Handheld electromechanical stapler with tissue thickness detection

Abstract

A surgical device includes a motor and a reload having a plurality of staples. The surgical device also includes an anvil assembly movable relative to the reload by the motor to clamp tissue therebetween. The device further includes a force sensor configured to measure force imparted on the anvil assembly. The device additionally includes a controller configured to compare the measured force to a target force, determine a distance at which the measured force matches the target force, and output the distance and the target force.

Description

BACKGROUND

Circular staplers are used in a surgical procedure to reattach rectum portions that were previously transected, or similar procedures. Conventional circular clamping, cutting and stapling instruments include a pistol or linear grip-styled structure having an elongated shaft extending therefrom and a staple cartridge supported on the distal end of the elongated shaft. In this instance, a physician may insert an anvil assembly of the circular stapling instrument through an incision and toward the transected rectum portion. The physician may then introduce the remainder of the circular stapling instrument (including the cartridge assembly) into a rectum of a patient and maneuver the device up the colonic tract of the patient toward the transected rectum portions. The anvil and cartridge assemblies are approximated toward one another, and staples are ejected from the cartridge assembly toward the anvil assembly to form the staples in tissue to affect an end-to-end anastomosis, and an annular knife is advanced to core a portion of the clamped tissue portions. After the end-to-end anastomosis has been affected, the circular stapling apparatus is removed from the surgical site.

Powered electromechanical surgical staplers, including battery power sources, utilize motors to actuate various components of the powered surgical stapler during clamping, stapling, and cutting portions of the anastomosis procedure. An unresolved issue with conventional powered staplers is that a user manually needs to estimate or measure appropriate tissue thickness and match an appropriate staple cartridge for that thickness.

Currently there is not a standard procedure for measurement of soft tissue thickness. Each company or individual that provides any tissue thickness measurements for development and usage of medical devices, research studies or such similar reasons has created a test method or product to fulfill this need. Since this measuring process is not standardized in the medical field, the tissue thicknesses compiled and reported by all institutions cannot be combined or compared quantitatively. Thus, there is a need for a powered surgical stapler configured to accurately measure tissue thickness by leverage precise electronic sensors of the powered surgical stapler.

SUMMARY

A powered circular stapler according to the present disclosure is used to create anastomoses on a variety of tissue types, thicknesses, and disease states across multiple surgical techniques. Depending on the tissue type, thickness, etc., the force required to approximate the tissue that forms the anastomosis may vary between procedures. In situations where the tissue is particularly thick or dense due to tissue type or condition, clamping at the same speed and force as for thinner tissue could result in tissue trauma, over compression, or an inability to compress tissue to a desired tissue gap.

The present disclosure provides a tissue thickness measuring algorithm that operates alongside a controlled tissue compression (“CTC”) algorithm. The CTC algorithm and the tissue thickness algorithm may be embodied as software instructions executed by a controller of a powered surgical stapler. The CTC algorithm control clamping of tissue prior to stapling and cutting processes of forming an anastomosis. The powered surgical stapler includes a strain gauge to measure force during clamping and continuously compare the measured force to a target force while simultaneously monitoring the distance traveled by an anvil. The distance at which the measured force is equal to the target force is logged by the controller and displayed on a display of the powered surgical stapler providing for an accurate measurement of tissue thickness. This allows the clinician to confirm that a reload is of an appropriate size and to use a different reload based on the measured thickness.

It is envisioned that the tissue thickness measuring algorithm according to the present disclosure may be implemented any powered stapling device, including linear staplers and robotic staplers.

According to one embodiment of the present disclosure, a surgical device may be disclosed. The surgical device includes a motor and a reload having a plurality of staples. The surgical device also includes an anvil assembly movable relative to the reload by the motor to clamp tissue therebetween. The device further includes a force sensor configured to measure force imparted on the anvil assembly. The device additionally includes a controller configured to compare the measured force to a target force, determine a distance at which the measured force matches the target force, and output the distance and the target force.

Implementations of the above embodiment may include one or more of the following features. According to one aspect of the above embodiment, the reload may include a storage device configured to store the target force. The surgical device may include a display. The controller may be further configured to output the distance at which the measured force matches the target force and the target force on the display. The controller may be further configured to maintain a timer and update the target force to the measured force obtained at expiration of the timer. The controller may be further configured to determine a distance at which the target force was updated. The controller may be configured to output an expiration time of the timer, the distance at which the target force was updated, and the target force on the display. The controller may be further configured to pulse the motor to maintain the target force prior to determining the distance. The controller may be further configured to maintain the target force for a preset time period.

