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148 A.R. Watson

14.1  Hematuria

The dipsticks are very sensitive for blood and can be positive at <5 RBCs per high power field. Evidence of red blood cells in the urine should be confirmed by microscopy which should be performed on fresh urine. Contrast microscopy has been advocated with anatomically normal red blood cells suggesting bleeding of lower urinary tract origin as distinct from dysmorphic red cells suggesting a higher (glomerular) source. However, the test is very rarely applied in pediatric practice. Microscopy of urine can help in diagnosis with the presence of red cell casts indicating glomerular bleeding.

Causes of “red urine” need to be excluded:

Urate crystals, especially in young infants giving “pink” nappies

Food coloring, e.g., beetroot or blueberries

Hemoglobinuria and intravascular hemolysis

Myoglobinuria, e.g., in rhabdomyolysis

Drugs, e.g., Rifampicin

External source, e.g., menstrual blood loss

Fictitious – consider if no cause found.

14.1.1  Important Points in the History

Symptoms suggestive of UTI, e.g., fever, frequency, and dysuria. UTI quoted as commonest cause for macroscopic and microscopic hematuria.

Urine red (more likely to be a local cause) or tea/coke colored (more likely to be glomerular with oxidized blood)

Is the hematuria at the beginning or end of the stream (bladder or urethral cause)

Is there colicky abdominal pain (suggesting stones)

History of trauma

Is there history of coagulopathy such as easy bruising

Is there a family history of hematuria or of renal disease and deafness (Alport’s syndrome) or sickle cell disease

Chapter 14.  Hematuria and Proteinuria 149

Examination will include palpation of the abdomen for abdominal masses, skin rashes and blood pressure

14.1.2  Causes of Hematuria

Urinary tract infections:

––Bacterial

––Viral (e.g., adenovirus in outbreaks)

––Schistosomiasis (history of foreign travel)

––Tuberculosis

Glomerular

––Post-infectious glomerulonephritis

––IgA nephropathy, Henoch-Schonlein purpura, SLE

––Hereditary – thin basement membrane, Alport’s syndrome

Urinary tract stones: hypercalciuria

Trauma

Other renal tract pathology

––Renal tract tumor

––Polycystic kidney disease

Vascular

––Renal vein thrombosis

––Arteritis

Hematological: coagulopathy/sickle cell disease

Drugs – cyclophosphamide

Exercise induced

14.1.3  Investigations

When evaluating childhood hematuria it is important to identify serious and progressive conditions. If macroor microscopic hematuria is found in the setting of an acute illness such as UTI then it needs to be confirmed by urine culture and the urine tested after the acute illness. Glomerulonephritis will require a full “nephritis work-up.” However, if the child presents with asymptomatic “benign” hematuria without growth failure, hypertension, edema, proteinuria, urinary casts or renal impairment then investigations can be arranged in the outpatient clinic.

150 A.R. Watson

Urine

––Microscopy to confirm RBCs and look for casts

––Culture for bacteria and possibly viruses

––Protein : creatinine ratio to define level of proteinuria if present (normal <20 mg protein/mmol creatinine) on an early morning urine

––Calcium : creatinine ratio on second morning urine to exclude hypercalciuria (normal <0.7 mmol calcium/ mmol creatinine)

Bloods

––U&E/creatinine/albumin/calcium/phosphate/alk phos

––FBC/clotting

––Complement: C3/C4

––ASOT and antihyaluronidase B titers

––ANA/anti-dsDNA and ANCA titers if nephritis suspected

Radiology

––Ultrasound of urinary tract of all patients with hematuria

––Further radiology will depend upon clinical situation and initial ultrasound

Test urine of parents and other children in clinic (hereditary causes)

Cystoscopy – not routine and rarely indicated in children. Heavy isolated hematuria, recurrent fresh bleeding and abnormal findings on ultrasound may provide indication

14.1.4  Management

If obvious cause such as UTI treat with antibiotics but will require at least renal tract ultrasound.

If impaired renal function, proteinuria or family history refer to pediatric nephrology unit.

If suspicious lesion on ultrasound of urinary tract or intermittent macroscopic hematuria (with IgA nephropathy excluded in an older child) then discuss with radiology/urology.

If no cause found and normal renal function, BP and no proteinuria monitor in clinic at 6-monthly intervals.

If persistent microscopic hematuria after one year or change in any of the above parameters then refer to pediatric nephrology unit for consideration of renal biopsy.2

Chapter 14.  Hematuria and Proteinuria 151

Pediatric nephrologists debate the role of renal biopsy in benign persistent microscopic hematuria. One approach is shown in Fig. 14.1. One cause of persistent microscopic hematuria is thin basement membrane nephropathy with abnormal thinning of the glomerular basement membrane. This is probably the commonest cause of benign familial hematuria. When thinning is combined with thickening of the glomerular basement membrane (basket weave appearance) and a

Hematuria

Non-glomerular causes excluded

 

 

 

 

 

 

Renal function tests

 

 

 

 

 

 

 

 

 

 

 

 

 

Complement studies

 

 

 

 

 

 

 

 

 

 

 

 

 

Streptococcal antibodies

 

 

 

 

 

 

 

 

 

 

 

 

 

Antinuclear factor

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Persistent creatinine

 

 

 

 

 

 

 

Proteinuria

 

 

 

 

 

 

Proteinuria

 

 

 

 

Low GFR

 

 

 

 

 

 

 

 

 

nil or

 

persistent,

 

 

 

Persistent C3

 

 

 

 

 

 

 

 

 

minimal

 

heavy

 

 

 

Hypertension

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Family +ve

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Test 1st degree

 

 

 

 

 

 

Renal biopsy

 

 

 

Relatives

 

 

 

 

 

 

 

 

 

Repeat tests

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

6 and 12

 

 

 

 

 

 

continuous

 

 

months

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Persistent microscopic hematuria

 

 

Family –ve

 

 

 

 

 

 

or increased anxiety

 

 

intermittent

 

 

 

 

 

 

 

 

 

 

 

 

hematuria

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Discharge

 

 

Follow up yearly

 

 

 

 

 

Reassure

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

If urine neg x

 

 

 

 

 

 

 

 

 

 

 

2 or

 

 

 

 

 

 

 

 

 

 

 

proteinuria nil

 

 

 

 

 

 

 

 

 

 

 

after 5 years

 

 

 

 

 

 

 

 

 

 

FIGURE 14.1.  A scheme for the management of children with hematuria­ .