์ธํฌํ์ฌ
์ธํฌํ์ฌ์ ๊ทธ๋ ์์ฑ๊ท ๋ฐ ๊ทธ๋ ์์ฑ๊ท ๋ชจ๋์ ๋ํด ๊ด๋ฒ์ํ ํญ๊ท ํ์ฑ์ ๊ฐ๋ **3์ธ๋ ์ฃผ์ฌ์ฉ ์ธํ๋ก์คํฌ๋ฆฐ** ํญ์์ ์ ๋๋ค. ์ฃผ์ ์์์ ํน์ง์ ๋ค์๊ณผ ๊ฐ์ต๋๋ค: * **ํ์ฅ๋ ๊ทธ๋ ์์ฑ๊ท ์ปค๋ฒ๋ฆฌ์ง**: ์ฅ๋ด์ธ๊ท ๊ณผ(์: ํด๋ ๋ธ์์๋ผ, ๋์ฅ๊ท , ์ด๋ชจ๋ฌ๋ผ, ํ๋กํ ์ฐ์ค)์ ๋งค์ฐ ํจ๊ณผ์ ์ ๋๋ค. * **ํ๊ธฐ์ฑ ๊ท ํ์ฑ**: ๋ฐํ ๋ก์ด๋ฐ์ค ํ๋ผ์ง๋ฆฌ์ค ๋ฐ ํด๋ก์คํธ๋ฆฌ๋์ ์ข ์ ํฌํจํ ๋ง์ ํ๊ธฐ์ฑ ๊ท ์ ํจ๊ณผ์ ์ ๋๋ค. * **์ค์ถ์ ๊ฒฝ๊ณ(CNS) ์นจํฌ**: 1์ธ๋ ๋ฐ ๋๋ถ๋ถ์ 2์ธ๋ ์ธํ๋ก์คํฌ๋ฆฐ๊ณผ ๋ฌ๋ฆฌ, ๋์๋ง์ ์ผ์ฆ์ด ์์ ๋ **๋์ฒ์์ก(CSF)**์์ ์น๋ฃ ๋๋์ ๋๋ฌํ๋ฏ๋ก ์ธ๊ท ์ฑ ๋์๋ง์ผ ๋ฐ ์ฒ์ ๊ฐ์ผ์ ์ ์ฉํ ์ต์ ์ ๋๋ค. * **ํฌ์ฌ**: ๊ฒฝ๊ตฌ๋ก ๊ฑฐ์ ํก์๋์ง ์์ผ๋ฏ๋ก ๋ฐ๋์ ๋น๊ฒฝ๊ตฌ(IV, IM, SC)๋ก ํฌ์ฌํด์ผ ํฉ๋๋ค. ๋ถ์์ฉ์ ์ต์ํํ๊ธฐ ์ํด ์ ๋งฅ ์ฃผ์ฌ๋ ์ฒ์ฒํ(3-5๋ถ ์ด์) ํฌ์ฌํด์ผ ํฉ๋๋ค. > **์์ ํ**: ๋ง์ ๊ทธ๋ ์์ฑ ํธ๊ธฐ์ฑ ๊ท ์ ๋ํด ์ฐ์ํ ํ์ฑ์ ๋ณด์ด์ง๋ง, ๋ น๋๊ท (Pseudomonas aeruginosa)์ ๋ํ ํจ๋ฅ์ ๋ณ๋์ฑ์ด ํฌ๋ฉฐ ์์์ ์ผ๋ก ์ค๋ง์ค๋ฌ์ด ๊ฒฝ์ฐ๊ฐ ๋ง์ต๋๋ค. ๋์คํฌ ํ์ฐ๋ฒ ๊ฐ์์ฑ ๊ฒ์ฌ ์ 30๋ง์ดํฌ๋ก๊ทธ๋จ ์ธํฌํ์ฌ ๋์คํฌ๋ฅผ ์ฌ์ฉํด์ผ ํฉ๋๋ค.
