The present disclosure relates generally to medical devices and surgical methods, more specifically to a patient support platform. Such devices as well as systems and methods for use therewith are described.
Millions of surgical procedures are performed in the U.S. alone every year. Patients undergoing surgery are positioned for preparation for surgery and/or during the surgical procedure. One of the more common ways a patient is positioned on an operating room table is by being freely placed in a supine position (i.e., lying horizontally with face and torso facing up) or a prone position (i.e., lying horizontally with face and torso facing down).
Many current surgical techniques were designed or have evolved to solve problems specific to the period of time in which the surgery occurs. Some of the factors that have been taken into account in the design of surgical techniques include: the maintenance and handling of the weight of a patient's body without significant movement; the maintenance of a sterile field; easy access by the hands of one or more surgeons or surgical assistants while maintaining safe, ergonomic body positioning of the surgeons or surgical assistants; ease of incorporation of imaging systems including radiographic, fluoroscopic, or other imaging systems; maintenance and continuous measurement of controlled blood pressure; maintenance and continuous measurement of other vital parameters, such as temperature, respiratory rate, heart rate and rhythm, EKG, blood oxygen saturation, anesthesia level, state of reflexes, interface with medical equipment, and many other others. Some of the surgical positions used include prone, supine, lateral, lithotomy, and variations of these positions, such as the Trendelenburg position, the reverse Trendelenburg position, the full or high Fowler's position, the semi-Fowler's position, the jackknife or Kraske position, the high and low lithotomy positions, the fracture table position, the knee-chest position, the Lloyd-Davies position, the kidney position, and the Sims' position.
However, a significant problem with current surgical systems and methods is that anatomical and physiological conditions normal to the patient, such as weight distribution when the patient is standing normally, are not present during preparation of surgery or during the surgical procedure. Thus, patients may experience post-operative problems when returning to normal (i.e., non-surgical) anatomical positions and physiology. Therefore, a need continues to exist for systems and methods for performing surgical procedures under physiological and anatomical conditions normally experienced by the patient in the course of the patient's normal daily activities (e.g., standing, sleeping, sitting).
The needs described above, as well as others, are addressed by embodiments of the systems and methods for controlling multiple surgical variables described in this disclosure (although it is to be understood that not all needs described above will necessarily be addressed by any one embodiment), as the systems and methods of the present disclosure are separable into multiple pieces and can be used independently or in combination.
The present disclosure provides for a surgical patient interface including a patient support platform having a first end and a second end and configured for secure placement with respect to at least one surface of a building structure. The patient support platform is configured to interface with a patient such that at least the torso of the patient extends in a generally vertical direction between the first end and the second end of the patient support platform. One or more patient supports couple to the patient support platform and are configured to secure the patient to the patient support platform, such that the at least the torso of the patient is held in a substantially static condition, and such that a target portion of the patient's skin is accessible for surgical puncture or incision.
The present disclosure further provides for a method for performing surgery. The method includes placing a surgical patient in a patient support platform having a first end and a second end and configured for secure placement with respect to at least one surface of a building structure. The patient support platform is configured to interface with the patient such that at least the torso of the patient extends in a generally vertical direction between the first end and the second end of the patient support platform. The patient support platform includes one or more patient supports coupled thereto and configured to secure the patient to the patient support platform, such that the at least the torso of the patient is held in a substantially static condition, and such that a target portion of the patient's skin is accessible for surgical puncture or incision. The method includes using one or more of the one or more patient supports to secure the surgical patient to the patient support platform, and performing surgery on the patient.
Embodiments of the present invention provide systems and methods for performing surgery on a patient such that patient anatomical and/or physiological conditions preparing for and during surgery are more closely reproduced to reflect anatomical and/or physiological conditions during normal patient activities (e.g., standing, sitting, sleeping) than current standard surgical techniques. Advantageously, the systems and methods of the present disclosure are capable of being used in conjunction with many current surgical positions. For example, the systems and methods of the present disclosure can be used with a patient placed in a prone position, which is used in a large percent of thoracic, lumbar, and sacral spine surgeries.
