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| United States Patent | 5009658 |
| Link to this page | http://www.wikipatents.com/5009658.html |
| Inventor(s) | Damgaard-Iversen; Karsten (Marietta, GA);
Morris; Robert C. (Morris County, NJ);
Chin; Timothy C. (Hunterdon County, NJ);
Kuper; Jerry W. (Somerset County, NJ) |
| Abstract | Method and apparatus are provided for laser lithotripsy by subjecting
calcified matter in the mammalian body, especially the human body, to two
spatially and temporally overlapping pulsed laser light beams in the
300-450 and 600-900 nanometer wavelength range. |
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Title Information  |
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Drawing from US Patent 5009658 |
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Dual frequency laser lithotripter |
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| Publication Date |
April 23, 1991 |
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| Filing Date |
April 14, 1989 |
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Title Information  |
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References  |
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| Market Size |
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| Reasonable Royalty |
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Public's "Guesstimation" of Royalty Value
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Market Review  |
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Technical Review  |
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Claims  |
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We claim:
1. A laser lithotripter system comprising, in combination:
a source of pulsed coherent radiation having a wavelength in the range of
from about 300 to about 450 nm, at an energy level of from about 2 to
about 30 mJ;
a source of pulsed coherent radiation having a wavelength from about 600 to
about 900 nm, at an energy level of from about 15 to about 100 mJ,
said pulses of coherent radiation achieving temporal overlap; an endoscopic
delivery system; and
mirror means for focusing said temporally overlapping pulses of coherent
radiation in spatially overlapped relationship into said endoscopic
delivery system for delivery to calcified matter located within a
mammalian body.
2. The laser lithotripter system of claim 1, wherein said source of pulsed
coherent radiation having a wavelength in the range of from about 600 to
about 900 nm comprises, at least, a first laser, and wherein said source
of pulsed coherent radiation in the wavelength range of from about 300 to
about 450 nm comprises, at least, means for frequency doubling the basic
laser output of said first laser.
3. The laser lithotripter system of claim 2, wherein said frequency
doubling means of said source of pulsed coherent radiation in the
wavelength range of from about 300 to about 450 nm comprises, at least, a
nonlinear crystal.
4. The laser lithotripter system of claim 2, further comprising, at least,
a first Q-Switch device associated with said source of pulsed coherent
radiation having a wavelength in the range of from about 600 to about 900
nm.
5. The laser lithotripter system of claim 4, further comprising at least a
second Q-Switch device associated with said source of pulsed coherent
radiation having a wavelength in the range of from about 300 to about 450
nm.
6. The laser lithotripter of claim 2, wherein said first laser is an
alexandrite laser.
7. The laser lithotripter system of claim 1, wherein said endoscopic
delivery system comprises, at least, a fiber-optic cable.
8. The laser lithotripter system of claim 1, wherein said mirror means
comprises means for focusing said temporally overlapping pulses of
coherent radiation in a completely spatially overlapped relationship into
said endoscopic delivery system.
9. The laser lithotripter system of claim 1, wherein said mirror means
comprises, at least, a front surface mirror.
10. The laser lithotripter system of claim 1, wherein said source of pulsed
coherent radiation having a wavelength in the range of from about 600 to
about 900 nm comprises, at least, a first laser, and wherein said source
of pulsed coherent radiation in the wavelength range of from about 300 to
about 450 nm comprises, at least, an independent, second laser.
11. A method for fragmentation of calcified matter in the mammalian body,
which method comprises the steps of:
initiating plasma sparking in the calcified matter by subjecting the
surface of the calcified matter to a first beam having a wavelength in the
range of from about 300 nanometers to about 450 nanometers; and
subjecting the calcified matter to a second beam having a wavelength in the
range of from about 600 nanometers to about 900 nanometers, the second
beam spatially and temporally overlapping the first beam.
12. Method of claim 11, wherein the step of subjecting the calcified matter
to a second beam comprises, at least, the step of:
subjecting the calcified matter to a second beam having a wavelength in the
range of from about 600 nanometers to about 900 nanometers, the second
beam being spatially and temporally coincident with the first beam.
13. The method of claim 11, wherein said first and second beams are pulsed.
14. The method of claim 13, wherein the initiating step further comprises
the step of subjecting the calcified matter to a first beam having an
energy level in the range of from about 2 to about 30 mJ; and wherein the
subjecting step further comprises the step of subjecting the calcified
matter to a second beam having an energy level of about 15 to about 100
mJ.
