์์ธํธ์๋ฏธ๋ ธํ (ํ๋ผ์ธํ๋ชฐ)
์์ธํธ์๋ฏธ๋ ธํ์ ๊ฒฝ๋ ๋ด์ง ์ค๋ฑ๋์ ํต์ฆ ๋ฐ ๋ฐ์ด์ ์กฐ์ ํ๊ธฐ ์ํด ์ฌ์ฉ๋๋ ์ค์ถ์ฑ ์งํตํด์ด์ ์ ๋๋ค. ์ ํต์ ์ธ NSAID์ ๋นํด ํญ์ผ์ฆ ํจ๊ณผ๋ ์ฝํ์ง๋ง ์์ฅ๊ด ๋ถ์์ฉ์ด ์ ์ ๊ฒ์ผ๋ก ์๋ ค์ ธ ์์ด ์๊ถค์ ํ์์๊ฒ ์ ์ฉํ ๋์์ด ๋ ์ ์์ต๋๋ค. ์ฃผ์ฌ์ฉ ์์ธํธ์๋ฏธ๋ ธํ์ ๊ฐ์์ ์์ ์ ํ ๋ณด์กฐ ์งํต์ ๋ก๋ ์ฌ์ฉ๋ฉ๋๋ค. > **์ฌ๊ฐํ ๊ฒฝ๊ณ :** ๊ณ ์์ด๋ ์ด ์ฝ๋ฌผ์ ์์ ํ๊ฒ ๋์ฌํ๋ ํจ์๊ฐ ๋ถ์กฑํ์ฌ ์น๋ช ์ ์ธ ๋ ์ฑ์ ์ ๋ฐํ๋ฏ๋ก ๊ณ ์์ด์๊ฒ๋ **์ ๋ ๊ธ๊ธฐ**์ ๋๋ค. **์์ ํ:** ํ๊ฐ๋ ์์์ฉ ๊ฒฝ๊ตฌ ์ ์ (Pardale-V)์๋ ์ฝ๋ฐ์ธ์ด ํฌํจ๋์ด ์์ผ๋, ๊ฐ์์๋ ์คํผ์ค์ด๋์ ์ดํ ํต๊ณผ ๋์ฌ์จ์ด ๋์ ์ฝ๋ฐ์ธ ์ฑ๋ถ์ ์์ฒด์ด์ฉ๋ฅ ์ด ๋ฎ์ผ๋ฉฐ ์งํต ํจ๊ณผ์ ํฌ๊ฒ ๊ธฐ์ฌํ์ง ์์ต๋๋ค.
์์ฉ ๊ธฐ์ : The exact mechanism of action remains partially unclear. It is proposed that its antipyretic and analgesic actions are due to: - Decreased **prostaglandin synthesis** specifically within the central nervous system (CNS). - Possible indirect actions on the **cannabinoid system**. Unlike traditional NSAIDs, it has minimal peripheral cyclooxygenase (COX) inhibition, which explains its lack of significant anti-inflammatory activity and reduced gastrointestinal toxicity.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Mild to moderate pain / Antipyretic ยท 10-20 mg/kg ยท PO/IV ยท q8h ยท 5-7 days (for acute pain) ยท For acute pain management, doses at the top of the range (20 mg/kg) can be used for up to 5-7 days.
- Mild to moderate pain (Pardale-V preparation) ยท 1 tablet per 12 kg body weight (equivalent to 33 mg/kg) ยท PO ยท q8h ยท Max 7 days before titrating down ยท Authorized dose for Pardale-V. After 7 days, titrate down to the lowest effective dose. Codeine component is not bioavailable.
- All indications ยท Do not use ยท PO/IV ยท N/A ยท N/A ยท Absolute contraindication. Fatal toxicosis due to methaemoglobinaemia.
์ฉ๋์ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์ฐธ๊ณ ์๋ฃ์ ๋๋ค. ํญ์ ์ต์ ๋ผ๋ฒจ๊ณผ ๊ฐ๋ณ ํ์์ ๋ํด ํ์ธํ์ญ์์ค.
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Cats (absolute contraindication due to fatal toxicosis)
- Patients with pre-existing severe hepatic impairment
์ด์๋ฐ์
- Hepatotoxicity (dose-dependent)
- Methaemoglobinaemia (especially in cats)
- Facial edema
- Cyanosis
์ฝ๋ฌผ ์ํธ์์ฉ
- Metoclopramide ยท Enhances the absorption of paracetamol, thereby enhancing its clinical and potentially toxic effects. ยท moderate
- Cytochrome P450 Inducers (e.g., Phenobarbital, certain NSAIDs) ยท May increase the production of toxic metabolites (NAPQI), enhancing the risk of hepatotoxicity. ยท major
๋ชจ๋ํฐ๋ง
- Liver enzyme panel (ALT, AST, ALP, Bilirubin) if prolonged use or overdose is suspected
- Clinical signs of toxicity (jaundice, vomiting, lethargy)
- Mucous membrane color (monitoring for cyanosis/brown blood indicative of methaemoglobinaemia)
๊ณผ์ฉ๋
Overdose of paracetamol causes severe liver damage. Metabolism produces the toxic intermediate **N-acetyl-p-aminobenzoquinonimine (NAPQI)**, which depletes hepatic glutathione, leading to hepatocyte cell death and centrilobular hepatic necrosis. In cats, it causes fatal methaemoglobinaemia. **Treatment:** - Decontamination (emesis/activated charcoal) if ingestion is recent. - **Antidote:** Oral **methionine** or IV **acetylcysteine (N-acetylcysteine)**. These are directed at replenishing hepatic glutathione stores to neutralize NAPQI, though clinical data in veterinary species is limited. - Supportive care (IV fluids, oxygen therapy, blood transfusions if severe methaemoglobinaemia occurs).
VetSheet ์ฝ๋ฌผ ๋ ํผ๋ฐ์ค๋ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์์ฌ๊ฒฐ์ ๋ณด์กฐ ๋๊ตฌ์ด๋ฉฐ, ์ ๋ฌธ์ ํ๋จ์ด๋ ์ ์กฐ์ฌ์ ์ต์ ๋ผ๋ฒจ์ ๋์ ํ์ง ์์ต๋๋ค.