Pain Experience, Physical Function, Pain Coping, and Catastrophizing in Children with Sickle Cell Disease who had Normal and Abnormal Sensory Patterns.

[1]  A. Ozkaraman,et al.  The Effect of Progressive Muscle Relaxation Exercises on Pain on Patients with Sickle Cell Disease: Randomized Controlled Study. , 2020, Pain management nursing : official journal of the American Society of Pain Management Nurses.

[2]  J. Bost,et al.  Acupuncture for pain management in children with sickle cell disease. , 2020, Complementary therapies in medicine.

[3]  A. Stone,et al.  Daily Associations between Child and Parent Psychological Factors and Home Opioid Use in Youth with Sickle Cell Disease. , 2019, Annals of behavioral medicine : a publication of the Society of Behavioral Medicine.

[4]  D. Lubeck,et al.  Estimated Life Expectancy and Income of Patients With Sickle Cell Disease Compared With Those Without Sickle Cell Disease , 2019, JAMA network open.

[5]  M. Hillegers,et al.  Systematic Review and Meta-analysis of Virtual Reality in Pediatrics: Effects on Pain and Anxiety , 2019, Anesthesia and analgesia.

[6]  S. Sil,et al.  Pediatric pain screening identifies youth at risk of chronic pain in sickle cell disease , 2018, Pediatric blood & cancer.

[7]  M. Treadwell,et al.  Virtual reality as complementary pain therapy in hospitalized patients with sickle cell disease , 2018, Pediatric blood & cancer.

[8]  C. Stucky,et al.  Children and adolescents with sickle cell disease have worse cold and mechanical hypersensitivity during acute painful events , 2018, Pain.

[9]  P. Fu,et al.  The Effects of a Single Electronic Music Improvisation Session on the Pain of Adults with Sickle Cell Disease: A Mixed Methods Pilot Study , 2018, Journal of music therapy.

[10]  V. Gordeuk,et al.  Characterization of opioid use in sickle cell disease , 2018, Pharmacoepidemiology and drug safety.

[11]  D. Weatherall,et al.  Sickle cell disease , 2018, Nature Reviews Disease Primers.

[12]  S. Bediako,et al.  Depressive Symptoms and Sickle Cell Pain: The Moderating Role of Internalized Stigma , 2017, Stigma and health.

[13]  James G. Taylor VI,et al.  Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia , 2017, Scandinavian journal of pain.

[14]  Soyang Kwon,et al.  Self-Reported Physical Activity and Exercise Patterns in Children With Sickle Cell Disease. , 2017, Pediatric exercise science.

[15]  R. Ware,et al.  Sickle cell disease , 2017, The Lancet.

[16]  F. Piel,et al.  Sickle Cell Disease. , 2017, The New England journal of medicine.

[17]  A. Douiri,et al.  Survival in adults with sickle cell disease in a high-income setting. , 2016, Blood.

[18]  K. James,et al.  Increased rates of body dissatisfaction, depressive symptoms, and suicide attempts in Jamaican teens with sickle cell disease , 2016, Pediatric blood & cancer.

[19]  C. Haywood,et al.  Chronic Opioid Therapy and Central Sensitization in Sickle Cell Disease. , 2016, American journal of preventive medicine.

[20]  Jill B. Hamilton,et al.  Perceptions of young adults with sickle cell disease concerning their disease experience. , 2016, Journal of advanced nursing.

[21]  J. Panepinto,et al.  Clinical Interpretation of Quantitative Sensory Testing as a Measure of Pain Sensitivity in Patients With Sickle Cell Disease , 2016, Journal of pediatric hematology/oncology.

[22]  E. Jacob,et al.  Depression, Anxiety, and Quality of Life In Children and Adolescents With Sickle Cell Disease. , 2016, Pediatric nursing.

[23]  P. Tanabe,et al.  Sickle Cell Disease: A Review of Nonpharmacological Approaches for Pain. , 2016, Journal of pain and symptom management.

[24]  C. Dobson Outcome results of self-efficacy in children with sickle disease pain who were trained to use guided imagery. , 2015, Applied nursing research : ANR.

[25]  S. McMillan,et al.  Role of self-care in sickle cell disease. , 2015, Pain management nursing : official journal of the American Society of Pain Management Nurses.

[26]  M. Sehlo,et al.  Depression and quality of life in children with sickle cell disease: the effect of social support , 2015, BMC Psychiatry.

[27]  D. Zurakowski,et al.  Sensory and Thermal Quantitative Testing in Children With Sickle Cell Disease , 2015, Journal of pediatric hematology/oncology.

[28]  D. Simone,et al.  Sensitization of nociceptive spinal neurons contributes to pain in a transgenic model of sickle cell disease , 2015, Pain.

