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Cerebrospinal Fluid
surrounds brain and spinal cord
from subarachnoid space
Function
Physical protection/cushion brain
supply nutrients / remove waste
Transport
Lumber tap (collection order, reason for collection)
3~4 tubes from L3 or L4 below
Remember from Heme: Tube allocation order by department
Chem
Micro
Heme
Extra
Reasons
CNS infection
demyelinating disease
malignancy
CNS hemmorrage
Characteristics of CSF
Color
red - hemorrhage or traumatic tap
always spin red CSF and check if the supernatant is xanthochromic (yellow)
checks how long it has been since the bleed
Clarity
turbid = infection?
Clot/hemosiderin-containing macrophages
Biomarkers for CSF (4)
Glucose
Protein
Lactate
Glutamate
CSF Glucose
CSF Glucose 2/3 (60-70%) of Plasma Glucose, until plasma glucose reaches >600 mg/dL
High CSF glucose not clinically significant
LOW CSF Glucose
glucose transport carrier disorder
increased metabolism by organism or cells (bacteria, tumor)
Increased lactate if glucose consumption increased
CSF Protein
0.5~1% of plasma total protein, fractional concentration NOT proportional to plasma protein
Must be compared to plasma protein
Decreased protein
Decrease inflow from plasma
Increased protein loss
Leakage in dura (tears from traumatic tap), ear, or nose (runny nose)
Detect leakage by testing for beta-transferrin (protein only in CSF)
Increased protein
clinically nonspecific
contamination from traumatic tap (plasma protein)
increased permeability of BBB (blood brain barrier) can be caused from bacterial/fungal infection
not diagnostic
Increased CNS protein production
Albumin and IgG in CSF
Albumin
produced in liver, not too much should be in csf
IgG
can be produced locally in CNS by plasma cells
CSF serum albumin index
(CSF albumin mg/dL)/(Serum albumin mg/dL)
Index value <9 intact BBB
Index vaule >9 damaged BBB
CSF IgG Index
CSF IgG/Serum IgG
Normal Index <0.73
Increase IgG index w/ no increase in albumin suggests local igG synthesis
MS or SSPE
Increase IgG index and albumin
Bacterial meningitis
CSF electrophoresis
Ran when etiology is unclear, normal CSF protein but show inflammation
Oligoclonal bands: multiple banding in the gamma region, usually seen with MS or SSPE
Lactate CSF
Indicator of anaerobic metabolism
Increased lactate, decreased glucose —> bacterial meningitis
Time-sensitive, collect in sodium fluoride tube
Glutamine CSF
ammonia + glutamate
ammonia test w/ in 30min
correlation of ammonia level in CNS
Increase in hepatic encephalopathy
Serous Membranes (2)
parietal membrane line cavity wall
visceral membrane line organ
Surrounds heart, lung, abdomin
Serous fluid (3 types and formation)
Pleural—lung
Pericardial—heart
Peritoneal--abdominal
Continuously formed, and circulated by hydrostatic pressure and oncotic pressure
ultrafiltrate of plasma
arterial capillaries - fluid moves out to interstitial space
Venous capillaries - fluid moves into capillaries from interstitial space
Lymphatics - excess fluid from interstitial space flows here
Effusion
Accumulation of serous fluid
Transudate
Effusion that occurs during various systemic disorders that disrupt fluid filtration, fluid reabsorption, or both
Congestive heart failure, hepatic cirrhosis, nephrotic syndrome
Exudate
Effusion that occurs during inflammatory processes that result in damage to blood vessel walls, body cavity membrane damage, or decreased reabsorption by the lymphatic system
Infections, inflammations, hemorrhages, malignancies
Differentiate exudate and transudate by testing for
Fluid appearance, specific gravity, amylase, glucose, lactate dehydrogenase (LD), proteins, ammonia, lipids, pH
Pleural Fluid
Enter as ultrafiltrate of plasma through parietal layer and exit through lymphatics of visceral layer
inner layer (visceral) - bronchial circulation
outer layer (parietal) - systemic circulation
Normal: 3-20mL
Thoracentesis
pleural (lung) fluid removal through chest
anticoagulant tubes
Pleural Transudate
Secondary to remote (non-pleural) systemic pathology
Have biochemical and cellular abnormalities consistent non-inflammatory changes in fluid dynamics
Ex: hypoproteinemia due to malnutrition—leads to decreased osmotic pressure and decrease in fluid resorption into the capillaries
Causes:
congestive heart failure ****most common
