Evidence map›Paper›PMID 16504026›Full record

Trial reportBMC psychiatry2006

Time to discontinuation of atypical versus typical antipsychotics in the naturalistic treatment of schizophrenia.

Haya Ascher-Svanum, Baojin Zhu, Douglas Faries, Ron Landbloom, Marvin Swartz, Jeff Swanson

Registry-linked trialOpen access · goldAbstract readClinical TrialComparative StudyMulticenter Study
In one paragraph

Trial report in BMC psychiatry, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01245348 (Relative Effectiveness of Schizophrenia Therapy), which is not on this map. Cited by 44 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 7 pooled it
6.5field-weighted citation impact, top 3% 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.

NCT01245348 completednot on this mapstarted 2010, after this paper: background citation

Relative Effectiveness of Schizophrenia Therapy (REST) Study

TypeobservationalSponsorMedco Health Solutions, Inc.Ran2010 to 2012Enrolled1,110ConditionsSchizophrenia, Bipolar DisorderArmsSULT4A1-1 genetic test
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 7 syntheses or guidelines pooled it, 110 citations in OpenAlex.

  1. Pooled it
  2. Quetiapine versus other atypical antipsychotics for schizophrenia.The Cochrane database of systematic reviews · 2013
    Pooled it
  3. Risperidone versus other atypical antipsychotics for schizophrenia.The Cochrane database of systematic reviews · 2011
    Pooled it
  4. Clozapine versus other atypical antipsychotics for schizophrenia.The Cochrane database of systematic reviews · 2010
    Pooled it
  5. Olanzapine versus other atypical antipsychotics for schizophrenia.The Cochrane database of systematic reviews · 2010
    Pooled it
  6. Quetiapine versus other atypical antipsychotics for schizophrenia.The Cochrane database of systematic reviews · 2010
    Pooled it
  7. Ziprasidone versus other atypical antipsychotics for schizophrenia.The Cochrane database of systematic reviews · 2009
    Pooled it
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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 2 institutions in 1 country.

Haya Ascher-SvanumLilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA. haya@lilly.com
Baojin Zhu
Douglas Faries
Ron Landbloom
Marvin Swartz
Jeff Swanson
Eli Lilly (United States) · USDuke Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is an ongoing debate over whether atypical antipsychotics are more effective than typical antipsychotics in the treatment of schizophrenia. This naturalistic study compares atypical and typical antipsychotics on time to all-cause medication discontinuation, a recognized index of medication effectiveness in the treatment of schizophrenia.

methodsWe used data from a large, 3-year, observational, non-randomized, multisite study of schizophrenia, conducted in the U.S. between 7/1997 and 9/2003. Patients who were initiated on oral atypical antipsychotics (clozapine, olanzapine, risperidone, quetiapine, or ziprasidone) or oral typical antipsychotics (low, medium, or high potency) were compared on time to all-cause medication discontinuation for 1 year following initiation. Treatment group comparisons were based on treatment episodes using 3 statistical approaches (Kaplan-Meier survival analysis, Cox Proportional Hazards regression model, and propensity score-adjusted bootstrap resampling methods). To further assess the robustness of the findings, sensitivity analyses were performed, including the use of (a) only 1 medication episode for each patient, the one with which the patient was treated first, and (b) all medication episodes, including those simultaneously initiated on more than 1 antipsychotic.

resultsMean time to all-cause medication discontinuation was longer on atypical (N = 1132, 256.3 days) compared to typical antipsychotics (N = 534, 197.2 days; p < .01), and longer on atypicals compared to typicals of high potency (N = 320, 187.5 days; p < .01), medium potency (N = 140, 213.5 days; p < .01), and low potency (N = 74, 208.7 days; p < .01). Among the atypicals, only clozapine, olanzapine, and risperidone had significantly longer time to all-cause medication discontinuation compared to typicals, regardless of potency level, and compared to haloperidol with prophylactic anticholinergic treatment. When compared to perphenazine, a medium-potency typical antipsychotic, only clozapine and olanzapine had a consistently and significantly longer time to all-cause medication discontinuation. Results were confirmed by sensitivity analyses.

conclusionIn the usual care of schizophrenia patients, time to medication discontinuation for any cause appears significantly longer for atypical than typical antipsychotics regardless of the typical antipsychotic potency level. Findings were primarily driven by clozapine and olanzapine, and to a lesser extent by risperidone. Furthermore, only clozapine and olanzapine therapy showed consistently and significantly longer treatment duration compared to perphenazine, a medium-potency typical antipsychotic.

Indexed as

AdultAntipsychotic AgentsBenzodiazepinesBiasClozapineDrug Administration ScheduleEpisode of CareFemaleFollow-Up StudiesHumansMaleOlanzapineOutcome Assessment, Health CarePerphenazineProportional Hazards ModelsResearch DesignAntipsychotic AgentsBenzodiazepinesClozapineOlanzapinePerphenazineRisperidone

Identifiers

PMID16504026
PMCPMC1402287
OpenAlexW1496843021

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.