Burden of sickle cell disease in paediatric patients admitted to Rundu Intermediate State Hospital, Namibia, over the 2-year period 2020 - 2021
PDF

Keywords

Malaria
Namibia
Prevalence
Sickle cell disease
Sickle cell anemia
Hemoglobin
Burden
Hemolytic crisis
Aplastic crisis
Vaso occlusive crisis
Sequestration
Admission

How to Cite

Burden of sickle cell disease in paediatric patients admitted to Rundu Intermediate State Hospital, Namibia, over the 2-year period 2020 - 2021. (2025). Undergraduate Research in Health Journal, 3(2), e3597. https://doi.org/10.1796/

Abstract

Background. Sickle cell disease (SCD) originated in the malarial regions of the tropics, where carriers are protected against death from malaria and hence enjoy an evolutionary advantage. The βS mutation is the archetypal example of natural selection in humans. Of the total population of Namibia (2.46 million), 72% are living in areas of active malaria transmission. Individuals with SCD suffer from various clinical manifestations.

Objectives. To document the clinical presentation and treatment outcome of paediatric patients with SCD admitted to Rundu State Intermediate Hospital in 2020 and 2021.

Methods. This was a retrospective cross-sectional study using paediatric hospital records for patients admitted to Rundu Hospital.

Results. Over the 2-year study period, a total of 3 168 children were admitted to Rundu Hospital, with 1 527 and 1 641 admitted in 2020 and 2021, respectively. Of these children, 103 had SCD, which constituted a prevalence of 3.3%. Many of the children with SCD were male, aged between 1 and 5 years, and suffering from vaso-occlusive crisis.

Conclusion. The burden of SCD among admitted patients at Rundu Hospital was high, and vaso-occlusive crisis was the main clinical manifestation. Patients with SCD had access to adequate management. SCD should be diagnosed in newborns before the development of complications, and comprehensive care must be offered in the future in Namibia.

PDF

References

1. Sawe HR, Reynolds TA, Mfinaga JA, et al. The clinical presentation, utilisation, and outcome of individuals with sickle cell anaemia presenting to urban emergency department of a tertiary hospital in Tanzania. BMC Hematol 2018;18:25. https://doi.org/10.1186/s12878-018-0122-3

2. Chakravorty S, Williams TN. Sickle cell disease: A neglected chronic disease of increasing global health importance. Arch Dis Child 2015;100(1):48-53. https://doi.org/10.1136/archdischild-2013-303773

3. Murayama M. Structure of sickle cell hemoglobin and molecular mechanism of the sickling phenomenon. Clin Chem 1967;13(7):578-588. https://doi.org/10.1093/clinchem/13.7.578

4. Inusa BPD, Hsu LL, Kohli N, et al. Sickle cell disease – genetics, pathophysiology, clinical presentation and treatment. Int J Neonatal Screen 2019;5(2):20. https://doi.org/10.3390/ijns5020020

5. Jastaniah W. Epidemiology of sickle cell disease in Saudi Arabia. Ann Saudi Med 2011;31(3):289-293.

https://doi.org/10.4103/0256-4947.81540

6. Karayalcin G, Rosner F, Kim KY, Chandra P, Aballi AJ. Sickle cell anemia – clinical manifestations in 100 patients and review of the literature. Am J Med Sci 1975;269(1):51-68. https://doi.org/10.1097/00000441- 197501000-00007

7. Oluleye TS, Brown BJ, Olawoye O. Ocular manifestations of children with sickle cell disease in Ibadan, Nigeria. East Afr Med J 2018;94(10):812-819. https://doi.org/10.4314/eamj.v94i10

8. Da Silva Filho IL, Ribeiro GS, Moura PG, Vechi ML, Cavalcante AC, de Andrada-Serpa MJ. Sickle cell disease: Acute clinical manifestations in early childhood and molecular characteristics in a group of children in Rio de Janeiro. Rev Bras Hematol Hemoter 2012;34(3):196-201. https://doi.org/10.5581/1516- 8484.20120049

9. Mustafa AEM, Abdlgadir O, Elsheikh NMH. A clinical and hematological study on the sickle cell anemia among children in El Obeid hospitals, Sudan. Int J Med Res Health Sci 2018;7(11):66-71.

