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Psychological therapies for sickle cell disease and pain
Abstract
Background Sickle cell disease comprises a group of genetic blood disorders, and occurs when the sickle haemoglobin gene is inherited from both parents. The effects of the condition are: varying degrees of anaemia which if severe reduce the capacity for mobility; predisposition to obstruction of small blood capillaries causing pain in muscle and bone known as "crises"; damage to major organs such as the spleen, liver, kidneys, and lungs; and increased vulnerability to severe infections. There are both medical and non-medical complications, and treatment is usually symptomatic and palliative in nature. Psychological intervention for individuals with sickle cell disease seems viable in complementing current medical treatment, and studies examining their efficacy appear to have also yielded encouraging results. Objectives To examine the evidence that in patients with sickle cell disease, psychological treatment improves the ability to cope with the condition. Search strategy The Cochrane Cystic Fibrosis and Genetic Disorders Group specialist trials register which comprises references from comprehensive electronic database searches. Also, hand searching relevant journals, hand searching abstract books of conference proceedings, and searches on the Internet were performed. Date of the most recent search of the Group's specialised register: January 2001. Selection criteria All randomised or quasi-randomised controlled trials comparing the use of psychological intervention to no (ps…
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“There is a pressing need for effective and practical approaches to help adolescents with SCD pain improve their functioning and quality of life (13,14).”
From Ecological system influences in the treatment of pediatric chronic pain (2012) · cites this paper as [13]
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- 1991, Self-help in sickle-cell disease in Nigeria, Health Promotion International, 6, 241, 10.1093/heapro/6.4.241 · DOI
- Broome, 2001, An intervention to increase coping and reduce health care utilization for school-age children and adolescents with sickle cell disease, Journal of National Black Nurses Association, 12, 6
- Gil, 2000, Follow-up of coping skills training in adults with sickle cell disease: Analysis of daily pain and coping practice diaries, Health Psychology, 19, 85, 10.1037/0278-6133.19.1.85 · DOI
- Gil, 1996, Effects of cognitive coping skills training on coping strategies and experimental pain sensitivity in African American adults with sickle cell disease, Health Psychology, 15, 3, 10.1037/0278-6133.15.1.3 · DOI
- Gil, 2001, Daily coping practice predicts treatment effects in children with sickle cell disease, Journal of Pediatric Psychology, 26, 163, 10.1093/jpepsy/26.3.163 · DOI
- Gil, 1997, Cognitive coping skills in children with sickle cell disease, International Journal of Behavioral Medicine, 4, 365, 10.1207/s15327558ijbm0404_7 · DOI
- Kaslow, 1997, Empirically validated family intervention for pediatric psychology: Sickle cell disease as an exemplar, Journal of Pediatric Psychology, 22, 213, 10.1093/jpepsy/22.2.213 · DOI
- Kaslow, 2000, The efficacy of a pilot family psychoeducational intervention for pediatric sickle cell disease (SCD), Family, Systems and Health, 18, 381, 10.1037/h0091863 · DOI
- Thomas, 2000, Cognitive behavioural therapy in pain management for sickle cell disease, International Journal of Palliative Nursing, 6, 434, 10.12968/ijpn.2000.6.9.9055 · DOI
- Thomas, 1999, Cognitive-behaviour therapy for the management of sickle cell disease pain: An evaluation of a community-based intervention, British Journal of Health Psychology, 4, 209, 10.1348/135910799168588 · DOI
- Applegate, 2003, Improving parent participation at pediatric diabetes and sickle cell appointments using a brief intervention, Children's Health Care, 32, 125, 10.1207/S15326888CHC3202_4 · DOI
- Barakat, 2007, Negative thinking as a coping strategy mediator of pain and internalizing symptoms in adolescents with sickle cell disease, Journal of Behavioral Medicine, 30, 199, 10.1007/s10865-007-9103-x · DOI
