Literature DB >> 33723587

Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease: A Preliminary Investigation.

Megan M Miller1, Deanna D Rumble2, Adam T Hirsh1, Tine Vervoort3, Lori E Crosby4, Avi Madan-Swain5, Jeffrey Lebensburger5, Anna M Hood6, Zina Trost7.   

Abstract

OBJECTIVES: Sickle cell disease (SCD) is a genetic disorder that affects approximately 100,000 Americans, the majority of whom are African American. SCD-related pain often has deleterious effects on functioning and quality of life. The inherited nature of SCD, SCD-related stigma, and serious physical and functional impact of SCD-related pain create a situation ripe for individuals to appraise their SCD-related pain as unfair or unjust. The aim of this preliminary investigation is to explore the extent to which pediatric patients with SCD appraise their pain as unjust and how these appraisals relate to functioning.
METHODS: Participants were youth with SCD (N = 30, mean age = 11.3, 57% boys) who attended a hematology clinic visit. Patients were invited to complete paper-based questionnaires assessing pain-related injustice appraisals, pain catastrophizing, pain and hurt, functional disability, depression, anxiety, and peer relationships.
RESULTS: Results of hierarchical regressions indicate that pain-related injustice significantly predicted functional disability, depression, and anxiety after controlling for patient pain and catastrophizing.
CONCLUSIONS: These findings suggest that pain-related injustice appraisals are an important contributor to the pain experience of youth with SCD. Early identification and remediation of pain-related injustice appraisals could have long-term functional benefits for youth with SCD.
© The Author(s) 2021. Published by Oxford University Press on behalf of the American Academy of Pain Medicine. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Anxiety; Depression; Functioning; Sickle Cell; Youth;  Injustice

Mesh:

Year:  2021        PMID: 33723587      PMCID: PMC8677454          DOI: 10.1093/pm/pnab001

Source DB:  PubMed          Journal:  Pain Med        ISSN: 1526-2375            Impact factor:   3.750


  83 in total

1.  It's not fair: an Interpretative Phenomenological Analysis of discourses of justice and fairness in chronic pain.

Authors:  Joanna L McParland; Christopher Eccleston; Mike Osborn; Louisa Hezseltine
Journal:  Health (London)       Date:  2010-12-15

2.  Longitudinal relationships of depressive symptoms to pain intensity and functional disability among children with disease-related pain.

Authors:  Ahna L Hoff; Tonya M Palermo; Mark Schluchter; Kathy Zebracki; Dennis Drotar
Journal:  J Pediatr Psychol       Date:  2005-09-08

3.  Racism and Health-Related Quality of Life in Pediatric Sickle Cell Disease: Roles of Depression and Support.

Authors:  Ifigenia Mougianis; Lindsey L Cohen; Sarah Martin; Caitlin Shneider; Meredith Bishop
Journal:  J Pediatr Psychol       Date:  2020-09-01

Review 4.  Sickle cell disease.

Authors:  P A Lane
Journal:  Pediatr Clin North Am       Date:  1996-06       Impact factor: 3.278

Review 5.  History and current status of newborn screening for hemoglobinopathies.

Authors:  Jane M Benson; Bradford L Therrell
Journal:  Semin Perinatol       Date:  2010-04       Impact factor: 3.300

6.  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

7.  Pain catastrophizing in children with chronic pain and their parents: proposed clinical reference points and reexamination of the Pain Catastrophizing Scale measure.

Authors:  Melissa Pielech; Maggie Ryan; Deirdre Logan; Karen Kaczynski; Matthew T White; Laura E Simons
Journal:  Pain       Date:  2014-08-29       Impact factor: 6.961

8.  Clinical utility and validity of the Functional Disability Inventory among a multicenter sample of youth with chronic pain.

Authors:  Susmita Kashikar-Zuck; Stacy R Flowers; Robyn Lewis Claar; Jessica W Guite; Deirdre E Logan; Anne M Lynch-Jordan; Tonya M Palermo; Anna C Wilson
Journal:  Pain       Date:  2011-03-31       Impact factor: 6.961

9.  Parent perceptions of adolescent pain expression: the adolescent pain behavior questionnaire.

Authors:  Anne M Lynch-Jordan; Susmita Kashikar-Zuck; Kenneth R Goldschneider
Journal:  Pain       Date:  2010-10-18       Impact factor: 6.961

10.  PROMIS(®) pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions.

Authors:  Darren A DeWalt; Heather E Gross; Debbie S Gipson; David T Selewski; Esi Morgan DeWitt; Carlton D Dampier; Pamela S Hinds; I-Chan Huang; David Thissen; James W Varni
Journal:  Qual Life Res       Date:  2015-02-26       Impact factor: 4.147

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  1 in total

1.  Mechanisms of injustice: what we (do not) know about racialized disparities in pain.

Authors:  Vani A Mathur; Zina Trost; Miriam O Ezenwa; John A Sturgeon; Anna M Hood
Journal:  Pain       Date:  2021-11-01       Impact factor: 7.926

  1 in total

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