Vaginal dilatation device, and, methods for dilating a vagina during labor pains and for preventing

专利摘要:
VAGINAL DILATING DEVICE, AND, METHODS FOR DILATING A VAGINA DURING BIRTH PAINS AND FOR AVOIDING TISSUE DAMAGE DURING LABOR A vaginal dilatation device is provided that may include any of many features. A feature of the vaginal dilatation device is that it is configured to dilate vaginal tissue during labor pains to prevent tissue damage. Another feature of the vaginal dilation device is that it can be manually controlled to dilate vaginal tissue, or it can be automatically controlled to dilate vaginal tissue. In some embodiments, the vaginal dilator device is configured to measure a force applied by the device to tissue. In other embodiments, the vaginal dilatation device is configured to apply a constant force to the tissue. In other embodiments, the vaginal dilator device is configured to expand at a constant rate. Methods associated with the use of the vaginal dilatation device are also provided.
公开号:BR112012008679B1
申请号:R112012008679-0
申请日:2010-10-13
公开日:2022-01-25
发明作者:Mark Juravic；Michael Stewart
申请人:Materna Medical, Inc；
IPC主号:

专利说明:

CROSS REFERENCE OF RELATED ORDERS
This application claims benefit under 35 U.S.C. 119 of the U.S. Provisional Patent Application At the. 61/278,687, filed October 13, 2009, titled “Method to Prevent Vaginal Lacerations During Childbirth.” This application is incorporated herein by reference in its entirety. MERGER BY REFERENCE
All publications, including patents and patent applications,* mentioned in this report are hereby incorporated by reference in their entirety to the same extent as if each individual publication were specifically and individually indicated to be incorporated by reference. FIELD OF THE INVENTION
Devices and methods are generally described in connection with preparing tissue for childbirth. More specifically, the devices and methods described herein are intended to prepare and dilate vaginal tissue during labor so as to prevent pelvic floor damage, and vaginal and perineal lacerations. FUNDAMENTALS OF THE INVENTION
Approximately 134 million women worldwide give birth each year, of which 3.0 million give birth by vaginal delivery in the 25 United States. Approximately 8 out of 10 women who give birth by vaginal delivery will experience some degree of vaginal tearing. in the U.S. about 1.2 million, or 40%, experience a spontaneous tear or episiotomy (surgical cut planned for high-risk patients) that requires surgical repair. Between 1.5% and 15% of lacerations are considered severe and require prolonged healing time and pain control, and can result in difficult reconstructive surgery and a considerable increase in the quality of vital measurements. Additionally, 15-35% of women experience damage to their pelvic floor muscles, where the muscles are being physically pulled out of the pelvic bone or overstretched to the point where they become functionally impaired. The direct costs of treating perineal lacerations to the health care system are estimated to total over $650 million per year, with treatments targeting even greater future pelvic floor disorders.
Specific risk factors for perineal lacerations during childbirth have been identified, leading to an above-average incidence of patient populations. These risk factors include nulliparity (first pregnancy, first pregnancy), short perineal body, instrumental delivery (forceps-assisted delivery, vacuum-assisted delivery), prolonged second stage of labor (>1 hour), epidural analgesia, intrapartum infant factors (birth weight above 4 kg, persistent occipitoposterior position, shoulder dystocia), episiotomy, mediolateral or midline, previous anal sphincter tear, maternal age > 30, and Asian ethnicity. In addition to the risk factors listed above, perineal tears have been linked to a higher incidence of many pelvic floor disorders, such as infection, incontinence, or prolapse. In general, pregnancy and birth have been linked as a cause of many pelvic floor disorders. However, the exact physiological mechanisms that lead to many of these disorders are under investigation. Damage to the pelvic floor musculature during childbirth is considered to be one of the most significant causes of pelvic floor disorders.
During vaginal delivery, labor and delivery are clinically divided into three stages. The first stage begins with cervical effacement, and concludes with full cervical dilatation that will allow the fetus to pass through the birth canal. The second stage is defined by the passage of the fetus through the birth canal, described as the Cardinal Movements of Labor. It begins with complete cervical effacement and dilation and ends with delivery of the fetus. The third stage is comprised of the separation and expulsion of the placenta.
