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Haematogenous Osteoarticular Infections in Paediatric Sickle Cell Trait Patients: A Reality in a Tertiary Centre in West Africa

BACKGROUND: Sickle cell trait (SCT) affects at least 5.2% of the world population, and it is considered asymptomatic by medical practitioners. There is a paucity of data regarding SCT paediatric patients and haematogenous osteoarticular infections (HOAIs). In our practice, some children with SCT pre...

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Autores principales: Yaokreh, Jean Baptiste, Thomas, Helen Audrey, Ekobo, Paule-Christine, Kouamé, Guy-Serge Yapo, Kouamé, Bertin Dibi, Ouattara, Ossénou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8109757/
https://www.ncbi.nlm.nih.gov/pubmed/33595545
http://dx.doi.org/10.4103/ajps.AJPS_114_20
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author Yaokreh, Jean Baptiste
Thomas, Helen Audrey
Ekobo, Paule-Christine
Kouamé, Guy-Serge Yapo
Kouamé, Bertin Dibi
Ouattara, Ossénou
author_facet Yaokreh, Jean Baptiste
Thomas, Helen Audrey
Ekobo, Paule-Christine
Kouamé, Guy-Serge Yapo
Kouamé, Bertin Dibi
Ouattara, Ossénou
author_sort Yaokreh, Jean Baptiste
collection PubMed
description BACKGROUND: Sickle cell trait (SCT) affects at least 5.2% of the world population, and it is considered asymptomatic by medical practitioners. There is a paucity of data regarding SCT paediatric patients and haematogenous osteoarticular infections (HOAIs). In our practice, some children with SCT presented HOAIs. This study aims to describe the pattern of HOAIs in children with SCT admitted in our unit. MATERIALS AND METHODS: A single-centre retrospective study of medical records of SCT paediatric patients treated for HOAIs between January 2012 and June 2019 was performed. The data extracted were epidemiologic (gender, age at diagnosis, history of haemoglobinopathy and ethnic group), diagnostic (time to diagnosis, type of infection and fraction of haemoglobin S [HbS] at standard electrophoresis of Hb), germs and complications. RESULTS: Among 149 patients with haemoglobinopathy treated for HOAIs, 52 have SCT. The prevalence of SCT patients was 34.9%. Thirty-nine (n = 39) records were retained for the study. The average age at diagnosis was 7.18 ± 4.59 years (7 months–15 years). The Malinké ethnic group was found in 22 (56.4%) cases. The mean HbS fraction was 37.2% ± 4.3% (30%–46%). Septic arthritis and osteoarthritis involved the hip in 11 cases, the shoulder in 4 and the knee in 2. Osteomyelitis was acute in 5 cases (11.1%) and chronic in 16 (35.5%). None of the patients has multifocal involvements. Bacterial identification was positive in 17 cases (37.8%). Staphylococcus aureus was involved in 9 cases (52.9%), and in one case, it was Mycobacterium tuberculosis. This patient has abscess of the psoas. No patient was infected by human immunodeficiency virus. The sequelae were joint destruction (n = 2), epiphysiodesis (n = 5) and retractile scars (n = 2). CONCLUSION: Relatively infrequent in our daily practice, SCT patients present with HOAIs. These infections had characteristics that are not very different from the series of the literature.
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spelling pubmed-81097572021-05-18 Haematogenous Osteoarticular Infections in Paediatric Sickle Cell Trait Patients: A Reality in a Tertiary Centre in West Africa Yaokreh, Jean Baptiste Thomas, Helen Audrey Ekobo, Paule-Christine Kouamé, Guy-Serge Yapo Kouamé, Bertin Dibi Ouattara, Ossénou Afr J Paediatr Surg Original Article BACKGROUND: Sickle cell trait (SCT) affects at least 5.2% of the world population, and it is considered asymptomatic by medical practitioners. There is a paucity of data regarding SCT paediatric patients and haematogenous osteoarticular infections (HOAIs). In our practice, some children with SCT presented HOAIs. This study aims to describe the pattern of HOAIs in children with SCT admitted in our unit. MATERIALS AND METHODS: A single-centre retrospective study of medical records of SCT paediatric patients treated for HOAIs between January 2012 and June 2019 was performed. The data extracted were epidemiologic (gender, age at diagnosis, history of haemoglobinopathy and ethnic group), diagnostic (time to diagnosis, type of infection and fraction of haemoglobin S [HbS] at standard electrophoresis of Hb), germs and complications. RESULTS: Among 149 patients with haemoglobinopathy treated for HOAIs, 52 have SCT. The prevalence of SCT patients was 34.9%. Thirty-nine (n = 39) records were retained for the study. The average age at diagnosis was 7.18 ± 4.59 years (7 months–15 years). The Malinké ethnic group was found in 22 (56.4%) cases. The mean HbS fraction was 37.2% ± 4.3% (30%–46%). Septic arthritis and osteoarthritis involved the hip in 11 cases, the shoulder in 4 and the knee in 2. Osteomyelitis was acute in 5 cases (11.1%) and chronic in 16 (35.5%). None of the patients has multifocal involvements. Bacterial identification was positive in 17 cases (37.8%). Staphylococcus aureus was involved in 9 cases (52.9%), and in one case, it was Mycobacterium tuberculosis. This patient has abscess of the psoas. No patient was infected by human immunodeficiency virus. The sequelae were joint destruction (n = 2), epiphysiodesis (n = 5) and retractile scars (n = 2). CONCLUSION: Relatively infrequent in our daily practice, SCT patients present with HOAIs. These infections had characteristics that are not very different from the series of the literature. Wolters Kluwer - Medknow 2021 2021-02-16 /pmc/articles/PMC8109757/ /pubmed/33595545 http://dx.doi.org/10.4103/ajps.AJPS_114_20 Text en Copyright: © 2021 African Journal of Paediatric Surgery https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Yaokreh, Jean Baptiste
Thomas, Helen Audrey
Ekobo, Paule-Christine
Kouamé, Guy-Serge Yapo
Kouamé, Bertin Dibi
Ouattara, Ossénou
Haematogenous Osteoarticular Infections in Paediatric Sickle Cell Trait Patients: A Reality in a Tertiary Centre in West Africa
title Haematogenous Osteoarticular Infections in Paediatric Sickle Cell Trait Patients: A Reality in a Tertiary Centre in West Africa
title_full Haematogenous Osteoarticular Infections in Paediatric Sickle Cell Trait Patients: A Reality in a Tertiary Centre in West Africa
title_fullStr Haematogenous Osteoarticular Infections in Paediatric Sickle Cell Trait Patients: A Reality in a Tertiary Centre in West Africa
title_full_unstemmed Haematogenous Osteoarticular Infections in Paediatric Sickle Cell Trait Patients: A Reality in a Tertiary Centre in West Africa
title_short Haematogenous Osteoarticular Infections in Paediatric Sickle Cell Trait Patients: A Reality in a Tertiary Centre in West Africa
title_sort haematogenous osteoarticular infections in paediatric sickle cell trait patients: a reality in a tertiary centre in west africa
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8109757/
https://www.ncbi.nlm.nih.gov/pubmed/33595545
http://dx.doi.org/10.4103/ajps.AJPS_114_20
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