Google
Trusted Resources: Evidence & Education
Scientific literature and patient education texts
Sleep Problem Risk for Adolescents With Sickle Cell Disease: Sociodemographic, Physical, and Disease-Related Correlates
source: Journal of Pediatric Hematology/Oncology
year: 2018
authors: Valrie CR, Trout KL, Bond KE, Ladd RJ, Huber NL, Alston KJ, Sufrinko AM, Everhart E, Fuh BR
summary/abstract:The aims of the current study were to investigate whether SCD incurs an additional risk for poor sleep over and above the influence of sociodemographic factors (ie, race and sex) during adolescence, and to explore the relationships between sociodemographic, physical (ie, age and pubertal status), and disease-related factors (ie, SCD genotype and hydroxyurea use) on sleep problem risk during adolescence.
Black adolescents (age, 12 to 17 y) with SCD (n=53) were recruited from regional pediatric SCD clinics in the southeast and a sample of healthy black adolescents (n=160) were recruited from middle and high schools. Regression analyses indicated that SCD was uniquely related to sleeping more, and worse sleep quality over and above the influence of sociodemographic factors. Having a more severe SCD genotype was related to worse sleep quality and higher pubertal status was related to sleeping longer during the week. Results indicate the need for systematic assessments of sleep problems, with more a focus on youth with more severe genotypes and higher pubertal status.
Future research should focus on characterizing trajectories of sleep problems in this population, identifying key risk factors, and elucidating mechanisms linking risk factors to sleep problem risk to aid in tailoring interventions for this population.
organization: Virginia Commonwealth University, USA; University of Nebraska Medical Center, USA; Medical University of South Carolina, USA; University of Mississippi Medical Center, USA; University of Pittsburgh Medical Center, USA; Pediatrics, East Carolina University, USADOI: 10.1097/MPH.0000000000001067
read more full text
+myBinderRelated Content
-
Sickle Cell Treatment ‘Life-Changing’ for Brockton BrothersEmmanuel “Manny” Johnson, 21, of Bro...
-
Rare patients with sickle cell disease live nearly twice national averageWith a national median life expectancy o...
-
Today’s Faces of Sickle Cell Disease: Marjorie DeJoie-Brewer, MDIt wasn’t until her second year in med...
-
Predictive factors of daily opioid use and quality of life in adults with sickle cell diseaseObjectives: In adults with sickle cell ...
-
Billy Garrett Jr. Chases Dream in the G LeagueOn a frigid New York Friday evening in F...
-
Brandi Abernethy: Nursing Student, Patient, Single MomWhen she was growing up in St. Petersbur...
-
Implementation of an Educational Intervention to Optimize Self-Management and Transition Readiness in Young Adults W...Background: The transition from the ped...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.