λμμ‘±μ¬μ΄λ
λμμ‘±μ¬μ΄λ(Diazoxide)λ λΉμ΄λ¨μ± ν°μμ§λ μ λ체λ‘, μμνμμλ μ£Όλ‘ κ°μ νλΏμ **μΈμλ¦°μ’ **(μΈμλ¦° λΆλΉ μ·λ μΈν¬ μ’ μ)μ λ΄κ³Όμ κ΄λ¦¬μ μ¬μ©λ©λλ€. κ°λ ₯ν μ§μ νκ΄ νμ₯ νΉμ±(μΈμ²΄μμλ κ³ νμ μκΈ μν©μ μ λ§₯ ν¬μ¬λ¨)μ κ°μ§κ³ μμ§λ§, λλ¬Όμμμ 경ꡬ μ¬μ©μ μ£Όλ‘ κ·Έ κ°λ ₯ν **νλΉ μμΉ** λΆμμ©μ νμ©ν©λλ€. μΈμλ¦° λ°©μΆμ κΈΈνν¨μΌλ‘μ¨ λμΉμ± μ νλΉμ¦ νμμ νλΉ μμΉλ₯Ό μμ μν€λ λ° λμμ μ€λλ€. **μμ μμ :** - μμ΄ κ΄λ¦¬(μλμ© μμ£Ό κΈμ¬)μ κΈλ£¨μ½μ½λ₯΄ν°μ½μ΄λ(μ: νλ λλμ) λ¨λ μΌλ‘ μ νλΉ μκΈ°λ₯Ό ν΅μ νμ§ λͺ»ν λ μ’ μ’ λ³μ©νμ¬ μ¬μ©λ©λλ€. - ν°μμ§λ μ΄λ¨μ μ ꡬ쑰μ μΌλ‘ μ μ¬νμ¬ λνΈλ₯¨ λ° μλΆ μ λ₯λ₯Ό μ λ°ν μ μμΌλ, μ΄λ¨ ν¨κ³Όλ μμ΅λλ€.
μμ© κΈ°μ : Diazoxide exerts its hyperglycemic and vasodilatory effects via multiple mechanisms: - **K+ ATP Channel Activation**: It binds to the sulfonylurea receptor 1 (SUR1) subunit of the **ATP-sensitive potassium (K+ ATP) channels** on pancreatic beta cells β channel opening β cellular hyperpolarization β decreased intracellular **calcium (Ca2+)** influx β **inhibition of insulin exocytosis** from secretory granules. - **Beta-Adrenergic Stimulation**: Stimulates the release of **epinephrine**, which promotes hepatic glycogenolysis and inhibits peripheral cellular glucose uptake. - **Vasodilation**: Directly relaxes arteriolar smooth muscle by opening K+ ATP channels in vascular smooth muscle cells β hyperpolarization β vasodilation β decreased peripheral vascular resistance and blood pressure.
λλ¬Ό μ’ λ³ μ©λ
- Hypoglycemia secondary to insulin secreting islet cell tumors Β· Initially, 5 mg/kg PO twice daily; increase to a maximum of 30 mg/kg PO twice daily to control clinical signs Β· PO Β· q12h Β· Insulinomas are very rare in cats; little experience with this drug in this species.
- Hypoglycemia secondary to insulin secreting islet cell tumors Β· Begin at 5-10 mg/kg PO q12h. Β· PO Β· q12h Β· Add diazoxide when clinical signs cannot be controlled with prednisone alone. At same time prednisone dosage may be lowered.
- Hypoglycemia secondary to insulin secreting islet cell tumors Β· Initially, 5 mg/kg PO twice daily; increase to a maximum of 30 mg/kg PO twice daily to control clinical signs Β· PO Β· q12h
- Hypoglycemia secondary to insulin secreting islet cell tumors (refractory) Β· Initially at 10 mg/kg divided twice a day. May gradually increase dosage to 60 mg/kg/day as tolerated and add hydrochlorothiazide (2-4 mg/kg/day). Β· PO Β· Divided twice a day Β· Used if frequent feedings and glucocorticoids fail or cause Cushingoid appearance.
