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    NordOpedic AB

    Surgical technique

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    PF Posterior Fixator

    The posterior Fixator is a rigid xation for the treatment of fractures and malalignment

    of the spine. The device allows easy reduction of the spine in all planes and can be

    used as a single or multiple level xator. The device is a rigid xator in which the pe-

    dicle screws are independently placed in the vertebra.

    Benets

    When in place the device is adjustible without any restrictions.

    Precise compression / distraction with pedicle screws locked in angle to the construct.

    Reposition of fracture deformities is performed with simple reduction instruments in a

    controlled and careful mode.

    The different reduction planes are all separately locked.

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    Surgical technique

    Pre operative planning

    Prior to the operation the actual cross sectional size of the pedicle should be check-

    ed by CT-scan. The rear part of all pedicle screws have a diameter of 6.35mm.

    However two different screw diameters are available; 5 and 6mm. The 5mm screws

    are usually used in the thoracic spine from T5 downwards. The 6mm screws should

    be used whenever possible, typically from T12 downwards including the sacrum.

    The device should be placed as close as possible to the level of the lesion, thereby

    immobilizing the minimum number of segments.

    Patient positioning

    The patient is placed prone on a radiolucent operating table in such a way that the

    C-arm image-intensier can be placed under the patient. Reduction is facilitated by

    initial positioning in hyperextension by external means.

    Indications for use:

    1. Fractures of the lower thoracic and lumbar spine.

    2. Posttraumatic spinal deformity.

    3. Vertebral tumors, metastasis, infections and cases with imminent instability.

    4. Spondylolisthesis and lumbar scoliosis.

    5. Spondylolysis

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    Preparation for screw placement. An

    awl is used to penetrate the cortex at

    the intersection of the dotted lines. The

    tap is used to prepare the screw canal

    down into the pedicle. Use the tap that

    corresponds to the desired screw

    diameter.

    STEP 1

    Use the tap to measure the depth of the canal. Add 15 mm for the protruding part of

    the screw. The pedicle screws are inserted, do not turn down the screws all the way,

    the nal tightening of the pediclescrews can be done when the blocks are in place.

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    STEP 3

    The rod and blocks are slid over the screw lengthener on to the pediclescrews. Let

    the proximal block slide on rst. The distance between the blocks is regulated

    by turning the rod (shortening gives compression - Lengthening gives distraction).

    The PF-blocks are assembled on to the spindle bolt outside the patient.

    The threaded block is mounted on the hexagonal side of the rod and the

    unthreaded block on the opposite side. Make sure that both blocks can rotate fre-ely on the rod (do not overtighten the locking screws in the blocks).

    STEP 2

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    STEP 4

    C

    ompression or distraction can be achieved by turning the spindle bolt with the

    angled screwdriver. The screwdriver is inserted into the hexagonal hole at either

    the cranial or caudal side of the bolt.

    By turning the pedicle screws the rod and block assembly can be lowered against

    the lamina, achieving a minimum of protrusion.

    CAUTION!The length of the pedicle screw in the vertebra has to be monitored withX-ray.

    STEP 5

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    STEP 6

    Reduction handles are mounted over the blocks. The handle is placed over the

    block and the plug is inserted into the block as shown below.

    STEP 7

    With the reduction handles in place the fracture can be reduced. The distance between

    A and B should be normalized both anteriorly and posteriorly.

    Reduction - Correction

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    STEP 8

    C

    orrection is done as follows: Assemble the reduction clamps on the ends

    of the reduction handles. Reduction starts by turning the clamping rod. The

    distance A - B should be carefully monitored during the correction procedure.

    Caution: Kyphotic deformity often requires a shortening of the device to be able

    to achieve sufcient lordosis.

    Use the angular screwdriver to compensate for shortening. A ball headedhexagonal screwdriver may be used instead of the angled screwdriver ifthat feels more comfortable.

    STEP 9

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    With the oblique clamp mounted on the reduction handles. Translatory de-

    formity can easily be corrected.

    STEP 10

    STEP 11

    Finally all locking screws are tightened and the implantation is completed.

