Methods
The University College Hospital Ibadan is a large tertiary care referral centre located in Ibadan, the capital city of Oyo State, in South West, Nigeria. Patients come from Ibadan, other parts of Oyo State and beyond. Approximately 68% of the population of Nigeria live below the United Nations Children’s Fund (UNICEF) poverty line of 1.25 dollars per day [
14]. Patients are required to pay out-of-pocket for medical care, including RRT. The National Health Insurance is limited to a minority of employees of the Federal Government as of now and does not include the cost of dialysis or kidney transplantation.
According to the 2006 national census, Oyo State has a population of 5,580,894 and a growth rate of 3.35%. The population of children aged ≤ 14 years in Oyo state is 2,099,694, while that of children aged 5-14 years is 1,385,660. While Ibadan, the capital city, has a population of 2,560,573 with populations of children aged ≤ 14 years and those aged between 5-14 years in Ibadan 949,639 and 608,012 respectively [
15‐
17].
The hospital’s paediatric nephrology unit is the only one in Oyo state. It offers acute peritoneal dialysis with rigid or adapted catheters and acute haemodialysis [
18]. Chronic dialysis is not available due to barriers related to cost. Kidney transplantation have recently become available in the adult nephrology unit (four have been performed) and there are ongoing efforts to extend these services to children.
As a retrospective study, case records of all the patients who were managed for ESRD in the Paediatric Nephrology Unit of the hospital from January 2005 to December 2012 (96 months) were reviewed. Demographic, clinical, anthropometric, laboratory, aetiology of ESRD, and RRT modality data were extracted and entered into a questionnaire and subsequently into the Statistical Package for Social Sciences (SPSS) version 17 (Reproduced 2008, SPSS Statistics for Windows, Version 17. Chicago: SPSS Inc.) spread sheet.
ESRD was defined as need for dialysis, commencement of dialysis or death from renal failure in patients with chronic kidney disease (CKD) [
19]. Chronic kidney disease was defined as kidney damage or glomerular filtration rate of <60 ml/min/1.73 m
2 for ≥ 3 months, and kidney damage was defined as pathologic abnormalities or markers of damage on urine, blood or imaging tests [
19]. For patients who presented to us in ESRD and were followed up for less than 3 months, the diagnosis of background CKD was made from the patient’s clinical history or if the patient was stunted (height < 3
rd percentile) [
20]. Chronic Kidney disease was also diagnosed if the patient had congenital anomalies of the kidneys and urinary tract (CAKUT) or ultrasound finding of shrunken kidneys [
19,
21]. Nephrotic syndrome was defined as massive proteinuria (dipstick urinalysis ≥ 3+ proteinuria or 24 hour urinary protein of 40 mg/m
2/hour) with serum albumin of <2.5 g/dl, oedema and hyperlipidaemia [
22]. Chronic glomerulonephritis (CGN) was characterized by hypertension, renal failure, proteinuria and haematuria. The term glomerulonephritis referred to nephrotic syndrome or CGN [
22] CAKUT were diagnosed on the basis of ultrasound, micturating cysthourethrogram, or autopsy findings.
A primary outcome measure of in-hospital mortality was determined as a recording of mortality was only available for patients who died while admitted. The secondary outcome measure was the duration of survival in ESRD. Mean or median and inter quartile range (IQR) was calculated for continuous variables. Proportions were determined for categorical variables. The numerator for annual incidence of ESRD was children who reached ESRD in the respective year, who were domiciled in Ibadan and were managed in our hospital. The denominator for the incidence of ESRD incidence was the age related population of children in Ibadan for the year based on the 2006 national census [
15‐
17]. Incidence of ESRD was not calculated for children aged 15 years and above because patients in this age group variably present to and are managed in the adult nephrology unit. Data of patients managed in the adult unit were not included in this study.