15. The method of claim 14, wherein the mammalian body is a human, and
wherein the initiating step further comprises the step of subjecting the
calcified body to a first beam having pulse durations of from about 50
nanoseconds (ns) to about 300 ns, and wherein the subjecting step further
comprises the step of subjecting the calcified body to a second beam
having pulse durations of from about 50 nanoseconds (ns) to about 300 ns.
16. The method of claim 11, wherein the mammalian body is a human body.
17. The method of claim 11, wherein the mammalian body is a human body, and
wherein the method further comprises the steps of generating the second
beam by a laser, and frequency doubling at least a portion of the second
beam to create the first beam.
18. The method of claim 17, wherein the step of generating the second beam
by a laser comprises the step of generating the second beam by an
alexandrite laser.
19. The method of claim 17, wherein the step of generating the second beam
further comprises the step of Q-switching the laser; and wherein the
method further comprises the steps of:
developing the first and second beams with energy levels in the range of
from about 2 to about 30 mJ and of from about 15 to about 100 mJ,
respectively; and
developing the first and second beams with pulse durations of from about 50
nanoseconds (ns) to about 300 ns.
20. The method of claim 17, wherein the generating step further comprises
the step of generating the first beam with a wavelength in the range of
from about 365 nm to about 390 nm; and
generating the second beam with a wavelength of from about 730 nm to about
780 nm.
21. The method of claim 11, wherein the mammalian body is a human body, and
wherein the method further comprises the steps of generating the first
beam by a first laser and generating the second beam by an independent
second laser.
22. The method of claim 21, wherein the step of generating the first beam
further comprises the steps of:
Q-switching the first laser;
generating the first beam with energy levels in the range of from about 2
to about 30 mJ; and
generating the first beam with pulse durations of from about 50 nanoseconds
(ns) to about 300 ns; and wherein the step of generating the second beam
further comprises the steps of:
Q-switching the second laser;
generating the second beam with energy levels in the range of from about 15
to about 100 mJ; and
generating the second beam with pulse durations of from about 50
nanoseconds (ns) to about 300 ns.
23. The method of claim 21, wherein the generating steps further comprises
the steps of:
generating the first beam with a wavelength in the range of from about 365
nm to about 390 nm; and
generating the second beam with a wavelength of from about 730 nm to about
780 nm.
24. The method of claim 21, wherein the step of generating the second beam
comprises the step of generating the second beam by an independent,
alexandrite laser.
25. A method of fragmentation of calcified matter in the mammalian body,
which method comprises the steps of:
initiating plasma sparking in the calcified matter and creating an acoustic
wave by subjecting the surface of the calcified matter to a first beam
having a wavelength in the range of from about 300 nanometers to about 450
nanometers; and
subjecting the calcified matter to a second beam having a wavelength in the
range of from about 600 nanometers to about 900 nanometers, the energy of
the second beam being absorbed by the plasma and thereby amplifying the
plasma sparking,
whereby the calcified matter is fragmented.
26. Method of claim 25, wherein the step of subjecting the calcified matter
to a second beam comprises, at least, the step of:
subjecting the calcified matter to a second beam having a wavelength in the
range of from about 600 nanometers to about 900 nanometers, the second
beam being spatially and temporally coincident with the first beam.
27. The method of claim 25, wherein said first and second beams are pulsed.
28. The method of claim 27, wherein the initiating step further comprises
the step of subjecting the calcified matter to a first beam having an
energy level in the range of from about 2 to about 30 mJ; and wherein the
subjecting step further comprises the step of subjecting the calcified
matter to a second beam having an energy level of about 15 to about 100
mJ.
29. The method of claim 28, wherein the mammalian body is a human, and
wherein the initiating step further comprises the step of subjecting the
calcified body to a first beam have pulse durations of from about 50
nanoseconds (ns) to about 300 ns, and wherein the subjecting step further
comprises the step of subjecting the calcified body to a second beam have
pulse durations of from about 50 nanoseconds (ns) to about 300 ns.
30. The method of claim 25, wherein the mammalian body is a human body.
31. The method of claim 25, wherein the mammalian body is a human body, and
wherein the method further comprises the steps of generating the second
beam by a laser, and frequency doubling at least a portion of the second
beam to create the first beam.
32. The method of claim 31, wherein the step of generating the second beam
by a laser comprises the step of generating the second beam by an
alexandrite laser.