According to another embodiment of the present disclosure, a surgical device is disclosed. The surgical device includes a motor and a reload including a plurality of staples. The surgical device also includes an anvil assembly movable relative to the reload by the motor to clamp tissue therebetween in a first phase and a second phase and a force sensor configured to measure force imparted on the anvil assembly. The surgical device also includes a controller coupled to the motor and the force sensor. During the first phase, the controller is configured to: compare the measured force to a target force, determine a distance at which the measured force matches the target force, and output the distance and the target force.

Implementations of the above embodiment may include one or more of the following features. According to one aspect of the above embodiment, during the first phase the anvil assembly may be moved at a constant speed. During the second phase the anvil assembly may be moved at a varying speed. The reload may include a storage device configured to store the target force. The surgical device may include a display. The controller may be further configured to output the distance at which the measured force matches the target force and the target force on the display. The controller may be further configured to maintain a timer and update the target force to the measured force obtained at expiration of the timer. The controller may be further configured to determine a distance at which the target force was updated. The controller may be further configured to output an expiration time of the timer, the distance at which the target force was updated, and the target force on the display. The controller may be further configured to pulse the motor to maintain the target force prior to determining the distance. The controller may be further configured to maintain the target force for a preset time period.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the present disclosure are described herein with reference to the accompanying drawings, wherein:

FIG. 1 is a perspective view of a handheld surgical instrument including a handle assembly, an adapter assembly, and an end effector, according to an embodiment of the present disclosure;

FIG. 2 is a schematic diagram of the handle assembly, the adapter assembly, and the end effector of FIG. 1;

FIG. 3 is a side perspective view of the adapter assembly and the end effector, an annular reload and an anvil assembly, attached to the adapter assembly of FIG. 1 according to an embodiment of the present disclosure;

FIG. 4 is a perspective view of a clamping transmission assembly disposed within the adapter assembly of FIG. 1, shown partially in phantom;

FIG. 5 is a perspective view of a stapling transmission assembly disposed within the adapter assembly of FIG. 1, shown partially in phantom;

FIG. 6 is a cross-sectional view of a reload of the end effector of FIG. 1;

FIG. 7 is a perspective view of the adapter assembly, shown partially disassembled, with a strain gauge assembly;

FIG. 8 is a method for controlling the surgical instrument of FIG. 1 during the clamping sequence according to an embodiment of the present disclosure;

FIG. 9 is a schematic diagram illustrating travel distance and speed of the anvil assembly and a corresponding motor during a clamping sequence performed by the handheld surgical device of FIG. 1 according to an embodiment of the present disclosure; and

FIG. 10 is a method for controlling the surgical instrument of FIG. 1 during a tissue thickness measuring sequence according to an embodiment of the present disclosure.

DETAILED DESCRIPTION OF EMBODIMENTS

Embodiments of the presently disclosed surgical devices, and adapter assemblies for surgical devices and/or handle assemblies are described in detail with reference to the drawings, in which like reference numerals designate identical or corresponding elements in each of the several views. As used herein the term “distal” refers to that portion of the surgical instrument, or component thereof, farther from the user, while the term “proximal” refers to that portion of the surgical instrument, or component thereof, closer to the user.

The present disclosure provides a powered circular stapler 10 having a handle assembly, an adapter assembly coupled to the handle assembly, and an end effector coupled to the adapter assembly. The stapler allows for full, independent control of three functions: clamping, stapling, and cutting. This allows certain portions of the stapler to adapt if the tissue presents a non-ideal situation.

FIG. 1 illustrates a surgical device, such as, for example, a powered circular stapler 10 for forming end-to-end anastomosis (“EEA”), including a handle assembly 100, which is configured for selective connection with an adapter assembly 200. The adapter assembly 200 is configured for selective connection with an end effector 300, which includes a reload 400 and an anvil assembly 500. The end effector 300 is configured to produce a surgical effect on tissue of a patient, namely, forming an anastomosis by connecting two portions of a structure (e.g., intestine, colon, etc.) by clamping, stapling, and cutting tissue grasped within the end effector 300.

The handle assembly 100 includes a power handle 101 and an outer shell housing 11 configured to selectively receive and encase power handle 101. The shell housing 11 includes a distal half-section 10a and a proximal half-section 10b pivotably connected to distal half-section 10a. When joined, distal and proximal half-sections 10a, 10b define a shell cavity therein in which power handle 101 is disposed.