Kaplan Meier survival analysis was used to determine the median survival time from the day of presentation in ESRD to in-hospital mortality. Patients who were not hospitalized or who were discharged home were censored. Cox proportional hazard regression analysis model was used to assess the effect of gender, age, presentation in ESRD, aetiology of ESRD and acute dialysis, on duration of survival in ESRD. For this analysis, age was grouped as 9 years and below versus 10 years and above; and aetiology of ESRD was grouped as CAKUT and acquired (glomerulonephritis and malignancy) causes. Patients were also grouped into those who received any form of dialysis and those who did not. Statistical analysis was done with the SPSS version 17 software.
Ethical approval for the study was obtained from the University of Ibadan/University College Hospital (UI/UCH) Ethics Committee and the study was performed in line with the Declaration of Helsinki.
Discussion
Children in ESRD are the most severely ill in the spectrum of childhood chronic kidney disease (CKD), and carry the highest risk for mortality. There are few studies on childhood ESRD from sub-Saharan Africa [
1,
2,
12,
13]. To the best of our knowledge none of the studies were reported exclusively on children in ESRD and therefore, our study adds important new information to the epidemiology of ESRD among Nigerian children. Our study showed that the incidence of paediatric ESRD was higher than previously reported from our sub region [
1,
2,
13] but lower than those reported in developed countries [
8,
9,
11,
23]. Glomerulonephritis was the commonest cause, followed by CAKUT. Management of the patients was hampered by lack of funds and facilities for chronic RRT resulting in high mortality.
This study noted a variation in the distribution of ESRD within Oyo state with virtually all patients domiciled in the state, coming from within Ibadan, the capital city, where our hospital is located. This variation is most likely due to differences in referral patterns of ESRD within the state. Awareness, recognition and referral of children with ESRD may be higher from communities that are closer to the University College Hospital which is the sole centre offering paediatric dialysis services in Oyo State. Variation in reporting of ESRD by accessibility to health services has been previously documented with higher reporting from metropolitan areas noted in Jamaica and Chile [
4,
24]. Concentration of main health resources and technology for the diagnosis and treatment of renal diseases in metropolitan areas and under reporting of kidney disease from other areas are assumed to be reasons for differential referral patterns [
4,
24].
The few studies on childhood ESRD from sub-Saharan Africa, mainly from Nigeria [
1,
2] and South Africa [
13], also included patients with other stages of CKD and found a CKD incidence of 1-3 per million children. The present study found an ESRD incidence of 4 per million children in Ibadan which was higher than findings from other parts of Nigeria [
1,
2] or South Africa [
13]. The higher incidence of ESRD in our study compared to the other Nigerian studies may be due to differences in referral patterns, while the higher incidence compared to findings in South Africa may be related to variations in genetic or environmental factors.
Additionally we found an increasing incidence of paediatric ESRD over the 4 year bands 2005-2008, and 2009-2012. This is similar to a report from the United Kingdom which also noted a rising incidence in paediatric RRT for ESRD over 3 consecutive 5 year bands from 1996-2010 [
25]. The rising incidence of RRT in the United Kingdom was attributed to increased provision of dialysis to younger children due to improvements in techniques for nutritional and dialysis support and increasing referral of children who are younger than 16 years of age to paediatric units [
25]. The rising incidence of ESRD in the present study may be due to increasing recognition and referral of children in ESRD.
The incidence of childhood ESRD observed in this study is lower than that reported from many developed countries. In the United States and Canada an ESRD incidence of 9-16 per million is recorded for children aged 0-19 years [
11]. The North American registries included patients in the 15-19 year age group an age group reportedly having the highest incidence of paediatric ESRD [
9,
11,
23]. The incidence in Ibadan was also less than the mean of 5.3 per million for children less than 14 years old reported in European countries [
8], or 10.9 per million children as noted in Turkey [
26]. It was however much less than the 17 per million children noted in Kuwait in the Middle East, where hereditary renal diseases are common due to high prevalence of consanguinity [
27]. Poor health seeking behaviour, under-reporting of cases and referral patterns in poor resource settings may also contribute to the low incidence in Ibadan compared to developed nations. Additionally, the lack of resources for appropriate consultations, medications, chronic dialysis and kidney transplantation for children accelerates mortality in patients with both acute and chronic kidney diseases leading to a lower incidence and prevalence of ESRD in Ibadan and indeed in many parts of sub-Saharan Africa.