33. The method of claim 31, wherein the step of generating the second beam
further comprises the step of Q-switching the laser; and wherein the
method further comprises the steps of:
developing the first and second beams with energy levels in the range of
from about 2 to about 30 mJ and of from about 15 to about 100 mJ,
respectively; and
developing the first and second beams with pulse durations of from about 50
nanoseconds (ns) to about 300 ns.
34. The method of claim 31, wherein the generating step further comprises
the step of generating the first beam with a wavelength in the range of
from about 365 nm to about 390 nm; and
generating the second beam with a wavelength of from about 730 nm to about
780 nm.
35. The method of claim 25, wherein the mammalian body is a human body, and
wherein the method further comprises the steps of generating the first
beam by a first laser and generating the second beam by an independent
second laser.
36. The method of claim 35, wherein the step of generating the first beam
further comprises the steps of:
Q-switching the first laser;
generating the first beam with energy levels in the range of from about 2
to about 30 mJ; and
generating the first beam with pulse durations of from about 50 nanoseconds
(ns) to about 300 ns; and wherein the step of generating the second beam
further comprises the steps of:
Q-switching the second laser;
generating the second beam with energy levels in the range of from about 15
to about 100 mJ; and
generating the second beam with pulse durations of from about 50
nanoseconds (ns) to about 300 ns.
37. The method of claim 35, wherein the generating steps further comprise
the steps of:
generating the first beam with a wavelength in the range of from about 365
nm to about 390 nm; and
generating the second beam with a wavelength of from about 730 nm to about
780 nm.
38. The method of claim 35, wherein the step of generating the second beam
comprises the step of generating the second beam by an independent,
alexandrite laser. |
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Claims  |
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Description  |
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FIELD OF THE INVENTION
The present invention relates generally to laser lithotripsy, and more
particularly to an improved laser lithotripter comprising a dual
wavelength pulsed laser for fragmentation of calcified matter in the human
body such as biliary and urinary calculi.
BACKGROUND OF THE INVENTION
One method of laser lithotripsy known in the art is that disclosed in PCT
Publication No. WO 86/6269 of Furumoto et al. Furumoto discusses the use
of a laser lithotripter delivering pulsed laser light at a single
wavelength in the 350-550 nanometer (nm) range. Although Furumoto
contemplates use of pulse energy levels in the range of 5 -200 millijoules
(mJ), in practice the energy range for achieving effective fragmentation
is in the order of 20-200 mJ. Furumoto's wavelength of 350 -550 nm lies
within a range of significant energy absorption by water and hemoglobin,
and thus poses risk of damage to the surrounding tissue during treatment.
Further, while in its preferred embodiment operating at a wavelength of
504 nm and pulse energy levels of 30-60 mJ, this modality is effective for
fragmentation of many urinary and biliary calculi, however, cystine
stones, brushite stones, as well as certain calciumoxalate monohydrate and
uric acid stones cannot be treated without the use of undesirably higher
pulse energy levels and/or shorter wavelengths.
We have investigated the use of a Q-switched alexandrite laser lithotripter
to address tissue damage concerns. In our experiments the laser
lithotripter delivered pulsed laser light in the wavelength range of
730-780 nm, where the energy absorption by hemoglobin and water is
significantly lower than in the 350-550 nm range. This lithotripter was
capable of generating energy in the 0-300 mJ range; in practice, the
energy range which is effective for stone fragmentation is in the order of
30-120 mJ. A detailed in vitro study of the Q-switched alexandrite laser
lithotripter has disclosed that the energy threshold for achieving the
plasma sparking at the surface of the targeted calculi, which is the
driving force in the fragmentation process, is undesirably high for many
stone compositions. By plasma sparking we mean the initiation of
dielectric breakdown of the targeted material, a process which includes
the emission of a bright flash of white light and the launching of an
audible acoustic wave. Indeed, the pulse energy levels and associated peak
power densities required to achieve plasma sparking in certain stone
compositions exceeds the transmission capabilities of the fused silica
fibers preferably used for clinical laser lithotripsy and generates
violent forces which propel the calculi and its larger fragments away from
the fiber tip. As a result of these phenomena the range of different
compositions of calculi which can be effectively fragmented with the
Q-switched alexandrite laser lithotripter is less than that obtainable
with the Furumoto apparatus.