Distal and proximal half-sections 10a, 10b of shell housing 11 are divided along a plane that traverses a longitudinal axis “X” of adapter assembly 200. Distal half-section 10a of shell housing 11 defines a connecting portion 20 configured to accept a corresponding drive coupling assembly 210 (FIG. 3) of adapter assembly 200. Distal half-section 10a of shell housing 11 supports a toggle control button 30. Toggle control button 30 is capable of being actuated in four directions (e.g., a left, right, up and down).

With reference to FIGS. 1 and 2, the power handle 101 includes a main controller circuit board 142, a rechargeable battery 144 configured to supply power to any of the electrical components of handle assembly 100, and a plurality of motors 152 coupled to the battery 144. The power handle 101 also includes a display 146. In embodiments, the motors 152 may be coupled to any suitable power source configured to provide electrical energy to the motor 152, such as an AC/DC transformer. Each of the motors 152 is coupled a motor controller 143 which controls the operation of the corresponding motor 152 including the flow of electrical energy from the battery 144 to the motor 152. A main controller 147 is provided that controls the power handle 101. The main controller 147 is configured to execute software instructions embodying algorithms disclosed herein, such as clamping, stapling, and cutting algorithms which control operation of the power handle 101.

The motor controller 143 includes a plurality of sensors 408a . . . 408n configured to measure operational states of the motor 152 and the battery 144. The sensors 408a-n include a strain gauge 408b and may also include voltage sensors, current sensors, temperature sensors, telemetry sensors, optical sensors, and combinations thereof. The sensors 408a-408n may measure voltage, current, and other electrical properties of the electrical energy supplied by the battery 144. The sensors 408a-408n may also measure angular velocity (e.g., rotational speed) as revolutions per minute (RPM), torque, temperature, current draw, and other operational properties of the motor 152. The sensor 408a also includes an encoder configured to count revolutions or other indicators of the motor 152, which is then use by the main controller 147 to calculate linear movement of components movable by the motor 152. Angular velocity may be determined by measuring the rotation of the motor 152 or a drive shaft (not shown) coupled thereto and rotatable by the motor 152. The position of various axially movable drive shafts may also be determined by using various linear sensors disposed in or in proximity to the shafts or extrapolated from the RPM measurements. In embodiments, torque may be calculated based on the regulated current draw of the motor 152 at a constant RPM. In further embodiments, the motor controller 143 and/or the main controller 147 may measure time and process the above-described values as a function of time, including integration and/or differentiation, e.g., to determine the rate of change in the measured values. The main controller 147 is also configured to determine distance traveled of various components of the adapter assembly 200 and/or the end effector 300 by counting revolutions of the motor 152.

The motor controller 143 is coupled to the main controller 147, which includes a plurality of inputs and outputs for interfacing with the motor controller 143. In particular, the main controller 147 receives measured sensor signals from the motor controller 143 regarding operational status of the motor 152 and the battery 144 and, in turn, outputs control signals to the motor controller 143 to control the operation of the motor 152 based on the sensor readings and specific algorithm instructions. The main controller 147 is also configured to accept a plurality of user inputs from a user interface (e.g., switches, buttons, touch screen, etc. coupled to the main controller 147).

The main controller 147 is also coupled to a memory 141. The memory 141 may include volatile (e.g., RAM) and non-volatile storage configured to store data, including software instructions for operating the power handle 101. The main controller 147 is also coupled to the strain gauge 408b of the adapter assembly 200 using a wired or a wireless connection and is configured to receive strain measurements from the strain gauge 408b which are used during operation of the power handle 101.

The power handle 101 includes a plurality of motors 152 each including a respective motor shaft (not explicitly shown) extending therefrom and configured to drive a respective transmission assembly. Rotation of the motor shafts by the respective motors function to drive shafts and/or gear components of adapter assembly 200 in order to perform the various operations of handle assembly 100. In particular, motors 152 of power handle 101 are configured to drive shafts and/or gear components of adapter assembly 200 in order to selectively extend/retract a trocar member 274 (FIG. 4) of a trocar assembly 270 of adapter assembly 200. Extension/retraction of the trocar member 274 opens/closes end effector 300 (when anvil assembly 500 is connected to trocar member 274 of trocar assembly 270), fire an annular array of staples 423 of reload 400, and move an annular knife (not explicitly shown) of reload 400.