A surgical patient 10 is shown in
As shown in
If one of the intervertebral lumbar discs (i.e., 122, 124, 126, 128, 130) is diseased, degenerated, or damaged or if one of the zygapophysial joints 125 is diseased, degenerated, or damaged, that disc or joint can be at least partially treated using an implanted device that provides rigid fixation, dynamic fixation, or adjustable fixation, including noninvasively-adjustable fixation. For example, a disc replacement device can be inserted into one of the intervertebral lumbar disc (e.g., 122, 124, 126, 128, 130) or one or more of the zygapophysial joints (e.g., 125).
In humans who are standing in a neutral position, a normal lumbar spine may be described as having a lumbar lordosis angle (LLA) 127 in the sagittal plane (i.e., the anatomical plane which divides the body into right and left halves) between about 20° and 40°. An LLA less than 20° is frequently considered lumbar hypolordosis and an LLA greater than 40° is frequently considered lumbar hyperlordosis. Similarly, the normal thoracic spine may be described as having a thoracic kyphosis of between about 20° and 50°, or between about 20° and 45°, or between about 25° and 45°. The lumbar region 102 is one of the key support elements for the upper portion of the body, weight (W) of which may, in many persons, constitute 50% or more of the persons' total body weight. The lordosis of the lumbar spine critically contributes to the lumbar region's 102 ability to support large amounts of weight. It is also important (along with the thoracic kyphosis) to a person's balance. When describing a patient's full or complete body herein (or simply “patient's body”), the term should be inclusive of all parts of the body, including the head and feet. Other modifiers may be used to denote specific portions of the patient's body (e.g., “upper body portion”).
Attempts may be made to position the body during prone lumbar spine surgery (such as illustrated in
Numerous types of surgery are performed with a primary purpose of improving the patient's mobility by changing the shape or condition of a portion of the patient's skeletal system. These surgeries may also reduce pain that the patient feels when in certain positions or when performing certain movements. Many of the higher stress positions or movements (and therefore, the positions and movements commonly responsible for increased pain) occur when a patient is in an erect (e.g., standing, walking, running) or a sitting position. In both erect and sitting positions, the lumbar region 102 of the vertebral column 100 fully or partially supports the upper body portion weight W. Oftentimes, the effect of a surgical procedure on the lumbar region 102 is not fully known until a patient has recovered, at least partially and sometimes fully, from surgery, and is able to engage in common movements and/or positions (e.g., run, walk, stand, sit), and thereby judge whether balance has improved, pain has diminished, stiffness has decreased, mobility has increased, or other factors have improved (e.g., in a noticeable fashion). Because the mechanical/physical conditions experienced by patients during surgery are so unlike the key high-stress positions and/or actions the patient typically experiences, the surgical technique tends to be based on a certain amount of conjecture or guess-work.
Examples of surgeries in the lumbar region 102 area include, but are not limited to: Anterior Lumbar Interbody Fusion (commonly known as “ALIF”), Foraminotomy, Forminectomy, Kyphoplasty, Laminectomy, Laminoplasty, Laminotomy, Posterior Lumbar lnterbody Fusion (commonly known as “PLIF”), Scoliosis correction, including modifying a coronal plane deformity, Spinal Decompression, Spinal Fusion, Spinal Osteotomy, and Transforamenal Lumbar lnterbody Fusion (commonly known as “TLIF”). Along with these procedures, a discectomy or microdiscectomy may be performed. Lasers may be used in such surgical procedures. The procedures may be performed with normal incisions, or with smaller incisions (e.g., minimally invasive surgery). Some procedures may be performed endoscopically. Thoroscopic surgery may include, for example, thoroscopic release. In a large number of procedures, spinal instrumentation may be implanted to fixate or “instrument” a portion of the spine. This may include holding one or more vertebrae static with respect to one or more other vertebrae, for example, to aid fusion. Spinal instrumentation may include metal rods, screws, hooks, wires, and/or other materials, including polymers like PEEK.
