Evidence map›Paper›PMID 35510346›Full record

SynthesisBritish journal of clinical pharmacology2022

Ketamine treatment for refractory anxiety: A systematic review.

Jamie L Tully, Amelia D Dahlén, Connor J Haggarty, Helgi B Schiöth, Samantha Brooks

Open access · hybridAbstract readSystematic Review
In one paragraph

Synthesis in British journal of clinical pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 3 pooled it
13.9field-weighted citation impact, top 1% 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

30 citing papers in PubMed, 3 syntheses or guidelines pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Ketamine treatment for refractory anxiety: A systematic review.British journal of clinical pharmacology · 2022
    Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Article
  10. Review
  11. Article
  12. Review
  13. Difficult-to-Treat Anxiety: A Neurocomputational Framework.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2025
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Ketamine-assisted buprenorphine initiation: a pilot case series.Addiction science & clinical practice · 2024
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 3 countries.

Jamie L TullyCollege of Life and Environmental Sciences, University of Exeter, Exeter, UK.ORCID 0000-0002-3049-5011
Amelia D DahlénDepartment of Surgical Sciences, University of Uppsala, Uppsala, Sweden.
Connor J HaggartyHuman Behavioral Pharmacology Lab, Biological Sciences Division, University of Chicago, USA.
Helgi B SchiöthDepartment of Surgical Sciences, University of Uppsala, Uppsala, Sweden.
Samantha BrooksFaculty of Health, Liverpool John Moores University, Liverpool, UK.
Uppsala University · SELiverpool John Moores University · GBUniversity of Chicago · USUniversity of Exeter · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a growing interest in the psychiatric properties of the dissociative anaesthetic ketamine, as single doses have been shown to have fast-acting mood-enhancing and anxiolytic effects, which persist for up to a week after the main psychoactive symptoms have diminished. Therefore, ketamine poses potential beneficial effects in patients with refractory anxiety disorders, where other conventional anxiolytics have been ineffective. Ketamine is a noncompetitive antagonist of the N-methyl-d-aspartate (NMDA) glutamate receptor, which underlies its induction of pain relief and anaesthesia. However, the role of NMDA receptors in anxiety reduction is still relatively unknown. To fill this paucity in the literature, this systematic review assesses the evidence that ketamine significantly reduces refractory anxiety and discusses to what extent this may be mediated by NMDA receptor antagonism and other receptors. We highlight the temporary nature of the anxiolytic effects and discuss the high discrepancy among the study designs regarding many fundamental factors such as administration routes, complementary treatments and other treatments.

Indexed as

Anti-Anxiety AgentsKetamineAnxietyAnxiety DisordersHumansReceptors, N-Methyl-D-AspartateAnti-Anxiety AgentsKetamineReceptors, N-Methyl-D-Aspartateanxietyanxiolyticdepressionketamineketamine infusionrefractory anxietytreatment-resistant depression

Identifiers

PMID35510346
PMCPMC9540337
OpenAlexW4229020297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.