
Minimally Invasive Spine Surgery (MIS)
January, 2009
Minimally invasive spine surgery (MIS) was first performed in the 1980s, but
has recently seen rapid advances. Technological advances have enabled spine
surgeons to expand patient selection and treat an evolving array of spinal
disorders, such as degenerative disc disease, herniated disc, fractures, tumors,
infections, instability, and deformity.
One potential downside of traditional, open lumbar (back) surgeries is the
damage that occurs from the 5- to 6-inch incision. There are many potential
sources for damage to normal tissue: the muscle dissection and retraction required
to uncover the spine (which contributes to the formation of scar and fibrotic
tissue), the need for blood vessel cauterization, and the necessity of bone
removal. Disrupting natural spinal anatomy is necessary to facilitate decompression
of pinched nerves and the placement of screws and devices to stabilize the
spine. This may lead to lengthy hospital stays (up to five days or longer),
prolonged pain and recovery periods, the need for postoperative narcotic use,
significant operative blood loss, and risk of tissue infection.
MIS was developed to treat disorders of the spine with less disruption to
the muscles. This can result in quicker recovery, decrease operative blood
loss, and speed patient return to normal function. In some MIS approaches,
also called "keyhole surgeries," surgeons use a tiny endoscope with a camera
on the end, which is inserted through a small incision in the skin. The camera
provides surgeons with an inside view, enabling surgical access to the affected
area of the spine.
Not all patients are appropriate candidates for MIS procedures. It is important
to keep in mind that there needs to be certainty that the same or better results
can be achieved through MIS techniques as with the respective open procedure.
As with all non-emergency spinal surgeries, the patient should undergo an
appropriate period of conservative treatment, such as physical therapy, pain
medication, or bracing, without showing improvement, before surgery is considered.
The time period of this varies depending on the specific condition and procedure,
but is generally six weeks to six months. The benefits of surgery should always
be weighed carefully against its risks. Although a large percentage of patients
report significant symptom and pain relief, there is no guarantee that surgery
will help every individual.
Many MIS procedures can be performed on an outpatient basis. In some cases,
the surgeon may require a hospital stay, typically less than 24 hours to 2
days, depending on the procedure.
Benefits
The potential benefits of MIS include:
- Smaller incisions
- Smaller scars/less scar tissue
- Reduced blood loss
- Less pain
- Less soft tissue damage
- Reduced muscle retraction
- Decreased postoperative narcotics
- Shorter hospital stay
- Possibility of performing on outpatient basis
- Faster recovery
- Quicker return to work and activities
Surgery Risks
As with any spinal surgical procedure, there are risks, including:
- Allergic reaction
- Anesthesia reaction
- Bleeding
- Blood vessel damage
- Blood clots
- Bruising
- Death
- Dissatisfactory instrumentation placement; may require re-operation
- Headache
- Incision problems
- Infection
- Need for further surgery
- Pain or discomfort
- Paralysis
- Pneumonia
- Spinal fluid leakage
- Stroke
Conditions Treated using MIS Procedures
Glossary of Select Spine-Related Surgical Terms
Bone spur: bony growth or rough edges of bone.
Decompression: a surgical procedure performed to relieve pressure and alleviate
pain caused by the impingement of bone and/or disc material on the spinal cord
or nerves.
Disc degeneration: degeneration or wearing out of a disc. A disc in the spine
may deteriorate or wear out over time. A deteriorated disc may or may not cause
pain.
Discectomy: the surgical removal of part or all of an intervertebral disc,
performed to relieve pressure on a nerve root or the spinal cord.
Excision: removal by cutting away material, as in removing a disc.
Facet: a posterior structure of a vertebra which articulates (joins) with
a facet of an adjacent vertebra to form a facet joint that allows motion in
the spinal column. Each vertebra has a right and left superior (upper) facet
and a right and left inferior (lower) facet.
Foramen: a normal occurring opening or passage in the vertebrae of the spine
through which the spinal nerve roots travel.
Foraminotomy: surgical opening or enlargement of the bony opening traversed
by a nerve root as it leaves the spinal canal, to help increase space over
a nerve canal. This surgery can be done alone or together with a laminotomy.