Certain types of spinal instrumentation allow a finite, controlled amount of movement between bones (e.g., vertebrae); these types of spinal instrumentation are often called dynamic stabilization instrumentation. Other types of spinal instrumentation include adjustable spinal instrumentation. These include instrumentation that may be adjusted (e.g., lengthened or distracted) via a minimally invasive puncture or small incision. For example, through such a minimally invasive puncture or incision, a screw may be loosened, then a spinal rod may be lengthened, and then the screw may be retightened to again hold the spinal rod. Some such instrumentation has been named “growing rods.” One such implant is the VEPTR® or VEPTR II™ (Vertical Expandable Prosthetic Titanium Rib), manufactured by DePuySynthes, West Chester, Pa., USA. Recently, non-invasively adjustable spinal instrumentation has been developed which allows non-invasive post-surgical adjustment (e.g., lengthening, shortening). That is, no additional incision is required. For example, the MAGEC® system, manufactured by Ellipse Technologies, Inc., Irvine, Calif., USA, is a magnetically adjustable implant that may be lengthened or shortened after implantation by the use of an externally-applied magnetic field (e.g., a rotating magnetic field).
In addition to the changes in normal anatomy and physiology described above, a prone surgical position may place blood vessels in vulnerable positions, including, but not limited to, the vena cava, the aorta, the carotid artery, and/or the saphenous vein. The prone position may also make the patient's body susceptible to hyperextension of joints, and may increase the chance of damage to nerves including, but not limited to, the radial, brachia I, median, and/or ulnar nerves. The prone position may additionally place undesirable stress(es) on the lungs and/or other portions of the respiratory system.
In order to maintain the patient in a stable, substantially static condition during vertical surgery, one or more patient supports 240 may be coupled to the platform 224, and may include straps 242, 244, 246, 248, 250, and/or bolsters 258, 260, 262. In some embodiments, the straps 242, 244, 246, 248, 250 may include one or more of a hole, a pocket, a hook and loop fastener feature, a tie-off, an adhesive feature, a clamp, and a groove. In some embodiments, the bolsters 258, 260, 262 may include one or more of a pillow, a rod, a tube, a mound, a bag, a pad, an inflated structure, a filled structure, and a buttress. The bolsters 258, 260, 262 may be configured to at least partially support at least one of a head, a neck, a shoulder, an arm, and elbow, a hand, a chest, a waist, a hip portion, a leg, a knee, an ankle, a foot, or any combination thereof. The patient 10 may be secured to the platform 224 using the patient supports 240 such that the patient's weight is well supported (e.g., evenly, securely, firmly, immovably) in the vertical position of
The platform 224, in its entirety or a portion thereof, may be adjustable in relation to the base 220. The first end 254 or the second end 256 may be adjustable, such as angularly, rotationally, linearly, or in multiple axis, in relation to the base 220. The platform 224 may be locked in relation to the base 220.
The orientation of each of the patient supports 240 is such that an open, accessible area 266 in the skin may be left available for surgical preparation. Depending on the configuration of the patient supports 240 chosen, that area 266 may be at least 60 cm2, at least 120 cm2, or at least 200 cm2. The area 266 may be rectangular, square, circular, or any other shape that facilitates a surgical procedure, regardless of invasiveness (e.g., whether the surgery is minimally invasive or maximally invasive). In some embodiments, the vertical orientation of the patient may be adjusted to be partially vertical (i.e., from 90° to 60° from the direction of gravity), mostly vertical (i.e., from 20° to 60° from the direction of gravity), or substantially vertical (i.e., 0° to 20° from the direction of gravity). In some embodiments, the vertical orientation may be changed by around 180 degrees (e.g., from about positive vertical (i.e., feet down/head up) to about negative vertical (i.e., feet up/head down)). Adjustment away from vertical may be used to change (e.g., slightly change) the effective body weight of the patient, or the effective upper body portion weight W, which exerts force in the direction of gravity.
