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MAST QUADRANT. Medial Lateral Blades Procedural Solutions Technique
MAST QUADRANT. Medial Lateral Blades Procedural Solutions Technique
As described by:
Charles L. Branch, Jr., M.D.
Wake Forest University
Baptist Medical Center
Winston-Salem, NC
Arthur H. Conley, M.D.
Oklahoma Sports Sciences
and Orthopedics
Oklahoma City, OK
MAST QUADRANT™ Unilateral and Bilateral Technique
Table of Contents
Access
MAST QUADRANT™ Unilateral and Bilateral Technique
Access
Patient Positioning
The patient is positioned prone on an appropriate table for fluoroscopy.
Two Flexible Arms may be required depending upon surgeon technique.
The NIM-SPINE™ System may be utilized for nerve monitoring.
NIM-SPINE™ System
MAST QUADRANT™ Unilateral and Bilateral Technique
Access
For PLIF, the incision is made approximately 3.0 to 4.0cm For TLIF, the incision is made approximately 4.0 to 4.5cm
off midline. After the tube insertion, the trajectory may off midline. This trajectory allows direct access to both
be shifted medial to accommodate the interbody portion disc space and pedicles.
of the procedure and lateral to target the Pedicle Screws.
MAST QUADRANT™ Unilateral and Bilateral Technique
Access
Access
Access
Access
Retractor
Access
Access
Access
Access
If needed, the MAST QUADRANT™ medial lateral blades may be added at this time.
The blades slide onto the medial lateral rack and sit between the existing medial
MAST QUADRANT™ Retractor.
14 MAST QUADRANT™ Unilateral and Bilateral Technique
Access
Perform the same dilation steps on the contralateral side to gain bilateral access.
MAST QUADRANT™
Unilateral and Bilateral Technique
Interbody
Implant Insertion
16 MAST QUADRANT™ Unilateral and Bilateral Technique
Bony Exposure
A facetectomy is performed ipsilaterally or bilaterally.
Using a Bone Rongeur, Osteotome, or Drill remove the
superior and inferior facets.
The extent of facetectomy is determined by the need for
visualization of the disc space and decompression of the
neural elements.
MAST QUADRANT™ Unilateral and Bilateral Technique 17
EMG Monitoring
18 MAST QUADRANT™ Unilateral and Bilateral Technique
Endplate Preparation
Using various Curettes and Scrapers, remove the cartilaginous material from the disc space and the endplates.
Thorough endplate preparation should be accomplished prior to insertion of the interbody construct.
Unilateral Bilateral
EMG Monitoring
MAST QUADRANT™ Unilateral and Bilateral Technique 21
Unilateral Bilateral
MAST QUADRANT™
Unilateral and Bilateral Technique
Fixation
MAST QUADRANT™ Unilateral and Bilateral Technique 23
Fixation
The MAST QUADRANT™ Retractor may now be Angulation may also be achieved.
translated to gain pedicle access.
Fixation
Fixation
NIM-PAK™ Needle
MAST QUADRANT™ Unilateral and Bilateral Technique 27
Fixation
Guidewire Insertion
The inner stylet of the NIM-SPINE™ Pedicle Access
Needle is removed to allow the Guidewire to be inserted
into the pedicle. Be extremely careful with regards to the
position of the Guidewire. Unintentional advancement
of the wire can potentially be very dangerous. Once the
Guidewire is inserted, the NIM-SPINE™ Pedicle Access
Needle may be removed.
In dense bone, where the Screw may be difficult to
advance, ensure that the pedicle is fully prepared by using
a Tap the same size as the inserted Screw to avoid pos-
sible Screwdriver damage. Fluoroscopy should be used to
verify the position of the Guidewire and the Tap during
this step. The threaded portion of the Tap is 45mm in
length. This allows you to determine Screw length.
