Evidence map›Paper›PMID 38741224›Full record

ReviewHarm reduction journal2024

High-dose naloxone formulations are not as essential as we thought.

Paige M Lemen, Daniel P Garrett, Erin Thompson, Megan Aho, Christina Vasquez, Ju Nyeong Park

Abstract readReview
In one paragraph

Review in Harm reduction journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Observational
  2. Naloxone Administration in Relation to Fentanyl, Xylazine, CNS Depressants, and Stimulants Exposure After Suspected Opioid Overdose: A Pilot Study.Academic emergency medicine : official journal of the Society for Academic Emergency Medicine · 2026
    Observational
  3. Article
  4. Article
  5. An antifentanyl monoclonal antibody reverses fentanyl-induced apnea in pigs.The Journal of pharmacology and experimental therapeutics · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Paige M LemenTennessee Harm Reduction, 1989 Madison Avenue, 7, Memphis, TN, 38104, USA. plemen1@uthsc.edu.
Daniel P GarrettTennessee Harm Reduction, 1989 Madison Avenue, 7, Memphis, TN, 38104, USA.
Erin ThompsonHarm Reduction Innovation Lab, Rhode Island Hospital, Providence, RI, USA.
Megan AhoHarm Reduction Innovation Lab, Rhode Island Hospital, Providence, RI, USA.
Christina VasquezHarm Reduction Innovation Lab, Rhode Island Hospital, Providence, RI, USA.
Ju Nyeong ParkHarm Reduction Innovation Lab, Rhode Island Hospital, Providence, RI, USA.

Funding

Project 4: Neonatal Abstinence Syndrome (NAS): Fetus to First YearsP20GM125507 · NIGMS · RHODE ISLAND HOSPITAL · PI Brandon David Lewis Marshall · 2018 to 2026
$23.4M
Enhancing FDA's opioids systems modeling efforts to more comprehensively address fentanyl, stimulants, polysubstance use, and associated outcomesU01FD007455 · FDA · MASSACHUSETTS GENERAL HOSPITAL · PI JALALI, MOHAMMAD S. · 2021 to 2021
$1.2M
FDA HHS U01 FD007455NIGMS NIH HHS P20 GM125507
6 · The paper itself

Abstract

Naloxone is an effective FDA-approved opioid antagonist for reversing opioid overdoses. Naloxone is available to the public and can be administered through intramuscular (IM), intravenous (IV), and intranasal spray (IN) routes. Our literature review investigates the adequacy of two doses of standard IM or IN naloxone in reversing fentanyl overdoses compared to newer high-dose naloxone formulations. Moreover, our initiative incorporates the experiences of people who use drugs, enabling a more practical and contextually-grounded analysis. The evidence indicates that the vast majority of fentanyl overdoses can be successfully reversed using two standard IM or IN dosages. Exceptions include cases of carfentanil overdose, which necessitates ≥ 3 doses for reversal. Multiple studies documented the risk of precipitated withdrawal using ≥ 2 doses of naloxone, notably including the possibility of recurring overdose symptoms after resuscitation, contingent upon the half-life of the specific opioid involved. We recommend distributing multiple doses of standard IM or IN naloxone to bystanders and educating individuals on the adequacy of two doses in reversing fentanyl overdoses. Individuals should continue administration until the recipient is revived, ensuring appropriate intervals between each dose along with rescue breaths, and calling emergency medical services if the individual is unresponsive after two doses. We do not recommend high-dose naloxone formulations as a substitute for four doses of IM or IN naloxone due to the higher cost, risk of precipitated withdrawal, and limited evidence compared to standard doses. Future research must take into consideration lived and living experience, scientific evidence, conflicts of interest, and the bodily autonomy of people who use drugs.

Indexed as

NaloxoneNarcotic AntagonistsAdministration, IntranasalAnalgesics, OpioidDrug OverdoseFentanylHumansOpiate OverdoseAnalgesics, OpioidFentanylNaloxoneNarcotic AntagonistsLiterature reviewNaloxoneOpioid overdose

Identifiers

PMID38741224
PMCPMC11089786

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.