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Hematuria
   Dr Muzammil Koshish
   DCH, DNB Resident,
   JLN Hospital and Research
   Centre, Bhillai
Red or brown color change of urine



Intermittent red or brown color urine a/w variety of clinical setting

              Medications (phenazopyridine, microbid, NSAID)
              Ingestion of beets or certain dyes
              Metabolities
              Myoglobinuria or hemoglobinuria
              Hematuria
Work up

Centrifuge the specimen,

Supernatant be tested for
heme (hemoglobin or myoglobin) with a urine dipstick.
APPROACH TO A PATIENT WITH RED OR BROWN COLOURED URINE
CAUSES OF HEME-NEGATIVE RED URINE


Medications       Food dyes                      Metabolities

Doxorubicin       Beets (in selected patients)   Bile pigments

Chloroquine       Blackberries                   Homogentisic acid

Desferoxamine     Food coloring                  Melanin

Ibuprofen                                        Methemoglobin

Iron sorbitol                                    Porphyrin

Nitrofurantoin                                   Tyrosinosis

Phenazopyridine                                  Urates

Phenolphthalein

Rifampin
Hematuria


      Microscopic hematuria
          > 50 RBCs / μl ( 5 RBCs / HPF )
      Gross hematuria
          > 2500 RBCs / μl


•American Urological Association
The evaluation should address the following three
questions

1. Are there any clues from the history or physical
   examination that suggest a particular diagnosis?

2. Does the hematuria represent glomerular or
extraglomerular bleeding?

3. Is the hematuria transient or persistent?
a three-tube test may also help to
locate the source of bleeding in
selected cases.



         Urethral: First 10-15 mL
         Bladder: Final 10-30 mL
         Upper urinary tract: Throughout
History and Physical
Examination
History
   Abdominal or flank pain
􀂄   Dysuria, frequency, urgency
􀂄   Trauma
􀂄   Strenuous exercise
􀂄   Menstruation
􀂄   Recent URI/ sore throat
􀂄   Skin rashes/ skin infection
􀂄   Diarrhea (especially bloody)
􀂄   Joint pains/swellings
􀂄   Medications/toxins
􀂄   h/o sickle cell disease or sickle trait
Family history
 Hematuria ,
Hearing loss,
HTN,
Stones,
Renal disease,
Dialysis or transplant,
Sickle cell trait
Coagulopathy,
Medication Hx
Substances and Medications Affecting Urine Color
Artificial food coloring
Beets
Berries
Chloroquine (Aralen)
Furazolidone (Furoxone)
Hydroxychloroquine (Plaquenil)
Nitrofurantoin (Furadantin)
Phenazopyridine (Pyridium)
Phenolphthalein
Rifampin (Rifadin)
  Information from Restrepo NC, Carey PO. Evaluating hematuria in adults.
    Am Fam Physician 1989; 40(2):149-56, and Drugdex system. Englewood:
                      Colo.: Micromedex, Inc., 1999. Accessed Sept. 24, 1998.
MECHANISM BY WHICH SELECTED DRUGS CAN CAUSE HEMATURIA

Interstitial nephritis       Captopril (Capoten)
                             Cephalosporins
                             Chlorothiazide (Diuril)
                             Ciprofloxacin (Cipro)
                             Furosemide (Lasix)
                             NSAIDs
                             Olsalazine (Dipentum)
                             Omeprazole (Prilosec)
                             Penicillins
                             Rifampin (Rifadin)
                             Silver sulfadiazine (Silvadene)
                             Trimethoprim-sulfamethoxazole (Bactrim, Septra

Papillary necrosis           Acetylsalicylic acid (aspirin)
                             NSAIDs
Hemorrhagic cystitis         Cyclophosphamide (Cytoxan)
                             Ifosfamide (Ifex)
                             Mitotane (Lysodren)
Urolithiasis                 Carbonic anhydrase inhibitors
                             Dichlorphenamide (Daranide)
                             Indinavir (Crixivan)
                             Mirtazapine (Remeron)
                             Ritonavir (Norvir)
                             Triamterene (Dyrenium)
Physical Exam

