Literature DB >> 21927581

"Sickle Cell Disease in the Emergency Department: Atypical Complications and Management"

Amanda M Brandow1, Robert Liem.   

Abstract

Sickle cell disease is the most common inherited blood disorder in the United States. This disorder of hemoglobin structure leads to a chronic hemolytic anemia and complex chronic disease manifested by sudden, severe, and life-threatening complications. These acute complications can occur in any organ system beginning in early childhood and lasting throughout life. The intermittent nature and acuity of these complications lend the emergency department to be an important site of care. The hallmark of sickle cell disease is the vasoocclusive painful event. Other more "typical" complications include fever, acute chest syndrome, priapism, and ischemic stroke. Children with sickle cell disease can also present with other "atypical" complications that can have devastating consequences if they are unrecognized. Detailed discussion of these "atypical" sickle cell disease complications, organized by organ system involved, will be the focus of this article.

Entities:  

Year:  2011        PMID: 21927581      PMCID: PMC3172721          DOI: 10.1016/j.cpem.2011.07.003

Source DB:  PubMed          Journal:  Clin Pediatr Emerg Med        ISSN: 1522-8401


  51 in total

Review 1.  Sickle cell hepatopathy.

Authors:  S Banerjee; C Owen; S Chopra
Journal:  Hepatology       Date:  2001-05       Impact factor: 17.425

2.  Orbital compression syndrome presenting as orbital cellulitis in a child with sickle cell anemia.

Authors:  Miltiadis Douvoyiannis; Esra Fakioglu; Nathan Litman
Journal:  Pediatr Emerg Care       Date:  2010-04       Impact factor: 1.454

3.  The burden of emergency department use for sickle-cell disease: an analysis of the national emergency department sample database.

Authors:  Sophie Lanzkron; C Patrick Carroll; Carlton Haywood
Journal:  Am J Hematol       Date:  2010-10       Impact factor: 10.047

4.  Biomarkers of splenic function in infants with sickle cell anemia: baseline data from the BABY HUG Trial.

Authors:  Zora R Rogers; Winfred C Wang; Zhaoyu Luo; Rathi V Iyer; Eglal Shalaby-Rana; Stephen D Dertinger; Barry L Shulkin; John H Miller; Bea Files; Peter A Lane; Bruce W Thompson; Scott T Miller; Russell E Ware
Journal:  Blood       Date:  2011-01-07       Impact factor: 22.113

Review 5.  Human parvovirus B19: general considerations and impact on patients with sickle-cell disease and thalassemia and on blood transfusions.

Authors:  Svetoslav N Slavov; Simone Kashima; Ana Cristina Silva Pinto; Dimas Tadeu Covas
Journal:  FEMS Immunol Med Microbiol       Date:  2011-06-15

6.  Delayed hemolytic transfusion reaction in children with sickle cell disease.

Authors:  Mariane de Montalembert; Marie-Dominique Dumont; Claire Heilbronner; Valentine Brousse; Oussama Charrara; Béatrice Pellegrino; Christophe Piguet; Valérie Soussan; France Noizat-Pirenne
Journal:  Haematologica       Date:  2011-02-17       Impact factor: 9.941

7.  Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial.

Authors:  A Ferster; C Vermylen; G Cornu; M Buyse; F Corazza; C Devalck; P Fondu; M Toppet; E Sariban
Journal:  Blood       Date:  1996-09-15       Impact factor: 22.113

8.  Antithrombotic therapy for venous thromboembolic disease: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition).

Authors:  Clive Kearon; Susan R Kahn; Giancarlo Agnelli; Samuel Goldhaber; Gary E Raskob; Anthony J Comerota
Journal:  Chest       Date:  2008-06       Impact factor: 9.410

9.  Acute sickle cell hepatopathy represents a potential contraindication for percutaneous liver biopsy.

Authors:  Nada Zakaria; Alex Knisely; Bernard Portmann; Giorgina Mieli-Vergani; Julia Wendon; Roopen Arya; John Devlin
Journal:  Blood       Date:  2002-08-15       Impact factor: 22.113

Review 10.  Sickle cell lung disease and sudden death: a retrospective/prospective study of 21 autopsy cases and literature review.

Authors:  Jason K Graham; Marina Mosunjac; Randy L Hanzlick; Mario Mosunjac
Journal:  Am J Forensic Med Pathol       Date:  2007-06       Impact factor: 0.921

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  1 in total

1.  Hospitalization Events among Children and Adolescents with Sickle Cell Disease in Basra, Iraq.

Authors:  Zeina A Salman; Meaad K Hassan
Journal:  Anemia       Date:  2015-10-26
  1 in total

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