Herniated disc: a condition, also known as a slipped or ruptured disc, in
which the gelatinous core material of a disc bulges out of position and puts
painful pressure on surrounding nerve roots.
Intervertebral foramen: An opening between vertebrae through which nerves
leave the spine and extend to other parts of the body. Also known as neural
foramen.
Kyphosis: a condition in which the upper back curves forward, sometimes leading
to the appearance of a hump in the back. Kyphosis may result from years of
poor posture, spine fractures associated with osteoporosis, trauma, or developmental
problems.
Lamina: the flattened or arched part of the vertebral arch, forming the roof
of the spinal canal.
Laminectomy: surgical removal of the rear part of a vertebra in order to gain
access to the spinal cord or nerve roots, to remove tumors, to treat injuries
to the spine, or to relieve pressure on a nerve root.
Laminotomy: an opening made in a lamina, to relieve pressure on the nerve
roots.
Lordosis: Lordotic curves refer to the inward curve of the lumbar spine. In
some patients, this may represent a spinal deformity, also called swayback,
which occurs when the lower back curves inward more than normal. Pathologic
or excessive lordosis may be caused by osteoporosis or spondylolisthesis. Obesity,
congenital disorders, or overcompensation for kyphosis may contribute to this
condition.
Medial facetectomy: a procedure in which a part of the facet is removed to
increase space in the spinal canal.
Nerve roots: the initial portion of a spinal nerve; the nerve root is an extension
of the central nervous system that begins at the spinal canal and ends in the
extremities (fingers, toes). Its purpose is to send sensory information from
the extremity to the brain, and a motor commands from the brain to the extremity.
Pedicle: the bony part of each side of the neural arch of a vertebra that
connects the lamina (back part) with the vertebral body (front part).
Percutaneous: effected, occurring, or performed through the skin.
Pseudoarthrosis: the movement of a bone at the location of a fracture or a
fusion resulting from inadequate healing of the fracture or failure of the
fusion to mature properly. This can also result from a developmental failure.
Scoliosis: lateral (sideways) curvature of the spine.
Spinal stenosis: abnormal narrowing of the vertebral column that may result
in pressure on the spinal cord, spinal sac, or nerve roots arising from the
spinal cord.
Spinous process: a slender projection of bone from the back of a vertebra
to which muscles and ligaments are attached.
Spondylitis: inflammation of vertebrae.
Spondylolisthesis: the forward displacement of one vertebra on another.
Spondylosis: degenerative bone changes in the spine, most commonly affecting
the vertebral joints.
Device Technology
Endoscope: a thin, fiber optic tube with a light and lens, used to examine
the interior of the patient’s body; provides minimally invasive access for
diagnostic and surgical procedures. Currently only a small number of spinal
surgeries can be performed utilizing an endoscopic approach.
Fluoroscope: an imaging device that uses x-rays to view internal body structures on
a screen, intraoperatively.
Laparoscope: an instrument which enables visualization of specific structures
within the body. A small surgical incision is made through which the laparoscope
is fed. An array of tubes can be guided through the same incision or other
small incisions, permitting the use of probes and other instruments.
Minimally invasive tubular retractor (MITR): muscle-splitting technology first
introduced in 1995 in conjunction with microendoscopic discectomy. The tubular
retractor is used to create a tunnel down to the spinal column, and measures
1.6 cm in diameter (about ¾ of an inch). The actual skin incision is a little
larger, but is generally about 2.5 cm in length. A "muscle splitting" approach
is employed, in which the tubular retractor is passed through a tunnel in the
muscles of the back, rather than stripping the muscles away from the spine,
as is done in open procedures. This approach limits damage to the muscles around
the spine and decreases blood loss during surgery.
Portals: devices that provide a passage through which the surgeon operates.
After the incision is made, dilators are used to reach the area of the spine
that the surgeon is working on. Fluoroscopy is used to locate the right level
at time of surgery. During the procedure, instruments are used to continue
the dissection through the portal. When the portal is removed, all the tissue
falls back into place. In order to avoid damaging the tissue by moving instruments
in and out of the passage, the portal or tubular retractor is placed into the
incision to hold the tissue apart and left in place throughout the procedure.
