Clinical Chemistry – Flashcards
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Unlock answersTests fof Glucurine |
Glucserum> 180mg/dL=> +Glucurine - dipstick--> gluc oxidase & peroxidase--> sensitive gluc--> gluconate + hydrogen peroxide - Copper sulfate method - Copper sulfate method --> low senstivity |
Which Urine proteins are detected with the dipstick method? |
Only Albumin |
Detection of Bence-Jones proteins |
1.Unique solubility property of light chain proteins Precipitate-400C & Re-dissolve - 100oC when cooled--> Precipitate-600C & Re-dissolve-40oC 2.Urine protein electrophoresis |
Dipstick test sensitivity for Ketones |
Sensitive only--> acetoacetic acid |
DDx for Dipstick + Hgb |
- 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 |
Nitriteurine + --> Dx? |
UTI --> most organisms = nitrite + (E.coli) !!! - = enterococci, N. gonorrhea, M tb |
Leukocyte esterase + --> DDx? |
UTI--> screen -->reflection of urinary neutrophils # !!!false + <-- trichomonads & eosinophils |
Fixed Urinespecgrav = 1.010= Glomerular filtratespecgrav Term & cause |
Isosthenuria tubular damage-- renal medullary dysfunction Sickle Cell disease |
Renal tubular acidosis and pHurine |
Kidney cannot acidify the urine beyond pH 6.5 => Inappropriately alkaline relative to pHblood |
Ascorbic Acid and dipstick tests |
Ascorbate --> inhibits Dipstick tests: Gluc, Hgb, Bilirubin, nitrite, leukocyte esterase |
Calcium oxalate stones Causes of Oxaluria |
Crohn's, s/p small bowel resection/bypass, ingestion of excessive amounts of oxalate(rhubarbs, spinach, nuts) 10 hyperoxaluria --> stones in childhood |
pHurine and kidney stones |
--> little effect on Calcium oxalate crystallization --> elevated pH--> Calcium Phosphate stones, struvite --> acidotic pH--> urate stones |
X linked nephrolithiasis (Dent disease) |
Mutation in the voltage gated chloride channel5 gene=> hypercalciuria--> stone |
UTI w Proteus mirabilis a/w whict type of stones? |
Struvite --> urea-splitting organisms=> alkalotic pH |
Common stones in Pts s/p colectomy Rx |
Urate stones-Hyperuricosuria-Rx: 1.allopurinol=xanthine oxidase inhibitor--> reduces endogenous urate 2.Urine alkalization |
Cystine stone formation - Cause? |
cystinuria--> autosomal recessive-->defect in renal/intestinal dibasic AACOLA transport--> Cystein = least soluble -->Rx: Urinealkaline ,Proteinrestriction |
2,8-Dihydroxyadenine stones-Cause? Rx? |
deficiency - Adenine phosphoribosyl transferase -->purine metabolism Rx: Allopurinol |
Urine Crystals Envelopes ~ dumpells |
Calcium oxalate Dihydrate(envelopes)/monohydrate (dumpells,spindle/oval) "recieved the -envelope late-> dump it" |
Pleomorphic crystals most often--> diamond/square/rod polarize in a variety of colors yellow-brown rhombic/hexagonal plates, needles/rosettes |
Uric acid DDx:Sulfonamide crystals-->soluble in acetone "URing w shapes/diamonds/colors"
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Urine crystals? "Coffin lids" |
Struvite-Triple Phosphate (Mg, ammonium phosphate) --> alkaline pH, staghorn calculi "Coffin of Proteus-->staghorn-->struvite " |
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Cysteine --> cystinuria "Cola --> hexagonal glass bottle"
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Urine crystals? yellow brown needles |
Bilirubin "Bins and needles" |
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Sulfadiazine <-- trimethoprim-sulfadiazine administration |
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Cholesterol "cholesterol results-->broke the glass" |
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Tyrosine <--severe liver disease |
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Ammonium biurate "thorn=ankathi"
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Urine crystals? "Maltese cross" under polarized light |
Leucine "Leukos cross" |
Leucine and Tyrosine urine crystals Causes? |
often--> severe liver disease rare: Tyrosinosis, "Maple syrup disease" |
