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Eur J Hosp Pharm 20:100-105 doi:10.1136/ejhpharm-2012-000222
  • Research
  • Original article

Development of a standardised method to recommend protective measures to handle hazardous drugs in hospitals

  1. Pascal Bonnabry1,2
  1. 1Department of Pharmacy, University Hospitals of Geneva, Geneva, Switzerland
  2. 2School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, Geneva, Switzerland
  3. 3Department of Occupational Medicine, University Hospitals of Geneva, Geneva, Switzerland
  4. 4Service of Clinical Pharmacology and Toxicology, University Hospitals of Geneva, Geneva, Switzerland
  1. Correspondence to Laure-Zoé Kaestli, Department of Pharmacy, University Hospitals of Geneva, Rue Gabrielle-Perret-Gentil 4, CH-1211 Geneva 14, Switzerland; laure.z.kaestli{at}hcuge.ch
  • Received 10 September 2012
  • Revised 8 November 2012
  • Accepted 14 November 2012
  • Published Online First 12 December 2012

Abstract

Purpose Healthcare professionals frequently have to handle hazardous drugs in the hospital setting. Data on the inherent toxicity of drugs cannot be directly applied to occupational exposure. We developed a standardised method to evaluate occupational risks and to recommend protective measures.

Methods Step 1: evaluation of chronic and acute toxicities and toxicity for reproduction. Step 2: toxicity weighting according to risk of exposure related to drug formulations. Step 3: definition of protective measures. Step 4: toxicity assessment of drugs used in our institution and comparison with hazardous drug lists published in the literature.

Results The whole process resulted in a standardised evaluation algorithm. Risks of exposure were determined by a panel of experts to balance intrinsic toxicity of each drug formulation or administration route. Protective measures were recommended. 80 substances (109 drug formulations) were screened for toxicity. Centralisation of compounding in the pharmacy was recommended for 12/24 (50%) of intravenous liquids, 19/32 (60%) of intravenous powders and 7/26 (27%) tablets (crushing). We found a slightly different estimation of risk for only two products (prednisone and mycophenolate mofetil) compared with the literature lists (National Institute for Occupational and Safety in Health Alert and University Health System Consortium Consensus).

Conclusions We developed a simple standardised method to generate a list of hazardous drugs in our hospital according to the risk of exposure. We determined reasonable protective measures that could be easily introduced into practice to protect healthcare workers.

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