nephrotic syndrome
hypoproteinemia
hepatic cirrhosis
chronic renal failure
Pleural exudate
Primary involvement of the pleura and lung (ex. Infection)
Requires immediate attention
Ex: infection-mediated damage to the membranes allowing increased fluid entry into the pleural space
Causes
bacterial pneumonia ****
tuberculosis
pulmonary abscess
malignancy causing lymphatic obstruction
viral/fungal infection
lymphoma
Pleural transudate Lights criteria (PF/Serum protein and LD ratio and PF LD)
PF/Serum protein <0.5
PF/Serum Lactate dehydrogenase (LD) <0.6
PF LD <2/3URL
Pleural exudate Lights criteria (PF/Serum protein and LD ratio and PF LD)
PF/Serum protein >=0.5
PF/Serum Lactate dehydrogenase (LD) >=0.6
PF LD >=2/3URL
Pleural fluid other tests
Fluid cholesterol
Exudates cholesterol >60 mg/dL
Fluid to serum cholesterol ratio
Exudates ratio >0.3
Fluid to serum bilirubin ratio
Exudates ratio ≥0.6
Further characterization
Glucose, lactate, amylase, triglyceride, pH, or uric acid
Inflammation: decreased glucose or increased lactate
Pancreatitis: increased amylase
Triglyceride: (grossly elevated 2-10x serum levels) thoracic duct leakage
pH: <7.2 infection; close to 6.0 esophageal rupture
Uric acid: levels significantly lower in exudates
Pericardial fluid
Normal <50mL
effusions almost always exudate and caused by damage to mesothelium
pericardiocenthesis - procedure is dangerous to perform, rare
Pericardiocentesis
needle inserted through chest with electrocardiographic monitoring to find heart
DANGEROUS
Peritoneal Fluid
AKA ascitic fluid
abdomen
paracenthesis
Ascites
excess peritoneal fluid
>50mL indicate disease
peritoneal transudate
secondary pathology
most common - portal hypertension
Peritoneal exudate
primary pathology
metastatic ovarian, prostate, colon cancers OR infective peritonitis
PMN>250 cells/um in infective peritonitis
Serum ascite albumin gradient (SAAG)
SAAG = serum albumin - ascitic albumin
> 1.1 g/dL Transudate
<1.1 g/dL Exudate
Amniotic fluid source
Maternal plasma and later, mostly fetal urine
controlled by fetal swallowing of fluid
Fetal skin also permeable to fluid, becomes less permeable as gestation goes on
Extracting amniotic fluid
amniocentesis
ultra sound guided
used to test for hemolytic disease of new born, neural tube defect, fetal lung development
Hemolytic disease of new born
caused by maternal antibody against fetal RBC. bilirubin in amniotic fluid
Neural tube defects
Test for alpha-fetoprotein and compare multiple median
test maternal plasma
test again if high
ultrasound
amniocentesis
Fetal lung maturity
Main reason for amniocentesis
phosphatidylglycerol and lectin-sphingomyelin checked
PG increased proportionally to L/S
Lamellar body checked
phospholipid produced by type II alveolar cells
run on heme analyzer bc size similar to PLT
Lamellar body count of mature lung
>50,000/uL
Lamellar body count of immature lung
<15,000/uL
Synovial fluid sample collection and prep
arthrocentesis, treat with hyaluronidase
Synovial fluid total protein
normal 1-3g/L
increased in arthritis, gout, ulcerative colitis, ankylosing spondylitis
Synovial fluid glucose
10 mg/dL lower than serum glucose
decreased ratio suggest inflammation or infection
Synovial fluid uritic acid
GOUT
Synovial fluid lactic acid
septic arthritis
Normal synovial fluid
colorless
high viscosity
mucin clot good
<150 WBC <25% PMN
Glucose blood:SF 0-10
Non inflammatory synovial fluid
yellow, slightly cloudy
decreased viscosity
mucin clot fair
<1000 WBC <35% PMN
Glucose blood:SF 0-10
Inflammatory synovial fluid
white, yellow, grey, turbid
no viscosity
mucin clot poor
<100,000 WBC >50% PMN
Glucose blood:SF 0-4
Septic synovial fluid
white, yellow, grey, cloudy
no viscosity
mucin clot poor
50,000-200,000 WBC >90% PMN
Glucose blood:SF 20-100
cultures positive
Crystal induced synovial fluid
white, cloudy, milky
no viscosity
mucin clot poor
50,000-200,000 WBC <90% PMN
Glucose blood:SF 0-80
crystals present
Hemorrhagic synovial fluid
red, brown, xanthochromic, cloudy
no viscosity
mucin clot poor
50-10,000 WBC <50% PMN
Glucose blood:SF 0-20
RBC present
Sweat
Only tested for cystic fibrosis using sweat chloride test
autosomal recessive disorder that affects exocrine glands and causes electrolyte and mucus secretion abnormalities
>60 mmol/L is a positive test