Idiopathic Nephrotic Syndrome in Children in Chad: Epidemiology and Clinical Outcomes

• Published in: Journal of clinical medicine 2023-12, Vol.12 (24), p.7626
• Main Authors: Mahamat Abderraman, Guillaume, Djidita Hagré, Youssouf, Mahamat, Hissein Ali, Charfadine, Senoussi, Amne, Ali Sakine, Khadidja, Adoum Attimer, Rostaing, Lionel
• Format: Article
• Language: English
• Subjects: Biopsy; Children; Children & youth; Corticosteroids; Creatinine; Diseases; Edema; Epidemiology; Health risk assessment; Hematuria; Hospitals; Hypertension; Hypertension in children; Kidney diseases; Nephrotic syndrome; Patient outcomes; Patients; Pediatrics; Proteins; Remission (Medicine); Software; Steroids; Urine
• ISSN: 2077-0383; 2077-0383
• DOI: 10.3390/jcm12247626

Nephrotic syndrome (NS) remains the most common presentation of glomerular diseases in children. Moreover, NS is primarily idiopathic, accounting for 90% of cases, with an average onset age between 2 and 10 years. The objective of our study was to describe the characteristics and outcomes of NS in children from three major hospitals in one of the world's poorest countries, Chad. This observational, cross-sectional, descriptive, and multicenter study took place over a period of 36 months (1 January 2019-31 December 2021) and was carried out in three hospitals in N'Djamena, Chad. Children aged 1-15 years presenting with NS were included in the study. Out of 16,776 children hospitalized or followed up with in outpatient clinics, 24 cases of NS were identified, yielding a prevalence of 0.14%. The median age at presentation was 6.16 years (1-10). Nineteen children were male (sex ratio 3.8). Eight cases were classified as impure NS (33.3%). Edema was present in all patients, while oliguria was present in 29.16% ( = 7), and arterial hypertension was present in 20.83% ( = 5) of cases. Mean proteinuria, albuminemia, and total proteins were 2.86g/L, 19.13g/L and 30.41g/L, respectively. The median serum creatinine was 87.3 µmol/L (75-1375 µmol/L). Three patients experienced acute renal failure upon admission. Four patients had secondary NS. All idiopathic NS patients ( = 20) who had received corticosteroid therapy had a 90% response rate to steroids. Non-responsive or relapsed patients underwent kidney biopsy ( = 7), revealing focal segmental glomerulosclerosis (FSGS; = 4) as the most common histological lesion, followed by minimal change disease ( = 2) and membranoproliferative glomerulonephritis ( = 1). The median length of hospitalization stay was 10.67 (5-27) days. None of the patients with idiopathic NS died. At the last follow-up, sixteen patients (80%) achieved long-term complete remission with normal renal function; however, four of those had subsequent relapses. One patient with secondary NS died. In Chad, childhood idiopathic nephrotic syndrome predominantly affects young males; steroid sensitivity is as high as 95%, and in the long-term, 80% of patients achieve remission with normal renal function.