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Dr. Sanjeev Mehta MDDr. Sanjeev Mehta MD
Ahmedabad, INDIAAhmedabad, INDIAwww.urolab.net
Metabolic Evaluation&Stone Analysis
Practical implications
Role of laboratory
• What lab can not tell you, you will not know.• What it tells you in error, you will not
correct by using your instincts, your medical experience or your art.
• Misdirected treatment : unreasonable expenses.
• The Kidney Stone Handbook; Gail Savitz & co auth.
Stone : Supersaturation of Urine
Stone Promoting and Inhibiting Factors
PROMOTORS INHIBITORS
Calcium Inorganic : Magnesium
Sodium Phosphorus
Oxalate Citrate
Urate Organic : Nephrocalcin
Cystine Tomm-Horsfall Protein
Low Urine Ph Urinary Prothrombin fragment.
Tomm-Horsfall Protein
Bacterial products
Evaluation of Stone Disease
ROUTINE BLOOD AND URINE TESTSSTONE ANALYSIS.24 HRS URINE METABOLIC PROFILE
New advances in Stone analysis, Blood and Urinary Chemical analysis can find out 90-95% cause.
Clinical usefulness
1.Identify treatable metabolic abnormality2.Identify underlying medical disease that
predisposes to stone formation.3.Outline a treatment plan.
A. Routine Tests
BLOOD low K, and HCO3- RTA High Uric acid - Uric acid
diathesisHigh Calcium- pri
hyperparathyroidism Low phosphorus- renal
phosphorus leak. Parathyroid ; sos
URINEpH > 7.5 – infection
lithiasis pH < 5.5 – Uric acid lithiasisSediments for crystalluriaUrine cultureQualitative cystine
Renal Stone Analysis
• Essential step in the examination and initial treatment of Urolithiasis.
• Yields fundamental information about ;- Metabolic abnormality.- Presence of infection.- Possible artifacts.- Drug metabolism.
Technique
Integrated analysis with Infra-red spectrometryXenthene and Ca.oxalate Dihydrite
INTEGRETED ANALYSIS ;Mixed Stone
11
Actually up to 65 different chemical compounds are found in urinary calculi.
Clinical significance of Stone analysis• Three categories :1.Composition and hardness of Renal
Stones.2.Composition and its predictive value.3.Composition and related metabolic
abnormalities. Kourambas J, Aslan P, Teh CL, Mathias BJ, Preminger GM.J Endourol. 2001
Mar;15(2):181-6
Clinical Significance: Hardness pattern in Stone.• Useful in describing consistency in individual.• Formulation of treatment strategies. - Number of re-treatments. - Number of Shock waves. • Energy index (KV x number of shock waves).
Ringdén I, Tiselius HG, Scand J Urol Nephrol. 2007;41(4):316-23
Hardness Factor of Stone
Calcium Oxalate Dihydrate 1.0Calcium Oxalate Monohydrate 1.3Hydroxy-peptite 1.1Brushite 2.2Uric Acid/ Urate 1.0Cystine 2.4Carbonate Apatite 1.3Struvite 1.0Mixed Stone 1.0* Ringden I, Scand J Urol Nephrol.2007;41(4):316-23
Clinical value : Calcium
• Present in approximately 80% stones.• Combines with phosphate or oxalate or both.• Risk factors : hypercalciuria, Hyperoxaluria. hyperuricosuria. predominantly acid or alk urine. hypocitraturia. low urine volume.
Calcium Stones …..
Pure calcium Stones
• More Acid urine• Low Urine volume• High Oxalate
excretion
Mixed Stone formers
• pH is higher• High Calcium • High Calcium
excretion• High recurrence rate
* Schroeppel j Smith et all ; J Am Soc Nephrol 1997;8:568A
Calcium Stone…..
Ca-oxalate Monohydrate
• Hypo- megnesuria• Acidic Urine• Low Urine volume• Hardness +
• Ca-ox Dihydrate
• Hyper-calciuria• Alkaline Urine• Hypo-citraturia• Hardness ; less
Renal tubular acidosis
Carbonate apattite
• Consider RTA• Increases with amount • (5-39%)
Brushite Stones
• Consider RTA
Struvite Stone Magnesium Ammonium Phosphate
• Mixed Stone : Infection. ‘Proteus’ • Strains of staphylococci, pseudomonas and
kelbsiella. • Rarely; E.coli.• Urine Ph. Is < 7.5
Ammonium Urate
• Calcium oxalate – containing calculi, may start hyperuricosuria.
• Elders : associated with infection.• Children : May as result of hyperuricosuria,
but No UTI
Brushite : Amm. Calcium Phosphate
• Sizable stone burden. Increasing trend • High recurrence rate , 3 yrs• Familial tendency• Hypercalciurea and underlying metabolic
abnormality. • Extreme Alkaline Urine.
J Urol. Oct 2010; 184(4): 1367–1371.
Dahilite ( Carbonate apatite)
• Phosphate stone• Infection in body.• May not accompanying sign of disease.• RTA• Disorder of phosphate metabolism. • Rare in pure form ( 2-3%).
Uric Acid
URIC ACID• Hyperuricemia, hyperuricosuria.• Low Urine Ph. < 6.2• Causes: - Gout. - Myeloproliferative dis. - Chemotherapy and Radiotherapy.
Cystine
CYSTINE• Cysteinuria.• Autosomal recessive
disorder.• Occurs predominantly
in pure form.
• XENTHENE Most frequent causes:- Xanthinuria. - Absence of Xanthene
oxidase.• Genetic autosomal
hereditary recessive enzyme disorder.
• Trigger : Allopurinol Treating Gout.
Urine: Metabolic Evaluation24 hrs Urine collections: multiple parameters Stone risk factors : Quantitation Volume and pH Calcium Oxalate Citrate Uric acid. Creatinine
Metabolic Evaluation: 24 hrs Urine
• Dietary risk factors: Sodium, Potassium Magnesium Urinary analysts : phosphorus, sulphate, Urea Children : state sample Repeat 24 hrs Urine collection 4-6 weeks post
interventi
GOLD STANDARDSupersaturation value.
•High risk parameter can be monitored.
Graphic presentation
Super-saturation : Gold standard….
Conclusion
• Advancement in laboratory can now diagnose cause of stone formation uo tp 90% cases.
• By appropriate Stone analysis and metabolic
evaluation can effectively treat impact of Nephrolithiasis and prevent recurrence .
Conclusion: Significance
• Advancement in laboratory can diagnise cause of Stone disease up to 90%
• Impact mitigated by appropriate metabolic evaluation.
• Identify risk factor.• Focused medical treatment • Significantly reduces recurrence• Social and financial burden. • Batter quality of life
Thank you !
For further details contact:
Phone: +91 79 40380380