Literature DB >> 32287106

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

Soumitri Sil1,2, Lindsey L Cohen2,3, Nitya Bakshi1,2, Amanda Watt2, Morgan Hathaway2, Farida Abudulai2, Carlton Dampier1,2.   

Abstract

OBJECTIVES: This study aimed to: (1) examine changes in pain, psychosocial functioning, and health care utilization among children and adolescents with sickle cell disease (SCD) over a 2-year period and (2) identify baseline biopsychosocial variables associated with the development and maintenance of chronic SCD pain at follow-up.
MATERIALS AND METHODS: Forty-two youth (8 to 18 y old) with SCD completed a battery of self-report measures at baseline and 2-year follow-up. Analgesic, Anesthetic, and Addiction Clinical Trial Translational Innovations Opportunities and Networks and American Pain Society Pain Taxonomy (AAPT) diagnostic criteria were used to categorize patients into pain frequency groups at both timepoints: chronic (pain on most [≥15] d/mo for the past 6 mo, per AAPT diagnostic criteria), episodic (pain on 1 to 14 d/mo), or asymptomatic (0 d/mo).
RESULTS: At baseline, 31% (n=13) had chronic pain, 50% (n=21) episodic pain, and 19% (n=8) were asymptomatic. At follow-up, 40.5% (n=17) had chronic pain, 52.4% (n=22) episodic pain, and 7.1% (n=3) were asymptomatic. Between baseline and 2-year follow-up, 12% (n=5) developed chronic SCD pain. Depressive symptoms and admissions for pain significantly increased over time for youth with chronic pain (Ps<0.05). An interaction effect revealed that baseline pain groups differed in their change in pain intensity over time (P<0.01). Baseline psychosocial factors (ie, higher functional disability, greater depressive symptoms, higher pain catastrophizing, and lower quality of life) were significantly associated with chronic pain at follow-up. DISCUSSION: Biopsychosocial factors may be associated with the development and maintenance of chronic SCD pain and their relative contributions warrant further study.

Entities:  

Year:  2020        PMID: 32287106      PMCID: PMC7233325          DOI: 10.1097/AJP.0000000000000827

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


  53 in total

1.  Peer relationships and emotional well-being of youngsters with sickle cell disease.

Authors:  R B Noll; K Vannatta; K Koontz; K Kalinyak; W M Bukowski; W H Davies
Journal:  Child Dev       Date:  1996-04

2.  Child and Family Antecedents of Pain During the Transition to Adolescence: A Longitudinal Population-Based Study.

Authors:  Emily Incledon; Meredith O'Connor; Rebecca Giallo; George A Chalkiadis; Tonya M Palermo
Journal:  J Pain       Date:  2016-08-04       Impact factor: 5.820

3.  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

4.  Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell disease.

Authors:  Cheryl A Hillery; Patrick C Kerstein; Daniel Vilceanu; Marie E Barabas; Dawn Retherford; Amanda M Brandow; Nancy J Wandersee; Cheryl L Stucky
Journal:  Blood       Date:  2011-06-27       Impact factor: 22.113

5.  The cost of health care for children and adults with sickle cell disease.

Authors:  Teresa L Kauf; Thomas D Coates; Liu Huazhi; Nikita Mody-Patel; Abraham G Hartzema
Journal:  Am J Hematol       Date:  2009-06       Impact factor: 10.047

6.  Pediatric Sickle Cell Disease and Parent and Child Catastrophizing.

Authors:  Soumitri Sil; Carlton Dampier; Lindsey L Cohen
Journal:  J Pain       Date:  2016-06-03       Impact factor: 5.820

7.  The child version of the pain catastrophizing scale (PCS-C): a preliminary validation.

Authors:  Geert Crombez; Patricia Bijttebier; Chris Eccleston; Tamara Mascagni; Gustaaf Mertens; Liesbet Goubert; Katrien Verstraeten
Journal:  Pain       Date:  2003-08       Impact factor: 6.961

8.  Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease.

Authors:  Bryce B Reeve; Lloyd J Edwards; Byron C Jaeger; Pamela S Hinds; Carlton Dampier; Debbie S Gipson; David T Selewski; Jonathan P Troost; David Thissen; Vaughn Barry; Heather E Gross; Darren A DeWalt
Journal:  Qual Life Res       Date:  2017-09-07       Impact factor: 4.147

9.  Trajectories of pain in adolescents: a prospective cohort study.

Authors:  Kate M Dunn; Kelvin P Jordan; Lloyd Mancl; Mark T Drangsholt; Linda Le Resche
Journal:  Pain       Date:  2010-10-23       Impact factor: 7.926

10.  Depression and quality of life in children with sickle cell disease: the effect of social support.

Authors:  Mohammad Gamal Sehlo; Hayat Zakaria Kamfar
Journal:  BMC Psychiatry       Date:  2015-04-11       Impact factor: 3.630

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  1 in total

1.  Caregivers' experience of seeking care for adolescents with sickle cell disease in a tertiary care hospital in Bahrain.

Authors:  Khadija Al Saif; Fatema Mohamed Abdulla; Anwaar Alrahim; Sara Abduljawad; Zainab Matrook; Jenan Jaafar Abdulla; Fatima Bughamar; Fatema Alasfoor; Rana Taqi; Amna Almarzooq; Jamil Ahmed
Journal:  PLoS One       Date:  2022-04-07       Impact factor: 3.240

  1 in total

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