The reload 400 includes a storage device 402 configured to store operating parameters of the reload 400 including starting clamping force, maximum clamping force, a force factor, and the like. Each type of reload 400 may have a corresponding starting clamping force, which the main controller 147 may obtain automatically by reading the starting clamping force value from the storage device 402 and/or set manually by the user by selecting either the type of the reload 400 or the clamping force directly. Starting clamping force may be any suitable threshold from about 100 pounds to about 200 pounds, in embodiments, the target clamping force may be approximately 150 pounds. In embodiments, a 33 mm sized reload 400 may have a clamping force of about 150 lbs.

Turning now to FIGS. 3 and 4, adapter assembly 200 includes an outer knob housing 202 and an outer tube 206 extending from a distal end of knob housing 202. Knob housing 202 and outer tube 206 are configured and dimensioned to house the components of adapter assembly 200. The knob housing 202 includes an electrical connector 312 and a storage device 310 coupled thereto. The storage device 310 is configured to store various operating parameters pertaining to the adapter assembly 200. Adapter assembly 200 is configured to convert rotation of coupling shafts (not explicitly shown) of handle assembly 100 into axial translations useful for operating trocar assembly 270 of adapter assembly 200, anvil assembly 500, and/or staple driver 430 or knife assembly (not explicitly shown) of reload 400.

Adapter assembly 200 further includes the trocar assembly 270 removably supported in a distal end of outer tube 206. Trocar assembly 270 includes a trocar member 274 and a drive screw 276 operably received within trocar member 274 for axially moving trocar member 274 relative to outer tube 206. A distal end 274b of trocar member 274 is configured to selectively engage anvil assembly 500, such that axial movement of trocar member 274, via a rotation of drive screw 276, results in a concomitant axial movement of anvil assembly 500.

With reference to FIG. 4, a clamping transmission assembly 240 includes first rotatable proximal drive shaft 212 coupled to one of the motors 152, a second rotatable proximal drive shaft 281, a rotatable distal drive shaft 282, and a coupling member 286, each of which are supported within the outer tube 206 of adapter assembly 200. Clamping transmission assembly 240 functions to extend/retract trocar member 274 of trocar assembly 270 of adapter assembly 200, and to open/close the anvil assembly 510 when anvil assembly 510 is connected to trocar member 274.

With reference to FIG. 5, the adapter assembly 200 includes a stapling transmission assembly 250 for interconnecting one of the motors 152 and a second axially translatable drive member of reload 400, wherein the stapling transmission assembly 250 converts and transmits a rotation of one of the motors 152 to an axial translation of an outer flexible band assembly 255 of adapter assembly 200, and in turn, the staple driver 430 of reload 400 to fire staples 423 from the reload 400 and against anvil assembly 510.

The stapling transmission assembly 250 of adapter assembly 200 includes the outer flexible band assembly 255 secured to staple driver coupler 254. A second rotatable proximal drive shaft 220 is coupled to one of the motors 152 and is configured to actuate that staple driver coupler 254, which converts rotational movement into longitudinal movement. Outer flexible band assembly 255 includes first and second flexible bands 255a, 255b laterally spaced and connected at proximal ends thereof to a support ring 255c and at distal ends thereof to a proximal end of a distal pusher 255d. Each of first and second flexible bands 255a, 255b is attached to support ring 255c and distal pusher 255d. Outer flexible band assembly 255 further includes first and second connection extensions 255e, 255f extending proximally from support ring 255c. First and second connection extensions 255e, 255f are configured to operably connect outer flexible band assembly 255 to staple driver coupler 254 of stapling transmission assembly 250.

With reference to FIG. 6, staple driver 430 of reload 400 includes a staple cartridge 420 having a driver adapter 432 and a driver 434. A proximal end 432a of driver adapter 432 is configured for selective contact and abutment with distal pusher 255d of outer flexible band assembly 255 of stapling transmission assembly 250 of adapter assembly 200. In operation, during distal advancement of outer flexible band assembly 255, as described above, distal pusher 255d of outer flexible band assembly 255 contacts proximal end 432a of driver adapter 432 to advance driver adapter 432 and driver 434 from a first or proximal position to a second or distal position. Driver 434 includes a plurality of driver members 436 aligned with staple pockets 421 of staple cartridge 420 for contact with staples 423. Accordingly, advancement of driver 434 relative to staple cartridge 420 causes ejection of the staples 423 from staple cartridge 420.

