Renal/urinary Flashcards
What is glomerulonephritis?
Acute and chronic
Damage inflicted by the formation of immune complexes, most commonly post streptococcal infection –> haematuria, brown urine, oedema (peri-orbital and ankles)
Why is important to check the BP when investigating haematuria?
HTN indicates kidney pathology - child needs to be admitted
What is the most common cause of haematuria in children?
UTI
What is the most common type of tumour that will cause haematuria in children?
Wilm’s tumour - should be palpable mass in the loin
Investigations for a child with haematuria?
Urine - MSU dip and culture
Bloods
- FBC, ESR, CRP, clotting screen
- plasma urea, creatinine, eGFR, U+Es, albumin, phosphate
If suggestive of renal pathology - screen for hepatitis, renal biospy, throat swab (+ ASO titre for streptococcal)
What is haemolytic uraemic syndrome (HUS)?
A triad of AKI, microangiopathic haemolytic anaemia and thrombocytopaenia
Typically affects children 3mo-3yrs after a GI infection (e.coli or shighella)
Toxins damage the renal endothelium –> intravascular thrombogenesis
No consumption of clotting factors but consumption of platelets
Symptoms and signs of HUS?
Diarrhoea and colitis from GI infection
Oliguria, pallor, jaundice, encephalopathy
Investigations of HUS?
Bloods:
- High LDH (tissue damage)
- High WCC
- Coombes -ve
- Decreased PCV (% of RBC in blood)
- Fragmented RBCs
What is nephrotic syndrome?
Oedema + hypoalbuminaemia + proteinuria
Due to increased permeability of the glomerular capillary wall –> increased loss of protein in urine
Cause = minimal change glomeurlonephritis (80%)
Presentation of nephrotic syndrome?
- peri-orbital oedema –> becomes more generalised (pitting oedema of legs/ankles and oedema of scrotum, vulva)
- Ascites and pulmonary effusion (SOB/respiratory distress)
Investigations in nephrotic syndrome?
MSU dip and culture - increased protein, may have microscopic haematuria
Bloods - FBC, U+Es, ESR
Decreased levels of albumin, increased levels of cholesterol
Renal biospy if not typical minimal change disease (85% of cases) or if haven’t responded to steroid treatment
Management of nephrotic syndrome?
2-4 weeks prednisolone and then wean down to low-dose for 4-6 weeks
If persistent recurrence treat with cyclophosphamide
Refer to specialist if symptoms do not improve with steroid treatment
Presentation of glomerulonephritis?
haematuria, oedema, HTN, oliguira +/- proteinuria
Aetiology of glomerulonephritis?
Autoimmune - SLE, IgA nephropathy, membranoproliferative
Post infection (~1-2 weeks after URTI)
Bacterial - strep, stap A, salmonella
Viral - CMV, EBV, Varicella
Fungal - aspergillus, candida
Toxins/drugs e.g. gentamicin
Symptoms/signs of glomerulonephritis?
Often asymptomatic
Nephrotic syndrome - oedema, Proteinuria, hypoalbuminaemia
Nephritic syndrome - nephrotic + haematuria
Lethargy, malaise, anorexia
Pruritis
Oliguria
Pulmonary oedema