Adjustment and coping in adults with sickle cell disease: An assessment of research evidence

British Journal of Health Psychology

Volumn 1, Issue 2, 1996, Pages 95-111

  Midence, Kenny ^a   Elander, James ^b  

^a BANGOR UNIVERSITY   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0002783088     PISSN: 1359107X     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.2044-8287.1996.tb00495.x     Document Type: Article

References (14)

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2. Anderson, L. P. & Rehm, L. P. (1984). The relationship between strategies of coping and perception of pain in three chronic pain groups. Journal of Clinical Psychology, 40, 1170-1177.
3. Aschenbrenner, J. (1975). Lifelines: Black Families in Chicago. New York: Holt, Rinehart & Winston.
4. Atkin, K. & Rollings, J. (1992). Informal care in Asian and Afro-Caribbean communities: A literature review. British Journal of Social Work, 22, 405-418.
5. Barrett, D. H., Wisotzek, I. E., Abel. G. G., Rouleau, J. L., Platt, A..F., Pollard, W. E. & Eckman, J. R. (1988). Assessment of psychosocial functioning of patients with sickle cell disease. Southern Medical Journal, 81, 745-750.
6. Baum, K. F., Dunn, D. T., Maude, G. H. & Serjeant, G. R. (1987). The painful crisis of homozygous sickle cell disease: A study of risk factors. Archives of Internal Medicine, 147, 1231-1234.
7. Benjamin, S. (1989). Psychological treatment of chronic pain: A selective review. Journal of Psychosomatic Research, 33, 121-131.
8. Bertram, R. A., Webster, G. D. & Carson, C. C. (1985). Priapism: Aetiology, treatment and results in a series of 35 presentations. Urology, 26, 229-231.
9. Black, J. & Laws, S. (1986). Living with SCD: An Enquiry into the Need for Health and Social Service Provision for Sickle Cell Sufferers in Newbam. London: East London Sickle Cell Society.
10. Bobo, L., Miller, S. T., Smith, W. R., Elam, J. T., Rosmarin, P. C. & Lancaster, D. J. (1989). Health perceptions and medical care opinions of inner-city adults with sickle cell disease or asthma compared with those of their siblings. Southern Medical Journal, 82, 9-12.
11. Broome, M. & Monroe, S. (1979). Sickle Cell Anemia: A Patient-Perceived Needs Assessment. San Francisco, CA: Sickle Cell Anemia Research & Education Inc.
12. Brozovic, M. & Davies, S. C. (1987). Management of sickle cell disease. Postgraduate Medical Journal, 63, 605-609.
13. Vichinski, E. P., Johnson, R. & Lubin, B. H. (1982). Multidisciplinary approach to pain management in SCD. American Journal of Pediatric Hematology and Oncology, 4, 328-333.
14. Williams, I., Earles, A. N. & Pack, B. (1983). Psychological considerations in sickle cell disease. Nursing Clinics of North America, 18, 215-229.