 􀂄 Vital sign: BP, T, HR
 Skin: Rashes, evidence of trauma, bruising
 􀂄 Abdomen for masses, tenderness (flank,
suprapubics), bruits
 􀂄 CVS: irregular irregular
 􀂄 Edema (especially periorbital)
 􀂄 Joint erythema, swelling, warmth
 􀂄 Paleness, jaundice
 􀂄 Careful inspection of external genitalia

•If BP is elevated, further evaluation is immediately warranted
Clues from the history and physical examination
    that point toward a specific diagnosis

1. Concurrent pyuria and dysuria, indicate UTI.


2. A recent URI, raise the possibility of either post infectious
    glomerulonephritis or IgA nephropathy


3. A positive family history of renal disease give suspicion of hereditary
    nephritis, polycystic kidney disease, or sickle cell disease.


4. Unilateral flank pain radiating to the groin, suggesting ureteral
    obstruction. Flank pain that is persistent or recurrent can also occur in
    the rare loin pain hematuria syndrome.
Clues from the history and physical examination that
    point toward a specific diagnosis
5. Recent vigorous exercise or trauma


6. History of a bleeding disorder or bleeding from multiple sites due to
coagulopathy.


7. Medications that might cause nephritis (usually with other findings,
typically with renal insufficiency).


8. All should be screened for sickle cell trait or disease, which can lead to
papillary necrosis and hematuria.


9.Sterile pyuria with hematuria, which may occur with renal tuberculosis,
analgesic nephropathy and other interstitial diseases.
Glomerular or Extra Glomerular bleeding?
Microscopic hematuria DDx

    Glomerular

 primary nephritis (post streptococcal glomerulonephritis, Ig A
nephropathy, Anti-GBM disease)

 IInd nephritis (SLE, goodpasture’s syndrome, ANCA related
       vasculitis)
 Alport’s syndrome (hereditary nephritis)

 Thin basement membrane nephropathy (benign familial hematuria)

•
Microscopic hematuria DDx

   Non-glomerular
 Renal

 Malignancy
 vascular disease (malignant hypertension, AVM,
                    nutcracker syndrome, renal vein
                    thrombosis, sickle cell trait/disease,
                     papillary necrosis)
 infection (pyelonephritis, TB, CMV, EBV)
 Hypercalciuria
 hereditary disease (polycystic kidney disease, medullary
      sponge kidney)
   Nonrenal

 Nephrolithiasis
 Coagulopathy
 Trauma
Rare cause of Microscopic Hematuria
 Arteriovenous malformations and
 fistulas

 Nutcracker syndrome


 Loin pain-hematuria syndrome
Arteriovenous malformations and fistulas —                        An AV
malformation (AVM) or fistula of the urologic tract may be either congenital or
acquired. The primary presenting sign is gross hematuria, but high-output heart
failure and hypertension also may be seen . The latter is presumably due to
activation of the renin-angiotensin system resulting from ischemia distal to the
AVM
Nutcracker syndrome — The nutcracker syndrome refers to compression
of the left renal vein between the aorta and proximal superior mesenteric artery.
Nutcracker syndrome can cause both microscopic and gross hematuria, primarily in
children (but also adults) in Asia . The hematuria is usually asymptomatic but may be
associated with left flank pain. Nutcracker syndrome has also been associated with
orthostatic proteinuria.

Loin pain-hematuria syndrome — The loin pain-hematuria syndrome
is a poorly defined disorder characterized by loin or flank pain that is often severe
and unrelenting, and hematuria with dysmorphic red cell features suggesting a
glomerular origin. Affected patients usually have normal kidney function.
Extraglomerular vs Glomerular
                 Extraglomerular   Glomerular



Color (if
                 Red or pink       Red, smoky brown, or "Coca-Cola"
macroscopic)



Clots            May be present    Absent


Proteinuria      <500 mg/day       May be >500 mg/day


RBC morphology   Normal            Dysmorphic


RBC casts        Absent            May be present
Dysmorphic erythrocytes are characterized by an irregular outer cell membrane and
suggest hematuria of glomerular origin.