10. Schnog JB, Duits AJ, Muskiet FA, Ten Cate H, Rojer RA, Brandjes DP. Sickle cell disease; a general overview. Neth J Med 2004;62(10):364-374.

11. Piel FB, Steinberg MH, Rees DC. Sickle cell disease. N Engl J Med 2017;376(16):1561-1573. https://doi. org/10.1056/NEJMra1510865

12. Oyetunji IA, Amoo AJ, Adeyemo TA, Ojewunmi OO. Asymptomatic malaria infection among children with sickle cell anaemia: The role of IL-10 and possible predisposing factors. PAMJ One Health 2020;2:7. https:// doi.org/10.11604/pamj-oh.2020.2.7.22892

13. Aloni MN, Tshimanga BK, Ekulu PM, Ehungu JLG, Ngiyulu RM. Malaria, clinical features and acute crisis in children suffering from sickle cell disease in resource-limited settings: A retrospective description of 90 cases. Pathog Glob Health 2013;107(4):198-201. https://doi.org/10.1179/2047773213Y.0000000089

14. Bansil NH, Kim TY, Tieu L, Barcega B. Incidence of serious bacterial infections in febrile children with sickle cell disease. Clin Pediatr (Phila) 2013;52(7):661-666. https://doi.org/10.1177/0009922813488645

15. Gbadoé, AD, Guédénon KM, N’zounou M, et al. Severe acute bacterial infections in children with sickle cell disease in Togo. J Pediatr Hematol Oncol 2023;45(7):404-408. https://doi.org/10.1097/ MPH.0000000000002710

16. Makani J, Cox SE, Soka D, et al. Mortality in sickle cell anemia in Africa: A prospective cohort study in Tanzania. PLoS ONE 2011;6(2):e14699. https://doi.org/10.1371/journal.pone.0014699

17. Uyoga S, Macharia AW, Mochamah G, et al. The epidemiology of sickle cell disease in children recruited in infancy in Kilifi, Kenya: A prospective cohort study. Lancet Global Health 2019;7(10):e1458-e1466. https:// doi.org/10.1016/S2214-109X(19)30328-6

18. Lamprecht H. Namibia making strides in battle against malaria. Republikein, 26 January 2021. https:// www.republikein.com.na/nuus/namibia-making-strides-in-battle-against-malaria2021-01-26 (accessed 20 October 2025).

19. World Health Organization. Sickle-cell disease: A strategy for the WHO African Region. Report AFR/ RC60/8. 22 June 2010. https://www.afro.who.int/sites/default/files/2017-06/afr_rc60_8.pdf (accessed 18 February 2021).

20. World Health Organization. Sickle-cell anemia: Report by the Secretariat. Fifty-ninth World Health. Assembly provisional agenda item 11.4. A59/9. 24 April 2006. https://apps.who.int/gb/archive/pdf_files/ WHA59/A59_9-en.pdf (accessed 18 February 2021).

21. Mandema SM, Sheehama J, Nakashwa N. Prevalence of malaria and risk factors among residents in Rundu District, Kavango East Region. Am J Biomed Sci Res 2024;23(2). https://doi.org/10.34297/ AJBSR.2024.23.003065

22. Namibia Statistics Agency. Namibia 2023 housing and population census. 2024. https://nsa.org.na/census/ wp-content/uploads/2024/10/2023-Population-and-Housing-Census-Main-Report-28-Oct-2024.pdf (accessed 16 October 2024).

23. Namibia Statistics Agency. Namibia inter-censal demographic survey 2016 report. 2017. https://cms.my.na/ assets/documents/NIDS_2016.pdf (accessed 28 April 2023).

24. American Society of Hematology. ASH statement on FDA’s approval of new sickle cell disease gene therapies. 8 December 2023. https://www.hematology.org/newsroom/press-releases/2023/ash-statement-on-fda- approval-of-new-sickle-cell-disease-gene-therapies (accessed 7 October 2024).

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Copyright (c) 2025 C N Sanzila, R Mashingaidze-Mano