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Dive into the research topics where Rebecca H. Bitsko is active.

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Featured researches published by Rebecca H. Bitsko.


American Journal of Epidemiology | 2009

Control Selection and Participation in an Ongoing, Population-based, Case-Control Study of Birth Defects The National Birth Defects Prevention Study

Mary E. Cogswell; Rebecca H. Bitsko; Marlene Anderka; Alissa R. Caton; Marcia L. Feldkamp; Stacey M. Hockett Sherlock; Robert E. Meyer; Tunu A. Ramadhani; James M. Robbins; Gary M. Shaw; T. J. Mathews; Marjorie Royle; Jennita Reefhuis

To evaluate the representativeness of controls in an ongoing, population-based, case-control study of birth defects in 10 centers across the United States, researchers compared 1997-2003 birth certificate data linked to selected controls (n = 6,681) and control participants (n = 4,395) with those from their base populations (n = 2,468,697). Researchers analyzed differences in population characteristics (e.g., percentage of births at > or =2,500 g) for each group. Compared with their base populations, control participants did not differ in distributions of maternal or paternal age, previous livebirths, maternal smoking, or diabetes, but they did differ in other maternal (i.e., race/ethnicity, education, entry into prenatal care) and infant (i.e., birth weight, gestational age, and plurality) characteristics. Differences in distributions of maternal, but not infant, characteristics were associated with participation by selected controls. Absolute differences in infant characteristics for the base population versus control participants were < or =1.3 percentage points. Differences in infant characteristics were greater at centers that selected controls from hospitals compared with centers that selected controls from electronic birth certificates. These findings suggest that control participants in the National Birth Defects Prevention Study generally are representative of their base populations. Hospital-based control selection may slightly underascertain infants affected by certain adverse birth outcomes.


American Journal of Obstetrics and Gynecology | 2010

Mental health and access to services among US women of reproductive age

Sherry L. Farr; Rebecca H. Bitsko; Donald K. Hayes; Patricia M. Dietz

OBJECTIVE The objective of the study was to estimate prevalence of depression and serious psychological distress (SPD) and mental health service receipt among reproductive-age women. STUDY DESIGN We used 2006-2007 nationally representative data to estimate the prevalence of depression and SPD among nonpregnant women aged 18 to 44 years. Using logistic regression, we individually examined predictors of depression and SPD and characteristics associated with clinical diagnosis and current treatment. RESULTS More than 14% of women had current depression and 2.7% had current SPD. Risk factors for major depression and SPD included older age, less education, being unmarried, inability to work/unemployed, and low income. Among depressed women, 18-24 year-olds, nonwhite women, those with children, the employed, and urban women had lower odds of clinical diagnosis. Among women with SPD, Hispanic, employed, and those without health insurance had lower odds of receiving treatment. CONCLUSION Mental health conditions are prevalent among women of reproductive age and a substantial proportion goes untreated.


Pediatrics | 2009

Unmet Health Care Needs Among CSHCN With Neurologic Conditions

Rebecca H. Bitsko; Susanna N. Visser; Laura A. Schieve; Danielle S. Ross; David J. Thurman; Ruth Perou

OBJECTIVE Children with neurologic conditions require a variety of services. With this study we examined health care needs and unmet needs among children with neurologic conditions. METHODS Cross-sectional data reported by parents of 3-to 17-year-olds in the 2005–2006 National Survey of Children With Special Health Care Needs were analyzed. Demographic characteristics, health care needs, and unmet needs of children with special health care needs (CSHCN) and neurologic conditions were descriptively compared with an independent referent group of children without special health care needs; statistical contrasts were performed as a function of the type (conditions included in the Diagnostic and Statistical Manual of Mental Disorders [DSM] or not) and number of reported neurologic conditions. RESULTS Compared with the parents of children without special health care needs, parents of CSHCN with neurologic conditions were more likely to report unmet health care needs for their child. After adjustment for demographic factors and severity of functional limitation, CSHCN with at least 2 conditions had more visits to a health care provider, needed more services, and reported more unmet needs than CSHCN with a single DSM condition. The magnitude of need among CSHCN was greatest among those with at least 1 of each type of neurologic condition. CONCLUSIONS Unmet health care needs exist among CSHCN with neurologic conditions and are particularly pronounced among children with a combination of both DSM and non-DSM disorders. The health care needs among CSHCN with multiple neurologic conditions may be better served by targeted efforts to improve care coordination.


