US20100318161A1 - Light therapy methods - Google Patents
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- US20100318161A1 US20100318161A1 US12/834,601 US83460110A US2010318161A1 US 20100318161 A1 US20100318161 A1 US 20100318161A1 US 83460110 A US83460110 A US 83460110A US 2010318161 A1 US2010318161 A1 US 2010318161A1
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- A61N5/00—Radiation therapy
- A61N5/06—Radiation therapy using light
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- A—HUMAN NECESSITIES
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- A61N5/06—Radiation therapy using light
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- A61N2005/0629—Sequential activation of light sources
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N5/00—Radiation therapy
- A61N5/06—Radiation therapy using light
- A61N2005/0635—Radiation therapy using light characterised by the body area to be irradiated
- A61N2005/0643—Applicators, probes irradiating specific body areas in close proximity
- A61N2005/0645—Applicators worn by the patient
- A61N2005/0647—Applicators worn by the patient the applicator adapted to be worn on the head
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- A—HUMAN NECESSITIES
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- A61N5/06—Radiation therapy using light
- A61N2005/065—Light sources therefor
- A61N2005/0651—Diodes
- A61N2005/0652—Arrays of diodes
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- A—HUMAN NECESSITIES
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- A61N2005/0658—Radiation therapy using light characterised by the wavelength of light used
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Definitions
- This invention relates to light therapy.
- Apparatus and methods according to the invention may be applied to the treatment of bone disorders and the biostimulation of bone and soft tissue.
- Embodiments of the invention provide apparatus for irradiating tissues of the face and jaw with biologically effective doses of light.
- Light therapy involves irradiating tissues with light.
- Light can stimulate a variety of biological activities in cells and tissues that are compromised in function.
- Light therapy treatment is typically administered by a physician or therapist who directs light from a hand-held light emitting device at an affected area.
- Light emitting devices can be difficult to position consistently over the affected area.
- a tattoo is used to identify the affected area.
- even with a tattoo or other reference mark it is difficult to consistently deliver light therapy treatments to an affected area.
- Light therapy typically involves repeated treatments over at least several days. Thus, patients undergoing light therapy may be required to make multiple visits to a practitioner's office or clinic in order to complete a therapy regimen. Such repeated visits may be time consuming and/or expensive.
- LEDs and other light sources suitable for generating light for light therapy can get hot when they operate. Such light sources can be inefficient at higher temperatures. Hot apparatus can also be uncomfortable or even dangerous to patients.
- the inventor has identified a need or desire for light therapy apparatus which can deliver consistent treatments, particularly to tissues in the dental and maxillofacial areas. There is a particular need or desire for such apparatus that is sufficiently cost-effective and foolproof to be used at home by patients. There is also a need for such apparatus that can be operated without exposing a patient to high temperature surfaces.
- One aspect of this invention provides apparatus for delivering light to tissues of a patient's dental and maxillofacial areas.
- the apparatus comprises a support that registers against one or more anatomical features of a patient's head and one or more light sources mounted to the support.
- the light sources illuminate selected tissues of a patient's dental and maxillofacial areas from outside of the patient's mouth.
- the light sources comprise arrays of LEDs in some embodiments.
- the support comprises an intra-oral tray connected to an extra-oral bridge.
- a light source such as a light emitting diode (“LED”) array, is mounted to the extra-oral bridge.
- LED light emitting diode
- the support comprises a head-set that registers on the bridge of a patient's nose and the patient's ears.
- a light source such as a light emitting diode (“LED”) array, is mounted to the head-set.
- LED light emitting diode
- FIG. 1 is a view from the front side of an extra-oral light therapy device having an intra-oral tray, an extra-oral bridge, and left and right side extra-oral LED arrays.
- FIGS. 1A , 1 B and 1 C are respectively a cross-section, a front side elevation and a rear elevation of a light source having a cooling fan, a heat sink and two arrays of light emitters.
- FIG. 2 is a right side view of the device of FIG. 1 with the end of the extra-oral bridge attached to the extra-oral LED array.
- FIG. 3 is a view from the front-left side of the extra-oral bridge, intra-oral tray and extra-oral LED array of FIG. 1 .
- FIG. 4 is a view from the rear right side of the extra-oral bridge, intra-oral tray and extra-oral LED array of FIG. 1 .
- FIG. 5 is a view from the left rear side of the extra-oral bridge, intra-oral tray and extra-oral LED array of FIG. 1 with the intra-oral tray detached.
- FIG. 6 is a top view of a programmable controller for use with light therapy apparatus.
- FIG. 7 is a perspective view of a light therapy device according to an alternative embodiment in which an LED array is supported by a head-set.
- FIG. 7A is a perspective view of a light therapy device according to another alternative embodiment in which an LED array is supported by a head-set.
- FIG. 8 is a side view of the light therapy device of FIG. 7 .
- FIG. 9 is a front view of at least one LED array, and a connector detached from the head-set.
- FIG. 10 is a front view of an external light therapy device having two LED arrays, a hinge-like member, and an attaching means.
- FIG. 11 is a cross-sectional view of an LED array mounted onto a substrate.
- FIG. 11A is a schematic cross section through a portion of a light source having a light emitter and a reflector.
- FIG. 12 is a cross-sectional view of an LED array detached from the substrate.
- FIG. 1 shows an example light therapy apparatus 2 that comprises an extra-oral light source 4 having a right side 1 and a left side 3 (as viewed from the front of the device), an extra-oral bridge 5 , and an intra-oral tray 7 .
- Intra-oral tray 7 registers to a patient's teeth.
- Light source 4 is rigidly connected to intra-oral tray 7 by extra-oral bridge 5 . Therefore, a patient can position light source 4 accurately and repeatedly to illuminate a desired location in the patient's dental and maxillofacial areas by inserting intra-oral tray 7 into his or her mouth and biting intra-oral tray 7 so that it registers to at least some of the patient's teeth. This stabilizes light therapy apparatus 2 and positions light source 4 at a desired position.
- the consistent alignment and targeting of light from light source 4 during subsequent treatments makes the treatments more repeatable.
- extra-oral bridge 5 is removable from extra-oral light source 4 and intra-oral tray 7 .
- Providing a light therapy apparatus 2 having major components that are detachably connectable to one another adds versatility.
- a design which permits the major components of the light therapy apparatus to be disassembled and reassembled while preserving alignment of extra-oral light source 4 to intra-oral tray 7 has the advantage that the apparatus can be disassembled for storage or transportation and then used immediately after assembly.
- FIG. 3 shows light therapy apparatus 2 with extra-oral light source left side 3 detached from extra-oral bridge 5 .
- Extra-oral bridge 5 , extra-oral light source right side 1 , and extra-oral light source left side 3 may be secured together via a suitable connector.
- extra-oral bridge 5 , the extra-oral light source right side 1 , and the extra-oral light source left side 3 may be connected by inserting male connector portions 6 A of the extra-oral light source right and left sides 1 and 3 into corresponding female connector portions 8 A of extra-oral bridge 5 (see FIG. 3 ).
- the suitable connector allows extra-oral light source right and left sides 1 and 3 to be detached from extra-oral bridge 5 for ease of use and flexibility.
- extra-oral light source right and left sides 1 and 3 are rotatable between a sagittal orientation (as shown in FIG. 1 ) and a vertical orientation (indicated in dotted outline in FIG. 1 ).
- Light source right and left sides 1 and 3 can be locked at a desired angle of rotation by any suitable mechanism. This permits light source right and left sides 1 and 3 to be arranged so that the light that they emit fully covers the desired treatment areas.
- Intra-oral tray 7 may be connected to extra-oral bridge 5 by way of another suitable connector.
- a male portion 6 B of intra-oral tray 7 is removably received in a female portion 8 B of extra-oral bridge 5 .
- extra-oral bridge 5 may be reused for other patients (after suitable sterilization).
- Intra-oral tray 7 may be disposed of after it is no longer required by a patient.
- extra-oral bridge 5 is non-removably attached to intra-oral tray 7 .
- Intra-oral tray 7 is intended for insertion into a patient's mouth and is suitably shaped to fit around a patient's teeth. Intra-oral tray 7 may register with a few selected teeth (for example, intra-oral tray 7 may comprise a bite tab) or may fit around the patient's full set of teeth.
- the intra-oral tray 7 comprises a frame of a plastic or other suitable material that can serve as a skeleton for a settable material. The frame may be perforated to aid retention of the settable material.
- the frame may comprise extra-oral bridge 5 or a connector to connect to extra-oral bridge 5 .
- the frame for intra-oral tray 7 may be filled with a suitable settable material (for example a clear vinyl siloxane gel or similar material) which sets around the patient's teeth and subsequently allows repeatable alignment of intra-oral tray 7 in the patient's mouth.
- a suitable settable material for example a clear vinyl siloxane gel or similar material
- intra-oral tray 7 could be in the path of light as it travels from light source 4 to target tissues, the material of intra-oral tray 7 should be transparent to the light.
- Extra-oral bridge 5 preferably conforms around the jaw line of a patient.
- the light source right and left sides 1 and 3 are respectively positioned on the right and left sides of a patient's face along the patient's jaw line.
- Extra-oral bridge 5 may be adjustable to permit alignment of light source left and right sides 1 and 3 with target areas to be irradiated.
- Light source left and right sides 1 and 3 are extra-oral (outside of the patient's oral cavity). Light can pass from left and right sides 1 and 3 through tissues of the patient's lips and cheeks into target areas on the patient's gums and/or in the patient's jaws.
- Light source 4 emits light toward the patient.
- the light is not necessarily visible light.
- the light may include or consist of infrared light.
