Literature DB >> 9637327

The role of cognitive-behavioural therapy in the management of pain in patients with sickle cell disease.

V N Thomas1, J Wilson-Barnett, F Goodhart.   

Abstract

Painful crisis is the most common manifestation of sickle cell disease and accounts for the second greatest number of admissions with an average length of stay of 7 days in central London. Despite this frequency of admissions, the management of pain is fraught with problems. This is not surprising since the psychological challenges presented by sickle cell disease are manifold, resulting in significant psychological distress for some individuals. This paper considers the literature on the psychosocial impact of sickle cell disease, and the American research evidence which suggests that pain management strategies that incorporate a psychological intervention can significantly reduce psychological distress as well as hospital admissions. Britain has been slow to incorporate psychology in the pain management strategies, and we have embarked on research to fill this gap. Although this research constitutes work in progress, an argument is put forward for utilizing the cognitive-behavioural perspective in the management of pain in sickle cell disease and we conclude by giving a brief summary of pilot work which is both the foundation and justification for the current ongoing research.

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Year:  1998        PMID: 9637327     DOI: 10.1046/j.1365-2648.1998.00584.x

Source DB:  PubMed          Journal:  J Adv Nurs        ISSN: 0309-2402            Impact factor:   3.187


  5 in total

1.  Using Quality Improvement Methods to Implement an Electronic Medical Record (EMR) Supported Individualized Home Pain Management Plan for Children with Sickle Cell Disease.

Authors:  Lori E Crosby; Kenya Simmons; Peggy Kaiser; Blair Davis; Patricia Boyd; Tiffany Eichhorn; Tracy Mahaney; Naomi Joffe; Darice Morgan; Kathy Schibler; Viia Anderson; Charles T Quinn; Karen A Kalinyak
Journal:  J Clin Outcomes Manag       Date:  2014-05

Review 2.  A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.

Authors:  Christopher L Edwards; Mischca T Scales; Charles Loughlin; Gary G Bennett; Shani Harris-Peterson; Laura M De Castro; Elaine Whitworth; Mary Abrams; Miriam Feliu; Stephanie Johnson; Mary Wood; Ojinga Harrison; Alvin Killough
Journal:  Int J Behav Med       Date:  2005

Review 3.  Pain management in children with sickle cell disease.

Authors:  Jennifer Stinson; Basem Naser
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

4.  Do chronic pain and comorbidities affect brain function in sickle cell patients? A systematic review of neuroimaging and treatment approaches.

Authors:  Joyce T Da Silva; Janelle E Letzen; Jennifer A Haythornthwaite; Patrick H Finan; Claudia M Campbell; David A Seminowicz
Journal:  Pain       Date:  2019-09       Impact factor: 7.926

5.  A Stress and Pain Self-management mHealth App for Adult Outpatients With Sickle Cell Disease: Protocol for a Randomized Controlled Study.

Authors:  Miriam O Ezenwa; Yingwei Yao; Molly W Mandernach; David A Fedele; Robert J Lucero; Inge Corless; Brenda W Dyal; Mary H Belkin; Abhinav Rohatgi; Diana J Wilkie
Journal:  JMIR Res Protoc       Date:  2022-07-29
  5 in total

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