Journal of the American Academy of Child & Adolescent Psychiatry
New researchTrends in Serious Emotional Disturbance Among Youths Exposed to Hurricane Katrina
Section snippets
Sample
We recruited English-speaking adults (≥18 years of age) for the initial survey either by random-digit–dial telephone calls of households in the FEMA-defined disaster area or from a random selection of families applying for assistance from the American Red Cross database. The initial CAG interviews were carried out in three waves (Table 1). The first wave was collected 5 to 7 months after the hurricane (n = 1,043; 41.9% cooperation rate); the second wave was carried out 7 to 10 months
Estimated prevalence and trends in SED
The estimated prevalence of SED decreased significantly from 15.1% at the baseline survey (18-27 months post-hurricane) to 11.5% at the follow-up survey (36-39 months post-hurricane) (t = 2.1, p = .03). (Table 2) The estimated prevalence of H-SED decreased from baseline (9.3%) to the follow-up (7.5%). A similar decrease was observed for the estimated prevalence of NH-SED (5.7% and 4.1%, respectively), although this decrease was not statistically significant for either H-SED or NH-SED.
Discussion
The estimated prevalence of SED among children and adolescents exposed to Hurricane Katrina decreased significantly from 15.1% at our baseline assessment 18 to 27 months after the storm to 11.5% at our assessment 12 to 18 months later. This reduction is not surprising, given that the prevalence of youth mental health problems following natural disasters tends to decrease over time.6, 17 However, the prevalence of SED among youths exposed to Katrina continues to be considerably greater than the
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This study is supported by National Institutes of Health (NIH) Research Grants R01 MH070884-01A2 and R01 MH081832 from the US Department of Health and Human Services, NIH, the Office of the Assistant Secretary of Planning and Evaluation, the Federal Emergency Management Agency, and the Administration for Children and Families.
Supplemental material cited in this article is available online.
Disclosure: Dr. Kessler has served as a consultant for GlaxoSmithKline, Inc., Kaiser Permanente, Pfizer Inc., Sanofi-Aventis, Shire Pharmaceuticals, and Wyeth-Ayerst. He has served on the advisory boards for Eli Lilly and Co., and Wyeth-Ayerst. He has received research support from Bristol-Myers Squibb, Eli Lilly and Co., GlaxoSmithKline, Inc., Johnson and Johnson Pharmaceuticals, Ortho-McNeil Pharmaceuticals, Inc., Pfizer Inc., and Sanofi-Aventis. Drs. McLaughlin, Fairbank, Jones, Osofsky, and Pfefferbaum, and Mr. Gruber, and Mrs. Sampson report no biomedical financial interests or potential conflicts of interest.