Forces during an actuation of trocar member 274, closing of end effector 300 (e.g., a retraction of anvil assembly 500 relative to reload 400), and ejecting staples 423 from the reload 400, and advancement of the knife assembly 440 may be measured by the strain gauge 408b in order to monitor and control various processes, such as firing of staples 423 from reload 400; monitor forces during a firing and formation of the staples 423 as the staples 423 are being ejected from reload 400; optimize formation of the staples 423 (e.g., staple crimp height) as the staples 423 are being ejected from reload 400 for different indications of tissue; and monitor and control a firing of the annular knife of reload 400.

With reference to FIG. 7, the strain gauge 408b of adapter assembly 200 is disposed within a strain gauge housing 320. The strain gauge 408b measures and monitors the retraction of trocar member 274 as well as the ejection and formation of the staples 423 from the reload 400. During the closing of end effector 300, when anvil assembly 500 contacts tissue, an obstruction, a tissue-contacting surface of the reload 400, staple ejection, or the like, a reaction force is exerted on anvil assembly 500 which is in a generally distal direction. This distally directed reaction force is communicated from anvil assembly 500 to the strain gauge 408b. The strain gauge 408b then communicates signals to main controller circuit board 142 of power handle 101 of handle assembly 100. Graphics are then displayed on the display 146 of handle assembly 100 to provide the user with real-time status information.

The trocar assembly 270 is axially and rotationally fixed within outer tube 206 of adapter assembly 200. With reference to FIG. 6, adapter assembly 200 includes a support block 292 fixedly disposed within outer tube 206. The strain gauge housing 320 is disposed between the support block 292 and a connector sleeve 290. The reload 400 is removably coupled to the connector sleeve 290.

In operation, strain gauge 408b of adapter assembly 200 measures and monitors the retraction of trocar member 274, which passes through the strain gauge 408b. The strain gauge 408b of adapter assembly 200 also measures and monitors ejection of the staples 423 from the reload 400, since the first and second flexible bands 255a, 255b also pass through the strain gauge 408b. During clamping, stapling and cutting, a reaction force is exerted on anvil assembly 500 and the reload 400, which is communicated to support block 292, which then communicates the reaction force to a strain sensor of the strain gauge 408b.

Strain sensor of strain gauge 408b may be any device configured to measure strain (a dimensionless quantity) on an object that it is adhered to (e.g., support block 292), such that, as the object deforms, a metallic foil of the strain sensor is also deformed, causing an electrical resistance thereof to change, which change in resistance is then used to calculate loads experienced by trocar assembly 270. Strain gauge 408b provides a closed-loop feedback to a firing/clamping load exhibited by first, second and third force/rotation transmitting/converting assemblies.

Strain sensor of strain gauge 408b then communicates signals to main controller circuit board 142. Graphics are then displayed on display 146 of handle assembly 100 to provide the user with real-time information related to the status of the firing of handle assembly 100. Strain gauge 408b is also electrically connected to the electrical connector 312 (FIG. 3) via proximal and distal harness assemblies 314, 316.

For further details regarding the construction and operation of the circular stapler and its components, reference may be made to International Application Publication No. PCT/US2019/040440, filed on Jul. 3, 2019, the entire contents of which being incorporated by reference herein.

The user commences a surgical procedure by positioning the adapter assembly 200, including the trocar member 274 and the anvil assembly 510, within the colorectal or upper gastrointestinal region. The user presses the toggle control button 30 to extend the trocar member 274 until it pierces tissue. During operation, the anvil assembly 500 (after being positioned by surgeon at the tissue site where anastomosis is being performed) is attached to the trocar member 274 and the user begins the clamping process on the tissue interposed between reload 400 and the anvil assembly 500 by pressing on the bottom of the toggle control button 30. After extension of the trocar member 274, the anvil assembly 510 that was previously positioned by surgeon is attached to the trocar member 274. The surgeon then begins the clamping process on the tissue interposed between reload 400 and the anvil assembly 510 by pressing on the bottom portion of the toggle control button 30.

During clamping, the anvil assembly 500 is retracted toward the reload 400 until reaching a preset, fully clamped position (i.e., the fourth position 604). The preset clamped position varies for each of the different types of reloads. While clamping, the strain gauge 408b continuously provides measurements to the main controller 147 on the force imparted on the trocar member 274 as it moves the anvil assembly 500 to clamp tissue between the anvil assembly 500 and the reload 400.

