Author: Dr Sibel Demir-Deviren University of California San Francisco 2008-07-10
Introduction
Spinal
pain is the most common of all chronic pain disorders. The number of
individuals that have, at some point in their life, experienced spinal
pain has been reported as 54 to 80%. After the initial painful episode,
the prevalence of persistent low back and neck pain ranges from 26 to
75%.
Axial
(neck or low back pain) and radicular pain (radiating pain to arm or
leg) may arise from any anatomic structure capable of transmitting pain
(the pain generator). Pain generators include vertebral
discs, nerve roots, dura (the outer layer of membrane surrounding the
brain and spinal cord), muscles, fascia (soft, connective tissue),
ligaments, and facet joints. Injury to any of these structures results
in the release of inflammatory mediators. Epidural injection of steroid
(cortisone, corticosteroid) is one of the most commonly used
interventions to decrease the inflammation in managing persistent spinal
pain.
Historically,
the epidural steroid injection is the first-line invasive therapeutic
procedure of choice in patients with spinal pain. In 1901, the first
independent reports on the use of caudal epidural injections in the
treatment of lumbar nerve root compression were published. The first
reportedly successful use of lumbar epidural injections as a treatment
for sciatica was in 1909. In 1930, a success rate of 61% was reported
for the treatment of sciatica following the caudal injection of large
volumes of local anesthetic and saline. The first reported use of
epidural steroids was in 1957 as a treatment for radicular leg pain.
Mechanisms of Action
Patho-anatomic
evidence shows that spinal discs can produce pain in the neck and upper
extremities, thoracic spine, chest and abdominal walls, low back, and
lower extremities. Disc related pain is caused by disc degeneration,
disc herniation, or by biochemical effects including inflammation.
Traditionally, compression of nerve roots by disc herniation has been
regarded as the cause of radiating pain to arm or leg, but during the
past decade, the pivotal role of multiple causes has been implicated.
Chemical mediators, such as phospholipase A2,
play integral roles in the development of pain when released from a
herniated disc. In addition, prostaglandins and leukotrienes have been
demonstrated to sensitize pain receptors and enhance pain generation.
Steroids inhibit phospholipase A2, thereby limiting the formation of prostaglandins and leukotrienes.
Both
mechanical compression and chemical irritation of nerve roots have been
shown to cause nerve root inflammation. Injected steroids possess
potent anti-inflammatory effects that are more pronounced when
administered at the site of the pain generation.
In
addition, one mechanism by which injured nerves cause chronic pain is
by generating abnormal (ectopic) discharges in nerve fibers. When
injected locally, steroids have been shown to prevent ectopic discharge
from injured nerves and suppress the ongoing neural activity, which also
contributes to pain.
Purported
advantages of epidural steroids over oral delivery include direct
deposition of the drug into the affected area, use of much smaller
dosages with fewer side effects, and longer duration of pain relief.
Anatomic Consideration
The
epidural space lies between bony-ligamentous structure lining the
vertebral canal and the dural membrane surrounding the spinal cord and
the nerve roots. Each nerve root exits the spine via an intervertebral
foramen (canal/hole).
1) Interlaminar epidural steroid injection
2) Caudal epidural steroid injection
3) Transforaminal epidural steroid injection
There are two different modes of access used to reach the cervical (neck) or thoracic (upper and lower back) epidural spaces:
1) Interlaminar epidural steroid injection
2) Transforaminal epidural steroid injection
1) Interlaminar epidural steroid injection
2) Transforaminal epidural steroid injection
Is Fluoroscopy (C-Arm, x-ray machine) medically necessary?
Historically,
the epidural space was accessed from the back through the interlaminar
approach or inferiorly through the caudal approach, often without the
use of fluoroscopy, an imaging technique, similar to an x-ray, used by
physicians to obtain real-time images of internal structures. A major
criticism of these blind approaches (without fluoroscopy) is lack of
target specificity. Even when performed by experienced clinicians, blind
epidural injections result in incorrect placement of the needle 25 to
40 % of the time. Injection of contrast medium (substance used to make
structures more visible) is also strongly recommended to confirm correct
needle placement within the epidural space. For these reasons, blind
epidural injections have been abandoned in favor of a fluoroscopically
guided approach.
