Chapter 52 Hematuria
ETIOLOGY
What Causes Hematuria?
A list of the common causes of hematuria is found in Table 52-1.
Parenchymal Source | Urinary Tract Source |
---|---|
Glomerulonephritis | Stones, hypercalciuria |
Pyelonephritis | Hemorrhagic cystitis (usually viral), urethritis |
Less common | |
Trauma | Exercise (bladder trauma) |
Arteriovenous malformations | Tumors |
Anatomic malformations (polycystic kidney disease or ureteropelvic junction obstruction) | Coagulation disorder (von Willebrand’s disease, etc.) |
EVALUATION
How Do I Evaluate Persistent Microscopic Hematuria?
Most patients who have asymptomatic persistent microscopic hematuria have no history of gross hematuria and have age-appropriate growth, development, blood pressure, and renal function. Proteinuria is not present on urinalysis. Such patients have, at most, mild renal disorders, which have little chance of progressing to renal failure. Treatment does not alter the management or natural history. A limited workup is appropriate for these patients, including random urine calcium-to-creatinine ratio, and screening for microscopic hematuria in family members to detect familial glomerulonephritis (Chapter 65). A complete workup, as outlined later for gross hematuria, would be necessary if the physician or family wishes to rule out all significant renal diseases or if the patient has microscopic hematuria plus other associated signs or symptoms.
How Do I Evaluate Gross Hematuria?
If your patient has visible blood in the urine a complete workup is needed. A thorough history, physical examination, and urinalysis can usually determine whether the hematuria originates in the renal parenchyma or the collecting system (Table 52-2). If the source is identified, perform the pertinent workup, as discussed later. If you cannot determine the source of hematuria with any reasonable degree of accuracy, do further testing as dictated by the patient’s condition. Referral to a nephrologist or urologist is justified.
Clinical Finding | Source of Bleeding | |
---|---|---|
Parenchyma (Intrarenal) | Collecting System Ureter, Bladder (Extrarenal) | |
Appearance of urine | “Tea colored” | Bright red or blood clots |
Urinary symptoms | Painless hematuria | Dysuria, urgency, frequency |
Associated symptoms | Sore throat Hypertension, edema | Fever and colicky pain |
Family history | Deafness, renal failure | Renal stones, UTI |
Proteinuria | > 2+ on dipstick Urine protein-to-creatinine ratio > 1 | Trace to 1+ on dipstick |
Other | RBC casts (high specificity but low sensitivity) | Crystals in urine |
RBC, Red blood cell; UTI, urinary tract infection.