- Light source 4 comprises an array of light-emitting diodes (LEDs) in some embodiments.
- Light source 4 has an inner surface 13 (see FIG. 4 ) that is placed near or against the patient's skin adjacent to the tissues that it is desired to treat. Light is emitted is from inner surface 13 toward the area of treatment.
- left and right sides 1 and 3 of light source 4 each have a length similar to a significant fraction of the length of a human jaw.
- left and right sides 1 and 3 may each have a length of about 20 mm to about 90 mm in some embodiments and about 25 to about 45 or 60 mm in some embodiments.
- light source 4 may be smaller in extent.
- light source 4 has optics that emit light in the form of diverging beams.
- light source 4 may be somewhat smaller than the area of tissues to be treated because light from light source 4 will spread somewhat as it passes through the tissues of the patient's lips and cheeks before reaching the tissues of the jaw and or gums to be treated.
- Light source 4 may be wide enough to illuminate both upper and lower jaws of a patient simultaneously although in some embodiments light source 4 may be narrower.
- light source 4 has a width in the range of 12 mm to about 40 mm in some embodiments (e.g. about 15 to 17 mm in some embodiments).
- the light is emitted by arrays of discrete LEDs.
- the LEDs may be arranged in any of a wide variety of patterns.
- the LEDs may be arranged in staggered parallel rows to maximize the density of LEDs in the LED array.
- the LEDs may be arranged to achieve substantially uniform optical intensity over the light-emitting inner surface 13 of light source 4 .
- each array comprises 50 to 100 LEDs or other light emitters.
- the average light intensity produced by light source 4 is at least about 10 mW/cm 2 .
- light source 4 has an average intensity that is, or can be adjusted to be, in the range of 20 mW/cm 2 to about 60 mW/cm 2 .
- the output of light source 4 is pulsed.
- the peak light intensity may be significantly higher than 50 mW/cm 2 .
- right light source 4 or its components are flexible so that they can be bent in one or two dimensions (i.e. molded) to conform to the contours of the patient's face.
- light source 4 may comprise an array of light emitters mounted to a flexible sheet of material that will hold a shape when it is bent.
- the flexible material can advantageously comprise a metal sheet that can serve as a heat sink or as a thermal path to a heat sink for heat generated by the light emitters.
- the flexible sheet may be molded to conform to the contours of the patient's face while light therapy apparatus 2 is being fitted.
- Light source 4 may include optical elements such as lenses and reflectors to focus and direct light from light source 4 onto a target area. Such optical elements may be suitably encapsulated in plastic or similar material.
- FIG. 11A shows a portion of a light source 4 .
- a light emitter 11 (which may, for example, comprise a junction in a light-emitting diode or other light-emitting semiconductor device) is located adjacent to a reflective backing 11 A.
- a curved light-reflecting recess 11 B is provided adjacent to light emitter 11 . Light from light source 11 is reflected in recess 11 B to form a beam.
- the beams from all light emitters of light source 4 combine to illuminate the target tissues. The area covered by the beam will depend upon the tissues which it is desired to treat.
- the beams of light emitted by light source 4 diverges to cover an area of tissue larger than the area of the light-emitting part of light source 4 .
- the emitted light converges to provided increased light intensity at the location of the tissues that it is desired to treat.
- the emitted light diverges in a beam having an included angle ⁇ in the range of about 45-60°.
- light source 4 may comprise a system for forced air or liquid cooling.
- a cooling system allows for treatment without the danger of potential burns to the patient and allows for greater efficiency and control of the device.
- Extra-oral light source right and left sides 1 and 3 may comprise thermally-conductive LED wafers mounted on a suitable heat sink. Heat from the LED wafers is conducted into the heat sink and dissipated.
- FIGS. 1A , 1 B and 1 C show a light source 100 of a type that may be used as light source right and left sides 1 and 3 .
- Light source 100 comprises arrays 102 of LEDs that are mounted to a heat sink 104 .
- Heat sink 104 has pins 106 projecting from its face that is away from LED arrays 102 .
- a fan 110 causes air to flow past pins 106 to carry away excess heat.
- the light from light source 4 at the tissues to be treated should have at least a threshold intensity.
- Light source 4 may be operated in a pulsed mode to facilitate cooling of light source 4 while ensuring that when light source 4 is emitting light, the intensity of emitted light at the tissues to be treated is sufficient to be effective.
- the duty cycle of light source 4 is 1:1 or less, in some embodiments 1:2 or less (for each interval in which light source 4 is on, light source 4 is off for two equal intervals).
- the pulsing of light source 4 may be performed fast enough that light source 4 does not visibly flicker (e.g. at 25 Hz or more) although this is not mandatory.
- the character of the light emitted by light source right and left sides 1 and 3 will depend upon the nature of the LEDs or other light emitters in light source 4 . It is generally desirable that the emitted light include light in the wavelength range of 620 nm to 1000 nm. In some embodiments the emitted light includes light having a wavelength in at least one of the following wavelength ranges: about 820 to about 890 nm and about 620 to about 680 nm. Light having wavelengths corresponding to one or more of the following ranges may be particularly effective:
- the range 613 nm to 624 nm corresponds to a band at which reduced cytochrome c oxidase absorbs light.
- the range 812 nm to 846 nm corresponds to a band at which oxidized cytochrome c oxidase absorbs light.
- the light is substantially monochrome in some embodiments although this is not mandatory. Providing light emitters that emit at multiple wavelengths allows for irradiation over multiple wavelengths for greater biological activity.
- the light may comprise incoherent light although this is not mandatory.
- the light may be delivered continuously or pulsed at suitable frequencies and duty cycles.
- Invisible infrared light can be clinically effective.
- the emitted light includes infrared light
- the emitted light also includes bright visible light.
- the bright visible light deters users from looking into the light source when it is operating, provides a perceptible indication that the apparatus is operating, and may be useful in properly positioning the device.
- the visible light may be, but is not necessarily in a wavelength range that is beneficial for light therapy.
- the ratio of the intensities of the visible and infrared components of the light is 1 part or less visible light to 5 parts or more infrared light.
- the treatment area and desired light characteristics will vary from patient to patient.
- a physician, dentist or other therapist can determine a light treatment regime for a patient and set up light therapy apparatus 2 to operate light emitters in light source 4 to provide the desired treatment.
- FIG. 6 illustrates a programmable controller 15 of a type that may be used to control the operation of light therapy apparatus 2 (or other light therapy apparatus as described below).
- Programmable controller 15 may be a separate, remote unit or may be directly connected to or integrated with light source 4 .
- Programmable controller 15 may comprise a microprocessor, data store, power supply, clock and associated electronic circuitry. Control parameters are stored in the data store. Programmable controller 15 operates light source 4 according to the parameters in the data store. The parameters may specify one or more of:
- light therapy apparatus has sets of light emitters having different characteristics (e.g. sets of LED that emit light at different wavelengths or sets of light emitters that illuminate target tissues in different locations) then separate control parameters may be provided for different sets of the light emitters.
- different sets of parameters are specified for different segments (intervals) of a light treatment.
- light therapy treatments may be defined for a set of intervals each lasting from a few seconds to a few hundred seconds or a fraction of an hour. Different parameters may be specified for each of the intervals. The intervals are not necessarily equal in length.
- different sets of parameters may be specified for different areas of light source 4 .
- some areas of light source 4 may be turned off because the treatment plan for a patient does not require light to be delivered at locations corresponding to those parts of the light source 4 .
- a physician, dentist, or therapist may program a patient's treatment regimen into programmable controller 15 . This may be done, for example, with the aid of suitable software running on a computer that is in data communication with programmable controller 15 or by way of a suitable user interface built into programmable controller 15 .
- Programmable controller 15 may have one or more pre-set programs built in. As an alternative to, or as an aid to programming controller 15 the physician, dentist, or therapist may select a pre-set program that is appropriate for controlling light therapy apparatus 2 to deliver light to a patient.
- a typical treatment regimen provides a dose of light daily.
- Each of the daily doses of light may be delivered over a period lasting between a few minutes and an hour or so.
- daily 1 ⁇ 2 hour doses of light can be effective and are not unduly inconvenient for patients.
- a single daily dose appears to be as effective as dividing the same dose into multiple sessions delivered at different times during the day. Examples of possible treatment regimens are
- Programmable controller 15 may maintain a log of treatments that have been delivered. For example, controller 15 may log the date and time that each treatment was initiated, the duration of the treatment, and whether or not the treatment was completed. This log can be subsequently reviewed by a dentist, physician, or the like to evaluate whether or not the patient has complied with the prescribed treatment regimen.
- Programmable controller 15 has a button or other suitable user patient interface that allows a patient to initiate a treatment according to previously-set parameters in the data store.
- the patient interface is preferably very simple such that minimal instruction is required to explain to a patient how to use light therapy apparatus 2 .
- Programmable controller 15 may include an audible or visual indicator that generates a signal to remind a patient that it is time for a treatment (or that a scheduled treatment is overdue).
- a patient can use light therapy apparatus 2 at home or in another location by operating programmable controller 15 to initiate delivery of a treatment.
- Programmable controller 15 may comprise circuitry that monitors temperature at one or more locations in light source 4 .
- the circuitry may monitor a signal modulated by a temperature sensor in light source 4 .
- programmable controller 15 may monitor the current and voltage driving LEDs in light source 4 .
- the current/voltage relationship is temperature-dependent. Thus, by monitoring the current/voltage relationship programmable controller 15 can determine whether the LED is at an undesirably high temperature.
- Programmable controller 15 may shut off or reduce current to light source 4 (or part of light source 4 ) when it detects that the temperature of light source 4 is undesirably high (or is trending towards being undesirably high). If light source 4 is equipped with a cooling fan then programmable controller 15 may optionally control the speed of the cooling fan in response to the monitored temperature.
