Literature DB >> 1592957

Sickle cell disease pain: 2. Predicting health care use and activity level at 9-month follow-up.

K M Gil1, M R Abrams, G Phillips, D A Williams.   

Abstract

This study examined 9-month follow-up data obtained from adults with sickle cell disease (SCD) participating in a longitudinal study of pain-coping strategies. Of 99 subjects completing the baseline assessment of pain-coping strategies, 89 (90%) completed a structured pain interview assessing health care use and activity reduction during painful episodes over the follow-up period. Regression analyses controlling for demographics and disease severity revealed that baseline Negative Thinking and Passive Adherence was associated with greater activity reduction and more frequent health care contacts during the subsequent 9 months. Additional correlational analyses revealed that if levels of Negative Thinking and Passive Adherence increased from baseline to follow-up, this increase was associated with even further reductions in activity level during painful episodes. Changes in disease severity were not associated with any of the follow-up measures. Comparing pain-coping strategies assessed at baseline to pain-coping strategies measured at follow-up revealed that, without intervention, pain-coping strategies were relatively stable over time.

Entities:  

Mesh:

Year:  1992        PMID: 1592957     DOI: 10.1037//0022-006x.60.2.267

Source DB:  PubMed          Journal:  J Consult Clin Psychol        ISSN: 0022-006X


  18 in total

1.  Awareness and identification of athletes with sickle cell disorders at historically black colleges and universities.

Authors:  J D Jones; D M Kleiner
Journal:  J Athl Train       Date:  1996-07       Impact factor: 2.860

2.  Health status in sickle cell disease: examining the roles of pain coping strategies, somatic awareness, and negative affectivity.

Authors:  J D McCrae; M A Lumley
Journal:  J Behav Med       Date:  1998-02

3.  Pain and stress in sickle cell disease: an analysis of daily pain records.

Authors:  L S Porter; K M Gil; J A Sedway; J Ready; E Workman; R J Thompson
Journal:  Int J Behav Med       Date:  1998

4.  Predictive Ability of Intermittent Daily Sickle Cell Pain Assessment: The PiSCES Project.

Authors:  Wally R Smith; Donna K McClish; James Levenson; Imoigele Aisiku; Bassam Dahman; Viktor E Bovbjerg; Susan Roseff; John Roberts
Journal:  Pain Med       Date:  2018-10-01       Impact factor: 3.750

5.  Health-related quality of life and adaptive behaviors of adolescents with sickle cell disease: stress processing moderators.

Authors:  Maisa S Ziadni; Chavis A Patterson; Elizabeth R Pulgarón; M Renée Robinson; Lamia P Barakat
Journal:  J Clin Psychol Med Settings       Date:  2011-12

6.  Interventional pain medicine: retreat from the biopsychosocial model of pain.

Authors:  Randy S Roth; Michael E Geisser; David A Williams
Journal:  Transl Behav Med       Date:  2012-03       Impact factor: 3.046

7.  Respect, trust, and the management of sickle cell disease pain in hospital: comparative analysis of concern-raising behaviors, preliminary model, and agenda for international collaborative research to inform practice.

Authors:  James Elander; Mary Catherine Beach; Carlton Haywood
Journal:  Ethn Health       Date:  2011 Aug-Oct       Impact factor: 2.772

Review 8.  Sickle Cell Disease: A Review of Nonpharmacological Approaches for Pain.

Authors:  Hants Williams; Paula Tanabe
Journal:  J Pain Symptom Manage       Date:  2015-11-17       Impact factor: 3.612

9.  Psychosocial factors and adjustment to chronic pain in spinal cord injury: replication and cross-validation.

Authors:  Ivan R Molton; Brenda L Stoelb; Mark P Jensen; Dawn M Ehde; Katherine A Raichle; Diana D Cardenas
Journal:  J Rehabil Res Dev       Date:  2009

10.  Parental report of health-related quality of life in children with sickle cell disease.

Authors:  Tonya Mizell Palermo; Lisa Schwartz; Dennis Drotar; Kathryn McGowan
Journal:  J Behav Med       Date:  2002-06
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