1) Interlaminar Epidural Steroid Injections (ESI)
The
interlaminar epidural approach involves insertion of an epidural needle
midway between two adjacent vertebrae. For lumbar and thoracic
interlaminar epidural injections, 6 to 8 ml of steroid, local anesthetic
and sterile saline injection mixture is recommended. For cervical
interlaminar epidural injections, 4 to 6 ml of total volume of steroid,
local anesthetic, and sterile saline mixture is used.
The clinical evidence supporting use of interlaminar ESI is conflicting. Almost half of the studies report positive results and half report negative results. Based on a recent review, the use of interlaminar ESI to control lumbar radiating pain shows that interlaminar ESI provide good short term relief (6 weeks) but limited long term relief (6-12 months). In the management of cervical radiating pain with cervical interlaminar ESI, the evidence is moderate for both short and long term improvement.
2) Caudal Epidural Steroid Injections
The
caudal epidural approach involves insertion of a spinal needle into the
sacral hiatus, a hole located just above the tailbone. Caudal epidural
injections require larger volumes of injected fluids than lumbar,
thoracic and cervical ESI. Depending on the proposed pain generator, 10
to 15 ml of injection mixtures is recommended. This will often require
dilution of steroid with sterile saline and local anesthetic.
3) Transforaminal Epidural Steroid Injections (TFE)
Over
the last 10 years, the wide variations in reported success rates with
interlaminar ESI have generated intense interest in the use of
transforaminal epidural injections (TFE). The transforaminal epidural
steroid injection involves insertion of a spinal needle into the upper
portion of an intervertebral foramen (hole) where the nerve root is
exiting the spine. The medication mixture goes to epidural space and
nerve root sleeve which is responsible from the patient's pain. TFE
require 2 ml of steroid and local anesthetic mixture for the lumbar and
thoracic spine. For the cervical spine 1 to 1.5 ml of steroid and local
anesthetic mixture is recommended.
TFE
provides several advantages over traditional interlaminar and caudal
ESI. These include direct deposition of steroid at the level and side of
the pain generator, having a greater percentage of injected steroid
reach the ventral epidural space (the site of most inflammation), and
dramatic reduction in or even elimination of the risk of spinal
headache. Based on multiple studies, TFE is more effective than
interlaminar and caudal ESI. Because of its advantages, TFE under
fluoroscopic guidance has emerged as the preferred approach to deliver
steroids to the epidural space. Forty to eighty five percent of patients
have successful long-term (more than 3 months) pain relief. Both the
duration and the amount of pain relief depend on the pain generator or
generators, diagnosis, severity of the problem, and the patients’
functional limitations. The best candidates for TFE are patients with
acute radiating pain to arm or leg whose symptoms correlate with imaging
studies or electrodiagnostic testing. The response to TFE is also
helpful to find out the potential success rate of surgery, if needed.
Patients who had 70-80% relief from the TFE are shown to have greater
than 95% success in achieving average of 90% pain relief after the
surgery.
4) Selective Nerve Root Blocks (SNRB)
4) Selective Nerve Root Blocks (SNRB)
Although
the terms TFE and SNRB are sometimes used interchangeably, they are
separate procedures with minimal differences in the needle location.
SNRB is often overlooked as a diagnostic tool and as a potential
temporizing pain relief therapy. SNRB delivers a low volume (1 – 1.5 ml)
of concentrated medication (mixture of steroid and local anesthetic)
directly into the nerve root sleeve in question.
SNRB
is most appropriately used in patients with radiating pain. In many
instances, the source of the radiating pain can be diagnosed with
imaging studies and careful examination. However, there are patients
with radiating symptoms for whom results of an examination may be
equivocal and an imaging study may demonstrate nonspecific findings at
one or more levels. When careful evaluation and imaging studies do not
make diagnosis clear in patients with radicular or radicular like
symptoms, SNRB is considered to be a pivotal diagnostic test in making a
determination for surgery. This test uses pain relief as a diagnostic
endpoint to detect the nerve root responsible from the symptoms. In
patients with multilevel imaging abnormalities, or in the case of
postoperative patient, SNRB can help guide the surgeon to the proper
level or levels where the pain is originating. This information may help
to limit the extent of surgery or in some cases may prevent surgery.
