Professional Documents
Culture Documents
6 0
sophisticated bacteriologic, biochemical, cytologic, and serologic techniques were introduced. In 1919 Dandy reported on
replacing CSF with air to determine normal brain anatomy
and to identify pathologic changes.3 Water-soluble contrast
media have since been used to delineate the spinal subarachnoid space and cerebral cisterns. Other uses of spinal dural
puncture include drainage of fluids and injection of anesthetic
agents, chemotherapeutic agents, and antibiotics.
Brian D. Euerle
HISTORICAL PERSPECTIVE
In 1885, Corning punctured the subarachnoid space to induce
cocaine anesthesia in a living patient.1 In 1891, Quincke first
removed CSF in a diagnostic study and introduced the use of
a stylet.2 He studied the cellular contents and measured
protein and glucose levels. Quincke was also the first to record
CSF pressure with a manometer. Subsequently, increasingly
Spinal Puncture
Indications
Equipment
Lidocaine
Syringe
Contraindications
Absolute:
Presence of infection near the puncture site
Relative:
Coagulopathy
Presence of increased intracranial pressure caused by
a space-occupying lesion
Severe thrombocytopenia
Complications
Brain herniation
Cauda equina syndrome
Cranial nerve VI palsy
Epidermoid tumor
Epidural cerebrospinal fluid collection
Epidural hematoma
Meningitis
Minor backache
Postdural puncture headache
Retroperitoneal abscess
Subarachnoid hemorrhage
Subdural hematoma
Antiseptic
and applicator
3-way
stopcock
Spinal needles
Needles for
anesthetic
Sterile drape
Manometer
6-inch
extension
tubing
Collection tubes
Review Box 60-1 Spinal puncture: indications, contraindications, complications, and equipment.
1218
CHAPTER
1219
1220
SECTION
X NEUROLOGIC PROCEDURES
Figure 60-1 This computed tomography scan demonstrates a lowdensity mass lesion with an enhancing rim and surrounding edema
in an immunosuppressed patient with an Aspergillus abscess. Lumbar
puncture in such a patient would be contraindicated. (From Zitelli BJ
and Davis HW: Atlas of Pediatric Physical Diagnosis. 5th ed. Philadelphia: Saunders; 2007.)
CHAPTER
1221
EQUIPMENT
Assemble the standard equipment for a spinal puncture before
starting the procedure. Place it where the operator can easily
access it. A standard-point Quincke cutting needle is most
often used and supplied with the kit. Some operators prefer
to use a Sprotte needle (Havels, Inc., Cincinnati, OH)
or a Whitacre needle (Becton Dickinson and Company,
Rutherford, NJ) to minimize any dural injury associated
with passage of the needle (Fig. 60-2). These styletted needles
have a side port for withdrawal of fluid and, theoretically, are
more likely to separate than cut the dural tissue.
Although commercial kits provide most of the items
needed for lumbar puncture, the operator should bring
additional supplies, including supplemental spinal needles,
specimen tubes, gauze, antiseptic solution, additional local
anesthetic, needles and syringes, and extra sterile gloves of the
appropriate size (see Review Box 60-1).
PROCEDURE
Lumbar puncture is commonly carried out with the patient
in the lateral recumbent position (Fig. 60-3). A line connecting the posterior superior iliac crests intersects the midline at
approximately the L4 spinous process (Fig. 60-4). Spinal
needles entering the subarachnoid space at this point are well
below the termination of the spinal cord, and the only important neurologic structure is the cauda equina. Generally, the
needle pushes isolated nerves to the side during advancement.
The adjacent interspace above or below may be used, depending on which area appears to be most accessible to palpation.
The space between the lumbar vertebrae is relatively wide. In
the thoracic region, the spinous processes overlap and are
directed caudally; therefore, there is no midline area free of
overlying bone. In adults, the spinal cord extends to the lower
level of L1 or the body of L2 in 31% of persons, thus eliminating higher levels as sites for puncture. Puncture in adults
and older children may be performed from the L2-L3 interspace to the L5-S1 interspace.
Developmentally, the spinal canal and the spinal cord are
of equal length in the fetus. Growth of the cord does not
keep pace with the longitudinal growth of the spinal canal.
At birth, the cord ends at the level of the L3 vertebra.
Consequently, in infants the needle should be placed at the
L4-L5 or L5-S1 interspace. The subarachnoid space extends
to the S2 vertebral level; however, the overlying bony mass
prevents entry into this lowermost portion of the subarachnoid space.
