Evidence map›Paper›PMID 31839014›Full record

ArticleEpidemiology and psychiatric sciences2019

Childhood adversity and clinical and psychosocial outcomes in psychosis.

S Turner, C Harvey, L Hayes, D Castle, C Galletly, S Sweeney, S Shah, L Keogh, M J Spittal

Abstract read
In one paragraph

Article in Epidemiology and psychiatric sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
–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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. The Australian and New Zealand journal of psychiatry · 2026
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  7. Synergistic pathways to psychosis: understanding developmental risk and resilience factors.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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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

9 authors.

S TurnerQuality and Service Improvement, NorthWestern Mental Health, 300 Grattan St, Parkville, Victoria3050, Australia.
C HarveyDepartment of Psychiatry, The University of Melbourne, Parkville, Victoria3010, Australia.
L HayesParenting Research Centre, 232 Victoria Parade, East Melbourne, Victoria3002, Australia.
D CastleDepartment of Psychiatry, The University of Melbourne, Parkville, Victoria3010, Australia.
C GalletlyDiscipline of Psychiatry, University of Adelaide, Adelaide, South Australia5005, Australia.
S SweeneyDiscipline of Psychiatry, University of Adelaide, Adelaide, South Australia5005, Australia.
S ShahNeuropsychiatric Epidemiology Research Unit, School of Psychiatry and Clinical Neurosciences, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia6009, Australia.
L KeoghMelbourne School of Population and Global Health, The University of Melbourne, Parkville, Victoria 3010, Australia.
M J SpittalMelbourne School of Population and Global Health, The University of Melbourne, Parkville, Victoria 3010, Australia.ORCID https://orcid.org/0000-0002-2841-1536

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsAssociations between childhood abuse and various psychotic illnesses in adulthood are commonly reported. We aim to examine associations between several reported childhood adverse events (sexual abuse, physical abuse, emotional abuse, neglect and interpersonal loss) among adults with diagnosed psychotic disorders and clinical and psychosocial outcomes.

methodsWithin a large epidemiological study, the 2010 Australian National Survey of Psychosis (Survey of High Impact Psychosis, SHIP), we used logistic regression to model childhood adverse events (any and specific types) on 18 clinical and psychosocial outcomes.

resultsEighty percent of SHIP participants (1466/1825) reported experiencing adverse events in childhood (sexual abuse, other types of abuse and interpersonal loss). Participants reporting any form of childhood adversity had higher odds for 12/18 outcomes we examined. Significant associations were observed with all psychosocial outcomes (social dysfunction, victimisation, offending and homelessness within the previous 12 months, and definite psychosocial stressor within 12 months of illness onset), with the strongest association for homelessness (odds ratio (OR) = 2.82). Common across all adverse event types was an association with lifetime depression, anxiety and a definite psychosocial stressor within 12 months of illness onset. When adverse event types were non-hierarchically coded, sexual abuse was associated with 11/18 outcomes, other types of abuse 13/18 and, interpersonal loss occurring in the absence of other forms of abuse was associated with fewer of the clinical and psychosocial outcomes, 4/18. When adverse events types were coded hierarchically (to isolate the effect of interpersonal loss in the absence of abuse), interpersonal loss was associated with lower odds of self-reproach (OR = 0.70), negative syndrome (OR = 0.75) and victimisation (OR = 0.82).

conclusionsAdverse childhood experiences among people with psychosis are common, as are subsequent psychosocial stressors. Mental health professionals should routinely enquire about all types of adversities in this group and provide effective service responses. Childhood abuse, including sexual abuse, may contribute to subsequent adversity, poor psychosocial functioning and complex needs among people with psychosis. Longitudinal research to better understand these relationships is needed, as are studies which evaluate the effectiveness of preventative interventions in high-risk groups.

Indexed as

AdolescentAdultAdult Survivors of Child Adverse EventsAgedAnxietyAustraliaChildChild AbuseChild Abuse, SexualDepressionFemaleHumansLife Change EventsMaleMiddle AgedPrevalenceAdverse life eventschild abusechildhood sexual abusechildhood traumapsychosis

Identifiers

PMID31839014
PMCPMC8061294

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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.