Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study. Issue 6 (June 2020)
- Record Type:
- Journal Article
- Title:
- Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study. Issue 6 (June 2020)
- Main Title:
- Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease
- Authors:
- Sil, Soumitri
Cohen, Lindsey L.
Bakshi, Nitya
Watt, Amanda
Hathaway, Morgan
Abudulai, Farida
Dampier, Carlton - Abstract:
- 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 ( P s<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 depressiveAbstract : 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 ( P s<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. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- Clinical journal of pain. Volume 36:Issue 6(2020)
- Journal:
- Clinical journal of pain
- Issue:
- Volume 36:Issue 6(2020)
- Issue Display:
- Volume 36, Issue 6 (2020)
- Year:
- 2020
- Volume:
- 36
- Issue:
- 6
- Issue Sort Value:
- 2020-0036-0006-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-06
- Subjects:
- sickle cell disease -- chronic pain -- pediatric -- biopsychosocial -- longitudinal
Pain -- Periodicals
Pain -- Treatment -- Periodicals
Analgesia -- Periodicals
616.047205 - Journal URLs:
- http://journals.lww.com/clinicalpain/pages/default.aspx ↗
http://ovidsp.tx.ovid.com/sp-3.8.1a/ovidweb.cgi?&S=KBIDFPKNAEDDLKHNNCOKIBOBIMNEAA00&Browse=Toc+Children%7cNO%7cS.sh.2.14.27%7c629%7c50 ↗
http://www.clinicalpain.com ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/AJP.0000000000000827 ↗
- Languages:
- English
- ISSNs:
- 0749-8047
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.294200
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- 13761.xml