Laser apparatus have previously been employed for invasive surgery in the
human body. For example, U.S. Pat. No. 4,791,927 to Menger describes a
dual-wavelength laser scalpel for both cutting and coagulating tissue
employing a laser beam in the wavelength range of 500-800 nm for
cauterizing bleeding blood vessels through photocoagulation, and a laser
bean in the wavelength range from 250-400 nm for cutting tissue by
photoablation.
There is, accordingly, a need for an improved lithotripsy method and
apparatus which mainly utilizes the laser light in the long (600-900 nm)
wavelength range to effectively treat most urinary and biliary calculi and
minimize the total laser pulse energy required to obtain effective stone
fragmentation.
Accordingly, it is an object of the present invention to provide a method
and related apparatus for improved effectiveness of laser lithotripsy.
Another object of the present invention is to provide an effective laser
lithotripter which can fragment most calcified matter while exposing the
calcified matter and surrounding tissue to minimum amounts of short
wavelength light.
SUMMARY OF THE INVENTION
Briefly described, the present invention provides a method (and related
apparatus) for fragmentation of calcified matter in the human body which
method comprises the simultaneous irradiation of the calcified matter by
pulsed coherent radiation at two separate wavelengths (short and long),
(1) a short wavelength (SW) in the range of 300-450 nm, which acts as an
igniter which initiates plasma sparking in the calculi; and
(2) a long wavelength (LW) in the range of 600-900 nm, which is readily
absorbed in the plasma generated by the short wavelength pulse and
amplifies the plasma sparking, thus amplifying the the resultant
fragmentation of the object calculi. The initially formed plasma thus acts
as a black body absorber.
The short wavelength pulses are administered at a relatively lower energy
of from about 2 to about 30 mJ, desirably at an energy level of from about
2 to about 16 mJ, and preferably at an energy level of from about 2 to
about 12 mJ, at pulse duration of from about 50 to about 300 nanoseconds
(ns), preferably of from about 75 to about 150 ns.
The long wavelength pulses are administered at an energy level of from
about 15 to about 100 mJ, desirably at an energy level of from about 15 to
about 75 mJ, and preferably at an energy level of from about 15 to about
60 mJ, at pulse duration of from about 50 to about 300 nanoseconds (ns),
preferably of from about 85 to about 165 ns.
This synergistic interaction between the two wavelengths enhances the
fragmentation effect of the long wavelength and enables its participation
in the plasma sparking process at energy levels significantly below the
threshold for plasma sparking experienced with this wavelength alone. The
two wavelength pulses are administered in a manner which utilizes the
minimum necessary energy in the SW pulse to initiate sparking in
conjunction with moderate energy in the LW pulse to produce effective
fragmentation. Because the plasma lifetime is short compared to the
duration of the laser pulses, this process is most effective when the SW
and LW laser pulses completely overlap. More desirably, the SW pulse
should be timed to overlap the initial part of the LW temporal pulse, so
as to initiate the plasma sparking before the LW pulse has achieved its
intensity maximum. Therefore, tissue exposure by the potentially harmful
short wavelength of laser light is thus minimized by primarily relying on
the laser light in the long wavelength range to accomplish the
fragmentation of calculi. One preferred embodiment of the present
invention utilizes long wavelength coherent radiation of about 730-780 nm
and short wavelength coherent radiation of about 365 -390 nm.
Briefly described, the apparatus of the present invention comprises a laser
generating and delivering device, or devices, being capable of providing
the above-mentioned two wavelengths at pulse energies, pulse durations,
pulse temporal sequencing, and pulse repetition rates in accordance with
the method of the present invention; and capable of delivering the two
wavelengths substantially simultaneously to the targeted calcified matter.
In the preferred embodiment, the apparatus comprises a Q-switched
alexandrite laser generating light in the long wavelength spectrum and
provided with a frequency doubling crystal for converting a portion of the
output laser pulse into its second harmonic in the short wavelength
spectrum. A focusing device coincidentally focuses both the LW and SW
light at a selected point, which may be the calcified matter itself or,
preferably, the collecting end of a fused silica fiber optic cable, by
means of which the combined laser pulses are delivered to the calcified
matter.
