Sentanyl: a comparison of blood fentanyl concentrations and naloxone dosing after non-fatal overdose.


Journal

Clinical toxicology (Philadelphia, Pa.)
ISSN: 1556-9519
Titre abrégé: Clin Toxicol (Phila)
Pays: England
ID NLM: 101241654

Informations de publication

Date de publication:
Feb 2022
Historique:
pubmed: 20 7 2021
medline: 31 3 2022
entrez: 19 7 2021
Statut: ppublish

Résumé

Non-pharmaceutical fentanyl and its analogs have driven striking increases in opioid-associated overdose deaths. These highly potent opioids can be found at low concentrations in biological specimens. Little is known regarding the concentrations of these substances among survivors of non-fatal overdoses. In a locale where fentanyl is responsible for the majority of non-fatal opioid overdoses, we compared the concentration of fentanyl in blood to naloxone dosing in the presence and absence of a concurrent sedative-hypnotic exposure. In this pilot study, we enrolled adult patients presenting to the emergency department (ED) who: (1) arrived after an overdose requiring naloxone for the reversal of respiratory depression; and (2) who required venipuncture or intravenous access as part of their clinical care. Blood specimens ( Nineteen of twenty participants (95%) were exposed to fentanyl prior to their overdose; the remaining participant tested positive for heroin metabolites. No participants reported pharmaceutical fentanyl use. Fentanyl analogs - acetylfentanyl or carfentanil - were present in three specimens. In 11 cases, fentanyl and its metabolites were the only opioids identified. Among the fentanyl-exposed, blood concentrations ranged from <0.1-19 ng/mL with a mean of 6.2 ng/mL and a median of 3.6 ng/mL. There was no relationship between fentanyl concentration and naloxone dose administered for reversal. We detected sedative-hypnotics (including benzodiazepines, muscle relaxants, and antidepressants) in nine participants. Among the sedative-hypnotic exposed, fentanyl concentrations were lower, but naloxone dosing was similar to those without a concomitant exposure. In this study, we found that: 1) fentanyl was present in the blood of nearly all participants; 2) fentanyl concentrations were lower among study participants with concomitant sedative-hypnotic exposure; and 3) the dose of naloxone administered for overdose reversal was not associated with the measured fentanyl concentration in blood specimens. Our results underscore the role that tolerance and concomitant drug exposure play in the precipitation and resuscitation of management of opioid overdose.

Identifiants

pubmed: 34278904
doi: 10.1080/15563650.2021.1948558
doi:

Substances chimiques

Analgesics, Opioid 0
Narcotic Antagonists 0
Naloxone 36B82AMQ7N
Heroin 70D95007SX
Fentanyl UF599785JZ

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

197-204

Auteurs

Alex J Krotulski (AJ)

Center for Forensic Science Research and Education, Fredric Rieders Family Foundation, Willow Grove, PA, USA.
College of Life Sciences, Thomas Jefferson University, Philadelphia, PA, USA.

Brittany P Chapman (BP)

Department of Emergency Medicine, Division of Medical Toxicology, University of Massachusetts Medical School, Worcester, MA, USA.

Sarah J Marks (SJ)

Department of Emergency Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Sam T Ontiveros (ST)

Department of Emergency Medicine, Division of Medical Toxicology, University of Massachusetts Medical School, Worcester, MA, USA.

Katharine Devin-Holcombe (K)

Department of Emergency Medicine, Division of Medical Toxicology, University of Massachusetts Medical School, Worcester, MA, USA.

Melissa F Fogarty (MF)

Center for Forensic Science Research and Education, Fredric Rieders Family Foundation, Willow Grove, PA, USA.

Hai Trieu (H)

College of Life Sciences, Thomas Jefferson University, Philadelphia, PA, USA.

Barry K Logan (BK)

Center for Forensic Science Research and Education, Fredric Rieders Family Foundation, Willow Grove, PA, USA.
College of Life Sciences, Thomas Jefferson University, Philadelphia, PA, USA.
Toxicology Department, NMS Labs, Horsham, PA, USA.

Roland C Merchant (RC)

Department of Emergency Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Kavita M Babu (KM)

Department of Emergency Medicine, Division of Medical Toxicology, University of Massachusetts Medical School, Worcester, MA, USA.

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Classifications MeSH