Chronic Kidney Disease: Epidemiological, Clinical, and Paraclinical Characteristics at the Nephrology Unit of the Fousseyni Daou Hospital in Kayes, Mali ()
1. Introduction
Chronic kidney disease (CKD) is a major public health problem. CKD is the progressive and irreversible loss of kidney function. It results from a reduction in functional renal parenchyma. It is diagnosed based on a decrease in glomerular filtration rate (GFR), which results in a gradual increase in plasma creatinine concentrations [1]. Its incidence continues to rise in developed countries due to the ageing population and the increase in vascular diseases, which affect the kidneys and can lead to CKD [1]. In Africa, changes in people’s eating habits and lifestyles have led to the emergence of certain diseases such as diabetes and high blood pressure (HBP), which are complicated by CRF in most patients in our context due to the lack of early screening and medical follow-up. Madore F [2] reported that patients starting dialysis were diabetic and hypertensive in 54% and 96% of cases, respectively. In addition, the persistence of neglected tropical diseases such as urinary bilharzia and other infectious diseases that are not adequately treated, as well as self-medication encouraged by the increased availability of street drugs, are other equally important risk factors for CRF in our context [3].
In Côte d’Ivoire, CKD is the second leading cause of death in the internal medicine department of the Treichville University Hospital [4] and accounts for 4 to 20% of deaths at the Yalgado Ouédraogo National Hospital in Burkina Faso [5]. Its prevalence is underestimated given its silent progression in the early stages.
In Mali, it accounts for 15.98% of admissions to the nephrology department of Point G University Hospital [6].
Extrarenal purification (ERP) by haemodialysis (HD) forms the basis of the medical management of end-stage CRF in our countries. In Mali, 20% of patients reaching the CRF stage benefit from this technique [7].
In Kayes, there are little data on CRF, hence the interest of our study, which aimed to describe the epidemiological, clinical, and paraclinical profile of patients with chronic renal failure in the nephrology unit of the Fousseyni Daou Hospital in Kayes.
2. Materials and Methods
This was a prospective, single-centre, cross-sectional, and descriptive study conducted from 1 January to 31 December 2022. All patients diagnosed with chronic renal failure in the aforementioned department during the study period with a complete medical record were included. Patients seen outside the study period, those without CRF, or those with incomplete medical records were not included.
The variables studied were:
Sociodemographic data: age, gender, occupation, marital status, place of residence, and ethnicity.
2.1. Clinical Data
Reason for hospitalization or consultation
Medical, urological, nephrological, and surgical history.
Cardiovascular risk factors: age, gender, smoking, hypertension, diabetes, dyslipidaemia, obesity, heredity, sedentary lifestyle, and alcohol consumption.
General signs: blood pressure, temperature, weight, pulse, height, BMI, and urine output.
Symptoms: oedema of the lower limbs, facial swelling, anorexia, vomiting, nausea, insomnia, drowsiness, diarrhoea, pruritus, asthenia, dizziness, muscle cramps, headache, tinnitus, lower back pain, chest pain, etc.
Physical signs: oedema, uraemic frost, crackles, jugular turgidity, hepatojugular reflux, abdominal mass, bladder globe, pericardial friction, etc.
2.2. Paraclinical Data
2.2.1. Biological
1=CMI (GFR ≥ 90); 2=mild CRF (GFR = 60 - 89); 3=moderate CRF (3A GFR = 45 - 59 and 3B GFR = 30 - 44); 4=severe CRF (GFR = 15 - 29); 5=end-stage CRF (GFR < 15)
Blood urea and uric acid levels: these levels were used to assess the extent of nitrogen retention.
Complete blood count (CBC): to check for anaemia defined by an Hb level < 11 g/dl, as well as other CBC abnormalities.
Complete blood ionogram (sodium, potassium, calcium, and phosphorus levels, PTH, vitamin D): to check for water-electrolyte imbalances and calcium-phosphorus metabolism disorders.
24-hour proteinuria test Proteinuria: Minimal: < 1 g/24 h; Moderate: 1 to 3 g/24 h; Massive: > 3 g/24 h
Cytological and bacteriological examination of urine (ECBU): ECBU to check for leukocyturia, hematuria, and urinary tract infection.
