Clinical and laboratory profile of patients with sickle cell anemia
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , |
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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Revista brasileira de hematologia e hemoterapia (Online) |
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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 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842017000100040 |
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 |
eu_rights_str_mv |
openAccess |
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) |
repository.mail.fl_str_mv |
sbhh@terra.com.br||secretaria@rbhh.org |
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1754213112871911424 |