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Psychotropic Drug Therapy and Psychiatric Symptoms in HIV-infected and -uninfected Children and Adolescents Enrolled in PACTG P1055
Miriam C Chernoff*1, S Nachman2, P Williams1, P Brouwers3, J Heston4,5, J Heston4,5, J Hodge6, V Di Poalo7, N Deygoo8, K Gadow2, and PACTG P1055 Study Team
1Harvard Sch of Publ Hlth, Boston, MA, US; 2Stony Brook Univ Sch of Med, NY, US; 3Natl Inst of Mental Hlth, NIH, Rockville, MD, US; 4St Jude Children's Res Hosp, Memphis, TN, US; 5Child and Adolescent Psychiatry Assoc PLLC, Memphis, TN, US; 6Frontier Sci & Tech Res Fndn, Amherst, NY, US; 7Robert Wood Johnson Univ Hosp, Hazlet, NJ, US; and 8New York Univ Sch of Med, NY, US
Background: Perinatally HIV-infected youth often receive
psychotropic medication for the management of emotional or behavioral problems
that may be linked to the virus or its treatments. Nevertheless, little is
known about this aspect of clinical management. We describe psychotropic drug
therapy and its association with psychiatric symptoms, in HIV+ and HIV–
(control) children and adolescents.
Methods: The study sample consisted of 6- to 17-year-olds,
291 HIV+ and 246 controls, enrolled in Pediatric AIDS Clinical
Trials Group (PACTG) 1055, a prospective, observational study of psychiatric
symptoms. Youth and their primary caregivers completed Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) -referenced
rating scales (ie, Child and Adolescent Symptom Inventories—4) for their and their
children’s symptoms. Screening cut-off scores were computed for
attention-deficit or hyperactivity disorder, generalized anxiety disorder, major
depression, and dysthymia. Lifetime psychotropic drug therapy and ART histories
were obtained.
Results: Overall, 93 (17%) participants had received at
least 1 psychotropic drug therapy during their lifetime: stimulants (13%), neuroleptics (3%), and selective
serotonin reuptake inhibitor (SSRI)
antidepressants (6%). More HIV+ (22%) than controls (11%) were
administered psychotropic drug therapies (OR 2.1, 95%CI 1.3 to 3.4), specifically,
stimulants (p = 0.02) or SSRI (p <0.001). Males were twice as likely
as females to have been treated (OR 2.0, 95%CI 1.2 to 3.2). Of the 478 youth who
self-reported, 28% obtained an screening cut-off score for at least 1 targeted psychiatric
disorder in contrast to 14% of 519 caregiver-reports. Where both reported, youth
showed significantly higher prevalence (29%) than did caregivers (15%, McNemar p <0.001, n = 465) and overall agreement was weak (κ= 0.20, 95%CI 0.10
to 0.29). The odds of receiving psychotropic drug therapy was greater for
youths with caregiver symptom endorsement than for those with only child
self-reports (OR 4.1, 95%CI 1.9 to 8.9). Based on youth self-report, 86% of younger
children (<12 years) and 67% of older children (≥12 years) who obtained
at least 1 screening cut-off score for a psychiatric disorder never received psychotropic
drug therapy but may have received non-medication intervention.
Conclusions: Perinatally HIV-infected children are twice as
likely to be prescribed psychotropic medication as controls. Additional
research on biologic, psychological, and social variables that influence both the
etiology of emotional and behavioral problems and the complex psychiatric
treatment decisions in this clinical population is needed.
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