Restriction of oxycodone in the emergency department (ROXY-ED): A randomised controlled trial

Author:

Mitra Biswadev12ORCID,Roman Cristina134ORCID,Wu Bertha1,Luckhoff Carl1,Goubrial Diana134,Amos Timothy1,Bannon-Murphy Holly1,Huynh Ronald1,Dooley Michael34,Smit De Villiers12,Cameron Peter A.12

Affiliation:

1. Emergency & Trauma Centre, The Alfred Hospital, Melbourne, VIC, Australia

2. School of Public Health & Preventive Medicine, Monash University, Melbourne, VIC, Australia

3. Pharmacy Department, Alfred Health, Melbourne, VIC, Australia

4. Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Melbourne, VIC, Australia

Abstract

Background The prescription of opioids in emergency care has been associated with harm, including overdose and dependence. The aim of this trial was to assess restriction of access to oxycodone (ROXY), in combination with education and guideline modifications, versus education and guideline modifications alone (standard care) to reduce oxycodone administration in the Emergency Department (ED). Methods An unblinded, active control, randomised controlled trial was conducted in an adult tertiary ED. Participants were patients aged 18–75 years who had analgesics administered in the ED. The primary intervention was ROXY, through removal of all oxycodone immediate release tablets from the ED imprest, with availability of a small supply after senior clinician approval. The intervention did not restrict prescription of discharge medications. The primary outcome measure was oxycodone administration rates. Secondary outcomes were administration rates of other analgesic medications, time to initial analgesics and oxycodone prescription on discharge. Results There were 2258 patients eligible for analysis. Oxycodone was administered to 80 (6.1%) patients in the ROXY group and 221 (23.3%) patients in the standard care group (relative risk (RR) 0.26; 95% CI: 0.21 to 0.33; p < .001). Tapentadol was prescribed more frequently in the ROXY group (RR 2.17; 95% CI: 1.71–2.74), while there were no differences in prescription of other analgesic medications. On discharge, significantly fewer patients were prescribed oxycodone (RR 0.51; 95% CI: 0.39–0.66) and no differences were observed in prescription rates of other analgesic medications. There was no difference in time to first analgesic (HR 0.94; 95% CI: 0.86–1.02). Conclusions Restricted access to oxycodone was superior to education and guideline modifications alone for reducing oxycodone use in the ED and reducing discharge prescriptions of oxycodone from the ED. The addition of simple restrictive interventions is recommended to enable rapid changes to clinician behaviour to reduce the potential harm associated with the prescribing of oxycodone in the ED.

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine

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