๋ํฐ์์ ฌ
๋ํฐ์์ ฌ์ **๋น๋ํ๋๋กํผ๋ฆฌ๋๊ณ ์นผ์ ์ฑ๋ ์ฐจ๋จ์ **์ด์ **์ 4๊ตฐ ํญ๋ถ์ ๋งฅ์ **๋ก, ์์ํ์์๋ ์ฃผ๋ก ๊ณ ์์ด์ ์์ฌ์ค์ฑ ๋น๋งฅ(SVT), ์ ์ ๊ณ ํ์, ํ๋๋งฅ ๊ณ ํ์ ๋ฐ ๋น๋์ฑ ์ฌ๊ทผ๋ณ์ฆ(HCM) ๊ด๋ฆฌ์ ์ฌ์ฉ๋ฉ๋๋ค. * **์ฌํ๊ด๊ณ ํจ๊ณผ:** ์ฃผ๋ก ๋ฐฉ์ค๊ฒฐ์ (AV node) ์ ๋๋ฅผ ๋ฆ์ถ๊ณ ํ๊ด ํ์ฅ์ ์ด์งํ์ฌ ์ฌ๋ฐฉ์ธ๋์ ์ฌ๋ฐ์ ์กฐ์ ์ ๋งค์ฐ ํจ๊ณผ์ ์ ๋๋ค. * **์์์ ์ ์ฉ์ฑ:** ๊ณผ๊ฑฐ์๋ ๊ณ ์์ด HCM ์น๋ฃ์ ํต์ฌ์ด์์ผ๋, ์ต๊ทผ์๋ ๋ค๋ฅธ ์น๋ฃ๋ฒ์ด ์ ํธ๋๋ฉด์ ์ด ์ ์์ฆ์ ๋ํ ์ฌ์ฉ์ด ๊ฐ์ํ์ต๋๋ค. ํ์ง๋ง ๋น๋งฅ์ฑ ๋ถ์ ๋งฅ ์น๋ฃ์๋ ์ฌ์ ํ ์ค์ํ ์ฝ๋ฌผ์ ๋๋ค. * **์์ ์์ :** ๊ฐ๋ ฅํ ๋ง์ด ํ๊ด ํ์ฅ์ ์ธ ๋ํ๋๋กํผ๋ฆฌ๋๊ณ(์: ์๋ก๋ํ)์ ๋ฌ๋ฆฌ, ๋ํฐ์์ ฌ์ ์ฌ์ฅ ์ ๋์ ๋ฏธ์น๋ ์ํฅ์ด ๋ ์ปค์ ๋ฆฌ๋ฌ ์กฐ์ ์๋ ์ฐ์ํ์ง๋ง ์ค์ฆ ์ ์ ๊ณ ํ์์ ๋ํ ๊ฐ์ ํจ๊ณผ๋ ์๋์ ์ผ๋ก ์ฝํฉ๋๋ค.
์์ฉ ๊ธฐ์ : Diltiazem exerts its effects by binding to the alpha-1 subunit of **L-type voltage-gated calcium channels**. * **Mechanism:** Inhibits transmembrane influx of extracellular calcium ions โ decreases intracellular calcium in myocardial cells and vascular smooth muscle. * **Cardiac Conduction:** Slows **AV node conduction** and prolongs refractory times (negative dromotropic effect). It rarely affects SA node conduction except in sick sinus syndrome. * **Vasodilation:** Relaxes vascular smooth muscle โ dilates main systemic and coronary arteries โ reduces total peripheral resistance, blood pressure, and cardiac afterload. * **Inotropy:** Can cause mild negative inotropic effects, though rarely of clinical significance compared to verapamil.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Treatment of hypertrophic cardiomyopathy (Option A) ยท 7.5 mg (total dose) PO q8-12h; Long-acting forms: Cardizem CD Capsules: 10 mg/kg once daily. Dilacor XR Capsules: 15-30 mg total dose q12-24h. ยท PO ยท q8-24h ยท Some cats tolerate 60 mg daily, but vomiting may be a problem.
- Treatment of hypertrophic cardiomyopathy (Option B) ยท 1.75-2.5 mg/kg PO q8h or sustained release (Dilacor) dosed at 30 mg (total dose) PO q12h ยท PO ยท q8-12h
- Treatment of hypertrophic cardiomyopathy (Option C) ยท 7.5-15 mg (total dose) per cat PO q8h. Alternatively, the sustainedrelease products Cardizem CD at 45 mg (total dose) PO q24h or Dilacor XR at 30 mg (total dose; 1/2 of one of the 60 mg tablets found within the capsule) PO q12h can be used. ยท PO ยท q8-24h
- Treatment of hypertrophic cardiomyopathy (Option D) ยท If using standard release formulations: 1-2.5 mg/kg PO q8h; if using sustained release formations: 30-60 mg (total dose per cat) q24h. ยท PO ยท q8-24h ยท Also indicated for supraventricular arrhythmias.