์์ฉ ๊ธฐ์ : Cefotaxime is a **time-dependent, bactericidal** antibiotic. * **Mechanism**: It binds to specific **penicillin-binding proteins (PBPs)** located inside the bacterial cell wall โ inhibits the third and final stage of bacterial cell wall peptidoglycan synthesis โ leads to cell lysis and death mediated by bacterial cell wall autolytic enzymes (autolysins). * **Metabolism**: It is partially metabolized in the liver to **desacetylcefotaxime**, an active metabolite that works synergistically with the parent compound to enhance antibacterial activity.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Soft tissue infections ยท 22 mg/kg IV, IM or SC q8h for 7 days or less or 50 mg/kg IV or IM q12h for 7 days or less ยท IV, IM, SC ยท q8h or q12h ยท 7 days or less
- Orthopedic infections ยท 20-40 mg/kg IV, IM or SC q6-8h for 7 days or less ยท IV, IM, SC ยท q6-8h ยท 7 days or less
- Severe bacteremia ยท 20-80 mg/kg IV q6h or 10-50 mg/kg IV q4-6h for as long as necessary ยท IV ยท q4-6h ยท As long as necessary
- Susceptible infections ยท 25-50 mg/kg IV, IM or SC q8h ยท IV, IM, SC ยท q8h
- Sepsis ยท 20-80 mg/kg IV, IM q8h ยท IV, IM ยท q8h
- CNS infections (spinal cord) ยท 25 mg-50 mg/kg IV, IM q8h ยท IV, IM ยท q8h
- Acute sepsis or serious susceptible infections ยท 40-50 mg/kg ยท IV/IM/SC ยท q8h ยท Until clinical resolution ยท Standard recommended dose.
- Susceptible infections ยท 10-20 mg/kg ยท IV/IM/SC ยท q12h ยท Until clinical resolution ยท Lower dose suggested by some authors to have good clinical efficacy.
- Susceptible infections (most birds) ยท 50-100 mg/kg IM three times a day ยท IM ยท TID ยท May be used with aminoglycosides, but nephrotoxicity may occur. Reconstituted vial good for 13 weeks if frozen.
- Bacterial infections, bacterial hepatitis ยท 75-100 mg/kg IM or IV q4-8h ยท IM, IV ยท q4-8h
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Patients with a documented history of hypersensitivity to cephalosporins
์ด์๋ฐ์
- Pain at the IM injection site
- Thrombophlebitis (after IV administration)
- Hypersensitivity reactions (rashes, fever, eosinophilia, anaphylaxis)
- Antibiotic-associated diarrhea (alteration of gut flora)
- Sterile abscesses or local tissue reactions
- Rarely: Nephrotoxicity, neurotoxicity (at high doses), neutropenia, agranulocytosis, thrombocytopenia, hepatitis
์ฝ๋ฌผ ์ํธ์์ฉ
- Aminoglycosides / Nephrotoxic drugs (e.g., amphotericin B) ยท Potential for additive nephrotoxicity. In vitro studies show synergistic antibacterial activity, but they must NOT be mixed in the same syringe or fluid bag.
- Probenecid ยท Competitively blocks the renal tubular secretion of cefotaxime, significantly increasing its serum levels and prolonging its elimination half-life.
- Oxytetracycline ยท Bacteriostatic agents may antagonize the bactericidal activity of cephalosporins. ยท moderate
- Erythromycin ยท Bacteriostatic agents may antagonize the bactericidal activity of cephalosporins. ยท moderate
- Aminoglycosides ยท Synergistic antibacterial effect, but do not mix in the same syringe due to chemical incompatibility. ยท minor
- Amphotericin B ยท Increased risk of nephrotoxicity. ยท major
- Furosemide ยท Loop diuretics may increase the risk of nephrotoxicity when used with cephalosporins. ยท major
๋ชจ๋ํฐ๋ง
- Clinical efficacy (resolution of infection signs)
- Renal function parameters (BUN, creatinine, urinalysis) in compromised patients or those on concurrent nephrotoxic drugs
๊ณผ์ฉ๋
Acute cephalosporin overdoses are unlikely to cause significant life-threatening problems. However, massive overdoses may exacerbate adverse effects, potentially leading to **neurotoxicity** (seizures, encephalopathy), **nephrotoxicity**, or severe gastrointestinal upset. Treatment should consist of standard supportive care and monitoring.
VetSheet ์ฝ๋ฌผ ๋ ํผ๋ฐ์ค๋ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์์ฌ๊ฒฐ์ ๋ณด์กฐ ๋๊ตฌ์ด๋ฉฐ, ์ ๋ฌธ์ ํ๋จ์ด๋ ์ ์กฐ์ฌ์ ์ต์ ๋ผ๋ฒจ์ ๋์ ํ์ง ์์ต๋๋ค.