Lumbar puncture is a procedure that is often performed in the emergency department to obtain information about the cerebrospinal fluid (CSF).[1, 2, 3, 4] Although usually used for diagnostic purposes to rule out potential life-threatening conditions (eg, bacterial meningitis or subarachnoid hemorrhage), it is also sometimes used for therapeutic purposes (eg, treatment of pseudotumor cerebri). CSF fluid analysis can also aid in the diagnosis of various other conditions (eg, demyelinating diseases and carcinomatous meningitis).
Lumbar puncture should be performed only after a neurologic examination but should never delay potentially life-saving interventions, such as the administration of antibiotics and steroids to patients with suspected bacterial meningitis.[5]
The lumbar spine consists of 5 moveable vertebrae numbered L1-L5.The lumbar vertebrae have a vertical height that is less than their horizontal diameter. They are composed of the following 3 functional parts:
The vertebral body, designed to bear weight
The vertebral (neural) arch, designed to protect the neural elements
The bony processes (spinous and transverse), which function to increase the efficiency of muscle action
The lumbar vertebral bodies are distinguished from the thoracic bodies by the absence of rib facets. The lumbar vertebral bodies (vertebrae) are the heaviest components, connected together by the intervertebral discs. The size of the vertebral body increases from L1 to L5, indicative of the increasing loads that each lower lumbar vertebra absorbs. Of note, the L5 vertebra has the heaviest body, smallest spinous process, and thickest transverse process.
For more information about the relevant anatomy, see Lumbar Spine Anatomy.
Lumbar puncture should be performed for the following indications:
Suspicion of meningitis
Suspicion of subarachnoid hemorrhage (SAH)
Suspicion of nervous system diseases such as Guillain-Barré syndrome[6] and carcinomatous meningitis
Therapeutic relief of pseudotumor cerebri[7]
Absolute contraindications for lumbar puncture are the presence of infected skin over the needle entry site and the presence of unequal pressures between the supratentorial and infratentorial compartments. The latter is usually inferred from the following characteristic findings on computed tomography (CT) of the brain:
Midline shift
Loss of suprachiasmatic and basilar cisterns
Posterior fossa mass
Loss of the superior cerebellar cistern
Loss of the quadrigeminal plate cistern
Relative contraindications for lumbar puncture include the following:
Increased intracranial pressure (ICP)
Coagulopathy
Brain abscess
Indications for performing brain CT scanning before lumbar puncture in patients with suspected meningitis include the following[8] :
Patients who are older than 60 years
Patients who are immunocompromised
Patients with known CNS lesions
Patients who have had a seizure within 1 week of presentation
Patients with an abnormal level of consciousness
Patients with focal findings on neurologic examination
Patients with papilledema seen on physical examination, with clinical suspicion of an elevated ICP
Cranial CT scanning should be obtained before lumbar puncture in all patients with suspected SAH in order to diagnose obvious intracranial bleeding or any significant intracranial mass effect that might be present in awake and alert SAH patients with a normal neurologic examination.[9, 10]
The following measures should be taken to help minimize complications of lumbar puncture:
Explain the procedure, benefits, risks, complications, and alternative options to the patient or the patient’s representative, and obtain a signed informed consent
Before performing the lumbar puncture, ensure that patients are hydrated so as to avoid a dry tap
Never allow a lumbar puncture or a pre–lumbar puncture CT scan to delay administration of intravenous (IV) antibiotics; meningitis can usually be inferred from the cell count, antigen detection, or both
Avoid lumbar puncture in patients in whom the disease process has progressed to the neurologic findings associated with impending cerebral herniation (ie, deteriorating level of consciousness and brainstem signs that include pupillary changes, posturing, irregular respirations, and very recent seizure)[11, 12]
The smaller the needle used for the lumbar puncture, the lower the risk that the patient will experience a post–lumbar puncture headache. Data suggest an inverse linear relation between needle gauge and headache incidence, and some authors recommend using a 22-gauge needle regardless of what size needle is supplied with the kit.[13]
The use of atraumatic needles has been shown to significantly reduce the incidence of post–lumbar puncture headache (3%) when compared to the use of standard spinal needles (approximately 30%).[14, 15] In addition, it may lead to cost savings.[16] However, obtaining pressures can be more difficult with atraumatic needles.
