Evidence map›Paper›PMID 39655766›Full record

SynthesisJournal of psychopharmacology (Oxford, England)2025

Antipsychotic polypharmacy and high-dose antipsychotic therapy compared to antipsychotic monotherapy at standard doses in schizophrenia - a systematic review.

Christopher Lawrence, Chloe Roberts, Chloe Galides, Samuel R Chamberlain, Ruihua Hou

Abstract readSystematic ReviewComparative Study
In one paragraph

Synthesis in Journal of psychopharmacology (Oxford, England), 2025. 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
–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

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
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

5 authors.

Christopher LawrenceFaculty of Medicine, Clinical and Experimental Sciences, University of Southampton, Southampton, UK.ORCID 0000-0002-0188-2127
Chloe RobertsDorset Healthcare University Foundation Trust, Poole, Dorset, UK.
Chloe GalidesHampshire and Isle of Wight Healthcare NHS Foundation Trust, Southampton, UK.
Samuel R ChamberlainFaculty of Medicine, Clinical and Experimental Sciences, University of Southampton, Southampton, UK.
Ruihua HouFaculty of Medicine, Clinical and Experimental Sciences, University of Southampton, Southampton, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundSchizophrenia is considered to have a lifetime prevalence of around 1%. Up to 30% of patients diagnosed with schizophrenia are subsequently categorised as treatment resistant. Current guidelines advise against the use of antipsychotic polypharmacy (APP) or high-dose antipsychotic therapy (HDAT) in the treatment of schizophrenia; however, these treatment approaches continue to be used in up to 25% of cases.

aimsThis review was to evaluate the evidence for the efficacy and tolerability of APP and HDAT as an alternative to antipsychotic monotherapy at standard doses in the treatment of schizophrenia.

methodsThis is a systematic review. We searched PubMed, EMBASE and PsycINFO, for eligible trials published prior to 24 March 2023. The protocol was registered on PROSPERO (CRD42023408785). Quality assessment was conducted using the Revised Cochrane risk-of-bias tool for randomised trials.

resultsA total of 14 studies were included in this review. Two studies demonstrated clinically significant improvement with APP compared to standard treatment. There was no clear evidence that APP or HDAT is definitively less tolerable than antipsychotic monotherapy at a standard dose.

conclusionsThis review found limited evidence for the efficacy of APP and HDAT in the treatment of schizophrenia over the use of antipsychotic monotherapy at a standard dose. The relative tolerability was unclear. Management of treatment-resistant schizophrenia remains a prominent clinical issue and further research, including high-quality large-scale Randomised Controlled Trials (RCTs) of APP and HDAT in patients who have been unresponsive to clozapine, would be of significant benefit to the field of psychiatry.

Indexed as

Antipsychotic AgentsPolypharmacySchizophreniaDose-Response Relationship, DrugDrug Therapy, CombinationHumansRandomized Controlled Trials as TopicAntipsychotic Agentsantipsychotic polypharmacydopamine receptor antagonistsdopamine receptor partial agonistsdrugs for psychosishigh-dose antipsychotic therapySchizophreniatreatment-resistant schizophrenia

Identifiers

PMID39655766
PMCPMC11831860

What OpenQuestion holds

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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.