Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study

Detalhes bibliográficos
Autor(a) principal: Hamerschlak,Nelson
Data de Publicação: 2005
Outros Autores: Maluf,Eliane, Pasquini,Ricardo, Eluf-Neto,José, Moreira,Frederico Rafael, Cavalcanti,Alexandre Biasi, Okano,Íria Ruriko, Falcão,Roberto Passeto, Pita,Marimília Teixeira, Loggetto,Sandra Regina, Rosenfeld,Luiz Gastão, Lorand-Metze,Irene Gyongyvér Heidemarie
Tipo de documento: Artigo
Idioma: eng
Título da fonte: São Paulo medical journal (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802005000300002
Resumo: CONTEXT AND OBJECTIVE: Aplastic anemia and agranulocytosis are rare but life-threatening disorders, often caused by drugs and other environmental exposures. Reported incidence of these diseases seems to vary between different geographic regions, and few data on their incidence are available for Latin American countries. The aim of this work is to determine the incidence of agranulocytosis and aplastic anemia in Brazil. DESIGN AND SETTING: Incidence study. Seven centers took part in the pilot phase, so as to represent all Brazilian regions. METHODS: Each center conducted an active search for new cases in a defined region by means of regular contacts with all hematologists, main clinical laboratories and clinicians in hospitals of the region. RESULTS: 74 patients with aplastic anemia and 16 with agranulocytosis were identified. Patients with agranulocytosis had a median age of 31 years (interquartile range, IQR: 12.5-48.2); 32.2% were male and 81.2% were white. The median age of aplastic anemia patients was 21 years (IQR 15.0-35.2); 62.2% were male, 50.0% were white and 39.2% mulatto. The incidence of agranulocytosis was estimated to be 0.5 cases per million individuals per year, ranging from 0.0 to 1.1 cases per million per year between regions. The incidence of aplastic anemia was 2.7 cases per million per year, ranging from 1.1 to 7.1 cases per million per year between regions. CONCLUSIONS: Aplastic anemia and agranulocytosis are rare diseases in Brazil. However, there is considerable variability in their incidences between different regions.
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spelling Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN studyAplastic anemiaAgranulocytosisIncidenceRisk factorsGranulocytesCONTEXT AND OBJECTIVE: Aplastic anemia and agranulocytosis are rare but life-threatening disorders, often caused by drugs and other environmental exposures. Reported incidence of these diseases seems to vary between different geographic regions, and few data on their incidence are available for Latin American countries. The aim of this work is to determine the incidence of agranulocytosis and aplastic anemia in Brazil. DESIGN AND SETTING: Incidence study. Seven centers took part in the pilot phase, so as to represent all Brazilian regions. METHODS: Each center conducted an active search for new cases in a defined region by means of regular contacts with all hematologists, main clinical laboratories and clinicians in hospitals of the region. RESULTS: 74 patients with aplastic anemia and 16 with agranulocytosis were identified. Patients with agranulocytosis had a median age of 31 years (interquartile range, IQR: 12.5-48.2); 32.2% were male and 81.2% were white. The median age of aplastic anemia patients was 21 years (IQR 15.0-35.2); 62.2% were male, 50.0% were white and 39.2% mulatto. The incidence of agranulocytosis was estimated to be 0.5 cases per million individuals per year, ranging from 0.0 to 1.1 cases per million per year between regions. The incidence of aplastic anemia was 2.7 cases per million per year, ranging from 1.1 to 7.1 cases per million per year between regions. CONCLUSIONS: Aplastic anemia and agranulocytosis are rare diseases in Brazil. However, there is considerable variability in their incidences between different regions.Associação Paulista de Medicina - APM2005-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802005000300002Sao Paulo Medical Journal v.123 n.3 2005reponame:São Paulo medical journal (Online)instname:Associação Paulista de Medicinainstacron:APM10.1590/S1516-31802005000300002info:eu-repo/semantics/openAccessHamerschlak,NelsonMaluf,ElianePasquini,RicardoEluf-Neto,JoséMoreira,Frederico RafaelCavalcanti,Alexandre BiasiOkano,Íria RurikoFalcão,Roberto PassetoPita,Marimília TeixeiraLoggetto,Sandra ReginaRosenfeld,Luiz GastãoLorand-Metze,Irene Gyongyvér Heidemarieeng2006-01-20T00:00:00Zoai:scielo:S1516-31802005000300002Revistahttp://www.scielo.br/spmjhttps://old.scielo.br/oai/scielo-oai.phprevistas@apm.org.br1806-94601516-3180opendoar:2006-01-20T00:00São Paulo medical journal (Online) - Associação Paulista de Medicinafalse
