Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in Nigeria

Aim:Nigeria has the highest number of children with sickle cell disease (SCD) with a consistent prevalence of 2 to 3% despite increased awareness and widespread premarital screening. In our practice, we observed that complaints of haemoglobin phenotype misdiagnosis are common among parents of childr...

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Main Authors: Motunrayo Oluwabukola Adekunle, Oyesola Ojewunmi, Adeola Barakat Animasahun, Faith Ozavisa Lawani, Peter Odion Ubuane
Format: Article
Language:English
Published: Galenos Yayinevi 2021-09-01
Series:Journal of Pediatric Research
Subjects:
Online Access: http://jpedres.org/archives/archive-detail/article-preview/prevalence-determinants-and-mpact-of-haemoglobin-p/48637
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author Motunrayo Oluwabukola Adekunle
Oyesola Ojewunmi
Adeola Barakat Animasahun
Faith Ozavisa Lawani
Peter Odion Ubuane
author_facet Motunrayo Oluwabukola Adekunle
Oyesola Ojewunmi
Adeola Barakat Animasahun
Faith Ozavisa Lawani
Peter Odion Ubuane
author_sort Motunrayo Oluwabukola Adekunle
collection DOAJ
description Aim:Nigeria has the highest number of children with sickle cell disease (SCD) with a consistent prevalence of 2 to 3% despite increased awareness and widespread premarital screening. In our practice, we observed that complaints of haemoglobin phenotype misdiagnosis are common among parents of children living with SCD. The present study was thus carried out to identify the prevalence, determinants, as well as the perceived impacts of haemoglobin phenotype misdiagnosis in Lagos, Nigeria. Materials and Methods:This study included the parents of children with SCD aged below 18 years. Interviewer administered questionnaires were used to obtain relevant biodata, sociodemographic data and an assessment of the perceived impact from both caregivers and their children, between May and July 2019.Results:Fifty-nine (32.4%) out of the 182 parents recruited had a previous haemoglobin phenotype misdiagnosis. Misdiagnosis was significantly more in individuals in the upper social class and those that had their tests performed in private laboratories. Clinical, psychosocial and economic impacts of having an affected child with SCD were reported.Conclusion:The frequency of wrong haemoglobin phenotype diagnosis is alarmingly rampant amongst the parents of children with SCD. This is potentially devastating to these families and to society; hence, the government needs to act by auditing and enforcing regulatory oversight of laboratories as well as instituting a nationwide new-born screening programme to replace the existing widespread use of haemoglobin electrophoresis for the diagnosis of SCD.
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spelling doaj.art-d7879cf6b2a845cc87596333330de9bf2023-02-15T16:12:11ZengGalenos YayineviJournal of Pediatric Research2147-94452587-24782021-09-018323924510.4274/jpr.galenos.2020.5436613049054Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in NigeriaMotunrayo Oluwabukola Adekunle0Oyesola Ojewunmi1Adeola Barakat Animasahun2Faith Ozavisa Lawani3Peter Odion Ubuane4 Lagos State University Teaching Hospital, Department of Paediatrics, Lagos, Nigeria DNA Laboratory, Sickle Cell Foundation Nigeria, Lagos, Nigeria Lagos State University College of Medicine, Department of Paediatrics and Child Health, Lagos, Nigeria Lagos State University Teaching Hospital, Department of Paediatrics, Lagos, Nigeria Lagos State University Teaching Hospital, Department of Paediatrics, Lagos, Nigeria Aim:Nigeria has the highest number of children with sickle cell disease (SCD) with a consistent prevalence of 2 to 3% despite increased awareness and widespread premarital screening. In our practice, we observed that complaints of haemoglobin phenotype misdiagnosis are common among parents of children living with SCD. The present study was thus carried out to identify the prevalence, determinants, as well as the perceived impacts of haemoglobin phenotype misdiagnosis in Lagos, Nigeria. Materials and Methods:This study included the parents of children with SCD aged below 18 years. Interviewer administered questionnaires were used to obtain relevant biodata, sociodemographic data and an assessment of the perceived impact from both caregivers and their children, between May and July 2019.Results:Fifty-nine (32.4%) out of the 182 parents recruited had a previous haemoglobin phenotype misdiagnosis. Misdiagnosis was significantly more in individuals in the upper social class and those that had their tests performed in private laboratories. Clinical, psychosocial and economic impacts of having an affected child with SCD were reported.Conclusion:The frequency of wrong haemoglobin phenotype diagnosis is alarmingly rampant amongst the parents of children with SCD. This is potentially devastating to these families and to society; hence, the government needs to act by auditing and enforcing regulatory oversight of laboratories as well as instituting a nationwide new-born screening programme to replace the existing widespread use of haemoglobin electrophoresis for the diagnosis of SCD. http://jpedres.org/archives/archive-detail/article-preview/prevalence-determinants-and-mpact-of-haemoglobin-p/48637 misdiagnosishaemoglobin-phenotypesickle cell diseaselaboratorynigeria
spellingShingle Motunrayo Oluwabukola Adekunle
Oyesola Ojewunmi
Adeola Barakat Animasahun
Faith Ozavisa Lawani
Peter Odion Ubuane
Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in Nigeria
Journal of Pediatric Research
misdiagnosis
haemoglobin-phenotype
sickle cell disease
laboratory
nigeria
title Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in Nigeria
title_full Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in Nigeria
title_fullStr Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in Nigeria
title_full_unstemmed Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in Nigeria
title_short Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in Nigeria
title_sort prevalence determinants and impact of haemoglobin phenotype misdiagnosis among parents of children living with sickle cell disease in nigeria
topic misdiagnosis
haemoglobin-phenotype
sickle cell disease
laboratory
nigeria
url http://jpedres.org/archives/archive-detail/article-preview/prevalence-determinants-and-mpact-of-haemoglobin-p/48637
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