Literature DB >> 3375880

Assessment of psychosocial functioning of patients with sickle cell disease.

D H Barrett1, I E Wisotzek, G G Abel, J L Rouleau, A F Platt, W E Pollard, J R Eckman.   

Abstract

The Chronic Illness Problem Inventory (CIPI) was used to assess level of psychosocial functioning in 89 patients with sickle cell disease. The results indicated that sickle cell patients have significant psychosocial distress in the areas of employment and finances, sleeping and eating, and performance of normal daily activities. Fear and anxiety regarding body deterioration, and lack of assertiveness in social relationships were also found. These findings suggest that depression may be a common problem among sickle cell patients. Treatment alternatives that address these areas are reviewed.

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Year:  1988        PMID: 3375880     DOI: 10.1097/00007611-198806000-00015

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  8 in total

1.  A biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease.

Authors:  Lou Ella V Taylor; Nancy A Stotts; Janice Humphreys; Marsha J Treadwell; Christine Miaskowski
Journal:  Pain Manag Nurs       Date:  2011-12-14       Impact factor: 1.929

2.  Paradigms and politics: shaping health care access for sickle cell patients through the discursive regimes of biomedicine.

Authors:  Carolyn Moxley Rouse
Journal:  Cult Med Psychiatry       Date:  2004-09

3.  Depression and functioning in relation to health care use in sickle cell disease.

Authors:  M M Grant; K M Gil; M Y Floyd; M Abrams
Journal:  Ann Behav Med       Date:  2000

4.  Depression, disease severity, and sickle cell disease.

Authors:  J J Wison Schaeffer; K M Gil; M Burchinal; K D Kramer; K B Nash; E Orringer; D Strayhorn
Journal:  J Behav Med       Date:  1999-04

5.  Depression in sickle cell disease.

Authors:  Syed Parwez Hasan; Shahzad Hashmi; Mohammed Alhassen; William Lawson; Oswaldo Castro
Journal:  J Natl Med Assoc       Date:  2003-07       Impact factor: 1.798

6.  The role of depression in hospital admissions and emergency treatment of patients with sickle cell disease.

Authors:  F Z Belgrave; S D Molock
Journal:  J Natl Med Assoc       Date:  1991-09       Impact factor: 1.798

7.  Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.

Authors:  Marsha J Treadwell; Kathryn Hassell; Roger Levine; San Keller
Journal:  Clin J Pain       Date:  2014-10       Impact factor: 3.442

8.  Daily functioning and quality of life in children with sickle cell disease pain: relationship with family and neighborhood socioeconomic distress.

Authors:  Tonya M Palermo; Craig A Riley; Brian A Mitchell
Journal:  J Pain       Date:  2008-06-12       Impact factor: 5.820

  8 in total

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