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    Postoperative regime

    Early mobilization is advocated, i.e. as soon as the postoperative pain has resol-

    ved, which is usually within 3-5 days after injury or surgery. Heavy patients (over

    75-80 kg) and patients with major instability should wear a threepoint corset for 2-3months. Extension injuries which can be stabilized by compression and exion com-

    pression injuries suitable for management via the tension band principle should not

    require any postoperative support.

    Patients without neurological decit usually require to be off work for 4-6 months

    after which sound union can normally be anticipated. The device may be removed

    after 8 months but in most instances leaving it in-situ has no adverse effect.

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    ImplantsItem no.

    Fixation blocksPF-blocks w/o thread, set of 2 ST250-005

    PF-blocks with thread, set of 2 ST250-006

    Rods 7 mmSpindle bolt 35 mm ST250-235

    Spindle bolt 45 mm ST250-245

    Spindle bolt 55 mm ST250-255

    Spindle bolt 65 mm ST250-265

    Spindle bolt 75 mm ST250-275

    Spindle bolt 85 mm ST250-285

    Spindle bolt 95 mm* ST250-295

    Spindle bolt 105 mm* ST250-305

    Spindle bolt 115 mm* ST250-315

    Spindle bolt 125 mm* ST250-325Spindle bolt 150 mm* ST250-350

    Pedicle screws 5 mm Pedicle screw 45 mm ST250-545

    Pedicle screw 50 mm ST250-550

    Pedicle screw 55 mm ST250-555

    Pedicle screw 60 mm ST250-560

    Pedicle screw 65 mm ST250-565

    Pedicle screw 70 mm ST250-570

    Pedicle screw 75 mm ST250-575

    Pedicle screws 6 mmPedicle screw 45 mm ST250-645Pedicle screw 50 mm ST250-650

    Pedicle screw 55 mm ST250-655

    Pedicle screw 60 mm ST250-660

    Pedicle screw 65 mm ST250-665

    Pedicle screw 70 mm ST250-670

    Pedicle screw 75 mm ST250-675

    Pedicle screw 80 mm ST250-680

    Pedicle screws 7 mmPedicle screw 60 mm ST250-760

    Pedicle screw 65 mm ST250-765Pedicle screw 70 mm ST250-770

    Pedicle screw 75 mm ST250-775

    Pedicle screw 80 mm ST250-780

    Additional implantsIntermediate block, 10 mm offset* ST250-850

    Intermediate block, 13 mm offset ST250-860

    *Sizes marked with * are made to order, the delivery

    time for these sizes may vary.

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    Instruments

    Screwdriver handle "Snap on" 20-001

    Bit for "Snap-on" screwdriver 20-003

    Screwdriver "Multi tip" 20-002Angular screwdriver 50-001

    Round bit for Multi tip screwdriver 20-352

    Straight bit for Multi tip screwdriver 20-353

    Crown bit for Multi tip screwdriver 50-602

    Tap 5 mm (for 5mm screws) 40-500

    Tap 6 mm (for 6 & 7mm screws) 40-600

    Reduction handles, set of 2 90-004

    Reduction clamps, set of 2 20-007

    Open key 6 mm 50-009Screw lenghtener 50-010

    Ring key 50-011

    Block releaser 90-002

    20-002

    20-003

    50-001

    40-500 / 40-600

    90-004

    20-007

    50-011

    50-010

    50-009

    90-002

    120-001

    20-352

    20-353

    50-602

    20-001

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    Postal adress: Anatomica AB, Stora vgen 25, SE-436 34 Askim, SWEDENTelephone: +46 (0)31-748 89 00, Fax: +46 (0)31-28 72 76E-mail: [email protected], Web: www.anatomicaspine.com

    Anatomica design, manufactureand supply Orthopaedic Products tohospitals and distributors all overthe world.

    The company was founded in 1981and our head quarter is located inGothenburg, Sweden.

    In 1981 an agreement was signedwith Biomet Inc for distribution of

    their products. Today Anatomicaalso distributes products from othermanufacturers, mainly from the USAand the European Union.

    In 2001 Anatomica aquired thecompany Nordopedic from professorSven Olerud. This gave us the opp-ortunity to develop and manufacturespinal products.

    Our Quality and environmental sys-tem is certifed according to the ISO13485 and ISO 14000 standards.

    Anatomica stands for Quality, Safety

    and a High Level ofService.