2.2.2. Radiological
Abdominal ultrasound to assess the size and echostructure of the kidneys, as well as the condition of the excretory tracts.
Frontal chest X-ray: to check for cardiomegaly, pulmonary oedema, or pleuro-parenchymal involvement.
Cardiac ultrasound: to check for hypertrophy and/or dilation of the heart chambers, heart failure, pericarditis, valvular heart disease, or pericardial effusion.
ECG: to check for LVH and other signs.
Fundus examination: to check for retinopathy
Diabetic retinopathy, if associated with diabetes:
Absence of diabetic retinopathy Minimal non-proliferative DR
Moderate non-proliferative DR
Severe non-proliferative RD
Early proliferative RD
Moderate proliferative RD
Severe proliferative RD
Complicated proliferative RD
Oedematous maculopathy
Ischemic maculopathy
Hypertensive retinopathy is associated with hypertension (Kirkendall classification):
I: severe and widespread arterial narrowing,
stage II: haemorrhages and/or exudates,
stage III: dysoric nodules/papillary oedema.
3. Operational Definitions
CKD: elevated creatinine levels for > 3 months + reduced kidney size (<10 cm or 3 vertebrae)
Chronic kidney disease: morphological abnormality of the kidneys and/or proteinuria and/or urinary sediment abnormality without impaired kidney function (creatinine clearance is normal), persisting for more than three (3) months.
Criteria for chronic kidney failure:
Medical history criteria: history of elevated creatinine levels for more than 3 months.
Morphological criteria: reduction in kidney size to less than 10 cm in length on ultrasound (except in cases of diabetes, hydronephrosis, and polycystic kidney disease)
Biological criteria: normochromic normocytic aregenerative anaemia, hypocal- caemia with hypocalciuria.
For patients with a history of pathological creatinine levels that was unknown, the chronic nature of renal failure was confirmed based on the presence of morphological and biological criteria and the lack of recovery of renal function after 3 months of follow-up.
Glomerular nephropathy: PU/24 h ˃ 2 g or PU/24 h ˂ 2 g + hematuria.
Vascular nephropathy (nephroangiosclerosis): HTN + PU < 1 g/24 h + IR + hypertensive retinopathy at the back of the eye;
HIV-associated nephropathy (HIN): PU > 3 g/24 h – HTN + severe and rapidly progressive IR from the outset + patient infected with HIV;
Diabetic nephropathy (DN): PU > 500 mg/24 h + diabetic retinopathy at the back of the eye;
Favorable outcome: an outcome characterized by the absence of worsening and/or partial recovery from renal insufficiency due to conservative treatments throughout the study period. It excludes all cases of vision loss or those requiring renal replacement therapy.
4. Results
Of the 169 patients under follow-up, 77 met our inclusion criteria, representing a frequency of 45.56%. Of the 92 patients not included in the study, 54 were excluded due to acute kidney failure, 20 because the data were unusable due to a lack of financial resources to perform the tests necessary for diagnosing chronic kidney disease, and 18 due to conditions other than kidney failure. Women accounted for 53% with a sex ratio of 0.8. The average age was 50.97 ± 16.33 years, with extremes of 11 and 80 years. The 16 to 45 age group accounted for 40.2% of cases (see Table 1).
Housewives accounted for 49.3% of cases. Elevated creatinine levels were the main reason for consultation in 89.6% (69 cases), while the other reasons (10 cases) were oedema syndrome (1); OAP (1); anaemia (1); bilateral renal hypotrophy (1); papillary oedema (1); hypersalivation (1); renal distress on ultrasound (1); vomiting (1). The emergency department was the main referral service for patients, accounting for 45.5% (35 cases), followed by cardiology and private practitioners, accounting for 15.9% (12 cases) and 14.3% (11 cases), respectively (see Table 2).
Table 1. Distribution of patients by age.
Age (year) |
Workforce |
Percentages (%) |
[0 - 15] |
2 |
2.6 |
[16 - 30] |
5 |
6.5 |
[31 - 45] |
26 |
33.7 |
[46 - 60] |
17 |
22.1 |
>60 |
27 |
35.1 |
Total |
77 |
100 |
Table 2. Distribution of patients by referral service.