Red blood cell casts are also associated with a glomerular cause of hematuria.

 FIGURE 2. Dysmorphic erythrocytes from a urine specimen. These cells suggest a
 glomerular cause of microscopic hematuria. (phase contrast microscopy, 3 100)
Transient or persistent hematuria
Transient hematuria

Transient microscopic hematuria is a common problem in
adults
Fever, infection, trauma, and exercise are potential causes
It is reasonable to repeat an abnormal urinalysis in a few
days
Persistent hematuria

When persistent hematuria is essentially the only manifestation of glomerular
disease, one of three disorders is most likely


IgA nephropathy, in which there is often gross hematuria, and sometimes a
positive family history but without any clear pattern of autosomal inheritance


 Alport syndrome (hereditary nephritis), in which gross hematuria can occur
in association with a positive family history of renal failure, and sometimes
deafness or corneal abnormalities.


Thin basement membrane nephropathy (also called thin basement
membrane disease or benign familial hematuria), in which gross hematuria is
unusual and the family history may be positive (with an autosomal dominant
pattern of inheritance) for microscopic hematuria but not for renal failure .
Persistent hematuria

Underlying malignancy is greater in patients with persistent hematuria in
whom there is no obvious cause from the history

The primary underlying cancers are bladder, renal, and, much less
often, prostate
Laboratory Tests (initial work up)

• UA and  microscopy to determine the number and morphology of
        RBC, crystal and casts
•   Consider urine Cx
•   CBC, PT, INR, electrolytes, kidney function
•   Serum chemistries and serologic studies for glomerular causes of
        hematuria as directed by the medical history
•   Repeat UA in a few days

    Further urologic evaluation is warranted if more than five
    RBC/phf are found on at least two of three properly
    collected urine specimens or if high-grade microscopic
    hematuria (more than 100 red blood cells per high-power
    field) is found on a single urinalysis.17
Further Work up


•Glomerular causes:
    Consider a refer to nephrology for further
   evaluation and possible renal biopsy
Renal Biopsy
A biopsy is not usually performed for isolated
glomerular hematuria (i.e., no proteinuria or renal
insufficiency,) since there is no specific therapy for
these conditions


However, biopsy should be considered if there is
evidence of progressive disease as manifested by an
elevation in the plasma creatinine concentration,
increasing protein excretion, or an otherwise
unexplained rise in blood pressure, even when the
values remain within the normal range
Further Work up

•Non-glomerular causes:

   CT, renal US, and/or IVP: to search for lesions in the
   kidney, collecting system, ureters, and bladder


   Consider a referral to urology for cystoscopy
RADIOLOGIC AND OTHER TESTS FOR THE EVALUATION OF HEMATURIA
Test                          Advantages                            Disadvantages
                              Excellent visualization of the        May miss bladder lesions; can
Intravenous pyelogram (IVP)   kidney, collecting system, and        cause nephrotoxicity,
                              ureter                                idiosyncratic reactions (1/10,000)
                              Best way to examine the bladder,
                                                                    Invasive, uncomfortable and
Cystoscopy                    which is not as well visualized by
                                                                    expensive
                              IVP or ultrasound
                              If of good quality, as sensitive as
                                                                    Less sensitive than IVP for ureter
Ultrasound                    IVP for renal lesions, with less
                                                                    and bladder
                              morbidity and cost
                              The best test for examing the         Invasive, not useful for
Retrograde pyelography        ureters, can be combined with         examining other parts of the
                              cystoscopy                            urinary collecting system
                              Sensitivity 67 percent, specificity
                                                                    Useful only for cancer, mainly of
Urinary cytology              96 percent for uroepithelial
                                                                    the bladder
                              cancer
                              Excellent for examining the
CT scan, DTPA, DMSA           renal parenchyma and                  Expensive
                              functioning
                              Useful for gross hematuria when
                              other tests have not revealed the
Angiography                                                         Invasive, expensive
                              cause; the only good test for
                              vascular malformations
SCREENING FOR HEMATURIA