- Programmable controller 15 may be configured to maintain a log of treatments delivered by light therapy apparatus 2 .
- the log may be reviewed by a physician, dentist or technician to verify that light therapy device has been used as prescribed by a patient.
- the log may track the times and durations of light therapy treatments delivered by light therapy apparatus 2 and may also track other features such as operating temperatures, operational status and the like.
- FIGS. 7 and 8 show a light therapy apparatus 2 A having a head-set style arrangement.
- Light therapy apparatus 2 A comprises a head-set 17 and at least one extra-oral light source 19 mounted to head-set 17 by way of a suitable connector 21 .
- Head-set 17 may have the general form of a frame for eyeglasses.
- headset 17 has arms 27 that fit above and around the patient's ears and a frame 29 that fits over the bridge of the patient's nose.
- Head-set 17 may also include lenses (not shown).
- the lenses may be made of a material that blocks radiation at wavelengths emitted by light source 19 so that the patient's eyes are protected from the radiation.
- Light source 19 may comprise an array of LEDs or other light emitters.
- Head-set 17 When head-set 17 has been adjusted to fit an individual patient, frame 29 registers with the bridge of the patient's nose and arms 27 sit on the patient's ears. Head-set 17 will sit on the patient's head in the same way each time it is put on. Head set 17 may be adjusted for fit by adjusting arms 27 which may be made of a firm, resilient material that allows for some flexibility for a better and more secure fit for individual users. In some embodiments, arms 27 can also be adjusted horizontally along their axis. Frame 29 can also be adjustable, for example, by bending to allow for a better and more secure fit. An elastic keeper such as an elastic strap may be provided to hold head-set 17 in place during use.
- arms 27 may be made of a firm, resilient material that allows for some flexibility for a better and more secure fit for individual users.
- arms 27 can also be adjusted horizontally along their axis.
- Frame 29 can also be adjustable, for example, by bending to allow for a better and more secure fit.
- An elastic keeper such as an
- connector 21 permits the position of light source 19 to be adjusted both along a horizontal axis 30 A and a vertical axis 30 B relative to head-set 17 .
- a yoke 31 A is mounted to head-set 17 by screws 31 B which pass through slot 31 C.
- the position of light source 19 in horizontal direction 30 A can be adjusted by loosening screws 31 B, sliding yoke 31 A to a desired position along slot 31 C and retightening screws 31 B.
- Light source 19 is connected to arms 31 D of yoke 31 A by screws 31 E which pass through slots 31 F.
- the vertical position of light source 19 may be adjusted by loosening screws 31 E, sliding light source 19 up or down along slots 31 F to a desired vertical position and then retightening screws 31 E.
- slot 31 C is curved when viewed from above.
- Slot 31 C generally follows the curvature of a typical maxillary bone such that light source 19 can effectively be applied against the patient's skin for a range of positions of light source 19 along slot 31 C.
- connector 21 may hold light source 19 so that it is tilted with its lower edge projecting more in the direction of the patient than its upper edge.
- the angle of tile of light source 19 is adjustable. Head-set 17 may be adjusted so that light source 19 is biased against the patient's face when head set 17 is being worn by a patient.
- connector 21 may comprise a bar, rod or similar device that can be clamped or otherwise fastened to head-set 17 and a clip or similar mechanism that fastens light source 19 to the bar, rod or similar device.
- light source 19 can be removably detached from head-set 17 . This can be convenient for storage or transportation of light therapy apparatus 2 A.
- head-set 17 comprises an adjustable strap (not shown) which fits around the crown of a patient's head for securing the extra-oral light therapy device 2 A.
- the adjustable strap can also fit around a patient's chin and extend back to the crown and around the crown of a patient's head.
- the adjustable strap may be made of a flexible, elastic woven material.
- FIG. 10 shows a light therapy apparatus 34 comprising at least one light source 35 .
- Light source 35 comprises at least one light emitter, for example an LED array, mounted on a thin molded substrate 51 ( FIG. 11 ). More than one array of light emitters may be provided in light source 35 .
- the light source 35 shown in FIG. 10 has two arrays of LEDs.
- Arrays 36 of light emitters may be arranged in lower level 45 and an upper level 47 .
- the upper and lower levels may be separately controlled.
- the upper and lower levels respectively irradiate tissues of the upper and lower jaws.
- An attaching means 43 is provided for securing the device to the area of treatment.
- a power source and controller which may comprise a programmable controller 15 as described above, operate light source 35 to emit light according to a desired protocol.
- light source 35 has a right section 37 , a center section 39 and a left section 41 .
- Right section 37 and the left section 41 are respectively supported on the right and left sides of a patient's face.
- a light source 35 as shown in FIG. 10 may be supported by way of any suitable attaching means including:
- the LED arrays may be removably attached to light source 35 by suitable connectors 38 such as ribbon connectors or may be more permanently integrated into light source 35 as illustrated in FIG. 11 .
- suitable connectors 38 such as ribbon connectors or may be more permanently integrated into light source 35 as illustrated in FIG. 11 .
- Providing removable, repositionable LED arrays on a light source 35 permits LED arrays to be arranged on light source 35 so as to optimally illuminate target tissues. LED arrays may be concentrated to illuminate target tissues while areas of light source 35 that overly non-target tissues do not need to have any LED arrays.
- FIG. 12 shows a cross-section of an LED array 36 of external light therapy device 34 detached from substrate 51 .
- a clip or similar attaching means 53 allows the at least one LED array 36 to be mounted onto substrate 51 .
- Substrate 51 serves as a heat sink as described above.
- Substrate 51 may be made of aluminum or similar metal that is a good heat conductor.
- Substrate 51 may be moldable (i.e. flexible in one or two dimensions so that it can be formed to follow contours of a patient's face and, once formed, will retain its shape).
- Hinge-like members 49 may be provided between arrays 36 to allow light source 35 to be bent to provide a better fit around the facial area.
- Hinge-like member 49 may comprise a thin crease 50 or other bend line set into the substrate material, as illustrated in FIG. 11 .
- Hinge-like member 49 allows the center section 39 to fit around a patient's mouth and the right section 37 and the left section 41 to fit around a patient's face.
- Apparatus as described herein may be applied to treat a variety of conditions including:
- jaw osteonecrosis permits treatment of a condition for which existing treatments are highly invasive. Treating osteonecrosis using light therapy is significantly more cost-effective and comfortable for the patient than existing surgical treatment options.
- the apparatus may be applied by fitting a support to a patient.
- the support may comprise a head-set, intra-oral tray, a bite tab, or the like.
- one or more light sources are mounted to the support at locations where light from the light sources can illuminate a treatment area.
- a treatment regimen is then established.
- the physician, dentist, or therapist at his office or a patient at his home then performs the prescribed extra-oral light therapy treatment.
- intra-oral tray 7 Prior to extra-oral light therapy treatment, intra-oral tray 7 is prepared by filling it with a suitable settable material such as a clear vinyl siloxane gel or similar material. The intra-oral tray is then placed around the patient's teeth to obtain an impression of the patient's teeth. After the settable material sets, intra-oral tray 7 can be used to achieve consistent targeting of light to target tissues bone during subsequent treatments.
- a suitable settable material such as a clear vinyl siloxane gel or similar material.
- a physician, dentist, or therapist programs a patient's prescribed treatment regimen into a programmable controller 15 (see FIG. 6 , for example).
- Programmable controller 15 controls parameters of a light therapy treatment to be delivered by light therapy apparatus 2 .
- controller 15 may control the duration of the treatment, light intensity, pulse frequency, etc.
- Programmable controller 15 runs a patient's prescribed treatment regimen causing the at least one light source 4 to emit pulsed or continuous light according to the prescribed parameters onto the treatment area. Therefore, stimulating and accelerating bone formation and healing at a patient's treatment area for the treatment of jaw bone disorders and jaw osteonecrosis.
- the invention also relates to a method for the treatment and stimulation of soft and hard tissue and the biostimulation of bone.
- a light source 35 which may comprise at least one LED array 36 is first attached to the desired area of treatment.
- a physician, dentist, or therapist programs a patient's prescribed treatment regimen into a programmable controller 15 .
- Programmable controller 15 controls the energy density, pulse frequency and duration of the external light therapy device 34 .
- the programmable controller 15 runs a patient's prescribed treatment regimen causing the at least one LED array 35 to emit pulsed or continuous light at the predetermined rates and frequencies onto the treatment area.
- the light therapy device can provide effective, stabilized, repeatable, accurate, programmable, and consistent light therapy for the treatment and stimulation of soft and hard tissue and the biostimulation of bone.
- Exclusion criteria included: 1) a medical condition associated with abnormal bone growth or remodeling, such as Paget's disease of bone, fibrous dysplasia, osteopetrosis, severe systemic osteoporosis, etc.; 2) unwillingness to sign informed consent form; 3) inability to perform daily LED treatments at home; 4) inability to obtain high quality QUS scans of the jaws.
- An exclusion waiver for the research was provided by the Committee for the Protection of Human Subjects of the University of Texas in Houston and informed consent was obtained from all subjects.
- III Cube shows moderate loss of column height in more than 1 ⁇ 2 of columns (32 columns); and/or severe loss of column height in 1 ⁇ 4 to 1 ⁇ 2 of columns (17-32 columns).
- IV Cube shows severe loss of column height in more than 1 ⁇ 2 of columns (32 columns).
- the investigational OsseoPulseTM (Version 1.0) device made by Biolux Research Ltd., Vancouver, Canada.
