Evidence map›Paper›PMID 34676067›Full record

ArticleTherapeutic advances in psychopharmacology2021

Outcomes in treatment-resistant schizophrenia: symptoms, function and clozapine plasma concentrations.

Amir Krivoy, Eromona Whiskey, Henrietta Webb-Wilson, Dan Joyce, Derek K Tracy, Fiona Gaughran, James H MacCabe, Sukhwinder S Shergill

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in psychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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 2 countries.

Amir KrivoyGeha Mental Health Center, Petach-Tikva, Israel.ORCID https://orcid.org/0000-0003-2218-3250
Eromona WhiskeyNational Psychosis Service, South London and Maudsley NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0002-6146-0073
Henrietta Webb-WilsonNational Psychosis Service, South London and Maudsley NHS Foundation Trust, London, UK.
Dan JoyceNational Institute of Health Research Oxford Health Biomedical Research Center and Department of Psychiatry, Warneford Hospital, University of Oxford, Oxford, UK.
Derek K TracyDepartment of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.ORCID https://orcid.org/0000-0002-3609-9407
Fiona GaughranNational Psychosis Service, South London and Maudsley NHS Foundation Trust, London, UK.
James H MacCabeNational Psychosis Service, South London and Maudsley NHS Foundation Trust, London, UK.
Sukhwinder S ShergillNational Psychosis Service, South London and Maudsley NHS Foundation Trust, London, UK.
King's College London · GBSouth London and Maudsley NHS Foundation Trust · GBTel Aviv University · ILWarneford Hospital · GB

Funding

Medical Research Council G0901868
6 · The paper itself

Abstract

backgroundClozapine is the only medication licenced for treating patients with treatment-refractory schizophrenia. However, there are no evidence-based guidelines as to the optimal plasma level of clozapine to aim for, and their association with clinical and functional outcome.

objectiveWe assessed the relationship between clinical and functional outcome measures and blood concentrations of clozapine among patients with treatment-refractory psychosis.

methodsData were reviewed in 82 patients with treatment-refractory psychosis admitted to a specialised tertiary-level service and treated with clozapine. Analysis focussed on the relationship between clozapine and norclozapine plasma concentrations and the patient's clinical symptoms and functional status.

resultsClinical symptom improvement was positively correlated with norclozapine plasma concentrations and inversely correlated with clozapine to norclozapine plasma concentrations ratio. Clozapine concentrations showed a bimodal association with clinical improvement (peaks around 350 and 660 ng/ml). Clinical symptom improvement correlated with functional outcomes, although there was no significant correlation between the latter and clozapine or norclozapine plasma concentrations.

conclusionClozapine treatment was associated with optimal clinical improvement at two different peak plasma concentrations around 350 and 650 ng/ml. Clinical improvement was associated with functional outcome; however, functionality was not directly associated with clozapine concentrations. A subset of patients may require higher clozapine plasma concentrations to achieve clinical improvement.

Indexed as

clozapinenorclozapinepsychosis

Identifiers

PMID34676067
PMCPMC8524694
OpenAlexW3202939786

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.