These and other objects, features and advantages of the present invention
will become more readily apparent and understood upon reading and
comprehending this specification in conjunction with the accompanying
drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a schematic presentation of a dual wavelength lithotripter device
of the present invention employing a single laser cavity;
FIG. 2 is a schematic of a dual laser lithotripter system of the invention;
FIG. 3 is an oscilloscope trace of long and short wavelength laser pulses
for laser lithotripsy in accordance with the invention;
FIG. 4 is a schematic for an endoscope probe for delivering laser pulses;
FIG. 5 shows the relative absorption in the light spectrum by water,
hemoglobin and melanin;
FIG. 6 summarizes comparative in vitro lithotripsy test results employing
single frequency laser light at 504 nm;
FIG. 7 summarizes in vitro lithotripsy test results employing dual
frequency (378 nm together with 755 nm) laser light in accordance with the
invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
Referring now in greater detail to the drawings in which like numerals
represent like components throughout the several views, FIG. 1 shows a
schematic representation of a dual wavelength lithotripter 19 in
accordance with a preferred embodiment of the present invention. The
preferred lasing medium is an alexandrite rod 5 which is a broadly tunable
solid state chromium doped berylium aluminate material, such as is shown
in U.S. Pat. Nos. 3,997,853 and 4,272,733, which are owned by
Allied-Signal, Inc., Morristown, N.J. There are a variety of alternate
laser materials that are capable of providing laser pulses of the desired
characteristics: for example, Nd:BEL, Cr:GSGG, Ti:A1204, Ti:BeA1204,
Cr:SrA1F5, excimer, ruby, emerald and dye lasers, whose output can be
shifted using standard frequency shifting techniques to provide either the
long or short wavelength laser energy.
A laser of the present invention is depicted schematically in FIG. 1. The
laser comprises laser medium 5 in a resonant cavity defined by mirrors 1
and 2, of which 2 is partly reflecting (50% R typically). A Q-switch
device 3 is provided in the cavity in order to provide a single high peak
power laser pulse output (50-300 ns pulse) as is generally understood by
those knowledgeable in the art. When medium 5 is excited by a conventional
pulsed pump source 13, coherent radiation is emitted through mirror 2 as
permitted by the intracavity Q-switch device 3 and passes through beam
shifting means 6, which is typically a nonlinear mixing crystal of the
type well known in the art. In a preferred embodiment, the present
invention employs a beta barium borate frequency doubling crystal which
provides greater than 15% conversion of the long wavelength output into
the short wavelength spectrum. Thereafter, the beam, including the long
and short wavelengths, passes to a front surface mirror 7 which
coincidently focusses the two wavelengths into a beam delivery means 8,
which may, for example, be a fiber optic cable. FIG. 1 also depicts a beam
attenuator means 14 (i. e. neutral density filters, color filters,
polarization) which may be used to selectively adjust the power ratio of
the two wavelengths in the beam. Additionally, the coating applied to the
focusing mirror 7 can be adjusted to provide the proper ratio of short to
long wavelength pulse energy in the beam. Another optional device shown in
FIG. 1 is an intracavity tuning device 4 which can be used to select a
specific output wavelength from a broadly tunable lasing medium's emission
bandwidth, such as alexandrite (720-790 nm), thus enhancing its beam
shifting efficiency and interaction with target materials.
An example of the performance characteristics of a dual wavelength
alexandrite laser system is as follows: a) an output of 0-200 mJ/pulse at
755 nm at 15 Hertz (Hz); b) a pulse width of the 755 nm output 100-300 ns
full width half maximum (FWHM); c) a 15% doubling efficiency using beta
barium borate to provide 0-30 mJ/pulse at 378 nm; d) 85 -245 ns pulse
width at 378 nm FWHM; e) a focusing mirror 7 having a 50 millimeter (mm)
focal length, which coincidently focusses the two laser output beams to a
full beam diameter of less than 300 microns; and f) an intracavity 4-plate
birefringent filter which provides tunable 0.1 nm bandwidth from 730-780
nm.
An alternate laser system for the embodiment of the present invention is
depicted schematically in FIG. 2. In this device two laser systems 15 and
16 are employed to provide the laser pulses at the long and short
wavelengths, respectively. In combination, the lasers of this embodiment
function as the one described above, the difference being that the dual
wavelengths (long and short) are created in two different laser systems.
The laser output beams are combined with the aid of mirrors 10 and 12
which serve to spatially overlap the two beams into a single beam. These
combined beams are then coincidentally focused by mirror 7 into the
delivery means 8. Optionally, a means 17 and 18 (i.e. neutral density
filters) is provided to selectively attenuate the individual laser beams
to produce the desired ratio of long to short wavelength pulse energy. The
temporal sequencing of these two laser pulses should follow the
description provided in the text.