- the device consists of an extra-oral array of highly-efficient light emitting diodes (LED) producing non-coherent continuous wave monochromatic light in the visible far red (660 nm @ 15 mW/cm2) and infra-red range (840 nm @ 20 mW/cm2).
- LED highly-efficient light emitting diodes
- the OsseoPulse device was placed on the facial surface for 15 minutes daily, 5 days a week for 12 weeks on each treatment side.
- the dose per session per treatment area was approximately 200 Joules per square inch.
Abstract
An extra-oral light therapy device comprises a support that registers against features of a patient's head. A light source is mounted to the support. The light source may comprise an array of light emitting diodes (“LEDs”). A controller controls the extra-oral light therapy device. The support may comprise a tray fitted to the patient's teeth or a head-set fitted to the patient's ears and the bridge of the patient's nose. An external light therapy device has a thin, molded substrate, at least one array of light emitters mounted onto the thin, molded substrate, an attaching means for removably attaching the device to an area of treatment, and a controller for controlling the external light therapy device. Methods for supporting light sources adjacent desired treatment locations and for treating jaw bone disorders and jaw osteonecrosis and biostimulating bone and soft tissue are also disclosed.
Description
- This application is a division of U.S. patent application Ser. No. 11/767,302, filed Jun. 22, 2007, which is a continuation-in-part of U.S. patent application Ser. No. 11/355,583, filed Feb. 16, 2006, which claims the benefit of U.S. Provisional Application No. 60/705,753, filed on Aug. 5, 2005 and U.S. Provisional Application No. 60/653,828, filed Feb. 17, 2005, the contents of each of which is incorporated herein by reference in its entirety.
- This invention relates to light therapy. Apparatus and methods according to the invention may be applied to the treatment of bone disorders and the biostimulation of bone and soft tissue. Embodiments of the invention provide apparatus for irradiating tissues of the face and jaw with biologically effective doses of light.
- Light therapy involves irradiating tissues with light. Light can stimulate a variety of biological activities in cells and tissues that are compromised in function. Light therapy treatment is typically administered by a physician or therapist who directs light from a hand-held light emitting device at an affected area. Light emitting devices can be difficult to position consistently over the affected area. Sometimes a tattoo is used to identify the affected area. However, even with a tattoo or other reference mark it is difficult to consistently deliver light therapy treatments to an affected area.
- Light therapy typically involves repeated treatments over at least several days. Thus, patients undergoing light therapy may be required to make multiple visits to a practitioner's office or clinic in order to complete a therapy regimen. Such repeated visits may be time consuming and/or expensive.
- LEDs and other light sources suitable for generating light for light therapy can get hot when they operate. Such light sources can be inefficient at higher temperatures. Hot apparatus can also be uncomfortable or even dangerous to patients.
- The inventor has identified a need or desire for light therapy apparatus which can deliver consistent treatments, particularly to tissues in the dental and maxillofacial areas. There is a particular need or desire for such apparatus that is sufficiently cost-effective and foolproof to be used at home by patients. There is also a need for such apparatus that can be operated without exposing a patient to high temperature surfaces.
- One aspect of this invention provides apparatus for delivering light to tissues of a patient's dental and maxillofacial areas. The apparatus comprises a support that registers against one or more anatomical features of a patient's head and one or more light sources mounted to the support. The light sources illuminate selected tissues of a patient's dental and maxillofacial areas from outside of the patient's mouth. The light sources comprise arrays of LEDs in some embodiments.
- In some embodiments the support comprises an intra-oral tray connected to an extra-oral bridge. A light source, such as a light emitting diode (“LED”) array, is mounted to the extra-oral bridge.
- In some embodiments, the support comprises a head-set that registers on the bridge of a patient's nose and the patient's ears. A light source, such as a light emitting diode (“LED”) array, is mounted to the head-set.
- Other aspects of the invention provide methods for preparing light therapy apparatus and methods for delivering light therapy.
- Further aspects of the invention and features of various example embodiments of the invention are described below and/or shown in the accompanying drawings.
- The appended drawings illustrate non-limiting example embodiments of the invention.
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FIG. 1 is a view from the front side of an extra-oral light therapy device having an intra-oral tray, an extra-oral bridge, and left and right side extra-oral LED arrays. -
FIGS. 1A , 1B and 1C are respectively a cross-section, a front side elevation and a rear elevation of a light source having a cooling fan, a heat sink and two arrays of light emitters. -
FIG. 2 is a right side view of the device ofFIG. 1 with the end of the extra-oral bridge attached to the extra-oral LED array. -
FIG. 3 is a view from the front-left side of the extra-oral bridge, intra-oral tray and extra-oral LED array ofFIG. 1 . -
FIG. 4 is a view from the rear right side of the extra-oral bridge, intra-oral tray and extra-oral LED array ofFIG. 1 . -
FIG. 5 is a view from the left rear side of the extra-oral bridge, intra-oral tray and extra-oral LED array ofFIG. 1 with the intra-oral tray detached. -
FIG. 6 is a top view of a programmable controller for use with light therapy apparatus. -
FIG. 7 is a perspective view of a light therapy device according to an alternative embodiment in which an LED array is supported by a head-set. -
FIG. 7A is a perspective view of a light therapy device according to another alternative embodiment in which an LED array is supported by a head-set. -
FIG. 8 is a side view of the light therapy device ofFIG. 7 . -
FIG. 9 is a front view of at least one LED array, and a connector detached from the head-set. -
FIG. 10 is a front view of an external light therapy device having two LED arrays, a hinge-like member, and an attaching means. -
FIG. 11 is a cross-sectional view of an LED array mounted onto a substrate. -
FIG. 11A is a schematic cross section through a portion of a light source having a light emitter and a reflector. -
FIG. 12 is a cross-sectional view of an LED array detached from the substrate. - Throughout the following description specific details are set forth in order to provide a more thorough understanding to persons skilled in the art. However, well known elements may not have been shown or described in detail to avoid unnecessarily obscuring the disclosure. Accordingly, the description and drawings are to be regarded in an illustrative, rather than a restrictive, sense.
-
FIG. 1 shows an examplelight therapy apparatus 2 that comprises anextra-oral light source 4 having aright side 1 and a left side 3 (as viewed from the front of the device), anextra-oral bridge 5, and anintra-oral tray 7. Intra-oral tray 7 registers to a patient's teeth.Light source 4 is rigidly connected tointra-oral tray 7 byextra-oral bridge 5. Therefore, a patient can positionlight source 4 accurately and repeatedly to illuminate a desired location in the patient's dental and maxillofacial areas by insertingintra-oral tray 7 into his or her mouth and bitingintra-oral tray 7 so that it registers to at least some of the patient's teeth. This stabilizeslight therapy apparatus 2 andpositions light source 4 at a desired position. The consistent alignment and targeting of light fromlight source 4 during subsequent treatments makes the treatments more repeatable. - In the illustrated embodiment,
extra-oral bridge 5 is removable from extra-orallight source 4 andintra-oral tray 7. Providing alight therapy apparatus 2 having major components that are detachably connectable to one another adds versatility. A design which permits the major components of the light therapy apparatus to be disassembled and reassembled while preserving alignment of extra-orallight source 4 tointra-oral tray 7 has the advantage that the apparatus can be disassembled for storage or transportation and then used immediately after assembly.FIG. 3 showslight therapy apparatus 2 with extra-oral light sourceleft side 3 detached fromextra-oral bridge 5. -
Extra-oral bridge 5, extra-oral light sourceright side 1, and extra-oral light sourceleft side 3 may be secured together via a suitable connector. For example,extra-oral bridge 5, the extra-oral light sourceright side 1, and the extra-oral light sourceleft side 3 may be connected by insertingmale connector portions 6A of the extra-oral light source right and leftsides female connector portions 8A of extra-oral bridge 5 (seeFIG. 3 ). Suitably, the suitable connector allows extra-oral light source right and leftsides extra-oral bridge 5 for ease of use and flexibility. - In some embodiments, extra-oral light source right and left
sides FIG. 1 ) and a vertical orientation (indicated in dotted outline inFIG. 1 ). Light source right and leftsides sides -
Intra-oral tray 7 may be connected toextra-oral bridge 5 by way of another suitable connector. In the embodiment illustrated inFIG. 5 , amale portion 6B ofintra-oral tray 7 is removably received in afemale portion 8B ofextra-oral bridge 5. Whereintra-oral tray 7 is removable fromextra-oral bridge 5,extra-oral bridge 5 may be reused for other patients (after suitable sterilization).Intra-oral tray 7 may be disposed of after it is no longer required by a patient. In some embodiments,extra-oral bridge 5 is non-removably attached tointra-oral tray 7. -
Intra-oral tray 7 is intended for insertion into a patient's mouth and is suitably shaped to fit around a patient's teeth.Intra-oral tray 7 may register with a few selected teeth (for example,intra-oral tray 7 may comprise a bite tab) or may fit around the patient's full set of teeth. In one embodiment, theintra-oral tray 7 comprises a frame of a plastic or other suitable material that can serve as a skeleton for a settable material. The frame may be perforated to aid retention of the settable material. The frame may compriseextra-oral bridge 5 or a connector to connect toextra-oral bridge 5. - Prior to being used in the delivery of light therapy, the frame for
intra-oral tray 7 may be filled with a suitable settable material (for example a clear vinyl siloxane gel or similar material) which sets around the patient's teeth and subsequently allows repeatable alignment ofintra-oral tray 7 in the patient's mouth. Whereintra-oral tray 7 could be in the path of light as it travels fromlight source 4 to target tissues, the material ofintra-oral tray 7 should be transparent to the light. -
Extra-oral bridge 5 preferably conforms around the jaw line of a patient. The light source right and leftsides Extra-oral bridge 5 may be adjustable to permit alignment of light source left andright sides right sides right sides -