Referral services |
Workforce |
Percentages (%) |
Emergency |
35 |
45.5 |
Cardiology |
12 |
15.6 |
Private structure |
11 |
14.3 |
Internal medicine |
7 |
9 |
Self-reference |
6 |
7.8 |
Hepatology and Gastroenterology |
2 |
2.6 |
Others* |
4 |
5.2 |
Total |
77 |
100 |
Others*: Gynaecology and obstetrics (1); Pulmonology (1); Traumatology (1); Senior healthcare technician (1).
High blood pressure (67.5% or 52 cases) and diabetes (7.8% or 6 cases) were the main medical conditions in our patients. Nocturia accounted for 33.8% of cases (Table 3).
Table 3. Distribution of patients according to urological and nephrological history.
Urological and nephrological history |
Workforce |
Percentages (%) |
Nocturia |
26 |
33.8 |
Edema of the lower limbs |
20 |
26 |
Burning sensation when urinating |
17 |
22.1 |
Pollakiuria |
15 |
19.5 |
Dysuria |
8 |
10.4 |
Gross hematuria |
5 |
6.5 |
Polyuria |
4 |
5.2 |
Pathological creatinine |
3 |
3.9 |
others* |
8 |
10.4 |
Others*: oliguria (2), earache (2), ear discharge (2), tonsillitis (1), urinary incontinence (1).
Phytotherapy was used in 51.9% of our patients (see Table 4). Self-medication was found in 12 patients, or 15.6%.
Table 4. Distribution of patients according to previous treatment.
History of medication use |
Workforce |
Percentages (%) |
Herbal medicine |
40 |
51.9 |
Antihypertensive |
33 |
42.9 |
Antibiotic |
23 |
29.9 |
Nonsteroidal anti-inflammatory drug |
9 |
11.7 |
Antimalarial |
7 |
9.1 |
Diuretic |
11 |
14.3 |
Allopurinol |
6 |
7.8 |
Others* |
21 |
27.3 |
Vomiting accounted for 55.8% (43 cases), headache for 40.3% (31 cases), and vertigo for 39% (30 cases) (see Table 5).
Table 5. Distribution of patients according to clinical symptoms.
Symptoms |
Workforce |
Percentages (%) |
Vomiting |
43 |
55.8 |
Headache |
31 |
40.3 |
Vertigo |
30 |
39 |
Anorexia |
23 |
29.9 |
Asthenia |
23 |
29.9 |
Shortness of breath |
20 |
26 |
Edema of the lower limbs |
16 |
20.6 |
Nausea |
14 |
18.2 |
Cough |
9 |
11.7 |
Insomnia |
8 |
10.4 |
Abdominal pain |
8 |
10.4 |
Epigastric pain |
7 |
9.1 |
Facial swelling |
7 |
9.1 |
Tinnitus |
5 |
6.5 |
Phosphenes |
5 |
6.5 |
Hemorrhagic syndrome |
5 |
6.5 |
Diarrhea |
4 |
5.2 |
Lower back pain |
4 |
5.2 |
Pollakiuria |
3 |
3.9 |
others* |
11 |
14.3 |
Others*: tremor (2); burning sensation when urinating (1); dysuria (1); pruritus (1); muscle cramps (1); hypersalivation (1); dysgeusia (1); dysarthria (1); hemiplegia (1); plantar warmth (1).
More than half of the patients had serum creatinine levels above 800 µmol/l (see Table 6). The mean creatinine level was 1200.81 µmol/l, with extremes of 208 and 3453 µmol/l.
Table 6. Distribution of patients according to serum creatinine levels.
Creatinine level (µmol/L) |
Workforce |
Percentages (%) |
[150 - 300] |
4 |
5.2 |
[301 - 600] |
23 |
29.9 |
[601 - 800] |
7 |
9.1 |
>800 |
43 |
55.8 |
Total |
77 |
100 |
Renal failure was end-stage in 80.5% (62 cases), severe in 18.2% (14 cases), and moderate in 1.3% (1 case). The average blood urea nitrogen level was 31.23 mmol/l, with extremes of 4 and 66 mmol/l. It was above 30 mmol/l in 39 patients (50.6%) and below 30 mmol/l in 38 patients (49.4%). The average uric acid level was 543.5 µmol/l, with extremes of 262 and 930 µmol/l. It was above 600 µmol/l in 50 (64.9%) patients and below 600 µmol/l in 27 patients (5.1%).
