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COMMON PRESENTATION
AND INVESTIGATION OF
RENAL DISEASES
By Ezmeer Emiral
Cross Section of Kidney
Nephron
Normal function of kidney
1. Excretion of waste product .
2. Regulation of fluid, electrolyte and acid-base
balance.
3. Production of erythropoitein, renin,
prostagladins.
4. Metabolism of vitamin D.
Presenting features of renal disease
1. Dysuria.
- urethritis and cystitis.
- inflammation of vagina and penis.
2. Polyuria and nocturia.
- > 3 L/ day.
- solute diuresis, diabetes insipidus, CRF.
3. Oliguria.
- < 300 ml/ day.
- hypotension, hypovolaemia.
- intrinsic renal disease.
- urinary tract obstruction.
4. Haematuria.
- blood in the urine, arise anywhere in renal
tract.
- start of micturition- urethral disease.
- throughout the urine-comes from bladder
and above
- end of micturition- prostate/bladder base.
5. Renal pain.
- dull constant pain in the loin.
- dt renal obstruction, acute pyelonephritis, acute
nephritic syndrome, polycystic kidney, renal infart.
6.Ureteric colic.
- Severe loin pain, waxes and wanes, a/w fever,
vomiting, radiate to abdomen, groin, upper thigh.
- Renal calculus, clot.
Outlines
• Features of common renal diseases
-Glomerulopathies (GN)
-Urinary tract infection
-Urinary tract obstruction
-Renal failure
-Polycystic Kidney Disease
-Others
Acquired
Congenital
Glomerulopathies(GN)
• Glomerulopathies are the third most common
cause of endstage renal disease.
• Glomerulopathy is a general term for a group of
disorders in which:
-The kidneys are involved symmetrically.
-There is primarily an immunologically mediated
injury to glomeruli.
-May be part of a generalized disease eg:SLE
• Classification of glomerulopathies
-Nephrotic syndrome.
-Nephritic syndrome.
Nephrotic syndrome
1. Proteinuria ( >3.5 g/ day).
2. Hypoalbuminaemia( <30 g/L).
3. Oedema.
4. Hyperlipidaemia ( ↑ LDL & cholesterol).
Causes of neprotic syndrome
1. Primary
- minimal change GN
- membranous GN
- focal segmental glomerulosclerosis
- Ig A nephropathy
2. Secondary
- infection; HBV, HIV,CMV,
- malignancy; leukemia, lymphoma
- drug/toxin; NSAID, mercury
- CT disease; SLE
- metabolic disease;DM
Nephritic syndrome
• Haematuria
• Hypertension
• Oliguria
• Uraemia
Causes of nephritic syndrome
1. Primary
- lg A nephropathy
- membranoproliferative GN
- rapidly progressive GN
2. Secondary
- infection: post- strep GN, IE
- multisystem disease: SLE, Henoch-Scholein
purpura, Goodpasture’s syndrome
Clinical presentations of GN
1. Hypoalbuminemia.
• Pedal oedema , Ascites , Anasarca ,Pleural
Effusion.
2. Protenuria
• Frothy urine.
3. Hematuria
• Microscopic or bloody urine.
4. Hypertension.
• Asymptomatic.
• Headache, confusion,seizure (hypertensive crisis).
5. Fluid retention.
• Reduced effort tolerance, orthopnea.
• Acute pulmonary edema.
• Reduced urine output (oliguria).
6. Uremia.
• Nausea, vomiting .
• Confusion , seizure.
Systemic disease associated with
glomerulopathy
1. Post-strep GN.
- child, strep infection 1-3 wks before with
tonsilitis, otitis media, cellulitis or impetigo.
2. Multiple myeloma.
-Bone pain,recurrent infection,lethargy.
3. Diabetes Mellitus.
-History of chronic DM,multiple DM end organ
damage.
4. SLE.
-Oral ulcer,malar rash.
-Alopecia,athralgia.
5.Cryoglubulinemia.