Light source 4 emits light toward the patient. The light is not necessarily visible light. For example, the light may include or consist of infrared light.Light source 4 comprises an array of light-emitting diodes (LEDs) in some embodiments.Light source 4 has an inner surface 13 (seeFIG. 4 ) that is placed near or against the patient's skin adjacent to the tissues that it is desired to treat. Light is emitted is frominner surface 13 toward the area of treatment. In some embodiments, left andright sides light source 4 each have a length similar to a significant fraction of the length of a human jaw. For example, left andright sides light source 4 is intended to treat a localized condition, thenlight source 4 may be smaller in extent. In some embodiments,light source 4 has optics that emit light in the form of diverging beams. In such cases,light source 4 may be somewhat smaller than the area of tissues to be treated because light fromlight source 4 will spread somewhat as it passes through the tissues of the patient's lips and cheeks before reaching the tissues of the jaw and or gums to be treated. -
Light source 4 may be wide enough to illuminate both upper and lower jaws of a patient simultaneously although in some embodimentslight source 4 may be narrower. For example,light source 4 has a width in the range of 12 mm to about 40 mm in some embodiments (e.g. about 15 to 17 mm in some embodiments). - In some embodiments, the light is emitted by arrays of discrete LEDs. The LEDs may be arranged in any of a wide variety of patterns. For example, the LEDs may be arranged in staggered parallel rows to maximize the density of LEDs in the LED array. The LEDs may be arranged to achieve substantially uniform optical intensity over the light-emitting
inner surface 13 oflight source 4. In some embodiments, each array comprises 50 to 100 LEDs or other light emitters. - It is desirable that the average light intensity produced by
light source 4 is at least about 10 mW/cm2. In some embodiments,light source 4 has an average intensity that is, or can be adjusted to be, in the range of 20 mW/cm2 to about 60 mW/cm2. In some embodiments the output oflight source 4 is pulsed. In such embodiments, the peak light intensity may be significantly higher than 50 mW/cm2. - In some embodiments right
light source 4 or its components are flexible so that they can be bent in one or two dimensions (i.e. molded) to conform to the contours of the patient's face. For example,light source 4 may comprise an array of light emitters mounted to a flexible sheet of material that will hold a shape when it is bent. The flexible material can advantageously comprise a metal sheet that can serve as a heat sink or as a thermal path to a heat sink for heat generated by the light emitters. The flexible sheet may be molded to conform to the contours of the patient's face whilelight therapy apparatus 2 is being fitted. -
Light source 4 may include optical elements such as lenses and reflectors to focus and direct light fromlight source 4 onto a target area. Such optical elements may be suitably encapsulated in plastic or similar material.FIG. 11A shows a portion of alight source 4. A light emitter 11 (which may, for example, comprise a junction in a light-emitting diode or other light-emitting semiconductor device) is located adjacent to areflective backing 11A. A curved light-reflectingrecess 11B is provided adjacent tolight emitter 11. Light fromlight source 11 is reflected inrecess 11B to form a beam. The beams from all light emitters oflight source 4 combine to illuminate the target tissues. The area covered by the beam will depend upon the tissues which it is desired to treat. In some embodiments, the beams of light emitted bylight source 4 diverges to cover an area of tissue larger than the area of the light-emitting part oflight source 4. In other embodiments the emitted light converges to provided increased light intensity at the location of the tissues that it is desired to treat. In some embodiments, the emitted light diverges in a beam having an included angle ÿ in the range of about 45-60°. - Since LEDs and other light emitters give off heat when they are operated, it is desirable to provide a suitable mechanism for dissipating the heat to prevent any parts of
light therapy apparatus 2 that could come into contact with a patient's skin from getting too hot. For example,light source 4 may comprise a system for forced air or liquid cooling. A cooling system allows for treatment without the danger of potential burns to the patient and allows for greater efficiency and control of the device. - Extra-oral light source right and left
sides FIGS. 1A , 1B and 1C show alight source 100 of a type that may be used as light source right and leftsides Light source 100 comprisesarrays 102 of LEDs that are mounted to aheat sink 104.Heat sink 104 haspins 106 projecting from its face that is away fromLED arrays 102. Afan 110 causes air to flowpast pins 106 to carry away excess heat. - To be most effective, the light from
light source 4 at the tissues to be treated should have at least a threshold intensity.Light source 4 may be operated in a pulsed mode to facilitate cooling oflight source 4 while ensuring that whenlight source 4 is emitting light, the intensity of emitted light at the tissues to be treated is sufficient to be effective. In some embodiments, the duty cycle oflight source 4 is 1:1 or less, in some embodiments 1:2 or less (for each interval in whichlight source 4 is on,light source 4 is off for two equal intervals). The pulsing oflight source 4 may be performed fast enough thatlight source 4 does not visibly flicker (e.g. at 25 Hz or more) although this is not mandatory. - While the invention is described herein as usefully employing LEDs, other light sources such as lasers could suitably be employed. The character of the light emitted by light source right and left
sides light source 4. It is generally desirable that the emitted light include light in the wavelength range of 620 nm to 1000 nm. In some embodiments the emitted light includes light having a wavelength in at least one of the following wavelength ranges: about 820 to about 890 nm and about 620 to about 680 nm. Light having wavelengths corresponding to one or more of the following ranges may be particularly effective: - 613 nm to 624 nm
- 667 nm to 684 nm
- 750 nm to 773 nm
- 812 nm to 846 nm.
- The range 613 nm to 624 nm corresponds to a band at which reduced cytochrome c oxidase absorbs light. The range 812 nm to 846 nm corresponds to a band at which oxidized cytochrome c oxidase absorbs light.
- The light is substantially monochrome in some embodiments although this is not mandatory. Providing light emitters that emit at multiple wavelengths allows for irradiation over multiple wavelengths for greater biological activity. The light may comprise incoherent light although this is not mandatory. The light may be delivered continuously or pulsed at suitable frequencies and duty cycles.
- Invisible infrared light can be clinically effective. In some embodiments in which the emitted light includes infrared light, the emitted light also includes bright visible light. The bright visible light deters users from looking into the light source when it is operating, provides a perceptible indication that the apparatus is operating, and may be useful in properly positioning the device. The visible light may be, but is not necessarily in a wavelength range that is beneficial for light therapy. In some embodiments, the ratio of the intensities of the visible and infrared components of the light is 1 part or less visible light to 5 parts or more infrared light.
- The treatment area and desired light characteristics will vary from patient to patient. A physician, dentist or other therapist can determine a light treatment regime for a patient and set up
light therapy apparatus 2 to operate light emitters inlight source 4 to provide the desired treatment. -
FIG. 6 illustrates aprogrammable controller 15 of a type that may be used to control the operation of light therapy apparatus 2 (or other light therapy apparatus as described below).Programmable controller 15 may be a separate, remote unit or may be directly connected to or integrated withlight source 4.Programmable controller 15 may comprise a microprocessor, data store, power supply, clock and associated electronic circuitry. Control parameters are stored in the data store.Programmable controller 15 operateslight source 4 according to the parameters in the data store. The parameters may specify one or more of: -
- treatment duration;
- light intensity during the treatment;
- whether light emitters operate continuously or are pulsed;
- if the light emitters are pulsed, the rate at which light emitters are pulsed;
- if the light emitters are pulsed, the duty cycle at which the light emitters are pulsed;
- etc.
- If light therapy apparatus has sets of light emitters having different characteristics (e.g. sets of LED that emit light at different wavelengths or sets of light emitters that illuminate target tissues in different locations) then separate control parameters may be provided for different sets of the light emitters. In some embodiments, different sets of parameters are specified for different segments (intervals) of a light treatment. For example, light therapy treatments may be defined for a set of intervals each lasting from a few seconds to a few hundred seconds or a fraction of an hour. Different parameters may be specified for each of the intervals. The intervals are not necessarily equal in length.
- In some embodiments, different sets of parameters may be specified for different areas of
light source 4. In some cases, some areas oflight source 4 may be turned off because the treatment plan for a patient does not require light to be delivered at locations corresponding to those parts of thelight source 4. - A physician, dentist, or therapist may program a patient's treatment regimen into
programmable controller 15. This may be done, for example, with the aid of suitable software running on a computer that is in data communication withprogrammable controller 15 or by way of a suitable user interface built intoprogrammable controller 15. -
Programmable controller 15 may have one or more pre-set programs built in. As an alternative to, or as an aid toprogramming controller 15 the physician, dentist, or therapist may select a pre-set program that is appropriate for controllinglight therapy apparatus 2 to deliver light to a patient. - A typical treatment regimen provides a dose of light daily. Each of the daily doses of light may be delivered over a period lasting between a few minutes and an hour or so. For example. the inventor has found that daily ½ hour doses of light can be effective and are not unduly inconvenient for patients. A single daily dose appears to be as effective as dividing the same dose into multiple sessions delivered at different times during the day. Examples of possible treatment regimens are
-
- Enhancement of bone density by applying light in 5 treatments per week for 12 weeks. Each treatment lasts ½ hour and illuminates the tissues of a patient's jaw with light having wavelengths of 660 nm and 840 nm. The 660 nm light has an intensity of about 20 mW/cm2 at the skin's surface The 840 nm light has an intensity of about 10 mW/cm2 at the skin's surface.
- Accelerating healing of bone grafts by applying light in daily treatments for 21 days. Each treatment lasts between 20 minutes and one hour and illuminates the tissues of a patient's jaw with light having a wavelength of 618 nm and an intensity of 20 mW/cm2 at the skin's surface.
