๋ํธ๋กํธ๋ํ ์ธ
**๋ํธ๋กํธ๋ํ ์ธ (Nitrofurantoin)**์ ์ฃผ๋ก **์๋ก ๋ฐฉ๋ถ์ /ํญ๊ท ์ **๋ก ์ฌ์ฉ๋๋ ํฉ์ฑ ๋ํธ๋กํธ๋๊ณ ํญ๊ท ์ ์ ๋๋ค. * **๋ถ์ ํน์ด์ ํจ๋ฅ**: ์๋ณ์ผ๋ก ๋น ๋ฅด๊ฒ ๋ฐฐ์ค๋๊ธฐ ๋๋ฌธ์ ํ๋ถ ์๋ก์์๋ ๋์ ๋๋์ ๋๋ฌํ์ง๋ง, ์ ์ ํ๋ฅ๋ ์กฐ์ง์์๋ ์น๋ฃ ๋๋์ ๋๋ฌํ์ง *์์ต๋๋ค*. ๋ฐ๋ผ์ **ํ๋ถ ์๋ก ๊ฐ์ผ(UTI)**์๋ ๋งค์ฐ ํจ๊ณผ์ ์ด์ง๋ง ์ ์ ๊ฐ์ผ, ์ ์ฐ์ ์ผ(์ ์ฅ ๊ฐ์ผ) ๋๋ ์ ์ฃผ์ ๋์์๋ **ํจ๊ณผ๊ฐ ์์ต๋๋ค**. * **ํญ๊ท ์คํํธ๋ผ**: ๋์ฅ๊ท (*E. coli*), ํด๋ ๋ธ์์๋ผ(*Klebsiella*), ํฌ๋์๊ตฌ๊ท (*Staphylococcus*), ์ฅ๊ตฌ๊ท (*Enterococcus*)์ ํฌํจํ ๋ง์ ๊ทธ๋ ์์ฑ๊ท ๋ฐ ๊ทธ๋ ์์ฑ๊ท ์ ํ์ฑ์ ๋ํ๋ ๋๋ค. ์๋๋ชจ๋์ค(*Pseudomonas* spp.) ๋ฐ ๋๋ถ๋ถ์ ํ๋กํ ์ฐ์ค(*Proteus*) ๊ท ์ฃผ์๋ ํจ๊ณผ๊ฐ ์๋ค๋ ์ ์ ์ ์ํด์ผ ํฉ๋๋ค. * **์์์ ์์ **: 1์ฐจ ํญ์์ ์ ๋ํ ๋ด์ฑ์ด ์ฆ๊ฐํจ์ ๋ฐ๋ผ, ๋ํธ๋กํธ๋ํ ์ธ์ ํนํ ๋ด์ฑ ๋์ฅ๊ท ์ด๋ ์ฅ๊ตฌ๊ท ์ ์ํด ๋ฐ์ํ๋ ๋ค์ ๋ด์ฑ ํ๋ถ ์๋ก ๊ฐ์ผ์ ์ํด ๋ณด๋ฅ๋๋ ๊ฒฝ์ฐ๊ฐ ๋ง์ต๋๋ค.
์์ฉ ๊ธฐ์ : Nitrofurantoin can be bacteriostatic or bactericidal depending on the concentration and organism susceptibility. * **Mechanism**: Inside the bacterial cell, nitrofurantoin is reduced by bacterial **flavoproteins** to highly reactive intermediate compounds. * **Pathway**: Reactive intermediates โ attack bacterial **ribosomal proteins** and other macromolecules โ inhibit protein synthesis, aerobic energy metabolism (specifically **acetyl coenzyme A**), DNA synthesis, RNA synthesis, and cell wall synthesis. * **Environmental Factor**: It exhibits significantly greater antibacterial activity in **acidic environments**.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Susceptible bacterial urinary tract infections ยท 5 mg/kg ยท PO ยท q8h
- Recurrent UTI (Conventional dose) ยท 4 mg/kg ยท PO ยท q8h
- Recurrent UTI (Prophylactic dose) ยท 3-4 mg/kg ยท PO ยท q24h ยท Should be given at night after micturition and immediately before bedtime.
- Susceptible bacterial urinary tract infections ยท 4 mg/kg ยท PO ยท q6-8h
- Urinary tract infections (lower UTI only) ยท 4.4-5 mg/kg ยท PO ยท q8h ยท As directed by culture and sensitivity ยท For urinary tract infections only. Not for pyelonephritis.