Prophylactic bed rest after lumbar puncture has not been shown to be of benefit and should not be recommended.[17, 18, 19]
The overall risk of post dural puncture headache (PDPH) does not appear to be influenced by opening pressure, closing pressure, and volume of cerebrospinal fluid removed in instances of high-volume removal.[20]
A spinal or lumbar puncture tray (see the image below) should include the following items:
Sterile dressing
Sterile gloves
Sterile drape
Antiseptic solution with skin swabs
Lidocaine 1% without epinephrine
Syringe, 3 mL
Needles, 20 and 25 gauge
Spinal needles, 20 and 22 gauge
Three-way stopcock
Manometer
Four plastic test tubes, numbered 1-4, with caps
Local anesthesia is employed for lumbar puncture (see Technique and Local Anesthetic Agents, Infiltrative Administration).
The patient is placed in the lateral recumbent position (see the image below) with the hips, knees, and chin flexed toward the chest so as to open the interlaminar spaces. A pillow may be used to support the head. In a single-center prospective study, performance of lumbar puncture in the extended rather than the flexed lateral recumbent position yielded a statistically significant decrease in the cerebrospinal fluid (CSF) opening pressure, but the difference (mean, 0.6 ± 2.2 cm water) was small and of doubtful clinical significance.
The sitting position (see the image below) may be a helpful alternative, especially in obese patients, because it makes it easier to confirm the midline. In order to open the interlaminar spaces, the patient should lean forward and be supported by a Mayo stand with a pillow on it, by the back of a stool, or by another person.
If the procedure is performed with the patient in the sitting position and an opening pressure is required (as in the case of pseudotumor cerebri), replace the stylet and have an assistant help the patient into the left lateral recumbent position. There are no data suggesting that a position change will increase the risk of spinal headache or transection of the spinal nerves. Take care, however, not to change the orientation of the spinal needle during this maneuver.
Wearing nonsterile gloves, locate the L3-L4 interspace by palpating the right and left posterior superior iliac crests and moving the fingers medially toward the spine (see the image below). Palpate that interspace (L3-L4), the interspace above (L2-L3), and the interspace below (L4-L5) to find the widest space. Mark the entry site with a thumbnail or a marker. To help open the interlaminar spaces, ask the patient to practice pushing the entry site area out toward the practitioner.
Open the spinal tray, change to sterile gloves, and prepare the equipment. Open the numbered plastic tubes, and place them upright (see the image below). Assemble the stopcock on the manometer, and draw the lidocaine into the 10-mL syringe.
Use the skin swabs and antiseptic solution to clean the skin in a circular fashion, starting at the L3-L4 interspace and moving outward to include at least 1 interspace above and 1 below (see the video below). Just before applying the skin swabs, warn the patient that the solution is very cold; application of an unexpectedly cold solution can be unnerving for the patient.
Place a sterile drape below the patient and a fenestrated drape on the patient (see the video below). Most spinal trays contain fenestrated drapes with an adhesive tape that keeps the drape in place.
Use the 10-mL syringe to administer a local anesthetic (see the video below). Raise a skin wheal using the 25-gauge needle, then switch to the longer 20-gauge needle to anesthetize the deeper tissue. Insert the needle all the way to the hub, aspirate to confirm that the needle is not in a blood vessel, and then inject a small amount as the needle is withdrawn a few centimeters. Continue this process above, below, and to the sides very slightly (using the same puncture site).
This process anesthetizes the entire immediate area so that if redirection of the spinal needle is necessary, the area will still be anesthetized. For this reason, a 10-mL syringe may be more beneficial than the usual 3-mL syringe supplied with the standard lumbar puncture kit. The 20-gauge needle can also be used as a guide for the general direction of the spinal needle. In other words, the best direction in which to aim the spinal needle can be confirmed if the 20-gauge needle encounters bone in one direction but not in another.
