Evidence map›Paper›PMID 33692392›Full record

SynthesisScientific reports2021

A network meta-analysis of the dose-response effects of lurasidone on acute schizophrenia.

Manit Srisurapanont, Sirijit Suttajit, Surinporn Likhitsathian, Benchalak Maneeton, Narong Maneeton

Open access · goldAbstract readComparative StudySystematic ReviewNetwork Meta-Analysis
In one paragraph

Synthesis in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Lurasidone versus typical antipsychotics for schizophrenia.The Cochrane database of systematic reviews · 2025
    Pooled it
  3. Observational
  4. Review
  5. Article
  6. Review
  7. Article
  8. Does the Ranking Matter? A Retrospective Cohort Study Investigating the Impact of theCanadian journal of psychiatry. Revue canadienne de psychiatrie · 2023
    Article
  9. Review
  10. 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

5 authors at 1 institution in 1 country.

Manit SrisurapanontDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Si Phum, 110 Inthawarorot Road, Mueang, 50200, Chiang Mai, Thailand. manit.s@cmu.ac.th.
Sirijit SuttajitDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Si Phum, 110 Inthawarorot Road, Mueang, 50200, Chiang Mai, Thailand.
Surinporn LikhitsathianDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Si Phum, 110 Inthawarorot Road, Mueang, 50200, Chiang Mai, Thailand.
Benchalak ManeetonDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Si Phum, 110 Inthawarorot Road, Mueang, 50200, Chiang Mai, Thailand.
Narong ManeetonDepartment of Psychiatry, Faculty of Medicine, Chiang Mai University, Si Phum, 110 Inthawarorot Road, Mueang, 50200, Chiang Mai, Thailand.
Chiang Mai University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We compared the efficacy, safety, and acceptability of lurasidone at different doses to establish the dose-response relationships of lurasidone therapeutic and adverse effects in acute schizophrenia. Included trials were 4- to 16-week, fixed-dose, randomized controlled trials of lurasidone in adults with acute schizophrenia. Different doses of lurasidone, other antipsychotics, and placebo were considered as independent treatments. Apart from all-cause dropout rates, four therapeutic and four adverse outcomes were included in the frequentist network meta-analysis (NMA). Lurasidone 160, 120, 80, 40, and 20 mg/day were studied in ten trials of 3,366 adults with schizophrenia exacerbation. Lurasidone 160 mg/day reduced Positive and Negative Syndrome Scale (PANSS) total scores significantly more than lurasidone 120, 80, 40, and 20 mg/day (mean differences = - 7.63, - 7.04, - 8.83, and - 12.25, respectively). All-cause dropout rates were significantly lower in participants receiving lurasidone 160 mg/day and 80 mg/day compared with those taking placebo. The half-maximal effective doses of lurasidone for PANSS total, PANSS positive, and MADRS score reductions were higher than 80 mg/day. The confidence of all NMA estimates was low or very low. Lurasidone 160 mg/day is currently the most efficacious and acceptable dose for acute schizophrenia. Its maximal effective doses may be higher than 160 mg/day.

Indexed as

Acute DiseaseDose-Response Relationship, DrugDouble-Blind MethodHumansLurasidone HydrochlorideRandomized Controlled Trials as TopicSchizophreniaLurasidone Hydrochloride

Identifiers

PMID33692392
PMCPMC7946927
OpenAlexW3134710682

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.