RENAL-UA Flashcards

1
Q

Pt states his urine is foamy and he is swollen, recent wt gain swollen eyes in am, ankles at night. Weak and tired.
UA dipstick protein >150mg/24 hrs. What is condition?

A

Proteinuria defined
asymptomatic until severe
UA (dipstick)

Miscellaneous Causes
Exercise
Fever, 
systemic stress, 
concentrated urine, 
UTI
Orthostatic - Split urine test, during day and first morning sample - normal when supine
Preeclampsia - >20wks
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2
Q

Which protein is is restricted by glomerular capillaries?

A

Albumin – relatively high molecular weight (smaller)

Multiple types, all are filtered by the glomerulus and reabsorbed PCT

Sick glomeruli = increased permeability

Tubular proteinuria results

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3
Q

Who gets it Glomerular Proteinuria?

A

Inc permeability of GM
Albumin +, MOD- (AKA microabluminuria)
Large amounts for DX 300-500mg/day

Diabetics – mod. albuminuria*** earliest diabetic nephropathy

Non-diabetic CKD (HTN)

Conditions causing the Nephrotic Syndrome

Orthostatic proteinuria - benign
<30yo, <2g/day, nl CrCl, >upright, 16hr collection

Exercise - benign

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4
Q

Pt describes long terms use of NSAIDs and recent ABX d/t car accident and sever blood loss. She was septic and also and CT w/ contrast. FH of Wilson DZ adn Faconi syndrome. U/A Dip NEG. What is MOST likely conditions?

A

Tubular Proteinuria
Small light chain proteins d/t Tubular dysfx
Acute (and chronic) interstitial nephritis (AIN)

Acute tubular necrosis (ATN)
Myoglobinuria - rhabdomyolysis
Trauma, hemolysis, sepsis, low perfusion ischemia

Toxic injury – drugs (OD’s), contrast dye (ATN)
Hereditary disorders
Wilson’s Dz- rare, copper excretion into bile
Kayser-Fiesher ring cornea
KID w/ Proteinuria and Pysche is Key

Fanconi- PCT injury, unable to resor gluc, phos, bicarb. Dehydration. Protein. Kids, Adult-amionglycosides. RENAL TUBULAR Acidosis

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5
Q

Pt was diagnosed with Multiple Myeloma d/t Bence Jones proteins. PHM of OD and stones, rhabdomyoiss, and hemolysis. What is the condition?

A
Multiple Myeloma (overproduction)
Plasma cell malignancy
25% - “Myeloma kidney”
Bence Jones proteins present
Causes tubular toxicity and obstruction
Back pain and chest
Anemias
Inc. Ca+
Waxy cast
Osteolytic lesion-fx, weak bone
PET scan
Tx- chemo, bone marrow transplant
Older PT bone pain, proteinuria, inc Ca, ARF is key

Rhabdomyolysis (overload from ATN)
Hemolysis (overload from ATN)

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6
Q

What is the first step in DX fo proteinuria?

A

Dipstick-Indicates presence only ***

Trace to 4+ - rough estimates, not good for true or type
1+ = <100mg/dL
2+ = 100 to 300mg/dL
3+ = 300 to 1000mg/dL
4+ = >1000mg/dL

albumin but not small amounts; positive at ~300-500mg/24hrs
Positive = glomerular etiology
Early diabetic nephropathy is not reliably detected on dipstick
Does not detect small, light chain proteins

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7
Q

Pt 1 has Dipstick positive but no Sx’s or risks? What is the status? and next step?

Pt 2 has the follow but no risk What is the status?and next step.

A
Pt1 -Transient 
Urine micro (casts), if dipstick 2+ or > repeat 1 month 

Pt2 Persistent
UA micro, chem panel, esp if with hematuria
Culture for amount and type
Consider urine protein immunoelectrophoresis for light chain proteins IF Sx’s, Family Hx suggest Myeloma
Risks? Diabetic, HTN, CHF?
Screen all for albuminuria early, monitor
Persistent proteinuria reflects underlying renal or systemic disorder – work it up

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8
Q

What is important prognostic indicator for secondary glomerular disease = end-organ damage?

A

AMOUNT
Moderately increased albuminuria:
30-300mg/day of albumin

Benign, isolated proteinuria <1-2 gm/day; dipstick +

Foamy urine? >2 gm protein/24hrs

Nephrotic range >3 grams/24hrs

Diabetic nephropathy
Hypertensive nephropathy – proteinuric, non-diabetic chronic kidney disease (CKD)

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9
Q

Which one is which…
>30 abnormal

> 0.2 abnormal

A

Urine microalbumin (random sample): first test
AKA: urinary albumin-to-creatinine ratio (UACR): >30 abnormal
Screening for diabetic nephropathy
HTN, glomerular Dz

UPCR: urine protein-to-creatinine ratio
>0.2 abnormal

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10
Q

What does Moderately increased albuminuria Dx relies on?