   Not recommended
Reference:
1.  Significance of microhaematuria in young adults. AU Froom P; Ribak J; Benbassat J SO Br Med J (Clin Res Ed)
    1984 Jan 7;288(6410):20-2.
2. Asymptomatic microhematuria and urologic disease. A population-based study
3. Asymptomatic microscopic hematuria in adults: summary of the AUA best practice policy recommendations. AU
    Grossfeld GD; Wolf JS Jr; Litwan MS; Hricak H; Shuler CL; Agerter DC; Carroll PR SO Am Fam Physician 2001
    Mar 15;63(6):1145-54.U Mohr DN; Offord KP; Owen RA; Melton LJ 3d SO JAMA 1986 Jul 11;256(2):224-9
4. The left renal entrapment syndrome: diagnosis and treatment. AU Zhang H; Li M; Jin W; San P; Xu P; Pan S SO
    Ann Vasc Surg. 2007 Mar;21(2):198-203.
5. Heavy phenacetin use and bladder cancer in women aged 20 to 49 years. AU Piper JM; Tonascia J; Matanoski GM
    SO N Engl J Med 1985 Aug 1;313(5):292-5.
6. Recent advances in the diagnosis and treatment of renal arteriovenous malformations and fistulas. AU Crotty KL;
    Orihuela E; Warren MM SO J Urol 1993 Nov;150(5 Pt 1):1355-9.
7. Evaluation of Asymptomatic Microscopic Hematuria in Adults. TIMOTHY R. THALLER, M.D
    University of Kansas Medical Center, Kansas City, Kansas LESTER P. WANG, M.D. Valley Urology
    Center, Renton, Washington
8. Am Fam Physician 1989; 40(2):149-56, and Drugdex system. Englewood: Colo.: Micromedex, Inc., 1999.
    Accessed Sept. 24, 1998.
9. Am Fam Physician 1989; 40(2):149-56, and Drugdex system. Englewood: Colo.: Micromedex, Inc., 1999.
    Accessed Sept. 24, 1998.
10. Urothelial tumors of the urinary tract. In: Walsh PC, ed. Campbell's Urology. 7th ed. Philadelphia:
    Saunders, 1998:2327-410.
11. A quick reference for urologist, AUA 2006
12. Up to date 2008
Thank you
Hematuria

