Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Cecelia R Valrie"'
Publikováno v:
Frontiers in Pain Research, Vol 4 (2023)
Sickle cell disease (SCD) is a prevalent and complex inherited pain disorder that can manifest as acute vaso-occlusive crises (VOC) and/or chronic pain. Despite their known risks, opioids are often prescribed routinely and indiscriminately in managin
Externí odkaz:
https://doaj.org/article/d956465d83694b469465d90e21e58467
Autor:
Cynthia W Karlson, Kimberly G Barajas, Samantha R Seals, Anna B Britt, Alyssa M Schlenz, Erin A Jackson, Dereck B Davis, Matthew C Morris, Cecelia R Valrie
Publikováno v:
Journal of Pediatric Psychology.
Objective Despite the identified pathophysiology of vaso-occlusive pain in sickle cell disease (SCD), predictors of pain in youth with SCD remain elusive. In this study, we measured changes in pain frequency, intensity, and interference over 1 year a
Autor:
Cecelia R. Valrie, Kristen Alston, Krystal Morgan, Rebecca Kilpatrick, India Sisler, Beng Fuh
Publikováno v:
Health Psychol
The current study investigated the role of affect in the daily sleep quality-pain severity relationship in youth with sickle cell disease (SCD). Previous investigations have not allowed researchers to examine whether positive and negative affect work
Publikováno v:
Journal of Pediatric Psychology
This introduction to the special issue on Addressing Health Disparities in Pediatric Psychology provides context for why this special issue is needed, reviews key findings of the accepted articles, and discusses future directions for advancing the fi
Autor:
David W. Sosnowski, Cecelia R. Valrie, Ananda B. Amstadter, Zewelanji Serpell, Marcia A. Winter, Wendy Kliewer
Publikováno v:
Child Development. 92:746-759
Childhood adversity is linked to shortened telomere length (TL), but behavioral indicators of telomere attrition remain unclear. This study examined the association between adverse childhood experiences (ACEs) and child TL, and if ACEs were indirectl
Publikováno v:
Journal of Pain Research. 13:729-736
Purpose Youth with sickle cell disease (SCD), a genetic disorder of red blood cells, may experience acute pain episodes lasting 2 to 3 days on average. While existing research has demonstrated associations between SCD pain and poor social functioning
Autor:
Tiffany L. Green, Nao Hagiwara, Rosalie Corona, Jelaina Shipman, Shawn Valiani, Tatiana Kohlmann, Cecelia R. Valrie
Publikováno v:
J Racial Ethn Health Disparities
INTRODUCTION: A growing literature documents the associations between discrimination and health. Emerging evidence suggests that among Hispanic/Latinx immigrants, discrimination leads to the deterioration of health outcomes over time. While sleep has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b87f556a20f92d6aa7fe860f0986761f
https://europepmc.org/articles/PMC10168626/
https://europepmc.org/articles/PMC10168626/
Autor:
Rebecca L. Kilpatrick, Beng Fuh, Kristen J. Alston, Cecelia R. Valrie, India Sisler, Krystal L. Trout, Rupa Redding-Lallinger
Publikováno v:
Journal of Pediatric Psychology. 44:323-332
Objectives The current study utilized mHealth technologies that were objective (e.g., sleep actigraphy and pulse oximetry) and time-sensitive (e.g., ecological momentary assessments [EMAs]) to characterize sleep in youth with sickle cell disease (SCD
Autor:
Erik Everhart, Alicia Sufrinko, Cecelia R. Valrie, Nichelle L. Huber, Kayzandra E. Bond, Rebecca J. Ladd, Beng Fuh, Kristen J. Alston, Krystal L. Trout
Publikováno v:
Journal of Pediatric Hematology/Oncology. 40:116-121
The aims of the current study were to investigate whether SCD incurs an additional risk for poor sleep over and above the influence of socio-demographic factors (i.e., race and sex) during adolescence, and to explore the relationships between socio-d
Sleep Moderating the Relationship Between Pain and Health Care Use in Youth With Sickle Cell Disease
Publikováno v:
Clin J Pain
Objectives The purpose of the current study was to investigate the influence of sleep on the relationship between pain and health care use (HCU) in youth with sickle cell disease (SCD). It was hypothesized that poor sleep would be related to higher H