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Clinical Biochemistry of Domestic Animals (Sixth Edition) - UMK ...

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784<br />

Chapter | 26 Cerebrospinal Fluid<br />

people with brain injury, but its utility in veterinary medicine<br />

is unproven ( Shimada et al., 2005 ). The usefulness <strong>of</strong> these<br />

substances in veterinary medicine has yet to be established.<br />

G . Concentration Gradient along the<br />

Neuraxis<br />

In cats (Hochwald et al., 1969 ), dogs (Bailey and Higgins,<br />

1985 ; Vaughn et al., 1988b ), horses (Andrews et al., 1 990a ;<br />

Vaughn and Smyth, 1989 ), rhesus macaques ( Smith and<br />

Lackner, 1993 ), and people ( Davson and Segal, 1996 ;<br />

Fishman, 1992 ), the total protein concentration increases<br />

along the neuraxis from rostral to caudal. For example, in<br />

people the total protein concentration <strong>of</strong> ventricular, cerebellomedullary<br />

cistern, and lumbar subarachnoid fluid is about 26,<br />

32, and 42 mg/dl, respectively ( Weisner and Bernhardt, 1978 ).<br />

Total protein, albumin, and globulin content <strong>of</strong> cerebellomedullary<br />

cistern and lumbar subarachnoid CSF for dogs,<br />

cats, and horses is given in Tables 26.5, 26.6, and 26.7 , respectively.<br />

The concentration <strong>of</strong> the albumin and globulin fractions<br />

also increases from ventricular to lumbar fluid. The increased<br />

protein content may be the result <strong>of</strong> a greater permeability <strong>of</strong><br />

the spinal blood-CSF barrier than <strong>of</strong> the ventricular barrier to<br />

albumin ( Fishman, 1992 ), additions <strong>of</strong> protein from adjacent<br />

nervous tissue (e.g., IgG from lymphocytes located in or near<br />

the CSF pathway ( Weisner and Bernhardt, 1978 ), progressive<br />

equilibration <strong>of</strong> CSF with plasma through the capillary walls<br />

( Weisner and Bernhardt, 1978 ), and low flow rates <strong>of</strong> lumbar<br />

CSF ( Davson and Segal, 1996 ).<br />

A study <strong>of</strong> healthy dogs also identified a small but significant<br />

gradient for the CSF WBCs; lumbar fluid contained<br />

significantly fewer cells than cerebellomedullary fluid<br />

( Bailey and Higgins, 1985 ). Another study did not find a<br />

difference in WBC counts between fluids from the two sites<br />

(Vaughn et al., 1988b ). However, 4 <strong>of</strong> the 10 dogs in this<br />

study had CSF total WBC counts 3/ μ l, and none <strong>of</strong> the<br />

dogs was necropsied to verify its health. Therefore, some <strong>of</strong><br />

these dogs may have had subclinical neurological disease,<br />

disguising a small cellular gradient. The small number <strong>of</strong><br />

WBCs in normal fluid may make a cellular gradient more<br />

<strong>of</strong> a theoretical issue than a practical issue, however. If a<br />

cellular gradient exists, it may be due to fewer cells entering<br />

the lumbar CSF than the cerebellomedullary CSF, a greater<br />

rate <strong>of</strong> cell lysis in the lumbar CSF, a greater migration rate<br />

<strong>of</strong> WBCs from lumbar CSF back into the blood, or loss <strong>of</strong><br />

WBCs that entered the CSF rostrally and lysed as CSF circulated<br />

to the caudal subarachnoid space.<br />

A gradient has also been reported for CSF neurotransmitter<br />

metabolites in the dog ( Vaughn et al., 1988b ) and the<br />

horse ( Vaughn and Smyth, 1989 ). In each species, the neurotransmitter<br />

metabolite content <strong>of</strong> cerebellomedullary CSF<br />

was greater than that <strong>of</strong> lumbar subarachnoid CSF. This gradient<br />

probably reflects the major source <strong>of</strong> the neurotransmitter<br />

(brain) and transport <strong>of</strong> the metabolite from the CSF<br />

into the blood along the spinal axis ( Vaughn et al., 1988a ).<br />

VI . CSF COLLECTION AND ANALYTICAL<br />

TECHNIQUES<br />

A . Collection<br />

1 . General Techniques<br />

Specific details about the collection <strong>of</strong> CSF from the various<br />

species are covered in many excellent articles and textbooks<br />

( Boogerd and Peters, 1986 ; Brewer, 1983 , 1987, de<br />

Lahunta, 1983 ; Fowler, 1989 ; Holbrook and White, 1992 ;<br />

Kornegay, 1981 ; Mayhew, 1989 ) and will not be covered<br />

here except for the authors ’ preferred technique for collection<br />

from the cerebellomedullary cistern <strong>of</strong> dogs and cats<br />

(discussed later). Considerations that apply regardless <strong>of</strong> species<br />

are sterility, use <strong>of</strong> a specialized spinal needle, and collection<br />

from animals with increased intracranial pressure. To<br />

prevent iatrogenic central nervous system infection, sterility<br />

during the collection procedure is essential. A generous area<br />

around the puncture site should be clipped and surgically prepared.<br />

Preparation <strong>of</strong> too small an area can lead to contamination<br />

if any difficulty in palpating landmarks or entering the<br />

subarachnoid site is encountered. Additionally, the use <strong>of</strong> a<br />

fenestrated drape is highly recommended. Spinal puncture is<br />

contraindicated in an area <strong>of</strong> severe pyoderma/furunculosis<br />

or cellulitis. A needle with a stylet (spinal needle) should be<br />

used to prevent implantation <strong>of</strong> a plug <strong>of</strong> epidermis in the subarachnoid<br />

space that not only could lead to infection but also<br />

could seed an epidermoid tumor. Replacement <strong>of</strong> the stylet<br />

upon withdrawal is controversial, either preventing or causing<br />

entrapment and severance or dislocation <strong>of</strong> nerve root filaments<br />

( Fishman, 1992 ). Collection <strong>of</strong> CSF from animals with<br />

increased intracranial pressure may result in brain herniation.<br />

Appropriate anesthetic agents, hyperventilation, and mannitol<br />

(to treat intracranial hypertension) may decrease the probability<br />

<strong>of</strong> herniation. Use <strong>of</strong> the smallest gauge needle possible<br />

may also help prevent herniation by decreasing CSF leakage<br />

through the puncture hole in the meninges. Only the minimal<br />

amount <strong>of</strong> CSF necessary to perform the desired tests should<br />

be withdrawn. Brain herniation can occur following lumbar<br />

taps as well as cerebellomedullary cistern taps.<br />

2 . Collection Site<br />

Cerebellomedullary puncture should be done under general<br />

anesthesia. In most instances, lumbar puncture can be done<br />

with sedation and local anesthesia. Therefore, if general anesthesia<br />

is contraindicated, a lumbar puncture should be done.<br />

The choice <strong>of</strong> collection site is influenced by the species<br />

and breed <strong>of</strong> animal, the location <strong>of</strong> the neurological<br />

lesion, and anesthetic considerations. The size <strong>of</strong> some animals<br />

may make lumbar subarachnoid puncture difficult, if<br />

not impossible. However, cerebellomedullary puncture usually<br />

can be accomplished even in large or obese animals.<br />

Because <strong>of</strong> differences in anatomy, the type or breed influences<br />

the exact site for lumbar puncture in the dog; L4-5 is

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