Burden and Risk Factors of Chronic Kidney Disease in Children with Sickle Cell Anaemia Aged 5 – 16 Years at the University Teaching Hospital, Lusaka - Zambia

  • Nchimunya Machila University Teaching Hospital, Department of Paediatrics and Child Health, Private bag RW1X, Lusaka, Zambia.
  • Chishala Chabala
  • Chisambo Mwaba
  • Catherine Chunda-Liyoka
Keywords: Chronic kidney disease, sickle cell anaemia, Nephropathy.

Abstract

Background: Improved medical care has led to improved life expectancy of sickle cell anaemia (SCA) patients hence complications associated with SCA such as chronic kidney disease (CKD) are being seen more frequently. Globally, nephropathy of varying severity occurs in 5 to 18 % of the SCA population across all age groups with a third of the adults proceeding to develop CKD while over 30 % of paediatric SCA patients have CKD in Africa. The mortality rate in SCA patients CKD is high. This study sought to determine the prevalence and risk factors of CKD in SCA, information that was not available in Zambia prior to this study.This information will guide in targeting and timing of screening for CKD in SCA in children in our population Objectives:To determine prevalence of haematuria, proteinuria, abnormal estimated glomerular filtration rate (eGFR), CKD, and risk factors of CKD among the steady state SCA patients aged 5 to 16 years at the University Teaching Hospital (UTH), Lusaka. Methodology:This was a prospective cross - sectional study of 197 children aged 5 to 16 years with SCA at the UTH - Lusaka conducted from August 2014 to July 2015. Demographic and clinical data were collected using a structured questionnaire. Urine and blood samples were used to determine the urine albumin creatinine ratio (ACR) and full blood count /blood biochemistry respectively. CKD was defined and determined using the Kidney Disease Outcome Quality Initiative 2012 guidelines employing urine ACR, dipstick urinalysis and eGFR. In this study, spot urine ACR and dipstick urinalysis were done and repeated three months later if initial tests were abnormal. Data was analysed using SPSS version 21. Chi square and t test were used to compare proportions between groups. Relation between study variables and CKD were examined using logistic regression Results: The mean age of the participants was 9.6 years (SD ±3.6). Male to female ratio was 1:1. The median age at diagnosis of SCA was 22 months (IQR = 44). The prevalence of haematuria, proteinuria and CKD among the study participants was 14.2%, 36% and 36 % respectively. Low haemoglobin and elevated mean corpuscular volume (MCV) were associated with CKD-AOR 0.62, 95% CI; 0.46-0.84 and 1.04, 95% CI; 1.01 – 1.08 respectively. Recurrent admissions (due to VOCs, severe anaemia and febrile illness) were also risk factors associated with CKD- AOR 0.52, 95% CI; 0.27-0.98. CKD was not associated with age at enrolment, sex, age at diagnosis of SCA, recurrent Vaso-occlusive crisis (VOCs) or abnormal liver function tests. Conclusion: The prevalence of CKD among the SCA patients at UTH- Lusaka is high (36%) with lower Haemoglobin, elevated MCV and recurrent admissions being risk factors for developing CKD. SCA patients should be screened for CKD routinely at least once a year. Interventions such as early introduction of hydroxyurea, proactive blood transfusions and ACE inhibitors can reduce the risk of CKD and its progression to end stage renal disease.

References

1 DeBaun MR and Vichinsky E.Nelsons text book of paediatrics 18th edition (2007), Saunders, an imprint of Elsevier Inc.
2 Makani J, Ofori-AcquahSF, Nnodu O, Wonkam A and Ohene-Frempong K. Sickle cell disease: New opportunities and challenges for Africa. The scientific world journal, Volume 2013, article ID 193252, pages 1 -16.
3 Scheinmann JI: Sickle cell nephropathy. In: Pediatric Nephrology, edited by Holliday M, Barratt TM, Avner ED, Baltimore, Williams & Wilkins, 1994, pages 908–919.
4 Powars DR, Elliot-Mills MDD, Chan L, Hiti AL, Opas LM and Johnson C. Chronic renal failure in sickle cell disease, Risk factors, clinical course and mortality, Ann intern Med 115: 614-620, 1991.
5 Aleem A. Renal abnormalities in patients with sickle cell disease: a single center report from Saudi Arabia. Saudi J Kidney Dis Transpl 2008; 19(2): 194-199.
6 Bodas P, Huang A, O’Riordan AN, Sedor JR and KD.The prevalence of hypertension and abnormal kidney function in children with sickle cell disease- a cross sectional review Nephrology 2013, 14: 237. http://www.biomedcentral.com/1471-2369/14/237
7 Silva Junior GB, Loborio AB, Viera APF, ACX Bem, Filho ASL, ACF Filho et al. Evaluation of renal function in sickle cell disease in Brazil, Brazilian Journal of medical and Biological research (2012) b45: 652 – 655.
8 Yee MM, Jabbar SF, Osunkwo I Clement L, Lane PA, Eckman JR et al. Chronic kidney disease and albuminuria in children with sickle cell disease. Clin J Am SOC Nephrol 6: 2628- 2633, 2011.
9 Aneke JC, Adegoke AO, Oyekunle AA et al, degreesof kidneydisease in Nigerian adults with Sickle cell disease, medical principle and practice 2014;23:271–274, DOI: 10.1159/000361029
10 Madu AJ, A Ubesie, Ocheni S, Chinawa J, Madu KA, Ibegbulam OG et al. Important clinical and laboratory correlates of glomerular filtration rate in sickle cell anaemia, Nigerian Journal of clinical practice, Sep-Oct 2015. Volume 18. Issue 5.
11 Ephraim RKD, Osakunor DNM and Cudjoe O, Oduro EA, Asante-Asamani, Mitchell J et al, Chronic kidney disease is common in sickle cell disease: a cross-sectional study in the Tema Metropolis, Ghana, BMC Nephrology (2015) 16:75, DOI 10.1186/s12882-015-0072-y
12 Chansa C. Prevalence of Iron deficiency anaemia in adult patients with sickle cell anaemia at the University Teaching Hospital in Lusaka, Zambia. Dissertation study, March 2012.
13 Musonda C. Renal abnormalities among sickle cell anaemia patients aged 10 years and above at the University Teaching Hospital, Lusaka, Zambia. Dissertation study, 2010.
14 Alleyne GAO, Statius van Eps LW and Addac SK: The kidney in sickle cell anemia. (editorial review) Kidney Int 7:371–379, 1975.
15 Aygun B, Mortier NA, Smeltzer MP, Hankins JS, and Ware RE. Glomerular hyper filtration and albuminuria in children with sickle cell anemia. Pediatr Nephrol (2011) 26: 1285-1290.
16 Guash A, Cua M and You W. Sickle cell anemia causes a distinct pattern of glomerular dysfunction. Kidney int 1997: 51: 826-33.
Published
2020-09-30
How to Cite
1.
Machila N, Chabala C, Mwaba C, Chunda-Liyoka C. Burden and Risk Factors of Chronic Kidney Disease in Children with Sickle Cell Anaemia Aged 5 – 16 Years at the University Teaching Hospital, Lusaka - Zambia. Journal of Agricultural and Biomedical Sciences [Internet]. 30Sep.2020 [cited 23Nov.2024];4(3):40-8. Available from: https://humanities.unza.zm/index.php/JABS/article/view/397
Section
Biomedical Sciences