[29]  R. Hoffmann,et al.  The Use of Neuropathic Pain Drugs in Children With Sickle Cell Disease Is Associated With Older Age, Female Sex, and Longer Length of Hospital Stay , 2015, Journal of pediatric hematology/oncology.

[30]  Matthew T. White,et al.  Pain catastrophizing in children with chronic pain and their parents: Proposed clinical reference points and reexamination of the Pain Catastrophizing Scale measure , 2014, PAIN®.

[31]  M. Beach,et al.  Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease. , 2014, Journal of pain and symptom management.

[32]  M. Beach,et al.  Perceived Discrimination, Patient Trust, and Adherence to Medical Recommendations Among Persons with Sickle Cell Disease , 2014, Journal of General Internal Medicine.

[33]  B. Yawn,et al.  Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members. , 2014, JAMA.

[34]  D. Wilkie,et al.  Adolescent pediatric pain tool for multidimensional measurement of pain in children and adolescents. , 2014, Pain management nursing : official journal of the American Society of Pain Management Nurses.

[35]  E. Jacob,et al.  Pain, coping, and sleep in children and adolescents with sickle cell disease. , 2014, Journal of child and adolescent psychiatric nursing : official publication of the Association of Child and Adolescent Psychiatric Nurses, Inc.

[36]  M. Byrne,et al.  Original Research: Using Guided Imagery to Manage Pain in Young Children with Sickle Cell Disease , 2014, The American journal of nursing.

[37]  M. Crawford,et al.  Thermal Pain and Sensory Processing in Children With Sickle Cell Disease , 2014, The Clinical journal of pain.

[38]  S. Hay,et al.  Global Burden of Sickle Cell Anaemia in Children under Five, 2010–2050: Modelling Based on Demographics, Excess Mortality, and Interventions , 2013, PLoS medicine.

[39]  Sylvia T. Brown,et al.  A Pilot Study , 2013, Journal of holistic nursing : official journal of the American Holistic Nurses' Association.

[40]  J. Stinson,et al.  Facilitating pediatric patient-provider communications using wireless technology in children and adolescents with sickle cell disease. , 2013, Journal of pediatric health care : official publication of National Association of Pediatric Nurse Associates & Practitioners.

[41]  T. Palermo,et al.  Perception versus ability: physical function in pediatric sickle cell disease , 2013 .

[42]  M. Beach,et al.  The impact of race and disease on sickle cell patient wait times in the emergency department. , 2013, The American journal of emergency medicine.

[43]  Eufemia Jacob,et al.  Remote monitoring of pain and symptoms using wireless technology in children and adolescents with sickle cell disease , 2013, Journal of the American Association of Nurse Practitioners.

[44]  C. Stucky,et al.  Patients with sickle cell disease have increased sensitivity to cold and heat , 2013, American journal of hematology.

[45]  Azeem Majeed,et al.  Trends in hospital admissions for sickle cell disease in England, 2001/02-2009/10. , 2012, Journal of public health.

[46]  Mario Gerla,et al.  Usability Testing of a Smartphone for Accessing a Web-based e-Diary for Self-monitoring of Pain and Symptoms in Sickle Cell Disease , 2012, Journal of pediatric hematology/oncology.

[47]  M. Hollins,et al.  Detecting the emergence of chronic pain in sickle cell disease. , 2012, Journal of pain and symptom management.

[48]  T. Eckle,et al.  Ischemia and reperfusion—from mechanism to translation , 2011, Nature Medicine.

[49]  S. Ballas Update on Pain Management in Sickle Cell Disease , 2011, Hemoglobin.

[50]  S. Bediako,et al.  Race and social attitudes about sickle cell disease , 2011, Ethnicity & health.

[51]  S. Kashikar-Zuck,et al.  Clinical utility and validity of the Functional Disability Inventory among a multicenter sample of youth with chronic pain , 2011, PAIN®.

[52]  M. Mitchell,et al.  Disease management, coping, and functional disability in pediatric sickle cell disease. , 2011, Journal of the National Medical Association.

[53]  N. Powe,et al.  The Association of Provider Communication with Trust among Adults with Sickle Cell Disease , 2010, Journal of General Internal Medicine.

[54]  D. Mark Courtney,et al.  A Comparison of Analgesic Management for Emergency Department Patients With Sickle Cell Disease and Renal Colic , 2010, The Clinical journal of pain.

[55]  Tsveti Markova,et al.  Aversive Racism and Medical Interactions with Black Patients: A Field Study. , 2010, Journal of experimental social psychology.

[56]  K. Lemanek,et al.  A randomized controlled trial of massage therapy in children with sickle cell disease. , 2009, Journal of pediatric psychology.