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Hematuria

  • 1. Hematuria Dr Muzammil Koshish DCH, DNB Resident, JLN Hospital and Research Centre, Bhillai
  • 2. Red or brown color change of urine Intermittent red or brown color urine a/w variety of clinical setting Medications (phenazopyridine, microbid, NSAID) Ingestion of beets or certain dyes Metabolities Myoglobinuria or hemoglobinuria Hematuria
  • 3. Work up Centrifuge the specimen, Supernatant be tested for heme (hemoglobin or myoglobin) with a urine dipstick.
  • 4. APPROACH TO A PATIENT WITH RED OR BROWN COLOURED URINE
  • 5. CAUSES OF HEME-NEGATIVE RED URINE Medications Food dyes Metabolities Doxorubicin Beets (in selected patients) Bile pigments Chloroquine Blackberries Homogentisic acid Desferoxamine Food coloring Melanin Ibuprofen Methemoglobin Iron sorbitol Porphyrin Nitrofurantoin Tyrosinosis Phenazopyridine Urates Phenolphthalein Rifampin
  • 6. Hematuria Microscopic hematuria > 50 RBCs / μl ( 5 RBCs / HPF ) Gross hematuria > 2500 RBCs / μl •American Urological Association
  • 7. The evaluation should address the following three questions 1. Are there any clues from the history or physical examination that suggest a particular diagnosis? 2. Does the hematuria represent glomerular or extraglomerular bleeding? 3. Is the hematuria transient or persistent?
  • 8. a three-tube test may also help to locate the source of bleeding in selected cases. Urethral: First 10-15 mL Bladder: Final 10-30 mL Upper urinary tract: Throughout
  • 10. History  Abdominal or flank pain 􀂄 Dysuria, frequency, urgency 􀂄 Trauma 􀂄 Strenuous exercise 􀂄 Menstruation 􀂄 Recent URI/ sore throat 􀂄 Skin rashes/ skin infection 􀂄 Diarrhea (especially bloody) 􀂄 Joint pains/swellings 􀂄 Medications/toxins 􀂄 h/o sickle cell disease or sickle trait
  • 11. Family history  Hematuria , Hearing loss, HTN, Stones, Renal disease, Dialysis or transplant, Sickle cell trait Coagulopathy,
  • 12. Medication Hx Substances and Medications Affecting Urine Color Artificial food coloring Beets Berries Chloroquine (Aralen) Furazolidone (Furoxone) Hydroxychloroquine (Plaquenil) Nitrofurantoin (Furadantin) Phenazopyridine (Pyridium) Phenolphthalein Rifampin (Rifadin) Information from Restrepo NC, Carey PO. Evaluating hematuria in adults. Am Fam Physician 1989; 40(2):149-56, and Drugdex system. Englewood: Colo.: Micromedex, Inc., 1999. Accessed Sept. 24, 1998.
  • 13. MECHANISM BY WHICH SELECTED DRUGS CAN CAUSE HEMATURIA Interstitial nephritis Captopril (Capoten) Cephalosporins Chlorothiazide (Diuril) Ciprofloxacin (Cipro) Furosemide (Lasix) NSAIDs Olsalazine (Dipentum) Omeprazole (Prilosec) Penicillins Rifampin (Rifadin) Silver sulfadiazine (Silvadene) Trimethoprim-sulfamethoxazole (Bactrim, Septra Papillary necrosis Acetylsalicylic acid (aspirin) NSAIDs Hemorrhagic cystitis Cyclophosphamide (Cytoxan) Ifosfamide (Ifex) Mitotane (Lysodren) Urolithiasis Carbonic anhydrase inhibitors Dichlorphenamide (Daranide) Indinavir (Crixivan) Mirtazapine (Remeron) Ritonavir (Norvir) Triamterene (Dyrenium)
  • 14. Physical Exam 􀂄 Vital sign: BP, T, HR  Skin: Rashes, evidence of trauma, bruising 􀂄 Abdomen for masses, tenderness (flank, suprapubics), bruits 􀂄 CVS: irregular irregular 􀂄 Edema (especially periorbital) 􀂄 Joint erythema, swelling, warmth 􀂄 Paleness, jaundice 􀂄 Careful inspection of external genitalia •If BP is elevated, further evaluation is immediately warranted
  • 15. Clues from the history and physical examination that point toward a specific diagnosis 1. Concurrent pyuria and dysuria, indicate UTI. 2. A recent URI, raise the possibility of either post infectious glomerulonephritis or IgA nephropathy 3. A positive family history of renal disease give suspicion of hereditary nephritis, polycystic kidney disease, or sickle cell disease. 4. Unilateral flank pain radiating to the groin, suggesting ureteral obstruction. Flank pain that is persistent or recurrent can also occur in the rare loin pain hematuria syndrome.
