Comparison of medication error rates and clinical effects in three medication prescription‐dispensation systems
Author:
Belén Jiménez Muñoz Ana,Muiño Miguez Antonio,Paz Rodriguez Pérez María,Esther Durán Garcia María,Sanjurjo Saez María
Abstract
PurposeMedication errors (MEs) are important in terms of their magnitude and severity, and there are numerous systems in place to reduce their occurrence. However, the ideal system has not yet been identified. The authors' institution uses three different medication prescription‐dispensation systems which operate simultaneously. ME rates were compared, overall and by phase (prescription, transcription and administration) and their overall and specific clinical impact.Design/methodology/approachThe administration of medicinal products was observed directly and compared with medical and nursing prescriptions. Errors and adverse events were classified by a consensus of experts.FindingsIn the traditional system the error prevalence rate was 13.59 per cent, (99 per cent CI, 12.15‐14.61 per cent), in the single dose system it was 6.43 per cent (99 per cent CI, 5.53‐7.32) and in the electronic prescription system it was 8.86 per cent (99 per cent CI, 7.33‐10.17). The highest error rates in all phases were found in the traditional system. The phase affected by most errors in all three models was transcription, and the least affected was administration, except for the single dose system, in which prescription was the worst. The effects of errors in the administration phase are greater, although less so than with the automated system.Research limitations/implicationsThe dispensation phase was not analyzed.Practical implicationsA study of errors will enable us to reduce their occurrence if we know the most frequent types and in which phase they are produced, we will be able to prioritise the areas in which to work and select the necessary preventive measures.Originality/valueIt is possible that automated medication dispensation systems reduce error rates and the severity of their effects.
Subject
Health Policy,General Business, Management and Accounting
Reference31 articles.
1. AJHP (1995), “Understanding and preventing drug misadventures. Introduction”, American Journal of Health‐System Pharmacy, Vol. 52 No. 11, p. 373. 2. Baker, G.R., Norton, P.G., Flintoft, V., Blais, R., Brown, A., Cox, J., Etchells, E., Ghali, W.A., Hébert, P., Majumdar, S.R., O'Beirne, M., Palacios‐Derglingher, L., Reid, R.J., Sheps, S. and Tamblyn, R. (2004), “The Canadian adverse events study: the incidence of adverse events among hospital patients in Canada”, Canadian Medical Association Journal, Vol. 170 No. 11, pp. 1678‐86. 3. Barker, K.N., Flynn, E.A., Pepper, G.A., Bates, D.W. and Mikeal, R.L. (2002), “Medication errors observed in 36 health care facilities”, Archives of Internal Medicine, Vol. 162 No. 16, pp. 1897‐903. 4. Bates, D.W. (2005), “Preventing medication errors: a summary”, Drug Safety, Vol. 28 No. 12, pp. 1119‐29. 5. Bobb, A., Gleason, K., Husch, M., Feinglass, J., Yarnold, P.R. and Noskin, G.A. (2004), “The epidemiology of prescribing errors”, Archives of Internal Medicine, Vol. 164 No. 7, pp. 785‐92.
Cited by
11 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|