์๋ฐํธ์ฐ ์นผ์ ์ด๋ํธ๋ฅจ
์๋ฐํธ์ฐ ์นผ์ ์ด๋ํธ๋ฅจ(CaEDTA)์ ์์ํ์์ ์ฃผ๋ก **๋ฉ** ๋ฐ **์์ฐ** ์ค๋ ์น๋ฃ์ ์ฌ์ฉ๋๋ ์ค๊ธ์ ํฌ๋ ์ดํธ์ ์ ๋๋ค. ์๋๋ฌผ์ ๋ฉ ์ค๋ ์น๋ฃ์๋ ๊ฒฝ๊ตฌ ํฌ์ฌ๊ฐ ๊ฐ๋ฅํ๊ณ ์ ๋ ์ฑ์ด ๋ฎ์ ์์๋จธ(DMSA)๊ฐ ์ ์ ๋ ์ ํธ๋๊ณ ์์ง๋ง, ๋๋๋ฌผ ๋ฐ ์กฐ๋ฅ์์๋ ์ฌ์ ํ ์ค์ํ ์ฃผ์ฌ์ฉ ํด๋ ์ ์ ๋๋ค. > **์ค์ํ ์์์ ์ฃผ์์ฌํญ:** ๋ฐ๋์ **์นผ์ ์ด๋ํธ๋ฅจ(Calcium Disodium)** ํํ์ EDTA๋ฅผ ์ฌ์ฉํด์ผ ํฉ๋๋ค. ์นผ์์ด ์๋ ์๋ฐํธ์ฐ ์ด๋ํธ๋ฅจ(Na2EDTA)์ ํฌ์ฌํ๋ฉด ํ์์ ๋ด์ธ์ฑ ํ์ฒญ ์นผ์์ ๊ฐ๋ ฅํ๊ฒ ํฌ๋ ์ดํธํ์ฌ ๋น ๋ฅด๊ณ ์น๋ช ์ ์ธ ์ ์นผ์ํ์ฆ์ ์ ๋ฐํ ์ ์์ต๋๋ค. CaEDTA๋ ์์ฉ์ฑ์ด ๋งค์ฐ ๋๊ณ ์ ์ฅ ๋ฐฐ์ค์ ํฌ๊ฒ ์์กดํ๋ฏ๋ก ์น๋ฃ ์ค ์ ์ ํ ์๋ถ ๊ณต๊ธ๊ณผ ์ ์ฅ ๊ธฐ๋ฅ ๋ชจ๋ํฐ๋ง์ด ํ์์ ์ ๋๋ค.
์์ฉ ๊ธฐ์ : CaEDTA works via **competitive chelation**. The calcium ion in the CaEDTA complex has a lower binding affinity than heavy metals. When introduced into the bloodstream, divalent or trivalent heavy metals (such as Pb2+ or Zn2+) displace the calcium: **CaEDTA + Pb2+ โ PbEDTA + Ca2+** The resulting heavy metal-EDTA complex is highly stable, water-soluble, and is rapidly excreted by the kidneys into the urine. * Theoretically, 1 gram of CaEDTA binds 620 mg of lead, but in vivo, only about 5 mg of lead is excreted per gram of drug. * It effectively chelates lead and zinc, and to a lesser extent cadmium, copper, iron, and manganese. * It is **ineffective** for mercury, gold, or arsenic poisoning.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Lead poisoning (Psittacines) ยท 35 mg/kg IM twice daily for 5-7 days. ยท IM ยท q12h ยท 5-7 days ยท After initial therapy, may give orally until all lead fragments are dissolved and/or passed from GI tract.
- Lead poisoning (Raptors/Falcons) ยท 100 mg/kg q12h for 5-25 consecutive days. (25% CaEDTA given undiluted IM) ยท IM ยท q12h ยท 5-25 days ยท Treated if blood lead was >65 micrograms/dL for 5 day courses, until blood lead was <20 micrograms/dL.
- Lead or zinc poisoning ยท 30-35 mg/kg IM q12h x 3-5 days, off 3-5 days, may repeat and/or use another chelator. ยท IM ยท q12h ยท 3-5 days ยท Maintain hydration. Do not give orally. Can be used IV short term (48 hrs) at 20-35 mg/kg diluted in saline.
- Lead poisoning ยท 75 mg/kg IV slowly in D5W or saline daily for 4-5 days (may divide daily dose into 2-3 administrations per day). ยท IV ยท q24h or divided q8-12h ยท 4-5 days ยท Stop therapy for 2 days and repeat for another 4-5 days. Give adequate supportive and nutritional therapy.
- Lead poisoning ยท 100 mg/kg SC divided into 4 daily doses in 5% dextrose for 5 days. May require second course of treatment, particularly if blood lead levels >0.10 ppm. Do not exceed 2 g/day and do not treat for more than 5 consecutive days. ยท SC ยท divided q6h ยท 5 days ยท Be sure there is no lead in GI tract before using.
- Lead poisoning ยท 25 mg/kg SC four times daily for 5 days. Give as 1% solution in D5W. ยท SC ยท q6h ยท 5 days ยท Provide a 5-7 day rest period between courses of treatment to minimize potential for nephrotoxicity.
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Patients with anuria
- Oral (PO) administration in the presence of lead in the GI tract (enhances absorption)
์ด์๋ฐ์
- Renal toxicity (renal tubular necrosis)
- Depression (dogs)
- Vomiting
- Diarrhea
- Zinc deficiency (with chronic therapy)
- Pain at IM injection site
์ฝ๋ฌผ ์ํธ์์ฉ
- Glucocorticoids ยท May enhance the renal toxicity of CaEDTA
- Insulin (NPH, PZI) ยท Concurrent administration will decrease the sustained action of the insulin preparation due to zinc chelation
- Nephrotoxic drugs (e.g., aminoglycosides, amphotericin B) ยท Increased risk of nephrotoxicity; use with extreme caution
๋ชจ๋ํฐ๋ง
- Blood lead or zinc levels (serial monitoring)
- Urine d-ALA
- Renal function tests (BUN, Creatinine)
- Urinalyses (monitor for casts/glucose indicating tubular damage)
- Hydration status
- Serum phosphorus and calcium values
- Periodic cardiac rate/rhythm monitoring
๊ณผ์ฉ๋
Doses greater than 12 g/kg are lethal in dogs. Acute toxicity primarily manifests as severe **renal tubular necrosis**. It can also cause profound depression, vomiting, and diarrhea. Treatment of overdose is largely supportive, focusing on maintaining diuresis and managing uremia.
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