Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease-Reference-Cited by-同舟云学术

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Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease

Published:2020-04-13 Issue:6 Volume:36 Page:463-471
ISSN:0749-8047
Container-title:The Clinical Journal of Pain
language:en
Short-container-title:

Author:

Sil Soumitri,Cohen Lindsey L.,Bakshi Nitya,Watt Amanda,Hathaway Morgan,Abudulai Farida,Dampier Carlton

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine,Clinical Neurology

Reference58 articles.

1. Health-related quality of life in children with sickle cell disease: a report from the Comprehensive Sickle Cell Centers Clinical Trial Consortium;Dampier;Pediatr Blood Cancer,2010

2. Acute care utilization and rehospitalizations for sickle cell disease;Brousseau;JAMA,2010

3. The cost of health care for children and adults with sickle cell disease;Kauf;Am J Hematol,2009

4. Characteristics of pain managed at home in children and adolescents with sickle cell disease by using diary self-reports;Dampier;J Pain,2002

5. Daily assessment of pain in adults with sickle cell disease;Smith;Ann Intern Med,2008

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1. Unmet Need: Mechanistic and Translational Studies of Sickle Cell Disease Pain as a Whole-Person Health Challenge;The Journal of Pain;2024-10

2. The medication usage pattern and prevalence of polypharmacy among patients with sickle cell disease: a population-based study in southern Iran;Expert Review of Hematology;2024-07-29

3. A Systemic Review of the Psychosocial Aspects of Chronic Pain in Youth With Sickle Cell Disease;Pain Management Nursing;2024-06

4. Investigating home‐based opioid use among youth with sickle cell disease using ecological momentary assessment;Pediatric Blood & Cancer;2024-05-27

5. Pain screening in youth with sickle cell disease: A quality improvement study;Pediatric Blood & Cancer;2024-02-13

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