Proteinuria
   Dr. Sachin Verma MD, FICM, FCCS, ICFC
      Fellowship in Intensive Care Medicine
         Infection Control Fellows Course
 Consultant Internal Medicine and Critical Care
           Ivy Hospital Sector 71 Mohali
Web:- http://www.medicinedoctorinchandigarh.com
              Mob:- +91-7508677495
Proteinuria – early indicator of renal disease

   Increases the risk of renal impairment,
    hypertension & cardiovascular disease.

   Proteinuria of 1+ or more persisting on 2
    subsequent dipstick tests at weekly intervals –
    requires further investigations.

   Causes of transient proteinuria to be excluded.
CAUSES
   Transient proteinuria
       UTI
       Fever
       Heavy exercise
       Pregnency
       Orthostatic proteinuria - not found in early morning
        sample, uncommon over age of 30 yrs
       Vaginal mucus
Persistant proteinuria
   Primary renal disease
       Glomerular – GN
       Tubular
   Secondary renal disease
       DM
       CTD
       Vasculitis
       Amyloidosis
       Myeloma
       CCF
       Hypertension
Evaluation
   History
       Symptoms of renal failure
       CTD – arthralgia, mouth ulcers, rashes.
       Past h/o DM, HTN, CCF, CTD
       H/O drugs ass. with proteinuria – NSAIDs,
        captopril, penicillamine
       Family h/o PCKD, reflux nephropathy, CTD.
Examination
   Look for signs of Nephrotic syndrome
   Signs of multisystem dis – rashes, splinter
    haemorrhage, bruits.
   B.P
   Urine dipstick test to check for microscopic
    haematuria – if + go for urine microscopy.
   Rule out Diabetes and UTI
Quantification of proteinuria
   24 hr urinary collection
   Spot morning protein/creatinine ratio – simpler & as
    accurate.
   24 hr urinary protein excretion (mg/24hrs) can be
    approximated as (mg/l protein) / ( mmol/l creatinine)
    × 10 or (mg/l creatinine ) × 100.
   More than 150 mg in 24 hr or protein to creatinine
    ratio of 15 mg/mmol or 150 mg/mg is abnormal
   Nephrotic range - >3.5 g/24 hr or a ratio > 3500 -
    check for serum albumin and cholesterol.
Assessment of renal function
   Check serum creatinine, urea, electrolytes.
   Creatinine clearance gives more accurate
    picture of renal function than creatinine alone,
    can be calculated by Cockcroft- Gault formula.
   Best to estimate GFR by MDRD formula
   GFR or creatinine clearance > 90ml/min can
    be considered normal. Lower values may be
    normal in old age and in people with low
    muscle mass.
   Significant proteinuria > 100 mg/mmol
    although values > 50 may be significant if
    other features of renal disease are present like
       Impaired renal function
       Coexistant microscopic haematuria
       Hypertension
       Features underlying systemic disease.
Further investigations
   Renal tract USG
   Immunology
       Serum and urine protein electrophoresis
       ANA
       ANCA
       Complements
   Hepatitis B & C serology
Follow-up
   Review after six months and then annualy to
    reassess quantity of proteinuria, renal function
    and blood pressure.

   Any hypertension if present – to be treated
    aggressively with an ACE inhibitor or ARB.

Proteinuria

  • 1.
    Proteinuria Dr. Sachin Verma MD, FICM, FCCS, ICFC Fellowship in Intensive Care Medicine Infection Control Fellows Course Consultant Internal Medicine and Critical Care Ivy Hospital Sector 71 Mohali Web:- http://www.medicinedoctorinchandigarh.com Mob:- +91-7508677495
  • 2.
    Proteinuria – earlyindicator of renal disease  Increases the risk of renal impairment, hypertension & cardiovascular disease.  Proteinuria of 1+ or more persisting on 2 subsequent dipstick tests at weekly intervals – requires further investigations.  Causes of transient proteinuria to be excluded.
  • 3.
    CAUSES  Transient proteinuria  UTI  Fever  Heavy exercise  Pregnency  Orthostatic proteinuria - not found in early morning sample, uncommon over age of 30 yrs  Vaginal mucus
  • 4.
    Persistant proteinuria  Primary renal disease  Glomerular – GN  Tubular  Secondary renal disease  DM  CTD  Vasculitis  Amyloidosis  Myeloma  CCF  Hypertension
  • 5.
    Evaluation  History  Symptoms of renal failure  CTD – arthralgia, mouth ulcers, rashes.  Past h/o DM, HTN, CCF, CTD  H/O drugs ass. with proteinuria – NSAIDs, captopril, penicillamine  Family h/o PCKD, reflux nephropathy, CTD.
  • 6.
    Examination  Look for signs of Nephrotic syndrome  Signs of multisystem dis – rashes, splinter haemorrhage, bruits.  B.P  Urine dipstick test to check for microscopic haematuria – if + go for urine microscopy.  Rule out Diabetes and UTI
  • 7.
    Quantification of proteinuria  24 hr urinary collection  Spot morning protein/creatinine ratio – simpler & as accurate.  24 hr urinary protein excretion (mg/24hrs) can be approximated as (mg/l protein) / ( mmol/l creatinine) × 10 or (mg/l creatinine ) × 100.  More than 150 mg in 24 hr or protein to creatinine ratio of 15 mg/mmol or 150 mg/mg is abnormal  Nephrotic range - >3.5 g/24 hr or a ratio > 3500 - check for serum albumin and cholesterol.
  • 8.
    Assessment of renalfunction  Check serum creatinine, urea, electrolytes.  Creatinine clearance gives more accurate picture of renal function than creatinine alone, can be calculated by Cockcroft- Gault formula.  Best to estimate GFR by MDRD formula  GFR or creatinine clearance > 90ml/min can be considered normal. Lower values may be normal in old age and in people with low muscle mass.
  • 9.
    Significant proteinuria > 100 mg/mmol although values > 50 may be significant if other features of renal disease are present like  Impaired renal function  Coexistant microscopic haematuria  Hypertension  Features underlying systemic disease.
  • 10.
    Further investigations  Renal tract USG  Immunology  Serum and urine protein electrophoresis  ANA  ANCA  Complements  Hepatitis B & C serology
  • 11.
    Follow-up  Review after six months and then annualy to reassess quantity of proteinuria, renal function and blood pressure.  Any hypertension if present – to be treated aggressively with an ACE inhibitor or ARB.