1222
SECTION
X NEUROLOGIC PROCEDURES
Sprotte
Quincke
Whitacre
Standard point
(Quincke)
Pencil point
(Whitacre)
patients greatly fear lumbar puncture, and hence some clinicians provide routine preprocedure sedation or analgesia if not
clinically contraindicated. Intravenous midazolam and fentanyl are useful adjuncts, but practices vary and there is no
consensus on standards with regard to the use or nonuse of
preprocedure medications. In anxious patients it is reasonable
to give a benzodiazepine agent parenterally (e.g., midazolam,
0.1 to 2.5mg intravenously for a healthy adult younger than
60 years of age) to facilitate the procedure. Fentanyl at a dose
of 0.5 to 1.5g/kg (adults) is a reasonable alternative.
The next important step is positioning the patient. Generally, place older children and adults in the lateral decubitus
position for the procedure. Give the patient a pillow to keep
the head in line with the vertebral axis. Position the shoulders
and hips perpendicular to the stretcher or table. Use a firm
table or bed when available. Because flexion of the neck does
not facilitate the procedure to any great extent and severe
flexion may add to the patients discomfort, this step may be
omitted. Severe flexion of the neck in an infant may cause
airway compromise. Pull the knees up to the chest and arch
the lower part of the patients back toward the clinician by
having the patients knees drawn toward the chest.
Some clinicians place the patient in an upright sitting position because the midline is more easily identified. This position can be used in both adults and infants (Fig. 60-5). The
higher CSF hydrostatic pressure while sitting may aid flow of
CSF in a dehydrated patient. Observe caution regarding
orthostatic changes in blood pressure and airway maintenance. Generally, allow a sitting patient to lean onto a bedside
stand and use a pillow to rest the head and arms. Have an
assistant support the patient during the procedure. Radiographic studies by Fisher and colleagues have demonstrated
the advantages of hip flexion when the sitting position is
used.33 To accomplish hip flexion, use a stool to support the
patients feet, which pulls the knees up toward the chest. This
increases lumbar interspinous width, which may increase the
success and ease of needle passage.
Iatrogenic infection after lumbar puncture is extremely
rare. Use sterile gloves during the procedure, but the need for
face masks is debatable.34-36 Apply the same guidelines for
control of central line infection (caps, gowns, gloves, and
masks) to lumbar puncture.37 Wash the patients back with an
antiseptic solution applied in a circular motion and increase
the circumference of the cleansed area with each motion.
Place a sterile towel or drape between the patients hip and
the bed. Commercial trays have a second sterile drape with a
hole that may be centered over the site selected for the
procedure.
Infiltrate the skin and deeper subcutaneous tissue generously with local anesthetic. Buffered or warmed 1% lidocaine
is preferred. Warn the patient about transient discomfort
from the anesthetic. Anesthetizing the deeper subcutaneous
tissue significantly reduces procedural discomfort. Merely
raising a skin wheal is insufficient anesthesia. Some operators
not only anesthetize the interspinous ligament but also apply
local anesthetic in a vertically fanning distribution on both
sides of the spinous processes near the lamina. Such a field
block on each side of the spinous processes anesthetizes the
recurrent spinal nerves that innervate the interspinous ligaments and muscles.
While waiting for the anesthetic to take effect, connect the
stopcock and manometer and ensure that the valve is working.
Commonly, a 3.5-inch, 20-gauge needle is used in adults, and
CHAPTER
1223
SPINAL PUNCTURE
1
2
Level of
iliac crest
Anatomic
midline
Consider mild
sedation or analgesia
when clinically
appropriate.
Attach the
manometer and
measure the
opening pressure.
10
1224
SECTION
X NEUROLOGIC PROCEDURES
L3 L4 L5
Iliac crest
L3
L4
L5
Spinal cord
L5 L 4 L3 L2 L1
Cauda equina
Iliac crest
B
Figure 60-6 Various ways to hold the spinal needle.
Iliac crest
L4-L5 landmark
B
Figure 60-5 A, Many clinicians prefer the sitting position for
lumbar puncture because of the ease of entering the dural space.
However, the opening pressure obtained in this position is not accurate. If possible, place the patient in the lateral decubitus position for
measurement of pressure, usually after fluid has been collected.
B, Upright positioning in an infant. (A, From Thomsen T, Setnik G,
eds. Procedures ConsultEmergency Medicine Module. Copyright
2008 Elsevier Inc. All rights reserved. B, from Dieckmann R, Selbst S,
eds. Pediatric Emergency and Critical Care Procedures. St. Louis:
Mosby; 1997.)