-
Programmable controller 15 may maintain a log of treatments that have been delivered. For example,controller 15 may log the date and time that each treatment was initiated, the duration of the treatment, and whether or not the treatment was completed. This log can be subsequently reviewed by a dentist, physician, or the like to evaluate whether or not the patient has complied with the prescribed treatment regimen. -
Programmable controller 15 has a button or other suitable user patient interface that allows a patient to initiate a treatment according to previously-set parameters in the data store. The patient interface is preferably very simple such that minimal instruction is required to explain to a patient how to uselight therapy apparatus 2.Programmable controller 15 may include an audible or visual indicator that generates a signal to remind a patient that it is time for a treatment (or that a scheduled treatment is overdue). - A patient can use
light therapy apparatus 2 at home or in another location by operatingprogrammable controller 15 to initiate delivery of a treatment. -
Programmable controller 15 may comprise circuitry that monitors temperature at one or more locations inlight source 4. The circuitry may monitor a signal modulated by a temperature sensor inlight source 4. In the alternative,programmable controller 15 may monitor the current and voltage driving LEDs inlight source 4. The current/voltage relationship is temperature-dependent. Thus, by monitoring the current/voltage relationshipprogrammable controller 15 can determine whether the LED is at an undesirably high temperature.Programmable controller 15 may shut off or reduce current to light source 4 (or part of light source 4) when it detects that the temperature oflight source 4 is undesirably high (or is trending towards being undesirably high). Iflight source 4 is equipped with a cooling fan thenprogrammable controller 15 may optionally control the speed of the cooling fan in response to the monitored temperature. -
Programmable controller 15 may be configured to maintain a log of treatments delivered bylight therapy apparatus 2. The log may be reviewed by a physician, dentist or technician to verify that light therapy device has been used as prescribed by a patient. The log may track the times and durations of light therapy treatments delivered bylight therapy apparatus 2 and may also track other features such as operating temperatures, operational status and the like. -
FIGS. 7 and 8 show alight therapy apparatus 2A having a head-set style arrangement.Light therapy apparatus 2A comprises a head-set 17 and at least one extra-orallight source 19 mounted to head-set 17 by way of asuitable connector 21. Head-set 17 may have the general form of a frame for eyeglasses. In the illustrated embodiment,headset 17 hasarms 27 that fit above and around the patient's ears and aframe 29 that fits over the bridge of the patient's nose. Head-set 17 may also include lenses (not shown). Suitably, the lenses may be made of a material that blocks radiation at wavelengths emitted bylight source 19 so that the patient's eyes are protected from the radiation.Light source 19 may comprise an array of LEDs or other light emitters. - When head-set 17 has been adjusted to fit an individual patient,
frame 29 registers with the bridge of the patient's nose andarms 27 sit on the patient's ears. Head-set 17 will sit on the patient's head in the same way each time it is put on. Head set 17 may be adjusted for fit by adjustingarms 27 which may be made of a firm, resilient material that allows for some flexibility for a better and more secure fit for individual users. In some embodiments,arms 27 can also be adjusted horizontally along their axis.Frame 29 can also be adjustable, for example, by bending to allow for a better and more secure fit. An elastic keeper such as an elastic strap may be provided to hold head-set 17 in place during use. - In the embodiment shown in
FIG. 7A ,connector 21 permits the position oflight source 19 to be adjusted both along ahorizontal axis 30A and avertical axis 30B relative to head-set 17. Ayoke 31A is mounted to head-set 17 byscrews 31B which pass throughslot 31C. The position oflight source 19 inhorizontal direction 30A can be adjusted by looseningscrews 31B, slidingyoke 31A to a desired position alongslot 31C and retightening screws 31B.Light source 19 is connected toarms 31D ofyoke 31A byscrews 31E which pass throughslots 31F. The vertical position oflight source 19 may be adjusted by looseningscrews 31E, slidinglight source 19 up or down alongslots 31F to a desired vertical position and then retighteningscrews 31E. - In the illustrated
embodiment slot 31C is curved when viewed from above.Slot 31C generally follows the curvature of a typical maxillary bone such thatlight source 19 can effectively be applied against the patient's skin for a range of positions oflight source 19 alongslot 31C. Since the lower portions of people's faces are typically narrower than upper portions,connector 21 may holdlight source 19 so that it is tilted with its lower edge projecting more in the direction of the patient than its upper edge. In some embodiments the angle of tile oflight source 19 is adjustable. Head-set 17 may be adjusted so thatlight source 19 is biased against the patient's face when head set 17 is being worn by a patient. - Many alternative designs for
connector 21 may be provided. For example,connector 21 may comprise a bar, rod or similar device that can be clamped or otherwise fastened to head-set 17 and a clip or similar mechanism that fastenslight source 19 to the bar, rod or similar device. - As shown in
FIG. 9 , in some embodimentslight source 19 can be removably detached from head-set 17. This can be convenient for storage or transportation oflight therapy apparatus 2A. - In another embodiment, head-set 17 comprises an adjustable strap (not shown) which fits around the crown of a patient's head for securing the extra-oral
light therapy device 2A. The adjustable strap can also fit around a patient's chin and extend back to the crown and around the crown of a patient's head. The adjustable strap may be made of a flexible, elastic woven material. -
FIG. 10 shows alight therapy apparatus 34 comprising at least onelight source 35.Light source 35 comprises at least one light emitter, for example an LED array, mounted on a thin molded substrate 51 (FIG. 11 ). More than one array of light emitters may be provided inlight source 35. For example, thelight source 35 shown inFIG. 10 has two arrays of LEDs. Arrays 36 of light emitters may be arranged inlower level 45 and anupper level 47. The upper and lower levels may be separately controlled. The upper and lower levels respectively irradiate tissues of the upper and lower jaws. An attaching means 43 is provided for securing the device to the area of treatment. - A power source and controller, which may comprise a
programmable controller 15 as described above, operatelight source 35 to emit light according to a desired protocol. - In the
example apparatus 34 shown inFIG. 10 ,light source 35 has aright section 37, acenter section 39 and aleft section 41.Right section 37 and theleft section 41 are respectively supported on the right and left sides of a patient's face. Alight source 35 as shown inFIG. 10 may be supported by way of any suitable attaching means including: -
- a head-set 17 as described above;
- an
intra-oral tray 7 which may comprise a full tray or one or more bite tabs as described above; - an adhesive such as double-sided adhesive tape;
- a strap or set of straps; or
- the like.
- The LED arrays may be removably attached to
light source 35 bysuitable connectors 38 such as ribbon connectors or may be more permanently integrated intolight source 35 as illustrated inFIG. 11 . Providing removable, repositionable LED arrays on alight source 35 permits LED arrays to be arranged onlight source 35 so as to optimally illuminate target tissues. LED arrays may be concentrated to illuminate target tissues while areas oflight source 35 that overly non-target tissues do not need to have any LED arrays. -
FIG. 12 shows a cross-section of an LED array 36 of externallight therapy device 34 detached fromsubstrate 51. A clip or similar attachingmeans 53 allows the at least one LED array 36 to be mounted ontosubstrate 51.Substrate 51 serves as a heat sink as described above.Substrate 51 may be made of aluminum or similar metal that is a good heat conductor.Substrate 51 may be moldable (i.e. flexible in one or two dimensions so that it can be formed to follow contours of a patient's face and, once formed, will retain its shape). - Hinge-
like members 49 may be provided between arrays 36 to allowlight source 35 to be bent to provide a better fit around the facial area. Hinge-like member 49 may comprise athin crease 50 or other bend line set into the substrate material, as illustrated inFIG. 11 . Hinge-like member 49 allows thecenter section 39 to fit around a patient's mouth and theright section 37 and theleft section 41 to fit around a patient's face. - Apparatus as described herein may be applied to treat a variety of conditions including:
- jaw osteonecrosis,
- other jaw bone disorders,
- periodontitis,
- malocclusion and other conditions treated by orthodontics,
- stimulation and acceleration of healing after oral surgery or periodontal surgery,
- stimulation of the healing of wounds at the locations of bone grafts,
- healing and acceleration of osseo-integration of endosseous dental implants; and,
- the like.
- The application to jaw osteonecrosis permits treatment of a condition for which existing treatments are highly invasive. Treating osteonecrosis using light therapy is significantly more cost-effective and comfortable for the patient than existing surgical treatment options.
- The apparatus may be applied by fitting a support to a patient. The support may comprise a head-set, intra-oral tray, a bite tab, or the like. When the support has been fitted so that it can be repeatably worn by the patient one or more light sources are mounted to the support at locations where light from the light sources can illuminate a treatment area. A treatment regimen is then established. The physician, dentist, or therapist at his office or a patient at his home then performs the prescribed extra-oral light therapy treatment.