During the first phase of labor, the birth canal is functionally closed and held in position by several layers of muscle and connective tissue that collectively form the pelvic floor. During the second stage of labor, the present part of the fetal head descends into the birth canal and exerts direct pressure on the pelvic floor. The fetus passes through the birth canal stretching the fibers of the levator ani muscle and connective tissues, dramatically straining and damaging the pelvic floor musculature, and stretching the perineum into a thin membranous structure that often tears during delivery. .
Pelvic and perineal floor tissues dilate rapidly during the second stage of labor. The introitus, or opening of the vagina, for the average female, has a baseline resting diameter of about 2.6 cm. During the first stage of labour, while the cervix is dilating, the vagina remains at this baseline diameter, and only when the baby has passed through the cervix does this tissue dilate from 2.6 cm to 10 cm, the diameter of average head of a newborn. This 3.8-fold diameter expansion and approximately 15-fold area expansion occur in a matter of seconds to minutes.
Currently, there are no devices or tools that have been proven to significantly reduce trauma to the pelvic floor during vaginal delivery, and there are no other devices that can be used to isolate variables associated with pelvic floor disorders resulting from childbirth. There are no effective treatments to help a woman precondition the tissues of the vagina and perineum before and during labor.
Historically, ever-larger gourds were used in Africa in an attempt to prepare the tissue for labor. Today, there are techniques such as perineal massage, warm compresses and “functional” delivery that can be performed in the hospital and have shown curiously promise, but none of these have proven to be effective in the clinical trial setting.
A device previously introduced for the purpose of pre-stretching tissue to prevent lacerations is called the Epi-No. The Epi-No is a small balloon that was intended to be used at home by the pregnant woman, 1 -3 months before the baby is born. The objective was to inflate the balloon to approximately 5 cm, at which point the woman would exercise then expel the device. One problem with this type of balloon-style dilator is that it can change shape and size during expansion, which can result in poor stability of the device in the vagina and an inability to measure and control the amount of dilation. SUMMARY OF THE INVENTION
A vaginal dilator device is provided comprising a handle, a plurality of arms coupled to the handle, each arm having a pad disposed thereon which is formed and configured to conform to a vagina, an expansion mechanism coupled to the arms and configured to move the arms and pads radially outward from the device, and a force sensor disposed on the device and configured to measure a force applied against the pads.
In some embodiments, each of the plurality of arms comprises a scissor-like assembly coupled to each of the pads. The expansion mechanism can be coupled to a central rod which is attached to the wrist and arms, characterized by the fact that axial movement of the central rod changes a distance of the pads from the central rod.
In one embodiment, actuation of the expansion mechanism is configured to move the central rod proximally toward the wrist in order to move the arms and pads radially away from the central rod.
In some embodiments, the pads are arranged in a substantially parallel configuration as the arms and pads move radially outward.
In some embodiments, the vaginal dilator device 10 further comprises a closed configuration, where the pads are arranged circumferentially around the central shaft, and an expanded configuration, where the pads are extended away from the central shaft and away from the pads. adjacent. In one embodiment, an outside diameter of the pads in the closed configuration is less than 4 cm. In another embodiment, an outside diameter of the pads in the expanded configuration is approximately 8-10 cm.
In one embodiment, the vaginal dilatation device further comprises a quick release mechanism configured to rapidly reduce an outside diameter of the device. In some embodiments, the device further comprises an actuation mechanism disposed on the handle that is configured to engage the quick release mechanism. In another embodiment, the device further comprises a shock absorber element disposed in a distal portion of the device which is configured to engage the quick release mechanism.
In some embodiments, the shock absorber element is configured to be engaged by a baby entering a birth canal.
In some embodiments, a center of mass of the vaginal dilator device moves forward under the pads as the device is expanded from the closed configuration to the expanded configuration.
In one embodiment, the vaginal dilation device further comprises a diameter sensor configured to indicate a dilation diameter of the vagina.
