Evidence map›Paper›PMID 25387562›Full record

ArticleJournal of medical toxicology : official journal of the American College of Medical Toxicology2015

Evolution of the NBOMes: 25C- and 25B- Sold as 25I-NBOMe.

Larissa K Laskowski, Faesal Elbakoush, Jessica Calvo, Gina Exantus-Bernard, Jane Fong, Justin L Poklis, Alphonse Poklis, Lewis S Nelson

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of medical toxicology : official journal of the American College of Medical Toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
6.5field-weighted citation impact, top 4% of its field
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

11 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. DARK Classics in Chemical Neuroscience: NBOMes.ACS chemical neuroscience · 2020
    Review
  4. Article
  5. Article
  6. Article
  7. 25C-NBOMe Ingestion.Clinical practice and cases in emergency medicine · 2017
    Article
  8. Article
  9. Review
  10. Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Larissa K LaskowskiNew York University School of Medicine/New York City Poison Control Center, 455 First Avenue Room 123, New York, NY, 10016, USA, larissa.laskowski@nyumc.org.
Faesal Elbakoush
Jessica Calvo
Gina Exantus-Bernard
Jane Fong
Justin L Poklis
Alphonse Poklis
Lewis S Nelson
Bronx-Lebanon Hospital Center · USNew York University · USVirginia Commonwealth University · USWoodhull Medical and Mental Health Center · US

Funding

VCU Center for Drug Addiction ResearchP30DA033934 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI YAN ZHANG · 2014 to 2026
$13.8M
NIDA NIH HHS P30 DA033934NIDA NIH HHS P30DA033934
6 · The paper itself

Abstract

introductionThe NBOMes (N-benzyl-oxy-methyl derivatives of known 2C phenylethylamines) are a new and growing class of potent synthetic stimulants. Case reports provide the bulk of available safety and clinical data for clinicians. We report two cases of NBOMe intoxication with 25C-NBOMe (the first lab-confirmed US case) and 25B-NBOMe, respectively, both confirmed via triple quadrapole mass spectrometry. CASE REPORTS: Case 1: A 16-year-old girl had a generalized seizure after reported use of 25I-NBOMe. She presented with altered mental status, lower extremity rigidity, and elevated CPK (6042 U/L). Despite treatment with benzodiazepines, her lower extremity rigidity persisted and CPK peaked at 47,906 U/L. She was discharged on hospital day 8. Serum and urine specimens confirmed presence of 25C-NBOMe. Case 2: A 15-year-old boy developed bizarre behavior after reported use of 25I-NBOMe. In the ED, he had two generalized seizures and persistent muscle rigidity. CPK peaked at 429 U/L. Seizures were managed with benzodiazepines, and he was discharged within 24 h. Serum specimens revealed 25B-NBOMe. DISCUSSION: NBOMes are amphetamine derivatives and highly potent 5-HT(2A) receptor agonists. Clinical manifestations are a product of enhanced central sympathetic and serotonergic tone. We report two cases of NBOMe intoxication in patients who believed they used 25I-NBOME, while lab confirmation proved otherwise. Whether unique clinical manifestations are specific to the NBOMe variant, dose, route of administration, or other factors is unknown. Laboratory confirmation may play a role in identifying unexpected NBOMe variants, while contributing to the epidemiologic data on these novel substances.

Indexed as

AdolescentAnisolesBenzodiazepinesCentral Nervous System StimulantsCreatine KinaseDesigner DrugsDimethoxyphenylethylamineFemaleHumansHypnotics and SedativesMaleMass SpectrometryMental DisordersMuscle RigidityPhenethylaminesReceptor, Serotonin, 5-HT2A2-(4-bromo-2,5-dimethoxyphenyl)-N-((2-methoxyphenyl)methyl)ethanamine2-(4-iodo-2,5-dimethoxyphenyl)-N-(2-methoxybenzyl)ethanamineAnisolesBenzodiazepinesCentral Nervous System StimulantsCreatine KinaseDesigner DrugsDimethoxyphenylethylamineHypnotics and SedativesPhenethylaminesReceptor, Serotonin, 5-HT2ASerotonin 5-HT2 Receptor Agonists

Identifiers

PMID25387562
PMCPMC4469725
OpenAlexW2050354078

What OpenQuestion holds

Textmetadata
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.