Literature DB >> 30296396

Relationship Between Adverse Childhood Experience Survey Items and Psychiatric Disorders.

David Cawthorpe1, Brian Marriott2, Jaime Paget3, Iraj Moulai4, Sandra Cheung5.   

Abstract

CONTEXT: Developmental psychopathology theory suggests a relationship between early childhood adversity and mental disorder.
OBJECTIVE: To examine the relationship between the specific items on the Adverse Childhood Experiences (ACE) survey and the International Classification of Diseases, Tenth Revision (ICD-10) categories of psychiatric diagnoses in a pediatric sample.
DESIGN: The sample included patients enrolled in the Child and Adolescent Addiction Mental Health and Psychiatry Program with both a completed ACE survey and at least 1 diagnosis of record (per admission). These criteria yielded 2 samples for each sex (ACE survey item frequencies and values in collapsed and multiple-admission groups). Data were analyzed employing tetrachoric correlation, hierarchical regression, and polychoric factor analysis.
RESULTS: Hierarchical regression analysis identified that ICD-10 diagnostic categories, except for substance disorders, were not consistently related to ACE total score and tended to reduce the magnitude of the ACE total score in the multiple-admission group. Tetrachoric correlation revealed very low (< 0.4) positive and negative correlations between ICD-10 categories and ACE items in both multiple-admission and collapsed sample groups. Polychoric factor analysis indicated that the ACE survey items and the ICD-10 categories for both sexes were independent, with only the diagnostic ICD-10 category substance disorders being marginally associated with the ACE items factor for females.
CONCLUSION: The nominal relationship between ACE items and ICD-10 diagnostic categories indicates the need to include ACE assessment in advance of differential diagnosis and implementation of conventional mental health interventions for children and adolescents.

Entities:  

Mesh:

Year:  2018        PMID: 30296396      PMCID: PMC6175599          DOI: 10.7812/TPP/18-001

Source DB:  PubMed          Journal:  Perm J        ISSN: 1552-5767


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