WO2001028623A2 - Split beam transducer - Google Patents
Split beam transducer Download PDFInfo
- Publication number
- WO2001028623A2 WO2001028623A2 PCT/US2000/041226 US0041226W WO0128623A2 WO 2001028623 A2 WO2001028623 A2 WO 2001028623A2 US 0041226 W US0041226 W US 0041226W WO 0128623 A2 WO0128623 A2 WO 0128623A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- region
- tissue
- treated
- ultrasound
- surrounding
- Prior art date
Links
- 238000002604 ultrasonography Methods 0.000 claims abstract description 62
- 238000011282 treatment Methods 0.000 claims abstract description 43
- 238000000034 method Methods 0.000 claims abstract description 16
- 210000001519 tissue Anatomy 0.000 description 31
- 230000003902 lesion Effects 0.000 description 17
- 210000002307 prostate Anatomy 0.000 description 13
- 238000003384 imaging method Methods 0.000 description 11
- 241000282472 Canis lupus familiaris Species 0.000 description 7
- 238000002560 therapeutic procedure Methods 0.000 description 7
- 241000288147 Meleagris gallopavo Species 0.000 description 6
- 206010060862 Prostate cancer Diseases 0.000 description 6
- 208000000236 Prostatic Neoplasms Diseases 0.000 description 6
- 210000000481 breast Anatomy 0.000 description 6
- 230000017074 necrotic cell death Effects 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 4
- 238000004088 simulation Methods 0.000 description 4
- 238000001356 surgical procedure Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229920002799 BoPET Polymers 0.000 description 3
- 238000001727 in vivo Methods 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 229920005372 Plexiglas® Polymers 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000003491 array Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005094 computer simulation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 210000003708 urethra Anatomy 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 description 1
- 206010020843 Hyperthermia Diseases 0.000 description 1
- 238000012404 In vitro experiment Methods 0.000 description 1
- 239000005041 Mylar™ Substances 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 208000004403 Prostatic Hyperplasia Diseases 0.000 description 1
- 206010072587 Rectal injury Diseases 0.000 description 1
- 230000008081 blood perfusion Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000036031 hyperthermia Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- 238000004861 thermometry Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N7/00—Ultrasound therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B8/00—Diagnosis using ultrasonic, sonic or infrasonic waves
- A61B8/08—Clinical applications
- A61B8/0833—Clinical applications involving detecting or locating foreign bodies or organic structures
Definitions
- This invention relates to methods and apparatus for the treatment of disease. It is disclosed in the context of high-intensity focused ultrasound (hereinafter sometimes HIFU) treatment of prostate cancer. However, it is believed to be useful in other applications as well.
- HIFU high-intensity focused ultrasound
- HIFU treatment of benign prostatic hyperplasia typically only prostate tissue surrounding the urethra is ablated. This treatment results in necrosis of prostate tissue adjacent the urethra, thereby relieving symptoms of BPH.
- a number of systems are known for the generation of treatment-intensity ultrasound in general, and the HIFU treatment of BPH in particular. There are, for example, the systems described in U.S.
- HIFU treatment of prostate cancer treatment of the whole prostate to eradicate all the cancerous cells and surrounding tissue are the objective. Using a single HIFU beam, such procedures to treat prostate cancer can dictate very long treatment times. There is a need to improve the treatment time for the HIFU treatment of prostate cancer, while maintaining efficacy and safety.
- a method of treating tissue includes providing an ultrasound transducer having a surrounded ultrasound generating region and a surrounding ultrasound generating region.
- the surrounded region and surrounding region are separately actuable to generate ultrasound.
- At least the surrounding region has a focus.
- the ultrasound transducer is placed adjacent the tissue to be treated so that the focus of the surrounding region lies adjacent a first treatment site.
- the surrounding region is actuated while the surrounded region is maintained unactuated to treat the tissue to create a first treated region in the tissue.
- the method further includes moving the ultrasound transducer to another location adjacent the tissue to be treated so that the focus of the surrounding region lies adjacent a second treatment site.
- the surrounding region is again actuated and the surrounded region is again maintained unactuated to treat the tissue to create a second treated region in the tissue.
- an apparatus for treating tissue includes an ultrasound transducer having a surrounded ultrasound generating region and a su ⁇ ounding ultrasound generating region. At least the surrounding region has a focus.
- the apparatus further includes a first driver for driving the surrounded region to generate ultrasound, and a second driver for driving the surrounding region to generate ultrasound.
