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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
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.
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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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