BODY FLUIDS 2 Flashcards

1
Q

Evaluation of Stone Disease

A
  • Routine Blood and Urine Tests
  • Stone Analysis
  • 24hrs urine metabolic profile
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2
Q

Renal Stone Analysis yields fundamental information about:

A
  • Metabolic abnormality
  • Presence of infection
  • possible artifacts
  • drug metabolism
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3
Q

Calcium Stone Characteristics: Pure Calcium Stones

A
  • More acid in urine
  • Low urine volume
  • high oxalate excretion
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4
Q

Calcium Stone Characteristics: Mixed Stone Formers

A
  • pH is higher
  • high calcium
  • high calcium excretion
  • high recurrence rate
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5
Q

Calcium Stone Characteristics: Co-oxalate Monohydrate

A
  • hypo-megnesuria
  • acidic urine
  • low urine volume
  • hardness (+)
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6
Q

Calcium Stone Characteristics: Ca-oxa Dihydrate

A
  • hypercalciuria
  • alkaline urine
  • hypocitraturia
  • hardness; less
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7
Q

Renal Tubular Acidosis: Carbonate apattite

A
  • COnsider RTA

- Increases with amount (5-39%)

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8
Q

Renal Tubular Acidosis: Brushite Stones

A

consider RTA

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9
Q

Characteristics:

Struvite Stone: Magnesium Ammonium Phosphate

A
  • Mixed Stone: Infection
  • “Proteus’
  • Strains of Staphylococci, pseudomonas and klebsiella
  • Rarely; E. coli
  • Urine pH: <7.5
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10
Q

Characteristics of Ammonium Urate

A
  • Calcium oxalate- containing calculi, may start hyperuricosuria
  • Elders: ass. w/ infection
  • Children: may as result of hyperuricosuria, but no UTI
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11
Q

Characteristics of Dahilite (Carbonic apetite)

A
  • phosphate stones
  • infection in body
  • may not accompanying sign of disease
  • RTA
  • Disorder of phosphate metabolism
  • rare in pure form (2-3%)
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12
Q

Characteristics of Uric Acid

A
  • hyperuricemia, hyperuricosuria
  • low urine pH: <6.2
  • Causes: gout, myeloproliferative dis., chemotherapy, radiotherapy
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13
Q

Causes of Cystine:

A
  • Cyateinuria
  • Autosomal recessive disorder
  • Occurs predominantly in pure form
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14
Q

Causes of Xenthene:

A
  • Xanthinuria
  • Absence of xanthene oxidase
  • genetic autosomal hereditary recessive enzyme disorder
  • Trigger: Allopurinol treating gout
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15
Q

is a fibrin degradation product (or FDP), a small protein fragment present in the blood after a blood clot is degraded through fibrinolysis, by enzyme plasmin.

A

D-dimer

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16
Q

is of clinical use when there is a suspicion of deep venous thrombosis (DVT), pulmonary embolism (PE) or disseminated intravascular coagulation (DIC). It is under
investigation in the diagnosis of aortic dissection.

A

D-dimer testing

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17
Q

A negative D-dimer test will virtually rule out

A

thromboembolism

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18
Q

Reference Ranges for D-dimer:

  • Non pregnant adult
  • 1st Trimester
  • 2nd Trimester
  • 3rd Trimester
A
  • Non pregnant adult: <0.5mg/L or ug/mL
  • 1st Trimester: 0.05–.95mg/L or ug/mL
  • 2nd Trimester: 0.32-1.29 mg/L or ug/mL
  • 3rd Trimester: 0.13-1.7mg/L or ug/mL
19
Q

False positive readings of D-dimer can be due to various causes:

A
  • liver disease,
  • high rheumatoid factor,
  • inflammation,
  • malignancy,
  • trauma,
  • pregnancy,
  • recent surgery
  • advanced age
20
Q

False negative readings can occur if:

A
  • sample is taken either too early after thrombus formation
  • testing is delayed for several days
  • presence of anticoagulation since it prevent thrombus extension
21
Q

is defined as excretion of albumin between 20 and 200 micrograms/min

A

Microalbuminuria

22
Q

Uses of Micral Test

A

(a) in diabetes, for early diagnosis of diabetic nephropathy;
(b) in patients with hypertension, as an indicator of end-organ damage associated with a lowered life expectancy;
(c) in pregnancy, as a possible predictor of developing preeclampsia.