- Purpura, arthralgia, leg ulcers, Raynaud’s
phenomenon, evidence of systemic vasculitis,
polyneuropathy and hepatic involvement.
6.Wegener’s granulomatosis.
- Sinusitis, recurrent nasal congestion, hemoptysis.
Urinary tract infection (UTI)
Presence of pure growth of >100000 colony
forming units/ml in urine with pyuria.
UTI sites: bladder (cystitis), prostate (prostatitis),
kidney (pyelonephritis)
Cystitis: frequency, dysuria, urgency,
haematuria, suprapubic pain
Pyelonephritis: fever, rigors, vomiting, loin pain,
tenderness, oliguria (if ARF)
Prostatitis: flu-like symptoms, low backache,
swollen and tender prostate
Renal calculi
Consist mainly of crystal aggregates, form in the
Collecting Duct and deposited anywhere in UT
• Asymptomatic.
• Loin pain, renal colic (radiates from loin to
groin).
• Haematuria, sterile pyuria, calculus anuria
Urinary tract obstruction
- Any point btw kidney and urethral meatus
- Dilatation of UT, hydronephrosis
- Causes of UTO :
1)within lumen: calculi, tumour, blood clot
2)within the wall : stricture, neuropathic
bladder, obstructive megaureter
3)from outside: pelvic tumour, retroperitoneal
fibrosis
Urinary tract obstruction(UTO)
Presentation:
- Loin pain
- Complete anuria
- Polyuria
- Intermittent anuria and polyuria
- Hesitancy, narrowing and diminished force of
urinary stream, terminal dribbling, sense of
incomplete bladder emptying
Renal Failure
Acute Renal failure
Definition:
- Significant deterioration in renal function occur
over hrs or days.
- Reversible over days /weeks(injury to kidney is
short term and potentially reversible)
- Clinically no symptom or sign but oliguria
( < 400 ml/day) common.
- No long term complication seen in CKD eg:renal
anemia,renal bone disease.
Causes:
1.Prenal
- failure or perfusion of kidney
- hypovolaemia,↓CO, renal artery obstruction
2. Intrinsic renal failure
- acute tubular necrosis, acute interstitial nephritis,
acute GN
3. Post-renal
- UTO
Renal
Post-Renal
Acute Renal
Failure
Pre-Renal
Clinical feature:
- Early stage asymptomatic
- ARF does not produce a classic set of symptoms. The
most common symptom is decreased urine output,
which occurs in 70% of patients.
Chronic Kidney Disease
• Definition
-CKD implies long-standing, and usually
progressive, impairment in renal function.
-In many instances, no effective means are
available to reverse the primary disease
process.
Symptoms and sign of
chronic renal failure
• Produces symptoms when renal function – which is measured as the
glomerular filtration rate (GFR) – falls below 30 milliliters per minute (<30
mL/min). This is approximately 30% of the normal value.
• When GFR slows to below 30 mL/min, signs of uremia (high blood level of
protein by-products, such as urea) may become noticeable. When the GFR
falls below 15 mL/min most people become increasingly symptomatic.
Clinical features of severe uraemia:
1.Anaemia
- Pallor; fatigue; malaise; SOB
2.Platelet abnormality
- Epistaxis, bruishing
3.GI
- Anorexia; nausea; vomiting; metallic taste; hiccups
4.CNS
- Confusion;Irritability; poor concentration; insomnia; restless legs;
twitching;coma;fits
5. Skin
- hyperpigmentation, pruritis
6.Cardiovascular system
- Uraemic pericarditis, HPT, PVD, HF
7.Renal
- Nocturia, polyuria, salt & water retention cause
edema.