There are open and sealed portals. The portals used in the thoracic spine are
usually 11 to 12 mm, while portals used in the abdominal cavity tend to be
larger. All of the instruments and implants must be designed to fit through
these small passages and perform surgical functions once they reach the site.
Creating the Operating Space
In the thoracic spine, the lung is deflated to provide operating space. The
anesthesiologist places a special breathing tube down the trachea into the
large airway of each lung. The patient is under general anesthesia and breathing
with only one lung, which is considered very safe and a common practice. This
allows the opposite lung to deflate and falls out of the way of the spine.
The portals are placed and the spinal procedure is begun.
Spinal Fusion
Spinal fusion is an operation that creates a solid union between two or more
vertebrae. This procedure may assist in strengthening and stabilizing the spine
and may thereby help to alleviate severe and chronic back pain. The best clinical
results are generally achieved in single-level fusion, although fusion at two
levels may be performed in properly selected patients.
Almost all of the surgical treatment options for fusing the spine involve
placement of a bone graft between the vertebrae. Bone grafts may be taken from
the hip or from another bone in the same patient (autograft) or from a bone
bank (allograft). Bone graft extenders and bone morphogenetic proteins (hormones
that cause bone to grow inside the body) can also be used to reduce or eliminate
the need for bone grafts.
Fusion may or may not involve use of supplemental hardware (instrumentation)
such as plates, screws, and cages. This fusing of the bone graft with the bones
of the spine will provide a permanent union between those bones. Once that
occurs, the hardware is no longer needed, but most patients prefer to leave
the hardware in place rather than go through another surgery to remove it.
Fusion can sometimes be performed via smaller incisions through MIS techniques.
The use of advanced fluoroscopy and endoscopy has improved the accuracy of
incisions and hardware placement, minimizing tissue trauma while enabling an
MIS approach.
MIS Fusion Procedures
- Minimally Invasive Lateral Interbody Fusion (XLIF and DLIF)
- Minimally Invasive Posterior Lumbar Interbody Fusion (PLIF)
- Minimally Invasive Transforaminal Lumbar Interbody Fusion (TLIF)
- Minimally Invasive Posterior Thoracic Fusion
Lumbar fusion
procedures at a glance |
Procedure |
Approach |
Incision Size(s) |
Surgery Duration |
XLIF and DLIF |
side |
5-cm and 2.5-cm |
1 to 1 ½ hours |
PLIF |
back |
two 2.5-cm |
3 to 3 ½ hours |
TLIF |
back and side |
2- to 4-cm |
2 ½ hours |
Minimally Invasive Lateral Interbody Fusion
eXtreme Lateral Interbody Fusion (XLIF)
Direct Lateral Interbody Fusion (DLIF)
These are MIS procedures performed in patients with spinal instability caused
by degenerative discs and/or facet joints that cause unnatural motion and pain,
loss of height of the disc space between the vertebrae that causes pinching
of the spinal nerves exiting the spinal canal, slippage of one vertebra over
another, and/or changes in the normal curvature of the spine. The primary difference
in these approaches is the area of the body through which the spine is accessed.
To access the anterior spine and disc space, a 5-cm incision is made on the
patient's side, usually with a second 2.5-cm incision just behind the first
one. Special retractors are utilized, in addition to fluoroscopy, which provides
intraoperative x-ray images of the spine. A tubular retractor or portal is
passed and positioned along the lateral aspect of the vertebral bodies being
operated upon. Monitoring equipment is used to determine the placement of the
instruments in relationship to the spinal nerves. Disc material is removed
from the spine and replaced with a bone graft, along with structural support
from a cage made of bone, titanium, carbon-fiber, or a polymer. This provides
extra stability and helps the bone heal. Sometimes, surgeons will position
small screws in the spine posteriorly through an additional procedure. This
procedure is limited to one or two levels, and only vertebra that can be clearly
accessed from the side of the body can be operated on. This procedure typically
takes about 1 to 1 ½ hours to perform.
Outcome
Because this is a fairly new procedure, there is very little long-term outcome
data available. In general, there is very little blood loss with this procedure.
Many patients are ambulatory within a few hours and discharged from the hospital
the next day. Patients are often back to work within a few weeks.
