Liver unit admission following paracetamol overdose with concentrations below current UK treatment thresholds

被引:31
作者
Beer, C.
Pakravan, N.
Hudson, M.
Smith, L. T.
Simpson, K.
Bateman, D. N.
Thomas, S. H. L. [1 ]
机构
[1] Univ Newcastle Upon Tyne, Sch Clin & Lab Sci, Wolfson Unit Clin Pharmacol, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Freeman Rd Hosp, Newcastle Upon Tyne Hosp NHS Trust, Liver Unit, Newcastle Upon Tyne NE7 7DN, Tyne & Wear, England
[3] Royal Infirm, Scottish Poisons Informat Bur, Edinburgh, Midlothian, Scotland
[4] Royal Infirm, Scottish Liver Transplant Unit, Edinburgh, Midlothian, Scotland
关键词
D O I
10.1093/qjmed/hcm003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: It has been suggested that current UK thresholds for treating paracetamol overdose should be reduced, following case reports of patients developing fatal liver failure after presenting with paracetamol concentrations below these thresholds. Aim: To determine the frequency of severe liver dysfunction following paracetamol overdose when paracetamol concentrations are below current UK antidote thresholds. Design: Retrospective case note review. Methods: Details were collected from all patients admitted to liver transplant units in Newcastle and Edinburgh with paracetamol-induced hepatotoxicity. Results: Of 696 patients admitted to the two liver units following paracetamol overdose, 14 presented between 4 and 15 h after overdose with paracetamol concentrations below current UK treatment thresholds (estimated annual population rate 0.15/million person-years). Over the period of study, > 100 000 presentations with paracetamol overdose would be expected in the catchment populations for these liver units. Discussion: In view of the rarity of this event, this research does not suggest a need to lower the current thresholds for antidotal treatment.
引用
收藏
页码:93 / 96
页数:4
相关论文
共 7 条
[1]   Lesson of the week - Deaths from low dose paracetamol poisoning [J].
Bridger, S ;
Henderson, K ;
Glucksman, E ;
Ellis, AJ ;
Henry, JA ;
Williams, R .
BRITISH MEDICAL JOURNAL, 1998, 316 (7146) :1724-1725
[2]   The Australasian clinical toxicology investigators collaboration randomized trial of different loading infusion rates of N-acetylcysteine [J].
Kerr, F ;
Dawson, A ;
Whyte, IM ;
Buckley, N ;
Murray, L ;
Graudins, A ;
Chan, B ;
Trudinger, B .
ANNALS OF EMERGENCY MEDICINE, 2005, 45 (04) :402-408
[3]   Impact of paracetamol pack size restrictions on poisoning from paracetamol in England and Wales: an observational study [J].
Morgan, O ;
Griffiths, C ;
Majeed, A .
JOURNAL OF PUBLIC HEALTH, 2005, 27 (01) :19-24
[4]   Restricting paracetamol in the United Kingdom to reduce poisoning: a systematic review [J].
Morgan, O ;
Majeed, A .
JOURNAL OF PUBLIC HEALTH, 2005, 27 (01) :12-18
[5]   INTRAVENOUS N-ACETYLCYSTEINE - TREATMENT OF CHOICE FOR PARACETAMOL POISONING [J].
PRESCOTT, LF ;
ILLINGWORTH, RN ;
CRITCHLEY, JAJH ;
STEWART, MJ ;
ADAM, RD ;
PROUDFOOT, AT .
BRITISH MEDICAL JOURNAL, 1979, 2 (6198) :1097-1100
[6]   Risk factors in the development of adverse reactions to N-acetylcysteine in patients with paracetamol poisoning [J].
Schmidt, LE ;
Dalhoff, K .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 51 (01) :87-91
[7]   Paracetamol poisoning in the North East of England: presentation, early management and outcome [J].
Thomas, SHL ;
Horner, JE ;
Chew, K ;
Connolly, J ;
Dorani, B ;
Bevan, L ;
Bhattacharyya, S ;
Bramble, MG ;
Han, KH ;
Rodgers, A ;
Sen, B ;
Tesfayohannes, B ;
Wynne, H ;
Bateman, DN .
HUMAN & EXPERIMENTAL TOXICOLOGY, 1997, 16 (09) :495-500