8.Renal osteodystrophy
- osteomalacia, muscle weakness, bone pain,
hyperPTH, osteoslerosis
9.Endocrine
- amenorrhoe, erectile impotence, infertility
Polycystic renal disease
Autosomal dominant disease with formation of
multiple cyst associated with extrarenal
abnormalities-hepatic and CVS. May present as:
- Loin pain or haematuria due to haemorrhage into a
cyst, cyst infection or urinary tract stone formation
- Loin or abdominal discomfort
- Hypertension
Investigations
• EXAMINATION OF URINE
- Appearance,Volume,Specific gravity&
osmolality,Urinary pH
- Chemical (Stix) testing
- Urine microscopy
• BLOOD AND QUANTITATIVE TESTS
- Urea,creatinine&GFR
- ANCA,Immunofluroscene,&complement
Investigations
• IMAGING TECHNIQUES
- Abdominal X-ray,Ultrasonography,CT,MRI
- Excretion urography
- Antegrade pyelography
- Retrograde pyelography
- Micturating cystourethrography
- Aortography
- Scintigraphy
• Transcutaneous renal biopsy
• Appearance
-causes of discoloration of urine include cholestatic jaundice,
haemoglobinuria, drugs such as rifampicin, use of fluorescein or
methylthioninium chloride(methylene blue), and ingestion of
beetroot.
• Volume
-CKD or diabetes insipidus, impairment of concentrating ability
requires increased volumes of urine to be passed, given the same
daily solute output.
• Specific gravity
-Measurement of the weight of dissolved particles in urine.
-Specific gravity is usually fixed at 1.010 in CKD or acute tubular
necrosis as compared to prerenal acute kidney injury and
inappropriate ADH secretion where specific gravity is very high –
close to 1.025.
• pH (4.5-8)
Acid base balance disorder
Examination of urine
Chemical (Stix) testing
• Haematuria
- may be overt, with bloody urine, or microscopic
and found only on chemical testing.
- A positive Stix test must always be followed by
microscopy of fresh urine (with the exception of
menstruating women) to confirm the presence of
red cells and so exclude the relatively rare
conditions of haemoglobinuria or myoglobinuria.
• Proteinuria
-Most reagent strips can detect protein if
albuminuria exceeds 300 mg/d. They react
primarily with albumin and are relatively
insensitive to globulin and Bence Jones proteins.
> 3.5 g/ day: nephrotic syndrome.
- Timed 24-hour urinary excretion rates provide
the most precise measure of microalbuminuria.
- 30-300 mg/ day.
- can be early indicator of DM.
• Glucose
- Renal glycosuria is uncommon, so that a
positive test for glucose always requires
exclusion of diabetes mellitus.
• Bacteriuria
-based on the detection of nitrite produced
from the reduction of urinary nitrate by
bacteria and also for the detection of
leucocyte esterase, an enzyme specific for
neutrophils.
Microscopy
- White blood cells. The presence of 10 or more WBCs per
cubic millimetre in fresh unspun mid-stream urine samples
is abnormal and indicates an inflammatory reaction within
the urinary tract such as urinary tract infection (UTI),
stones, tubulointerstitial nephritis, papillary necrosis,
tuberculosis and interstitial cystitis.
- Red cells. The presence of one or more red cells per cubic
millimetre in unspun urine samples results in a positive Stix
test for blood and is abnormal.
- Casts (cylindrical bodies, moulded in the shape of
the distal tubular lumen) may be hyaline, granular or
cellular.
- Coarse granular casts occur with pathological
proteinuria in glomerular and tubular disease.
- Red-cell casts – even if only single – always indicate
renal disease. White cell casts may be seen in acute
pyelonephritis. They may be confused with the
tubular cell casts that occur in patients with acute
tubular necrosis.