A

1-Spot urine microalbumin (albumin-to-creatinine ratio)
>30mg albumin to 1g creatinine = microalbuminuria likely

2-Timed albumin excretion rate (24hr or 10hr urine collection)>30micrograms/minute = microalbuminuria likely

confirm it with repeat testing
2 of 3 specimens over 3-6 month period for diagnosis

Type 1 DM – test after 5yrs (rare prior) or at puberty

Type 2 DM – at diagnosis and yearly

HTN – yearly, q6mos if poor control

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11
Q

What is the non compliant gold standard, used less, difficult as outpatient?

A

24 hour urine protein studies

> 30 mg/min - moderately increased albuminuria

> 2g/24hrs likely glomerular type

> 3g/24hrs nephrotic range (glomerular problem)

<2g/24hrs likely tubular or overflow
Both can be >2g/24hrs if severe
Next: urine protein immunoelectrophoresis

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12
Q

What if Pt has Acute renal failure with negative dipstick?

A

tubular or overflow proteinuria
SSA-sulfosalicytic acid turbidity testing
Measures all proteins
Excess light chain proteins form casts making
supranatant turbid
Identifies Bence Jones proteins

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13
Q

Tx Peristent Proteinuria

A

Tight control diabetes, HTN

Early recognition, tx can slow/reverse dz

Proteinuria/CKD = increased cardiovascular risk

ACE inhibitors and ARB’s – best if poor control

Monitor renal function (BUN, creatinine) q 3mos

Renal ultrasound for structural abnormalities

Refer to nephrologist for renal biopsy (glomeruli), worsening renal function & bad proteinuria

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14
Q
Pt has the following present...
Proteinuria-urine is foamy, >3.5 grams per 24hrs
Edema
HYPOalbuminemia
HYPErlipidemia 
Dipstick +
A

Nephrotic Syndrome

Glomerular proteinuria -Albumin is the principal urinary protein

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15
Q

How does Hypoalbuminemia contribute to edema in Nephrotic Syndome?

A

produces dec in plasma/capillary osmoid/oncotic pressure - fluid seeps OUT of vessels into interstitial space. (plasm fluid {High}-moves to low)

Renal Na+ retention and fluid into ECF

Both lead to decreased intravascular volume**. HIGH ECF
Pitting, peripheral; dependent areas first
Can progress to anasarca - total body edema - ascites, scrotal, sacral, pleural/cardiac effusions

Albumin is dumped into the urine
Serum albumin <3g/dL (N 3.5-5.5g/dL)
Total serum protein <6g/dL (N 6.0-8.0g/dL)

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16
Q

What are the effect of Hypoalbuminemia and decreased plasma oncotic pressure?

A

Hyperlipidemia-stimulate lipoprotein synthesis in liver

LDL and VLDL increase; HDL levels decrease

Cholesterol and triglycerides increase

Lipiduria: active sediment on micro – Fatty casts
Oval fat bodies, “Maltese Cross”

17
Q

Umbrella:
Glomeunora Protenuria
Nephrotic Syndrome
Who gets it?

A

Idiopathic*
MC-Minimal change disease* (kids, glomeruli ok)
Focal glomerular sclerosis (heroin, HIV drugs)
Membranous nephropathy (older adults)
Membranoproliferative glomerulonephritis (<30yrs)

Kids adults
GM dz primary
1/3 systemic renal- ERSD
SLE
Amyloidosos- EC small light protein deposition, genetic, complex. Affect all systems. ASX, proteinuria, RF. Biopsy -GS. TX- transplant
18
Q

Treatment

A

Consult and referral early

Treat proteinuria: lower intraglomerular pressure
ACE inhibitor or angiotensen II receptor blocker

Treat edema w/ Na restriction, diuretic

Treat lipids w/ statin, behavioral

Prevent by monitoring renal function in high risk pt’s

19
Q

What pathogen is common in proteinuria/ NS Pts?

A

Complications
NS pt’s very susceptible - poorly understood
Pneumococcal

Hypercoagulability - thromboembolic events
DVT, PE, renal vein thrombosis, prophylactic anticoagulation

Renal Failure
Underlying glomerular disease
Hypovolemia
Decreased intravascular volume -> decrease in renal blood flow -> dec. GFR

Protein malnutrition
Loss of lean body mass, hidden by edema

GI symptoms - anorexia, vomiting
Edema of GI tract itself