Incidence of aplastic anemia and agranulocytosis in Latin America: the LATIN study
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , , , , , , , , , |
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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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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1754209261235208192 |