- Ketchen, 2006, STARBRIGHT World: a pilot study of a home-based sickle cell psychoeducational intervention, Children's Health Care, 35, 321, 10.1080/02739615.2006.12028049 · DOI
- Kinlow, 2001, Computer based interactive education programs for hospitalized children with asthma and sickle cell disease [abstract], Respiratory Care, 46, 1112
- Yerys, 2003, Memory strategy training in children with cerebral infarcts related to sickle cell disease, Journal of Pediatric Hematology/Oncology, 25, 495, 10.1097/00043426-200306000-00014 · DOI
- Anie, 2002, Self-help manual-assisted cognitive behavioural therapy for sickle cell disease, Behavioural and Cognitive Psychotherapy, 30, 451, 10.1017/S135246580200406X · DOI
- Ballas, 1998, Sickle cell pain (Progress in pain research and management), 11
- Ballas, 1999, Erythropoietic activity in patients with sickle cell anaemia before and after treatment with hydroxyurea, British Journal of Haematology, 105, 491, 10.1111/j.1365-2141.1999.01339.x · DOI
- Baum, 1987, The painful crisis of homozygous sickle cell disease: A study of risk factors, Archives of Internal Medicine, 147, 1231, 10.1001/archinte.1987.00370070045007 · DOI
- Brown, 1993, Neurocognitive aspects of sickle cell disease, Journal of Learning Disabilities, 26, 33, 10.1177/002221949302600104 · DOI
- Brozovic, 1987, Acute admissions of patients with sickle cell disease who live in Britain, British Medical Journal (Clinical Research Edition), 294, 1206, 10.1136/bmj.294.6581.1206 · DOI
- Charache, 1995, Effect of hydroxyurea on the frequency of painful crises in sickle cell anaemia, New England Journal of Medicine, 332, 1317, 10.1056/NEJM199505183322001 · DOI · Paper page
- Davies, 1997, Management of patients with sickle cell disease, BMJ, 315, 656, 10.1136/bmj.315.7109.656 · DOI
- Gil, 1989, Coping with sickle cell disease pain, Annals of Behavioral Medicine, 11, 49, 10.1207/s15324796abm1102_2 · DOI
- Higgins, 2003, Measuring inconsistence in meta-analyses, BMJ, 327, 557, 10.1136/bmj.327.7414.557 · DOI · Paper page
- The Nordic Cochrane Centre, The Cochrane Collaboration Review Manager (RevMan) 2008
- Roberts-Harewood, 1998, Current management in sickle cell disease, Hematology, 3, 419, 10.1080/10245332.1998.11746416 · DOI
- Schulz, 1995, Empirical evidence of bias. Dimensions of methodological quality associated with estimates of treatment in controlled trials, JAMA, 273, 408, 10.1001/jama.1995.03520290060030 · DOI
- Serjeant, 2001, Sickle Cell Disease
- Streetley A Maxwell K Meija A Sickle cell disorders in Greater London: a needs assessment of screening and care services Bexley and Greenwich Health Authority 1997 · DOI
- Walters, 2000, Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report, Blood, 95, 1918
- Williams, 1983, Psychological considerations in sickle cell disease, Nursing Clinics of North America, 18, 215, 10.1016/S0029-6465(22)01726-1 · DOI
- Anie, 2000, Psychological therapies for sickle cell disease and pain (Cochrane review), Cochrane Database of Systematic Reviews
Metadata
- Authors
- Anie, K. A., & Green, J.
- Affiliations
- Central Middlesex Hospital (GB)
- St Mary's Hospital (GB)
- Venue
- Cochrane Database of Systematic Reviews
- Publisher
- John Wiley & Sons, Ltd
- Published
- 2002-04-22
- Issue
- 2
- Pages
- CD001916-CD001916
- ISSN
- 1361-6137 (ISSN-L)
- OpenAlex
- W4241589215
- Cited by
- 22
- References
- 29
- Citations by year
- 2026: 1 · 2021: 1 · 2016: 2 · 2015: 3 · 2014: 1 · 2013: 1 · 2012: 1
- Type
- reference entry
- Language
- en
- Open access
- closed
- Locations
- Cochrane Database of Systematic Reviews (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Genetics (clinical) › Hemoglobinopathies and Related Disorders
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pediatric Pain Management Techniques
- Health Sciences › Nursing › Research and Theory › Nursing care and research
- Keywords
- sickle cell disease, psychotherapy, coping, family education, cognitive behavioral therapy, patient education, pain, crisis, palliative care
- MeSH terms
- Adaptation, Psychological, Adult, Child, Hemoglobin SC Disease, Humans, Psychotherapy, Randomized Controlled Trials as Topic, Outcome Assessment, Health Care, Pain Management
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