28 MAST QUADRANT™ Unilateral and Bilateral Technique
Fixation
Screw Insertion
With the pedicles prepared and the proper Screw lengths determined, fully insert the hex end of the Multi Axial
Screwdriver into the Screw head. Next thread the Screwdriver Sleeve into the Screw head. The combination of the
hex head and the threaded sleeve provide a stable insertion instrument for inserting the Multi Axial Screws bilaterally.
The Screw and Screwdriver are now placed over the Guidewire and inserted into the pedicle. Once your Screw has
interfaced with bone you may now remove the Guidewire. After final Screw placement, Screw positioning can be
verified with EMG monitoring by direct stimulation of the Screw.
MAST QUADRANT™ Unilateral and Bilateral Technique 29
Fixation
EMG Monitoring
30 MAST QUADRANT™ Unilateral and Bilateral Technique
Fixation
Rod Insertion
To place the Rod into the MAST Rod Inserter, press the thumbswitch
to the right and insert the Rod into the Inserter, then press the thumb-
switch to the left to grip the Rod.
Lower the Rod Inserter into the Retractor and squeeze the Rod Inserter
handles to rotate the Rod from the vertical to the horizontal position.
Place the Rod into the Screw heads making sure lordosis will be achieved.
Then, with the Rod seated in the Screw heads, move the thumbswitch to
the right to release the Rod.
Thumbswitch
MAST QUADRANT™ Unilateral and Bilateral Technique 31
Fixation
Rod Reduction
If the Rod is not fully seated into the bottom of the Screw head, the Beale Rod Reducer can be used to fully seat
the Rod and simplify the Plug insertion process.
NOTE: Care should be taken with any Rod reduction maneuver. Improper instrument use may dislodge the implants
or damage the bony or neurologic anatomy.
The Beale Rod Reducer is the preferred method for reduction when the Rod is lying even to the top of the implant
head. To use the Rod Reducer, position the Reducer so that the handles are parallel to the Rod and grasp the Screw
head from above. The Reducer handles are slowly compressed allowing the sleeve to slide down and seat the Rod.
The Plug Starter or Provisional Driver is then inserted through the Rod Reducer to insert the Set Screw into the
head of the Pedicle Screw.
Provisional Driver
32 MAST QUADRANT™ Unilateral and Bilateral Technique
Fixation
Fixation
Final Tightening
When all implants are securely in place, final tightening and breakoff of the Plug head are done. Insert the Self-Retaining
Break-Off Driver into the cannulated portion of the Counter Torque which should be positioned over the implant and
Rod. The T-handle on the Driver provides adequate leverage for the breakoff of the Plug head (between 88 – 106 in-lbs).
The handle of the Counter Torque device should be held firmly to prevent torquing of the construct while the Plug is
secured and sheared off.
34 MAST QUADRANT™ Unilateral and Bilateral Technique
It should be noted that where excessive bone or fibrous growth has occurred from the first surgery,
there may be added stress on the removal instruments and the implants. Both instrument and implant
may be prone to possible breakage. In this case it is necessary to first remove the bone and/or tissue
from around the implants.
Further Information :
In case of complaint, or for supplementary information, please contact MEDTRONIC SOFAMOR
DANEK.
Product Complaint :
Any Health Care Professionals (e.g., customer users of MEDTRONIC SOFAMOR DANEK
instruments), who have any complaint or who have experienced dissatisfaction in the product quality,
identity, durability, reliability, safety, effectiveness and/or performance, should notify the distributor,
MEDTRONIC SOFAMOR DANEK. Further, if any instrument ‘’malfunctions’’, (i.e., does not meet any
of its performance specifications or otherwise does not perform as intended), or is suspected of
doing so, the distributor or MEDTRONIC SOFAMOR DANEK should be notified immediately. If any
MEDTRONIC SOFAMOR DANEK product ever ‘’malfunctions’’ and may have caused or contributed
to the death or serious injury of a patient, the distributor or MEDTRONIC SOFAMOR DANEK should
be notified as soon as possible by telephone, FAX or written correspondence. When filing a complaint,
please provide the component(s) name and number, lot number(s), your name and address, and the
nature of the complaint.