In some embodiments, the vaginal dilatation device further comprises a controller coupled to the expansion mechanism and the force sensor, the controller configured to automatically move the arms and pads radially outward based on the force measured by the force sensor. For example, in some embodiments, the force sensor can measure a force applied by the pads, and the controller can automatically expand and contract the device based on the measured force. The controller can automatically increase the applied force if the measured force is too low, or it can automatically decrease the applied force if the measured force is too high (for example, the applied force is above a force threshold).
In some embodiments, the controller is configured to automatically move the arms and pads radially outward to apply a constant force to the vagina with the pads. In some embodiments, the vaginal dilatation device further comprises a motor coupled to the central shaft and a controller coupled to the force sensor and the motor, the controller configured to automatically move the central shaft axially, and the arms and pads radially outward, based on the force measured by the force sensor. In some embodiments, the device further comprises a controller coupled to the expansion mechanism and the force sensor, the controller configured to automatically move the arms and pads radially outward until the force measured by the force sensor exceeds a force threshold.
In other embodiments, the controller is configured to automatically move the central rod axially in order to apply a constant force with the pads.
In some embodiments, the expansion mechanism is configured to automatically move the arms and pads of the device radially outward at a constant force. In some embodiments, the expansion mechanism comprises a spring coupled to the central rod, characterized in that the spring biases against the central rod with a constant force to move the arms and pads radially away from the central rod. In one embodiment, the constant spring force is user adjustable.
Some embodiments of the vaginal dilator device further comprise an expandable housing disposed over the pads. Other embodiments further comprise a working channel arranged on or in the device.
In some embodiments of the vaginal dilatation device, the force sensor comprises a plurality of force sensors disposed on the pads. In other embodiments, the force sensor comprises a plurality of force sensors disposed under the pads. In other embodiments, the force sensor comprises a plurality of force sensors arranged in the plurality of arms.
Some embodiments of the vaginal dilator device further comprise a retention mechanism configured to prevent over-expansion of the pads. Further embodiments further comprise an automatic swing mechanism configured to prevent pressure necrosis.
In one embodiment of the vaginal dilator device, none of the pads contact a urethra or any bundles of nerves positioned along an anterior portion of the patient's vagina as the pads move radially out of the device. In other embodiments, none of the pads contact a patient's perineum as the pads move radially out of the device.
In some embodiments, the expansion mechanism is remotely coupled to the arms via a flexible assembly.
Another vaginal dilatation device is provided comprising a handle, a plurality of arms coupled to the handle, each arm having a pad disposed therein that is formed and configured to conform to a vagina, and an expansion mechanism coupled to the arms and configured to move the arms and pads radially out of the device at a constant force.
In some embodiments, each of the plurality of arms comprises a scissor-like assembly coupled to each of the pads. The expansion mechanism can be coupled to a central rod which is attached to the wrist and arms, characterized by the fact that axial movement of the central rod changes a distance of the pads from the central rod.
In one embodiment, actuation of the expansion mechanism is configured to move the central shaft proximally towards the wrist for the purpose of moving the arms and pads radially away from the central shaft.
In some embodiments, the pads are arranged in a substantially parallel configuration as the arms and pads move radially outward.
In some embodiments, the vaginal dilatation device further comprises a closed configuration characterized in that the pads are arranged circumferentially around the central shaft, and an expanded configuration characterized in that the pads are extended away from the central shaft and towards away from adjacent pads. In one embodiment, an outside diameter of the pads in the closed configuration is less than 4 cm. In another embodiment, an outside diameter of the pads in the expanded configuration is approximately 8-10 cm.
In one embodiment, the vaginal dilatation device further comprises a quick release mechanism configured to rapidly reduce an outside diameter of the device. In some embodiments, the device further comprises an actuation mechanism disposed on the handle which is configured to engage the quick release mechanism. In another embodiment, the device further comprises a shock absorber element disposed in a distal portion of the device which is configured to engage the quick release mechanism. In some embodiments, the shock absorber element is configured to be engaged by a baby entering a birth canal.
In some embodiments, a center of mass of the vaginal dilator device moves forward under the pads as the device is expanded from the closed configuration to the expanded configuration.
In one embodiment, the vaginal dilation device further comprises a diameter sensor configured to indicate a dilation diameter of the vagina.