Anaemia was present in 84.4% (65 cases) of our patients. It was normochromic normocytic, microcytic hypochromic, microcytic normochromic, and normocytic hypochromic in 50.76% (33 cases), 38.46% (25 cases), 7.70% (5 cases), and 3.08% (2 cases), respectively. Calcaemia was reduced in 45.5% of patients (see Table 7).
Table 7. Distribution of patients according to calcium and phosphorus levels and potassaemia.
Settings |
Decreased |
Augmented |
Normal |
Calcemia (n = 77) |
35 (45.5%) |
36 (46.8%) |
6 (7.8%) |
Phosphatemia (n = 22) |
- |
20 (90.9%) |
2 (9.1%) |
Active vitamin D (n = 13) |
5 (38.5%) |
- |
8 (61.5%) |
parathyroid hormone (n = 12) |
2 (16.7%) |
8 (66.6%) |
2 (16.7%) |
Kaliemia (n = 77) |
7 (9.1%) |
21 (27.3%) |
49 (63.6%) |
Kidney size was reduced, normal, and enlarged in 67.5% (52 cases), 28.6% (22 cases), and 3.9% (3 cases) of our patients, respectively. The kidneys were poorly differentiated and not dilated in 89.60% (69 cases) and 93.50% (72 cases), respectively. Urine culture performed in 43 patients revealed urinary tract infection in 81.4% (35 cases) with the presence of Enterococcus in 13 cases (37.14%), Escherichia coli in 11 cases (31.43%), and Staphylococcus aureus in 3 cases (8.57%). Proteinuria was found in 13 patients, 92.3% (12) of whom had minimal proteinuria (less than 1 g/24 h) in 12 cases (92.3%) and moderate proteinuria (1 - 3 g/24 h) in 1 case (7.7%). The most common complication was hyperkalaemia, occurring in 27.3% of cases (see Table 8).
Table 8. Distribution of patients according to severity criteria.
Severity criteria |
Workforce |
Percentages (%) |
Hyperkalemia |
21 |
27.3 |
Uremic coma |
14 |
18.3 |
Acute pulmonary edema |
10 |
13 |
Metabolic acidosis |
6 |
7.8 |
Pericarditis |
3 |
3.9 |
The most common cause of CRF was vascular nephropathy, accounting for 50.6% of cases (see Table 9).
Table 9. Distribution of patients according to aetiology.
Etiologies |
Workforce |
Percentages (%) |
High blood pressure |
39 |
50.6 |
Chronic glomerulonephritis |
15 |
19.5 |
Chronic interstitial nephritis |
11 |
14.3 |
Diabetes |
6 |
7.8 |
Undetermined |
5 |
6.5 |
Autoimmune (Lupus) |
1 |
1.3 |
Total |
77 |
100 |
5. Discussion
From 1 January to 31 December 2022, 169 patients were admitted to the nephrology unit, 77 of whom had CRF, representing a frequency of 45.6%. This frequency was 15.98% and 23.65%, respectively, according to studies conducted in 2008 and 2011 in the nephrology department of the Point G University Hospital [6] [8]. The average age was 50.97 ± 16.33 years, with extremes of 11 and 80 years. The 16 - 45 age group was the most common, accounting for 40.2%. Many African authors have reported a predominance of young people among patients with chronic renal failure [4] [6] [9]. In contrast, in developed countries, more than 50% of patients with chronic renal failure are over 60 years of age. This disparity could be explained by the ever-increasing life expectancy in these countries, but also by a predominantly ageing population. The prevalence of CRF increases with age. The incidence of end-stage renal disease increases with age, from 7 cases per million people under the age of 20 to 590 cases per million people over the age of 75; 64% of patients are over 65 years of age [10]. The predominance of women (sex ratio of 0.88) in our study was reported by Samaké M et al. [11]. This contrasts with the data from several studies [12]-[15] and could be explained by the high level of male migration in the region on the one hand, and the predominance of women in the general population on the other. In the literature, the prevalence is mainly male [6] [16] [17] because male sex hormones have a direct effect on the initiation and progression of chronic renal failure. Sex hormones play a role in the progression of chronic kidney disease by influencing the synthesis and activity of cytokines and vasoactive agents, as well as the generation of reactive oxygen species and the production of matrix components. Furthermore, the effects of oestrogen on these processes confer a protective role on females in the progression of chronic kidney disease, explaining the lower number of women in chronic kidney failure populations [18].
