ฑ ๊ฐ์ง์ ๋ณด์กฐ ์น๋ฃ์ ๋ก ์ฐ๊ตฌ๋๊ณ ์์ต๋๋ค.
์์ฉ ๊ธฐ์ : Verapamil exerts its effects by blocking the transmembrane influx of extracellular calcium ions through **L-type voltage-gated calcium channels** in myocardial cells and vascular smooth muscle cells. * **Cardiac Conduction (Primary Effect):** Blocks calcium channels in the SA and AV nodes โ **decreases AV node conduction velocity** and increases the effective refractory period โ slows ventricular response rate in supraventricular arrhythmias. * **Myocardial Contractility:** Exhibits a **negative inotropic effect** (decreases heart muscle contractility). * **Vascular Smooth Muscle:** Inhibits contractile mechanisms โ causes vasodilation and decreases peripheral vascular resistance (though less potently than amlodipine). * **Neurological:** Inhibits **P-glycoprotein (MDR1/ABCB1)** at the blood-brain barrier โ reduces the efflux of certain substrate drugs back into the systemic circulation.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Supraventricular tachycardia ยท Initial dose of 0.025 mg/kg IV slowly, can repeat every 5 minutes up to a total dose of 0.15-0.2 mg/kg; Oral Dose: 0.5-1 mg/kg PO q8h ยท IV/PO ยท q8h (for PO)
- Supraventricular tachyarrhythmias ยท 0.5-1 mg/kg ยท PO ยท q8h
- Supraventricular tachyarrhythmias (Acute) ยท 0.025 mg/kg ยท IV ยท once ยท over 5 minutes ยท Administer slowly with ECG monitoring. Up to 3 repeat IV administrations q5min if necessary.
- To control ventricular rate in atrial fibrillation ยท 0.025-0.05 mg/kg IV q 30 minutes; give less than 0.2 mg/kg total dose ยท IV ยท q 30 minutes ยท ARCI UCGFS CLASS 4 DRUG
- Cardiovascular disease ยท 0.25-0.5 mg (total dose per hamster) SC ยท SC ยท Hamsters
- Cardiovascular disease ยท 8-16 mg/kg PO + 0.5-2 mg/kg SC once daily (q24h) ยท PO/SC ยท q24h ยท Rabbits
- Supraventricular tachycardia ยท Initial dose of 0.05 mg/kg IV slowly, can repeat every 5 minutes up to a total dose of 0.15-0.2 mg/kg; Oral Dose: 0.5-2 mg/kg PO q8h ยท IV/PO ยท q8h (for PO)
- Treatment of hypertension ยท 1-5 mg/kg PO q8h ยท PO ยท q8h
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Cardiogenic shock
- Severe CHF (unless secondary to a supraventricular tachycardia amenable to verapamil)
- Hypotension (<90 mmHg systolic)
- Sick sinus syndrome
- 2nd or 3rd degree AV block
- Digoxin intoxication
- Hypersensitivity to verapamil
- Recent use (within a few hours) of IV beta-adrenergic blockers
- Hypotension
- Left ventricular dysfunction
- Heart failure
์ด์๋ฐ์
- Hypotension
- Bradycardia
- Tachycardia
- Exacerbation of congestive heart failure (CHF)
- Peripheral edema
- AV block
- Pulmonary edema
- Nausea
- Constipation
- Dizziness
- Headache
- Fatigue
- Precipitation or exacerbation of congestive heart failure
์ฝ๋ฌผ ์ํธ์์ฉ
- ACE Inhibitors ยท May cause additive hypotensive effects
- Alpha-Adrenergic Blockers (e.g., prazosin) ยท May cause additive hypotensive effects
- Beta-Adrenergic Blockers (e.g., propranolol) ยท May cause additive negative cardiac inotrope and chronotrope effects; IV combination is contraindicated
- Doxorubicin ยท Verapamil may increase doxorubicin concentrations
- COPP Chemotherapy ยท May decrease oral absorption of verapamil
- Cyclosporine ยท Verapamil may increase cyclosporine levels
- Dantrolene ยท Cardiovascular collapse reported in animals when used with verapamil
- Digoxin ยท Verapamil may increase blood levels of digoxin; monitoring recommended ยท major
- Disopyramide ยท May cause additive effects and impair left ventricular function; concurrent use within 24-48 hours not recommended
- Diuretics ยท May cause additive hypotensive effects
- Erythromycin, Clarithromycin ยท May increase verapamil levels
- Flecainide ยท Possible additive effects; concurrent use is to be avoided in humans
- Neuromuscular Blockers ยท Effects of nondepolarizing muscle relaxants may be enhanced by verapamil
๋ชจ๋ํฐ๋ง
- ECG
- Clinical signs of toxicity (hypotension, bradycardia, edema)
- Blood pressure (especially during acute IV therapy)
- Serum concentration (if efficacy or toxicity warrant; 100-300 ng/mL is considered therapeutic)
- ECG (especially during IV administration)
- Blood pressure
- Heart rate and rhythm
- Liver function (in patients with hepatic disease)
๊ณผ์ฉ๋
**Clinical Signs of Overdose:** Bradycardia, hypotension, hyperglycemia, junctional rhythms, and 2nd or 3rd degree AV block. **Treatment:** * **Decontamination:** If secondary to recent oral ingestion, consider gut emptying and activated charcoal administration. * **Supportive Care:** Vigorously monitor cardiac and respiratory function. * **Negative Inotropy:** Intravenous calcium salts (1 mL of 10% solution per 10 kg of body weight) may treat negative inotropic signs, but may not adequately resolve heart block. * **Hypotension:** Fluid therapy and pressor agents (e.g., dopamine, norepinephrine) may be utilized. * **AV Block / Bradycardia:** Treat with isoproterenol, norepinephrine, atropine, or cardiac pacing. * **Rapid Ventricular Rate:** Patients developing rapid ventricular rate due to antegrade conduction in flutter/fibrillation with WPW syndrome have been treated with D.C. cardioversion, lidocaine, or procainamide.
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