Clinical and laboratory profile of patients with sickle cell anemia

Detalhes bibliográficos
Autor(a) principal: Sant'Ana,Phelipe Gabriel dos Santos
Data de Publicação: 2017
Outros Autores: Araujo,Ariane Moreira, Pimenta,Cynthia Teixeira, Bezerra,Mário Lúcio Pacheco Ker, Borges Junior,Sílvio Pereira, Martins Neto,Viviana, Dias,Janaina Sousa, Lopes,Aline de Freitas, Rios,Danyelle Romana Alves, Pinheiro,Melina de Barros
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista brasileira de hematologia e hemoterapia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842017000100040
Resumo: Abstract Objective: This study aimed to describe and analyze clinical and laboratory characteristics of patients with sickle cell anemia treated at the Hemominas Foundation, in Divinópolis, Brazil. Furthermore, this study aimed to compare the clinical and laboratory outcomes of the group of patients treated with hydroxyurea with those patients that were not treated with hydroxyurea. Methods: Clinical and laboratorial data were obtained by analyzing medical records of patients with sickle cell anemia. Results: Data from the medical records of 50 patients were analyzed. Most of the patients were female (56%), aged between 20 and 29 years old. Infections, transfusions, cholecystectomy, splenectomy and systemic arterial hypertension were the most common clinical adverse events of the patients. The most frequent cause of hospitalization was painful crisis. The majority of patients had reduced values of hemoglobin and hematocrit (8.55 ± 1.33 g/dL and 25.7 ± 4.4%, respectively) and increased fetal hemoglobin levels (12 ± 7%). None of the clinical variables was statistically significant on comparing the two groups of patients. Among hematological variables only hemoglobin and hematocrit levels were statistically different between patients treated with hydroxyurea and untreated patients (p-value = 0.005 and p-value = 0.001, respectively). Conclusion: Sickle cell anemia requires treatment and follow-up by a multiprofessional team. A current therapeutic option is hydroxyurea. This drug reduces complications and improves laboratorial parameters of patients. In this study, the use of the drug increased the hemoglobin and hematocrit levels of patients.
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spelling Clinical and laboratory profile of patients with sickle cell anemiaSickle cell anemiaHydroxyureaHemoglobin SAbstract Objective: This study aimed to describe and analyze clinical and laboratory characteristics of patients with sickle cell anemia treated at the Hemominas Foundation, in Divinópolis, Brazil. Furthermore, this study aimed to compare the clinical and laboratory outcomes of the group of patients treated with hydroxyurea with those patients that were not treated with hydroxyurea. Methods: Clinical and laboratorial data were obtained by analyzing medical records of patients with sickle cell anemia. Results: Data from the medical records of 50 patients were analyzed. Most of the patients were female (56%), aged between 20 and 29 years old. Infections, transfusions, cholecystectomy, splenectomy and systemic arterial hypertension were the most common clinical adverse events of the patients. The most frequent cause of hospitalization was painful crisis. The majority of patients had reduced values of hemoglobin and hematocrit (8.55 ± 1.33 g/dL and 25.7 ± 4.4%, respectively) and increased fetal hemoglobin levels (12 ± 7%). None of the clinical variables was statistically significant on comparing the two groups of patients. Among hematological variables only hemoglobin and hematocrit levels were statistically different between patients treated with hydroxyurea and untreated patients (p-value = 0.005 and p-value = 0.001, respectively). Conclusion: Sickle cell anemia requires treatment and follow-up by a multiprofessional team. A current therapeutic option is hydroxyurea. This drug reduces complications and improves laboratorial parameters of patients. In this study, the use of the drug increased the hemoglobin and hematocrit levels of patients.Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular2017-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842017000100040Revista Brasileira de Hematologia e Hemoterapia v.39 n.1 2017reponame:Revista brasileira de hematologia e hemoterapia (Online)instname:Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)instacron:ABHHTC10.1016/j.bjhh.2016.09.007info:eu-repo/semantics/openAccessSant'Ana,Phelipe Gabriel dos SantosAraujo,Ariane MoreiraPimenta,Cynthia TeixeiraBezerra,Mário Lúcio Pacheco KerBorges Junior,Sílvio PereiraMartins Neto,VivianaDias,Janaina SousaLopes,Aline de FreitasRios,Danyelle Romana AlvesPinheiro,Melina de Barroseng2017-03-30T00:00:00Zoai:scielo:S1516-84842017000100040Revistahttp://www.rbhh.org/pt/archivo/https://old.scielo.br/oai/scielo-oai.phpsbhh@terra.com.br||secretaria@rbhh.org1806-08701516-8484opendoar:2017-03-30T00:00Revista brasileira de hematologia e hemoterapia (Online) - Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)false