CHAPTER
1225
Supraspinal
ligament
Filum
terminale
Body of L1
Interspinal
ligament
Conus
medullaris
Anulus
fibrosus
and
nucleus
pulposus of the
intervertebral
disk
Ligamentum
flavum
Cauda equina
in the subarachnoid
space
Spinous
process of L-4
Dura/arachnoid
Posterior
longitudinal
ligament
Epidural space
Termination of
the thecal sac
B
Figure 60-8 A, This 22-gauge spinal needle has struck bone during
advancement (notice the bend in the needle) and needs to be repositioned. B, If bone is encountered, it is usually the inferior spinous
process (red spinal needle). The needle must be partially withdrawn
into subcutaneous tissue and then readvanced in a more cephalad
direction (green needle).
Figure 60-9 The spinal needle is usually advanced one half to three
fourths of its length before the spinal canal is reached. In this obese
patient, the needle was advanced all the way to the hub of the needle
before spinal fluid was returned.
1226
SECTION
X NEUROLOGIC PROCEDURES
Traumatic taps are common and usually clinically inconsequential. Nevertheless, they can be minimized by proper
patient and needle positioning. A traumatic tap most commonly occurs when the subarachnoid space is transfixed at the
entrance of the ventral epidural space, where the venous
plexus is heavier. A plexus of veins forms a ring around the
cord, and these veins may be entered if the needle is advanced
too far ventrally or is directed laterally (Fig. 60-11). If
blood is encountered and the fluid does not clear, repeat the
procedure at a higher interspace with a fresh needle. A traumatic tap, per se, is not a particularly dangerous problem in
a patient with normal coagulation, and no specific precautions
are needed if blood-tinged fluid is obtained. However, observe
for signs of cord or spinal nerve compression from a hematoma developing within the first several hours in patients with
a coagulopathy.
Internal
vertebral
plexus
External
vertebral
plexus
Nerve roots
forming
the cauda
equina
Radiculomedullary
vein
Arachnoid
Lumbar
vein
Dura
mater
L5 nerve root
Internal
vertebral
plexus
Spinal
needle
Figure 60-11 The spinal contents at L4 and L5 show the relationship of a lumbar puncture needle to the major vessels at this level.
The major radiculomedullary vein, shown accompanying the L5
nerve root, is situated far lateral to a needle correctly positioned in
the midline of the dural sac. Note the avascular subdural space. (From
Edelson RN, Chernik IVL, Rosner JB. Spinal subdural hematomas. Arch
Neurol. 1974;31:134. Illustration by Lynn McDowell. Reproduced by
permission. Copyright 1974, American Medical Association.)
Interspinal
ligament
Supraspinal
ligament
Ligamentum
flavum
Erector
spinae
muscle
Articular process
Epidural
space
Dura/arachnoid
Body of L3
Figure 60-10 To measure the opening pressure, attach the manometer to the needle hub with a 3-way stopcock. The zero mark of
the manometer should be level with the site of needle entry.
Subarachnoid space
containing the cauda
equina and lumbar
puncture needles
Figure 60-12 Horizontal section through the body of L3. Note the
two puncture needles in the subarachnoid space. The medial needle
is in the midline. The lateral needle exemplifies the lateral approach,
which avoids the occasionally calcified supraspinal ligament. Note
the lateral needle piercing the intrinsic musculature of the back and
only one ligament, the ligamentum flavum. (From Lachman E.
Anatomy as applied to clinical medicine. New Physician. 1968;17:745.)
CHAPTER
1227
1228
SECTION
X NEUROLOGIC PROCEDURES
US probe,
transverse
orientation
Figure 60-US3 First use the ultrasound (US) probe in the transverse orientation at the level of the iliac crests, and obtain an image
with the shadow of the spinous process centered on the screen (as
in Fig. 60-US1). Mark the skin at the exact midpoint of the transducer. This represents the anatomic midline.
US probe,
longitudinal
orientation
COMPLICATIONS
Headache after Lumbar Puncture
A number of complications from lumbar puncture have been
reported.58 One of the most common is headache, which
CHAPTER
tinnitus, and stiff neck. The headache may change to a positional backache or neck ache.