- Adjunctive therapy of hypoglycemia secondary to insulin secreting non-islet cell (extra-pancreatic) tumors Β· 5-13 mg/kg PO three times daily Β· PO Β· q8h Β· May add hydrochlorothiazide 2-4 mg/kg/day.
μ©λμ λ©΄ν μμ μ λ¬Έκ°λ₯Ό μν μμ μ°Έκ³ μλ£μ λλ€. νμ μ΅μ λΌλ²¨κ³Ό κ°λ³ νμμ λν΄ νμΈνμμμ€.
ν¬μ¬ κ²½λ‘
κΈκΈ°
- Functional hypoglycemia
- Hypoglycemia secondary to insulin overdosage in diabetic patients
- Hypersensitivity to thiazide diuretics (unless benefits outweigh risks)
- Hypersensitivity to thiazides
- Functional hypoglycemia (non-insulinoma)
μ΄μλ°μ
- Anorexia
- Vomiting
- Diarrhea
- Hypersalivation
- Tachycardia
- Agranulocytosis
- Aplastic anemia
- Thrombocytopenia
- Diabetes mellitus
- Cataracts
- Sodium and water retention
- Malaise (ferrets)
- Bone marrow suppression (ferrets)
- Gastrointestinal upset (anorexia, vomiting, diarrhea)
- Hyperglycemia
- Cataracts (rare)
- Bone marrow suppression (rare)
μ½λ¬Ό μνΈμμ©
- Alpha-adrenergic agents (e.g., phenoxybenzamine) Β· May decrease the effectiveness of diazoxide in increasing glucose levels
- Hypotensive agents (e.g., hydralazine, prazosin) Β· Diazoxide may enhance the hypotensive actions of other hypotensive agents
- Phenothiazines (e.g., acepromazine, chlorpromazine) Β· May enhance the hyperglycemic effects of diazoxide
- Phenytoin Β· Diazoxide may increase the metabolism, or decrease the protein binding of phenytoin
- Thiazide diuretics (e.g., hydrochlorothiazide) Β· May potentiate the hyperglycemic effects of oral diazoxide. Can be used synergistically, but caution is advised as hypotension may occur
- Thiazide diuretics Β· Potentiate hyperglycemic and hyperuricemic effects Β· moderate
- Phenothiazines Β· May potentiate hyperglycemia Β· moderate
- Alpha-adrenergic blockers Β· May antagonize the effects of diazoxide Β· moderate
- Highly protein-bound drugs (e.g., NSAIDs, warfarin) Β· Diazoxide is highly protein-bound and may displace or be displaced by other drugs, altering free drug concentrations Β· moderate
λͺ¨λν°λ§
- Blood (serum) glucose
- CBC (at least every 3-4 months)
- Physical exam (monitor for clinical signs of adverse effects like edema, cataracts, or tachycardia)
- Blood glucose
- Electrolytes (sodium, potassium)
- Complete blood count (CBC) periodically
- Signs of fluid retention/edema
κ³Όμ©λ
Acute overdosage may result in severe **hyperglycemia** and **ketoacidosis**. - **Treatment**: Administer insulin, intravenous fluids, and correct electrolyte imbalances. - **Monitoring**: Intensive and prolonged monitoring of blood glucose and acid-base status is highly recommended.
VetSheet μ½λ¬Ό λ νΌλ°μ€λ λ©΄ν μμ μ λ¬Έκ°λ₯Ό μν μμ μμ¬κ²°μ 보쑰 λꡬμ΄λ©°, μ λ¬Έμ νλ¨μ΄λ μ μ‘°μ¬μ μ΅μ λΌλ²¨μ λμ νμ§ μμ΅λλ€.