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Profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote SS en phase inter critique chez l’enfant à Ziguinchor, Sénégal
Sickle cell disease poses a public health problem in Senegal. It mainly affects children and adolescents. This study aimed to determine the epidemiological, clinical and hematological profiles of homozygous (SS) sickle cell disease in a cohort of children followed-up at the Peace Hospital in Ziguinc...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The African Field Epidemiology Network
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5878839/ https://www.ncbi.nlm.nih.gov/pubmed/29610646 http://dx.doi.org/10.11604/pamj.2017.28.208.14006 |
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author | Thiam, Lamine Dramé, Assane Coly, Isabelle Zokébé Diouf, François Niokhor Seck, Ndiogou Boiro, Djibril Ndongo, Aliou Abdoulaye Basse, Idrissa Niang, Babacar Deme/Ly, Indou Sylla, Assane Diagne, Ibrahima Ndiaye, Ousmane |
author_facet | Thiam, Lamine Dramé, Assane Coly, Isabelle Zokébé Diouf, François Niokhor Seck, Ndiogou Boiro, Djibril Ndongo, Aliou Abdoulaye Basse, Idrissa Niang, Babacar Deme/Ly, Indou Sylla, Assane Diagne, Ibrahima Ndiaye, Ousmane |
author_sort | Thiam, Lamine |
collection | PubMed |
description | Sickle cell disease poses a public health problem in Senegal. It mainly affects children and adolescents. This study aimed to determine the epidemiological, clinical and hematological profiles of homozygous (SS) sickle cell disease in a cohort of children followed-up at the Peace Hospital in Ziguinchor. We conducted a retrospective study of the medical records from children with sickle cell disease. All patients aged between 2 months and 21 years with sickle cell disease SS during the intercritical period, hospitalized during the study period from 1(st) January 2015 to 31 August 2017 were included in our study. Compound heterozygous patients (SC, S Beta Thalassemia) were not included. We collected 46 medical records of patients with sickle cell disease SS (20 girls and 26 boys). The average age of children was 8,0 years [11 months-21 years]. Approximately 1/3 of children (39.1%) had an age less than or equal to 5 years. There was an ethnic diversity showing a predominance of the Diola (30.2%) followed by the Mandinga (27.9%) and the Poular (25.6%). The average age of children with first crisis was 35,5 months [7-192 months]. More than 1/3 of children (41.3%) had had first crisis before their second anniversary. In the child, first crisis was dominated by vaso-occlusive crisis (32.6%) followed by hand-foot syndrome (30.4%). Clinical signs during the intercritical period were pallor 95.6%), jaundice (36.9%) and splenomegaly (21.7%). Mean white blood cell count was 12465 leucocytes/mm(3) [5340-26900]. Hyperleukocytosis greater than 10 000 leucocytes/mm(3)was found in 34 patients (73.9%). All patients had anemia with an average hemoglobin of 08,6 g/dl [05,7-11,8]. Hemoglobin S rate ranged between 54.6 and 98.4%. Diagnosis and medical management of sickle cell disease SS are delayed in Ziguinchor. Neonatal screening may lead to improve early management of patients in the region. |
format | Online Article Text |
id | pubmed-5878839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-58788392018-04-02 Profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote SS en phase inter critique chez l’enfant à Ziguinchor, Sénégal Thiam, Lamine Dramé, Assane Coly, Isabelle Zokébé Diouf, François Niokhor Seck, Ndiogou Boiro, Djibril Ndongo, Aliou Abdoulaye Basse, Idrissa Niang, Babacar Deme/Ly, Indou Sylla, Assane Diagne, Ibrahima Ndiaye, Ousmane Pan Afr Med J Case Series Sickle cell disease poses a public health problem in Senegal. It mainly affects children and adolescents. This study aimed to determine the epidemiological, clinical and hematological profiles of homozygous (SS) sickle cell disease in a cohort of children followed-up at the Peace Hospital in Ziguinchor. We conducted a retrospective study of the medical records from children with sickle cell disease. All patients aged between 2 months and 21 years with sickle cell disease SS during the intercritical period, hospitalized during the study period from 1(st) January 2015 to 31 August 2017 were included in our study. Compound heterozygous patients (SC, S Beta Thalassemia) were not included. We collected 46 medical records of patients with sickle cell disease SS (20 girls and 26 boys). The average age of children was 8,0 years [11 months-21 years]. Approximately 1/3 of children (39.1%) had an age less than or equal to 5 years. There was an ethnic diversity showing a predominance of the Diola (30.2%) followed by the Mandinga (27.9%) and the Poular (25.6%). The average age of children with first crisis was 35,5 months [7-192 months]. More than 1/3 of children (41.3%) had had first crisis before their second anniversary. In the child, first crisis was dominated by vaso-occlusive crisis (32.6%) followed by hand-foot syndrome (30.4%). Clinical signs during the intercritical period were pallor 95.6%), jaundice (36.9%) and splenomegaly (21.7%). Mean white blood cell count was 12465 leucocytes/mm(3) [5340-26900]. Hyperleukocytosis greater than 10 000 leucocytes/mm(3)was found in 34 patients (73.9%). All patients had anemia with an average hemoglobin of 08,6 g/dl [05,7-11,8]. Hemoglobin S rate ranged between 54.6 and 98.4%. Diagnosis and medical management of sickle cell disease SS are delayed in Ziguinchor. Neonatal screening may lead to improve early management of patients in the region. The African Field Epidemiology Network 2017-11-07 /pmc/articles/PMC5878839/ /pubmed/29610646 http://dx.doi.org/10.11604/pamj.2017.28.208.14006 Text en © Lamine Thiam et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Series Thiam, Lamine Dramé, Assane Coly, Isabelle Zokébé Diouf, François Niokhor Seck, Ndiogou Boiro, Djibril Ndongo, Aliou Abdoulaye Basse, Idrissa Niang, Babacar Deme/Ly, Indou Sylla, Assane Diagne, Ibrahima Ndiaye, Ousmane Profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote SS en phase inter critique chez l’enfant à Ziguinchor, Sénégal |
title | Profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote SS en phase inter critique chez l’enfant à Ziguinchor, Sénégal |
title_full | Profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote SS en phase inter critique chez l’enfant à Ziguinchor, Sénégal |
title_fullStr | Profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote SS en phase inter critique chez l’enfant à Ziguinchor, Sénégal |
title_full_unstemmed | Profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote SS en phase inter critique chez l’enfant à Ziguinchor, Sénégal |
title_short | Profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote SS en phase inter critique chez l’enfant à Ziguinchor, Sénégal |
title_sort | profils épidemiologiques, cliniques et hématologiques de la drépanocytose homozygote ss en phase inter critique chez l’enfant à ziguinchor, sénégal |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5878839/ https://www.ncbi.nlm.nih.gov/pubmed/29610646 http://dx.doi.org/10.11604/pamj.2017.28.208.14006 |
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