In some embodiments, the vaginal dilatation device further comprises a controller coupled to the expansion mechanism and the force sensor, the controller configured to automatically move the arms and pads radially outward based on the force measured by the force sensor. For example, in some embodiments, the force sensor can measure a force applied by the pads, and the controller can automatically expand and contract the device based on the measured force. The controller can automatically increase the applied force if the measured force is too low, or it can automatically decrease the applied force if the measured force is too high (for example, the applied force is above or below a desired constant force threshold).
In some embodiments, the controller is configured to automatically move the arms and pads radially outward to apply a constant force to the vagina with the pads. In some embodiments, the vaginal dilatation device further comprises a motor coupled to the central shaft and a controller coupled to the force sensor and the motor, the controller configured to automatically move the central shaft axially, and the arms and pads radially outward, based on the force measured by the force sensor. In some embodiments, the device further comprises a controller coupled to the expansion mechanism and the force sensor, the controller configured to automatically move the arms and pads radially outward in order to maintain the force applied by the device at constant force. In other embodiments, the controller is configured to automatically move the central rod axially in order to apply a constant force with the pads.
In some embodiments, the expansion mechanism is configured to automatically move the arms and pads of the device radially outward at a constant force. In some embodiments, the expansion mechanism comprises a spring coupled to the central rod, characterized in that the spring biases against the central rod with a constant force to move the arms and pads radially away from the central rod. In one embodiment, the constant spring force is user adjustable.
Some embodiments of the vaginal dilator device further comprise an expandable housing disposed over the pads. Other embodiments further comprise a working channel arranged on or in the device.
In some embodiments of the vaginal dilatation device, the force sensor comprises a plurality of force sensors disposed on the pads. In other embodiments, the force sensor comprises a plurality of force sensors disposed under the pads. In other embodiments, the force sensor comprises a plurality of force sensors disposed on the plurality of arms.
Some embodiments of the vaginal dilator device further comprise a retention mechanism configured to prevent over-expansion of the pads. Further embodiments further comprise an automatic swing mechanism configured to prevent pressure necrosis.
In one embodiment of the vaginal dilator device, none of the pads contact a urethra or any bundles of nerves positioned along an anterior portion of the patient's vagina as the pads move radially out of the device. In other embodiments, none of the pads contact a patient's perineum as the pads move radially out of the device.
In some embodiments, the expansion mechanism is remotely coupled to the arms via a flexible assembly.
In some embodiments, the expansion mechanism is configured to move the arms and pads radially away from the device at constant force for a pre-set period of time. In some embodiments, the pre-set time period comprises 5-10 minutes. In other embodiments, the pre-set time period comprises 5-60 minutes. In additional embodiments, the pre-set time period comprises less than 2 hours.
In another embodiment, a vaginal dilatation device is provided comprising a handle, a plurality of arms coupled to the handle, each arm having a pad disposed therein which is formed and configured to conform to a vagina, an expansion mechanism coupled to the arms and configured to move the arms and pads radially away from the device, and a diameter sensor disposed in the device and configured to measure a diameter of the device.
In some embodiments, each of the plurality of arms comprises a scissor-like assembly coupled to each of the pads. The expansion mechanism can be attached to a central rod which is attached to the wrist and arms, characterized by the fact that axial movement of the central rod changes a distance of the pads from the central rod.
In one embodiment, the drive of the expansion mechanism is configured to move the center rod proximally toward the wrist to move the arms and pads radially away from the center rod.
In some embodiments, the pads are arranged in a substantially parallel configuration as the arms and pads move radially outward.
In some embodiments, the vaginal dilatation device further comprises a closed configuration characterized in that the pads are arranged circumferentially around the central shaft, and an expanded configuration characterized in that the pads are extended away from the central shaft and towards away from adjacent pads. In one embodiment, an outside diameter of the pads in the closed configuration is less than 4 cm. In another embodiment, an outside diameter of the pads in the expanded configuration is approximately 8-10 cm.
In one embodiment, the vaginal dilatation device further comprises a quick release mechanism configured to rapidly reduce an outside diameter of the device. In some embodiments, the device further comprises an actuation mechanism disposed on the handle which is configured to engage the quick release mechanism. In another embodiment, the device further comprises a shock absorber element disposed in a distal portion of the device which is configured to engage the quick release mechanism. In some embodiments, the shock absorber element is configured to be engaged by a baby entering a birth canal.