JAMA Pediatrics | 2013

Convergent Validity of Parent-Reported Attention-Deficit/Hyperactivity Disorder Diagnosis: A Cross-Study Comparison

Susanna N. Visser; Melissa L. Danielson; Rebecca H. Bitsko; Ruth Perou; Stephen J. Blumberg

Author Contributions: All authors had full access to the data used in analysis and take full responsibility for the integrity and accuracy of the results. Study concept and design: Hanks, Just, and Wansink. Acquisition of data: Hanks and Just. Analysis and interpretation of data: Hanks, Just, and Wansink. Drafting of the manuscript: Hanks, Just, and Wansink. Critical revision of the manuscript for important intellectual content: Hanks, Just, and Wansink. Statistical analysis: Hanks and Just. Obtained funding: Just and Wansink. Administrative, technical, and material support: Wansink. Study supervision: Just and Wansink.


Morbidity and Mortality Weekly Report | 2016

Health Care, Family, and Community Factors Associated with Mental, Behavioral, and Developmental Disorders in Early Childhood - United States, 2011-2012.

Rebecca H. Bitsko

Sociodemographic, health care, family, and community attributes have been associated with increased risk for mental, behavioral, and developmental disorders (MBDDs) in children (1,2). For example, poverty has been shown to have adverse effects on cognitive, socio-emotional, and physical development (1). A safe place to play is needed for gross motor development, and accessible health care is needed for preventive and illness health care (3). Positive parenting and quality preschool interventions have been shown to be associated with prosocial skills, better educational outcomes, and fewer health risk behaviors over time (2). Protective factors for MBDDs are often shared (4) and conditions often co-occur; therefore, CDC considered MBDDs together to facilitate the identification of factors that could inform collaborative, multidisciplinary prevention strategies. To identify specific factors associated with MBDDs among U.S. children aged 2-8 years, parent-reported data from the most recent (2011-2012) National Survey of Childrens Health (NSCH) were analyzed. Factors associated with having any MBDD included inadequate insurance, lacking a medical home, fair or poor parental mental health, difficulties getting by on the familys income, employment difficulties because of child care issues, living in a neighborhood lacking support, living in a neighborhood lacking amenities (e.g., sidewalks, park, recreation center, and library), and living in a neighborhood in poor condition. In a multivariate analysis, fair or poor parental mental health and lacking a medical home were significantly associated with having an MBDD. There was significant variation in the prevalence of these and the other factors by state, suggesting that programs and policies might use collaborative efforts to focus on specific factors. Addressing identified factors might prevent the onset of MBDDs and improve outcomes among children who have one or more of these disorders.


Preventing Chronic Disease | 2013

State-based and demographic variation in parent-reported medication rates for attention-deficit/hyperactivity disorder, 2007-2008.

Susanna N. Visser; Stephen J. Blumberg; Melissa L. Danielson; Rebecca H. Bitsko; Michael D. Kogan

Medication is the most effective treatment of attention-deficit/hyperactivity disorder (ADHD), a common neurobehavioral disorder of childhood. We used data from the 2007-2008 National Survey of Children’s Health to calculate weighted estimates of parent-reported ADHD and medication treatment among US children aged 4 to 17 years, by state and sex-stratified age. State-based rates of ADHD medication treatment ranged from 33% in Nevada to 79% in Mississippi; rates of medicated ADHD were higher among boys than girls at every age. State-based investigations of ADHD medication treatment factors are needed, and our findings may inform these public health efforts.


Depression and Anxiety | 2015

SUICIDAL THOUGHTS AND BEHAVIORS IN CHILDREN AND ADOLESCENTS WITH CHRONIC TIC DISORDERS

Eric A. Storch; Camille E. Hanks; Jonathan W. Mink; Joseph F. McGuire; Heather R. Adams; Erika F. Augustine; Amy Vierhile; Alyssa Thatcher; Rebecca H. Bitsko; Adam B. Lewin; Tanya K. Murphy

Despite evidence of elevated risk factors for suicidal thoughts and behavior in youth with Tourette syndrome and chronic tic disorders (CTD), few studies have actually examined that relationship. This study documented the frequency and clinical correlates of suicidal thoughts and behaviors in a sample of children and adolescents with CTD (N = 196, range 6–18 years old). The content is solely the responsibility of the authors and does not necessarily represent the official views of the Centers for Disease Control.