Minimally Invasive Posterior Lumbar Interbody Fusion (PLIF)
This is a MIS technique that is performed in patients with refractory mechanical
low back and radicular pain associated with spondylolisthesis, degenerative
disc disease, and recurrent disc herniation. The procedure is performed from
the back (posterior) with the patient on his or her stomach.
Using x-ray guidance, two 2.5-cm incisions are made on either side of the
lower back. The muscles are gradually dilated and tubular retractors inserted
to allow access to the affected area of the lumbar spine. The lamina is removed
to allow visualization of the nerve roots. The disc material is removed from
the spine and replaced with a bone graft and structural support from a cage
made of bone, titanium, carbon-fiber, or a polymer, followed by rod and screw
placement. The tubular retractors are removed, allowing the dilated muscles
to come back together, and the incisions are closed. This procedure typically
takes about 3 to 3 ½ hours to perform.
Outcome
In a study of 31 patients who underwent the MIS PLIF surgery, there was less
blood loss, tissue trauma and operative time, quick recovery and bony fusion.
In two patients, the pedicle screws were not ideally positioned, but there
was no nerve root irritation or fixation failure and thus no revision was required.
The overall short-term outcomes were excellent.
Minimally Invasive Transforaminal Lumbar Interbody Fusion (TLIF)
Also known as mini-open TLIF, this is a MIS technique that is performed in
patients with refractory mechanical low back and radicular pain associated
with spondylolisthesis, degenerative disc disease, and recurrent disc herniation.
The TLIF approach may also have potential in patients with low back pain caused
by postlaminectomy instability, spinal trauma, or for treating pseudoarthrosis.
This procedure is contraindicated in patients who have a conjoined nerve root
within the foramen, a very rare occurrence, but one that may present during
surgery. The procedure is performed from the back (posterior) with the patient
on his or her stomach. The major difference in the TLIF approach is that the
operation is performed unilaterally, and the bone graft is inserted into the
disc space through the side.
Using x-ray guidance, a 2- to 4-cm incision is made approximately 4 to 5 cm
lateral to the midline. The muscles are gradually dilated and a tubular retractor
inserted to allow access to the affected area of the lumbar spine. The lamina
is removed to allow visualization of the nerve roots, and the facet joints
may be trimmed or removed to allow more room for the nerve roots. The disc
material is removed from the spine and replaced with a bone graft and structural
support from a cage made of bone, titanium, carbon-fiber, or a polymer, followed
by rod and screw placement. Surgeons may position small screws on the other
side of the spine through a percutaneous technique to provide additional stability.
The tubular retractor is removed, allowing the dilated muscles to come back
together, and the incision is closed. This procedure typically takes about
2 ½ hours to perform.
Outcome
A comparison study of 20 patients who underwent endoscopic-assisted MIS TLIF
with a group of patients who underwent the open PLIF procedure for single-level
degenerative disease yielded the following results. In the TLIF group, there
was less intraoperative blood loss, a shorter hospital stay, and postoperative
narcotic use significantly decreased.
In a larger study of 49 patients (45 with both low back pain and radicular
pain in the legs), and the remaining four with low back pain, there were very
promising results. Eleven of the patients had previous surgeries at the same
levels of the spine. Post surgery, all 45 patients with both back and leg pain
reported improvement in their symptoms. The four patients with low back pain
also reported a decrease in pain. At 18 months post surgery, all the patients
had solid, successful fusions. The patients appeared to have less postoperative
pain than with the open TLIF procedure, with narcotic pain relief medications
discontinued 2-4 weeks postoperatively.
Minimally Invasive Posterior Thoracic Fusion
Thoracic spinal fusion may be indicated for the surgical treatment of a wide
range of conditions, including trauma, deformity, tumor, and infection. Conventional
open surgical procedures for treatment of thoracic spine disease can be associated
with significant approach-related morbidity. Recent advances in technology
have led to the development of posterior MIS approaches for thoracic fusion.
