Opioid doses and acute care utilization outcomes for adults with sickle cell disease: ED versus acute care unit

[1]  R. Fillingim,et al.  Safety and Utility of Quantitative Sensory Testing among Adults with Sickle Cell Disease: Indicators of Neuropathic Pain? , 2016, Pain practice : the official journal of World Institute of Pain.

[2]  D. Schriger,et al.  Looking through the retrospectoscope: reducing bias in emergency medicine chart review studies. , 2014, Annals of emergency medicine.

[3]  S. Ballas,et al.  Sickle cell pain: a critical reappraisal. , 1998, Blood.

[4]  L. Solomon,et al.  Pain management in adults with sickle cell disease in a medical center emergency department. , 2010, Journal of the National Medical Association.

[5]  C. Haywood,et al.  The burden of emergency department use for sickle‐cell disease: An analysis of the national emergency department sample database , 2010, American journal of hematology.

[6]  Hussain R Yusuf,et al.  Emergency department visits made by patients with sickle cell disease: a descriptive study, 1999-2007. , 2010, American Journal of Preventive Medicine.

[7]  A. Giardino,et al.  Healthcare utilization and expenditures for low income children with sickle cell disease , 2009, Pediatric blood & cancer.

[8]  M. Beavers,et al.  Treatment of uncomplicated vaso‐occlusive crises in children with sickle cell disease in a day hospital , 2008, Pediatric blood & cancer.

[9]  M. Steinberg,et al.  Effectiveness of a dedicated day hospital for management of acute sickle cell pain. , 2007, Haematologica.

[10]  P. Arbogast,et al.  Medical care utilization and mortality in sickle cell disease: A population‐based study , 2005, American journal of hematology.

[11]  D. Bareford,et al.  Day case management of sickle pain: 3 years experience in a UK sickle cell unit , 2004, British journal of haematology.

[12]  J. Eckman,et al.  Treating sickle cell pain: an update from the Georgia comprehensive sickle cell center. , 2002, Journal of emergency nursing: JEN : official publication of the Emergency Department Nurses Association.

[13]  L. Benjamin,et al.  Sickle cell anemia day hospital: an approach for the management of uncomplicated painful crises. , 2000, Blood.

[14]  I. Hambleton,et al.  Day‐care management of sickle cell painful crisis in Jamaica: a model applicable elsewhere? , 1999, British journal of haematology.

[15]  J. Steiner,et al.  Chart reviews in emergency medicine research: Where are the methods? , 1996, Annals of emergency medicine.

[16]  W. Holzemer,et al.  Postoperative analgesics for children and adolescents: prescription and administration. , 1994, Journal of pain and symptom management.

[17]  Y. Saunthararajah,et al.  Patient-reported outcomes: descriptors of nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle cell disease. , 2010, Journal of the National Medical Association.