Renal function test
For Na, K, Ca, urea, creatinine excretion
Plasma creatinine to calculate creatinine clearance
Creatinine clearance=U x V/P x 0.7
U= urine creatinine (mmol/L)
P= plasma creatinine (μmol/L)
V= 24H urine volume (mL)
• Low GFR (classic ARF)
Plasma: ↑urea, creatinine, K, H, urate,
phosphate, anion gap
↓Ca, bicarbonate
Other finding: Oliguria
Diagnosis: Low GFR (↓ creatinine clearance)
Causes: early acute oliguric RF, long standing CRF
• Chronic renal failure
Plasma: ↑ creatinine, urea, phosphate, urate,
K
↓ bicarbonate, Hb, pH
Other finding: Osteomalacia
Access of renal failure must be combined with other
investigations
Urinary tract imaging
• Abdominal x-ray
Look at kidneys, ureters and bladder
Abnormal calcification, eg. calculi (80%)
• Ultrasound
-Characterizing renal masses as cystic or solid.
-Diagnosing polycystic kidney disease.
-Detecting intrarenal and/or perinephric fluid (e.g. pus,
blood).
-Demonstrating renal arterial perfusion or detecting renal
vein thrombosis using Doppler.
• IV pyelography
-has largely been replaced by ultrasonography and CT
scanning.
• Retrograde pyelography
-Reasons for performing a retrograde pyelogram include
identification of filling defects (e.g. stones or tumors),
as an adjunct during the placement of ureteral stents
or ureteroscopy, or to delineate renal anatomy in
preparation for surgery.
• Antegrade pyelography/percutaneous nephrostomy
-involves percutaneous puncture of a pelvicalyceal system
with a needle and the injection of contrast medium to
outline the pelvicalyceal system and ureter to the level
of obstruction.
• CT scan
Renal calculi, characterization of masses, renal trauma,
retroperitoneal lesion
CT + IV contrast can reveals kidney function
• Renal angiography
Assessment of renal artery stenosis
• MRI
-to characterize renal masses, demonstrate the renal arteries
and cancer staging.
• Radionuclide imaging
-Dynamic scintigraphy:investigation of obstruction,RBF & GFR
-Static scintigraphy:Kidney visualization,localization of
infection,renal function.
Renal biopsy
-Renal biopsy is carried out under ultrasound
control in specialized centres and requires
interpretation by an experienced pathologist.
-Renal biopsy is helpful in the investigation
of the nephritic and nephrotic syndromes, acute
and chronic renal failure, haematuria after
urological investigations and renal graft
dysfunction.
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Common presentation and investigation of Kidney diseases

  • 1. COMMON PRESENTATION AND INVESTIGATION OF RENAL DISEASES By Ezmeer Emiral
  • 2.
  • 5. Normal function of kidney 1. Excretion of waste product . 2. Regulation of fluid, electrolyte and acid-base balance. 3. Production of erythropoitein, renin, prostagladins. 4. Metabolism of vitamin D.
  • 6. Presenting features of renal disease 1. Dysuria. - urethritis and cystitis. - inflammation of vagina and penis. 2. Polyuria and nocturia. - > 3 L/ day. - solute diuresis, diabetes insipidus, CRF.
  • 7. 3. Oliguria. - < 300 ml/ day. - hypotension, hypovolaemia. - intrinsic renal disease. - urinary tract obstruction.
  • 8. 4. Haematuria. - blood in the urine, arise anywhere in renal tract. - start of micturition- urethral disease. - throughout the urine-comes from bladder and above - end of micturition- prostate/bladder base.
  • 9. 5. Renal pain. - dull constant pain in the loin. - dt renal obstruction, acute pyelonephritis, acute nephritic syndrome, polycystic kidney, renal infart. 6.Ureteric colic. - Severe loin pain, waxes and wanes, a/w fever, vomiting, radiate to abdomen, groin, upper thigh. - Renal calculus, clot.
  • 10. Outlines • Features of common renal diseases -Glomerulopathies (GN) -Urinary tract infection -Urinary tract obstruction -Renal failure -Polycystic Kidney Disease -Others Acquired Congenital
  • 11. Glomerulopathies(GN) • Glomerulopathies are the third most common cause of endstage renal disease. • Glomerulopathy is a general term for a group of disorders in which: -The kidneys are involved symmetrically. -There is primarily an immunologically mediated injury to glomeruli. -May be part of a generalized disease eg:SLE • Classification of glomerulopathies -Nephrotic syndrome. -Nephritic syndrome.