©2006 MEDTRONIC SOFAMOR DANEK USA, Inc. All rights reserved.
36 MAST QUADRANT™ Unilateral and Bilateral Technique
Purpose : 1. Plug the connector end of the stimulating instrument into the cathode (-) connection on the NIM
This instrument is intended for use in surgical procedures. Patient Interface STIM 1.
2. Place a subdermal EMG needle electrode (included) in the desired location to serve as the ground,
Description: or anode (+) for the stimulator.
Monopolar Stimulator Instruments are available in a variety of designs. These instruments have a lead !USA For US Audiences Only
that ends with a connector that plugs into the NIM system.
CAUTION : FEDERAL (U.S.) LAW RESTRICTS THESE DEVICES TO SALE BY OR ON THE
Intended Use: ORDER OF A PHYSICIAN ONLY.
This device is intended for use as a stimulating accessory for the NIM system. The NIM system is This device should be used only by physicians familiar with the device, its intended use, any additional
intended for use in surgical procedures for patient-connected intraoperative nerve monitoring, i.e. instrumentation and any available surgical techniques.
assisting the surgeon in locating and mapping motor nerves through the use of electromyographic
(EMG) signals and electrical stimulus of nerves. Sterility:
Indications: MEDTRONIC SOFAMOR DANEK instruments may be supplied as either sterile or non-sterile.
Sterile instruments will be clearly labeled as such on the package label. The sterility of instruments
This device is indicated for locating and identifying cranial and peripheral motor nerves during supplied as sterile can only be assured if the packaging is intact. If this product is provided
surgery, including spinal nerve roots. STERILE, it is intended for SINGLE PATIENT USE ONLY. DO NOT RESTERILIZE THIS PRODUCT.
Contraindications: MEDTRONIC SOFAMOR DANEK ASSUMES NO LIABILITY FOR PRODUCTS WHICH HAVE BEEN
The use of paralyzing anesthetic agents will significantly reduce, if not completely eliminate, RESTERILIZED BY HEALTH CARE FACILITIES.
electromyography (EMG) responses to direct or passive neural stimulation. Whenever nerve paralysis Further Information :
is suspected, consult an anesthesiologist. In case of complaint, or for supplementary information, please see the address page of this
Warnings: information sheet.
• MEDTRONIC SOFAMOR DANEK does not and cannot warrant the use of these instruments nor Product Complaint :
any of the component parts upon which repairs have been made or attempted except as performed Any Health Care Professionals (e.g., customer users of MEDTRONIC SOFAMOR DANEK
by MEDTRONIC SOFAMOR DANEK or an authorized MEDTRONIC SOFAMOR DANEK repair instruments), who have any complaint or who have experienced dissatisfaction in the product quality,
representative. identity, durability, reliability, safety, effectiveness and/or performance, should notify the distributor,
• Implied warranties of merchantability and fitness for a particular purpose or use are specifically MEDTRONIC SOFAMOR DANEK. Further, if any instrument ‘’malfunctions’’, (i.e., does not meet any
excluded. See the MSD catalog for further information about warranties and limitations of liability. of its performance specifications or otherwise does not perform as intended), or is suspected of
• DO NOT IMPLANT THE INSTRUMENTS. doing so, the distributor or MEDTRONIC SOFAMOR DANEK should be notified immediately. If any
• The NIM does not prevent the surgical severing of nerves. If these devices are compromised, the MEDTRONIC SOFAMOR DANEK product ever ‘’malfunctions’’ and may have caused or contributed
surgical practitioner must rely on alternate methods, or surgical skill, experience and anatomical to the death or serious injury of a patient, the distributor or MEDTRONIC SOFAMOR DANEK should
knowledge to prevent damage to nerves. be notified as soon as possible by telephone, FAX or written correspondence. When filing a complaint,
• To avoid patient burns: please provide the component(s) name and number, lot number(s), your name and address, and the
– Do not activate electrosurgical instruments while the stimulator is in contact with tissue. nature of the complaint.