The male predominance noted in this study is similar to the observation in many other reports [
11,
23,
25‐
29] including studies done in Africa [
1,
2,
12,
13]. The male predominance, as in the other studies, is due to the higher proportion of males among patients with CAKUT. Furthermore, there are relatively few patients in the 0-5 year age group in our study compared to other age groups in our study. ESRD in younger children is mostly due to CAKUT, while the contribution of glomerulonephritis to ESRD increases with age [
1,
9,
25,
30,
31]. The low number of patients who are less than 5 years of age in our study may reflect the finding of low numbers of patients with CAKUT versus those with glomerulonephritis.
Glomerulonephritis was the leading cause of ESRD in our study, accounting for approximately 80% of cases. This was followed by CAKUT in approximately 20% of our patients. This is in contrast to reports from Europe [
8], Australia [
9], Japan [
23], Kuwait [
27], Turkey [
26] and among whites in the United States [
11] where CAKUT are the largest causes of ESRD and are responsible for 34% - 52% of cases of ESRD among children. Glomerulonephritis accounts for 14 - 30% childhood ESRD in these settings [
8,
9,
11,
23,
27]. Among African American children primary and secondary glomerulonephritis were the leading cause of ESRD [
11]. Reports from India, South East Asia and South America indicate that glomerulonephritis is the predominant cause of childhood CKD in developing countries [
3,
32‐
34]. Similarly in a South African study [
13] with 75% black participants and in other studies from sub-Saharan Africa [
1,
2,
12], glomerulonephritis was the largest cause of CKD occurring in 25.4 - 56.4% of children, while CAKUT occurred in 17.5-37.3% of children [
1,
2,
10,
11]. The predominance of glomerulonephritis followed by CAKUT among our patients is consistent with the observation in African Americans and in developing countries including those in sub-Saharan Africa [
1,
2,
11‐
13].
The large proportion of patients with glomerulonephritis compared to CAKUT in this study may be due to both genetic and environmental factors. The renal biopsies, although few were performed, predominantly showed FSGS. Among African American children, FSGS is three times more common than in Caucasian children, suggesting a genetic basis [
10,
28]. In Ibadan, where our hospital is located, a strong association was previously found between APOL 1 variants and their two allele gene haplotypes in a study of 166 adult Nigerian patients with non diabetic kidney disease [
35]. Furthermore, vesico-ureteral reflux, a congenital anomaly which is commonly associated with renal hypoplasia and dysplasia and reflux nephropathy among children in Europe, Asia, and the Middle East and also among white Americans is less common among African Americans and in sub-Saharan Africa [
1,
2,
12,
36‐
39].
The high prevalence of glomerulonephritis among children in developing countries and in sub-Saharan Africa has also been attributed to the high prevalence of bacterial, protozoal or viral infections [
40,
41]. In our study 20% of the patients with glomerulonephritis were either seropositive for HIV or Hepatitis B surface antigen. With increasing survival of HIV infected children and reduction in mortality from infectious diseases, HIV appears to be emerging as a cause of paediatric ESRD [
42‐
44]. It is not clear, however, if Hepatitis B virus infection was the aetiology of ESRD in our patients or if it was incidental [
45].
The high proportion of patients with glomerulonephritis among our patients compared with CAKUT might also be due to patient selection. Our study evaluated only children in ESRD. It is recognised that glomerulonephritis progresses to ESRD faster than CAKUT [
36,
46]. Additionally severe cases of CAKUT may have been missed as they might have died in infancy or early childhood without diagnosis.
The majority (60%) of our patients already had ESRD at the time of their initial presentation. This pattern of late presentation has been noted in developing countries like India [
31,
32], Jamaica [
4] and Syria [
47], where ESRD was present in 20-55.5% of children with CKD at presentation. Late presentation has also been noted among ethnic minorities in the UK [
48]. In contrast, among children in the North American Renal Transplant and Cooperative Study (NAPRTCS), with many of the contributing centres in developed countries, only 4.3% were in ESRD at entry into the study [
10]. The early features of CKD may not be overt and may have been missed by the caregivers leading to late presentation in some of our patients. Furthermore there may be low priority for screening and referral of children for kidney disease in many primary and secondary health facilities in Nigeria because chronic renal replacement is expensive and not readily available. Early diagnosis of kidney disease may, however, allow institution of therapy that will potentially prevent or slow the progression to ESRD [
22]. Efforts to increase awareness of childhood kidney disease among the public and health workers, to promote early diagnosis, referral and treatment of kidney disease among children are needed.
