์ธํฌ์ํด
์ธํฌ์ํด์ ์์ํ์์ ์ค์ฆ ๋๋ ํผํฉ ์ธ๊ท ๊ฐ์ผ์ ์น๋ฃํ๋ ๋ฐ ์ฌ์ฉ๋๋ **2์ธ๋ ์ฃผ์ฌ์ฉ ์ธํ๋ก์คํฌ๋ฆฐ**(์๋ฐํ ๋งํด ์ธํ๋ง์ด์ ์ผ๋ก ๋ถ๋ฅ๋จ)์ ๋๋ค. ์ฃผ์ ์ฝ๋ฆฌํ์ ํน์ง์ ๋ค์๊ณผ ๊ฐ์ต๋๋ค: * **ํ๊ธฐ์ฑ ์ธ๊ท ์ ๋ํ ํจ๋ฅ**: ๋ค๋ฅธ ์ด๊ธฐ ์ธ๋ ์ธํ๋ก์คํฌ๋ฆฐ๊ณผ ๋ฌ๋ฆฌ ์ธํฌ์ํด์ ๋ฐํ ๋ก์ด๋ฐ์ค ํ๋ผ์ง๋ฆฌ์ค(*Bacteroides fragilis*)๋ฅผ ํฌํจํ **ํ๊ธฐ์ฑ ์ธ๊ท **์ ๋งค์ฐ ํจ๊ณผ์ ์ ๋๋ค. * **๊ทธ๋ ์์ฑ๊ท ์คํํธ๋ผ**: 1์ธ๋ ์ฝ๋ฌผ์ ๋ด์ฑ์ ๋ณด์ผ ์ ์๋ ๋์ฅ๊ท (*E. coli*), ํด๋ ์์๋ผ(*Klebsiella*), ํ๋กํ ์ฐ์ค(*Proteus*)์ ๋ง์ ๊ท ์ฃผ์ ๋ํด ์ฐ์ํ ํ์ฑ์ ๋ํ๋ ๋๋ค. * **๊ทธ๋ ์์ฑ๊ท ์คํํธ๋ผ**: ๊ทธ๋ ์์ฑ ๊ตฌ๊ท ์ ๋ํ ํ์ฑ์ ์ ์งํ์ง๋ง, ๋์ผ ์ฉ๋ ๊ธฐ์ค 1์ธ๋ ์ธํ๋ก์คํฌ๋ฆฐ์ ๋นํด ํจ๋ฅ์ ์ฝ๊ฐ ๋จ์ด์ง๋๋ค. > **์์ ์์ **: ๊ฐ๋ ฅํ ํ๊ธฐ์ฑ ์ธ๊ท ์คํํธ๋ผ ๋๋ถ์ ์ธํฌ์ํด์ ํก์ธ์ฑ ํ๋ ด, ์ฅ ์ฒ๊ณต, ์ค์ฆ ์ฐ๋ถ์กฐ์ง ๊ฐ์ผ ๋๋ ํจํ์ฆ๊ณผ ๊ฐ์ ํผํฉ ๊ฐ์ผ์ ์์ฃผ ์ ํ๋ฉ๋๋ค.
์์ฉ ๊ธฐ์ : Cefoxitin is a **bactericidal** antibiotic that works by inhibiting bacterial cell wall synthesis. * It covalently binds to specific **Penicillin-Binding Proteins (PBPs)** located inside the bacterial cell wall. * Binding to PBPs โ **inhibits the transpeptidation enzyme** responsible for cross-linking peptidoglycan strands. * Lack of cross-linking โ weakens the bacterial cell wall โ leads to osmotic instability, cell lysis, and bacterial death. * As a cephamycin, cefoxitin is highly resistant to degradation by many **beta-lactamases**, particularly those produced by *Bacteroides* species.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Systemic infections ยท 25-30 mg/kg IV or IM q8h ยท IV/IM ยท q8h ยท Use as long as necessary to control initial infection, then switch to oral drugs
- Sepsis ยท 30 mg/kg IV q5h ยท IV ยท q5h
- Susceptible infections ยท 30 mg/kg IV q8h ยท IV ยท q8h
- Non-tuberculosis mycobacteria (NTM) - second line treatment ยท 30-40 mg/kg IV, IM or SC q6-8h ยท IV/IM/SC ยท q6-8h ยท Causes pain on injection with IM or SC
- Susceptible infections (Foals) ยท 20 mg/kg IV q4-6h ยท IV ยท q4-6h
- Mixed infections (e.g., aspiration pneumonia, bowel perforation) ยท 30 mg/kg SC q8h; 30 mg/kg IV q4-6h ยท SC/IV ยท q8h or q4-6h
- Sepsis ยท 30 mg/kg IV q5h ยท IV ยท q5h
- Soft tissue infections ยท 30 mg/kg SC q8h or 30 mg/kg IV q5h ยท SC/IV ยท q8h or q5h
- Bacteremia ยท 15-30 mg/kg IV, IM SC q6-8h ยท IV/IM/SC ยท q6-8h
- Orthopedic infections ยท 22 mg/kg IV, IM q6-8h ยท IV/IM ยท q6-8h ยท Use as long as necessary to control initial infection, then switch to oral drugs
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Patients with a history of hypersensitivity to cephalosporins
- Use with extreme caution in patients documented to be hypersensitive to other beta-lactams (penicillins, carbapenems)
์ด์๋ฐ์
- Hypersensitivity reactions (rashes, fever, eosinophilia, lymphadenopathy, anaphylaxis)
- Pain at the injection site (IM)
- Sterile abscesses or local tissue reactions
- Thrombophlebitis (IV administration)
- Antibiotic-associated diarrhea or altered gut flora
- Superinfections
- Nephrotoxicity (rare at clinical doses)
- Neurotoxicity, neutropenia, thrombocytopenia, hepatitis (associated with high doses or prolonged use)
์ฝ๋ฌผ ์ํธ์์ฉ
- Aminoglycosides / Nephrotoxic Drugs ยท Potential for additive nephrotoxicity. While in vitro synergy exists against certain bacteria, they should not be mixed in the same syringe or fluid bag.
- Probenecid ยท Competitively blocks the tubular secretion of cefoxitin, thereby increasing serum levels and prolonging elimination half-lives.
๋ชจ๋ํฐ๋ง
- Clinical efficacy (resolution of infection signs)
- Renal function (BUN, creatinine, urinalysis) in patients with diminished renal capacity
๊ณผ์ฉ๋
Acute oral cephalosporin overdoses are unlikely to cause significant problems other than **gastrointestinal distress**. Massive parenteral overdoses or prolonged accumulation (especially in renal failure) may lead to: * Neurotoxicity (seizures) * Neutropenia or thrombocytopenia * Hepatitis * Nephrotoxicity (tubular necrosis) Treatment is supportive and symptomatic.
VetSheet ์ฝ๋ฌผ ๋ ํผ๋ฐ์ค๋ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์์ฌ๊ฒฐ์ ๋ณด์กฐ ๋๊ตฌ์ด๋ฉฐ, ์ ๋ฌธ์ ํ๋จ์ด๋ ์ ์กฐ์ฌ์ ์ต์ ๋ผ๋ฒจ์ ๋์ ํ์ง ์์ต๋๋ค.