Take-home naloxone administered in emergency settings: feasibility of intervention implementation in a cluster randomized trial
Discuss this preprint
Start a discussion What are Sciety discussions?Listed in
This article is not in any list yet, why not save it to one of your lists.Abstract
Background
Opioids kill more people than any other class of drug. Naloxone is an opioid antagonist which can be distributed in kits for peer administration. We assessed the feasibility of implementing a Take-home Naloxone (THN) intervention in emergency settings, as part of designing a definitive randomised controlled trial (RCT).
Methods
We undertook a clustered RCT on sites pairing UK Emergency Departments (ED) and ambulance services. At intervention sites, we recruited emergency healthcare practitioners to supply THN to patients presenting with opioid overdose or related condition, with recruitment across 2019–2021. We assessed feasibility of intervention implementation against four predetermined progression criteria covering site sign up and staff training; identification of eligible patients; issue of THN kits and Serious Adverse Events.
Results
At two intervention sites, randomly selected from 4, 299/687 (43.5%) clinical staff were trained (ED1 = 107, AS1 = 121, ED2 = 25, AS2 = 46). Sixty THN kits were supplied to eligible patients (21.7%) (n: ED1 = 36, AS1 = 4, ED2 = 16, AS2 = 4). Across sites, kits were not issued to eligible patients on a further 164 occasions, with reasons reported including: staff forgot ( n = 136), staff too busy ( n = 15), and suspected intentional overdose ( n = 3), no kit available ( n = 2), already given by drugs nurse ( n = 4), other ( n = 4). Staff recorded 626 other patients as ineligible but considered for inclusion, with reasons listed as: patient admitted to hospital ( n = 194), patient absconded ( n = 161) already recruited ( n = 64), uncooperative or abusive ( n = 55), staff not trained ( n = 43), reduced consciousness level ( n = 41), lack of capacity ( n = 35), patient in custody ( n = 21), other ( n = 12). No adverse events were reported.
Conclusion
Staff and patient recruitment were low and varied widely by site. This feasibility study did not meet progression criteria; a fully powered RCT is not planned.
Trial Registration
ISRCTN13232859 (Registered 16/02/2018).