dc.title.none.fl_str_mv Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
title Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
spellingShingle Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
Hamerschlak,Nelson
Aplastic anemia
Agranulocytosis
Incidence
Risk factors
Granulocytes
title_short Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
title_full Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
title_fullStr Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
title_full_unstemmed Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
title_sort Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
author Hamerschlak,Nelson
author_facet Hamerschlak,Nelson
Maluf,Eliane
Pasquini,Ricardo
Eluf-Neto,José
Moreira,Frederico Rafael
Cavalcanti,Alexandre Biasi
Okano,Íria Ruriko
Falcão,Roberto Passeto
Pita,Marimília Teixeira
Loggetto,Sandra Regina
Rosenfeld,Luiz Gastão
Lorand-Metze,Irene Gyongyvér Heidemarie
author_role author
author2 Maluf,Eliane
Pasquini,Ricardo
Eluf-Neto,José
Moreira,Frederico Rafael
Cavalcanti,Alexandre Biasi
Okano,Íria Ruriko
Falcão,Roberto Passeto
Pita,Marimília Teixeira
Loggetto,Sandra Regina
Rosenfeld,Luiz Gastão
Lorand-Metze,Irene Gyongyvér Heidemarie
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Hamerschlak,Nelson
Maluf,Eliane
Pasquini,Ricardo
Eluf-Neto,José
Moreira,Frederico Rafael
Cavalcanti,Alexandre Biasi
Okano,Íria Ruriko
Falcão,Roberto Passeto
Pita,Marimília Teixeira
Loggetto,Sandra Regina
Rosenfeld,Luiz Gastão
Lorand-Metze,Irene Gyongyvér Heidemarie
dc.subject.por.fl_str_mv Aplastic anemia
Agranulocytosis
Incidence
Risk factors
Granulocytes
topic Aplastic anemia
Agranulocytosis
Incidence
Risk factors
Granulocytes
description CONTEXT AND OBJECTIVE: Aplastic anemia and agranulocytosis are rare but life-threatening disorders, often caused by drugs and other environmental exposures. Reported incidence of these diseases seems to vary between different geographic regions, and few data on their incidence are available for Latin American countries. The aim of this work is to determine the incidence of agranulocytosis and aplastic anemia in Brazil. DESIGN AND SETTING: Incidence study. Seven centers took part in the pilot phase, so as to represent all Brazilian regions. METHODS: Each center conducted an active search for new cases in a defined region by means of regular contacts with all hematologists, main clinical laboratories and clinicians in hospitals of the region. RESULTS: 74 patients with aplastic anemia and 16 with agranulocytosis were identified. Patients with agranulocytosis had a median age of 31 years (interquartile range, IQR: 12.5-48.2); 32.2% were male and 81.2% were white. The median age of aplastic anemia patients was 21 years (IQR 15.0-35.2); 62.2% were male, 50.0% were white and 39.2% mulatto. The incidence of agranulocytosis was estimated to be 0.5 cases per million individuals per year, ranging from 0.0 to 1.1 cases per million per year between regions. The incidence of aplastic anemia was 2.7 cases per million per year, ranging from 1.1 to 7.1 cases per million per year between regions. CONCLUSIONS: Aplastic anemia and agranulocytosis are rare diseases in Brazil. However, there is considerable variability in their incidences between different regions.
publishDate 2005
dc.date.none.fl_str_mv 2005-05-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802005000300002
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802005000300002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1516-31802005000300002
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Associação Paulista de Medicina - APM
publisher.none.fl_str_mv Associação Paulista de Medicina - APM
dc.source.none.fl_str_mv Sao Paulo Medical Journal v.123 n.3 2005
reponame:São Paulo medical journal (Online)
instname:Associação Paulista de Medicina
instacron:APM
instname_str Associação Paulista de Medicina
instacron_str APM
institution APM
reponame_str São Paulo medical journal (Online)
collection São Paulo medical journal (Online)
repository.name.fl_str_mv São Paulo medical journal (Online) - Associação Paulista de Medicina
repository.mail.fl_str_mv revistas@apm.org.br
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