Medications, Dose and Frequency
Commonly
used steroid preparations include betamethasone, dexamethasone,
triamcinolone and methylprednisolone. Of these, betamethasone and
dexamethasone have the strongest anti-inflammatory effects.
Unfortunately,
there is no consensus regarding the most effective medication, dose,
volume, or frequency. It is suggested that patients receive no more than
12 mg of betamethasone (or other corticosteroid equivalent) at one time
and no more than four steroid containing injections in any one year.
Betamethasone
is an equal mixture of two betamethasone salts and allows for both
immediate and delayed steroid responses. Immediate acting betamethasone
acts within hours, whereas the delayed acting salt is slowly absorbed
over approximately two weeks. Typically, epidural injection doses vary
with number of injections the patient is getting at the same time and
range from one to three ml (6-18 mg). Based on our clinical experience,
18 mg betamethasone is most likely to cause systemic side effects (see
below). Therefore in our practice, we avoid to use more than 12 mg
betamethasone in one set of injections.
Dexamethasone
has a rapid onset and long duration of action. Dexamethasone is the
only nonparticulate corticosteroid and is usually preferred in cervical
TFE. It usually is given in doses of 4-18 mg. Triamcinolone is available as three different salts. Triamcinolone acetonide (Kenalog) provides a long acting response like betamethasone and dexamethasone and is preferred in epidural injections. However, triamcinolone has 1/5 to 1/6 the steroid potency of betamethasone and dexamethasone.
Methylprednisolone has similar anti-inflammatory effects to triamcinolone. It has an intermediate duration of action. Typical doses range from 40 mg to 80 mg.
Indications for Epidural Steroid Injections
2) Spinal nerve root compression
3) Spinal nerve root inflammation
Indications for Selective Nerve Root Blocks
1) Evaluation of atypical extremity pain
2) To resolve discrepancies when imaging studies and clinical presentation do not correlate
3) Patients with multilevel imaging abnormalities, to more accurately define the levels for possible surgery
4) Both for diagnostic and therapeutic purposes in postoperative patients with unexplainable or complex recurrent pain
5) To assess anomalous innervations
6) To aid in the evaluation of patients with transitional vertebrae
Contraindications of Epidural Steroid Injections
1) Patients unwilling to consent to the procedure
2) True allergy to the local anesthetic, corticosteroid, or contrast agent
3) Infection at the site of injection
4) Systemic infection
5) Coagulopathy which causes internal bleeding after the injection (INR>1.2 or Platelets <100000/mm3)
6) Pregnancy
7) Unstable systemic diseases
Side Effects of the Medications
The
side effects of steroids are insomnia, mood swings, euphoria,
depression, post injection pain flare, facial redness, fluid retention,
hypertension, hyperglycemia, headache, gastritis, necrosis of hip,
suppression of adrenal glands, and menstrual irregularities. The most
common side effects are insomnia and facial redness. Side effects are
generally short lived.
The two most common systemic effects from
epidural local anesthetics involve the central nervous system (CNS) and
the cardiovascular system. Peak plasma concentration of epidural
anesthetics occurs 10-20 minutes after injection, so it is recommended
that patients be monitored for at least 30 minutes following an epidural
injection.
Complications of Epidural Corticosteroid Injections
Relatively few serious complications occur in patients receiving epidural steroid
injection from well-trained and experienced physicians. The most common complications are transient non positional headache for few days and increase in pain.
injection from well-trained and experienced physicians. The most common complications are transient non positional headache for few days and increase in pain.
1. Transient non positional headache
2. Increase in pain
3. Infection
4. Dural puncture headache
5. Nerve root injury
6. Epidural hematoma in the spine
7. Vasovagal attack and ataxia
8. Pneumothorax during thoracic injections
9. Paraplegia because of intraarterial injections during cervical injections which is preventable with a special imaging study known as digital subtraction angiography
2. Increase in pain
3. Infection
4. Dural puncture headache
5. Nerve root injury
6. Epidural hematoma in the spine
7. Vasovagal attack and ataxia
8. Pneumothorax during thoracic injections
9. Paraplegia because of intraarterial injections during cervical injections which is preventable with a special imaging study known as digital subtraction angiography
More Information
Web Resources
Key References
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