In a posterior thoracic fusion, the surgical approach to the spine is from
the back through a midline incision. Special retractors are utilized, in addition
to fluoroscopy, which provides intraoperative x-ray images of the spine. Monitoring
equipment is used to determine the placement of the instruments in relationship
to the spinal nerves. At present, thoracic MIS techniques are primarily used
for stabilizing traumatic injuries, although some surgeons may use these techniques
for treatment of tumors, infections, or degenerative disc disease. These procedures
typically take about 3 to 3 ½ hours to perform, although with more complex
spinal disorders, longer procedures may be necessary.
Outcome
A large study of 104 spine trauma patients who underwent MIS transmuscular
pedicle screw fixation of the thoracic and lumbar spine yielded the following
results. Overall, 87 percent of screws were judged to be good, 10 percent were
judged to be acceptable, and 3 percent were judged to be unacceptable. Immediate
surgical revision, which was always performed through MIS techniques, was necessary
in nine patients for pedicle screw repositioning and in two patients for incomplete
tightening of anchor bolts. In the entire patient group, two patients with
an unacceptable screw position had new radicular pain that resolved completely
after screw repositioning, and two patients had delayed wound healing. No patients
experienced new neurological deficits.
MIS Decompression and Fracture Treatment Procedures
- Microdiscectomy
- Microendoscopic Laminectomy
- Minimally Invasive Cervical Foraminotomy (MICF)
- Minimally Invasive X-STOP® IPD Procedure
- Vertebroplasty and Kyphoplasty
Microdiscectomy
Microdiscectomy, also called microlumbar discectomy (MLD), is a very common
MIS decompression procedure performed in patients with a symptomatic lumbar
herniated disc. The operation consists of removing the portion of the intervertebral
disc that is herniated and compressing a spinal nerve root. The procedure is
performed from the back (posterior) with the patient on his or her stomach.
A 1- to 2-cm longitudinal incision is made in the midline of the lower back,
directly over the area of the herniated disc. Special retractors and an operating
microscope are used to visualize the region of the spine, with minimal or no
cutting of the adjacent muscles and soft tissues. After the retractor is in
place, an x-ray is used to confirm that the appropriate disc is identified.
A small amount of bone of the superior lamina may be removed first to expose
the disc herniation. The nerve root and neurologic structures are protected
and carefully retracted so that the herniated disc can be removed. Surrounding
areas are checked to ensure that no additional disc fragments are remaining.
This procedure typically takes about 1 hour to perform.
Outcome
Numerous research studies published in medical journals show that 90-96 percent
of patients have good or excellent results from microdiscectomy surgery. Most
patients experience a rapid decrease in pain and return to normal function.
Microendoscopic Laminectomy
Microendoscopic laminectomy, also called microlaminectomy, is a MIS decompression
procedure performed in patients with symptomatic, painful lumbar spinal stenosis.
The operation consists of removing the large, arthritic bone spurs that are
compressing the spinal nerves. The procedure is performed from the back (posterior)
with the patient on his or her stomach.
A 2- to 3-cm longitudinal incision is made in the midline of the lower back,
directly over the area of the spinal stenosis. Special retractors and an operating
microscope are used to visualize the region of the spine, with minimal or no
cutting of the adjacent muscles and soft tissues. After the retractor is in
place, an x-ray is used to confirm that the appropriate spinal level is identified.
The surgeon will remove all or part of the lamina and may also perform a foraminotomy,
where bone overlying the affected nerve is removed with a small drill. The
nerve root and neurologic structures are protected and carefully retracted
so that the bone spurs can be removed. Surrounding areas are checked to ensure
that no additional bone or disc fragments are remaining. This procedure typically
takes about 1 to 1 ½ hours to perform.
Outcome
Numerous research studies published in medical journals show that 86-95 percent
of patients have good or excellent results from microendoscopic laminectomy
surgery. Most patients experience a rapid decrease in pain and return to normal
function.
Minimally Invasive Cervical Foraminotomy
This is a MIS decompression procedure that enlarges the space in which a
spinal nerve root exits the cervical spinal canal (intervertebral foramen).
This narrowing can be caused by a herniated disc, bone spurs, thickened ligaments
or joints, which may result in painful pinched nerves. The procedure is performed
from the back (posterior) with the patient on his or her stomach.