  • 16. Clues from the history and physical examination that point toward a specific diagnosis 5. Recent vigorous exercise or trauma 6. History of a bleeding disorder or bleeding from multiple sites due to coagulopathy. 7. Medications that might cause nephritis (usually with other findings, typically with renal insufficiency). 8. All should be screened for sickle cell trait or disease, which can lead to papillary necrosis and hematuria. 9.Sterile pyuria with hematuria, which may occur with renal tuberculosis, analgesic nephropathy and other interstitial diseases.
  • 17. Glomerular or Extra Glomerular bleeding?
  • 18. Microscopic hematuria DDx Glomerular  primary nephritis (post streptococcal glomerulonephritis, Ig A nephropathy, Anti-GBM disease)  IInd nephritis (SLE, goodpasture’s syndrome, ANCA related vasculitis)  Alport’s syndrome (hereditary nephritis)  Thin basement membrane nephropathy (benign familial hematuria) •
  • 19. Microscopic hematuria DDx Non-glomerular  Renal  Malignancy  vascular disease (malignant hypertension, AVM, nutcracker syndrome, renal vein thrombosis, sickle cell trait/disease, papillary necrosis)  infection (pyelonephritis, TB, CMV, EBV)  Hypercalciuria  hereditary disease (polycystic kidney disease, medullary sponge kidney)
  • 20. Nonrenal  Nephrolithiasis  Coagulopathy  Trauma
  • 21. Rare cause of Microscopic Hematuria Arteriovenous malformations and fistulas Nutcracker syndrome Loin pain-hematuria syndrome
  • 22. Arteriovenous malformations and fistulas — An AV malformation (AVM) or fistula of the urologic tract may be either congenital or acquired. The primary presenting sign is gross hematuria, but high-output heart failure and hypertension also may be seen . The latter is presumably due to activation of the renin-angiotensin system resulting from ischemia distal to the AVM Nutcracker syndrome — The nutcracker syndrome refers to compression of the left renal vein between the aorta and proximal superior mesenteric artery. Nutcracker syndrome can cause both microscopic and gross hematuria, primarily in children (but also adults) in Asia . The hematuria is usually asymptomatic but may be associated with left flank pain. Nutcracker syndrome has also been associated with orthostatic proteinuria. Loin pain-hematuria syndrome — The loin pain-hematuria syndrome is a poorly defined disorder characterized by loin or flank pain that is often severe and unrelenting, and hematuria with dysmorphic red cell features suggesting a glomerular origin. Affected patients usually have normal kidney function.
  • 23. Extraglomerular vs Glomerular Extraglomerular Glomerular Color (if Red or pink Red, smoky brown, or "Coca-Cola" macroscopic) Clots May be present Absent Proteinuria <500 mg/day May be >500 mg/day RBC morphology Normal Dysmorphic RBC casts Absent May be present
  • 24.
  • 25. Dysmorphic erythrocytes are characterized by an irregular outer cell membrane and suggest hematuria of glomerular origin. Red blood cell casts are also associated with a glomerular cause of hematuria. FIGURE 2. Dysmorphic erythrocytes from a urine specimen. These cells suggest a glomerular cause of microscopic hematuria. (phase contrast microscopy, 3 100)
  • 27. Transient hematuria Transient microscopic hematuria is a common problem in adults Fever, infection, trauma, and exercise are potential causes It is reasonable to repeat an abnormal urinalysis in a few days
  • 28. Persistent hematuria When persistent hematuria is essentially the only manifestation of glomerular disease, one of three disorders is most likely IgA nephropathy, in which there is often gross hematuria, and sometimes a positive family history but without any clear pattern of autosomal inheritance  Alport syndrome (hereditary nephritis), in which gross hematuria can occur in association with a positive family history of renal failure, and sometimes deafness or corneal abnormalities. Thin basement membrane nephropathy (also called thin basement membrane disease or benign familial hematuria), in which gross hematuria is unusual and the family history may be positive (with an autosomal dominant pattern of inheritance) for microscopic hematuria but not for renal failure .
  • 29. Persistent hematuria Underlying malignancy is greater in patients with persistent hematuria in whom there is no obvious cause from the history The primary underlying cancers are bladder, renal, and, much less often, prostate
