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Dr. Kaviayarasi muthamizhan
Final yr MBBS
Government thiruvannamalai medical college
Thiruvannamalai
DEFINITIONS
 GROSS /MACROSCOPIC HEMATURIA :
visible to the naked eye
 MICROSCOPIC HEMATURIA :
>5 RBCs/HPF in centrifuged sample
 TRANSIENT HEMATURIA:
usually microscopic and benign
fever, infections ,trauma and exercise
 PERSISTENT HEMATURIA:
Persistent finding of hematuria in atleast two or three
urinalyses performed over 2-3 weeks
CLINICAL TERMINOLOGIES FOR
PRESENTATION OF HEMATURIA
Gross
hematuria
Single
episode
recurrent
Microscopic
hematuria
isolated
With
proteinuria
CONFIRMATION OF HEMATURIA
Urine sample
Urine dipstick
Urine
microscopic exn
 urine dipstick identifies hemeprotein
( SENSITIVITY=100% SPECIFICITY – 99% in detecting 1-5
RBCs/HPF )
FALSE POSITIVE FALSE NEGATIVE
Oxidising substances Vitamin C
Alkaline ph >9 formalin
DIPSTICK
MICROSCOPY
Positive urine dipstick
Urine
microscopy
>5 RBC
HEMATURIA
NO RBC
HEMOGLOBINURIA
MYOGLOBINURIA
PLASMA
COLOR
RED
HEMOGLOBINURIA
CLEAR
MYOGLOBINURIA
HEMOGLOBINURIA MYOGLOBINURIA
NEGATIVE URINE
DIPSTICK
RBC
HEMOGLOBIN
MYOGLOBIN
But urine
red colour ??
All that is red is not blood
Search for other causes of
red urine
SUBSTANCES CAUSING
DISCOLARATION OF URINE
• RED OR PINK URINE
• Urates
• Porphyrins
• Beets,red dyes in food
• Drugs:chloroquine,desf
errioxime,pyridum
• DARK YELLOW/ORANGE
• Normal concentrated
urine
• Rifampicin
• Pyridium
• DARK BROWN/BLACK
• Methemoglobinemia
• metronidazole
• Confirmed true hematuria
• Next step???
• LOCALIZATION OF BLEEDING
glomerular vs non glomerular
CASE 1
A 7 year old girl presented with
• h/o cola coloured urine 4 days
• Swelling of face & legs -2 days
• Oliguria -2 days
• Breathlessness -1 day
• h/o sore throat 2 weeks back
• O/E edema,BP>99 th percentile,tender hepatomegaly
• Urinalysis appearance : brown
RBC- plenty
albumin- 5to6/hpf
CASE 2
• 10 year old boy with
• red coloured urine-2 days
• colicky pain in right flank
• dysuria , increased frequency, urgency,
stranguary
• no oliguria,edema, hypertension
• Urinalysis appearance : bright red
albumin trace
RBC- plenty
WBC 6-10 /HPF
FEATURES GLOMERULAR NON GLOMERULAR
HISTORY
Dysuria Absent Present in urethritis and
cystitis
Systemic complaints Edema, fever,
pharyngitis,rash, athralgia
Fever with UTI, pain with
calculi
Family history Deafness, hematuria in
alport syndrome
May be positive with
calculi and hypercalcemia
PHYSICAL EXAMINATION
Hypertension,edema Usually present Less common
Abdominal mass Absent Present in wilms tumor,
obstructive uropathy
Rash, arthritis Lupus erythematosus,
henoch schnolein purpura
Absent (unless drug
induced interstitial
nephritis)
URINARY
FINDING
GLOMERULAR
HEMATURIA
NON
GLOMERULAR
HEMATURIA
color Red or brown Usually red
clots absent May be present
proteinuria 2+ or more Less than 2+
RBC
morphology
dysmorphic Eumorphic
CASE 1
GLOMERULAR DISEASE
CASE 2
NON GLOMERULAR DISEASE
GLOMERULAR DISEASE
• Acute PIGN common
• PSGN
• Ig A nephropathy
• Benign familial
hematuria
• Membranoproliferative
• FSGS
• SLE
• Systemic infections
(malaria,
leptospirosis,infective,
endocarditis)
• HUS
• Henoch schnolein
purpura
• Alport’s syndrome
• Goodpasture’s syndrme
MECHANISM
RBC passes through
the damaged
basement
membrane
Morphology of RBC
will be deformable
Morphology of RBC is modified by
Intrinsic deformability
Intraglomerular capillary pressure
Size of the gap
Thickness of basement membrane
Variation in urine pH
Osmotic pressure
Effects of tubular enzymes
NON GLOMERULAR CAUSES
• UTI common
• Nephrolithiasis
• Hypercalciuria
• Viral haemorrhagic
cystitis
• Vascular abnormalities
• Trauma, tumours,
exercise
• Renal cystic disease
• Tuberculosis
• Munchaussen
syndrome
CASE 3
• 8 year old boy presented with
• Red coloured urine : 3 months
• Intermittent once every 2-3 weeks for 2-3 days
• Painless
• No h/o burning micturition, increased frequency
• No h/o periorbital puffiness, edema,
oliguria,hypertension
• Urinalysis: RBC- plenty