- An example method for treatment for jaw osteonecrosis, other jaw bone disorders, periodontitis, orthodontics, or for stimulation and acceleration of healing after oral surgery or periodontal surgery or for acceleration of osseo-integration of endosseous dental implants applies extra-oral
light therapy device 2. Prior to extra-oral light therapy treatment,intra-oral tray 7 is prepared by filling it with a suitable settable material such as a clear vinyl siloxane gel or similar material. The intra-oral tray is then placed around the patient's teeth to obtain an impression of the patient's teeth. After the settable material sets,intra-oral tray 7 can be used to achieve consistent targeting of light to target tissues bone during subsequent treatments. - A physician, dentist, or therapist programs a patient's prescribed treatment regimen into a programmable controller 15 (see
FIG. 6 , for example).Programmable controller 15 controls parameters of a light therapy treatment to be delivered bylight therapy apparatus 2. For example,controller 15 may control the duration of the treatment, light intensity, pulse frequency, etc.Programmable controller 15 runs a patient's prescribed treatment regimen causing the at least onelight source 4 to emit pulsed or continuous light according to the prescribed parameters onto the treatment area. Therefore, stimulating and accelerating bone formation and healing at a patient's treatment area for the treatment of jaw bone disorders and jaw osteonecrosis. - The invention also relates to a method for the treatment and stimulation of soft and hard tissue and the biostimulation of bone. In this method, a
light source 35 which may comprise at least one LED array 36 is first attached to the desired area of treatment. A physician, dentist, or therapist programs a patient's prescribed treatment regimen into aprogrammable controller 15.Programmable controller 15 controls the energy density, pulse frequency and duration of the externallight therapy device 34. Theprogrammable controller 15 runs a patient's prescribed treatment regimen causing the at least oneLED array 35 to emit pulsed or continuous light at the predetermined rates and frequencies onto the treatment area. The light therapy device can provide effective, stabilized, repeatable, accurate, programmable, and consistent light therapy for the treatment and stimulation of soft and hard tissue and the biostimulation of bone. - Several studies have been carried out to determine the effectiveness of the invention. In one, a retrospective record review of a cohort of 68 QUS (quantitative ultrasound) scanned dental patients from the private practices of two co-investigators as performed. All scans and treatments occurred between 2002 and 2005. Inclusion criteria included: 1) no surgical procedure at an investigative site during or less than one year prior to entry into the study; 2) pre-treatment and post-treatment QUS scans of the maxillofacial region; 3) LED therapy to one or more maxillofacial regions. Exclusion criteria included: 1) a medical condition associated with abnormal bone growth or remodeling, such as Paget's disease of bone, fibrous dysplasia, osteopetrosis, severe systemic osteoporosis, etc.; 2) unwillingness to sign informed consent form; 3) inability to perform daily LED treatments at home; 4) inability to obtain high quality QUS scans of the jaws. An exclusion waiver for the research was provided by the Committee for the Protection of Human Subjects of the University of Texas in Houston and informed consent was obtained from all subjects.
- QUS scans were made immediately prior to LED therapy and immediately thereafter. All scans were performed by the FDA cleared dental QUS device, the Cavitat 4000™ (Cavitat Medical Technologies, Inc, Aurora, Colo.). This device renders a series of 3-dimensional cube images from analog signals generated when an external transmitter sends 27,000 sound pulses per microsecond through the alveolar bone at a speed of 317.6 meters per second, 3.5 mHz, to an intraoral piezo screen held on the lingual aspect of the alveolus. The screen has 64 sensors which detect electrical changes in the screen as sound distorts it. The test is premised on the assumption that sound traveling through LBD (low bone density) becomes attenuated, hitting the receptor screen with less intensity than sound which has traveled through normal bone. The speed of sound is also diminished and so changes in speed are captured and accounted for by the device.
- All initial and follow-up QUS scans of alveolar bone were blindly and independently graded, after calibration, by two investigators according to an established 5-point scale, and the following results were shown (Table 1):
-
TABLE 1 Grading categories for individual 3-D cube images (64 columns in each) of the Cavitat QUS images. QUS Grade * Description ** 0 “Green bone.” Cube shows no loss of column height and is 100% green; or mild loss of column height in less than ¼ of columns (16 columns); and/or moderate to severe loss of column height in less than 4 non-adjacent columns. I Cube shows mild loss of column height in more than ¼ of columns; and/or moderate loss of column height in 1/16 to ¼ of the columns (5-16 columns); and/or severe loss of height in 1/16 to ⅛ of the columns (5-8 columns). II Cube shows moderate loss of column height in ¼ to ½ of columns (17-32 columns); and/or severe loss of height in ⅛ to ¼ of columns (8-16 columns). III Cube shows moderate loss of column height in more than ½ of columns (32 columns); and/or severe loss of column height in ¼ to ½ of columns (17-32 columns). IV Cube shows severe loss of column height in more than ½ of columns (32 columns). * high grade lesion = Grade III and IV scans; low-grade lesion = Grade I and II scans; “green bone” = normal or Grade 0 scan ** definition of loss of column height: mild (crown is green, less than ⅓ loss of height); moderate (crown is yellow or brown, ⅓ to ⅔ loss of height); severe (crown is orange or red, more than ⅔ loss of height) - In case of differences, a consensus grade was arrived at via discussion between the two. QUS grades of positive scans, i.e. scans with grades I-IV before LED therapy were compared with post-therapy scan grades using matched pair analysis.
- Patients were treated using the a device made in accordance with the present invention, the investigational OsseoPulse™ (Version 1.0) device (made by Biolux Research Ltd., Vancouver, Canada). The device consists of an extra-oral array of highly-efficient light emitting diodes (LED) producing non-coherent continuous wave monochromatic light in the visible far red (660 nm @ 15 mW/cm2) and infra-red range (840 nm @ 20 mW/cm2). In addition, there was an integral alignment device used to ensure that the LED array was repeatably and accurately positioned directly over the treatment sites. The OsseoPulse device was placed on the facial surface for 15 minutes daily, 5 days a week for 12 weeks on each treatment side. The dose per session per treatment area was approximately 200 Joules per square inch.
- Of 1,148 pre-treatment QUS jawbone scans, each representing the area of one tooth, 294 were positive for damaged or abnormal bone. Using the 5-point scale (0=normal; 4=most severe), half of these sites were low grade, i.e.
grades -
TABLE 2 Results of 294 QUS scans before and after 3 months of daily LED photobiomodulation. Grade Level * # at Pre-Treatment # at Post-Treatment 1 79 120 2 69 54 3 86 53 4 61 40 Mean: 2.43 1.33 * 1 = mild LBD/dehydration; 4 = severe LBD/dehydration - The average grade for all 294 positive sites was 2.43. After LED photomodulation the average grade was 1.33 and almost 42% of investigated sites had returned to completely normal bone, while another 54 (18.4%) sites were
grade 1 after therapy (Table 2). One would expect that the lower the pre-treatment grade, the larger would be the proportion which returned to normal, since it takes a much greater grade improvement to reach normal from the higher grades. This proved to be the case: regions with pre-treatment grades of 1, 2, 3 and 4 returned to green bone 68.4%, 46.4%, 30.2% and 13.3% of the time, respectively (Table 3): -
TABLE 3 Post-treatment changes for each pre-treatment grade level, 294 QUS scans. Number of Sites Number @ Grade for each Site at Grade at Post-Treatment* Avg. Level* Pre-Treatment 0** 1** 2** 3** 4** Change 1 79 54 15 8 2 0 −0.54 2 69 32 19 12 4 2 −1.32 3 86 26 17 22 16 5 −1.50 4 60 8 3 10 18 21 −1.32 Mean: 2.43 120 54 52 40 28 −1.11 *1 = mild LBD/dehydration; 4 = severe LBD/dehydration (see Table 1) **Represents grade levels, 0-4, as described in Table 1 - Almost 71% of the 294 treated sites demonstrated improvement of at least one QUS grade level, with most of those, 43.4%, dropping by one grade. The post-treatment grade change was relatively uniform all each pretreatment QUS grade level (Table 3). Overall the mean difference, i.e. improvement of bone quality, of −1.11 was very statistically significant (matched pair analysis: Std error 0.06914; t-Ratio −15.9896; DF 293; prob [t] less than 0.0001; 95% confidence interval 0.558-1.242).
- While in the foregoing specification this invention has been described in relation to certain preferred embodiments thereof, and many details have been set forth for the purpose of illustration, it will be apparent to those skilled in the art that the invention is susceptible to additional embodiments and that certain details described herein can be varied considerably without departing from the basic principles of the invention. For example:
-
-
Light therapy apparatus 34 may be applied for treatment and stimulation of other bone or soft tissues, such as the hip. In such applications,light source 35 can be attached to a treatment area with an adhesive such as double-sided adhesive tape (not shown). Alternatively, the externallight therapy apparatus 34 can be placed or sewn into a pouch, undergarment or similar garment and attached to the treatment area through means of a strap, button or similar attaching means (not shown). - It is not mandatory that a controller be programmable. For example, a controller may have controls that allow various parameters to be set. A physician, therapist or technician may set those controls so that an appropriate treatment is delivered when a patient initiates delivery of the treatment.
- Features or components described in relation to one of the embodiments described herein may be provided in combination with components or features of other ones of the example embodiments described herein. For example, the
controller 15 shown inFIG. 6 could be used in conjunction with any of the described embodiments. Light sources having a property or properties like those of thelight source 4 shown in the embodiments ofFIGS. 1 to 1C could be applied in other embodiments.
It is therefore intended that the following appended claims and claims hereafter introduced are interpreted to include all such modifications, permutations, additions and sub-combinations as are within their true spirit and scope.
-
Claims (74)
1. A method for preparing an apparatus useful for delivering light therapy to jaw tissues of a patient, the method comprising:
coupling an extra-oral light source to a support;
fitting the support to register with one or more anatomical features of the patient's head; and
aligning the light source toward the patient's facial skin covering the patient's jaw bone or soft tissue.
2. The method according to claim 1 wherein fitting the support comprises inserting an intra-oral tray into the patient's mouth.
3. The method according to claim 1 wherein fitting the support comprises adjusting a head set to register with the bridge of the patient's nose and the patient's ears.
4. A method for administering phototherapy to tissues of the jaw bone or soft tissue of a patient, the method comprising:
directing a light source toward the face of the patient;
allowing the light source to emit light; and
allowing the light to pass through the patient's facial skin covering the patient's jaw bone to irradiate target tissues in one or more of the patient's jaw bone or soft tissue.
