Pediatric pain screening identifies youth at risk of chronic pain in sickle cell disease
Author:
Affiliation:
1. Department of Pediatrics; Aflac Cancer and Blood Disorders Center; Emory University School of Medicine; Atlanta Georgia
2. Children's Healthcare of Atlanta; Atlanta Georgia
3. Department of Psychology; Georgia State University; Atlanta Georgia
Funder
National Center for Advancing Translational Sciences
National Heart, Lung, and Blood Institute
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.27538/fullpdf
Reference35 articles.
1. Characteristics of pain managed at home in children and adolescents with sickle cell disease by using diary self-reports;Dampier;J Pain,2002
2. Home management of sickle cell-related pain in children and adolescents: natural history and impact on school attendance;Shapiro;Pain,1995
3. Validation of the sickle cell disease pain burden interview-youth;Zempsky;J Pain,2013
4. Psychosocial and functional outcomes in youth with chronic sickle cell pain;Sil;Clin J Pain,2016
5. AAPT diagnostic criteria for chronic sickle cell disease pain;Dampier;J Pain,2017
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2. Feasibility and preliminary efficacy of the Balance Program to reduce pain‐related disability in pediatric sickle cell disease;Pediatric Blood & Cancer;2023-09-19
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4. Vaso-occlusive crisis pain intensity, frequency, and duration: which best correlates with health-related quality of life in adolescents and adults with sickle cell disease?;Pain;2023-08-11
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