WBC:3-4 pus cells
albumin: = +1 albumin
between the episodes normal
RECURRENT HEMATURIA
CAUSES OF RECURRENT HEMATURIA
GLOMERULAR CAUSES
• Ig A nephropathy
• Benign familial hematuria
• Alport’s syndrome
NON GLOMERULAR CAUSES
• Nephrolithiasis
• Hypercalciuria
• Tumours
• Sickle cell disease
• tuberculosis
MICROSCOPIC HEMATURIA
ISOLATED
WITH PROTEINURIA
ISOLATED MICROSCOPIC HEMATURIA
Urinalysis repeated twice within 2 weeks
If on suspected medicine – withold
& recheck …
careful reitertion of history, special
emphasis on family history
RFT, URINE ca:cr ratio, proteinuria, USG,
Hb electrophoresis, coagulation profile ,
test parents for hematuria
negative
negative
negative
positive
positive
Follow every
2-3 months
Identify the cause and treat accordingly
MICROSCOPIC HEMATURIA WITH
PROTEINURIA
• PIGN
• Minimal change nephrotic syndrome
• Ig A Nephropathy
• Membranoproliferative GN
• Alport’s syndrome
• Thin BMD
• Focal segmental glomerulosclerosis
• Membranous nephropathy
CASE 4
• 7 days old term male baby with
• Red staining of diapers
• No fever, feeding well, good activity
• No significant antenatal history
• Urinalysis : PUS- 10 to 15/hpf
RBC 8-10
CAUSES OF HEMATURIA IN THE
NEWBORN
• Renal vein thrombosis
• Renal artery thrombosis
• Autosomal recessive polycystic kidney disease
• Urinary tract infection
• Trauma
• Bladder catheterization
HEMATURIA – QUESTIONS TO ASK
Recent sore throat or skin
infection ?
POST STREPTOCOCCAL
GLOMERULONEPHRITIS
Associated fever, dysuria or
flank pain ?
PYELONEPHRITIS
History of high blood pressure
?
NEPHRITIC SYNDROME
Family history of
deafnessrenal disease ?
ALPORT SYNDROME
Chronic medical problems ? SLE, SICKLE CELL ANAEMIA
History of purpuric rash,
abdominal pain?
HENOCH SCHONLEIN PURPURA
History of trauma ? BLEED IN URINARY TRACT
APPROACH TO A CHILD WITH
HEMATURIA
Detailed history
Physical
examination
In true
hematuria –
localize bleeding
Glomerular or
non glomerular

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Approach to hematuria with case discussion

  • 1. Dr. Kaviayarasi muthamizhan Final yr MBBS Government thiruvannamalai medical college Thiruvannamalai
  • 2. DEFINITIONS  GROSS /MACROSCOPIC HEMATURIA : visible to the naked eye  MICROSCOPIC HEMATURIA : >5 RBCs/HPF in centrifuged sample  TRANSIENT HEMATURIA: usually microscopic and benign fever, infections ,trauma and exercise  PERSISTENT HEMATURIA: Persistent finding of hematuria in atleast two or three urinalyses performed over 2-3 weeks
  • 3. CLINICAL TERMINOLOGIES FOR PRESENTATION OF HEMATURIA Gross hematuria Single episode recurrent Microscopic hematuria isolated With proteinuria
  • 4. CONFIRMATION OF HEMATURIA Urine sample Urine dipstick Urine microscopic exn  urine dipstick identifies hemeprotein ( SENSITIVITY=100% SPECIFICITY – 99% in detecting 1-5 RBCs/HPF ) FALSE POSITIVE FALSE NEGATIVE Oxidising substances Vitamin C Alkaline ph >9 formalin
  • 6. Positive urine dipstick Urine microscopy >5 RBC HEMATURIA NO RBC HEMOGLOBINURIA MYOGLOBINURIA PLASMA COLOR RED HEMOGLOBINURIA CLEAR MYOGLOBINURIA
  • 8. NEGATIVE URINE DIPSTICK RBC HEMOGLOBIN MYOGLOBIN But urine red colour ?? All that is red is not blood Search for other causes of red urine
  • 9. SUBSTANCES CAUSING DISCOLARATION OF URINE • RED OR PINK URINE • Urates • Porphyrins • Beets,red dyes in food • Drugs:chloroquine,desf errioxime,pyridum • DARK YELLOW/ORANGE • Normal concentrated urine • Rifampicin • Pyridium • DARK BROWN/BLACK • Methemoglobinemia • metronidazole
  • 10. • Confirmed true hematuria • Next step??? • LOCALIZATION OF BLEEDING glomerular vs non glomerular
  • 11. CASE 1 A 7 year old girl presented with • h/o cola coloured urine 4 days • Swelling of face & legs -2 days • Oliguria -2 days • Breathlessness -1 day • h/o sore throat 2 weeks back • O/E edema,BP>99 th percentile,tender hepatomegaly • Urinalysis appearance : brown RBC- plenty albumin- 5to6/hpf
