์๋ฏธ์ค๋ค๋ก
์๋ฏธ์ค๋ค๋ก ์ ์ฃผ๋ก ์ค์ฆ์ ๋์น์ฑ ์ฌ์ค ๋ฐ ์์ฌ์ค์ฑ ๋ถ์ ๋งฅ์ ์ฌ์ฉ๋๋ ๊ฐ๋ ฅํ๊ณ ๊ด๋ฒ์ํ **์ 3ํ ํญ๋ถ์ ๋งฅ์ **์ ๋๋ค. ๋ณต์กํ ์ฝ๋ํ์ ํน์ฑ๊ณผ ์ฌ๊ฐํ ๋ ์ฑ ๊ฐ๋ฅ์ฑ ๋๋ฌธ์, ์ผ๋ฐ์ ์ผ๋ก ๊ธฐ์กด์ ๋ ์ฑ์ด ์ ์ ์น๋ฃ๋ฒ์ด ์คํจํ ๊ฒฝ์ฐ์๋ง ์ ํ์ ์ผ๋ก ์ฌ์ฉ๋ฉ๋๋ค. **์์ ์์ :** * ๊ตฌ์กฐ์ ์ผ๋ก ์๋ฏธ์ค๋ค๋ก ์ ์์ค๋ํ ๋ฒค์กฐํธ๋ ์ ๋์ฒด์ ๋๋ค. 200mg ์ ์ ํ๋์๋ ์ฝ 75mg์ ์์ค๋๊ฐ ํฌํจ๋์ด ์์ด ๊ฐ์์ ๊ธฐ๋ฅ์ ์ํฅ์ ์ค ์ ์์ต๋๋ค. * ์ง์ฉ์ฑ์ด ๋งค์ฐ ๋์ ์กฐ์ง์ ๊ด๋ฒ์ํ๊ฒ ๋ถํฌํ๊ณ ์ง๋ฐฉ ์กฐ์ง์ ์ถ์ ๋๋ฉฐ, ์ด๋ ๋ฐ๊ฐ๊ธฐ๊ฐ ๋งค์ฐ ๊ธธ๊ณ ๋ณ๋์ฑ์ด ํฐ ์์ธ์ด ๋ฉ๋๋ค. * ์์ํ์์๋ ํนํ ์ ์ฌ์ฑ ํ์ฅ์ฑ ์ฌ๊ทผ๋ณ์ฆ(DCM)์ด ์์ผ๋ฉด์ ๋น ๋ฅธ ๋์ QRS๊ตฐ ์ฌ์ค ๋น๋งฅ์ด๋ ์ค์ ์ ๋ณด์ด๋ ๋๋ฒ ๋ฅด๋ง ํ์ ์๊ฒ ๊ฐ์ฅ ํํ ์ฌ์ฉ๋ฉ๋๋ค. * ๋ถ์์ฉ(๊ฐ๋ ์ฑ ๋ฐ ๊ฐ์์ ๊ธฐ๋ฅ ์ฅ์ ํฌํจ)์ ์ํ์ด ๋์ผ๋ฏ๋ก ์ฒ ์ ํ ๋ชจ๋ํฐ๋ง์ด ํ์์ ์ ๋๋ค.
์์ฉ ๊ธฐ์ : Amiodarone is uniquely versatile, possessing properties of all four Vaughan-Williams antiarrhythmic classes, though it is primarily classified as a **Class III** agent. * **Class III (Primary):** Blocks **potassium (K+) channels** โ prolongs phase 3 repolarization, action-potential duration (APD), and the effective refractory period (ERP) in myocardial cells. * **Class I:** Blocks **fast sodium (Na+) channels** โ slows conduction velocity. * **Class II:** Non-competitively blocks **beta-adrenergic receptors** โ provides sympatholytic effects, reducing heart rate. * **Class IV:** Weakly blocks **calcium (Ca2+) channels** โ slows AV node conduction and suppresses automaticity. It is metabolized in the liver to its active metabolite, **desethylamiodarone**, which also contributes significantly to its antiarrhythmic effects.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- For atrial fibrillation or ventricular arrhythmias primarily in ambulatory patients ยท 8-10 mg/kg PO every 12 hours ยท PO ยท q12h ยท Use caution if patient has bradycardia, AV blocks, or thyroid disorders.
- For ventricular arrhythmias secondary to occult cardiomyopathy in Doberman pinschers ยท 10 mg/kg PO twice daily for one week and then 8 mg/kg PO once daily. After 6 months reduce to 5 mg/kg PO once daily. ยท PO ยท q12h then q24h ยท Long-term ยท For severe V-Tach, mexiletine is added at 5-8 mg/kg three times daily for one week. Once efficacy confirmed, patient weaned off mexiletine.
