Random and systematic medication errors in routine clinical practice: a multicentre study of infusions, using acetylcysteine as an example

被引:76
作者
Ferner, RE [1 ]
Langford, NJ
Anton, C
Hutchings, A
Bateman, DN
Routledge, PA
机构
[1] City Hosp, W Midlands Ctr Adverse Drug React Reporting, Birmingham B18 7QH, W Midlands, England
[2] Cardiff Univ, Llandough Hosp, Coll Med, Therapeut & Toxicol Ctr, Cardiff CF64 2XX, S Glam, Wales
[3] Royal Infirm, Scottish Poisons Informat Bur, Edinburgh EH3 9YW, Midlothian, Scotland
关键词
acetaminophen (paracetamol); acetylcysteine; infusions; intravenous; medication errors; quality control;
D O I
10.1046/j.0306-5251.2001.01490.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims The nature and incidence of errors in prescribing and giving medicines have previously been estimated by trained observers, or by retrospective analysis of incidents in which patients have come to harm. We have examined prospectively in routine clinical practice the concentrations of intravenous infusions of a drug (acetylcysteine) which is given according to a complicated dosing schedule. Methods We prospectively collected samples before and, where possible, after the infusion of acetylcysteine in 66 anonymous patients requiring treatment for acetaminophen (paracetamol) overdose in four centres in the United Kingdom. We measured the concentration in each infusion bag, and deduced from the weight of the patient the percentage of the anticipated dose that had actually been given. Results The experimentally determined dose was within 10% of the anticipated dose in 68 of 184 individual bags (37%), and within 20% of the anticipated dose in 112 bags (61%). Doses in 17 bags were more than 50% from the anticipated doses. In three patients, values in all three bags appeared to be systematically wrong by 50% or more; in a further seven cases, individual bags differed by 50% or more from the anticipated value. The median difference between pre- and post-infusion samples was 0% [interquartile range -5.2% to +14.6%], but 9% showed a disparity of greater than +/- 50%. Conclusions Our data suggest that there is large random variation in administered dosage of intravenous infusions. Systematic calculation errors occur ill about 5% [95% confidence interval 2, 8%] of cases, and major errors in drawing up in a further 3% [1, 7%], with inadequate mixing in 9% [4, 14%]. While we have no evidence that patients were adversely affected, and while the regime of administration of the drug studied (acetylcysteine) is complicated, these data suggest that the delivered dose often deviates from the intended dose, and that methods of quality control are needed.
引用
收藏
页码:573 / 577
页数:5
相关论文
共 13 条
  • [1] [Anonymous], 1988, STAT QUALITY CONTROL
  • [2] [Anonymous], ERR IS HUMAN BUILDIN
  • [3] Effect of computerized physician order entry and a team intervention on prevention of serious medication errors
    Bates, DW
    Leape, LL
    Cullen, DJ
    Laird, N
    Petersen, LA
    Teich, JM
    Burdick, E
    Hickey, M
    Kleefield, S
    Shea, B
    Vander Vliet, M
    Seger, DL
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (15): : 1311 - 1316
  • [4] COHEN MR, 1999, MED ERRORS
  • [5] DeVor R. E., 1992, STAT QUALITY DESIGN
  • [6] A REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ASSAY FOR THE DETERMINATION OF N-ACETYLCYSTEINE IN AQUEOUS FORMULATIONS
    FARQUHAR, J
    FINLAY, G
    FORD, PA
    MARTINSMITH, M
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1985, 3 (03) : 279 - 285
  • [7] Ferner RE, 1999, BRIT J CLIN PHARMACO, V47, P581
  • [8] FERNER RE, 1999, SIDE EFFECTS DRUGS A, pR23
  • [9] RECENT DEVELOPMENTS IN THE MANAGEMENT OF PARACETAMOL (ACETAMINOPHEN) POISONING
    JANES, J
    ROUTLEDGE, PA
    [J]. DRUG SAFETY, 1992, 7 (03) : 170 - 177
  • [10] KIRWAN B, 1994, GUIDE PRACTICAL HUMA, P379