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BNF for Children 2011-2012

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296 5.1.11 Metronidazole <strong>BNF</strong>C <strong>2011</strong>–<strong>2012</strong>5 InfectionsMetronidazole is well absorbed orally and the intravenousroute is normally reserved <strong>for</strong> severe infections.Metronidazole by the rectal route is an effective alternativeto the intravenous route when oral administrationis not possible. Intravenous metronidazole is used <strong>for</strong>the treatment of established cases of tetanus; diazepam(section 10.2.2) and tetanus immunoglobulin (section14.5.2) are also used.Topical metronidazole (section 13.10.1.2) reduces theodour produced by anaerobic bacteria in fungatingtumours; it is also used in the management of rosacea(section 13.6).Oral infections Metronidazole is an alternative to apenicillin <strong>for</strong> the treatment of many oral infectionswhere the patient is allergic to penicillin or the infectionis due to beta-lactamase-producing anaerobes (Table 1,section 5.1). It is the drug of first choice <strong>for</strong> the treatmentof acute necrotising ulcerative gingivitis (Vincent’sinfection) and pericoronitis; suitable alternatives areamoxicillin (section 5.1.1.3) and erythromycin (section5.1.5). For these purposes treatment with metronidazole<strong>for</strong> 3 days is sufficient, but the duration of treatmentmay need to be longer in pericoronitis. Tinidazole islicensed <strong>for</strong> the treatment of acute ulcerative gingivitis.METRONIDAZOLECautions disulfiram-like reaction with alcohol, clinicaland laboratory monitoring advised if treatmentexceeds 10 days; interactions: Appendix 1 (metronidazole)Hepatic impairment in severe liver disease reducetotal daily dose to one-third, and give once daily; usewith caution in hepatic encephalopathyPregnancy manufacturer advises avoidance of highdoseregimens; use only if potential benefit outweighsriskBreast-feeding significant amount in milk; manufactureradvises avoid large single doses though otherwisecompatible; may give milk a bitter tasteSide-effects gastro-intestinal disturbances (includingnausea and vomiting), taste disturbances, furred tongue,oral mucositis, anorexia; very rarely hepatitis,jaundice, pancreatitis, drowsiness, dizziness, headache,ataxia, psychotic disorders, darkening of urine,thrombocytopenia, pancytopenia, myalgia, arthralgia,visual disturbances, rash, pruritus, and erythemamulti<strong>for</strong>me; on prolonged or intensive therapy peripheralneuropathy, transient epilepti<strong>for</strong>m seizures,and leucopeniaIndication and doseProtozoal infections section 5.4.2Anaerobic infections (usually treated <strong>for</strong> 7 daysand <strong>for</strong> 10–14 days in Clostridium difficileinfection). By mouthChild 1–2 months 7.5 mg/kg every 12 hoursChild 2 months–12 years 7.5 mg/kg (max.400 mg) every 8 hoursChild 12–18 years 400 mg every 8 hours. By rectumChild 1 month–1 year 125 mg 3 times daily <strong>for</strong> 3days, then twice daily thereafterChild 1–5 years 250 mg 3 times daily <strong>for</strong> 3 days,then twice daily thereafterChild 5–10 years 500 mg 3 times daily, <strong>for</strong> 3 days,then twice daily thereafterChild 10–18 years 1 g 3 times daily <strong>for</strong> 3 days,then twice daily thereafter. By intravenous infusion over 20–30 minutesNeonate 7.5 mg/kg every 12 hoursChild 1–2 months 7.5 mg/kg every 12 hoursChild 2 months–18 years 7.5 mg/kg (max.500 mg) every 8 hoursPelvic inflammatory disease (see also Table 1,section 5.1). By mouthChild 12–18 years 400 mg twice daily <strong>for</strong> 14 daysAcute ulcerative gingivitis and other acutedental infections. By mouthChild 1–3 years 50 mg every 8 hoursChild 3–7 years 100 mg every 12 hoursChild 7–10 years 100 mg every 8 hoursChild 10–18 years 200–250 mg every 8 hoursHelicobacter pylori eradication section 1.3Surgical prophylaxis. By mouthChild 1 month–12 years 30 mg/kg (max. 500 mg)2 hours be<strong>for</strong>e the procedureChild 12–18 years 400–500 mg 2 hours be<strong>for</strong>ethe procedure; up to 3 further doses of 400–500 mgmay be given every 8 hours <strong>for</strong> high-risk procedures. By intravenous infusionNeonate under 40 weeks postmenstrual age10 mg/kg up to 30 minutes be<strong>for</strong>e the procedureNeonate over 40 weeks postmenstrual age 20–30 mg/kg up to 30 minutes be<strong>for</strong>e the procedureChild 1 month–12 years 30 mg/kg (max. 500 mg)up to 30 minutes be<strong>for</strong>e the procedureChild 12–18 years 500 mg up to 30 minutesbe<strong>for</strong>e the procedure; up to 3 further doses of500 mg may be given every 8 hours <strong>for</strong> high-riskprocedures. By rectumChild 5–10 years 500 mg 2 hours be<strong>for</strong>e surgery;up to 3 further doses of 500 mg may be given every8 hours <strong>for</strong> high-risk proceduresChild 10–18 years 1 g 2 hours be<strong>for</strong>e surgery; upto 3 further doses of 1 g may be given every 8hours <strong>for</strong> high-risk procedures

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