Tariq Azamgarhi1, Ashik Shah1, Simon Warren2. 1. Pharmacy Department, Royal National Orthopaedic Hospital NHS Trust, Brockley Hill, Stanmore, HA7 4LP, United Kingdom. 2. Bone Infection Unit, Royal National Orthopaedic Hospital NHS Trust, Brockley Hill, Stanmore, HA7 4LP, United Kingdom.
Abstract
AIMS: The aim of this paper is to determine the rate of true anaphylaxis to teicoplanin. METHODS: A case-series including all suspected anaphylactic reactions attributed to teicoplanin anaphylaxis within a single institution over a 29-month period were categorised according to the probability of true IgE-mediated anaphylaxis using previously published criteria. The number of patients who received teicoplanin was determined and used to calculate the rate of IgE-mediated anaphylaxis. RESULTS: Approximately 18 800-19 600 patients received teicoplanin during the study period, during which there were 14 cases of suspected anaphylaxis attributed to the administration of teicoplanin: five were categorised as definite IgE-mediated anaphylaxis, four as probable, two as uncertain and three were excluded. Of the excluded cases, two were found to have positive intradermal skin testing to alternative agents (rocuronium and chlorhexidine), and one did not meet the published clinical criteria. We therefore calculated the rate of IgE-mediated anaphylaxis to be between 0.046% and 0.059% (equating to between 1:2088 and 1:1655). CONCLUSIONS: This is the first study to calculate a rate of IgE-mediated anaphylaxis to teicoplanin in clinical practice. Our case series suggests that these life-threatening reactions occur less commonly than reported by the manufacturers. Mast cell tryptase is unreliable when used to predict the likelihood of IgE-mediated anaphylaxis to teicoplanin.
AIMS: The aim of this paper is to determine the rate of true anaphylaxis to teicoplanin. METHODS: A case-series including all suspected anaphylactic reactions attributed to teicoplanin anaphylaxis within a single institution over a 29-month period were categorised according to the probability of true IgE-mediated anaphylaxis using previously published criteria. The number of patients who received teicoplanin was determined and used to calculate the rate of IgE-mediated anaphylaxis. RESULTS: Approximately 18 800-19 600 patients received teicoplanin during the study period, during which there were 14 cases of suspected anaphylaxis attributed to the administration of teicoplanin: five were categorised as definite IgE-mediated anaphylaxis, four as probable, two as uncertain and three were excluded. Of the excluded cases, two were found to have positive intradermal skin testing to alternative agents (rocuronium and chlorhexidine), and one did not meet the published clinical criteria. We therefore calculated the rate of IgE-mediated anaphylaxis to be between 0.046% and 0.059% (equating to between 1:2088 and 1:1655). CONCLUSIONS: This is the first study to calculate a rate of IgE-mediated anaphylaxis to teicoplanin in clinical practice. Our case series suggests that these life-threatening reactions occur less commonly than reported by the manufacturers. Mast cell tryptase is unreliable when used to predict the likelihood of IgE-mediated anaphylaxis to teicoplanin.
Authors: Christopher Southan; Joanna L Sharman; Helen E Benson; Elena Faccenda; Adam J Pawson; Stephen P H Alexander; O Peter Buneman; Anthony P Davenport; John C McGrath; John A Peters; Michael Spedding; William A Catterall; Doriano Fabbro; Jamie A Davies Journal: Nucleic Acids Res Date: 2015-10-12 Impact factor: 16.971
Authors: Paul James Antony Sice; Sarah Ford; Andrew Francis Whyte; James Robertson Greig Journal: Br J Clin Pharmacol Date: 2018-11-12 Impact factor: 4.335