  • 12. Nephrotic syndrome 1. Proteinuria ( >3.5 g/ day). 2. Hypoalbuminaemia( <30 g/L). 3. Oedema. 4. Hyperlipidaemia ( ↑ LDL & cholesterol).
  • 13. Causes of neprotic syndrome 1. Primary - minimal change GN - membranous GN - focal segmental glomerulosclerosis - Ig A nephropathy 2. Secondary - infection; HBV, HIV,CMV, - malignancy; leukemia, lymphoma - drug/toxin; NSAID, mercury - CT disease; SLE - metabolic disease;DM
  • 14. Nephritic syndrome • Haematuria • Hypertension • Oliguria • Uraemia
  • 15. Causes of nephritic syndrome 1. Primary - lg A nephropathy - membranoproliferative GN - rapidly progressive GN 2. Secondary - infection: post- strep GN, IE - multisystem disease: SLE, Henoch-Scholein purpura, Goodpasture’s syndrome
  • 16. Clinical presentations of GN 1. Hypoalbuminemia. • Pedal oedema , Ascites , Anasarca ,Pleural Effusion. 2. Protenuria • Frothy urine. 3. Hematuria • Microscopic or bloody urine.
  • 17. 4. Hypertension. • Asymptomatic. • Headache, confusion,seizure (hypertensive crisis). 5. Fluid retention. • Reduced effort tolerance, orthopnea. • Acute pulmonary edema. • Reduced urine output (oliguria). 6. Uremia. • Nausea, vomiting . • Confusion , seizure.
  • 18. Systemic disease associated with glomerulopathy 1. Post-strep GN. - child, strep infection 1-3 wks before with tonsilitis, otitis media, cellulitis or impetigo. 2. Multiple myeloma. -Bone pain,recurrent infection,lethargy. 3. Diabetes Mellitus. -History of chronic DM,multiple DM end organ damage.
  • 19. 4. SLE. -Oral ulcer,malar rash. -Alopecia,athralgia. 5.Cryoglubulinemia. - Purpura, arthralgia, leg ulcers, Raynaud’s phenomenon, evidence of systemic vasculitis, polyneuropathy and hepatic involvement. 6.Wegener’s granulomatosis. - Sinusitis, recurrent nasal congestion, hemoptysis.
  • 20. Urinary tract infection (UTI) Presence of pure growth of >100000 colony forming units/ml in urine with pyuria. UTI sites: bladder (cystitis), prostate (prostatitis), kidney (pyelonephritis) Cystitis: frequency, dysuria, urgency, haematuria, suprapubic pain Pyelonephritis: fever, rigors, vomiting, loin pain, tenderness, oliguria (if ARF) Prostatitis: flu-like symptoms, low backache, swollen and tender prostate
  • 21. Renal calculi Consist mainly of crystal aggregates, form in the Collecting Duct and deposited anywhere in UT • Asymptomatic. • Loin pain, renal colic (radiates from loin to groin). • Haematuria, sterile pyuria, calculus anuria
  • 22. Urinary tract obstruction - Any point btw kidney and urethral meatus - Dilatation of UT, hydronephrosis - Causes of UTO : 1)within lumen: calculi, tumour, blood clot 2)within the wall : stricture, neuropathic bladder, obstructive megaureter 3)from outside: pelvic tumour, retroperitoneal fibrosis
  • 23. Urinary tract obstruction(UTO) Presentation: - Loin pain - Complete anuria - Polyuria - Intermittent anuria and polyuria - Hesitancy, narrowing and diminished force of urinary stream, terminal dribbling, sense of incomplete bladder emptying
  • 25. Acute Renal failure Definition: - Significant deterioration in renal function occur over hrs or days. - Reversible over days /weeks(injury to kidney is short term and potentially reversible) - Clinically no symptom or sign but oliguria ( < 400 ml/day) common. - No long term complication seen in CKD eg:renal anemia,renal bone disease.
