Acute kidney injury (AKI) |
-
Patients with moderate to severe degree of renal impairment due to acute illness
-
Including patients who may need acute renal replacement therapy
|
Chronic kidney disease (CKD) |
-
Stage III-V (GFR < 60 ml/min/1.73m²) CKD
|
End-stage kidney disease (ESKD) |
-
Stage V CKD (GFR < 15ml/min/1.73m²) requiring renal replacement therapy
|
Complicated nephrotic syndrome |
-
Congenital or infantile nephrotic syndrome
-
Nephrotic syndrome with atypical features requiring renal biopsy
-
Steroid dependent nephrotic syndrome on second line immunosuppressant
-
Steroid resistant nephrotic syndrome
-
Other types of nephrotic syndrome with complications or renal impairment
|
IgA nephropathy |
-
Proteinuria > 1g/1.73m²/day despite ACEI/ARB
-
Patients with renal impairment or nephrotic syndrome on presentation
|
HSP with nephritis |
-
Persistent proteinuria of > 1g/ 1.73m2/day despite ACEI/ARB
-
Patients with renal impairment or nephrotic syndrome on presentation
|
APSGN (or post infectious GN) |
-
Atypical or rapidly progressive disease with renal impairment
-
Persistent significant proteinuria
|
Lupus nephritis or Vasculitis |
-
Acute kidney injury or renal impairment
-
Acute nephritis, nephrotic, or nephritic-nephrotic syndrome
-
Persistent significant proteinuria despite treatment
|
Urinary tract infection (UTI) with congenital kidney and urinary tract abnormalities (CAKUT) |
-
Patients with complicated structural abnormalities of the kidney and urinary tract, including severe VUR or obstructions
|
Complex congenital abnormality of kidney and urinary tract (CAKUT) |
-
Patients with complicated anatomy requiring surgical intervention for prevention of infection or preservation of kidney function
|
Severe hypertension |
-
Stage II hypertension or above
-
Secondary hypertension
-
Suspected reno-vascular hypertension
|
Renal stone disease |
-
Paediatric renal stone disease for work up
-
Acute kidney injury, infection or renal impairment secondary to stones disease
|
Complicated cystic kidney diseases |
-
Autosomal-dominant polycystic kidney disease (ADPKD)
-
Autosomal-recessive polycystic kidney disease (ARPKD)
-
Other cystic kidney diseases with impaired renal function or anatomical concern
|
Rare kidney diseases (including metabolic diseases or rare familial kidney diseases) |
-
Any rare diseases with significant kidney involvement
|