The technique of spinal puncture probably has little to do
with the development of a postprocedure headache. The syndrome is widely thought to be caused by leakage of fluid
through the dural puncture site. This results in a reduction
in CSF volume below the cisterna magna and downward
movement of brain tissue, along with displacement and
stretching of pain-sensitive structures such as the meninges
and vessels, and causes a traction headache. The recumbent
position brings relief because the weight of the brain is shifted
cephalad. Another proposed mechanism is cerebral vasodilation. A more recent hypothesis suggests that the headache is
caused by an altered distribution of craniospinal elasticity and
acute intracranial venous dilation.68 Some authors have commented on the incidence and severity of postdural puncture
headache as being related to the orientation of the spinal
needle bevel and its type and size.69-79 It is clear that the incidence of postdural puncture headache is lower when the
bevel of the needle is oriented parallel to the longitudinal axis
of the spine. Until relatively recently the explanation for this
was that the parallel bevel would separate rather than cut the
longitudinal dural fibers and thus produce a smaller dural hole
and less CSF leakage. However, it is now known that the dural
fibers are oriented randomly, not longitudinally.80 Even with
random fiber orientation, back flexion is more likely to close
a dural hole in the longitudinal plane than a hole in the horizontal plane.
The two basic types of spinal needles are cutting (Quincke)
and noncutting or pencil point (Sprotte and Whitacre). Noncutting needles cause a lower incidence of headache after
dural puncture, perhaps because the tip of the needle tends
to separate rather than cut the dural fibers. It has traditionally
been thought that the dural hole resulting from puncture
with a noncutting needle is smaller than that created by puncture with a cutting needle; however, this may not be true.
The important difference may be that the cutting needle
causes a clean-cut opening in the dura whereas the noncutting needle produces a jagged opening with rough edges.81
The jagged opening may produce a more intense inflammatory response that results in edema and more complete
closure of the hole. The use of atraumatic spinal needles is
not routine.82 As more spinal kit manufacturers include them
in kits, their use might increase.83 A single-institution study
suggested that routine use of noncutting needles yields a
potential cost savings.84 However, in thick-skinned individuals, passage of a thin, noncutting needle may be technically
difficult. Making the initial pass with a thicker cutting needle
to the level of the interspinal ligament, followed by removal
and advancement of a noncutting needle in the same soft
tissue tract, can be helpful.
Use of a smaller-diameter needle is one intervention that
will probably cause a lower incidence of postpuncture headache because it creates a smaller dural hole. If diameter were
the only consideration, as small a needle as possible would be
used. However, a needle must provide adequate CSF flow
rates to allow timely CSF collection and pressure measurement. With a very small needle, a syringe may be needed to
withdraw fluid, and pressure cannot be recorded easily. In
addition, technically, a small needle such as a 26 gauge is difficult to place and manipulate into a position in which it does
not become intermittently obstructed by nerve roots. When
these characteristics are considered, a 20- to 22-gauge
1229
1230
SECTION
X NEUROLOGIC PROCEDURES
Infection
Spinal puncture is contraindicated in the presence of local
infection at the puncture site (cellulitis, suspected epidural
abscess, or furunculosis) because of the danger of inducing
meningitis. A large concentration of bacteria in the bloodstream at the time of CSF examination is associated with
meningitis. The meningitis could be coincidental (spontaneous) or could result from leakage of blood containing bacteria into the subarachnoid space after lumbar puncture
(induced). It is likely that many cases of puncture-induced
meningitis emerge after a cautious clinician performs a lumbar
puncture early in the course of meningitis, before the infection has had time to be reflected in CSF. A recent review
concluded that the majority of cases of postpuncture meningitis are probably caused by contamination of the site with
aerosolized bacteria from medical personnel, contamination
from skin flora, or least commonly, direct or hematogenous
spread from an endogenous infectious site.37 Suspected bacteremia is not a contraindication to lumbar puncture. Delay
in diagnosis because of concern regarding the risks associated
with lumbar puncture is probably more serious than the risk
of causing meningitis with the procedure.99,100
CHAPTER
1231
Epidermoid Tumor
An epidermoid tumor or cyst is a mass of desquamated cells
containing keratin within a capsule of well-differentiated
stratified squamous epithelium. Congenital lesions arise from
epithelial tissue that becomes sequestered at the time of
closure of the neural groove between the third and the fifth
weeks of embryonic life, but such lesions are rare. Acquired
intraspinal epidermoid tumors result from the implantation
of epidermoid tissue into the spinal canal at the time of
lumbar puncture performed with needles without stylets or
with ill-fitting stylets. The clinical syndrome consists of pain
in the back and lower extremities developing years after
spinal puncture. Failure to use a stylet on needle withdrawal
might also result in aspiration of a nerve root into the epidural space.
