Clinical Chemistry – Flashcards

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Tests fof Glucurine
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Glucserum> 180mg/dL=> +Glucurine

- dipstick--> gluc oxidase & peroxidase--> sensitive  

gluc--> gluconate + hydrogen peroxide

- Copper sulfate method

- Copper sulfate method --> low senstivity

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Which Urine proteins are detected with the dipstick method?
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Only Albumin
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Detection of Bence-Jones proteins
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1.Unique solubility property of light chain proteins

Precipitate-400C & Re-dissolve - 100oC

when cooled--> Precipitate-600C & Re-dissolve-40oC

2.Urine protein electrophoresis

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Dipstick test sensitivity for Ketones
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Sensitive only--> acetoacetic acid
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DDx for Dipstick + Hgb
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- Myoglobinuria--> Hx: severe muscle tenderness, elevated [CK/aldolase]serum, [haptoglobin]nml

- Hemoglobinuria <-- hematuria / Hemolysisintravascular

!!!Mgb = soluble in NH4SO4

 

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Bilirubinurine +

Urobilinogenurine +++

DDx

 

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Conjugated Hyperbilirubinemia

Hepatitis

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Nitriteurine + --> Dx?
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UTI --> most organisms = nitrite + (E.coli)

!!! - = enterococci, N. gonorrhea, M tb

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Leukocyte esterase  + --> DDx?
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UTI--> screen -->reflection of urinary neutrophils #

!!!false + <-- trichomonads & eosinophils

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Fixed Urinespecgrav = 1.010= Glomerular filtratespecgrav

Term & cause

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Isosthenuria

tubular damage-- renal medullary dysfunction

Sickle Cell disease

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Renal tubular acidosis and pHurine
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Kidney cannot acidify the urine beyond pH 6.5 => Inappropriately alkaline relative to pHblood
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Ascorbic Acid and dipstick tests
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Ascorbate --> inhibits

Dipstick tests: Gluc, Hgb, Bilirubin, nitrite, leukocyte esterase

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Calcium oxalate stones

Causes of Oxaluria

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Crohn's, s/p small bowel resection/bypass, ingestion of excessive amounts of oxalate(rhubarbs, spinach, nuts)

10 hyperoxaluria --> stones in childhood

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pHurine and kidney stones
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--> little effect on Calcium oxalate crystallization

--> elevated pH--> Calcium Phosphate stones, struvite

--> acidotic pH--> urate stones

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X linked nephrolithiasis (Dent disease)
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Mutation in the voltage gated chloride channel5 gene=>

hypercalciuria--> stone

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UTI w Proteus mirabilis a/w whict type of stones?
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Struvite

--> urea-splitting organisms=> alkalotic pH

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Common stones in Pts s/p colectomy

Rx

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Urate stones-Hyperuricosuria-Rx: 1.allopurinol=xanthine oxidase inhibitor--> reduces endogenous urate

2.Urine alkalization

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Cystine stone formation - Cause?
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cystinuria--> autosomal recessive-->defect in renal/intestinal dibasic AACOLA transport--> Cystein = least soluble -->Rx: Urinealkaline ,Proteinrestriction
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2,8-Dihydroxyadenine stones-Cause?

Rx?

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deficiency - Adenine phosphoribosyl transferase

-->purine metabolism

Rx: Allopurinol

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Urine Crystals

Envelopes

~ dumpells

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Calcium oxalate Dihydrate(envelopes)/monohydrate (dumpells,spindle/oval)

"recieved the -envelope late-> dump it"

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Pleomorphic crystals most often--> diamond/square/rod

polarize in a variety of colors

yellow-brown rhombic/hexagonal plates, needles/rosettes

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Uric acid

DDx:Sulfonamide crystals-->soluble in acetone

"URing w shapes/diamonds/colors"

 

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Urine crystals?

"Coffin lids"

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Struvite-Triple Phosphate (Mg, ammonium phosphate)

--> alkaline pH, staghorn calculi

"Coffin of Proteus-->staghorn-->struvite "

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[image]
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Cysteine --> cystinuria

"Cola --> hexagonal glass bottle"

 

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Urine crystals?

yellow brown needles

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Bilirubin

"Bins and needles"

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[image]
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Sulfadiazine

<-- trimethoprim-sulfadiazine administration

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[image]
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Cholesterol

"cholesterol results-->broke the glass"

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[image]
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Tyrosine

<--severe liver disease

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[image]
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Ammonium biurate

"thorn=ankathi"

 

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Urine crystals?

"Maltese cross" under polarized light

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Leucine

"Leukos cross"

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Leucine and Tyrosine urine crystals

Causes?