5. The method according to claim 4 wherein directing the light source comprises registering a frame to anatomical features of the patient's head and supporting the light source on the frame.
6. The method according to claim 4 wherein the emitted light comprises light in the wavelength range of about 820 to about 890 nm or about 620 to about 680 nm.
7. The method according to claim 4 wherein the emitted light comprises light in the wavelength ranges of:
613 nm to 624 nm,
667 nm to 684 nm,
750 nm to 773 nm, or
812 nm to 846 nm.
8. The method according to claim 4 wherein the emitted light comprises light of a wavelength corresponding to an absorption band of cytochrome c oxidase.
9. The method according to claim 8 wherein the absorption band is an absorption band of reduced cytochrome c oxidase.
10. The method according to claim 8 wherein the absorption band is an absorption band of oxidized cytochrome c oxidase.
11. The method according to claim 4 comprising allowing the light source to contact the skin of the patient's face.
12. The method according to claim 4 wherein allowing the light source to emit light comprises allowing the light source to emit pulses of light.
13. The method according to claim 12 wherein the emitted light has a time-averaged intensity of at least about 10 mW/cm2 at a light-emitting surface of the light source over a period of at least 10 seconds.
14. The method according to claim 13 wherein the time-averaged intensity is in the range of 20 mW/cm2 to about 60 mW/cm2.
15. The method according to claim 4 wherein the emitted light comprises visible and infrared light.
16. The method according to claim 15 wherein a ratio of the intensity of the visible light to the infrared light is 1 part or less visible light to 5 parts or more infrared light.
17. The method according to claim 4 comprising allowing the light source to emit light for a period determined by an automatic timer.
18. The method according to claim 4 comprising: prior to allowing the light source to emit light, forming the light source support to conform to contours of the face of the patient; and while allowing the light source to emit light, urging the light source against the face of the patient.
19. A method for treating a jaw bone disorder, comprising the steps of:
contacting at least one extra-oral light source against skin the face of a patient in need of jawbone-disorder treatment; and
administering to the patient an effective amount of the light through the patient's face to the patient's jaw or gums.
20. The method of claim 19 further comprising placing into the patient's mouth an intra-oral tray, the intra-oral tray being connected to an extra-oral bridge that is connected to the at least one extra-oral light source.
21. The method of claim 19 wherein the extra-oral light source is an extra-oral LED array.
22. The method of claim 19 wherein the emitted light comprises light in the wavelength range of about 820 to about 890 nm or about 620 to about 680 nm.
23. The method of claim 19 wherein the emitted light comprises light in the wavelength ranges:
613 nm to 624 nm,
667 nm to 684 nm,
750 nm to 773 nm, or
812 nm to 846 nm.
24. The method of claim 19 further comprising rotating the at least one extra-oral light source between a sagittal axis and a vertical axis.
25. The method of claim 19 wherein the jaw bone disorder is jaw osteonecrosis.
26. A method for biostimulating bone or soft tissue comprising the steps of:
contacting at least one extra-oral light source against skin the face of a patient in need of jawbone-disorder treatment; and
administering to the patient an effective amount of the light through the patient's face to the patient's jaw or gums.
27. The method of claim 26 further comprising placing into the patient's mouth an intra-oral tray, the intra-oral tray being connected to an extra-oral bridge that is connected to the at least one extra-oral light source.
28. The method of claim 26 wherein the extra-oral light source is an extra-oral LED array.
29. The method of claim 26 wherein the emitted light comprises light in the wavelength range of about 820 to about 890 nm or about 620 to about 680 nm.
30. The method of claim 26 wherein the emitted light comprises light in the wavelength ranges:
613 nm to 624 nm,
667 nm to 684 nm,
750 nm to 773 nm, or
812 nm to 846 nm.
31. The method of claim 26 further comprising rotating the at least one extra-oral light source between a sagittal axis and a vertical axis.
32. The method of claim 26 , wherein the patient was subjected to oral or periodontal surgery.
33. The method of claim 32 , wherein the biostimulation results in the acceleration of post-oral surgery healing or post-periodontal surgery healing.
34. The method of claim 26 , wherein the patient has an endosseous dental implant.
35. The method of claim 34 , wherein the biostimulation results in the acceleration of osseointegration of endosseous dental implants.
36. The method of claim 26 , wherein the method is used in orthodontics.
37. The method of claim 26 wherein the at least one extra-oral light source comprises optics which focus the light emitted from the at least one extra-oral light source at an angle approximately between 45-60°.
38. A method for orthodontic treatment, comprising the steps of:
contacting at least one extra-oral light source against skin the face of a patient in need of jawbone-disorder treatment; and
administering to the patient an effective amount of the light through the patient's face to the patient's jaw or gums.
39. The method of claim 38 , wherein the emitted light comprises light in at least one of the wavelength ranges: 613 nm to 624 nm, 667 nm to 684 nm, 750 nm to 773 nm, 812 nm to 846 nm, between about 820 to about 890 nm, and between about 620 to about 680 nm.
40. The method of claim 19 , 26 , or 38 wherein the extra-oral light source contacts a side of the person's face.
41. The method of claim 19 , 26 , or 38 wherein the light is substantially monochrome.
42. The method of claim 19 , 26 , or 38 wherein the light is pulsed.
43. The method of claim 19 , 26 , or 38 wherein the light has an average intensity of at least about 10 mW/cm2.
44. The method of claim 19 , 26 , or 38 wherein the light has an average intensity in the range of 10 mW/cm2 to about 60 mW/cm2.
45. The method of claim 19 , 26 , or 38 wherein the light has an average intensity in the range of 20 mW/cm2 to about 60 mW/cm2.
46. The method of claim 19 , 26 , or 38 wherein the light has a peak intensity higher than 50 mW/cm2.
47. The method of claim 19 , 26 , or 38 wherein the light radiates from a plurality of extra-oral light sources that contact the patient's face.
48. The method of claim 47 wherein the light passes through the left and right sides of the facial skin covering the patient's jaw bone.
49. The method of claim 19 , 26 , or 38 further comprising cooling the extra-oral light sources with a thermal cooling system.
50. The method of claim 49 wherein the thermal cooling system is configured for forced air or liquid cooling.
51. The method of claim 49 wherein the thermal cooling system comprises a heat sink.
52. The method of claim 19 , 26 , or 38, further comprising programming a controller to direct the at least one extra-oral light source to emit light, wherein the controller is programmed to direct the extra-oral light source to emit light at predetermined rates, durations of treatment, light intensity, or pulse frequency according to a prescribed treatment regimen.
53. The method of claim 52 wherein the controller comprises a fail-safe circuitry that shuts off current and light if heat from the extra-oral light source exceeds a preset level.
54. The method of claim 38 wherein the extra-oral light source is an extra-oral LED array.
55. The method of claim 19 , 26 , or 38 wherein the extra-oral light source comprises a laser.
56. The method of claim 54 wherein the extra-oral LED array capable of illuminating both upper and lower jaws of the patient simultaneously.
57. The method of claim 19 , 26 , or 38 wherein the light comprises multiple wavelengths.
58. The method of claim 19 , 26 , or 38 wherein the light comprises visible and infrared light.
59. The method of claim 58 wherein a ratio of the intensity of the visible light to the infrared light is 1 part or less visible light to 5 parts or more infrared light.
60. The method of claim 42 wherein the light is pulsed with a duty cycle of 1:2 (on:off, respectively) or less.
61. The method of claim 19 , 26 , or 38 wherein the extra-oral light source further comprises optics or reflectors to direct the light emitted from the extra-oral light source.
62. The method of claim 61 wherein the optics or reflectors are encapsulated in plastic.
63. The method of claim 19 , 26 , or 38 wherein the light is emitted by another extra-oral light source, wherein one extra-oral light source contacts the right side of the patient's face, and the other extra-oral light source contacts the left side of the patient's face.
64. The method of claim 19 , 26 , or 38 wherein the extra-oral light source attached to a head set.
65. The method of claim 64 wherein the head set comprises a frame adapted to fit on the bridge of the patient's nose.
66. The method of claim 65 wherein the frame has arms that fit above and around the patient's ears.
67. The method of claim 64 further comprising attaching the extra-oral light source to the head set or detaching the extra-oral light source from the head set.
68. The method of claim 67 wherein the extra-oral light source is attached by inserting a male portion of the extra-oral LED light source into a female portion of the head set.
69. The method of claim 64 further comprising adjusting the position of the extra-oral light source along a horizontal axis relative to the head set or a vertical axis relative to the head set.
70. The method of claim 69 wherein the position of the extra-oral light source is adjusted by loosening screws, sliding a yoke to a desired position along a slot, and retightening the screws.
71. The method of claim 70 wherein the slot follows the curvature of a maxillary bone.
72. The method of claim 38 , further comprising rotating the extra-oral light source between a sagittal axis and a vertical axis.
73. The method of claim 52 , wherein the controller separately controls a first light source with an upper level and a second light source with lower level of light emitters, wherein the upper level and lower levels irradiate tissues of upper and lower jaws, respectively, of the patient when in use.
74. The method of claim 52 , wherein the controller maintains a log of treatments that have been administered.
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Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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Also Published As
Publication number | Publication date |
---|---|
US9308389B2 (en) | 2016-04-12 |
US8900282B2 (en) | 2014-12-02 |
US20140121731A1 (en) | 2014-05-01 |
EP2164570A1 (en) | 2010-03-24 |
US20130253620A1 (en) | 2013-09-26 |
US20150079536A1 (en) | 2015-03-19 |
EP2164570A4 (en) | 2014-04-23 |
WO2009000075A1 (en) | 2008-12-31 |
US20070248930A1 (en) | 2007-10-25 |
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