1232
SECTION
X NEUROLOGIC PROCEDURES
INTERPRETATION
Pressure
CSF pressure is clinically important.115 Measure it accurately
whenever feasible. Unfortunately, in some cases it will be
logistically impossible to obtain. If the lumbar puncture is
being performed with the patient in a seated position, place
the patient in the lateral decubitus position before a measurement is obtained. This may be done initially, before fluid is
collected, or after fluid collection, in which case a closing
pressure is obtained. By repositioning the patient and measuring the pressure after fluid is collected, the likelihood of the
needle being displaced as a result of the repositioning is minimized.13,17 Accurate measurement depends on cooperation of
the patient. Measurements from struggling or agitated patients
will probably be inaccurate; in such cases, sedation may allow
more accurate readings to be obtained.
Normal CSF pressure is between 7 and 20cm H2O. Obese
patients may have a CSF pressure of up to 25cm H2O. Elevated pressure is abnormal. Opening pressure is taken
promptly, thereby avoiding falsely low values caused by
leakage through and around the needle. Herniating cerebellar
tonsils may occlude the foramen magnum and prevent
increased ICP from being reflected in the lumbar pressure
reading. Increased ICP can result from expansion of the brain
(edema, hemorrhage, or neoplasm), overproduction of CSF
(choroid plexus papilloma), a defect in absorption, or obstruction of flow of CSF through the ventricles. Cerebral edema
may be associated with meningitis, CO2 retention, SAH,
anoxia, congestive heart failure, or superior vena cava obstruction. Pressure may be falsely elevated in a tense patient when
the head is elevated above the plane of the needle and, possibly, in markedly obese patients and those experiencing
muscle contraction.21 Pressure is not usually measured in neonates because a struggling or crying child will have a falsely
elevated pressure. Avery and colleagues concluded that for
most children (1 to 18 years of age), an opening pressure
above 28cm H2O should be considered elevated.116
Low pressure suggests obstruction of the needle by the
meninges. Low pressure can also be seen with a spinal block.
Rarely, a primary low-pressure syndrome occurs in a setting
of trauma, after neurosurgical procedures, secondary to
subdural hematoma in elderly patients, with barbiturate
intoxication, and in cases of CSF leakage through holes in the
arachnoid.117,118
The Queckenstedt test is useful for demonstrating obstruction in the spinal subarachnoid space,4,21 but this test is seldom
performed today because myelographic techniques have been
refined and the availability of MRI has reduced the number
of myelograms and associated lumbar puncture studies.
However, because situations might arise when this simple and
reliable test is important diagnostically, the technique is
described here.
With the patient in the lateral recumbent position, compression of the jugular vein causes decreased venous return to
the heart. This distends the cerebral veins and causes a rise
in ICP, which is transmitted throughout the system and measured in the manometer. After 10 seconds of bilateral compression, CSF pressure usually rises to 15cm H2O over the
initial reading and returns to baseline 10 to 20 seconds after
release. If there is no change in lumbar pressure or if the rise
and fall are delayed, one may conclude that the spinal subarachnoid space does not communicate with the cranial subarachnoid space. In this situation, to facilitate subsequent
myelography, consider injecting Pantopaque before removing
the needle. This is necessary because the lumbar dural sac may
collapse and thus make it impossible to reenter the canal. If
cervical cord disease is suspected, repeat the test with the neck
in the neutral position, hyperextended, and flexed. When
lateral sinus obstruction is suspected, use unilateral jugular
venous compression (Tobey-Ayer test).
Appearance
If CSF is not crystal clear and colorless, a pathologic condition of the CNS should be suspected. The examiner should
compare the fluid with water and view down the long axis of
the tube or by holding both tubes against a white background.
A glass tube is preferred because plastic tubes are frequently
not clear. CSF will appear grossly bloody if more than 6000
red blood cells (RBCs)/L are present. Note that the fluid
may appear clear with as many as 400 RBCs/L and 200
WBCs/L.21 Xanthochromia, a yellow-orange discoloration
of the supernate of centrifuged CSF, is generally considered
to be the result of SAH of at least a few hours duration and
has been used to differentiate prior bleeding from a traumatic
tap. A traumatic tap does not usually exhibit xanthochromia
(see the later section The Traumatic Tap). Xanthochromia
is produced by red cell lysis and is caused by one or more
of the following pigments: oxyhemoglobin, bilirubin, or
methemoglobin
Traditionally, CSF samples have been assessed for xanthochromia by visual inspection by a laboratory technician after
centrifugation of a sample of CSF. Most hospitals still use this
method.119 Recently, spectrophotometry, designed to demonstrate both oxyhemoglobin and bilirubin, has been advocated
as a more precise way of determining xanthochromia. Oxyhemoglobin alone without bilirubin in a CSF sample is thought
to be artifactual (traumatic). Visually, bilirubin and oxyhemoglobin cannot be differentiated. Therefore, detection of bilirubin by spectrophotometry should define xanthochromia
and prompt additional investigation for SAH. Relying on
spectrophotometry to identify xanthochromia without
pigment differentiation will cause a high false-positive interpretation. The absence of both oxyhemoglobin and bilirubin
by spectrophotometry does not support the diagnosis of SAH.
