Literature DB >> 26379074

Psychosocial and Functional Outcomes in Youth With Chronic Sickle Cell Pain.

Soumitri Sil1, Lindsey L Cohen, Carlton Dampier.   

Abstract

OBJECTIVE: To describe chronic pain-pain that is present most days per month over the past 3 months-in youth with sickle cell disease (SCD). This study characterized differences in functional outcomes, psychosocial characteristics, and health care utilization for youth with SCD across 3 groups based on pain frequency: chronic pain, episodic pain, and no SCD pain in the past month.
MATERIALS AND METHODS: Children and adolescents (aged 8 to 18 y) with SCD and their parents (n=100) completed measures of functional disability, health-related quality of life, depressive symptoms, pain catastrophizing, pain beliefs, and health care utilization during an outpatient comprehensive sickle cell clinic appointment. On the basis of pain frequency and duration, patients were categorized as follows: (1) chronic (≥3 d of pain per week in the past month lasting ≥3 mo; range, 12 to 31 d/mo), (2) episodic (<3 d of pain per week for the past month; range, 1 to 10 d/mo), and (3) no SCD pain in the past month.
RESULTS: Consistent with other pediatric chronic pain conditions, youth characterized as having chronic sickle pain (n=40) reported significantly greater functional disability, depressive symptoms, and inpatient admissions for pain relative to patients characterized with having episodic SCD pain (n=40) or no SCD pain (n=20). The chronic and episodic pain groups had comparable levels of pain intensity, pain catastrophizing, and quality of life. DISCUSSION: Specific definitions and criteria for chronic sickle pain in youth are needed. Identifying risk and protective factors related to the transition from acute to chronic pain is important to facilitate improved psychosocial functioning.

Entities:  

Mesh:

Year:  2016        PMID: 26379074     DOI: 10.1097/AJP.0000000000000289

Source DB:  PubMed          Journal:  Clin J Pain        ISSN: 0749-8047            Impact factor:   3.442


  32 in total

1.  American Society of Hematology 2020 guidelines for sickle cell disease: management of acute and chronic pain.

Authors:  Amanda M Brandow; C Patrick Carroll; Susan Creary; Ronisha Edwards-Elliott; Jeffrey Glassberg; Robert W Hurley; Abdullah Kutlar; Mohamed Seisa; Jennifer Stinson; John J Strouse; Fouza Yusuf; William Zempsky; Eddy Lang
Journal:  Blood Adv       Date:  2020-06-23

Review 2.  Psychological Predictors of Pain in Children and Adolescents With Sickle Cell Disease: A Scoping Review.

Authors:  Clare Donohoe; Ellen Lavoie Smith
Journal:  J Pediatr Oncol Nurs       Date:  2018-12-19       Impact factor: 1.636

3.  Feasibility and Acceptability of Internet-delivered Cognitive Behavioral Therapy for Chronic Pain in Adolescents With Sickle Cell Disease and Their Parents.

Authors:  Tonya M Palermo; Joanne Dudeney; James P Santanelli; Alexie Carletti; William T Zempsky
Journal:  J Pediatr Hematol Oncol       Date:  2018-03       Impact factor: 1.289

4.  Parent pain catastrophizing predicts child depressive symptoms in youth with sickle cell disease.

Authors:  Alana Goldstein-Leever; Lindsey L Cohen; Carlton Dampier; Soumitri Sil
Journal:  Pediatr Blood Cancer       Date:  2018-03-07       Impact factor: 3.167

5.  iCanCope with Sickle Cell Pain: Design of a randomized controlled trial of a smartphone and web-based pain self-management program for youth with sickle cell disease.

Authors:  Tonya M Palermo; William T Zempsky; Carlton D Dampier; Chitra Lalloo; Amos S Hundert; Lexa K Murphy; Nitya Bakshi; Jennifer N Stinson
Journal:  Contemp Clin Trials       Date:  2018-10-11       Impact factor: 2.226

Review 6.  Optimizing the care model for an uncomplicated acute pain episode in sickle cell disease.

Authors:  Paul Telfer; Banu Kaya
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

7.  Executive Functioning Mediates the Relationship Between Pain Coping and Quality of Life in Youth With Sickle Cell Disease.

Authors:  Natasha N Ludwig; Soumitri Sil; Meena K Khowaja; Lindsey L Cohen; Carlton Dampier
Journal:  J Pediatr Psychol       Date:  2018-11-01

8.  Systematic Review: Pain and Emotional Functioning in Pediatric Sickle Cell Disease.

Authors:  Steven K Reader; Laura M Rockman; Katherine M Okonak; Nicole M Ruppe; Colleen N Keeler; Anne E Kazak
Journal:  J Clin Psychol Med Settings       Date:  2020-06

9.  Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study.

Authors:  Soumitri Sil; Lindsey L Cohen; Nitya Bakshi; Amanda Watt; Morgan Hathaway; Farida Abudulai; Carlton Dampier
Journal:  Clin J Pain       Date:  2020-06       Impact factor: 3.442

Review 10.  Key Components of Pain Management for Children and Adults with Sickle Cell Disease.

Authors:  Amanda M Brandow; Michael R DeBaun
Journal:  Hematol Oncol Clin North Am       Date:  2018-06       Impact factor: 3.722

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