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Hyaline casts = nonspecific <--Dehydration, vigorous exercise, renal disease |
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white cell cast and budding yeast <--Tubulointerstitial nephritis |
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Granular cast (acellular)~>nonspecific <--renal disease |
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Fatty cast<-- Nephrotic syndrome lipid droplets-->polarized light--> maltese cross |
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Red cell cast <-- glomerulonephritis |
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waxy cast <-- renal diseaserenal disease |
Acute renal failure Urine Micro: Erythrophagocytosis Dx? |
RPGN "Phagocytosis" |
Acute renal failure Urine Micro: numerous granulocytes( neutros & eos) Dx? |
AIN "Nephritis-numerous neutros" |
CSF pink / yellow-tinged fluid following centrifucation Term and etiology |
Xanthochromia Pink<-- free Hgb--> subarachnoid hemorrhage Yellow<--Bilirubin (12hrs,peak72hrs, t1/2=2wks) Artifactual: hyperbili,CSFprotein>150mg/dL, carotinoids, melanin,rifambin, >1hr processing delay |
Post traumatic rhinorrhea/otorrhea tests to r/o CSF leak |
[Gluc ] = [Gluc]CSF-->nonspecific Protein electrophoresis--> twin transferrin peak ,pre-albumin band [asialated transferrin] |
elevated IgGCSF:IgGserum Control: AlbuminCSF:Albuminserum Dx?
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MS IgG index =IgGCSF:IgGserum/ control --> exclude the effect of increase permeability |
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 |
Increased [IgA]CSF Dx? |
Cerebral Adrenoleukodystrophy |
[Gluc]CSF < 30% (normal 60%, 60mg/dL) Dx? |
Bacterial meningitis |
elevated [Glutamine]CSF Dx?
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Hepatic encephalopathy |
Neurosyphilis - Screening test? - Confirmatory test? |
CSF- FTA-ABS CSF-VDRL --> counter to serum |
CSF: Protein>100, Gluc <40 Leuko's count 1000 -10,000 diff predom Polys Dx? |
Bacterial meningitis ~ predom lymphos --> if partially treated |
CSF: Protein= 20-100, Gluc< 40 Leukos count=50-500, diff: polys Dx? |
early viral meningitis--> HSV (Gluc=decreased) lymphs--> late viral meningitis vs. fungal/mycobacterial( also Gluc-->decreased)
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Pleural effusions Transudate Causes |
Most common -->CHF (larger on the right) Cirrhosis, nephrotic syndrome--> decreased Osmotic pressure |
Pleural fluid chemistries: pH<7.2, LDH>700, Gluc<30 Dx? |
most common = RA collagen vascular diseases |
Pleural effusion elevated Amylase Causes? |
Malignancy Esophageal perforation--> pH<6.0 Pancreatitis--> left-sided |
Pleural fluid micro: Lymphocytic effusion sparse mesothelial cells Dx? |
s/o tuberculous effusion |
Pleural fluid micro: Eosinophils a/w? |
Following prior tap |
Pleural fluid micro: conspicuously decreased mesothelial cells DDX? |
RA/Tb/post-pleurodesis pleuritis |
Pleural effusion - milky Micro: lymphos Triglycerides > 110mg/dL Chylomicrons: electrophoresis + |
Chylous-chylothorax <--thoracic duct obstruction |
Pleural effusion - milky Micro: mixed leukos, cholesterol crystals Triglycerides < 50mg/dL Chylomicrons: electrophoresis - |
Pseudochylous effusion <-- gradual accumulation of lipids<--cellular break down <--Tb, RA, myxedema |
Peritoneal fluid AlbuminSerum - Albuminascites > 1.1g/dL Dx? |
Portal hypertension <1.1 <-- other causes |
+ Diagnostic Peritoneal Lavage --> Indication for exploratory labarotomy Criteria |
gross blood >15mL / RBCs > 100,000/mL WBCs>500/mL, Gram stain: bacteria Chest tube/ Foley catheter : peritoneal fluid |
Synovial fluid 1. elevated lactate (>250mg/dL) --> dx? 2. low complement --> ddx? |
1. septic artritis 2. RA / Lupus |
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Monosodium urate crystal |
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Corticosteroid crystal |
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Calcium pyrophosphate <--pseudogout |
Alizarin red S stain + crystals non-birefringent |
Hydroxyapatite |