1366 The Evolution of Pain During Hospitalization of Children with Painful Sickle Cell Crises
نویسندگان
چکیده
منابع مشابه
Nocturnal oxygen saturation and painful sickle cell crises in children.
The pathogenesis of acute painful crisis in children with sickle cell disease is poorly understood; suggested risk factors include sickle cell type, severity of anemia, fetal hemoglobin concentration, and hypoxemia from upper airway obstruction. In a cohort study of 95 patients the relationship between clinical, laboratory, and sleep study data and frequency of painful crisis was investigated. ...
متن کاملPredictive value of pain intensity in the clinical severity of painful crises in children and adolescents with sickle cell diseases
(1) Department of Pediatric Hematology and Oncology, Medical Faculty of Mustafa Kemal University, Hatay, Turkey. (2) Department of Pediatric, Medical Faculty of Mustafa Kemal University, Hatay, Turkey. (3) Department of Hematology, Hatay Antakya State Hospital, Hatay, Turkey. (4) Hemoglobinopathy Center, Hatay Antakya State Hospital, Hatay, Turkey. (5) Department of Internal Medicine, Medical F...
متن کاملManagement of acute painful crises in sickle cell disease.
Pain is a common mode of manifestation of sickle cell disease (SCD) but there is limited information on pain management in this disorder. This study examines the use of opioids and non-opioid analgesia in the management of painful crisis in adult SCD patients; the routine use of antimalarials and antibiotics as adjunct therapy was also examined. A total of 87% of the patients had had a form of ...
متن کاملPainful sickle cell crises precipitated by stopping prophylactic exchange transfusions.
A patient with homozygous sickle cell disease showed a reduced incidence of painful crises as a result of regular exchange transfusion, but on three occasions when transfusion treatment was interrupted, a painful crisis occurred. Onset of painful crisis was associated with raised packed cell volume (PCV) or percentage of haemoglobin S (HbS%), or both. Measurement of whole blood viscosity using ...
متن کاملRed blood cell changes during the evolution of the sickle cell painful crisis.
A longitudinal study of the red blood cell (RBC) deformability, percent of dense erythrocytes, and hematologic parameters has been conducted during 117 painful crises affecting 36 patients with sickle cell anemia between January, 1985 and December, 1990. RBC deformability was determined by osmotic gradient ektacytometry and the percentage of dense cells was quantitated by centrifugation on a di...
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ژورنال
عنوان ژورنال: Pediatric Research
سال: 2010
ISSN: 0031-3998,1530-0447
DOI: 10.1203/00006450-201011001-01366