The main reason for consultation was renal failure, with a predominance (55.8%) of plasma creatinine levels above 800 µmol/l. This finding has been reported by several authors [19]-[21]. This can be explained, on the one hand, by the fact that most practitioners reduce nephrology to the management of renal failure, due to a lack of information [22] [23] and training (practitioners’ lack of knowledge of risk factors and early markers of chronic kidney disease such as proteinuria and haematuria) and, on the other hand, by the absence of reasons that could justify referral to a nephrologist.
In Tunisia, ‘signs of renal impairment: oedema, deterioration in general health, oligo-anuria, and mental confusion’ are the most common reasons, accounting for 48.5% of cases. Sakandé J et al. reported high blood pressure (30.4%) followed by nephrotic syndrome (23.8%) as the main reasons for hospitalisation [5]. In the literature, hypertension has been found to be a pathological history in patients with CRF [24] [25]. Its association with diabetes further compromises the prognosis of diabetic patients.
The uraemic symptoms were very varied but were dominated by morning sickness (55.8%), asthenia (29.9%), and anorexia (29.9%). Lengani A. in Burkina Faso reported asthenia and vomiting in 78.2% and 63.2% of cases, respectively [15]. The polymorphism of these symptoms can be explained by the late treatment of patients, most of whom arrive at the terminal stage, which accounts for 80.5% of cases in our study, with an average plasma creatinine level of 1200.81 ± 853 µmol/l. Akinsola et al. in Nigeria [26] and Ramiltiana in Madagascar [27] reported mean creatinine levels of 1130 ± 576 and 911.3 µmol/l, respectively.
Chronic renal failure was terminal in 80.5% of cases. These data are consistent with those of Ouattara [12], Tia WM [16], and Yao [28], who reported rates of 82.4%, 91.33%, and 94.5%, respectively. This finding is a very relevant reminder of the importance of focusing on the prevention of factors contributing to CKD through public awareness campaigns on self-medication, high blood pressure, infections, and diabetes mellitus, as well as early screening for chronic kidney disease.
Urea, the main waste product of nitrogen metabolism, was elevated in almost all patients, i.e., 97.4% of cases. The average urea level in patients with CRF was 31.23 mmol/l. This level increases as glomerular filtration rate decreases, reflecting the severity of renal function loss. Ramiltian [27] observed an average urea level of 14.37 mmol/l.
Anaemia is a major characteristic of CRF. Anaemia in patients with CRF is multifactorial. It is due to a deficiency in erythropoietin, inhibition of erythropoiesis induced by uraemia, and an imbalance in iron homeostasis. In our study, 65 patients, or 84.4%, had anaemia. It was normocytic normochromic (50.76%), hypochromic microcytic (38.46%), normochromic microcytic (7.7%), and hypochromic normocytic (3.08%).
This frequency of microcytic anaemia in CRF has been found in several studies in Africa [27]. This can be explained by the fact that during CRF, the increase in plasma hepcidin concentration (promoted by an inflammatory syndrome) reduces the absorption of dietary iron and promotes iron sequestration in the cells of the reticuloendothelial system. This results in functional iron deficiency, which is often associated with absolute iron deficiency secondary to increased iron loss (microhemorrhages) on the one hand, and tropical parasitic diseases on the other [8] [29]. Hemorrhagic diathesis, encountered in the terminal stage, due to prolonged bleeding time, could be the most plausible explanation for the severity of anemia.
In general, in the West, anemia in CRF is normochromic, normocytic, and aregenerative in almost all patients, and hemoglobin levels vary between 8 and 10 g/dL [30].
The hemoglobin level was below 8 g/dL in 33.8% of our patients. This level was found in 58.3% of patients in the series by Abderahim.
