Method for reducing or removing biofilm
A method for reducing or removing biofilm on a target tissue or prosthesis surface includes providing a coupling space or antechamber between the operative tip or end of an ultrasonic probe and a target treatment surface, the space or antechamber being fillable with a liquid irrigant to transmit ultrasonic vibration and facilitate extraction of biofilm fragments including potentially pathogenic particles. A second phase of treatment in the case of organic tissue involves the attachment of one or more ultrasonic transducers to a patient over or near a surgical treatment site after surgery is terminated. Each applied ultrasonic transducer is used to vibrate the patient's tissues at the treatment site to disrupt biofilm formation.
1. A medical therapeutic method comprising:
providing an ultrasonic debridement instrument having a probe with an operative tip and a first channel, said instrument including a sheath or sleeve with a distal tip, said sheath or sleeve defining a second channel extending outside said probe, said second channel having an inlet proximate said distal tip;
manipulating said instrument to place said distal tip against a target surface, said sheath or sleeve extending in part distally of said operative tip and serving in part to maintain a spacing between said operative tip and the target surface, whereby the manipulating of said instrument to place said distal tip against the target surface inherently positions said operative tip at a distance from the target surface and defines or encloses an ultrasound coupling space or antechamber between said operative tip and the target surface;
during contact of said distal tip with the target surface, feeding an irrigation fluid through said first channel to said ultrasound coupling space or antechamber between said operative tip and the target surface;
also during contact of said distal tip with the target surface, generating an ultrasonic standing wave in said probe to vibrate said operative tip and thereby fragment undesired material at or on the target surface; and
during the generating of said ultrasonic standing wave, applying vacuum or negative pressure to said second channel to remove fluid from the target surface.
2. The method defined in claim 1 wherein said sheath or sleeve is longitudinally shiftable relative to said probe, further comprising shifting said sheath or sleeve in a proximal direction along said instrument prior to the manipulating of said instrument to place said distal tip against the target surface.
3. The method defined in claim 2 wherein said second channel is located between said sheath or sleeve and said probe of said instrument, further comprising: shifting said sheath or sleeve in a proximal direction after the generating of said ultrasonic standing wave; and thereafter applying a vacuum or negative pressure to said second channel to suck ambient air into and through said second channel.
4. The method defined in claim 1 wherein the target surface is tissue of a patient.
5. The method defined in claim 1 wherein said irrigation fluid includes hypochlorous acid, further comprising electrolytically generating the hypochorous acid on site.
6. A medical therapeutic method comprising:
providing an ultrasonic debridement instrument having aerobe with an operative tip and a first channel, said instrument including a sheath or sleeve with a distal tip, said sheath or sleeve defining a second channel extending outside said probe, said second channel having an inlet proximate said distal tip;
manipulating said instrument to place said distal tip against a target surface, said sheath or sleeve extending in part distally of said operative tip and serving in part to maintain a spacing between said operative tip and the target surface, whereby the manipulating of said instrument to place said distal tip against the target surface inherently positions said operative tip at a distance from the target surface;
during contact of said distal tip with the target surface, feeding an irrigation fluid through said first channel to a region between said operative tip and the target surface;
also during contact of said distal tip with the target surface, generating an ultrasonic standing wave in said probe to vibrate said operative tip and thereby fragment undesired material at or on the target surface; and
during the generating of said ultrasonic standing wave, applying vacuum or negative pressure to said second channel to remove fluid from the target surface,
wherein the target surface is a hard surface.
7. The method defined in claim 6 wherein the target surface is a surface of a prosthesis.
8. The method defined in claim 6 wherein the target surface is a surface of a surgical instrument.
9. A surgical device comprising:
an ultrasonic probe having an operative tip and a first channel extending longitudinally therein;
an electromechanical transducer operatively connected to said probe for generating an ultrasonic standing wave in said probe to vibrate said operative tip at ultrasonic frequency; and
at least one sheath or sleeve disposed about said probe and defining a second channel outside said probe, said second channel having at least a first port in a region about a distal end of said probe, proximate said operative tip, said sheath or sleeve having an operative configuration wherein a distal end portion of said sheath or sleeve extends distally beyond said operative tip of said probe to define an ultrasound coupling space between said operative tip and a target surface.
10. The surgical device defined in claim 9 wherein said sheath or sleeve is longitudinally slidable relative to said probe to shift between a distal position in said operative configuration and a proximal position.
11. The surgical device defined in claim 10 wherein said probe and said sheath or sleeve define a first space or channel and a second space or channel, said second space or channel being located proximally of said first space or channel and having a larger transverse cross-sectional area, in a plane orthogonal to an axis of said probe, than said first space or channel.
12. The surgical device defined in claim 11 wherein said probe is provided at or in a distal end portion with at least one aperture communicating with said first space or channel, said sheath being provided with an aspiration arm having an aspiration channel communicating with said first space or channel and said second space or channel.
13. The surgical device defined in claim 12 wherein said probe includes a proximal body section, a smaller-diameter horn section, and a probe head, the horn section extending distally of said body section, said head being formed at a distal end of said horn section.
14. The surgical device defined in claim 10 wherein said sheath or sleeve is configured to shift between a distal-most position wherein said probe head is covered and a proximal-most position wherein at least a portion of said probe head is exposed.
15. The surgical device defined in claim 9 wherein said distal end portion of said sheath or sleeve is formed with a plurality of longitudinally extending fingers separated by gaps or spaces.
16. The surgical device defined in claim 9 wherein said distal end portion of said sheath or sleeve has a distal-most edge and is provided with at least one aperture in a sidewall, said aperture being spaced from said edge.