- For ventricular tachycardia when other first line drugs (Class I antiarrhythmics ยฑ beta-blockers) are ineffective ยท 10 mg/kg PO q12h for one week and then 5 mg/kg PO q12h for maintenance. ยท PO ยท q12h ยท Long-term
- For SVTs or Vtach ยท 10-20 mg/kg PO once daily (q24h) loading for 5-7 days; 5-10 mg/kg PO once daily thereafter. ยท PO ยท q24h ยท Long-term
- Ventricular and supraventricular arrhythmias, atrial fibrillation, ventricular pre-excitation syndromes ยท Dose not specified in monograph ยท PO/IV ยท Not specified ยท Not specified ยท Use as an IV infusion for recent onset atrial fibrillation has variable efficacy for restoring sinus rhythm but a high frequency of severe adverse effects.
- For conversion of atrial fibrillation or ventricular tachycardia ยท 5 mg/kg/hr for one hour, followed by 0.83 mg/kg/hr for 23 hours and then 1.9 mg/kg/hour for the following 30 hours. ยท IV ยท CRI ยท Up to 54 hours ยท Infusion was discontinued when conversion occurred or when any side effects were noted. Regimen should be further adapted based upon PK/PD studies.
์ฉ๋์ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์ฐธ๊ณ ์๋ฃ์ ๋๋ค. ํญ์ ์ต์ ๋ผ๋ฒจ๊ณผ ๊ฐ๋ณ ํ์์ ๋ํด ํ์ธํ์ญ์์ค.
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Hypersensitivity to amiodarone or iodine
- Severe sinus-node dysfunction
- Severe sinus bradycardia
- 2nd or 3rd degree AV block
- Bradycardial syncope
์ด์๋ฐ์
- Vomiting
- Anorexia
- Hepatopathy (elevated liver enzymes, bilirubinemia)
- Bradycardia
- Neutropenia
- Thrombocytopenia
- Positive Coombs' test
- Corneal deposits
- Injection site pain (IV)
- Facial pruritus and hyperemia (IV)
- Hind limb weakness (horses)
- Diarrhea (horses)
์ฝ๋ฌผ ์ํธ์์ฉ
- Warfarin (Anticoagulants) ยท Significantly increases serum levels and/or pharmacologic/toxic effects of the anticoagulant.
- Digoxin ยท Significantly increases serum levels and/or toxic effects of digoxin. ยท major
- Cyclosporine ยท Increases cyclosporine levels; may increase creatinine.
- Lidocaine ยท Significantly increases serum levels and/or toxic effects of lidocaine. ยท moderate
- Methotrexate ยท Significantly increases serum levels and/or toxic effects with prolonged amiodarone administration. ยท major
- Phenytoin ยท Significantly increases serum levels and/or toxic effects of phenytoin.
- Procainamide ยท Significantly increases serum levels and/or toxic effects of procainamide.
- Quinidine ยท Significantly increases serum levels and/or toxic effects of quinidine.
- Azole Antifungals (ketoconazole, itraconazole) ยท Additive effects on QTc interval; possible serious arrhythmias.
- Cisapride ยท Additive effects on QTc interval; possible serious arrhythmias.
- Disopyramide ยท Additive effects on QTc interval; possible serious arrhythmias.
- Dolasetron ยท Additive effects on QTc interval; possible serious arrhythmias.
๋ชจ๋ํฐ๋ง
- ECG (for antiarrhythmic efficacy and proarrhythmic effects)
- Gastrointestinal signs (anorexia, vomiting)
- CBC (for neutropenia, thrombocytopenia)
- Serial liver enzymes and bilirubin (baseline and routine monitoring)
- Thyroid function tests
- Blood pressure
- Pulmonary radiographs (if clinical signs such as dyspnea or cough occur)
๊ณผ์ฉ๋
Clinical overdosage experience is limited. **Expected Signs:** * Hypotension * Bradycardia * Cardiogenic shock * AV block * Hepatotoxicity **Treatment:** * Therapy is primarily **supportive**. * Bradycardia may be managed with a pacemaker or beta-1 agonists (e.g., isoproterenol). * Hypotension may be managed with positive inotropic agents or vasopressors. * *Note:* Neither amiodarone nor its active metabolite are dialyzable.
VetSheet ์ฝ๋ฌผ ๋ ํผ๋ฐ์ค๋ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์์ฌ๊ฒฐ์ ๋ณด์กฐ ๋๊ตฌ์ด๋ฉฐ, ์ ๋ฌธ์ ํ๋จ์ด๋ ์ ์กฐ์ฌ์ ์ต์ ๋ผ๋ฒจ์ ๋์ ํ์ง ์์ต๋๋ค.