In some embodiments, a center of mass of the vaginal dilator device moves forward under the pads as the device is expanded from the closed configuration to the expanded configuration.
In some embodiments, the vaginal dilatation device further comprises a controller coupled to the expansion mechanism and the diameter sensor, the controller configured to automatically move the arms and pads radially outwardly based on the diameter measured by the diameter sensor. For example, in some embodiments, the diameter sensor can measure a diameter of the device, and the controller can automatically expand and contract the device based on the measured diameter. The controller can automatically increase the diameter if the measured diameter is too low, or it can automatically decrease the diameter if the measured diameter is too low.
In some embodiments, the vaginal dilatation device further comprises a motor coupled to the central shaft and a controller coupled to the diameter sensor and the motor, the controller configured to automatically move the central shaft axially, and the arms and pads radially outwardly a constant rate of expansion. In some embodiments, the device further comprises a controller coupled to the expansion mechanism and the diameter sensor, the controller configured to automatically move the arms and pads radially outward based on the diameter measured by the diameter sensor.
Some embodiments of the vaginal dilator device further comprise an expandable housing disposed over the pads.
Other embodiments further comprise a working channel arranged on or in the device.
Some embodiments of the vaginal dilator device further comprise a retention mechanism configured to prevent over-expansion of the pads. Further embodiments further comprise an automatic swing mechanism configured to prevent pressure necrosis.
In one embodiment of the vaginal dilator device, none of the pads contact a urethra or any bundles of nerves positioned along an anterior portion of the patient's vagina as the pads move radially out of the device. In other embodiments, none of the pads contact a patient's perineum as the pads move radially out of the device.
In some embodiments, the expansion mechanism is remotely coupled to the arms via a flexible assembly.
In some embodiments, the constant rate of dilation is user adjustable.
In some embodiments, the vaginal dilatation device further comprises a timer configured to prompt a user to increase the diameter of the device.
In one embodiment, the expansion mechanism comprises a trigger assembly configured to expand the device by a pre-set increment of expansion with a single actuation of the trigger assembly. In some embodiments, the pre-set dilation increment is user adjustable.
A method of dilating a vagina during labor is provided, comprising inserting a vaginal dilator device into the vagina, measuring a force applied to the vagina by the vaginal dilator device, and dilating the vagina with the vaginal dilator device.
In some embodiments, the method further comprises stopping dilation of the vagina with the vaginal dilator device when the force applied to the vagina by the vaginal dilator device increases to a first threshold force. In one embodiment, the method further comprises resuming dilation of the vagina when the force applied to the vagina by the vaginal dilation device decreases to a second force threshold. In another embodiment, the step of resuming dilation further comprises resuming dilation of the vagina with the vaginal dilation device until the force applied by the vaginal dilation device increases to the first force threshold. In one embodiment, the step of resuming dilation further comprises resuming dilation of the vagina with the vaginal dilation device until the force applied by the vaginal dilation device increases to a third force threshold, the third force threshold being greater than the first. strength threshold. In one embodiment, the first strength threshold is greater than the second strength threshold. In another embodiment, the first strength threshold is less than 8 lbs (3.6 kg) of strength.
In some embodiments of the method, the insertion step further comprises inserting the vaginal dilator device into the vagina during a first stage of labor. The method may further comprise removing the vaginal dilator device from the vagina prior to a second stage of labour.
In some embodiments, the step of measuring a force further comprises measuring the force with the vaginal dilator device.
In one embodiment, the method further comprises measuring a diameter of the vagina with the vaginal dilator device. The method may further comprise dilating the vagina with the vaginal dilator device based on the measured diameter.
In some embodiments, the dilating step further comprises dilating the vagina at a constant force with the vaginal dilator device. In other embodiments, the step of dilating further comprises manually dilating the vagina with the vaginal dilator device. In a further embodiment, the step of dilating further comprises automatically dilating the vagina with the vaginal dilator device.
In another embodiment, the dilating step further comprises dilating the vagina with the vaginal dilator device at a location distant from the patient.