In the preferred embodiment of the present invention, the most effective
time sequencing of the laser pulses is shown in FIG. 3. This is a
photograph of an oscilloscope trace of the two laser pulses temporal
overlap, short (lower) and long (upper) wavelengths. The peak of the short
wavelength pulse is achieved at about 15 nanoseconds (ns) before the peak
of the long wavelength pulse. This sequencing scheme allows the plasma to
ignite by the action of the short wavelength pulse before a significant
part of the long wavelength pulse has irradiated the object calculi; and
allows a significant part of the long wavelength pulse to irradiate the
object calculi during the plasma lifetime. This is the most efficient use
of the long wavelength pulse. Alternately, the long wavelength pulse may
directly coincide temporally or even precede the short wavelength pulse
but this would result in a diminished fragmentation efficiency of the
target calculi.
The preferred embodiment of lithotripter 19 further comprises a fused
silica fiber 32 or 200-400 micron core diameter. In the preferred
embodiment and as best seen in FIG. 4, the fiber 32 is a 300 micron core
fiber which is insertable into the working channel 33 of an endoscope or
ureterescope 38 for positioning adjacent to the targeted calcified matter
40. A conventional stone basket may be employed to grasp the targeted
matter 40 and hold it adjacent to the working end 32' of the optical fiber
32 so as to accurately aim the laser pulses into the matter 40. The
endoscope 38 may also include a conventional irrigation channel 35.
In Vitro Test Results
To enable a direct comparison of fragmentation performance and test the
concept of SW light acting as a plasma igniter in stones where LW light
alone cannot generate consistent plasma sparking, eleven (11) specific
samples of calculi were selected among a group of 47 different biliary and
urinary calculi samples which composition had been previously analyzed.
These eleven (11) test samples were selected as those being extremely
difficult or impossible to fragment when exposed to the 504 nm light of a
commercially available dye laser lithotripter or to the 755 nm LW light of
the Q-switched Alexandrite laser lithotripter.
In a series of experiments with a dual wavelength Alexandrite test laser
substantially similar to the one described herein as a preferred
embodiment and shown in FIG. 1, each of the eleven (11) calculi samples
were irradiated with different energy levels of SW and LW light which were
transmitted simultaneously through a tapered 500-300 micron fused silica
fiber. Substantially enhanced fragmentation performance, as well as, the
synergistic interaction of the SW and LW pulse components were clearly
demonstrated.
For example, white Apatit & Struvite stone #KI-XI, in which little or no
plasma sparking could be generated with up to 60 mJ of 504 nm light or up
to 100 mJ of 755 nm LW light, responded very effectively to the
combination of 4 mJ SW and 40 mJ LW light.
In the case of Cystine stone #KI-XVI, which did not respond at all to 60 mJ
of 504 nm light or 100 mJ of 755 nm LW light, fragmentation was readily
accomplished with a combination of 4 mJ of SW light and 32 mJ of LW light.
Removal of any of the two beam components during stone exposure, resulted
in instant reduction of fragmentation response.
Further, the hard Brushite surface layer of stone #KDI-8, in which no
plasma sparking at all could be obtained with 60 mJ of 504 nm light or 100
mJ of 755 nm LW light, responded with consistent plasma sparking when
irradiated with 7 mJ SW and 52 mJ LW light.
The experiments with the eleven (11) different stone samples have
established that the combination of 4-12 mJ of SW light and 15-35 mJ of LW
light generates pulses which ensure consistent plasma sparking and
fragmentation in most stones when delivered through a 300 micron fused
silica fiber.
The table in FIG. 6 summarizes the specific fragmentation responses of the
eleven (11) different stone samples to the 504 nm light of a commercially
available dye laser lithotripter, at energy levels of between 30 and 60 mJ
(a "prior art" method), as well as, the composition, color and surface
structure of the samples.
The table in FIG. 7 summarizes the fragmentation response of the same
eleven (11) stone samples, when tested with different levels of SW and LW
light generated by the dual wavelength Alexandrite test laser, in
accordance with the present invention, employing spatially and temporally
overlapped short wavelength and long wavelength light. A stone by stone
comparision of the fragmentation responses tabulated in FIG. 6 and FIG. 7,
clearly demonstrates the superior and consistent performance of the
invention method and apparatus.
Since various changes may be made in the invention without departing from
its spirit and essential characteristics, it is intended that all matter
contained in the description shall be interpreted as illustrative only and
not in a limiting sense, the scope of the invention being defined by the
appended claims.
* * * * *
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Description  |
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