SAEVA Proceedings 2016 | Page 151

  T - Types of drug and bacteria Select appropriate drugs based on empirical use guidelines Use cytology where possible Consider the dose and pharmacokinetics of the drugs selected Avoid empirical use of the highest priority critically important antimicrobials E - Employ narrow spectrum drugs wherever possible e.g. penicillin, rather than drug combinations. C - Culture and sensitivity Use bacterial culture promptly, especially when clinical response to empirical use is less than expected or when long term therapy is likely to be required T - Treat effectively Using enough drug for long enough then stop Standardize dosing frequency and dose rates across the practice, acknowledging that sometimes dosing intervals licenced in the marketing authorisation differ from current clinical evidence. As such it is important to review the veterinary literature to determine optimal dosing here. M - Monitor antimicrobial use, compliance and resistance Undertake a clinical audit of antimicrobial use within your practice Formulate a policy to record the use of ‘protected’ antimicrobials in your practice Formulate a policy to review antimicrobial susceptibility from any cultures obtained within the practice Audit emerging antimicrobial resistance and consider adapting guidelines for empirical use. E - Educate Inform your team and your clients Ensure that protocols and changes to protocols are cascaded through the entire team Educate your clients to reduce pressure for antimicrobial prescribing The important underlying principle of this protocol was that it should be established at a local practice level (or even within practices). Even the categorisation of antibiotics as ‘PROTECTED or ‘AVOIDED should be established locally, although the WHO highest priority antimicrobials were recommended as being classed as protected, while those in category 3 of the EMA guidance as ‘AVOIDED’. Experiences of PROTECT ME The release of these protocols has been widely adopted by practices in the UK, with over 66% of UK practices having adopted protocols based on the principles of this policy (BEVA membership survey 2013). An audit of use in one clinical setting demonstrated that use of quinolones fell by 97% after the adoption of persuasive policies for antimicrobial use using the PROTECT ME documents (unpublished data). A recent international survey of antibiotic use in equine practice (n=164) showed that, of those who had adopted antibiotics use protocols, 78% had adopted the PROTECT ME templates. These documents are available freely through a Creative Commons Licence at beva.org.uk/protectme. Of the category 3 (EMA) or AVOIDED (BEVA) antibiotics, the carbepenems are currently the most relevant to equine practice. The importance of the carbepenems to human health relates to their use in the treatment of Enterobacteriaceae. While the pharmacokinetics of imepenem has been established in the horse18, the use in equine practice is currently uncommon. The survey of antibiotic usage described above identified that imepenem has been used in 9.4% of responding clinics, with 15-­‐18  February  2016      East  London  Convention  Centre,  East  London,  South  Africa     150