Hyperkalemia is one of the complications of CRF, especially in the terminal stage. In our study, it was found in 21 patients, or 27.3%, with an average of 5.13 ± 1.39 mmol/L. Its etiology is mixed, with decreased renal function leading to inadequate potassium excretion at glomerular filtration rates < 15 - 20 ml/min/1.73 m² in the face of a potassium-rich diet, and metabolic acidosis promoting extracellular potassium transfer [31]. In addition to CKD, diabetes and heart failure are frequently encountered comorbidities that indicate treatment with RAAS blockers for their nephroprotective and cardioprotective effects. Associated with these comorbidities, this type of treatment increases the risk of hyperkalemia [32].
Phosphocalcic metabolism disorders (hypocalcemia and hyperphosphatemia) are common in CRF. In addition to bone damage, they are accompanied by metabolic and vascular risks, particularly due to the risks of hyperphosphatemia and hypercalcemia, which are frequently associated with them [33]. Hypocalcemia was present in 36 patients (46.8%), including 32 patients in the terminal stage, compared with 90.9% of cases of hyperphosphatemia. Similar results were reported by Bourquia A in Morocco [24].
Renal failure was vascular (50.6%), glomerular (19.5%), interstitial (14.3%), diabetic (7.8%), autoimmune (lupus 1.3%), and undetermined (6.5%) in origin. Alhadji Ahmadou Tounkara et al. [34] reported the respective etiologies as hereditary nephropathies (1.3%), chronic interstitial nephritis (15.5%), CKD (34.8%), vascular nephropathies (VN = 28.4%), myelomatous kidney (2.6%), diabetic nephropathy (9.03%), and unclassifiable nephropathies (8.38%). The main etiologies in Bouaké were vascular nephropathies linked to high blood pressure (34.7%), chronic glomerular nephropathies (29.3%), HIV-related nephropathies (11.4%), and diabetic nephropathies (9.3%) [16]. This predominance of high blood pressure was confirmed in a systematic review of 152 articles published between January 1, 1995, and April 7, 2017, on CRF in Africa [35].
The management of CRF remained difficult in our context given the lack of financial resources and adequate technical facilities, particularly the absence of functional dialysis in the public hospital. The outcome was favorable in 63.8% of our patients, with partial and stable recovery of renal function. 20.6% were lost to follow-up, 7.8% were referred to a center with functional and accessible dialysis facilities, and we recorded six (6) deaths, or 7.8% of cases, related to the lack of dialysis in an emergency setting.
6. Limitations of the Study
However, our study suffered from a few shortcomings:
The low socioeconomic status of our patients and the high cost of examinations.
Inadequate technical facilities.
The very fragile health of our patients, who were already at an advanced stage.
7. Conclusions
Chronic renal failure is a fairly common condition affecting young adults in disadvantaged areas. The clinical manifestations are polymorphic, dominated by uremic syndrome.
Its management remained difficult in our context, especially in the terminal stage, due to the limited financial resources of our patients and the poor technical facilities in our institutions.
Data Collection and Analysis
Data were collected using a survey form designed for this purpose, based on patients’ outpatient and hospitalization records. Data entry and analysis were performed using Word 2016, Excel 2016, and SPSS version 20.0 software.
Ethical Considerations
The free and informed verbal consent of each patient was obtained with strict respect for the anonymity of the survey form.
Author Contributions
Conceptualization, Magara Samake and Aboubacar Sidiki Fofana.; methodology, Moctar Coulibaly.; software, SPSS version 20.0.; validation, Famory Kamissoko, Seydou Sy, Hamadoun Yattara., and Goundo Soumbounou Sissoko.; formal analysis, Bakary Diarra; investigation, Sah dit Baba Coulibaly.; resources, Ousmane Youssouf Djiguiba Singadou.; data curation, Famory Kamissoko.; writing—original draft preparation, Magara Samake.; writing—review and editing, Niagale Diakite.; visualization, Sahare Fongoro.; supervision, Sahare Fongoro.; project administration, Seydou Sy.; funding acquisition, Magara Samake., Aboubacar Sidiki Fofana., Moctar Coulibaly. All authors have read and agreed to the published version of the manuscript.