  • 12. CASE 2 • 10 year old boy with • red coloured urine-2 days • colicky pain in right flank • dysuria , increased frequency, urgency, stranguary • no oliguria,edema, hypertension • Urinalysis appearance : bright red albumin trace RBC- plenty WBC 6-10 /HPF
  • 13. FEATURES GLOMERULAR NON GLOMERULAR HISTORY Dysuria Absent Present in urethritis and cystitis Systemic complaints Edema, fever, pharyngitis,rash, athralgia Fever with UTI, pain with calculi Family history Deafness, hematuria in alport syndrome May be positive with calculi and hypercalcemia PHYSICAL EXAMINATION Hypertension,edema Usually present Less common Abdominal mass Absent Present in wilms tumor, obstructive uropathy Rash, arthritis Lupus erythematosus, henoch schnolein purpura Absent (unless drug induced interstitial nephritis)
  • 14. URINARY FINDING GLOMERULAR HEMATURIA NON GLOMERULAR HEMATURIA color Red or brown Usually red clots absent May be present proteinuria 2+ or more Less than 2+ RBC morphology dysmorphic Eumorphic
  • 15. CASE 1 GLOMERULAR DISEASE CASE 2 NON GLOMERULAR DISEASE
  • 16. GLOMERULAR DISEASE • Acute PIGN common • PSGN • Ig A nephropathy • Benign familial hematuria • Membranoproliferative • FSGS • SLE • Systemic infections (malaria, leptospirosis,infective, endocarditis) • HUS • Henoch schnolein purpura • Alport’s syndrome • Goodpasture’s syndrme
  • 17. MECHANISM RBC passes through the damaged basement membrane Morphology of RBC will be deformable
  • 18. Morphology of RBC is modified by Intrinsic deformability Intraglomerular capillary pressure Size of the gap Thickness of basement membrane Variation in urine pH Osmotic pressure Effects of tubular enzymes
  • 19. NON GLOMERULAR CAUSES • UTI common • Nephrolithiasis • Hypercalciuria • Viral haemorrhagic cystitis • Vascular abnormalities • Trauma, tumours, exercise • Renal cystic disease • Tuberculosis • Munchaussen syndrome
  • 20. CASE 3 • 8 year old boy presented with • Red coloured urine : 3 months • Intermittent once every 2-3 weeks for 2-3 days • Painless • No h/o burning micturition, increased frequency • No h/o periorbital puffiness, edema, oliguria,hypertension • Urinalysis: RBC- plenty WBC:3-4 pus cells albumin: = +1 albumin between the episodes normal RECURRENT HEMATURIA
  • 21. CAUSES OF RECURRENT HEMATURIA GLOMERULAR CAUSES • Ig A nephropathy • Benign familial hematuria • Alport’s syndrome NON GLOMERULAR CAUSES • Nephrolithiasis • Hypercalciuria • Tumours • Sickle cell disease • tuberculosis
  • 23. ISOLATED MICROSCOPIC HEMATURIA Urinalysis repeated twice within 2 weeks If on suspected medicine – withold & recheck … careful reitertion of history, special emphasis on family history RFT, URINE ca:cr ratio, proteinuria, USG, Hb electrophoresis, coagulation profile , test parents for hematuria negative negative negative positive positive Follow every 2-3 months Identify the cause and treat accordingly
  • 24. MICROSCOPIC HEMATURIA WITH PROTEINURIA • PIGN • Minimal change nephrotic syndrome • Ig A Nephropathy • Membranoproliferative GN • Alport’s syndrome • Thin BMD • Focal segmental glomerulosclerosis • Membranous nephropathy
  • 25. CASE 4 • 7 days old term male baby with • Red staining of diapers • No fever, feeding well, good activity • No significant antenatal history • Urinalysis : PUS- 10 to 15/hpf RBC 8-10
  • 26. CAUSES OF HEMATURIA IN THE NEWBORN • Renal vein thrombosis • Renal artery thrombosis • Autosomal recessive polycystic kidney disease • Urinary tract infection • Trauma • Bladder catheterization
  • 27. HEMATURIA – QUESTIONS TO ASK Recent sore throat or skin infection ? POST STREPTOCOCCAL GLOMERULONEPHRITIS Associated fever, dysuria or flank pain ? PYELONEPHRITIS History of high blood pressure ? NEPHRITIC SYNDROME Family history of deafnessrenal disease ? ALPORT SYNDROME Chronic medical problems ? SLE, SICKLE CELL ANAEMIA History of purpuric rash, abdominal pain? HENOCH SCHONLEIN PURPURA History of trauma ? BLEED IN URINARY TRACT
  • 28. APPROACH TO A CHILD WITH HEMATURIA Detailed history Physical examination In true hematuria – localize bleeding Glomerular or non glomerular