23
Q

is a test strip now available that makes a semiquantitative assessment of the albumin concentration in the urine at various levels (0, 10, 20, 50, 100 mg/L).

A

Micral-Test

24
Q

For screening, a concentration of 20-200 mg/L of____ in the first morning urine has been proven to be a suitable indicator in Micral TEST.

25
Advantage of Micral Test
no influence on the measurement from interfering factors such as glucose concentration, pH value, ketonuria, storage of the sample, or bacterial contamination in the urine
26
This utilizes monoclonal antibodies tagged with fluorochromes which bind specifically to ‘GPI-AP’ on peripheral blood cells or FLAER [bacterial aerolysin tagged with fluorescent antibody] which binds directly to GPI anchor itself.
Multicolour Flow Cytometry Test
27
Gold standard test for diagnosis of PNH.
Multicolour Flow Cytometry Test
28
The name lupus was derived from the Latin for ”wolf”. Autoantibodies are a characteristic feature of systemic lupus erythematosus (SLE).
LE cell
29
Abortive nucleus in the process of being extruded, undergoes ‘nucleophagocytosis’ by Neutrophils is seen in:
- LE cells - bone marrow, peripheral blood, synovial fluid, cerebrospinal fluid and pericardial and pleural effusions from patients with SLE.
30
The detection of this in serum facilitates the diagnosis of patients with systemic lupus erythematosus (SLE) and related autoimmune diseases.
antinuclear antibodies (ANA)
31
ANA titers higher than 1/500 are usually very significant clinically, often found in:
spontaneous or drug-induced SLE and few other Auto-immune diseases.
32
is an immunologic marker in the body, found in low titer in a number of diseases, including infectious mononucleosis and other viral diseases, chronic bacterial infections, and other acute and chronic conditions.
RHEUMATOID FACTOR (RH FACTOR TEST)
33
The highest levels of rheumatoid factor are usually found in
rheumatoid arthritis
34
higher titers of RH factor tend to correlate with
- more severe and sustained disease, - joint deformities, - rheumatoid nodules, - other extra-articular features of the disease.
35
present in an estimated 60 to 80% of people with RA, according to the Arthritis Foundation.
ANTI-CYCLIC CITRULLINATED PEPTIDE (ANTI-CCP) TEST
36
Interpret anti-CCP >20 units per milliliter (u/ml)
increased risk of RA
37
detects the presence of CRP, which the liver produces in response to inflammation in the body.
C-reactive protein (CRP) Test
38
The presence of CRP can indicate
- inflammation anywhere in the body, just like RA | - obesity and infecton, increase CRP in blood
39
evaluates the risk that a seriously ill person is developing a systemic bacterial infection, (including chronic bacterial diseases such as tuberculosis)
PROCALCITONIN TEST
40
Uses of PROCALCITONIN TEST
a) It helps detect or rule out sepsis (it is best used during the first day of presentation.) b) distinguish between viral and bacterial meningitis, c) detect/rule out bacterial pneumonia in those who are seriously ill and in fever of unknown origin. d) in post- trauma or post-operative patient with viral pneumonia in order to detect the development of a secondary bacterial infection. e) may be used to monitor the effectiveness of antimicrobial treatment.
41
Low levels of procalcitonin indicates
= low risk of sepsis but do not exclude it. = indicate a localized infection that has not yet become systemic = or a systemic infection that is less than six hours old. = the person's symptoms are likely due to another cause
42
High levels of procalcitonin indicate:
high probability of sepsis
43
Reference Range of procalcitonin in Adult
<0.10 ng/mL
44
``` Neonate reference ranges of procalcitonin: Ages in hours:         At birth -  18-20 hours  - 48 hours  - ```
Ages in hours:         At birth -  <2.00 18-20 hours  - <20.00 48 hours  - <5.00