The surgical table 318 includes a load adjustment module 378. The load adjustment module 378 may be disposed at the first end 354 such that it is positioned proximate to the patient's upper body portion, such as the patient's shoulders or heads, when the patient 10 is positioned on table 318. First stop 368 and second stop 370, each of which are coupled to the platform 324, are adjustable to apply a linear compressive force Fon the patient 10. In other embodiments, each of the stops 368, 370 or both of the stops 368, 370 may be adjustable in relation to the platform 324. However, in
As described in relation to the embodiment of
Advantageously, the support structure(s) described herein is capable of replicating anatomical and physiological conditions that the patient experiences during the patient's normal activities, such as sleeping, standing, and sitting. In this way, the presently disclosed support structure(s) allow a surgeon to operate on a patient with the benefit of observing, during the operating procedure, the effects of the surgical technique target as well as enabling the surgeon to select surgical technique based on the anatomical and physiological conditions that the patient normally experiences. It is believed that this benefit of the present support structure(s) and methods of use will result in improved surgical outcomes for patients.
In relation to any of the embodiments disclosed herein, all of the patient's weight may be borne by the patient (e.g., the patient's feet). Alternatively, in relation to any of the embodiments disclosed herein, a portion may be borne by the patient (e.g., the patient's feet) while a portion is borne by a support structure (e.g., stop 368, 370, 468 or first platform portion 471). The embodiments described herein may be used in surgical procedures which use general anesthesia, conscious sedation, local anesthesia, or other varieties of anesthesia. One or more drugs may be given to modify muscle tone of the patient 10. Stimulation, for example electrical stimulation, may be used to modify muscle tone. Stimulation may be done percutaneously, transcutaneously, or via an open or minimally invasive incision. A sterile field may be maintained during open surgery in an upright patient, such as with tented sterile drapes may be used in any of the embodiments to prevent drifting or falling particulate from entering surgical wound. Filtered air handling equipment may be used to move clean air over patient and prevent particulate from entering surgical wound.
In an embodiment, a method of placing and manipulating a musculoskeletal implant in a patient is provided. The method includes positioning the patient such that the bones of the head, spine, pelvis, and lower extremity are oriented in an upright standing position. The method may include performing a surgical intervention, either through an open skin incision or with minimally invasive percutaneous methods. The surgical intervention may be performed with the use of a robotic or robot-assisted surgical system. The surgical intervention may be performed with the use of an image-guided navigation system. The surgical intervention is performed with the use of minimally invasive access cannulas, retractors, and surgical instruments. The surgical intervention may be performed with the use of a fiber optic visualization system. The surgical intervention may include non-invasively adjusting the implant with a transcutaneous device that activates the implant to manipulate internal anatomy. The surgical intervention may be performed to implant a device on or near the cervical spine, thoracic spine, lumbar spine, pelvis, one or more hip or knee joints, or any combination thereof. The implant may be: a lumbar pedicle fixation device that can modify sagittal spine curvature, a lumbar pedicle fixation device that can modify coronal spine curvature. The device may be adjusted to modify varus or valgus alignment of bones connected by a joint, and the device can be adjusted to address flexion-extension misalignment of bones connected by a joint.
In another embodiment, a method for performing a surgical procedure is provided. The method includes placing a patient in a patient support platform having a first end and a second end and configured for secure placement with respect to at least one surface of a building structure, wherein the patient support platform is configured to interface with a patient such that at least the torso of the patient extends in a generally vertical direction between the first end and the second end of the patient support platform, the patient support platform including one or more patient supports coupled thereto and configured to maintain the position of the patient with respect to the patient support platform, such that the at least the torso of the patient remains in a substantially static condition, and such that a target portion of the patient is accessible. The method includes placing an external adjustment device in proximity to the target portion of the patient, and performing an adjustment procedure on the patient. The external adjustment device may be a magnetic device and configured to adjust a magnetic implant within the patient. The anatomy of the patient 10 may be manipulated by non-invasive external remote control of the magnetic implant.