Another method of dilating a vagina during labor is provided, comprising inserting a vaginal dilator device into the vagina, and applying a constant force to the vagina with the vaginal dilator device to dilate the vagina. In some disciplines, the constant force is less than 8 lbs of force. In other embodiments, the constant force is adjustable.
In some embodiments of the method, the insertion step further comprises inserting the vaginal dilator device into the vagina during a first stage of labor. In other embodiments, the method comprises removing the vaginal dilator device from the vagina prior to a second stage of labor. In additional embodiments, the method comprises removing the vaginal dilator device from the vagina when the vagina is dilated to a diameter of approximately 8-10 cm.
In some embodiments, the method comprises measuring a diameter of the vagina with the vaginal dilator device.
In another embodiment, the application step further comprises automatically applying a constant force to the vagina with the vaginal dilator device to dilate the vagina. In one embodiment, the application step further comprises automatically applying constant force to the vagina with a constant force spring disposed in the vaginal dilator device. In another embodiment, the application step further comprises automatically applying constant force to the vagina with an automatic controller and a motor coupled to the vaginal dilatation device. In another embodiment, the application step further comprises applying constant force to the vagina with the vaginal dilator device for a pre-set period of time to dilate the vagina. In some embodiments, the pre-set time period comprises less than 5 minutes. In other embodiments, the pre-set time period comprises 5-10 minutes. In additional embodiments, the pre-set time period comprises 5-60 minutes. In yet another embodiment, the pre-set time period comprises less than 2 hours.
Another embodiment of the method comprises measuring a force applied to the vagina by the vaginal dilator device.
A method of preventing tissue damage during childbirth is provided, comprising inserting a vaginal dilator device into a patient's vagina during a first stage of labor, and dilating the patient's vagina with the vaginal dilator device.
In some embodiments, the method further comprises removing the vaginal dilator device from the patient's vagina prior to a second stage of labor.
In another embodiment, the dilation step comprises dilating the patient's vagina by approximately 7-10 cm with the vaginal dilator device. BRIEF DESCRIPTION OF THE DRAWINGS
Figs, la-Id illustrate some embodiments of a vaginal dilator device.
Fig. 2 is a view of a vaginal dilator device in an expanded configuration.
Figs. 3a-3d show cross-sectional views of a vaginal dilator device.
Figs. 4a-4b show cross-sectional views of an automatic vaginal dilator device.
Figs. 5a-5d illustrate various embodiments of pillow shapes for use with a vaginal dilator device.
Figs. 6a-6g illustrate various embodiments of force sensors disposed on or within a vaginal dilator device.
Figs. 7a-7b show embodiments of a vaginal dilatation device with a protective sheath.
Figs. 8a-8d illustrate various embodiments of a vaginal dilatation device having working channels or through holes.
Fig. 9 illustrates a vaginal dilatation device with a quick release mechanism.
Figs. 10a-10b illustrate a vaginal dilatation device with a quick release mechanism inserted into a female patient during labor.
Figs. 11-12 illustrate female reproductive anatomy.
Figs 13a-13b illustrate a vaginal dilatation device inserted into a female patient in either a closed or an expanded configuration respectively.
Figs. 14a-14d illustrate a vaginal dilatation device inserted into a female patient during labor.
Fig. 15 is a graph illustrating a method of dilating vaginal tissue during labor.
Fig. 16 is a graph illustrating another method of dilating vaginal tissue during labor.
Fig. 17 is a graph illustrating another method of dilating vaginal tissue during labor.
Fig. 18 is a graph illustrating an additional method of dilating vaginal tissue during labor.
Figs. 19a-19b illustrate yet another embodiment of a vaginal dilator device. DETAILED DESCRIPTION OF THE INVENTION
The devices and methods described herein are intended to prepare and dilate vaginal tissue during labor so as to prevent damage to pelvic floor, vaginal and perineal lacerations. Some embodiments of the device can stretch the perineal tissue until the diameter of the vaginal introitus has reached a target diameter of approximately 10 cm, roughly the size of the fetal head. In some embodiments, the device is a mechanical dilator that penetrates the first 3-4 cm of the vagina, the introitus, and gradually expands the vagina from a resting diameter of 2-3 cm to a total expanded diameter equal to the size of the fetus is rising, approximately 10 cm. Expansion can be controlled manually or via an automatic drive system, and the device can be quickly collapsed and removed if necessary.