- the first driver is separately actuable from the second driver and the second driver is separately actuable from the first driver.
- the first driver is actuable to cause the surrounded region to generate ultrasound to aid in placing the ultrasound transducer adjacent the tissue to be treated so that the focus of the surrounding region lies adjacent the treatment site.
- the second driver is actuable while the surrounded region is maintained unactuated to treat the tissue to create a first treated region in the tissue.
- the ultrasound transducer is adapted to be positioned at another location adjacent the tissue to be treated so that the focus of the surrounding region lies adjacent a second treatment site, the second driver then being further actuable to cause the surrounding region to produce ultrasound while the first driver is maintained unactuated to treat the tissue to create a second treated region in the tissue.
- the second treated region is at least adjacent the first treated region.
- the second treated region intersects the first treated region.
- the second treated region overlaps the first treated region.
- the first driver is actuable to cause the surrounded region to generate ultrasound to aid in placing the ultrasound transducer adjacent the tissue to be treated so that the focus of the surrounding region lies adjacent the first treatment site.
- the first driver is actuable to cause the surrounded region to generate ultrasound to aid in placing the ultrasound transducer adjacent the tissue to be treated so that the focus of the surrounding region lies adjacent the second treatment site.
- Fig. 1 illustrates a partly block and partly schematic diagram of a system constructed according to the invention
- Fig. 2 illustrates a transverse beam profile image of a sha ⁇ ly focused single beam pattern generated using a Schlieren imaging system
- Fig. 3 illustrates a negative of a longitudinal beam profile image of a sha ⁇ ly focused single beam pattern generated using a Schlieren imaging system
- Fig. 4 illustrates a transverse beam profile image of a beam having a reduced amplitude main lobe with four side lobes, sometimes referred to herein as a "split beam,” generated using a Schlieren imaging system;
- Fig. 5 illustrates a negative of a longitudinal beam profile image of a split beam generated using a Schlieren imaging system
- Fig. 6 illustrates illustrates a simulation result for the split beam format in the focal field
- Fig. 7 illustrates illustrates a simulation result for a single beam format in the focal field
- Fig. 8 illustrates lesions created by the single beam format and the split beam format on the surface of a polyester film, side by side for pu ⁇ oses of comparison
- Fig. 9 illustrates temperature profiles measured by the thermocouples; and, Fig. 10 illustrates a lesion created on the prostate gland of a test animal using a system according to the invention.
- the control of the imaging driver/receiver 10 which drives the imaging transducer portion 12 of the multiple section ultrasound transducer 14 was separated, 20, 13, 15, from the control of the therapy driver 16 so that the imaging portion 12 was not driven when the therapy portion 18 of the transducer 14 was.
- These changes were made in the control 20 and drive circuits 16, 10 of the treatment transducer 18 and the imaging transducer 12, respectively, to reduce the amplitude of the main beam and surround it with a number, four in the illustrated embodiment, of significant side lobes.
- the HIFU beam is spread to create a larger treatment volume per ultrasound exposure which can reduce the overall treatment time.
- Mylar is a registered trademark of E. I. Du Pont de Nemours and Company.
- Plexiglas is a registered trademark of Rohm and Haas Company and ELF Atochem S.
- tissue heat conduction has been demonstrated to bridge the lesions created by the central lobe 22 and the side lobes 24, resulting in a larger treated volume per ultrasonic irradiation cycle. Avoidance of a single intense beam 26 can also reduce the likelihood of vapor formation at the focal site.
- Computer simulations were performed to explore the effects and differences between the single lobe 26 configuration and central lobe 22-and-side lobes 24 configuration. The acoustic properties, beam patterns and power output were verificd by standard procedures. Then, /// vitro tests in turkey breast tissue and in vivo experiments in dog prostate were carried out and lesion volumes created by the split beam transducer were examined.
- the split beam 22, 24 format creates larger volumes of lesion than the single beam 26 in turkey breast tissue and in dog prostate.
- a step size of 1.8 mm was selected between adjacent HIFU lesions. This was done in an effort to promote connected necrosis.
- connected lesions in turkey breast tissue and in dog prostate were achieved using a step size of 2.8 mm. This resulted in a more than 30% reduction in treatment time for the same volume of tissue treatment.
- the results demonstrate that treatment using the split beam 22, 24 format results in larger lesion volumes than are achieved using the single beam 26 format in turkey breast tissue and also in dog prostate tissue.