FIG. 8 shows a clamping algorithm according to the present disclosure, which is described with reference to FIG. 9, which schematically illustrates the travel distance and speed of the anvil assembly 500 as it is retracted by the motor 152. The anvil assembly 500 is retracted, i.e., moved proximally, from a first fully open position 601 at a first speed for a first segment from the fully open position 601 to a second position 602, which is closer to the reload 400. This is done in response to user pressing the toggle control button 30. Thereafter, the anvil assembly 500 traverses proximally along a second segment from the second position 602 to a third position 603 at the second speed, which is slower than the first speed. As the anvil assembly 500 is traversing the second segment, the main controller 147 continuously verifies whether the measured force is within predefined parameters to determine if the measured force exceeds a high force threshold limit prior to reaching a starting compression distance. This measurement is used to detect obstruction, a mismatch between the anvil assembly 500 and the reload 400, and/or misalignment of the anvil assembly 500 with the reload 400. If the force is higher than the high force threshold, then the power handle 101 temporarily reverses the clamping transmission assembly 240 to retract the anvil assembly 500 to correct the misalignment. The main controller 147 then reattempts to continue clamping, i.e., moving the anvil assembly 500 proximally toward the reload 400, until a third position 603 is reached. If the third position 603 is not reached within a predetermined period of time, the main controller 147 then issues an error, including an alarm on the display screen 146 prompting the user to inspect the anvil assembly 500. After inspection and clearance of any obstruction, the user may then restart the clamping process.

Once the anvil assembly 500 reaches the third position 603, which is at the end of the second segment, the power handle 101 performs a rotation verification to check position of the anvil assembly 500. Then the main controller 147 commences a controlled tissue compression (“CTC”) algorithm. The CTC algorithm has two phases—the first CTC phase starts from the third position 603, during which the anvil assembly 500 is driven proximally to a fourth position 604 (i.e., a clamp gap position) at a varying speed based on a measured force.

Advancement of the anvil assembly 500 between the third position 603 and the fourth position 604 accounts for slow-changing and rapid-changing forces imparted on the tissue during compression with a second-order predictive force filter. As the predicted force approaches the target force, the clamping speed is slowed to prevent over-shoot. When the measured force reaches the target force and the clamp gap has not yet been achieved, clamping is stopped to allow for tissue relaxation. During tissue relaxation, after the measured force falls below the target clamping force, advancement recommences. The force exerted on tissue is derived from the strain measurements by the main controller 147 from the strain gauge 408b. This process continues until the fourth position 604 is reached.

Once the fourth position 604 has been reached, the anvil assembly 500 is advanced proximally to a fifth position 605, (i.e., extended clamp gap position or a zero gap position). The fifth position 605 may be adjusted based on a clamp offset distance, which may be read by the main controller 147 from a storage 310 of the adapter assembly 200. Before advancing the anvil assembly 500 to the fifth position 605, after reaching the fourth position 604, the anvil assembly 500 may be stopped temporarily, which may be from about 0.5 seconds to about 2 seconds. The distance between the fourth position 604 to the fifth position 605 may be from about 0.002″ to about 0.02″. The anvil assembly 500 is advanced proximally to the fifth position 605 based on measured force in the same manner as the clamping between the third position 603 and the fourth position 604. In particular, the anvil assembly 500 may be advanced from the fourth position 604 to the fifth position 605 using the same force feedback as used to advance to the fourth position 604.

Once the fifth position 605 is reached, a notification that the fifth position 605 has been reached may be displayed on the display 146 and audio tones may be output by the power handle 101. The anvil assembly 500 is maintained at the fifth position 605 for a predetermined period of time, which may be from about 1 second to about 12 seconds and in embodiments, may be from about 2 seconds to about 6 seconds. The anvil assembly 500 maintains a preset force on the tissue, which may be from about 80 lbs. to about 150 lbs., which in embodiments may be about 105 lbs.

Once the preset time has expired, the anvil assembly 500 is moved distally from the sixth position 606 to the fifth position 605. Maintaining the preset force for the preset time, followed by relaxation, i.e., distal of the anvil assembly back to the fifth position 605, results in decreased clamp force by leveraging tissue hysteresis, which is a material phenomenon whereby the stored mechanical energy is dissipated more rapidly during unclamping than during clamping.

The powered surgical stapler 10 is also configured to measure tissue thickness as the anvil assembly 500 travels from second position 602 to the fourth position 604 at a constant speed, i.e., a first phase, and during the CTC phase, i.e., second phase. The main controller 147 is configured to execute a tissue thickness measuring algorithm as shown in FIG. 10. The tissue thickness measuring algorithm continuously monitors force that is measured by the strain gauge 408b during the clamping process. The force is measured continuously at a preset rate, which may be from about 10 ms to about 500 ms. During this phase, the force is monitored to determine if the measured force is equal to a target force. The target force is based on optimal force for determining tissue thickness. The target force may be stored in the storage device 402 and may be specific to the reload 400 that is being used. The storage device 402 may also store other parameters pertaining to the reload 400, including timeout, correction factor.

