Haematuria
Blood in the urine (haematuria)
may be visible to the naked eye or it may be microscopic and detected only by
dipstick testing or by microscopy. The presence on microscopy of 10 or more
RBCs per high-power field is abnormal. Urinary dipsticks are very sensitive and
can be positive at <5 RBCs per high-power field. Asymptomatic haematuria is
found in about 0.5–2% of children.
•
Episode
of macroscopic haematuria (causes alarm to child/family).
•
Incidental
finding of microscopic haematuria.
•
Family
screening and routine urinalysis.
The following can usually be
distinguished from haematuria by taking a careful history, and with urine
dipstick testing and microscopy:
•
Haemoglobinuria/myoglobinuria.
•
Foods—colouring
(e.g. beetroot).
•
Drugs
(e.g. rifampicin).
•
Urate
crystals (in young infants, usually ‘pink’ nappies).
•
External
source (e.g. menstrual blood losses).
•
Fictitious—consider
if no cause found.
•
Urinary tract infections:
o
bacterial;
o
viral
(e.g. adenovirus in outbreaks);
o
schistosomiasis
(history of foreign travel);
o
tuberculosis.
•
Glomerular:
o
post-infectious
glomerulonephritis;
o
Henoch–Schönlein
purpura IgA nephropathy, SLE;
o
hereditary—thin
basement membrane, Alport’s syndrome.
•
Urinary tract stones: e.g. due to hypercalciuria.
•
Trauma.
•
Other
renal tract pathology:
o
renal
tract tumour;
o
polycystic
kidney disease.
•
Vascular:
•
renal
vein thrombosis;
•
arteritis.
•
Haematological: coagulopathy/sickle cell disease.
•
Drugs: cyclophosphamide.
•
Exercise-induced.
•
UTI: fever/frequency/dysuria.
•
Renal stones: colicky abdominal pain.
•
Glomerular: sore throat/rashes.
•
Coagulopathy: easy bruising.
•
Trauma.
•
Family history: haematuria, deafness (Alport’s),
sickle cell disease.
·BP.
•
Abdomen: palpable masses.
•
Skin: rashes.
•
Joints: pain/swelling.
It is important to identify
serious, treatable, and progressive conditions. During an acute illness,
exclude UTI by urine culture. Asymptomatic or ‘benign haematuria’ in children
without growth failure, hypertension, oedema, proteinuria, urinary casts, or
renal impairment is a frequent find-ing. Many such children require no
immediate investigation but need to be checked in the outpatient clinic to see
if the problem persists.
•
Urine:
· microscopy (look for
casts—suggestive of nephritis) and culture;
· protein:creatinine ratio (normal,
<20mg/mmol);
· calcium:creatinine ratio (normal,
<0.7mmol/mmol).
·Bloods:
•
U&E/creatinine/albumin;
•
FBC/clotting;
•
complement—C3/C4, ASOT titres;
•
ANA/anti-dsDNA.
•
US
urinary tract.
•
Urinalysis
of parents (hereditary causes).
•
Cystoscopy: rarely indicated in children.
•
If
obvious cause (e.g. UTI), treat.
•
If
complex diagnosis (impaired renal function, proteinuria, or family
•
history)
refer to paediatric nephrology unit.
•
If no
cause found and normal renal function, BP, and no proteinuria,
•
monitor
until resolves.
•
If no
resolution after 6mths or change in any of above parameters
•
refer
to paediatric nephrology unit.
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