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Published on: March 14, 2017
Otological burdens of Nigerian children with sickle cell disease
Oyebanji Anthony Olajuyin1, Oladele Simeon Olatunya2, Atilade Waheed Adegbiji1
1Department of Ear, Nose and Throat, Ekiti State University Teaching Hospital, Ado- Ekiti, Ekiti State, Nigeria.
Insights
Children with sickle cell disease (SCD) experience significantly more ear diseases, including hearing loss, than their non-SCD peers. This highlights the need for specialized otolaryngological care for SCD patients.
Area of Science:
- Pediatrics
- Otolaryngology
- Genetics
Background:
- Sickle cell disease (SCD) is a genetic disorder causing episodic illnesses and multi-systemic complications.
- Otolaryngological (ear, nose, and throat) issues are recognized complications of SCD.
- Data on otological disease burden in Nigerian children with SCD is limited.
Purpose of the Study:
- To describe and compare the prevalence of otological diseases in children with SCD versus non-SCD children.
- To investigate the hypothesis that children with SCD have a higher burden of ear diseases.
Main Methods:
- A cross-sectional study was conducted.
- Participants included children with SCD and age-matched non-SCD controls.
- Otologic diseases were assessed in both groups at a tertiary institution.
Main Results:
- Children with SCD had a significantly higher prevalence of otological diseases (47.62%) compared to non-SCD children (22.02%).
- Specific conditions like Sensorineural Hearing Loss (SNHL) and otosclerosis were more common in the SCD group.
- Neither hemoglobin concentration nor HbF levels correlated with SNHL in SCD patients.
Conclusions:
- Otological diseases are more prevalent in children with SCD.
- The findings underscore the need for targeted prevention of suppurative otitis media (SOM) in SCD children.
- Specialized otolaryngological care is recommended for children with SCD.
Introduction/Objective:
Sickle cell disease (SCD) is associated with episodic illnesses, multi-systemic affectations and end-organs damages. Otolaryngological related complications are not unexpected. Studies on the overall Otolaryngological pathologies in children with SCD relative to their non-SCD counterparts are scanty in Nigeria. We hypothesized that children with SCD are likely to have more otological burdens than their non-SCD counterparts. Thus, we embarked on this study to describe and compare the overall ear diseases burdens seen in children with sickle cell disease relative to their non-SCD counterparts.
Methodology:
A cross-sectional study of otologic diseases among children with SCD and their non-SCD counterparts attending the paediatrics and otolaryngological clinics of a Nigerian tertiary institution was conducted.
Results:
Overall, 80 (47.62%) of the 168 ears of SCD patients compared to 37 (22.02%) of the 168 ears of their non-SCD counterparts were affected by diseases (p < 0.0001). The diseases were Wax, Otitis Media with Effusion, Suppurative Otitis Media, Otosclerosis and Sensorineural Hearing Loss (SNHL). There was a significant difference in the prevalence of SNHL and solitary otosclerosis between the SCD patients and their non-SCD counterparts (P < 0.05) respectively. Both the Haemoglobin concentration and HbF did not discriminate between the SCD participants with or without SNHL (P > 0.05).
Conclusion:
This study showed that otological burdens are more prevalent in children with SCD than the non-SCD population. The microbiological peculiarity of suppurative otitis media (SOM) among participants stresses the need for concerted efforts at preventing SOM in SCD children. There is need for special Otolaryngological care for SCD children.
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