Back to Search Start Over

Naloxone interventions in opioid overdoses: a systematic review protocol

Authors :
Jason Curran
Jane A. Buxton
Jesse Godwin
Roy Purssell
Penelope M. A. Brasher
Mary M. Doyle-Waters
Lindsay Victoria Shaw
Jeffrey P. Hau
Jessica Moe
Corinne M. Hohl
Source :
Systematic Reviews, Vol 8, Iss 1, Pp 1-9 (2019), Systematic Reviews
Publication Year :
2019
Publisher :
BMC, 2019.

Abstract

Background North America is in the midst of an unabated opioid overdose epidemic due to the increasing non-medical use of fentanyl and ultra-potent opioids. Naloxone is an effective antidote to opioid toxicity, yet its optimal dosing in the context of fentanyl and ultra-potent opioid overdoses remains unknown. This review aims to determine the relationship between the first empiric dose of naloxone and reversal of toxicity, adverse events, and the total cumulative dose required among patients with undifferentiated opioid overdoses and those with suspected toxicity from ultra-potent opioids. Secondary objectives include evaluating the relationship between the cumulative naloxone dose and toxicity reversal and adverse events, among patients with undifferentiated opioid overdoses and those with suspected toxicity from ultra-potent opioids. Methods To identify studies, we will search MEDLINE, Embase, CENTRAL, DARE, CDAG, CINAHL, Science Citation Index, multiple trial registries, and the gray literature. Included studies will evaluate patients with suspected or confirmed opioid toxicity from undifferentiated opioids and ultra-potent opioids, who received an empiric and possibly additional doses of naloxone. The main outcomes of interest are the relationship between naloxone dose and toxicity reversal and adverse events. We will include controlled and non-controlled interventional studies, observational studies, case reports/series, and reports from poison control centers. We will extract data and assess study quality in duplicate with discrepancies resolved by consensus or a third party. We will use the Downs and Black and Cochrane risk of bias tools for observational and randomized controlled studies. If we find sufficient variation in dose, we will fit a random effects one-stage model to estimate a dose-response relationship. We will conduct multiple subgroup analyses, including by type of opioid used and by suspected high and low prevalence of ultra-potent opioid use based on geographic location and time of the original studies. Discussion Our review will include the most up-to-date available data including ultra-potent opioids to inform the current response to the opioid epidemic, addressing the limitations of recent reviews. We anticipate limitations relating to study heterogeneity. We will disseminate study results widely to update overdose treatment guidelines and naloxone dosing in Take Home Naloxone programs. Electronic supplementary material The online version of this article (10.1186/s13643-019-1048-y) contains supplementary material, which is available to authorized users.

Details

Language :
English
ISSN :
20464053
Volume :
8
Issue :
1
Database :
OpenAIRE
Journal :
Systematic Reviews
Accession number :
edsair.doi.dedup.....55f48d917cea2a588a57b08c4a9022e7
Full Text :
https://doi.org/10.1186/s13643-019-1048-y