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often--> severe liver disease

rare: Tyrosinosis, "Maple syrup disease"

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[image]
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Hyaline casts = nonspecific

<--Dehydration, vigorous exercise, renal disease

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[image]
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white cell cast and budding yeast

<--Tubulointerstitial nephritis

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[image]
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Granular cast (acellular)~>nonspecific

<--renal disease

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[image]
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Fatty cast<-- Nephrotic syndrome

lipid droplets-->polarized light--> maltese cross

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[image]
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Red  cell cast

<-- glomerulonephritis

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[image]
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waxy cast

<-- renal diseaserenal disease

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Acute renal failure

Urine Micro: Erythrophagocytosis

Dx?

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RPGN

"Phagocytosis"

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Acute renal failure

Urine Micro: numerous granulocytes( neutros & eos)

Dx?

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AIN

"Nephritis-numerous neutros"

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CSF

pink / yellow-tinged fluid following centrifucation

Term and etiology

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Xanthochromia

Pink<-- free Hgb--> subarachnoid hemorrhage

Yellow<--Bilirubin (12hrs,peak72hrs, t1/2=2wks)

Artifactual: hyperbili,CSFprotein>150mg/dL, carotinoids, melanin,rifambin, >1hr processing delay

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Post traumatic rhinorrhea/otorrhea

tests to r/o CSF leak

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[Gluc ] = [Gluc]CSF-->nonspecific

Protein electrophoresis--> twin transferrin peak ,pre-albumin band

[asialated transferrin]

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elevated IgGCSF:IgGserum

Control: AlbuminCSF:Albuminserum

Dx?

 

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MS

IgG index =IgGCSF:IgGserum/ control

--> exclude the effect of increase permeability

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CSF-Agarose gel electrophoresis/Isoelectric focusing:

Oligoclonal bands (g-region)

 

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MS

2 or >2 band = +

IEF (+IgG Ab) -->4 or > 4

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Increased [IgA]CSF

Dx?

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Cerebral Adrenoleukodystrophy
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[Gluc]CSF < 30% (normal 60%, 60mg/dL)

Dx?

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Bacterial meningitis
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elevated [Glutamine]CSF

Dx?

 

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Hepatic encephalopathy
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Neurosyphilis

- Screening test?

- Confirmatory test?

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CSF- FTA-ABS

CSF-VDRL

--> counter to serum

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CSF: Protein>100, Gluc <40

Leuko's count 1000 -10,000 diff predom Polys

Dx?

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Bacterial meningitis

~ predom lymphos --> if partially treated

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CSF: Protein= 20-100, Gluc< 40

Leukos count=50-500, diff: polys

Dx?

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early viral meningitis--> HSV (Gluc=decreased)

lymphs--> late viral meningitis vs. fungal/mycobacterial( also Gluc-->decreased) 

 

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Pleural effusions

Transudate

Causes

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Most common -->CHF (larger on the right)

Cirrhosis, nephrotic syndrome--> decreased Osmotic pressure

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Pleural fluid chemistries:

pH<7.2, LDH>700, Gluc<30

Dx?

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most common = RA

collagen vascular diseases

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Pleural effusion

elevated Amylase

Causes?

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Malignancy

Esophageal perforation--> pH<6.0

Pancreatitis--> left-sided

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Pleural fluid micro:

Lymphocytic effusion

sparse mesothelial cells

Dx?

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s/o tuberculous effusion
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Pleural fluid micro:

Eosinophils

a/w?

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Following prior tap
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Pleural fluid micro:

conspicuously decreased mesothelial cells

DDX?

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RA/Tb/post-pleurodesis pleuritis
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Pleural effusion - milky

Micro: lymphos

Triglycerides > 110mg/dL

Chylomicrons: electrophoresis +

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Chylous-chylothorax

<--thoracic duct obstruction

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Pleural effusion - milky

Micro: mixed leukos, cholesterol crystals

Triglycerides < 50mg/dL

Chylomicrons: electrophoresis -

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Pseudochylous effusion

<-- gradual accumulation of lipids<--cellular break down <--Tb, RA, myxedema

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Peritoneal fluid

AlbuminSerum - Albuminascites > 1.1g/dL

Dx?

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Portal hypertension

<1.1 <-- other causes

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+ Diagnostic Peritoneal Lavage --> Indication for exploratory labarotomy

Criteria

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gross blood >15mL / RBCs > 100,000/mL

WBCs>500/mL, Gram stain: bacteria

Chest tube/ Foley catheter : peritoneal fluid 

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Synovial fluid

1. elevated lactate (>250mg/dL) --> dx?

2. low complement --> ddx?

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1. septic artritis

2. RA / Lupus

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[image]
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Monosodium urate crystal
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[image]
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Corticosteroid crystal
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[image]
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Calcium pyrophosphate

<--pseudogout

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Alizarin red S stain + crystals

non-birefringent

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Hydroxyapatite
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