Fiber Optic Medical Systems and Devices with Atraumatic Tip

Abstract

Disclosed herein are medical systems and devices that include an elongate probe configured for insertion into a patient, where the elongate probe includes an atraumatic tip and where the atraumatic tip includes one or more of a loop, a curl, coil, a flexible distal tip section, a steerable distal tip section, a distal tip section configured to transition away from a first shape toward a second shape upon insertion of the elongate probe within the patient. The optical fiber includes sensing core fibers configured to facilitate a determination of a physical state of the elongate probe. The elongate probe is also configured to project illuminating light away from a distal end and receive imaging light at the distal end.

Description

Claims

1. A medical system comprising: a medical device comprising: an elongate probe configured for insertion into a patient body, the elongate probe including a lumen extending along the elongate probe between a proximal end and a distal end;an optical fiber disposed within the lumen; andan atraumatic tip at the distal end, wherein: the atraumatic tip defines two or more patient contact surfaces disposed along a distal tip section of the elongate probe, anda lateral separation distance between any two of the two or more patient contact surfaces is greater than a diameter of the elongate probe; anda console operatively coupled with the medical device at the proximal end, the console including a light source, an optical receiver, one or more processors, and a non-transitory computer-readable medium having stored thereon logic that, when executed by the one or more processors, causes operations that include at least one of projecting light away from the distal end of the elongate probe or determining a physical state of the elongate probe within the patient body.

2. The system of claim 1, wherein the distal tip section is formed into a loop to define the atraumatic tip.

3. The system of claim 1, wherein the atraumatic tip includes a coil member having a number of windings wrapped around the distal tip section.

4. The system of claim 1, wherein the distal tip section is formed into a curl to define the atraumatic tip, the curl having a number of windings wrapped around a winding axis oriented perpendicular to a longitudinal axis of the elongate probe.

5. The system of claim 1, wherein the distal tip section is radially expanded to define the atraumatic tip, the radial expansion defining a diameter greater than the diameter of the elongate probe.

6. The system of claim 5, wherein the radial expansion defines a bulbous shape.

7. The system of claim 1, wherein the atraumatic tip defines an attachment between the elongate probe and the optical fiber.

8. The system of claim 1, wherein the distal tip section defines a greater flexibility in bending than a main probe section, the main probe section extending proximally away from the distal tip section.

9. The system of claim 8, wherein: the distal tip section includes a varying flexibility in bending along a length of the distal tip section,the varying flexibility includes a first flexibility in bending adjacent a proximal end of the distal tip section transitioning toward a second flexibility in bending adjacent a distal end of the distal tip section, andthe second flexibility in bending is greater than the first flexibility in bending.

10. The system of claim 1, wherein: the elongate probe includes an actuator adjacent the proximal end;the actuator is operatively coupled with the distal tip section; andthe actuator is configured to cause the distal tip section to laterally deflect between a first shape and a second shape based on manipulation of the actuator by a clinician, the second shape different from the first shape.

11. The system of claim 1, wherein: the distal tip section includes a shape memory material having a shape transition temperature between about 20° C. and 37° C.,distal tip section defines a first transition shape below the transition temperature and a second transition shape above the transition temperature, andthe second transition shape is different from the first transition shape.

12. The system of claim 1, wherein: the optical fiber includes one or more of core fibers extending along a longitudinal length of the optical fiber, each of the one or more core fibers including a plurality of sensors distributed along the longitudinal length and each sensor of the plurality of sensors being configured to (i) reflect a light signal of a different spectral width based on received incident light at proximal end, and (ii) change a characteristic of the reflected light signal based on condition experienced by the optical fiber;the operations include determining the physical state;determining the physical state includes: providing an incident light signal to the optical fiber;receiving reflected light signals of different spectral widths of the incident light by one or more of the plurality of sensors; andprocessing the reflected light signals associated with the one or more of core fibers to determine the physical state; andthe physical state includes one or more of a three-dimensional (3D) shape of the elongate probe, a temperature experienced by the elongate probe, a pressure exerted on the elongate probe, or a fluid flow adjacent the elongate probe.

