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Intravenous N-acetylcystine: the treatment of choice for paracetamol poisoning.

BMJ · 1979 · Vol. 2(6198) · pp. 1097–1100
L. F. PrescottR. N. IllingworthJulia CritchleyM J StewartR D AdamA. T. Proudfoot

Abstract

One hundred cases of severe paracetamol poisoning were treated with intravenous N-acetylcysteine (acetyl-cysteine). There was virtually complete protection against liver damage in 40 patients treated within eight hours after ingestion (mean maximum serum alanine transaminase activity 27 IU/1). Only one out of 62 patients treated within 10 hours developed severe liver damage compared with 33 out of 57 patients (58%) studied retrospectively who received supportive treatment alone. Early treatment and acetylcysteine also prevented renal impairment and death. The critical ingestion-treatment interval for complete protection against severe liver damage was eight hours. Efficacy diminished progressively thereafter, and treatment after 15 hours was completely ineffective. Intravenous acetylcysteine was more effective than cysteamine and methionine and noticeably free of adverse effects. It is the treatment of choice for paracetamol poisoning.

Drug-Induced Hepatotoxicity and ProtectionMetabolism and Genetic DisordersPoisoning and overdose treatmentsMedicineAcetylcysteineIngestionCysteamineAntidoteAcetaminophenAdverse effectAnesthesiaAlanine transaminaseTransaminase

MeSH terms

AcetaminophenAcetylcysteineAdolescentAdultAgedCysteamineFemaleHumansInfusions, ParenteralKidney DiseasesLiver DiseasesMaleMethionineMiddle AgedRisk
Citations
662
FWCI
12.13
field-weighted impact
References
2
Percentile
99%
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Cited by
Kinetics and metabolism of paracetamol and phenacetin.
British Journal of Clinical Pharmacology · 1980 · 450 citations
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Intravenous N-acetylcystine: the treatment of choice for paracetamol poisoning. · Scinovex