  • 30. Laboratory Tests (initial work up) • UA and microscopy to determine the number and morphology of RBC, crystal and casts • Consider urine Cx • CBC, PT, INR, electrolytes, kidney function • Serum chemistries and serologic studies for glomerular causes of hematuria as directed by the medical history • Repeat UA in a few days Further urologic evaluation is warranted if more than five RBC/phf are found on at least two of three properly collected urine specimens or if high-grade microscopic hematuria (more than 100 red blood cells per high-power field) is found on a single urinalysis.17
  • 31. Further Work up •Glomerular causes:  Consider a refer to nephrology for further evaluation and possible renal biopsy
  • 32. Renal Biopsy A biopsy is not usually performed for isolated glomerular hematuria (i.e., no proteinuria or renal insufficiency,) since there is no specific therapy for these conditions However, biopsy should be considered if there is evidence of progressive disease as manifested by an elevation in the plasma creatinine concentration, increasing protein excretion, or an otherwise unexplained rise in blood pressure, even when the values remain within the normal range
  • 33. Further Work up •Non-glomerular causes: CT, renal US, and/or IVP: to search for lesions in the kidney, collecting system, ureters, and bladder Consider a referral to urology for cystoscopy
  • 34. RADIOLOGIC AND OTHER TESTS FOR THE EVALUATION OF HEMATURIA Test Advantages Disadvantages Excellent visualization of the May miss bladder lesions; can Intravenous pyelogram (IVP) kidney, collecting system, and cause nephrotoxicity, ureter idiosyncratic reactions (1/10,000) Best way to examine the bladder, Invasive, uncomfortable and Cystoscopy which is not as well visualized by expensive IVP or ultrasound If of good quality, as sensitive as Less sensitive than IVP for ureter Ultrasound IVP for renal lesions, with less and bladder morbidity and cost The best test for examing the Invasive, not useful for Retrograde pyelography ureters, can be combined with examining other parts of the cystoscopy urinary collecting system Sensitivity 67 percent, specificity Useful only for cancer, mainly of Urinary cytology 96 percent for uroepithelial the bladder cancer Excellent for examining the CT scan, DTPA, DMSA renal parenchyma and Expensive functioning Useful for gross hematuria when other tests have not revealed the Angiography Invasive, expensive cause; the only good test for vascular malformations
  • 35. SCREENING FOR HEMATURIA Not recommended
  • 36. Reference: 1. Significance of microhaematuria in young adults. AU Froom P; Ribak J; Benbassat J SO Br Med J (Clin Res Ed) 1984 Jan 7;288(6410):20-2. 2. Asymptomatic microhematuria and urologic disease. A population-based study 3. Asymptomatic microscopic hematuria in adults: summary of the AUA best practice policy recommendations. AU Grossfeld GD; Wolf JS Jr; Litwan MS; Hricak H; Shuler CL; Agerter DC; Carroll PR SO Am Fam Physician 2001 Mar 15;63(6):1145-54.U Mohr DN; Offord KP; Owen RA; Melton LJ 3d SO JAMA 1986 Jul 11;256(2):224-9 4. The left renal entrapment syndrome: diagnosis and treatment. AU Zhang H; Li M; Jin W; San P; Xu P; Pan S SO Ann Vasc Surg. 2007 Mar;21(2):198-203. 5. Heavy phenacetin use and bladder cancer in women aged 20 to 49 years. AU Piper JM; Tonascia J; Matanoski GM SO N Engl J Med 1985 Aug 1;313(5):292-5. 6. Recent advances in the diagnosis and treatment of renal arteriovenous malformations and fistulas. AU Crotty KL; Orihuela E; Warren MM SO J Urol 1993 Nov;150(5 Pt 1):1355-9. 7. Evaluation of Asymptomatic Microscopic Hematuria in Adults. TIMOTHY R. THALLER, M.D University of Kansas Medical Center, Kansas City, Kansas LESTER P. WANG, M.D. Valley Urology Center, Renton, Washington 8. Am Fam Physician 1989; 40(2):149-56, and Drugdex system. Englewood: Colo.: Micromedex, Inc., 1999. Accessed Sept. 24, 1998. 9. Am Fam Physician 1989; 40(2):149-56, and Drugdex system. Englewood: Colo.: Micromedex, Inc., 1999. Accessed Sept. 24, 1998. 10. Urothelial tumors of the urinary tract. In: Walsh PC, ed. Campbell's Urology. 7th ed. Philadelphia: Saunders, 1998:2327-410. 11. A quick reference for urologist, AUA 2006 12. Up to date 2008

