Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of cases
OBJECTIVE: To analyze the neonatal screening program for hemoglobinopathies in São Carlos, Southeast Brazil, by investigating a series of cases in which the screening test was abnormal. More specifically, it was aimed to know the information regarding the neonatal screening received by mothers at th...
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| Format: | Article |
| Language: | English |
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Sociedade de Pediatria de São Paulo
2015-03-01
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| Series: | Revista Paulista de Pediatria |
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| Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822015000100019&lng=en&tlng=en |
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| author | Camila de Azevedo Silva Letícia Botigeli Baldim Geiza César Nhoncanse Isabeth da Fonseca Estevão Débora Gusmão Melo |
| author_facet | Camila de Azevedo Silva Letícia Botigeli Baldim Geiza César Nhoncanse Isabeth da Fonseca Estevão Débora Gusmão Melo |
| author_sort | Camila de Azevedo Silva |
| collection | DOAJ |
| description | OBJECTIVE: To analyze the neonatal screening program for hemoglobinopathies in São Carlos, Southeast Brazil, by investigating a series of cases in which the screening test was abnormal. More specifically, it was aimed to know the information regarding the neonatal screening received by mothers at the hospital and at primary health care, in addition to information related to genetic counseling. METHODS: A descriptive study that enrolled 119 mothers, accounting for 73% of all children born between 2010 and 2011 with abnormal results of neonatal screening for hemoglobinopathies. The mothers completed a questionnaire that assessed the information received at hospital and primary health care, and issues related to genetic counseling. Descriptive statistics was performed. RESULTS: Of the 119 participating mothers, 69 (58%) had children with sickle cell trait, 22 (18.5%) with hemoglobin C trait, 18 (15.1%) with alpha thalassemia trait and, in 10 cases (8.4%), the result was inconclusive. At the hospital, 118 mothers (99.2%) received information about where to go to collect the test and 115 (96.6%) were informed about the correct time to collect the test. Only 4 mothers (3.4%) were informed about which diseases are investigated and the risks of not performing the screening. Seventeen mothers (14.3%) recognized the difference between trait and disease, and 42 (35.3%) considered that a positive screening test could have implications for future pregnancies. In 70 cases (58.8%), the child's physician was not informed about the screening test results. CONCLUSIONS: The neonatal screening program needs further improvement. In both scenarios investigated, health professionals demonstrated a lack of training in providing information to mothers and families. |
| first_indexed | 2024-12-18T04:04:39Z |
| format | Article |
| id | doaj.art-d0dc3573aed64475aa4dbf7d64302002 |
| institution | Directory Open Access Journal |
| issn | 1984-0462 |
| language | English |
| last_indexed | 2024-12-18T04:04:39Z |
| publishDate | 2015-03-01 |
| publisher | Sociedade de Pediatria de São Paulo |
| record_format | Article |
| series | Revista Paulista de Pediatria |
| spelling | doaj.art-d0dc3573aed64475aa4dbf7d643020022022-12-21T21:21:37ZengSociedade de Pediatria de São PauloRevista Paulista de Pediatria1984-04622015-03-01331192710.1016/j.rpped.2014.08.001S0103-05822015000100019Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of casesCamila de Azevedo SilvaLetícia Botigeli BaldimGeiza César NhoncanseIsabeth da Fonseca EstevãoDébora Gusmão MeloOBJECTIVE: To analyze the neonatal screening program for hemoglobinopathies in São Carlos, Southeast Brazil, by investigating a series of cases in which the screening test was abnormal. More specifically, it was aimed to know the information regarding the neonatal screening received by mothers at the hospital and at primary health care, in addition to information related to genetic counseling. METHODS: A descriptive study that enrolled 119 mothers, accounting for 73% of all children born between 2010 and 2011 with abnormal results of neonatal screening for hemoglobinopathies. The mothers completed a questionnaire that assessed the information received at hospital and primary health care, and issues related to genetic counseling. Descriptive statistics was performed. RESULTS: Of the 119 participating mothers, 69 (58%) had children with sickle cell trait, 22 (18.5%) with hemoglobin C trait, 18 (15.1%) with alpha thalassemia trait and, in 10 cases (8.4%), the result was inconclusive. At the hospital, 118 mothers (99.2%) received information about where to go to collect the test and 115 (96.6%) were informed about the correct time to collect the test. Only 4 mothers (3.4%) were informed about which diseases are investigated and the risks of not performing the screening. Seventeen mothers (14.3%) recognized the difference between trait and disease, and 42 (35.3%) considered that a positive screening test could have implications for future pregnancies. In 70 cases (58.8%), the child's physician was not informed about the screening test results. CONCLUSIONS: The neonatal screening program needs further improvement. In both scenarios investigated, health professionals demonstrated a lack of training in providing information to mothers and families.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822015000100019&lng=en&tlng=enHemoglobinopatiasTriagem neonatalAssistência à saúde |
| spellingShingle | Camila de Azevedo Silva Letícia Botigeli Baldim Geiza César Nhoncanse Isabeth da Fonseca Estevão Débora Gusmão Melo Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of cases Revista Paulista de Pediatria Hemoglobinopatias Triagem neonatal Assistência à saúde |
| title | Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of cases |
| title_full | Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of cases |
| title_fullStr | Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of cases |
| title_full_unstemmed | Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of cases |
| title_short | Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of cases |
| title_sort | neonatal screening program for hemoglobinopathies in the city of sao carlos state of sao paulo brazil analysis of a series of cases |
| topic | Hemoglobinopatias Triagem neonatal Assistência à saúde |
| url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822015000100019&lng=en&tlng=en |
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