The pain experience of patients with sickle cell anemia

Pain Management Nursing - Tập 2 - Trang 74-83 - 2001
Eufemia Jacob1
1Hematology/Oncology Unit, Children's Hospital Oakland, Oakland, CA

Tài liệu tham khảo

Akinola, 1992, Rheological changes in the prodromal and established phases of sickle cell vaso-occlusive crisis, British Journal of Haematology, 81, 598, 10.1111/j.1365-2141.1992.tb02998.x

Baldy, 1997, Red blood cell disorders, 202

Ballas, 1990, Treatment of pain in adults with sickle cell disease, American Journal of Haematology, 34, 49, 10.1002/ajh.2830340111

Ballas, 1991, Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of desnse cells, American Journal of Hematology, 36, 122, 10.1002/ajh.2830360211

Ballas, 1994, Neurobiology and treatment of pain, 745

Ballas, 1992, Red blood cell changes during the evolution of the sickle cell painful crisis, Blood, 79, 2154, 10.1182/blood.V79.8.2154.2154

Barbarin, 1994, Estimating rates of psychosocial problems in urban and poor children with sickle cell anemia, Health & Social Work, 19, 112, 10.1093/hsw/19.2.112

Barrett, 1988, Assessment of psychosocial functioningof patients with sickle cell disease, Southern Medical Journal, 81, 745, 10.1097/00007611-198806000-00015

Belgrave, 1991, The role of depression in hospital admissions and emergency treatment ofpaitents with sickle cell disease, Journal of the National Medical Association, 83, 777

Beyer, 1999, A chronology of pain and comfort in children with sickle cell disease, Archives of Pediatrics & Adolescent Medicine, 153, 913, 10.1001/archpedi.153.9.913

Billett, 1988, Evolution of laboratory parameters during sickle cell painful crisis: evidence compatible with dense red cell sequestration without thrombosis, American Journal of Medical Science, 31, 293, 10.1097/00000441-198811000-00001

Blei, 1993, Elevated levels of circulating intercellular adhesion molecule-1 (ICAM-1) in sickle cell disease

Bobo, 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, 81, 9, 10.1097/00007611-198901000-00004

Buchanan, 1978, Leukocyte counts inchildren with sickle cell disease. Comparatve values in the steady state, vaso-occlusive crisis, and bacterial infection, American Journal of Disease in Childhood, 132, 396, 10.1001/archpedi.1978.02120290068013

Charache, 1994, Natural history of disease: Adults, 395

Conyard, 1980, Psychosocial aspects of sickle cell anemia in adolescents, Health & Social Work, 5, 20, 10.1093/hsw/5.1.20

Diggs, 1965, Sickle cell crises, American Journal of Clinical Pathology, 44, 1, 10.1093/ajcp/44.1.1

Eaton, 1995, Hospitalizations for painful episodes: association with school absenteeism and academic performance in children and adolescents with sickle cell anemia, Issues in Comprehensive Pediatric Nursing, 18, 1, 10.3109/01460869509080953

Fowler, 1988, Neuropsychologic and academic functioning of children with sickle cell anemia, Developmental and Behavioral Pediatrics, 9, 213, 10.1097/00004703-198808000-00006

Fuggle, 1996, Pain, quality of life, and coping in sickle cell disease, Archives of Diseases in Childhood, 75, 199, 10.1136/adc.75.3.199

Hurtig, 1986, Psychosocial adjustment in children and adolescents with sickle cell disease, Journal of Pediatric Psychology, 14, 117, 10.1093/jpepsy/14.1.117

Katz, 1993

Konotey-Ahulu, 1991, Morphine for painful crises in sickle cell disese [Letter], British Medical Journal, 302, 1604, 10.1136/bmj.302.6792.1604-c

Kumar, 1976, Anxiety, self-concept, and personal and social adjustment in children with sickle cell anemia, Journal of Pediatrics, 88, 859, 10.1016/S0022-3476(76)81132-8

Midence, 1994

Morgan, 1986, Psychological and social concomitants of sickle cell anemia in adolescents, Journal of Pediatric Psychology, 11, 429, 10.1093/jpepsy/11.3.429

Morin, 1981, Depression and sickle cell anemia, Southern Medical Journal, 74, 766, 10.1097/00007611-198106000-00035

Murray, 1988, Painful crises in sickle cell disease-patients' perspectives, British Medical Journal, 297, 452, 10.1136/bmj.297.6646.452

Platt, 1991, Pain in sickle cell disease. Rates and risk factors [see comments], New England Journal of Medicine, 325, 11, 10.1056/NEJM199107043250103

Samuels-Reid, 1985, Painful crises and menstruation in sickle cell disease, Southern Medical Journal, 78, 384, 10.1097/00007611-198504000-00007

Savedra, 1993, Assessment of postoperation pain in children and adolescents using the adolescent pediatric pain tool, Nursing Research, 42, 5, 10.1097/00006199-199301000-00002

Serjeant, 1992, The painful crisis, 245

Serjeant, 1994, The painful crisis of hemozygous sickle cell disease: Clinical features, British Journal of Haematology, 87, 586, 10.1111/j.1365-2141.1994.tb08317.x

Shapiro, 1994, The Acute painful episode, 531

Shapiro, 1993, Patient-controlled analgesia for sickle cell-related pain, Journal of Pain & Symptom Management, 8, 22, 10.1016/0885-3924(93)90116-D

Shapiro, 1995, Home management of sickle cell-related pain in children and adolescents: Natural history and impact on school attendance, Pain, 61, 139, 10.1016/0304-3959(94)00164-A

Swerlick, 1993, Alpha-4 Beta-1-Integrin expression on sickle reticulocytes: Vascular cell adhesion molecule-1-dependent binding to endothelium, Blood, 82, 1891, 10.1182/blood.V82.6.1891.1891

Swift, 1989, Neurologic impairment in children with sickle cell anemia, Pediatrics, 84, 1077, 10.1542/peds.84.6.1077

Treadwell, 1994, Psychosocial aspects, 517

Valeriano-Marcet, 1991, Myonecrosis and myofibrosis as complication of sickle cell anemia, Annals of Internal Medicine, 115, 99, 10.7326/0003-4819-115-2-99

Wall, 1994

Williams, 1983, Psychological consideration in sickle cell disease, Nursing Clinics of North America, 18, 215, 10.1016/S0029-6465(22)01726-1