- Treatment of hypertrophic cardiomyopathy (Option E) ยท Dilacor XR 30 mg/cat PO q24h. ยท PO ยท q24h ยท If cat has minimal tachycardia and a loud S4 gallop, many prefer using diltiazem (over a beta blocker).
- Emergency treatment of supraventricular tachyarrhythmias ยท Initially, 0.25 mg/kg IV bolus given over 2 minutes; subsequent 0.25 mg/kg boluses may be repeated at 15 minute intervals until conversion occurs or to a maximum (total) dose of 0.75 mg/kg. ยท IV ยท q15min
- Acute management of supraventricular tachyarrhythmias ยท 0.125-0.35 mg/kg IV ยท IV ยท As directed
- Chronic management of supraventricular tachyarrhythmias ยท 7.5 mg (per cat) PO q8h ยท PO ยท q8h ยท Used in combination with digoxin for patients with CHF unless cat has hypertrophic cardiomyopathy and atrial fib, then digoxin not used.
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Severe hypotension (<90 mm Hg systolic)
- Sick sinus syndrome (unless functioning pacemaker is in place)
- 2nd or 3rd degree AV block (unless functioning pacemaker is in place)
- Acute myocardial infarction
- Radiographically documented pulmonary congestion
- Hypersensitivity to diltiazem
- Second or third degree AV block
- Marked hypotension
- Sick sinus syndrome
- Acute or decompensated congestive heart failure (relative contraindication)
์ด์๋ฐ์
- Dogs: Bradycardia (most prominent)
- Cats: Vomiting (especially with 60 mg sustained-release pellets)
- Lethargy
- Anorexia / GI distress
- Hypotension
- Heart block or rhythm disturbances
- CNS effects
- Skin rashes
- Elevations in liver enzymes
- Bradycardia (most common in dogs)
- Vomiting (most common in cats)
- AV block
์ฝ๋ฌผ ์ํธ์์ฉ
- Anesthetics, General ยท May increase cardiac depressant effects of diltiazem.
- Benzodiazepines ยท Diltiazem may increase benzodiazepine levels.
- Beta-Blockers ยท May increase the likelihood of bradycardia, AV block, or CHF. Diltiazem may substantially increase the bioavailability of propranolol.
- Buspirone ยท Diltiazem may increase buspirone levels.
- Cisapride ยท Could potentially increase risk for increased QT intervals.
- Digoxin ยท Data conflicts regarding pharmacokinetic effects; diligent monitoring of digoxin serum concentrations is required. ยท moderate
- Cimetidine ยท May increase plasma diltiazem concentrations; increased monitoring warranted. ยท moderate
- Ranitidine ยท May affect diltiazem concentrations, but to a lesser extent than cimetidine.
- Cyclosporine ยท Diltiazem may increase cyclosporine serum concentrations; monitoring and dosage adjustments may be required.
- Rifampin ยท May decrease diltiazem levels.
- Quinidine ยท Diltiazem may increase quinidine serum concentrations; monitoring and dosage adjustments may be required.
- Beta-adrenergic blockers (e.g., propranolol) ยท Additive negative inotropic and chronotropic effects. Co-administration is not recommended. ยท major
๋ชจ๋ํฐ๋ง
- ECG / Heart rate
- Blood pressure
- Adverse effects (vomiting, lethargy)
- Heart rate and rhythm (ECG)
- Renal and hepatic function (periodically)
- Serum digoxin levels (if used concurrently)
๊ณผ์ฉ๋
The oral LD50 in dogs is >50 mg/kg. * **Clinical Signs:** GI signs, heart block, severe bradycardia, hypotension, CNS depression, and heart failure. * **Treatment:** * Gut emptying protocols if recent ingestion. * **Bradycardia/AV Block:** Atropine. If unresponsive to vagal blockade, cautious use of isoproterenol. Fixed block may require temporary transvenous cardiac pacing. * **Hypotension/Heart Failure:** Inotropics (dobutamine, dopamine, isoproterenol) and pressors (norepinephrine). * **Antidote:** A slow intravenous calcium infusion (1 mL/10 kg body weight of 10% calcium gluconate) may be useful for severe acute toxicity.
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