In some embodiments, a method for performing surgery is provided. The method includes placing a surgical patient in a patient support platform having a first end and a second end and configured for secure placement with respect to at least one surface of a building structure, wherein the patient support platform is configured to interface with a patient such that at least the torso of the patient extends in a generally vertical direction between the first end and the second end of the patient support platform, the patient support platform including one or more patient supports coupled thereto and configured to secure the patient to the patient support platform, such that the at least the torso of the patient is held in a substantially static condition, and such that a target portion of the patient's skin is accessible for surgical puncture or incision. The method includes using one or more of the one or more patient supports to secure the surgical patient to the patient support platform, and performing surgery on the patient. The surgery may be performed through a window in the patient support platform.
In addition to performing surgery with a patient positioned using the various systems and methods disclosed herein, other procedures may be performed in a conscious (i.e., awake) and/or non-surgical patient. For example, patients who have been implanted with non-invasively adjustable spinal instrumentation, such as the MAGEC® system, may be placed in, on, adjacent, or against any of the embodiments described herein to have their non-invasive adjustment procedures performed. For example, a window in any embodiments disclosed herein, may be configured to allow the placement of an external adjustment device (e.g., magnetic external adjustment device) adjacent the skin of the patient to perform non-invasive adjustment (lengthening, shortening, etc.). Additionally, patients who have been implanted with implants which are adjustable via a minimally invasive procedure (e.g., growing rods, VEPTR®) may be placed in, on, adjacent, or against any of the embodiments described herein to have their minimally-invasive adjustment procedures performed.
Although this invention has been disclosed in the context of certain preferred embodiments and examples, it will be understood by those skilled in the art that the present invention extends beyond the specifically disclosed embodiments to other alternative embodiments and/or uses of the invention and obvious modifications and equivalents thereof. In addition, while a number of variations of the invention have been shown and described in detail, other modifications, which are within the scope of this invention, will be readily apparent to those of skill in the art based upon this disclosure. It is also contemplated that various combinations or sub-combinations of the specific features and aspects of the embodiments may be made and still fall within the scope of the invention. Accordingly, it should be understood that various features and aspects of the disclosed embodiments can be combined with or substituted for one another in order to form varying modes of the disclosed invention. Thus, it is intended that the scope of the present invention herein disclosed should not be limited by the particular disclosed embodiments described above, but should be determined only by a fair reading of the claims that follow.
Similarly, this method of disclosure is not to be interpreted as reflecting an intention that any claim requires more features than are expressly recited in that claim. Rather, as the following claims reflect, inventive aspects lie in a combination of fewer than all features of any single foregoing disclosed embodiment. Thus, the claims following the Detailed Description are hereby expressly incorporated into this Detailed Description, with each claim standing on its own as a separate embodiment.
The present application is a continuation of currently pending U.S. Non-Provisional Continuation application Ser. No. 16/058,750 filed on Aug. 8, 2018, which is a continuation application of PCT Application No. PCT/US17/17331 filed on Feb. 10, 2017, which claims the benefit of the priority date of U.S. Provisional Application No. 62/293,755 filed on Feb. 10, 2016. The entire contents of all these applications are hereby incorporated by reference into this disclosure as if set forth fully herein.
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Number | Date | Country | |
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20220183913 A1 | Jun 2022 | US |
Number | Date | Country | |
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62293755 | Feb 2016 | US |
Number | Date | Country | |
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Parent | 16058750 | Aug 2018 | US |
Child | 17689471 | US | |
Parent | PCT/US2017/017331 | Feb 2017 | US |
Child | 16058750 | US |