If the measured force is equal to a target force, then the main controller 147 logs the distance at which the target force was measured. The distance is measured relative to fifth position 605 (i.e., zero gap) and may be expressed as inches or mm. This distance is indicative of tissue thickness being clamped. The distance may be stored in the memory 141 and may be displayed on the display 146. If the measured force does not reach the target force an error may be output on the display 146 since this would be indicative of a lack of sufficient tissue being clamped. The main controller 147 may prompt the user to attempt to re-clamp and attempt force detection again.

The target force and the distance may be displayed using any suitable message, such as “[force] lbs. detected [distance] inches from zero gap,” where the [force] is the target force and the [distance] is the measured distance. Thus, the strain gauge 408b and distance calculation capabilities of the main controller 147 allow the powered surgical stapler 10 to accurately measure tissue thickness under precise pressure (i.e., force applied during clamping).

Upon reaching the target force, the anvil assembly 500 is held in place while maintaining the target force on the tissue by pulsing the motor 152 as tissue relaxes. Once the target force has been maintained for a preset time period, the distance to the main controller 147 logs the distance. Measuring the distance following tissue relaxation allows for a more accurate tissue thickness measurement by removing fluctuations in tissue thickness.

Once the measured force matching the target force has been detected during clamping from the second position 602 to the fourth position 604, the main controller 147 also stops looking for the force matching the target force (i.e., comparing the measured force to the target force) unless the user stops the clamping process, which may occur in response to the user pressing the “open” key of the toggle control button 30. When clamping resumes, the main controller 147 restarts looking for the measured force matching the target force. The main controller 147 may also output on the display 146 a message whether force detection is in progress (e.g., “Detection ON” or “Detection OFF”).

Tissue thickness is also be measured during a second phase, namely, the CTC phase (see FIG. 8). During the CTC phase the anvil assembly 500 is moved at a varying speed based on the measured force. Upon reaching the fourth position 604, at which CTC phase commences, a timer is initialized, i.e., set to zero. The CTC phase includes clamping tissue while maintaining the target force, which as noted above may be retrieved by the main controller 147 from the storage device 402 of the reload 400. This target force is maintained while the anvil assembly 500 is retracted toward the fifth position 605 until the timer reaches a preset time, which may also be stored in the storage device 402 and retrieved by the main controller 147.

If, after the timeout, i.e., measured time exceeds the preset time, the measured force as measured by the strain gauge 408b is higher than the target force, the target force is then updated to be the measured force. The main controller 147 may output on the display 146 a message that a timeout has occurred and target force is being updated (e.g., “Timeout elapsed, taking measurement . . . ”). The main controller 147 may also display the correction factor read from the storage device 402 and a corresponding distance at which the correction factor is to be applied (e.g., “Reload correction . . . Original distance . . . ”). This correction factor may be a negative or positive value and may be added to the distance between the fifth position 605 and the point at which the target force was measured during the CTC phase. The preset time acts as a stabilization time period, during which pressure is maintained on the clamped tissue while fluids are exuded from the clamped tissue. The target pressure is also maintained during the preset time period, prior to logging the force measurements (e.g., distance to fifth position 605).

The main controller 147 may also display the new target force and the distance at which the new target force was measured relative to the fifth position 605, i.e., the distance at which the timeout has occurred. The new target force and the distance may be displayed using any suitable message, such as “[force] lbs. detected after [time], [distance] inches from zero gap,” where the [force] is the target force, [time] is the time at which the force measurement occurred, 8 and the [distance] is the measured distance.

After updating the target force, the main controller 147 stops looking for the force matching the target force (i.e., comparing the measured force to the target force) unless the users stops the clamping process, which may occur in response to the user pressing the “open” key of the toggle control button 30. When clamping resumes, the main controller 147 begins looking for the measured force matching the target force. The main controller 147 may output on the display 146 a message whether force detection is in progress (e.g., “Detection ON” or “Detection OFF”).

