Evidence map›Paper›PMID 25886676›Full record

SynthesisCanadian journal of psychiatry. Revue canadienne de psychiatrie2015

Response trajectories to clozapine in a secondary analysis of pivotal trials support using treatment response to subtype schizophrenia.

William G Honer, Andrea A Jones, Allen E Thornton, Alasdair M Barr, Ric M Procyshyn, Fidel Vila-Rodriguez

Abstract readMeta-Analysis
In one paragraph

Synthesis in Canadian journal of psychiatry. Revue canadienne de psychiatrie, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2020
    Article
  7. Article
  8. Article
  9. The 10th Anniversary of the Eli Lilly Chair of Schizophrenia from the University of Montreal.Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2015
    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

6 authors at 1 institution in 1 country.

William G HonerProfessor and Head, Department of Psychiatry, University of British Columbia, Vancouver, British Columbia.
Andrea A JonesStudent, Department of Psychiatry, University of British Columbia, Vancouver, British Columbia.
Allen E ThorntonAssociate Professor, Department of Psychology, Simon Fraser University, Vancouver, British Columbia.
Alasdair M BarrAssociate Professor, Department of Anesthesia, Pharmacology, and Therapeutics, University of British Columbia, Vancouver, British Columbia.
Ric M ProcyshynClinical Associate Professor, Department of Psychiatry, University of British Columbia, Vancouver, British Columbia.
Fidel Vila-RodriguezClinical Assistant Professor, Department of Psychiatry, University of British Columbia, Vancouver, British Columbia.
University of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGroups of nonrefractory patients with schizophrenia, taking antipsychotics other than clozapine, show distinct trajectories of treatment response over time. Whether similar patterns of response occur with clozapine-treated patients remains uncertain.

methodWe used a cluster analysis approach for longitudinal data (k-means longitudinal) to analyze individual patient data from 2 pivotal studies of clozapine, compared with chlorpromazine. Trajectories and symptom severity were examined in a younger, less chronic, mixed-sample (study 16, n=100) and in treatment-refractory (study 30, n=257) patients.

resultsEarly-good and delayed-partial trajectory groups were observed, with the early-good trajectory group comprised of 73/100 (73.0%) from the mixed patient study, and 147/257 (57.2%) refractory patients. In the mixed patient sample, the distribution of clozapine and chlorpromazine treatments did not differ between the early-good and delayed-partial trajectory groups; in refractory patients proportionately more clozapine treatment was present in the early-good (87/147, 59.2%), compared with the delayed-partial (35/110, 31.8%), trajectory group. In the early-good trajectory group, improvement in mean symptom severity was 63% in mixed-study patients. Clozapine resistance appeared to be present in 10/50 (20.0%) mixed-study patients, and in 35/122 (28.9%) refractory patients.

conclusionsEarly-good and delayed-partial response trajectories are seen in clozapine studies. The advantage of clozapine over chlorpromazine is seen most clearly in previous refractory patients, within the early-good trajectory group. Good and partial or poor responders to clozapine may merit further investigation.

Indexed as

AdultAntipsychotic AgentsChlorpromazineClozapineHumansOutcome Assessment, Health CareSchizophreniaAntipsychotic AgentsChlorpromazineClozapine

Identifiers

PMID25886676
PMCPMC4418624
OpenAlexW1490837787

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.