– Do not leave stimulating instruments in surgical field. ©2006 MEDTRONIC SOFAMOR DANEK USA, Inc. All rights reserved.
– Do not store stimulating instruments in electrosurgical instrument holder
– Do not allow a second surgeon (i.e. fat harvesting) to use electrosurgical instrument while
stimulator is in use.
– If NIM accessories are used with stimulators other than the NIM System, do not exceed an energy
level of 50 mJ per pulse (measured into a 1 kilo-ohm load). Note: The NIM system does not
exceed 50 mJ per pulse (measured into a 1 kilo-ohm load).
– If using this accessory with other monitoring equipment than NIM Patient Interface STIM 1, special
operator attention may be required for current densities exceeding 2 mA RMS/cm2. Current, mA
RMS is generally lower than the stimulator current setting in mA. To calculate current, mA RMS,
waveform morphology, pulse width, repetition rate, and the stimulator current delivered must be
considered.
• High stimulator current may cause involuntary patient movement resulting in patient injury.
• Direct stimulator contact may disrupt the operation of active implanted devices.
• The surgical practitioner must choose the appropriate size instruments based on the procedure to
be performed and the stimulating current necessary for the application.
• Avoid trans-thoracic stimulation; when possible, maintain anode and cathode stimulating sites in
close proximity.
• False negative responses (failure to locate nerve) may result from:
– Shorted EMG electrode or cabling (conductive parts of applied needle electrodes or cables
contacting each other).
– Patient Interface STIM 1 or STIM 2 fuse blown.
– Patient Interface defective.
– Inadequate stimulus current.
– Inadequate current for stimulation of nerve through hardware, such as pedicle screws or stimulus
dissection instruments, may vary based on the physical size, shape characteristics, and design of
the hardware and proximity to the nerve.
– Neuromuscular fatigue from prolonged or repeated exposure to electrical stimuli.
• While stimulating, it is recommended to use EMG monitor(s) equipped with active audio and/or
visual current delivered feedback systems to ensure delivery of current to intended tissues.
• Proper handling, insertion, and placement of instruments is critical for safe and accurate EMG
monitoring:
– Improperly placed or bent needles increase the risk of needle breaking off in the patient.
– Do not attempt to straighten bent needles because this may cause stress and weaken device,
causing needle to break off in patient.
– Extreme care must be taken when handling instruments with sharp points or edges.
Precautions:
• Inadequate stimulus current flow may be caused by non-flush contact between the stimulating
instrument and the nerve, inadequate stimulator instrument electrical contact surface area, or high
impedance.
• Electrode integrity should be checked (by pressing electrodes check on the NIM) after electrode
insertion and before electrode removal to give additional assurance that electrode continuity was
maintained throughout the entire procedure. If electrode impedance is very high, discontinue use
and replace.
• Inability to deliver stimulus current flow may be caused by:
– Stimulator return electrode not connected, or other incomplete electrical connection between the
NIM, electrode and stimulator instrument.
– Patient Interface STIM 1 or STIM 2 fuse blown.
– Stimulus set to 0.00 mA.
– Defective instrument.
• Avoid accidental contact between connected but unapplied electrodes and other conductive parts.
• Reuse of single use instruments increase the risk of infection and may cause degraded or ineffective
monitoring.
• Contaminated single use instruments must be disposed of in an appropriate sharps biohazard
container in accordance with hospital or other user facilities policy.
Instructions for Use:
The surgical technique shown is for illustrative purposes only. The technique(s) actually employed in each case will always depend
upon the medical judgement of the surgeon exercised before and during surgery as to the best mode of treatment for each patient.
Please see the package insert for the complete list of indications, warnings, precautions, and other medical information.
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The Capstone® System incorporates technology
MLITQUDST6
IRN2889/066 developed by Gary K. Michelson, M.D.
©2006 Medtronic Sofamor Danek USA, Inc.
All Rights Reserved.