Next, stabilize the 20- or 22-gauge needle with the index fingers, and advance it through the skin wheal using the thumbs (see the video below). Orient the bevel parallel to the longitudinal dural fibers to increase the chances that the needle will separate the fibers rather than cut them; in the lateral recumbent position, the bevel should face up, and in the sitting position, it should face to one side or the other.
Insert the needle at a slightly cephalad angle, directing it toward the umbilicus. Advance the needle slowly but smoothly. Occasionally, a characteristic “pop” is felt when the needle penetrates the dura. Otherwise, the stylet should be withdrawn after approximately 4-5 cm and observed for fluid return. If no fluid is returned, replace the stylet, advance or withdraw the needle a few millimeters, and recheck for fluid return. Continue this process until fluid is successfully returned.
For measurement of the opening pressure, the patient must be in the lateral recumbent position. After fluid is returned from the needle, attach the manometer through the stopcock, and note the height of the fluid column. The patient’s legs should be straightened during the measurement of the open pressure, or a falsely elevated pressure will be obtained (see the video below).
Collect at least 10 drops of cerebrospinal fluid (CSF) in each of the 4 plastic tubes, starting with tube 1. If possible, the CSF that is in the manometer should be used for tube 1. If the CSF flow is too slow, ask the patient to cough or bear down (as in the Valsalva maneuver), or ask an assistant to press intermittently on the patient’s abdomen to increase the flow. Alternatively, the needle can be rotated 90° so that the bevel faces cephalad.
Replace the stylet, and remove the needle (see the video below). Clean off the skin preparation solution. Apply a sterile dressing, and place the patient in the supine position.
If the CSF has been collected under sterile conditions, microbiologic studies can now be performed. Stains, cultures, and immunoglobulin titers may be obtained; the last are of special importance with diseases in which peripheral manifestations fade while central nervous system (CNS) symptoms persist (eg, syphilis and Lyme disease).[1, 2, 3]
Different institutions have different protocols for the studies performed on the various CSF tubes. The classic approach is to send the 4 CSF tubes for the following studies:
Tube 1 - Cell count and differential
Tube 2 - Glucose and protein levels
Tube 3 - Gram stain, culture and sensitivity (C&S)
Tube 4 - Cell count and differential
At some institutions, only 3 tubes are sent for analysis, and tube 4 is reserved for special studies when indicated. In this approach, the following studies are done:
Tube 1 - Protein and glucose levels
Tube 2 - Gram stain, C&S
Tube 3 - Cell count and differential
When indicated, viral titers or cultures, Venereal Disease Research Laboratory (VDRL) tests, Cryptococcus antigen assays, India ink stains, angiotensin-converting enzyme (ACE) levels, or other studies are ordered. Additional tests may be warranted, depending on the clinical situation. All specimens should be taken to the laboratory promptly to prevent hemolysis and specimen misplacement.
Separate specimens should be sent for microscopic study and for centrifugation. The latter must be done promptly because red blood cells (RBCs) hemolyze within a few hours. The lymphocyte count in normal CSF may be as high as 5/µL.
A larger-than-usual number of white blood cells (WBCs) suggests an infection or, more rarely, leukemic infiltration. Although bacterial infections are traditionally associated with a preponderance of polymorphonuclear leukocytes (PMNs), many cases of viral meningitis and encephalitis also show a high percentage of PMNs in the acute phase of the illness (when most lumbar punctures are done). In addition, inflammation from any source (eg, CNS vasculitis) can raise the WBC count.
A traumatic tap, of course, introduces WBCs and RBCs into the CSF (see Complications). An approximation of 1 WBC for every 1000 RBCs can be made, though a repeat tap may be preferable. Although no normal value for RBCs in the CSF is known, an occasional RBC may be incident to the tap itself.
Multiple lumbar puncture examinations may be required in testing for leptomeningeal malignancies. At least 3 negative cytologic evaluations (ie, 3 separate samplings) are required to rule out leptomeningeal malignancy (eg, leptomeningeal carcinomatosis).