Oxyhemoglobin causes red coloration; bilirubin, yellow; and
methemoglobin, brown. Oxyhemoglobin is seen within 2
hours after subarachnoid bleeding and red cell lysis, but it may
be detected immediately if the bleeding is profuse. Formation
of oxyhemoglobin peaks 24 to 48 hours after hemorrhage, and
the discoloration disappears in 3 to 30 days.4
Blood must be present in CSF (in vivo) for a number of
hours for bilirubin to appear; it will not appear spontaneously
once CSF is in the collection tube. The appearance of bilirubin in CSF involves the conversion of oxyhemoglobin by the
CHAPTER
Cells
In adults, WBC counts higher than 5 cells/L indicate the
presence of a pathologic condition. A recent large study by
Kestenbaum and colleagues determined 95th percentile WBC
reference values in normal infants: 19 cells/L for infants 28
days of age or younger and 9 cells/L for those between the
ages of 29 and 56 days.121 A median CSF WBC count of 271
WBCs/L has been reported in infants with group B Streptococcus in the era of intrapartum antibiotic prophylaxis. The
CSF WBC count in infants is higher with gram-negative
meningitis than with gram-positive CNS infections. In
general, polymorphonuclear leukocytes are never seen in
normal adults. However, with use of the cytocentrifuge, an
occasional specimen from an otherwise normal individual may
show one to two neutrophils.122 More than three neutrophils
is always abnormal in an adult. Moreover, as many as 30% of
patients exhibit CSF pleocytosis after a generalized or focal
seizure. Nonetheless, such a finding should prompt culture of
CSF because the presence of neutrophilic pleocytosis is commonly associated with bacterial meningitis or the early stages
of viral or tuberculous meningitis. Small lymphocytes may be
seen in normal individuals. Small and large immunocompetent cells are found with a variety of bacterial, fungal, viral,
granulomatous, and spirochetal diseases.
Eosinophils always indicate an abnormal condition, most
commonly a parasitic infestation of the CNS. They may also
be seen after myelography and pneumoencephalography and,
to a minor degree, with other inflammatory diseases, including tuberculous meningitis and neurosyphilis. Normal CSF
RBC counts are lower than 10 cells/L. Herpes simplex virus
(HSV) encephalitis may elevate the RBC count. Finally,
myeloid and RBC precursors may contaminate CSF with
bone marrow cells from an adjacent vertebral body.123
Glucose
Glucose enters CSF by way of the choroid plexus, as well as by
transcapillary movement into the extracellular space of the
brain and the cord via carrier-mediated transport. It then
1233
Protein
The normal range of lumbar CSF protein is 15 to 45mg/dL.
Infants normally have a lower level than adults do, and protein
levels may drop after lumbar puncture. The concentration is
lower in the ventricles (5 to 15mg/dL) and the basilar cisterns
(10 to 25mg/dL) as a result of a gradient in the permeability
of capillary endothelial cells to proteins in blood. Levels of
CSF protein in premature infants and full-term neonates are
higher than in adults, with a mean of 90mg/dL; protein levels
decline by the age of 8 weeks because of maturation of the
blood-brain barrier.
Most of the proteins in CSF come from blood, which
normally has a protein concentration of up to 8000mg/dL.
1234
SECTION
X NEUROLOGIC PROCEDURES
Protein entry is determined by its molecular size and the relative impermeability of the blood-CSF barrier. A full range of
serum proteins is found in CSF at a several hundredfold
dilution.
An increase in the total CSF protein level is a nonspecific
abnormality associated with many disease states. Levels higher
than 500mg/dL are uncommon and seen mainly with meningitis, subarachnoid hemorrhage, and spinal tumors. The
high levels that occur with cord tumors result from an increase
in local capillary permeability. With high levels (generally
1000mg/dL), CSF may clot (Froins syndrome).
