Common presentation and investigation of Kidney diseases


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Common presentation and investigation of Kidney diseases

  2. 2. Cross Section of Kidney
  3. 3. Nephron
  4. 4. 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.
  5. 5. 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.
  6. 6. 3. Oliguria. - < 300 ml/ day. - hypotension, hypovolaemia. - intrinsic renal disease. - urinary tract obstruction.
  7. 7. 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.
  8. 8. 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.
  9. 9. Outlines • Features of common renal diseases -Glomerulopathies (GN) -Urinary tract infection -Urinary tract obstruction -Renal failure -Polycystic Kidney Disease -Others Acquired Congenital
  10. 10. 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.
  11. 11. Nephrotic syndrome 1. Proteinuria ( >3.5 g/ day). 2. Hypoalbuminaemia( <30 g/L). 3. Oedema. 4. Hyperlipidaemia ( ↑ LDL & cholesterol).
  12. 12. 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
  13. 13. Nephritic syndrome • Haematuria • Hypertension • Oliguria • Uraemia
  14. 14. 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
  15. 15. Clinical presentations of GN 1. Hypoalbuminemia. • Pedal oedema , Ascites , Anasarca ,Pleural Effusion. 2. Protenuria • Frothy urine. 3. Hematuria • Microscopic or bloody urine.
  16. 16. 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.
  17. 17. 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.
  18. 18. 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.
  19. 19. 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
  20. 20. 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
  21. 21. 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
  22. 22. 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
  23. 23. Renal Failure
  24. 24. 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.
  25. 25. 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
  26. 26. 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.
  27. 27. 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.
  28. 28. 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
  29. 29. 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
  30. 30. 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
  31. 31. 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
  32. 32. Investigations • IMAGING TECHNIQUES - Abdominal X-ray,Ultrasonography,CT,MRI - Excretion urography - Antegrade pyelography - Retrograde pyelography - Micturating cystourethrography - Aortography - Scintigraphy • Transcutaneous renal biopsy
  33. 33. • 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
  34. 34. 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.
  35. 35. • 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.
  36. 36. • 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.
  37. 37. 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.
  38. 38. - 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.
  39. 39. 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)
  40. 40. • 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
  41. 41. • 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
  42. 42. 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.
  43. 43. • 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.
  44. 44. • 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.
  45. 45. 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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