Assessment of CSF protein level, though nonspecific, can be a clue to otherwise unsuspected neurologic disease. The high protein levels in demyelinating polyneuropathies, or postinfectious states, can be informative. A traumatic tap can introduce protein into the CSF. An approximation of 1 mg of protein for every 750 RBCs may be used, but a repeat tap is preferable.
The CSF glucose level normally approximates 60% of the peripheral blood glucose level at the time of the tap. A simultaneous measurement of blood glucose (especially if the CSF glucose level is likely to be low) is recommended.
A low CSF glucose level is usually associated with bacterial infection (probably due to enzymatic inhibition rather than to actual bacterial consumption of the glucose). This finding is also seen in tumor infiltration and may be one of the hallmarks of meningeal carcinomatosis, even with negative cytologic findings. A high CSF glucose level has no specific diagnostic significance and is most often spillover from an elevated blood glucose level.
The best way of distinguishing RBCs related to intracranial bleeding is to examine the centrifuged supernatant CSF for xanthochromia (yellow color). Although xanthochromia can be confirmed visually, it is more accurately identified and quantified in the laboratory.
Although xanthochromia can be produced by spillover from a very high serum bilirubin level (> 15 mg/dL), patients with severe hyperbilirubinemia (eg, from jaundice or known liver disease). usually have been identified before lumbar puncture. With this exception, xanthochromia in a freshly spun specimen is evidence of preexistent blood in the subarachnoid space. However, it should be remembered that an extremely high CSF protein level, as seen in lumbar punctures below a complete spinal block, also renders the fluid xanthochromic, though without RBCs.
Xanthochromia can persist for as long as several weeks after a subarachnoid hemorrhage (SAH). Thus, it has greater diagnostic sensitivity than computed tomography (CT) of the head without contrast, especially if the SAH occurred more than 3-4 days before presentation. Patients with aneurysmal leaks (eg, sentinel hemorrhages) may present days after the onset of headache, and this increases the likelihood of a false-negative head CT scan.
In some cases, the CSF may be another color that strongly suggests a diagnosis. For example, pseudomonal meningitis may be associated with bright-green CSF.
Possible lumbar puncture–related complications include the following[1, 2, 3, 4] :
Post–spinal puncture headache
Bloody tap
Dry tap
Infection
Hemorrhage
Dysesthesia
Post–dural puncture cerebral herniation
Headache is the most common complication of lumbar puncture, observed in 20-70% of patients.[21, 22, 23, 24] It usually begins 24-48 hours after the procedure and is more common in young adults. The probable etiology is continued leakage of CSF from the puncture site.[25] The headache is usually fronto-occipital and improves in the supine position.
This condition is usually self-limited (≤7 days) and responds to analgesics and caffeine (300-500 mg every 4-6 hours). Severe cases can be treated with an epidural blood patch performed by an anesthesiologist or a pain specialist. Pencil-tip (Whitacre) needles are associated with a significantly lower incidence of post–spinal puncture headaches than are standard bevel-tip (Quincke) needles.[26]
More than 50% of lumbar punctures are falsely positive for RBCs in the CSF as a result of microtrauma caused by the spinal needle. This is an uncomplicated occurrence in healthy patients with a normal coagulation system.
Dry taps usually result from misplacement of the spinal needle. The most common mistake is a lateral displacement, which can easily be corrected by withdrawing the needle completely, reevaluating the patient’s anatomy, and reinserting the needle in the correct place and at the proper angle. In obese patients, the regular spinal needle might be too short, in which case a longer one should be used.
If the patient is dehydrated, a falsely negative dry tap may be obtained as a result of very low CSF volume and pressure. If this is suspected, attempt to rehydrate the patient before the procedure.
Cellulitis, skin abscesses, epidural abscesses, spinal abscesses, or diskitis can result from a contaminated spinal needle. Adherence to sterile technique, including gloves, gowns, hair covers, and face masks, as well as thorough skin cleansing and disinfecting, should minimize this risk.
Epidural, subdural, and subarachnoid hemorrhage are rare complications that might carry significant morbidity and mortality in coagulopathic patients. Lumbar puncture should be deferred in patients with low platelets counts (< 50,000/µL) or patients with other coagulopathies (eg, hemophilia or supratherapeutic international normalized ratio [INR]) until the abnormality is corrected.