Hemorrhage into CSF or the introduction of blood by a
traumatic tap increases CSF protein levels. If the serum
protein concentration is normal, the CSF protein level should
theoretically rise by 1mg/dL for every 1000 RBCs, but this
relationship varies. The inflammatory effect of hemolyzed
RBCs may also significantly increase CSF protein.
Selective measurement of immunoglobulin fractions in
CSF has proved to be of diagnostic value in suspected cases
of multiple sclerosis. Elevated CSF immunoglobulin levels
may reflect disruption of the blood-brain barrier or a local
antibody response to a CNS immune response.125 Stimuli may
be infectious or antigenic and produce an inflammatory
response. Elevated immunoglobulin levels have been found in
many conditions, including syphilis, viral encephalitis, subacute sclerosing panencephalitis, progressive rubella encephalitis, tuberculous meningitis, sarcoidosis, cysticercosis, and
acute inflammatory demyelinating polyneuropathy (GuillainBarr syndrome).
CHAPTER
1235
VIRAL MENINGITIS
Usually elevated
Usually normal
Elevated, 500-10,000+
Elevated, 6-1000
Differential count
Polymorphonuclear predominance
Lymphocytic predominance
Glucose level
Decreased, 0-40mg/dL
Usually normal
Protein level
Elevated, >50mg/dL
Opening pressure
3
Adapted from Fong B, Van Bendegem J. Lumbar puncture. In: Reichman E, Simon R, eds. Emergency Medical Procedures. New York: McGraw-Hill; 2004:875.
CSF, cerebrospinal fluid.
*This is only a guide. Care must be taken when interpreting these parameters, especially early in the clinical course.
1236
SECTION
X NEUROLOGIC PROCEDURES
PREDISPOSING FACTOR
Age
0-4wk
4-12wk
3mo-18yr
18-50yr
>50yr
ANTIMICROBIAL THERAPY
Immunocompromised
state
Third-generation cephalosporin
Cerebrospinal fluid
shunt
Cefotaxime or ceftriaxone.
CHAPTER
1237
Ampicillin
12g/day
Cefotaxime
8-12g/day
Ceftazidime
6g/day
6g/day
12-24
Chloramphenicol
4g/day
Gentamicin
2mg/kg IV load,
then 1.7mg/kg q8h
Tobramycin
2mg/kg IV load,
then 1.7mg/kg IV q8h
Vancomycin
2-3g/day
Ceftriaxone
DOSING
INTERVAL (hr)
4
4-6
8-12
TABLE 60-4 Recommended Total Daily Doses with Divided Dosing Intervals in Hours of Antimicrobial Agents
for Meningitis in Neonates, Infants, and Children with Normal Renal and Hepatic Function
ANTIMICROBIAL
AGENT*
Amikacin
15-20mg/kg/day
IV divided q12h
30mg/kg/day
IV divided q8h
15-22.5mg/kg/day IV divided
q8h (max dose 1.5g/day)
Ampicillin
200-300mg/kg/day
IV divided q8h
400mg/kg/day
IV divided q6h
300-400mg/kg/day IV divided
q3-4h (max dose 10-12g/day)
Cefotaxime
100-150mg/kg/day
IV divided q8-12h
200mg/kg/day
IV divided q6h
200-300mg/kg/day IV divided
q6-8h (max 12g/day)
Ceftazidime
100-150mg/kg/day
IV divided q8-12h
100mg/kg/day
IV divided q12h
150mg/kg/day IV divided
q8h (max 6g/day)
Ceftriaxone
Chloramphenicol
25-50mg/kg/day IV divided
q12-24h (initial loading
20mg/kg, then first
maintenance dose 12h later)
75-100mg/kg/day IV divided
q6h (max 2-4 g/day)
Gentamicin
2.5mg/kg/day IV divided
q8h*
4-5mg/kg/day IV divided
q12-48h*
Tobramycin
4-5mg/kg/day q24-48h*
4-5mg/kg/day IV divided
q12-48h*
Vancomycin
10-15mg/kg/day IV divided
q8-12h
45-60mg/kg/day IV divided
q8-12h
Smaller dosages and longer intervals of administration may be advisable for very-low-birth-weight neonates (<2000g).