Journal of Mental Health Research in Intellectual Disabilities | 2012

Does Childhood Disability Increase Risk for Child Abuse and Neglect

Rebecca T. Leeb; Rebecca H. Bitsko; Melissa T. Merrick; Brian S. Armour

In this article we review the empirical evidence for the presumptions that children with disabilities are at increased risk for child maltreatment, and parents with disabilities are more likely to perpetrate child abuse and neglect. Challenges to the epidemiological examination of the prevalence of child maltreatment and disabilities are discussed. We conclude that the evidence for the relationship between child maltreatment victimization of children with disabilities and perpetration by caregivers with disabilities remains equivocal due to variability in research samples, key definitions, and study methodology. Future research examining the link between disability and child maltreatment would benefit from more rigorous methodology and inclusion of a theoretical framework, such as the ecological model of child maltreatment. One potential pathway from disability to child maltreatment is presented. Knowing and understanding the link between disability and child abuse and neglect is an important step toward planning targeted and appropriate prevention and intervention activities.


Birth Defects Research Part A-clinical and Molecular Teratology | 2008

Periconceptional use of weight loss products including ephedra and the association with birth defects.

Rebecca H. Bitsko; Jennita Reefhuis; Carol Louik; Martha M. Werler; Marcia L. Feldkamp; D. Kim Waller; Jaime L. Frías; Margaret A. Honein

BACKGROUND : Weight loss products are frequently used by reproductive-aged women and these products may be taken (inadvertently or intentionally) during pregnancy. This study assessed the association between periconceptional use of weight loss products and major structural birth defects. METHODS : Mothers of infants with birth defects (case infants) and a random sample of livebirths (control infants) born during the period 1998-2003 in 10 states participated in the National Birth Defects Prevention Study. Adjusted ORs (aORs) for the association between self-reported use of weight loss products and 23 categories of birth defects were calculated. RESULTS : Mothers of control infants (2.4%) and 2.6% of mothers of case infants reported periconceptional use of weight loss products; 1.2% of mothers of control infants and 1.3% of mothers of case infants reported using an ephedra-containing product. Use of any weight loss product was associated with anencephaly (aOR 2.6; 95% CI: 1.3-5.3), dextro-transposition of the great arteries (aOR 2.1; 95% CI: 1.1-4.3), and aortic stenosis (aOR 3.4; 95% CI: 1.5-7.9). Use of products containing ephedra showed an increased aOR with anencephaly (aOR 2.8; 95% CI: 1.0-7.3), while other weight loss products were associated with dextro-transposition of the great arteries (aOR 1.8; 95% CI: 1.2-2.7), and aortic stenosis (aOR 2.1; 95% CI: 1.3-3.5). CONCLUSIONS : These results suggest an association between periconceptional use of weight loss products and certain birth defects but the possible mechanism is not clear. This is the first finding of such an association and, because we examined a large number of exposure-outcome associations in a hypothesis-generating analysis, these results might have been due to chance.


Journal of Child Neurology | 2013

Health Care Needs of Children with Tourette Syndrome

Rebecca H. Bitsko; Melissa L. Danielson; Michael King; Susanna N. Visser; Lawrence Scahill; Ruth Perou

To document the impact of Tourette syndrome on the health care needs of children and access to health care among youth with Tourette syndrome, parent-reported data from the 2007-2008 National Survey of Children’s Health were analyzed. Children with Tourette syndrome had more co-occurring mental disorders than children with asthma or children without Tourette syndrome or asthma and had health care needs that were equal to or greater than children with asthma (no Tourette syndrome) or children with neither asthma nor Tourette syndrome. Health care needs were greatest among children with Tourette syndrome and co-occurring mental disorders, and these children were least likely to receive effective care coordination. Addressing co-occurring conditions may improve the health and well-being of children with Tourette syndrome. Strategies such as integration of behavioral health and primary care may be needed to improve care coordination.

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Joseph R. Holbrook

Centers for Disease Control and Prevention

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Melissa L. Danielson

Centers for Disease Control and Prevention

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Susanna N. Visser

Centers for Disease Control and Prevention

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Stephen J. Blumberg

Centers for Disease Control and Prevention

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Ruth Perou

Centers for Disease Control and Prevention

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Reem M. Ghandour

United States Department of Health and Human Services

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Laura A. Schieve

Centers for Disease Control and Prevention

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Adam B. Lewin

University of South Florida

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