- the spherically focused transducer 14 of the Sonablate-200TM HIFU device contains dual elements 12, 18 on the same piezoelectric ceramic crystal.
- the center element 12 is used in both imaging and therapy, and the outer element 18 is used in therapy.
- Use of the inner element 12 and outer element 18 both in therapy mode produces a sha ⁇ ly focused beam 26 which is sometimes referred to herein as a "single beam.”
- a beam 22, 24 characterized by a reduced amplitude main lobe 22 with four side lobes 24 is produced when the outer element 18 is driven.
- Figs. 2 and 3 illustrate transverse and longitudinal beam profile images, respectively, of the sharply focused single beam 26 pattern. These images are generated using a Schlieren imaging system. Figs.
- FIGS. 4 and 5 illustrate transverse and longitudinal beam profile images, respectively, of a split beam having a reduced amplitude main lobe 22 with four side lobes 24, as a result of driving only the outer element 18. Again, these images are generated using a Schlieren imaging system.
- the beams 22, 24 and 26 were also analyzed by computer simulation using numerical integration techniques. The following parameters were used during the simulations: frequency, 4 MHz; focal length, 3.5 cm; transducer aperture, 30 mm x 22 mm; and, inner element diameter, 10 mm.
- Figs. 6 and 7 illustrate the simulation results for the split beam 22, 24 format and the single beam 26 format, respectively, in the focal field.
- Both beam formats were also tested using Mylar® strips placed in the focal plane.
- the lesions created on the surface are illustrated side-by-side for pu ⁇ oses of comparison in Fig. 8.
- the power levels used are the same in both trials, namely, 30 watts.
- the areas treated by the split beam 22, 24 are illustrated on the left. Again, the spacing between successive treatments is 2.8mm.
- the spaces between the centers of consecutive ultrasonic treatments using the split beam 22, 24 format are characterized by the presence of lesion. Also as illustrated, there are significant gaps between the lesions on the right side of Fig. 8 where the single beam format 26 is used.
- tissue necrosis achieved using the split beam format was wider than was achieved using the single beam format.
- the depths of the lesions were comparable.
- the lesion width at the focus achieved using the split beam format is estimated at greater than 3 mm.
- the temperature profiles measured by the thermocouples are illustrated in Fig. 9.
- Fig. 10 illustrates the lesion created on male dog prostate gland. At 2.8 mm spacing between the centers of consecutive exposures, the treatment time was reduced from one hour to thirty-five minutes. Necrosis of the treated prostate tissue volume was achieved without any rectal injury. This is believed to establish the improvement in performance and safety of the split beam format in prostate cancer treatment as compared to single beam treatment.
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Radiology & Medical Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Surgical Instruments (AREA)
- Transducers For Ultrasonic Waves (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00982685A EP1227763A4 (en) | 1999-10-18 | 2000-10-18 | Split beam transducer |
JP2001531451A JP2003512103A (en) | 1999-10-18 | 2000-10-18 | Split beam converter |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16022299P | 1999-10-18 | 1999-10-18 | |
US60/160,222 | 1999-10-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2001028623A2 true WO2001028623A2 (en) | 2001-04-26 |
WO2001028623A3 WO2001028623A3 (en) | 2001-09-13 |
Family
ID=22576022
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2000/041226 WO2001028623A2 (en) | 1999-10-18 | 2000-10-18 | Split beam transducer |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1227763A4 (en) |
JP (1) | JP2003512103A (en) |
WO (1) | WO2001028623A2 (en) |
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US6719755B2 (en) | 1996-10-22 | 2004-04-13 | Epicor Medical, Inc. | Methods and devices for ablation |
US6805129B1 (en) | 1996-10-22 | 2004-10-19 | Epicor Medical, Inc. | Apparatus and method for ablating tissue |
US6805128B1 (en) | 1996-10-22 | 2004-10-19 | Epicor Medical, Inc. | Apparatus and method for ablating tissue |
US6840936B2 (en) | 1996-10-22 | 2005-01-11 | Epicor Medical, Inc. | Methods and devices for ablation |
US6949095B2 (en) | 1996-10-22 | 2005-09-27 | Epicor Medical, Inc. | Apparatus and method for diagnosis and therapy of electrophysiological disease |
