System and methods for performing surgical procedures and assessments
The present invention involves systems and related methods for performing surgical procedures and assessments, including the use of neurophysiology-based monitoring to: (a) determine nerve proximity and nerve direction to surgical instruments employed in accessing a surgical target site; (b) assess the pathology (health or status) of a nerve or nerve root before, during, or after a surgical procedure; and/or (c) assess pedicle integrity before, during or after pedicle screw placement, all in an automated, easy to use, and easy to interpret fashion so as to provide a surgeon-driven system.
1. A surgical system for neural monitoring while forming an operative corridor in a trans-psoas approach to a spine, comprising:
a control unit configured to receive user input regarding delivery of a stimulation signal to a stimulation electrode and to display on a color display device neuromuscular response data detected in response to the stimulation signal;
a connector module that provides a plurality of EMG response channels and an electrical connection for at least one surgical access instrument, the connector module having a wire connection to the control unit so that the connector module is positionable apart from the control unit;
a plurality of EMG electrodes connectable to the plurality of EMG response channels of the connector module, the EMG electrodes mountable relative to selected muscles;
a sequential dilation access system comprising a plurality of dilating cannulas to form a trans-psoas corridor between a skin surface and a targeted spine site, at least one of the dilating cannulas fitting over another of the dilating cannulas when advanced in a trans-psoas path toward the targeted spine site; and
a stimulation element electrically connectable to the connector module to deliver the stimulation signal proximate to a distal end of at least one of the dilating cannulas when advanced in the trans-psoas path toward the targeted spine site.
2. The surgical system of claim 1 , wherein the sequential dilation access system comprises at least a first dilating cannula, a second dilating cannula that is slidable over the first dilating cannula.
3. The surgical system of claim 2 , further comprising a working corridor instrument that is slidable over the second dilating instrument to form a trans-psaos operative corridor to the targeted spine site.
4. The surgical system of claim 3 , wherein the stimulation element is an electrode arranged on the distal end of at least one of the dilating cannulas.
5. The surgical system of claim 4 , wherein the stimulation electrode is positioned on one of the dilating cannulas to deliver the stimulation signal proximate to the distal end of the dilating cannula when advanced in the trans-psoas path, the stimulation electrode being arranged in a fixed position relative to a longitudinal axis of the dilating cannula such that the stimulation electrode rotates with the dilating cannula when the dilating cannula is rotated about the longitudinal axis while maintained in a fixed axial position.
6. The surgical system of claim 4 , wherein each of the dilating cannulas in the sequential dilation access system comprises a corresponding stimulation electrode arranged on a distal end the dilating cannula.
7. The system of claim 1 , wherein the color display device of the control unit comprises a touchscreen device to receive the user input regarding delivery of a stimulation signal.
8. A surgical system for neural monitoring while forming an operative corridor in a trans-psoas approach to a spine, comprising:
a control unit configured to receive user input regarding delivery of a stimulation signal to a stimulation electrode and to display on a color display device neuromuscular response data detected in response to the stimulation signal;
a sequential dilation access system comprising a plurality of dilating cannulas to form a trans-psoas corridor between a skin surface and a targeted spine site, at least one of the dilating cannulas fitting over another of the dilating cannulas when advanced in a trans-psoas path toward the targeted spine site,
wherein the stimulation electrode is positioned on one of the dilating cannulas to deliver the stimulation signal proximate to a distal end of the dilating cannula when advanced in the trans-psoas path, the stimulation electrode being arranged in a fixed position relative to a longitudinal axis of the dilating cannula such that the stimulation electrode rotates with the dilating cannula when the dilating cannula is rotated about the longitudinal axis.
9. The surgical system of claim 8 , wherein the sequential dilation access system comprises at least a first dilating cannula, a second dilating cannula that is slidable over the first dilating cannula.
10. The surgical system of claim 9 , further comprising a working corridor instrument that is slidable over the second dilating instrument to form a trans-psaos operative corridor to the targeted spine site.
11. The surgical system of claim 10 , wherein the trans-psoas operative corridor to the spine is formed after the first and second dilating cannulas are removed from the working corridor instrument.
12. The surgical system of claim 8 , further comprising:
a connector module that provides EMG response channels and an electrical connection for at least one surgical access instrument, the connector module having a wire connection to the control unit; and
a plurality of EMG electrodes connectable to the EMG response channels of the connector module, the EMG electrodes mountable relative to selected muscles.
13. The system of claim 8 , wherein the color display device of the control unit comprises a touchscreen device to receive the user input regarding delivery of a stimulation signal.
14. The system of claim 8 , wherein the stimulation signal delivered by the stimulation electrode is positioned on one of the dilating cannulas comprises stimulation current pulses, and the neuromuscular response data displayed by the control unit comprises a numeric stimulation threshold current level that indicates an amplitude of the stimulation current pulses required to evoke an EMG response having an amplitude value greater than a predetermined voltage value.
15. The method of claim 14 , wherein the stimulation current pulses of the signal delivered by the stimulation electrode is positioned on one of the dilating cannulas comprises rectangular monophasic current pulses output from the stimulation electrode during formation of the trans-psoas corridor between the skin surface and the targeted spine site.