Access to chronic RRT has improved the outcome of ESRD in developed countries. The case fatality ratio decreased from 11.0 per 100 patient years in the 1960s to 1.3 per 100 patient years in 2002-2004 [
7,
49]. Long term survival rate for children on chronic RRT in developed countries is 79% at 10 years and 66% at 20 years [
6,
28]. Transplant patients consistently have a 4 fold survival advantage compared with dialysis patients [
6,
11]. Life expectancy among young adults who started RRT in childhood is 38 years for patients remaining on dialysis compared to 68 years for those with a functioning graft [
50]. In developed countries, deaths in children from ESRD now occur mainly from infections and cardiovascular disease rather than renal failure in contrast to the pattern in developing countries [
28]. Although we offered acute dialysis to more patients in ESRD than in previous Nigerian reports on paediatric ESRD, in the absence of chronic RRT outcome remained very poor. Patients who were discharged home would have died at home shortly after discharge in the absence of chronic RRT. Similar high mortality was noted in previous reports from Nigeria [
1,
2]. Some centres in the country, including ours, have started performing kidney transplantation, the financial implication (including cost of immunosuppressive medications) is, however, prohibitive for most Nigerians. The absence of chronic renal replacement therapy was the cause of the high mortality in our patients.
Our study has a number of limitations, one of which is that it reflects a single centre hospital based incidence and the data is likely an underestimate of the true incidence of ESRD since many patients may not present or continue follow up at a tertiary care centre. A prospective multicentre study may give a better estimate, although prospective community based study will be ideal. Another limitation of our study is that the aetiology of chronic glomerulonephritis was not determined in many of our patients and that few renal biopsies were performed. In sub-Saharan Africa late presentation and limited diagnostic facilities, including facilities for immunofluorescence and electron microscopy of renal biopsies, make it difficult to determine the aetiology of glomerulonephritis in many patients. Multicentre and prospective studies are needed to accurately determine the aetiology of chronic glomerulonephritis in sub-Saharan Africa. The study however indicates that the incidence of paediatric ESRD in the sub-region may be higher than previously reported and underscores the high mortality associated with this condition in sub-Saharan Africa.
In view of the high mortality associated with ESRD in settings with very limited access to chronic RRT, urgent steps need to be taken in the areas of preventive nephrology, development of a public-funded chronic RRT program, and setting up of a national registry for paediatric ESRD. Programs that increase awareness of kidney disease among the public and health workers may lead to earlier presentation, detection and management of kidney disease. Optimal management of patients with glomerulonephritis is needed with adequate laboratory back up and access to medications. Early diagnosis and appropriate management of children with CAKUT may reduce mortality; it is however unclear if management will improve long term renal outcomes especially with posterior urethral valves [
51,
52]. A public-funded chronic RRT program is therefore needed to improve access to dialysis and kidney transplantation and potentially lead to improved prognosis. Nigerian nephrologists and other stake holders should continue to provide advocacy for the National Health Insurance to be expanded to include a larger proportion of the population and the cost of chronic RRT. The setting up of a national registry of paediatric ESRD will provide important data for advocacy, to monitor outcome of interventions and national trends in paediatric ESRD. In addition to governmental support, that from non-governmental bodies and individuals is required to achieve sustained improvement of paediatric nephrology services and research in Nigeria and sub-Saharan Africa.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
AOA: Conceptualized the work, data interpretation, and revised the article critically for intellectual content. ADA: Performed data analysis and interpretation. OOO: Performed data interpretation and revised the article critically for the intellectual content. SAM: Performed data interpretation and revised the article critically for the intellectual content. All the authors approved the final version.