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Qual Saf Health Care doi:10.1136/qshc.2008.029785
  • Error management

Where errors occur in the preparation and administration of intravenous medicines: a systematic review and Bayesian analysis

  1. Sarah E McDowell1,
  2. Shahrul Mt-Isa2,
  3. Deborah Ashby2,
  4. R E Ferner1
  1. 1West Midlands Centre for Adverse Drug Reactions, City Hospital, Birmingham, UK
  2. 2Wolfson Institute of Preventive Medicine, Queen Mary, University of London, London, UK
  1. Correspondence to Professor RE Ferner, West Midlands Centre for Adverse Drug Reactions, City Hospital, Birmingham B18 7QH, UK; r.e.ferner{at}bham.ac.uk
  1. Contributors SEM carried out the literature searches, extracted data and contributed to the writing of the paper. SM-I designed and performed the statistical analyses, and contributed to the writing of the paper. DA advised on study design and statistical analyses, and contributed to the writing of the paper. REF had the idea for the study, contributed to the writing of the paper and will act as a guarantor for this paper.

  • Accepted 7 May 2009
  • Published Online First 11 January 2010

Abstract

Objective To investigate the overall probability of error in preparing and administering intravenous medicines; to identify at which stage of the process an error is most likely to occur; and to determine the impact of error correction on the error probability.

Design Systematic review and random-effects Bayesian conditional independence modelling.

Methods Medline and EMBASE were searched for studies on intravenous medicines. The error rates of each stage were extracted. These, expert estimates, and error rates from generic tasks, were used in a Bayesian conditional independence model to find error ‘hot-spots.’ The main outcome measure was the probability of at least one error occurring during intravenous therapy.

Results Nine published studies were identified for inclusion in the systematic review and meta-analysis. The overall probability of making at least one error in intravenous therapy was 0.73 (95% credible interval (CrI) 0.54 to 0.90). If error-checking was introduced at each stage of the process, the overall rate fell to 0.22 (95% CrI 0.14 to 0.31). Errors were most likely in the reconstitution step. Removing the reconstitution step by providing preprepared injections would reduce the overall error rate to 0.17 (95% CrI 0.09 to 0.27).

Conclusions Intravenous therapy is complex and error-prone. Error-checking at each stage could reduce the error probability. The use of preprepared injections may help by eliminating errors in the reconstitution of drug and diluent. However, it will be important to ensure that benefits are not outweighed by practical disadvantages such as an increase in selection errors.

Footnotes

  • Funding SEM was supported by the Antidote Trust Fund of Sandwell and West Birmingham Hospitals NHS Trust.

  • Competing interests None.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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