US7387126B2 (en) | 1996-10-22 | 2008-06-17 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Surgical system and procedure for treatment of medically refractory atrial fibrillation |
US7393325B2 (en) | 2004-09-16 | 2008-07-01 | Guided Therapy Systems, L.L.C. | Method and system for ultrasound treatment with a multi-directional transducer |
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US7530958B2 (en) | 2004-09-24 | 2009-05-12 | Guided Therapy Systems, Inc. | Method and system for combined ultrasound treatment |
US7559905B2 (en) | 2006-09-21 | 2009-07-14 | Focus Surgery, Inc. | HIFU probe for treating tissue with in-line degassing of fluid |
US7662114B2 (en) | 2004-03-02 | 2010-02-16 | Focus Surgery, Inc. | Ultrasound phased arrays |
US7824403B2 (en) | 1996-10-22 | 2010-11-02 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Methods and devices for ablation |
US8235902B2 (en) | 2007-09-11 | 2012-08-07 | Focus Surgery, Inc. | System and method for tissue change monitoring during HIFU treatment |
US8308719B2 (en) | 1998-09-21 | 2012-11-13 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Apparatus and method for ablating tissue |
US8709007B2 (en) | 1997-10-15 | 2014-04-29 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Devices and methods for ablating cardiac tissue |
US9039617B2 (en) | 2009-11-24 | 2015-05-26 | Guided Therapy Systems, Llc | Methods and systems for generating thermal bubbles for improved ultrasound imaging and therapy |
US9095695B2 (en) | 2005-07-08 | 2015-08-04 | Focus Surgery, Inc. | Method and apparatus for treatment of tissue |
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EP0627206B1 (en) * | 1993-03-12 | 2002-11-20 | Kabushiki Kaisha Toshiba | Apparatus for ultrasound medical treatment |
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US5984881A (en) * | 1995-03-31 | 1999-11-16 | Kabushiki Kaisha Toshiba | Ultrasound therapeutic apparatus using a therapeutic ultrasonic wave source and an ultrasonic probe |
-
2000
- 2000-10-18 EP EP00982685A patent/EP1227763A4/en not_active Withdrawn
- 2000-10-18 WO PCT/US2000/041226 patent/WO2001028623A2/en not_active Application Discontinuation
- 2000-10-18 JP JP2001531451A patent/JP2003512103A/en active Pending
Cited By (99)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8114069B2 (en) | 1996-10-22 | 2012-02-14 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Methods and devices for ablation |
US6719755B2 (en) | 1996-10-22 | 2004-04-13 | Epicor Medical, Inc. | Methods and devices for ablation |
US6805128B1 (en) | 1996-10-22 | 2004-10-19 | Epicor Medical, Inc. | Apparatus and method for ablating tissue |
US6840936B2 (en) | 1996-10-22 | 2005-01-11 | Epicor Medical, Inc. | Methods and devices for ablation |
US6858026B2 (en) | 1996-10-22 | 2005-02-22 | Epicor Medical, Inc. | Methods and devices for ablation |
US6949095B2 (en) | 1996-10-22 | 2005-09-27 | Epicor Medical, Inc. | Apparatus and method for diagnosis and therapy of electrophysiological disease |
US6971394B2 (en) | 1996-10-22 | 2005-12-06 | Epicor Medical, Inc. | Methods and devices for ablation |
US7387126B2 (en) | 1996-10-22 | 2008-06-17 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Surgical system and procedure for treatment of medically refractory atrial fibrillation |
US7674257B2 (en) | 1996-10-22 | 2010-03-09 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Apparatus and method for ablating tissue |
US8721636B2 (en) | 1996-10-22 | 2014-05-13 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Apparatus and method for diagnosis and therapy of electrophysiological disease |
US8535301B2 (en) | 1996-10-22 | 2013-09-17 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Surgical system and procedure for treatment of medically refractory atrial fibrillation |
US7824403B2 (en) | 1996-10-22 | 2010-11-02 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Methods and devices for ablation |
US6805129B1 (en) | 1996-10-22 | 2004-10-19 | Epicor Medical, Inc. | Apparatus and method for ablating tissue |
US8057465B2 (en) | 1996-10-22 | 2011-11-15 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Methods and devices for ablation |
US8002771B2 (en) | 1996-10-22 | 2011-08-23 | St. Jude Medical, Atrial Fibrillation Division, Inc. | Surgical system and procedure for treatment of medically refractory atrial fibrillation |
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EP1227763A4 (en) | 2005-06-15 |
WO2001028623A3 (en) | 2001-09-13 |
JP2003512103A (en) | 2003-04-02 |
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