Editor's Notes

  1. 16 TI Clinical practice. Microscopic hematuria. AU Cohen RA; Brown RS SO N Engl J Med 2003 Jun 5;348(23):2330-8.
  2. Concurrent pyuria and dysuria, which are usually indicative of a urinary tract infection, but may also occur with bladder malignancy. A recent upper respiratory infection, suggesting either postinfectious glomerulonephritis or IgA nephropathy (see &quot;Hematuria following an upper respiratory infection&quot;). A positive family history of renal disease, as in hereditary nephritis, polycystic kidney disease, or sickle cell disease. Unilateral flank pain, which may radiate to the groin, suggesting ureteral obstruction due to a calculus or blood clot, but can occasionally be seen with malignancy. Flank pain that is persistent or recurrent can also occur in the rare loin pain hematuria syndrome. (See &quot;Loin pain hematuria syndrome&quot;). Symptoms of prostatic obstruction in older men such as hesitancy and dribbling. The cellular proliferation in benign prostatic hyperplasia (BPH) is associated with increased vascularity, and the new vessels can be fragile. There is some controversy about whether hematuria is more common in these patients than in age-matched controls [11,17] . However, there is general agreement that the presence of BPH should not dissuade the clinician from pursuing further evaluation of hematuria, particularly since older men are more likely to have more serious disorders such as cancer of the prostate or bladder. Among those with gross hematuria in whom no other cause can be identified, finasteride usually suppresses the hematuria [18,19] . (See &quot;Medical treatment of benign prostatic hyperplasia&quot;). Recent vigorous exercise or trauma (see &quot;Exercise-induced hematuria&quot;). History of a bleeding disorder or bleeding from multiple sites due to uncontrolled anticoagulant therapy. In contrast, it should not be assumed that hematuria alone can be explained by chronic warfarin therapy. In one report of 243 patients prospectively followed for two years, the incidence of hematuria was similar to that in a control group not receiving warfarin [20] . Furthermore, evaluation of patients who developed hematuria revealed a genitourinary cause in 81 percent of cases. Infection was most common, but papillary necrosis, renal cysts, and several malignancies of the bladder were also found. A smaller study found significant urinary tract disease in nine of 30 patients, two of whom had bladder cancer [21] . These observations indicate that hematuria in an anticoagulated patient should generally be evaluated in the same fashion as in other patients unless there is evidence of bleeding from multiple sites with markedly abnormal coagulation studies.Cyclic hematuria in women that is most prominent during and shortly after menstruation, suggesting endometriosis of the urinary tract [22] . Contamination with menstrual blood is always a possibility, and should be ruled out by repeating the urinalysis when menstruation has ceased. Medications that might cause nephritis (usually with other findings, typically with renal insufficiency). Black patients should be screened for sickle cell trait or disease, which can lead to papillary necrosis and hematuria. (See &quot;Renal manifestations of sickle cell disease&quot;). Travel or residence in areas endemic for Schistosoma hematobium, or tuberculosis. Sterile pyuria with hematuria, which may occur with renal tuberculosis, analgesic nephropathy and other interstitial diseases. 22   Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 33-1992. A 34-year-old woman with endometriosis and bilateral hydronephrosis. N Engl J Med 1992; 327:481.