Irritation of nerves or nerve roots by the spinal needle can cause different lower-extremity dysesthesias. Withdrawing the needle without replacing the stylet can cause aspiration of a nerve or arachnoid tissue into the epidural space. To prevent this complication, always replace the stylet before moving the needle.
Cerebral herniation is the most serious complication of a lumbar puncture. It is very rare, and there is considerable debate in the literature regarding whether it is caused by the lumbar puncture or by the underlying disease process. There is increasing evidence that a diagnostic lumbar puncture is safe even in patients with increased intracranial pressure (ICP), such as most patients with meningitis, but there is no firm consensus regarding the safety of lumbar puncture in patients with ICP.
Until further data are available, a reasonable approach would be to avoid lumbar puncture when the disease process has progressed to the point where neurologic findings associated with impending cerebral herniation (deteriorating level of consciousness and brainstem signs including pupillary changes, posturing, irregular respirations, and very recent seizure) are seen.[11, 12]
Different institutions have different protocols for the studies performed on the cerebrospinal fluid. Typical studies include the following:
Cell count and differential
Glucose and protein levels
Gram stain, culture and sensitivity (C&S)
When indicated, viral titers or cultures, Venereal Disease Research Laboratory (VDRL) tests, Cryptococcus antigen assays, India ink stains, angiotensin-converting enzyme (ACE) levels, or other studies may also be ordered. Additional tests may be warranted, depending on the clinical situation.
A larger-than-usual number of white blood cells (WBCs) suggests an infection or, more rarely, leukemic infiltration. In addition, inflammation from any source can raise the WBC count. A traumatic tap, of course, introduces WBCs and red blood cells (RBCs) into the CSF. An approximation of 1 WBC for every 1000 RBCs can be made, though a repeat tap may be preferable. Although no normal value for RBCs in the CSF is known, an occasional RBC may be incident to the tap itself.
Assessment of CSF protein level, though nonspecific, can be a clue to otherwise unsuspected neurologic disease. The high protein levels in demyelinating polyneuropathies, or postinfectious states, can be informative. A traumatic tap can introduce protein into the CSF. An approximation of 1 mg of protein for every 750 RBCs may be used, but a repeat tap is preferable.
The CSF glucose level normally approximates 60% of the peripheral blood glucose level at the time of the tap. A simultaneous measurement of blood glucose (especially if the CSF glucose level is likely to be low) is recommended. A low CSF glucose level is usually associated with bacterial infection but is also seen in tumor infiltration. A high CSF glucose level has no specific diagnostic significance and is most often spillover from an elevated blood glucose level.
The amount of lidocaine provided in most kits is often inadequate. The authors recommend supplementing the kit with a 10-mL syringe and a bottle of 1% lidocaine. Make sure not to exceed the maximal recommend dose of 4.5 mg/kg of lidocaine. A smaller needle (27 gauge, 1.25 in.) may be used for infiltration. Smaller needles are shown to be associated with less pain during local anesthesia.
Local anesthetic agents are used to increase patient comfort during the procedure.
Lidocaine is an amide local anesthetic used in a 1-2% concentration. This agent inhibits depolarization of type C sensory neurons by blocking sodium channels. Epinephrine prolongs the effect and enhances hemostasis (maximum epinephrine dose, 4.5-7 mg/kg).
Overview
Where is lumbar puncture (LP) most often performed?
Why is lumbar puncture (LP) performed?
When should a lumbar puncture (LP) be performed?
How many moveable vertebrae are located in the lumbar spine?
What is the vertical height of the lumbar vertebrae?
What are the three functional parts of the lumbar vertebrae?
How are the lumbar vertebrae bodies distinguished from thoracic bodies in a lumbar puncture (LP)?
What are the heaviest components of the vertebrae?
How does the vertebral body increase its size?
Which vertebra has the heaviest body, smallest spinous process, and thickest transverse process?
Where can information about lumbar spine anatomy be found?