1238
SECTION
X NEUROLOGIC PROCEDURES
CHAPTER
pleocytosis are sufficient grounds to initiate empirical acyclovir therapy until the results of more definitive diagnostic data
from PCR are available.152
1239
Rapidly progressive
confusion, apathy,
weakness
Gait dysfunction, lower
extremity weakness
and stiffness, urinary
dysfunction
Fever, headache, neck
stiffness, memory loss
<200
<200
<100
<100
<50
<200
<200
Toxoplasma encephalitis
CNS lymphoma
Progressive multifocal
leukoencephalopathy
CMV encephalitis
Vacuolar myelopathy
Cryptococcus neoformans
meningitis
INITIAL SYMPTOMS
HIV dementia
CD4+ COUNT
(CELLS/mm3)
Lethargy, confusion,
meningeal signs, cranial
nerve palsies
Spastic paraparesis,
Babinskis signs, sensory
abnormalities
Dementia, cranial
neuropathies, spasticity
Dementia, hemiparesis,
aphasia
Dementia, ataxia,
hemiparesis
Dementia, spasticity,
psychosis
NEUROLOGIC SIGNS
DIAGNOSTIC STUDIES
Ganciclovir, foscarnet
Radiotherapy
Pyrimethamine, sulfadiazine,
clindamycin
THERAPY
SECTION
1240
X NEUROLOGIC PROCEDURES
Distal numbness,
paresthesias, pain
Progressive weakness,
paresthesias
Facial weakness,
footdrop, wristdrop
Lower extremity
weakness, paresthesias,
urinary dysfunction
<200
>500 (early),
<50 (late)
>500 (early),
<50 (late)
<50
Any
Distal symmetric
polyneuropathy
Inflammatory
demyelinating
polyneuropathy
Mononeuropathy
multiplex
Progressive
polyradiculopathy
Myopathy
Dementia, stroke,
meningeal or
myelopathic signs, cranial
nerve palsies
Zidovudine reduction or
withdrawal, corticosteroids
Ganciclovir, foscarnet
Early: none
Late: ganciclovir
Neurotoxin withdrawal,
analgesics, tricyclic
antidepressants,
anticonvulsants, capsaicin
CHAPTER
From Simpson DM, Tagliati M. Neurologic manifestations of HIV infection. Ann Intern Med. 1994;121:770.
CMV, cytomegalovirus; CNS, central nervous system; CSF, cerebrospinal fluid; CT, computed tomography; EMG, electromyography; HIV, human immunodeficiency virus; IT, intrathecal; IV, intravenous; IVIG, intravenous
immunoglobulin; MRI, magnetic resonance imaging; PCR, polymerase chain reaction; PMNs, polymorphonuclear leukocytes; VDRL, Venereal Disease Research Laboratory.
Muscle weakness,
myalgia, weight loss
Any
Neurosyphilis
60 Spinal Puncture and Cerebrospinal Fluid Examination
1241
1242
SECTION
X NEUROLOGIC PROCEDURES
Mycobacterial Tuberculosis
CNS mycobacterial infection is almost always the result of
infection with Mycobacterium tuberculosis. Infection typically
occurs in the setting of disseminated tuberculosis. Atypical
Mycobacterium infection in HIV-infected individuals uncommonly affects the CNS.
The clinical manifestation is meningitis (particularly meningitis involving the basal cisterns), encephalitis, or abscess
formation. If tuberculosis is suspected, a large volume of CSF
(10mL) is required for adequate culture. The cell count
varies from 100 to 400 cells/L, with a lymphocytic predominance; 30% may show predominantly neutrophils early in the
course of infection. Protein levels are elevated (100 to 500mg/
dL), and the CSF glucose level may be depressed. Acid-fast
stains should be examined by experienced technicians. Fluid
is inoculated onto Lwenstein-Jensen medium, and the
absence of visible growth on the medium should not be considered negative until 8 weeks has elapsed. CSF cultures are
more sensitive than stains.
Primary CNS Lymphoma
CNS lymphoma develops in 2% of AIDS patients. The signs
and symptoms resemble those of diffuse encephalopathy,
although focal neurologic deficits occur occasionally. Leptomeningeal spread of malignancy is reflected in a modest
lymphocytic pleocytosis with slightly elevated protein and
decreased glucose levels. Cytologic yield is improved by
repeated lumbar punctures and submitting large quantities of
CSF or fluid obtained by cisternal puncture.153
Acknowledgment
The editors and author acknowledge the contributions of Jon
Kooiker to this chapter in previous editions. The author
would like to thank Linda J. Kesselring, MS, ELS, for copyediting the manuscript and incorporating revisions into the
final document.
References are available at www.expertconsult.com
CHAPTER
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