[57]  Carmen E Sanchez,et al.  Use of handheld wireless technology for a home-based sickle cell pain management protocol. , 2009, Journal of pediatric psychology.

[58]  C. Quinn,et al.  Improved survival of children and adolescents with sickle cell disease. , 2008, Blood.

[59]  D. Zurakowski,et al.  Cutaneous sensory abnormalities in children and adolescents with complex regional pain syndromes , 2007, Pain.

[60]  Driscoll Mc Sickle Cell Disease , 2007 .

[61]  B. Horta,et al.  The worldwide prevalence of ADHD: a systematic review and metaregression analysis. , 2007, The American journal of psychiatry.

[62]  I. Rolle,et al.  Understanding African Americans’ views of the trustworthiness of physicians , 2006, Journal of General Internal Medicine.

[63]  R. Claar,et al.  Functional assessment of pediatric pain patients: Psychometric properties of the Functional Disability Inventory , 2006, Pain.

[64]  P. A. Kelly,et al.  Racial differences in trust and lung cancer patients' perceptions of physician communication. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[65]  R. Zachariae,et al.  Relationship of pain-coping strategies and pain-specific beliefs to pain experience in children with juvenile idiopathic arthritis. , 2005, Arthritis and rheumatism.

[66]  J. Mandelblatt,et al.  The role of trust in use of preventive services among low-income African-American women. , 2004, Preventive medicine.

[67]  S. Ballas,et al.  Non-pharmacologic Management of Sickle Cell Pain , 2004, Hematology.

[68]  G. Crombez,et al.  The child version of the pain catastrophizing scale (PCS-C): a preliminary validation , 2003, Pain.

[69]  K. Anie,et al.  A comparison of the outcome of cognitive behaviour therapy and hydroxyurea in sickle cell disease , 2003 .

[70]  John Green,et al.  SELF-HELP MANUAL-ASSISTED COGNITIVE BEHAVIOURAL THERAPY FOR SICKLE CELL DISEASE , 2002, Behavioural and Cognitive Psychotherapy.

[71]  Aneil Mishra,et al.  Trust in physicians and medical institutions: what is it, can it be measured, and does it matter? , 2001, The Milbank quarterly.

[72]  D. Zurakowski,et al.  Quantitative assessment of cutaneous thermal and vibration sensation and thermal pain detection thresholds in healthy children and adolescents , 2001, Muscle & nerve.

[73]  D. Thom,et al.  Physician behaviors that predict patient trust. , 2001, The Journal of family practice.

[74]  K. Gil,et al.  Daily coping practice predicts treatment effects in children with sickle cell disease. , 2001, Journal of pediatric psychology.

[75]  D. Mechanic,et al.  Concepts of trust among patients with serious illness. , 2000, Social science & medicine.

[76]  Nicky Thomas,et al.  Cognitive‐behaviour therapy for the management of sickle cell disease pain: An evaluation of a community‐based intervention , 1999 .

[77]  D. Ingram,et al.  Theory and Practice of Self-Induced Pain Management: Approaches Learned from Effective Copers , 1999 .

[78]  J. Telfair,,et al.  African American Adolescents with Sickle Cell Disease: Support Groups and Psychological Well-Being , 1999 .

[79]  P. McGrath,et al.  The Pain Coping Questionnaire: preliminary validation , 1998, Pain.

[80]  M. Orne,et al.  Self-hypnosis training as an adjunctive treatment in the management of pain associated with sickle cell disease. , 1997, The International journal of clinical and experimental hypnosis.

[81]  D. Thom,et al.  Patient-physician trust: an exploratory study. , 1997, The Journal of family practice.

[82]  K. Kramer,et al.  Self-Help for Sickle Cell Disease in African American Communities , 1993 .

[83]  D. Butler,et al.  Functions of an adult sickle cell group: education, task orientation, and support. , 1993, Health & social work.

[84]  L. Walker,et al.  The functional disability inventory: measuring a neglected dimension of child health status. , 1991, Journal of pediatric psychology.

[85]  W. Tryon,et al.  The effectiveness of biofeedback-assisted relaxation in modifying sickle cell crises , 1987, Biofeedback and self-regulation.

[86]  L. Zeltzer,et al.  Hypnotically induced pain control in sickle cell anemia. , 1979, Pediatrics.

[87]  M. Westerman,et al.  Acupuncture: An evaluation in the painful crises of sickle cell anaemia , 1979, Pain.

[88]  R. Wong,et al.  Social stigma as a barrier to diabetes self-management: implications for multi-level interventions. , 2003, Journal of clinical nursing.

[89]  K. Anie,et al.  Psychological therapies for sickle cell disease and pain. , 2002, The Cochrane database of systematic reviews.

[90]  Scott R. Bishop,et al.  The Pain Catastrophizing Scale: Development and validation. , 1995 .