Literature DB >> 11388088

Cognitive-behavioural therapy for the management of sickle cell disease pain: identification and assessment of costs.

V J Thomas1, R Gruen, S Shu.   

Abstract

OBJECTIVE: The aim of the present study was to investigate the economic validity of using a psychological intervention in the management of sickle cell disease (SCD). Thomas et al. (Br J Health Psychol 1999; 4: 209-29) concluded that cognitive-behaviour therapy (CBT) appears to be immediately effective for the management of SCD pain in terms of reducing psychological distress pain as well as improving coping.
METHOD: The costs of management of SCD were evaluated using a societal viewpoint. This approach includes health and social services as well as costs privately borne by informal carers, but it did not include the economic loss due to patients' foregone earnings. Cost profiles were constructed for each patient taking account of cost generating events 12 months before and 12 months after CBT.
RESULTS: The hypothesis of the present study, stating that CBT is economically efficient, was confirmed. However, analysis of longitudinal data suggests that CBT is most cost-effective during the first 6 months after the intervention.
CONCLUSION: The present findings suggest the need for CBT to be integrated into the normal package of care available for all patients with SCD. The clinical implication is that CBT should be routinely offered to patients on a 6-monthly basis.

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Mesh:

Year:  2001        PMID: 11388088     DOI: 10.1080/13557850123965

Source DB:  PubMed          Journal:  Ethn Health        ISSN: 1355-7858            Impact factor:   2.772


  5 in total

1.  Feasibility and Acceptability of Internet-delivered Cognitive Behavioral Therapy for Chronic Pain in Adolescents With Sickle Cell Disease and Their Parents.

Authors:  Tonya M Palermo; Joanne Dudeney; James P Santanelli; Alexie Carletti; William T Zempsky
Journal:  J Pediatr Hematol Oncol       Date:  2018-03       Impact factor: 1.289

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

3.  Parental problem-solving abilities and the association of sickle cell disease complications with health-related quality of life for school-age children.

Authors:  Lamia P Barakat; Lauren C Daniel; Kelsey Smith; M Renée Robinson; Chavis A Patterson
Journal:  J Clin Psychol Med Settings       Date:  2014-03

4.  Genomics and pain research in sickle cell disease: an explanation of heterogeneity?

Authors:  Maxine Adegbola
Journal:  ISRN Nurs       Date:  2011-04-20

Review 5.  Pain in sickle cell disease: current and potential translational therapies.

Authors:  Varun Sagi; Aditya Mittal; Huy Tran; Kalpna Gupta
Journal:  Transl Res       Date:  2021-03-09       Impact factor: 10.171

  5 in total

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