Co-morbidity of substance use disorder and psychopathology in women who use methamphetamine during pregnancy in the US and New Zealand |
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Authors: | Trecia A. Wouldes Linda L. LaGasse Chris Derauf Elana Newman Rizwan Shah Lynne M. Smith Amelia M. Arria Marilyn A. Huestis Sheri DellaGrotta Tara Wilcox Charles R. Neal Barry M. Lester |
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Affiliation: | 1. Department of Psychological Medicine, University of Auckland, New Zealand;2. Brown Center for the Study of Children at Risk, Warren Alpert Medical School and Women & Infants Hospital, United States;3. Division of Community Pediatric and Adolescent Medicine, Mayo Clinic, United States;4. Department of Psychology, The University of Tulsa, United States;5. Central Iowa Health – Des Moines, United States;6. Los Angeles Biomedical Research Institute at Harbor UCLA Medical Center, United States;7. Center on Young Adult Health and Development, University of Maryland School of Public Health, United States;8. Chemistry and Drug Metabolism Section, NIDA IRP, United States;9. Department of Pediatrics, John A Burns School of Medicine, University of Hawaii, United States |
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Abstract: | BackgroundMethamphetamine (MA) abuse is a worldwide problem. Little is known about the co-morbidity of substance use disorders (SUD) and other psychiatric disorders of mothers who use MA prenatally. The Infant Development, Environment and Lifestyle (IDEAL) Study is a prospective, investigation of prenatal MA use and child outcome in the United States (US) and New Zealand (NZ). This study examined prenatal MA use and the co-morbidity of SUD and psychiatric disorders at 1-month postpartum.MethodMothers who used MA (US = 127, NZ = 97) were compared to a matched comparison group (US = 193, NZ = 110). The Substance Abuse Subtle Screening Inventory-3 was used to measure the probability of a SUD. The Brief Symptom Inventory (BSI) was used to measure the likelihood of a positive diagnosis of a psychiatric disorder.ResultsIn the US and NZ, MA groups had lower SES, increased single parenting, delayed prenatal care, and increased polydrug use. In the US only, MA mothers had lower income than the comparison group. MA users were 10 times more likely to have a SUD and twice as likely to meet BSI criteria for a diagnosable psychiatric disorder. In NZ, but not the US, MA users were five times more likely to have co-morbidity of both. This disparity may be due to higher quantities of prenatal alcohol use associated with increased psychiatric symptoms.ConclusionThese findings suggest that addressing both substance abuse and psychiatric disorders in mothers who use MA may be required to effectively treat maternal MA use. |
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