- Susceptible urinary tract infections ยท 2.5-4.5 mg/kg ยท PO ยท q8h ยท Listed as three times daily.
- Susceptible urinary tract infections ยท 10 mg/kg ยท PO ยท q24h ยท Listed as daily.
- Prevention of re-infections with gram-negative organisms ยท 4 mg/kg ยท PO ยท q24h ยท Long-term ยท Give once a day immediately before bedtime after the dog has urinated. Only use after extensive search for underlying cause and after effective treatment of existing UTI.
- Recurrent UTI (Conventional dose) ยท 4 mg/kg ยท PO ยท q8h
- Recurrent UTI (Prophylactic dose) ยท 3-4 mg/kg ยท PO ยท q24h ยท Should be given at night after micturition and immediately before bedtime.
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Renal impairment (decreased efficacy and increased risk of systemic toxicity)
- Known hypersensitivity to nitrofurantoin
- Pregnant patients at term (risk of hemolytic anemia in neonates)
- Neonates
- Rats (high risk of neurotoxicity)
- Significant renal impairment (decreased excretion leads to toxic serum levels)
- Pregnancy (mutagenic properties)
- Pyelonephritis
- Systemic infections outside the urinary tract
- Food-producing animals
์ด์๋ฐ์
- Gastrointestinal disturbances (vomiting, nausea, diarrhea)
- Hepatopathy (can be severe or chronic)
- Myasthenic-like effects (rare, reversible in dogs)
- Infertility in male dogs
- Peripheral neuropathy (rare)
- Hemolytic anemia (rare)
- Pneumonitis (rare)
- Emesis
- Diarrhoea
- Gastrointestinal bleeding
- Hepatotoxicity
- Peripheral neuritis (rare)
- Pulmonary complications (rare)
- Thrombocytopenia (at high doses)
- Anaemia (at high doses)
- Leucopenia (at high doses)
์ฝ๋ฌผ ์ํธ์์ฉ
- Fluoroquinolones (e.g., enrofloxacin, ciprofloxacin) ยท Nitrofurantoin may antagonize the antimicrobial activity of fluoroquinolones; concomitant use should be avoided.
- Food or Anticholinergic drugs ยท May increase the oral bioavailability and absorption of nitrofurantoin.
- Magnesium trisilicate containing antacids ยท May inhibit the oral absorption of nitrofurantoin.
- Probenecid ยท May inhibit the renal excretion of nitrofurantoin, potentially increasing systemic toxicity and reducing its effectiveness in the urinary tract.
- Antimuscarinic drugs ยท Delays gastric emptying time and increases absorption/bioavailability of nitrofurantoin ยท moderate
- Food ยท Delays gastric emptying time and increases absorption/bioavailability of nitrofurantoin ยท minor
- Fluoroquinolones ยท Antagonism of antibacterial efficacy ยท major
- Spironolactone ยท May increase the hyperkalaemic effects of spironolactone ยท moderate
- Urine alkalinizing agents ยท Significantly decreases the antibacterial activity of nitrofurantoin ยท major
๋ชจ๋ํฐ๋ง
- Clinical efficacy (resolution of UTI symptoms, negative urine cultures)
- Adverse effects (especially GI upset)
- Periodic liver function tests (especially with chronic/prophylactic therapy)
- Resolution of clinical signs of UTI
- Urine culture and sensitivity
- Renal function (BUN, Creatinine)
- Complete Blood Count (CBC) if used long-term or at high doses
- Liver enzymes
๊ณผ์ฉ๋
Because the drug is rapidly absorbed and excreted, patients with normal renal function usually require little therapy for mild overdoses. * **Massive Overdose**: If ingestion was recent, empty the gut using standard protocols (emesis/gastric lavage). * **Monitoring**: Monitor closely for gastrointestinal distress, hepatotoxicity, and neurologic signs. Provide supportive care as needed.
VetSheet ์ฝ๋ฌผ ๋ ํผ๋ฐ์ค๋ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์์ฌ๊ฒฐ์ ๋ณด์กฐ ๋๊ตฌ์ด๋ฉฐ, ์ ๋ฌธ์ ํ๋จ์ด๋ ์ ์กฐ์ฌ์ ์ต์ ๋ผ๋ฒจ์ ๋์ ํ์ง ์์ต๋๋ค.