The role of catastrophizing in sickle cell disease – The PiSCES project

[1]  J. Riley,et al.  An evaluation of the measurement of pain catastrophizing by the coping strategies questionnaire , 2007, European journal of pain.

[2]  John D. Roberts,et al.  Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES Project. , 2006, Journal of women's health.

[3]  J. Passchier,et al.  Factors Related to the Quality of Life in Adolescents With Chronic Pain , 2006, The Clinical journal of pain.

[4]  S. Linton,et al.  How does persistent pain develop? An analysis of the relationship between psychological variables, pain and function across stages of chronicity. , 2005, Behaviour research and therapy.

[5]  John D. Roberts,et al.  Health related quality of life in sickle cell patients: The PiSCES project , 2005, Health and quality of life outcomes.

[6]  K. Anie.  Psychological complications in sickle cell disease , 2005, British journal of haematology.

[7]  S. Woby,et al.  Coping strategy use: does it predict adjustment to chronic back pain after controlling for catastrophic thinking and self-efficacy for pain control? , 2005, Journal of rehabilitation medicine.

[8]  John D. Roberts,et al.  Understanding pain and improving management of sickle cell disease: the PiSCES study. , 2005, Journal of the National Medical Association.

[9]  M. Sullivan,et al.  Catastrophizing: A Risk Factor For Postsurgical Pain , 2005, The Clinical journal of pain.

[10]  G. Bennett,et al.  A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease , 2005, International journal of behavioral medicine.

[11]  Paul Karoly,et al.  Comparing the experiential and psychosocial dimensions of chronic pain in african americans and Caucasians: findings from a national community sample. , 2005, Pain medicine.

[12]  W. Chaplin,et al.  Personality Factors in the Explanation of Sex Differences in Pain Catastrophizing and Response to Experimental Pain , 2004, The Clinical journal of pain.

[13]  R. Fillingim,et al.  Ethnic differences in pain coping: factor structure of the coping strategies questionnaire and coping strategies questionnaire-revised. , 2004, The journal of pain : official journal of the American Pain Society.

[14]  D. Ehde,et al.  Social environment moderates the association between catastrophizing and pain among persons with a spinal cord injury , 2003, Pain.

[15]  G. Crombez,et al.  Acceptance of pain is an independent predictor of mental well-being in patients with chronic pain: empirical evidence and reappraisal , 2003, Pain.

[16]  J. Romano,et al.  The relationship of attachment style to depression, catastrophizing and health care utilization in patients with chronic pain , 2003, Pain.

[17]  N. Rothrock,et al.  Coping strategies in patients with interstitial cystitis: relationships with quality of life and depression. , 2003, The Journal of urology.

[18]  A. Steptoe,et al.  Coping and health service utilisation in a UK study of paediatric sickle cell pain , 2002, Archives of disease in childhood.

[19]  Francis J. Keefe,et al.  Memory for Pain: The Relationship of Pain Catastrophizing to the Recall of Daily Rheumatoid Arthritis Pain , 2002, The Clinical journal of pain.

[20]  D. McGuire,et al.  Use of focus groups for pain and quality of life assessment in adults with sickle cell disease. , 2001, Journal of National Black Nurses' Association : JNBNA.

[21]  R. Fillingim,et al.  Race, ethnicity and pain , 2001, PAIN.

[22]  E. Jacob,et al.  The pain experience of patients with sickle cell anemia. , 2001, Pain management nursing : official journal of the American Society of Pain Management Nurses.

[23]  J. Vlaeyen,et al.  Pain Catastrophizing Predicts Pain Intensity, Disability, and Psychological Distress Independent of the Level of Physical Impairment , 2001, The Clinical journal of pain.

[24]  B. Weiner,et al.  A meta-analytic review of coping with illness: do causal attributions matter? , 2001, Journal of psychosomatic research.

[25]  F. Keefe,et al.  Theoretical perspectives on the relation between catastrophizing and pain. , 2001, The Clinical journal of pain.

[26]  I. Kirsch,et al.  Catastrophizing, depression and expectancies for pain and emotional distress , 2001, Pain.

[27]  M. Jensen,et al.  Coping with chronic pain: a comparison of two measures , 2001, Pain.

[28]  H. Alaranta,et al.  Coping strategies, pain, and disability in patients with hemophilia and related disorders. , 2001, Arthritis and rheumatism.

[29]  R. Spitzer,et al.  The PHQ-9: validity of a brief depression severity measure. , 2001, Journal of general internal medicine.

[30]  G. Affleck,et al.  The relationship of gender to pain, pain behavior, and disability in osteoarthritis patients: the role of catastrophizing , 2000, Pain.

[31]  S. Yale,et al.  Approach to the vaso-occlusive crisis in adults with sickle cell disease. , 2000, American family physician.

[32]  R. Spitzer,et al.  Validation and utility of a self-report version of PRIME-MD: the PHQ primary care study. Primary Care Evaluation of Mental Disorders. Patient Health Questionnaire. , 1999, JAMA.

[33]  O. Barbarin,et al.  The Social and Cultural Context of Coping with Sickle Cell Disease: I. A Review of Biomedical and Psychosocial Issues , 1999 .

[34]  Graham R Serjeant,et al.  Sickle-cell disease , 1984, The Lancet.

[35]  P. Lane.  Sickle cell disease. , 1996, Pediatric clinics of North America.

[36]  R. J. Thompson,et al.  Psychological adjustment of adults with sickle cell anemia: stability over 20 months, correlates, and predictors. , 1996, Journal of clinical psychology.

[37]  F. Keefe,et al.  Catastrophizing, depression and the sensory, affective and evaluative aspects of chronic pain , 1994, Pain.

[38]  M. Robinson,et al.  The Coping Strategies Questionnaire and Chronic Pain Adjustment: A Conceptual and Empirical Reanalysis , 1994, The Clinical journal of pain.

[39]  R. J. Thompson,et al.  Stress, coping, and psychological adjustment of adults with sickle cell disease. , 1992, Journal of consulting and clinical psychology.

[40]  K. Gil,et al.  Sickle cell disease pain: 2. Predicting health care use and activity level at 9-month follow-up. , 1992, Journal of consulting and clinical psychology.

[41]  M. Jensen,et al.  Coping with chronic pain: a critical review of the literature , 1991, Pain.

[42]  F. Keefe,et al.  Sickle cell disease pain: relation of coping strategies to adjustment. , 1989, Journal of consulting and clinical psychology.

[43]  A. Stewart,et al.  The MOS short-form general health survey. Reliability and validity in a patient population. , 1988, Medical care.

[44]  Francis J. Keefe,et al.  The use of coping strategies in chronic low back pain patients: Relationship to patient characteristics and current adjustment , 1983, Pain.