dc.title.none.fl_str_mv Clinical and laboratory profile of patients with sickle cell anemia
title Clinical and laboratory profile of patients with sickle cell anemia
spellingShingle Clinical and laboratory profile of patients with sickle cell anemia
Sant'Ana,Phelipe Gabriel dos Santos
Sickle cell anemia
Hydroxyurea
Hemoglobin S
title_short Clinical and laboratory profile of patients with sickle cell anemia
title_full Clinical and laboratory profile of patients with sickle cell anemia
title_fullStr Clinical and laboratory profile of patients with sickle cell anemia
title_full_unstemmed Clinical and laboratory profile of patients with sickle cell anemia
title_sort Clinical and laboratory profile of patients with sickle cell anemia
author Sant'Ana,Phelipe Gabriel dos Santos
author_facet Sant'Ana,Phelipe Gabriel dos Santos
Araujo,Ariane Moreira
Pimenta,Cynthia Teixeira
Bezerra,Mário Lúcio Pacheco Ker
Borges Junior,Sílvio Pereira
Martins Neto,Viviana
Dias,Janaina Sousa
Lopes,Aline de Freitas
Rios,Danyelle Romana Alves
Pinheiro,Melina de Barros
author_role author
author2 Araujo,Ariane Moreira
Pimenta,Cynthia Teixeira
Bezerra,Mário Lúcio Pacheco Ker
Borges Junior,Sílvio Pereira
Martins Neto,Viviana
Dias,Janaina Sousa
Lopes,Aline de Freitas
Rios,Danyelle Romana Alves
Pinheiro,Melina de Barros
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Sant'Ana,Phelipe Gabriel dos Santos
Araujo,Ariane Moreira
Pimenta,Cynthia Teixeira
Bezerra,Mário Lúcio Pacheco Ker
Borges Junior,Sílvio Pereira
Martins Neto,Viviana
Dias,Janaina Sousa
Lopes,Aline de Freitas
Rios,Danyelle Romana Alves
Pinheiro,Melina de Barros
dc.subject.por.fl_str_mv Sickle cell anemia
Hydroxyurea
Hemoglobin S
topic Sickle cell anemia
Hydroxyurea
Hemoglobin S
description Abstract Objective: This study aimed to describe and analyze clinical and laboratory characteristics of patients with sickle cell anemia treated at the Hemominas Foundation, in Divinópolis, Brazil. Furthermore, this study aimed to compare the clinical and laboratory outcomes of the group of patients treated with hydroxyurea with those patients that were not treated with hydroxyurea. Methods: Clinical and laboratorial data were obtained by analyzing medical records of patients with sickle cell anemia. Results: Data from the medical records of 50 patients were analyzed. Most of the patients were female (56%), aged between 20 and 29 years old. Infections, transfusions, cholecystectomy, splenectomy and systemic arterial hypertension were the most common clinical adverse events of the patients. The most frequent cause of hospitalization was painful crisis. The majority of patients had reduced values of hemoglobin and hematocrit (8.55 ± 1.33 g/dL and 25.7 ± 4.4%, respectively) and increased fetal hemoglobin levels (12 ± 7%). None of the clinical variables was statistically significant on comparing the two groups of patients. Among hematological variables only hemoglobin and hematocrit levels were statistically different between patients treated with hydroxyurea and untreated patients (p-value = 0.005 and p-value = 0.001, respectively). Conclusion: Sickle cell anemia requires treatment and follow-up by a multiprofessional team. A current therapeutic option is hydroxyurea. This drug reduces complications and improves laboratorial parameters of patients. In this study, the use of the drug increased the hemoglobin and hematocrit levels of patients.
publishDate 2017
dc.date.none.fl_str_mv 2017-03-01
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=S1516-84842017000100040
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.bjhh.2016.09.007
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
publisher.none.fl_str_mv Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
dc.source.none.fl_str_mv Revista Brasileira de Hematologia e Hemoterapia v.39 n.1 2017
reponame:Revista brasileira de hematologia e hemoterapia (Online)
instname:Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
instname_str Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron_str ABHHTC
institution ABHHTC
reponame_str Revista brasileira de hematologia e hemoterapia (Online)
collection Revista brasileira de hematologia e hemoterapia (Online)
repository.name.fl_str_mv Revista brasileira de hematologia e hemoterapia (Online) - Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
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