13. The system of claim 1, wherein the optical fiber further includes: one or more illuminating core fibers, each of the one or more illuminating core fibers configured to receive illuminating light from the console at the proximal end and project the illuminating light away from the distal end; andone or more imaging core fibers, each of the one or more imaging core fibers configured to receive imaging light at the distal end and propagate the imaging light along the optical fiber from the distal end to the console.

14. A medical system comprising: a medical device comprising: an elongate probe configured for insertion into a patient body, the elongate probe including a lumen extending along the elongate probe between a proximal end and a distal end;an optical fiber disposed within the lumen; andan atraumatic tip at the distal end, the atraumatic tip including a distal tip section that has a greater flexibility in bending than a main probe section, the main probe section extending proximally away from the distal tip section; anda console operatively coupled with the medical device at the proximal end, the console including a light source, an optical receiver, one or more processors, and a non-transitory computer-readable medium having stored thereon logic that, when executed by the one or more processors, causes operations that include at least one of projecting light away from the distal end of the elongate probe or determining a physical state of the elongate probe within the patient body.

15. The system of claim 14, wherein: the distal tip section includes a varying flexibility in bending along a length of the distal tip section,the varying flexibility includes a first flexibility in bending adjacent a proximal end of the distal tip section transitioning toward a second flexibility in bending adjacent a distal end of the distal tip section, andthe second flexibility in bending is greater than the first flexibility in bending.

16. The system of claim 14, wherein: the elongate probe includes an actuator adjacent the proximal end;the actuator is operatively coupled with the distal tip section; andthe actuator is configured to cause the distal tip section to laterally deflect between a first shape and a second shape based on manipulation of the actuator by a clinician, the second shape different from the first shape.

17. The system of claim 14, wherein: the distal tip section includes a shape memory material having a shape transition temperature between about 20° C. and 37° C.,distal tip section defines a first transition shape below the transition temperature and a second transition shape above the transition temperature, andthe second transition shape is different from the first transition shape.

18. The system of claim 14, wherein the atraumatic tip includes a loop formed along a portion of the distal tip section.

19. The system of claim 14, wherein the atraumatic tip includes a coil member having a number of coil windings wrapped around the distal tip section.

20. The system of claim 14, wherein the atraumatic tip includes a curl formed along a portion of the distal tip section, the curl having a number of curl windings wrapped around a winding axis oriented perpendicular to a longitudinal axis of the distal tip section.

21. The system of claim 14, wherein the atraumatic tip includes a radially expanded portion of the distal tip section, the radially expanded portion defining a diameter greater than a diameter of the elongate probe.

22. The system of claim 14, wherein the atraumatic tip defines an attachment between the elongate probe and the optical fiber.

23. The system of claim 14, wherein: the optical fiber includes one or more of core fibers extending along a longitudinal length of the optical fiber, each of the one or more core fibers including a plurality of sensors distributed along the longitudinal length and each sensor of the plurality of sensors being configured to (i) reflect a light signal of a different spectral width based on received incident light at proximal end, and (ii) change a characteristic of the reflected light signal based on condition experienced by the optical fiber;the operations include determining the physical state;determining the physical state includes: providing an incident light signal to the optical fiber;receiving reflected light signals of different spectral widths of the incident light by one or more of the plurality of sensors; andprocessing the reflected light signals associated with the one or more of core fibers to determine the physical state; andthe physical state includes one or more of a three-dimensional (3D) shape of the elongate probe, a temperature experienced by the elongate probe, a pressure exerted on the elongate probe, or a fluid flow adjacent the elongate probe.

24. The system of claim 14, wherein the optical fiber further includes: one or more illuminating core fibers, each of the one or more illuminating core fibers configured to receive illuminating light from the console at the proximal end and project the illuminating light away from the distal end; andone or more imaging core fibers, each of the one or more imaging core fibers configured to receive imaging light at the distal end and propagate the imaging light along the optical fiber from the distal end to the console.