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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 5
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Original Article

Comparison of Emergency Department Wait Times in Adults with Sickle Cell Disease Versus Other Painful Etiologies

Dianne PulteDivision of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany; ;Department of Medicine, Thomas Jefferson University, Philadelphia, PA, USA; Correspondence[email protected]
,
Paris B. LovettDepartment of Medicine, Thomas Jefferson University, Philadelphia, PA, USA; ;EMCare Physician Providers Inc., Green Village, CO, USA;
,
David AxelrodDepartment of Medicine, Thomas Jefferson University, Philadelphia, PA, USA;
,
Albert CrawfordJefferson College of Population Health, Thomas Jefferson University, Philadelphia, PA, USA
,
John McAnaJefferson College of Population Health, Thomas Jefferson University, Philadelphia, PA, USA
&
Rhea PowellDepartment of Medicine, Thomas Jefferson University, Philadelphia, PA, USA;
Pages 330-334 | Received 20 Apr 2016, Accepted 16 Jul 2016, Published online: 28 Sep 2016

Citations (7)

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Read on this site (1)

Ugochi O Ogu, Nnenna U Badamosi, Pamela E Camacho, Amado X Freire & Patricia Adams-Graves. (2021) Management of Sickle Cell Disease Complications Beyond Acute Chest Syndrome. Journal of Blood Medicine 12, pages 101-114.
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Articles from other publishers (6)

Deborah M. Jean-Baptiste, Maureen Wassef, Susan Sullivan Bolyai & Coretta Jenerette. (2022) Individuals with Sickle Cell Disease Using SBAR as a Communication Tool: A Pilot Study. International Journal of Environmental Research and Public Health 19:21, pages 13817.
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Kendall L. Moody. (2022) Healthcare utilization and the quality of life of children and adolescents with sickle cell disease. Pediatric Blood & Cancer 69:8.
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Charles R. Jonassaint. (2021) If you Can’t Assess It, How Can you Treat It? Improving Pain Management in Sickle Cell Disease. Journal of Emergency Nursing 47:1, pages 10-15.
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Aindrea B. Maddray & Shannon M. Phillips. (2020) Instruments to Measure Perceptions in the Emergency Department Provider-Patient with Sickle Cell Disease Interaction: Findings of an Integrative Review from a Ph.D. Project. The Open Nursing Journal 14:1, pages 263-284.
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Samir K. Ballas & Carlton Dampier. (2020) Risk factors associated with increased emergency department utilization in patients with sickle cell disease: a systematic literature review. Annals of Hematology 99:11, pages 2483-2495.
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Angie Mae Rodday, Kimberly S Esham, Nicole Savidge & Susan K Parsons. (2020) Patterns of healthcare utilization among patients with sickle cell disease hospitalized with pain crises. eJHaem 1:2, pages 438-447.
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