A 1- to 2-cm incision is made on the symptomatic side of the neck. Using
an operating microscope and x-ray guidance, the muscles are gradually dilated
and a tubular retractor inserted to allow access to the cervical spine. Bone
or disc material and/or thickened ligaments are then removed to decompress
and relieve pressure on the spinal cord and/or nerves. The tubular retractor
is removed, allowing the dilated muscles to come back together, and the incision
is closed. This procedure typically takes about 2 hours to perform.
Outcome
A multicenter retrospective chart review of 73 patients who had MICF showed
the following results within a 40-month follow-up period:
- At 40 months, 21 percent of patients had radicular symptoms with 11 percent
reporting recurrence of preoperative symptoms and 9 percent with radicular
symptoms of a different pattern. Nine of the 73 patients required cervical
fusion within the 40-month period.
Minimally Invasive X-STOP® IPD Procedure
This is a MIS procedure performed in patients with symptomatic, painful lumbar
spinal stenosis. An implant, called the X-STOP® IPD Implant is placed between
two bones called spinous processes in the back of the spine. The goal is to
help keep the space between the spinous processes open, thus alleviating the
painful pinched nerves that can result from lumbar spinal stenosis. The device
can be implanted at one or two levels of the lumbar spine. This procedure is
performed while the patient is on his or her side so that the spine is in a
bent position during insertion of the implant.
Utilizing x-ray guidance, the implant is inserted through a small incision
in the skin of the back. Once the implant is in place, the incision is closed.
This procedure typically takes about 45 minutes to 1 ½ hours to perform.
Patients with the following criteria may be suitable candidates for this procedure:
- Age 50 and older with a radiological diagnosis of lumbar spinal stenosis
- Moderately impaired ability to function, with pain relief when bending
forward
Patients with any of the following criteria are NOT suitable candidates for
this procedure:
- Allergic to titanium or titanium alloy
- Spinal anatomy that prevents implantation of the device or would cause
the device to be unstable in the body
- Cauda equina syndrome, a spinal nerve compression that causes bowel or
bladder dysfunction
- Bone fractures or severe osteoporosis
Outcome
The X-STOP® IPD®System was tested in a controlled two-year research study
on 100 patients in nine hospitals across the United States. Outcome was compared
to 91 patients who were treated through conservative, nonsurgical methods.
Clinical results beyond two years post surgery were not measured.
- About 50 percent of the surgical patients experienced a degree of pain
relief and ability to increase their activity levels that was sufficient
to be considered a successful outcome at two years post surgery.
- During the study, 6 percent of patients experienced a dissatisfactory treatment
outcome and opted for a laminectomy (removal of part of the vertebra in the
spine), at which time the X-STOP® IPD® device was removed.
- The implant dislodged in one patient after a fall, and the implant was
later removed.
- A revision operation was required in three patients.
Vertebroplasty and Kyphoplasty
Vertebroplasty for the treatment of vertebral compression fractures (VCFs)
was introduced in the United States in the early 1990s. The procedure is usually
done on an outpatient basis, although some patients stay in the hospital overnight.
The procedure may be performed with a local anesthetic and intravenous sedation
or general anesthesia. Using x-ray guidance, a small needle containing specially
formulated acrylic bone cement is injected into the collapsed vertebra. The
cement hardens within minutes, strengthening and stabilizing the fractured
vertebra. Most experts believe that pain relief is achieved through mechanical
support and stability provided by the bone cement. Vertebroplasty typically
takes about 1 to 2 hours to perform, depending on the number of vertebrae being
treated.
A newer procedure, called kyphoplasty, involves an added procedure performed
before the cement is injected into the vertebra. First, two small incisions
are made and a probe is placed into the vertebral space where the fracture
is located. The bone is drilled and one balloon (called a bone tamp) is inserted
on each side. The two balloons are then inflated with contrast medium (which
are visualized using image guidance x-rays) until they expand to the desired
height and removed. The spaces created by the balloons are then filled with
the cement. Kyphoplasty has the added benefit of restoring height to the spine.
Outcome
Complication rates for vertebroplasty and kyphoplasty have been estimated
at less than 2 percent for osteoporotic VCFs and up to 10 percent for malignant
tumor-related VCFs.