After updating the target force, the main controller 147 also stops the motor 152 and thereby, the movement of the anvil assembly 500. In addition, the main controller 147 may output an audio (e.g., multiple beeps) and/or visual indication on the display 146. The main controller 147 also resets the target force to a default force value, which may be a customary clinical value of about 15 lbs. After the second tissue thickness measurement, the clamping algorithm may continue as described above in FIG. 8.

After clamping is complete, the main controller 147 signals that tissue clamping was successful. Once clamping is successfully completed, the user initiates the stapling sequence. To initiate stapling sequence, the user presses one of the safety buttons 36 of the power handle 101, which acts as a safety and arms the toggle control button 30, allowing it to commence stapling. The user then presses down on the toggle control button 30, which moves the second rotation transmitting assembly 250 to convert rotation to linear motion and to eject and form staples from circular reload 400.

It will be understood that various modifications may be made to the embodiments of the presently disclosed powered surgical staplers. Therefore, the above description should not be construed as limiting, but merely as exemplifications of embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the present disclosure.

In one or more examples, the described techniques may be implemented in hardware, software, firmware, or any combination thereof. If implemented in software, the functions may be stored as one or more instructions or code on a computer-readable medium and executed by a hardware-based processing unit. Computer-readable media may include non-transitory computer-readable media, which corresponds to a tangible medium such as data storage media (e.g., RAM, ROM, EEPROM, flash memory, or any other medium that can be used to store desired program code in the form of instructions or data structures and that can be accessed by a computer).

Instructions may be executed by one or more processors, such as one or more digital signal processors (DSPs), general purpose microprocessors, application specific integrated circuits (ASICs), field programmable logic arrays (FPGAs), or other equivalent integrated or discrete logic circuitry. Accordingly, the term “processor” as used herein may refer to any of the foregoing structure or any other physical structure suitable for implementation of the described techniques. Also, the techniques could be fully implemented in one or more circuits or logic elements.

Claims

1. A surgical device comprising: a motor;a reload including a plurality of staples;an anvil assembly movable relative to the reload by the motor to clamp tissue therebetween;a force sensor configured to measure force imparted on the anvil assembly; anda controller configured to: compare the measured force to a target force;determine a distance at which the measured force matches the target force; andoutput the distance and the target force.

2. The surgical device according to claim 1, wherein the reload includes a storage device configured to store the target force.

3. The surgical device according to claim 1, further comprising a display.

4. The surgical device according to claim 3, wherein the controller is further configured to output the distance at which the measured force matches the target force and the target force on the display.

5. The surgical device according to claim 4, wherein the controller is further configured to: maintain a timer; andupdate the target force to the measured force obtained at expiration of the timer.

6. The surgical device according to claim 5, wherein the controller is further configured to: determine a distance at which the target force was updated.

7. The surgical device according to claim 6, wherein the controller is further configured to output an expiration time of the timer, the distance at which the target force was updated, and the target force on the display.

8. The surgical device according to claim 6, wherein the controller is further configured to pulse the motor to maintain the target force prior to determining the distance.

9. The surgical device according to claim 8, wherein the controller is further configured to maintain the target force for a preset time period.

10. A surgical device comprising: a motor;a reload including a plurality of staples;an anvil assembly movable relative to the reload by the motor to clamp tissue therebetween in a first phase and a second phase;a force sensor configured to measure force imparted on the anvil assembly; anda controller coupled to the motor and the force sensor, during the first phase, the controller is configured to: compare the measured force to a target force;determine a distance at which the measured force matches the target force; andoutput the distance and the target force.

11. The surgical device according to claim 10, wherein during the first phase the anvil assembly is moved at a constant speed.

12. The surgical device according to claim 10, wherein during the second phase the anvil assembly is moved at a varying speed.

13. The surgical device according to claim 10, wherein the reload includes a storage device configured to store the target force.

14. The surgical device according to claim 10, further comprising a display.

15. The surgical device according to claim 14, wherein the controller is further configured to output the distance at which the measured force matches the target force and the target force on the display.

16. The surgical device according to claim 15, wherein during the second phase, the controller is further configured to: maintain a timer; andupdate the target force to the measured force obtained at expiration of the timer.

17. The surgical device according to claim 16, wherein the controller is further configured to: determine a distance at which the target force was updated.

18. The surgical device according to claim 17, wherein the controller is further configured to output an expiration time of the timer, the distance at which the target force was updated, and the target force on the display.

19. The surgical device according to claim 17, wherein the controller is further configured to pulse the motor to maintain the target force prior to determining the distance.

20. The surgical device according to claim 19, wherein the controller is further configured to maintain the target force for a preset time period.