PROTEINURIA IN CHILDREN

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Presentation transcript:

PROTEINURIA IN CHILDREN Barbara Botelho M.D. Children’s Hospital & Research Center Oakland

A CASE 15 year old girl presents for a sports physical Found to have a U/A with: 1015/5/no blood/no sugar/no LE/no nitrites 100 mg/dL protein

MECHANISMS OF PROTEINURIA GLOMERULAR FEVER/EXERCISE/ORTHOSTATIC GLOMERULAR DISEASE TUBULAR LMW PROTEINS TUBULOINTERSTITIAL DISEASE FANCONI’S SYNDROME OVERFLOW PROTEINURIA

SYMPTOMATIC OR ASYMPTOMATIC PROTEINURIA? History: swelling, gross hematuria joint pains, rashes previous UTIs Physical: growth blood pressure edema

Our case: entirely asymptomatic with a benign exam Our case: entirely asymptomatic with a benign exam. She has never had a UTI.

HOW COMMON IS PROTEINURIA? 5-10% OF CHILDREN WILL HAVE 1+ OR GREATER 0.1% WILL HAVE PERSISTENT PROTEINURIA

IS THE PROTEINURIA REAL? Remember that the urine dipsticks only measure concentration. Evaluate urine protein/Cr ratio on a spot urine sample (normal <0.2) 24 hour urine collection

IS THE PROTEINURIA DANGEROUS? If the proteinuria is transient or orthostatic, it is benign.

EVALUATE FOR ORTHOSTATIC PROTEINURIA **Give patient urine collection cup to take home.*** Void before bed Upon awakening: quick sitz bath collect mid void sample refrigerate sample send for U/A and urine pro/cr

INTERPRETING THE FIRST AM VOID If the first AM void shows normal protein excretion, no further work-up is needed. If the first AM void is abnormal (urine pro/cr ratio >0.2): Repeat directions Repeat sample

ASYMPTOMATIC PROTEINURIA If proteinuria is persistent and not orthostatic: REFER TO A NEPHROLOGIST!!

DIFFERENTIAL DIAGNOSIS OF ASYMPTOMATIC PROTEINURIA Focal Segmental Glomerulosclerosis FSGS Reflux Nephropathy Glomerulonephritis Systemic Lupus Erythematosis

ASYMPTOMATIC PROTEINURIA: WHAT IT IS NOT. It is absolutely not Minimal Change Nephrotic Syndrome There is no indication for a steroid trial.

ASYMPTOMATIC PROTEINURIA: WORK-UP Renal function ***Albumin*** Glomerulonephritis work-up: C3, C4, CH50, Hepatitis B ANA, ds DNA, ?ANCA Renal ultrasound ?DMSA scan

NONORTHOSTATIC ASYMPTOMATIC PROTEINURIA Important to make a definitive diagnosis Renal Biopsy may be indicated.

FOCAL SEGMENTAL GLOMERULOSCLEROSIS Some parts of some glomeruli have scars Frequently presents as nephrotic syndrome May present as asymptomatic proteinuria High incidence of progression to renal failure

FSGS Hyperfiltration Immune mediated Reduced renal mass Hypertension Diabetes Mellitus Sickle Cell Nephropathy Immune mediated

FSGS: TREATMENT Hyperfiltration Immune mediated ACE inhibitors ARB Solumedrol Calcineurin inhibitors Mycophenylate

REFLUX NEPHROPATHY Renal scarring related to UTIs in association with vesicoureteral reflux. If bilateral, may cause renal failure If unilateral may cause asymptomatic proteinuria and hypertension.

REFLUX NEPHROPATHY: DIAGNOSIS DMSA Scan Consider even if there is not a clear history of UTIs Unilateral scarring may result in asymmetry of renal lengths on renal ultrasound

SCREENING U/As The only way to detect asymptomatic proteinuria Cost effectiveness? Screen first AM void Try to avoid unnecessary testing or referrals.

SYMPTOMATIC PROTEINURIA Symptoms/signs of glomerulonephritis gross hematuria hypertension renal insufficiency Nephrotic syndrome

We will focus on Nephrotic Syndrome.

A CASE Three year old boy with swelling

HISTORY Previously healthy URI 2-3 weeks ago Noted periorbital swelling one week ago Dx: Allergies

THE CASE CONTINUES Swelling worsens and now involves his entire body Diarrhea

PHYSICAL EXAM BP= 100/50 AF Marked periorbital edema Breath sounds clear but decreased at the bases Ascites, but nontender abdomen 3+ pitting edema to thigh Moderate scrotal edema

WORK-UP Urinalysis: Yellow Micro: s.g.= 1030 15-20 RBC glu=neg 0 WBC ket=neg 3-5 Granular casts bld=small protein=neg nitrites=neg

FURTHER WORK-UP BLOOD: BUN=30 Alb=1.5 Cr=0.5 Chol=360 Na=131 Trig=300 Cl=115 Bicarb=24

MORE URINE STUDIES Urine pro/cr ratio=15 >10 is considered nephrotic range proteinuria You consider a 24 hour urine collection but decide against it. Greater than 1000 mg/M2 is considered nephrotic range proteinuria

CXR Important to consider in child with anasarca Risk of pleural effusions Extremely unusual to see pulmonary edema with nephrotic syndrome, unless: renal insufficiency overly aggressive management with 25% albumin

