Literature DB >> 23284258

Emergency care necessity for sickle cell disease patients at Rio de Janeiro State Coordinating Blood Bank.

Mario Sant'anna Santoro1, Haroldo José de Matos, Delaine Fidlarczyk.   

Abstract

Hemoglobinopathies, in particular sickle cell disease, is the most prevalent group of genetically transmitted diseases in the Brazilian population and should thus be treated as a public health problem. Many of these patients frequently present with complications and require emergency care at the blood bank Coordinator in Rio de Janeiro. This study was developed with the aim of characterizing the emergency assistance required by sickle cell disease patients registered in the blood bank from January 2007 to December 2008. A retrospective study of medical records was made of 78, mostly children, patients from the date of their registration until December 2009. Most attendances (63.7%) were not considered emergency care. The use of specialized services for cases that do not require this level of complexity may saturate the capacity of these centers. However, delay of intervention for complications due to the transportation of patients to specialist centers may lead to deterioration in the clinical condition.

Entities:  

Keywords:  Anemia, sickle cell; Emergency medical services; Hospital Care; Retrospective studies

Year:  2011        PMID: 23284258      PMCID: PMC3520635          DOI: 10.5581/1516-8484.20110031

Source DB:  PubMed          Journal:  Rev Bras Hematol Hemoter        ISSN: 1516-8484


  5 in total

1.  Emergency department visits made by patients with sickle cell disease: a descriptive study, 1999-2007.

Authors:  Hussain R Yusuf; Hani K Atrash; Scott D Grosse; Christopher S Parker; Althea M Grant
Journal:  Am J Prev Med       Date:  2010-04       Impact factor: 5.043

2.  [Government Directive MS # 822/01: unique aspects of hemoglobinopathies for public health in Brazil].

Authors:  Antonio Sérgio Ramalho; Luís Alberto Magna; Roberto Benedito de Paiva-e-Silva
Journal:  Cad Saude Publica       Date:  2003-09-08       Impact factor: 1.632

3.  [Community-based programs for hereditary hemoglobinopathies in Brazilian high school students].

Authors:  M B Compri; N C Polimeno; M B Stella; A S Ramalho
Journal:  Rev Saude Publica       Date:  1996-04       Impact factor: 2.106

4.  [Evaluation of coverage by a neonatal screening program for hemoglobinopathies in the Recôncavo region of Bahia, Brazil].

Authors:  Wellington dos Santos Silva; Angel Lastra; Silviene Fabiana de Oliveira; Nazaré Klautau-Guimarães; Cesar Kope Grisolia
Journal:  Cad Saude Publica       Date:  2006-12       Impact factor: 1.632

5.  [Neonatal screening for hemoglobinopathies in Rio de Janeiro, Brazil].

Authors:  Clarisse Lopes de Castro Lobo; Leíse Marcelo Bueno; Patricia Moura; Leila Loureiro Ogeda; Shirley Castilho; Silvia Maia Farias de Carvalho
Journal:  Rev Panam Salud Publica       Date:  2003 Feb-Mar
  5 in total
  2 in total

1.  Comprehensive healthcare for individuals with sickle cell disease - a constant challenge.

Authors:  Rodolfo Delfini Cançado
Journal:  Rev Bras Hematol Hemoter       Date:  2011

2.  Sickle cell disease: looking back but towards the future.

Authors:  Rodolfo Delfini Cançado
Journal:  Rev Bras Hematol Hemoter       Date:  2012
  2 in total

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