When is lumbar puncture (LP) indicated?
What are the absolute contraindications for a lumbar puncture (LP)?
What are the relative contraindications for lumbar puncture (LP)?
When is a brain CT scan indicated prior to performing a lumbar puncture (LP)?
When is a cranial CT scan indicated prior to performing a lumbar puncture (LP)?
How is the risk for complications of lumbar puncture (LP) reduced?
How is the risk of a post-lumbar puncture (LP) headache reduced?
Which needle size lowers the risk of a post-lumbar puncture (LP) headache?
What is the benefit of prophylactic bed rest after a lumbar puncture (LP)?
Periprocedural Care
What items need to be included in a spinal or lumbar puncture (LP) tray?
What anesthesia is administered for a lumbar puncture (LP)?
How is the patient positioned during a lumbar puncture (LP)?
What is the best alternative position when performing a lumbar puncture (LP) in obese patients?
How is patient position changed during lumbar puncture (LP)?
Technique
What is the first step when performing a lumbar puncture (LP)?
What can be done to help open the interlaminar spaces during a lumbar puncture (LP)?
How should the surgical site be prepared for a lumbar puncture (LP)?
How should drapes be placed during a lumbar puncture (LP)?
What size syringe should be used to administer local anesthetic during a lumbar puncture (LP)?
What are the steps for administering local anesthesia prior to a lumbar puncture (LP)?
How is the needle used as a guide during a lumbar puncture (LP)?
What are the steps for needle insertion during a lumbar puncture (LP)?
What angle and direction should the needle be inserted during a lumbar puncture (LP)?
How is measurement of the opening pressure taken during a lumbar puncture (LP)?
How much cerebrospinal fluid (CSF) should be collected during a lumbar puncture (LP)?
What are the final steps of a lumbar puncture (LP)?
What tests are performed once CSF has been collected in a lumbar puncture (LP)?
Are there universal protocols when performing studies on CSF tubes from a lumbar puncture (LP)?
What is the classic approach when sending CSF for testing following a lumbar puncture (LP)?
What is the approach when special CSF testing is indicated following a lumbar puncture (LP)?
Which tests may be conducted using cerebrospinal fluid (CSF) from a lumbar puncture (LP)?
How are specimens of CSF from lumbar puncture (LP) sent to the lab for centrifugation?
Which CSF findings from lumbar puncture suggest a specific infection?
What does a finding of WBCs and RBCs in CSF following lumbar puncture (LP) suggest?
When may multiple lumbar punctures (LPs) be indicated?
What is the indication for protein assessment of CSF from lumbar puncture (LP)?
What is the indication for glucose assessment of CSF from lumbar puncture (LP)?
What is suggested by xanthochromia in CSF from lumbar puncture (LP)?
What are possible complications of lumbar puncture (LP)?
What is the most common complication of a lumbar puncture (LP)?
How long do headaches persist after a lumbar puncture (LP)?
How are severe cases of post-lumbar puncture (LP) headaches treated?
What is the prevalence of RBC in CSF caused by lumbar puncture (LP)?
What should be done if a lumbar puncture (LP) results in a dry tap?
What are possible complications of a contaminated spinal needle during a lumbar puncture (LP)?
What can be done to minimize the risk of infections during a lumbar puncture (LP)?
What are rare complications of lumbar puncture (LP) in patients with coagulopathy?
When should a lumbar puncture (LP) be deferred?
What causes dysesthesia during lumbar puncture (LP)?
How can dysesthesia be prevented during a lumbar puncture (LP)?
What is the most serious complication of a lumbar puncture (LP)?
When should a lumbar puncture (LP) be avoided?
What studies are typically performed on the CSF from lumbar puncture (LP)?
Which specific studies are performed on CSF from a lumbar puncture (LP)?
How are cytologic studies of CSF from lumbar puncture (LP) used?
How is glucose assessment of CSF from lumbar puncture (LP) used in the diagnosis of infection?
Medications
What medications are used in a lumbar puncture (LP)?
Which medications in the drug class Local Anesthetics are used in the treatment of Lumbar Puncture?