  • 26. Causes: 1.Prenal - failure or perfusion of kidney - hypovolaemia,↓CO, renal artery obstruction 2. Intrinsic renal failure - acute tubular necrosis, acute interstitial nephritis, acute GN 3. Post-renal - UTO Renal Post-Renal Acute Renal Failure Pre-Renal
  • 27. Clinical feature: - Early stage asymptomatic - ARF does not produce a classic set of symptoms. The most common symptom is decreased urine output, which occurs in 70% of patients.
  • 28. Chronic Kidney Disease • Definition -CKD implies long-standing, and usually progressive, impairment in renal function. -In many instances, no effective means are available to reverse the primary disease process.
  • 29. Symptoms and sign of chronic renal failure • Produces symptoms when renal function – which is measured as the glomerular filtration rate (GFR) – falls below 30 milliliters per minute (<30 mL/min). This is approximately 30% of the normal value. • When GFR slows to below 30 mL/min, signs of uremia (high blood level of protein by-products, such as urea) may become noticeable. When the GFR falls below 15 mL/min most people become increasingly symptomatic. Clinical features of severe uraemia: 1.Anaemia - Pallor; fatigue; malaise; SOB 2.Platelet abnormality - Epistaxis, bruishing 3.GI - Anorexia; nausea; vomiting; metallic taste; hiccups 4.CNS - Confusion;Irritability; poor concentration; insomnia; restless legs; twitching;coma;fits
  • 30. 5. Skin - hyperpigmentation, pruritis 6.Cardiovascular system - Uraemic pericarditis, HPT, PVD, HF 7.Renal - Nocturia, polyuria, salt & water retention cause edema. 8.Renal osteodystrophy - osteomalacia, muscle weakness, bone pain, hyperPTH, osteoslerosis 9.Endocrine - amenorrhoe, erectile impotence, infertility
  • 31. Polycystic renal disease Autosomal dominant disease with formation of multiple cyst associated with extrarenal abnormalities-hepatic and CVS. May present as: - Loin pain or haematuria due to haemorrhage into a cyst, cyst infection or urinary tract stone formation - Loin or abdominal discomfort - Hypertension
  • 32. Investigations • EXAMINATION OF URINE - Appearance,Volume,Specific gravity& osmolality,Urinary pH - Chemical (Stix) testing - Urine microscopy • BLOOD AND QUANTITATIVE TESTS - Urea,creatinine&GFR - ANCA,Immunofluroscene,&complement
  • 33. Investigations • IMAGING TECHNIQUES - Abdominal X-ray,Ultrasonography,CT,MRI - Excretion urography - Antegrade pyelography - Retrograde pyelography - Micturating cystourethrography - Aortography - Scintigraphy • Transcutaneous renal biopsy
  • 34. • Appearance -causes of discoloration of urine include cholestatic jaundice, haemoglobinuria, drugs such as rifampicin, use of fluorescein or methylthioninium chloride(methylene blue), and ingestion of beetroot. • Volume -CKD or diabetes insipidus, impairment of concentrating ability requires increased volumes of urine to be passed, given the same daily solute output. • Specific gravity -Measurement of the weight of dissolved particles in urine. -Specific gravity is usually fixed at 1.010 in CKD or acute tubular necrosis as compared to prerenal acute kidney injury and inappropriate ADH secretion where specific gravity is very high – close to 1.025. • pH (4.5-8) Acid base balance disorder Examination of urine
  • 35. Chemical (Stix) testing • Haematuria - may be overt, with bloody urine, or microscopic and found only on chemical testing. - A positive Stix test must always be followed by microscopy of fresh urine (with the exception of menstruating women) to confirm the presence of red cells and so exclude the relatively rare conditions of haemoglobinuria or myoglobinuria.
