Literature DB >> 16700347

Emergency management of sickle cell disease complications: review and practice guidelines.

John L Hick1, Stephen C Nelson, Karen Hick, M Obinna Nwaneri.   

Abstract

The prevalence of sickle cell disease (SCD) in Minnesota is increasing because of the influx of immigrants from Africa, India, and countries in Latin America. Clinicians, families, and individuals with the disease have expressed the need to educate health care professionals in emergency settings about the standards of care for treating pain and other complications of SCD. Late last year, the Minnesota Department of Health and the Minnesota Hemoglobinopathy Collaborative created guidelines for treating patients with complications of SCD in the emergency department. This article provides additional background information to support the guidelines.

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Year:  2006        PMID: 16700347

Source DB:  PubMed          Journal:  Minn Med        ISSN: 0026-556X


  3 in total

1.  A comparison of analgesic management for emergency department patients with sickle cell disease and renal colic.

Authors:  Matthew P Lazio; Heather H Costello; D Mark Courtney; Zoran Martinovich; Randall Myers; Amy Zosel; Paula Tanabe
Journal:  Clin J Pain       Date:  2010 Mar-Apr       Impact factor: 3.442

2.  Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS), a focus group and decision support tool development project.

Authors:  Paula Tanabe; Christopher Reddin; Victoria L Thornton; Knox H Todd; Ted Wun; John S Lyons
Journal:  Acad Emerg Med       Date:  2010-08       Impact factor: 3.451

3.  Adult emergency department patients with sickle cell pain crisis: results from a quality improvement learning collaborative model to improve analgesic management.

Authors:  Paula Tanabe; John W Hafner; Zoran Martinovich; Nicole Artz
Journal:  Acad Emerg Med       Date:  2012-04       Impact factor: 3.451

  3 in total

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