NEPHROTIC SYNDROME Criteria for diagnosis: Edema Nephrotic Range Proteinuria Hypoalbuminemia Hyperlipidemia

HOW YOU COULD BE FOOLED Hypoalbuminemia without significant proteinuria: Protein losing enteropathy Decreased albumin synthesis Lymphedema

WHAT GIVES YOU NEPHROTIC SYNDROME IN A TODDLER? Minimal Change Disease Focal Segmental Glomerulosclerosis Membranous Membranoproliferative GN

HOW TO BE EVEN MORE SURE THAT THIS IS MCNS Sudden presentation Normal blood pressure No hematuria Hematuria in 25% with MCNS Normal Creatinine Normal Complement levels Steroid responsiveness

OTHER BLOOD WORK TO BE DONE AT PRESENTATION Complement levels ANA Check on varicella status

IT IS NOT MINIMAL CHANGE DISEASE WHEN: Presentation as an infant Asymptomatic proteinuria Low complement levels Be suspicious in teenagers

SO WHAT IS MCNS? Minimally altered glomerular structure Fusion of podocytes Profound proteinuria Steroid responsiveness Relapsing course Can be outgrown

NEPHROTIC SYNDROME IN CHILDREN IS CHANGING Incidence of FSGS is on the rise Dramatic increase of around 300% since the 1960’s FSGS is much more prevalent in African Americans

FOCAL SEGMENTAL GLOMERULOSCLEROSIS Histologic Diagnosis More likely to be steroid resistant May present as asymptomatic proteinuria Higher chance of progression to renal failure

INCREASED INCIDENCE OF FSGS ??Related to the obesity epidemic?? Obesity induced FSGS Hypertension induced FSGS

OUR CASE We assume our patient has minimal change disease… No need for a renal biopsy Now what do we do?

TREATMENT OF NEPHROTIC SYNDROME Control the edema Prevent complications Stop the proteinuria Minimize medication side effects

WHY DO YOU GET EDEMATOUS? Starling equilibrium 80% of oncotic pressure is due to albumin With albumin less than 2.5 mg/dL edema forms Albumin infusions as treatment

GENERAL MEASURE Diet: Low salt Fluid restriction Diuretics?

NUTRITIONAL ADVICE No added salt No fast food No food in little plastic packets Limit milk and cheese 2 gm/day

DIURETICS Very tempting but potentially dangerous Potentiates intravascular depletion Increases risk of ATN Increases risk of thrombosis

COMPLICATIONS FROM EDEMA Spontaneous Peritonitis Cellulitis Pleural Effusions

COMPLICATIONS FROM INTRAVASCULAR DEPLETION Prerenal azotemia Acute tubular necrosis Thrombosis

WHEN TO GIVE ALBUMIN AND LASIX Peritonitis Pleural effusions Severe edema with skin breakdown/cellulitis

WHEN NOT TO GIVE ALUMIN AND LASIX AESTHETIC PURPOSES

HOW TO GIVE ALBUMIN AND LASIX 25% Albumin 1 gm/kg over 4 hours Lasix at hour #2 and upon completion Watch for hypertension and pulmonary edema

STOP THE PROTEINURIA Prednisone 2 mg/kg/day (Max 80 mg/d) 80% WILL RESPOND WITHIN 2 WEEKS Best predictor of MCNS

GOOD NEWS AND BAD NEWS MCNS will likely get better with steroids It will come back again and again and again Especially a risk with intercurrent illness

STRATEGIES TO PREVENT RELAPSES Prolong initial Prednisone therapy of 2 mg/kg/day for 6 weeks Taper off Prednisone over a 6 week interval

SOME DEFINITIONS Frequent relapses Steroid dependence 4 or more relapses within a year Steroid dependence 2 relapses consecutively on steroids or shortly after stopping Steroid resistance No response to steroids after 4 weeks

THE MORE RELAPSES THE MORE STEROIDS

SOMETIMES STEROIDS AREN’T SO GREAT Side effects of chronic steroid therapy: Obesity Poor growth Osteoporosis Cataracts Striae Diabetes

WHEN GOOD STEROIDS GO BAD When excessive steroids are required to control nephrosis, consider a steroid sparing agent. Don’t need to wait for development of steroid side effects.

STEROID SPARING AGENTS Cyclophosphamide Mycophenylate Calcineurin inhibitors Cyclosporine Tacrolimus

CHOICE OF STEROID SPARING AGENT Depends on specific tissue diagnosis

INDICATIONS FOR A RENAL BIOPSY Steroid resistance Need for a steroid sparing agent Adolescent Infant

MINIMAL CHANGE DISEASE Steroid sparing agent of choice: Cyclophosphamide 3 mg/kg/day over 8 weeks Monitor carefully for side effects

SIDE EFFECTS OF CYTOXAN Hemorrhagic Cystitis Encourage good intake of fluids Monitor urine specific gravity Neutropenia Frequent blood draws to follow ANC Infertility Hair loss Infections

ADVANTAGES OF CYTOXAN Can anticipate a prolonged (one year or more) medication free remission

TAKE HOME MESSAGE Taking care of patients with Nephrotic Syndrome is interesting and rewarding It is not too late to do a nephrology fellowship