  • 36. • Proteinuria -Most reagent strips can detect protein if albuminuria exceeds 300 mg/d. They react primarily with albumin and are relatively insensitive to globulin and Bence Jones proteins. > 3.5 g/ day: nephrotic syndrome. - Timed 24-hour urinary excretion rates provide the most precise measure of microalbuminuria. - 30-300 mg/ day. - can be early indicator of DM.
  • 37. • Glucose - Renal glycosuria is uncommon, so that a positive test for glucose always requires exclusion of diabetes mellitus. • Bacteriuria -based on the detection of nitrite produced from the reduction of urinary nitrate by bacteria and also for the detection of leucocyte esterase, an enzyme specific for neutrophils.
  • 38. Microscopy - White blood cells. The presence of 10 or more WBCs per cubic millimetre in fresh unspun mid-stream urine samples is abnormal and indicates an inflammatory reaction within the urinary tract such as urinary tract infection (UTI), stones, tubulointerstitial nephritis, papillary necrosis, tuberculosis and interstitial cystitis. - Red cells. The presence of one or more red cells per cubic millimetre in unspun urine samples results in a positive Stix test for blood and is abnormal.
  • 39. - Casts (cylindrical bodies, moulded in the shape of the distal tubular lumen) may be hyaline, granular or cellular. - Coarse granular casts occur with pathological proteinuria in glomerular and tubular disease. - Red-cell casts – even if only single – always indicate renal disease. White cell casts may be seen in acute pyelonephritis. They may be confused with the tubular cell casts that occur in patients with acute tubular necrosis.
  • 40. Renal function test For Na, K, Ca, urea, creatinine excretion Plasma creatinine to calculate creatinine clearance Creatinine clearance=U x V/P x 0.7 U= urine creatinine (mmol/L) P= plasma creatinine (μmol/L) V= 24H urine volume (mL)
  • 41. • Low GFR (classic ARF) Plasma: ↑urea, creatinine, K, H, urate, phosphate, anion gap ↓Ca, bicarbonate Other finding: Oliguria Diagnosis: Low GFR (↓ creatinine clearance) Causes: early acute oliguric RF, long standing CRF
  • 42. • Chronic renal failure Plasma: ↑ creatinine, urea, phosphate, urate, K ↓ bicarbonate, Hb, pH Other finding: Osteomalacia Access of renal failure must be combined with other investigations
  • 43. Urinary tract imaging • Abdominal x-ray Look at kidneys, ureters and bladder Abnormal calcification, eg. calculi (80%) • Ultrasound -Characterizing renal masses as cystic or solid. -Diagnosing polycystic kidney disease. -Detecting intrarenal and/or perinephric fluid (e.g. pus, blood). -Demonstrating renal arterial perfusion or detecting renal vein thrombosis using Doppler.
  • 44. • IV pyelography -has largely been replaced by ultrasonography and CT scanning. • Retrograde pyelography -Reasons for performing a retrograde pyelogram include identification of filling defects (e.g. stones or tumors), as an adjunct during the placement of ureteral stents or ureteroscopy, or to delineate renal anatomy in preparation for surgery. • Antegrade pyelography/percutaneous nephrostomy -involves percutaneous puncture of a pelvicalyceal system with a needle and the injection of contrast medium to outline the pelvicalyceal system and ureter to the level of obstruction.
  • 45. • CT scan Renal calculi, characterization of masses, renal trauma, retroperitoneal lesion CT + IV contrast can reveals kidney function • Renal angiography Assessment of renal artery stenosis • MRI -to characterize renal masses, demonstrate the renal arteries and cancer staging. • Radionuclide imaging -Dynamic scintigraphy:investigation of obstruction,RBF & GFR -Static scintigraphy:Kidney visualization,localization of infection,renal function.
  • 46. Renal biopsy -Renal biopsy is carried out under ultrasound control in specialized centres and requires interpretation by an experienced pathologist. -Renal biopsy is helpful in the investigation of the nephritic and nephrotic syndromes, acute and chronic renal failure, haematuria after urological investigations and renal graft dysfunction.
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