The devices described here can be inserted during the first stage of labor and removed shortly before the second stage of labor, allowing the rest of the birthing process to proceed as usual. The device is intended to be used before the second stage of labor to prevent a baby from coming into contact with the device during delivery. Depending on the time it takes to achieve full vaginal dilation of approximately 10 cm, the device can be inserted as early as the first stage of labor with only very small amounts of dilation. The target dilatation diameter of 10 cm means that the device must be used in a hospital under the supervision of trained obstetricians and nurses. The device can be used without any anesthesia, or with local anesthesia. The tissue can also be prepared after administering an epidural, which would eliminate any pain or discomfort the device might cause. Local anesthesia can also be given to the tissue-contacting surfaces of the device to minimize pain.
Figs 11-1c illustrate one embodiment of a vaginal dilator device 100. The vaginal dilator device 100 may include rigid or semi-rigid pads 102, arms 104, handle 106, and expansion mechanism 108. In the embodiment of Figs, lc, device 100 includes four sets of pads 102 and arms 104. In other embodiments, any number of pads and arms may be used. For example, one embodiment comprises only 2 or 3 sets of pads and arms, and other embodiments may include more than four sets of pads and arms, such as 5, 6, 7, or even 8 or more sets of pads and arms. The sets of pads and arms can be arranged symmetrically or asymmetrically around a central axis of the device.
Pads 102 can be coupled to arms 104, which can be coupled to a central rod (not shown) that extends along a longitudinal axis of the device, through handle 106, and is coupled to expansion mechanism 108. Pads that contact the tissue 102 can be designed to maintain stability through all diameters of expansion. In some embodiments, the pads may have a saddle shape that maintains a constant waist size and height when expanded. These pads can be overmolded with a biocompatible elastomeric material in great compliance to help evenly distribute force against tissue and prevent trauma. Additional pillow shapes and designs will be covered below.
In the embodiment shown in Figs, 11-1c, the arms 104 comprise a scissor-like assembly, and include rods 110 and 112 which rotate about pivot 114. The rods 110 and 112 can be coupled to the pads and the central rod. In Figs, la-1c, the expansion mechanism 108 comprises a mechanical button configured to expand the arms of the vaginal dilator device. Manual rotation of the knob can cause the knob to move away from the handle and center rod in order to move proximally to the handle, allowing rods 110 and 112 to rotate about pivot 114 and to push pads 102 radially off the rod. device center. Since the arms 104 comprise a scissor-like assembly, the pads 102 can remain parallel to the device and to each other during expansion, which keeps the orientation of the pads to the tissue stable during dilation. Additionally, keeping the pads in a parallel orientation can help keep the device in place on the tissue while maximizing force distribution across the pads.
Rotating the knob in the opposite direction can cause the center rod to move distally, causing the scissors-like assembly to collapse and move the pads inward toward the center rod. In some embodiments, the arm sets 104 can have varying radii of curvature, which can expand the arms outward at different rates if desired.
Although most of the embodiments described here show the arms as a scissor-like assembly, it is important to understand that other methods and apparatus for expanding the pads may be used. For example, the arms may be single arms affixed to the pads (eg, similar to a speculum).
The vaginal dilator device can be sized, shaped and configured to penetrate approximately the first third, or 3-4 cm, of the vagina and gradually expand the vaginal introitus from a resting diameter of approximately 2 cm to a fully dilated diameter of approximately 10 cm. Vaginal dilatation device 100 can be configured to expand from a closed, compact configuration, as shown in Fig. la, for an expanded configuration, as shown in Fig. ic When the device is in the closed configuration, the pads can be perfectly closed against each adjacent pad to form a solid shape (eg, circle, oval, etc.).
When the device is in the closed configuration of Fig. There, the pads 102 can be configured to rest against each adjacent pad so as to reduce the outside diameter of the device. In some embodiments, the diameter of the pads in the closed configuration may be less than 4 cm. In one embodiment, the outside diameter of the pads in the closed configuration is approximately 2-4 cm. In other embodiments, the pads do not rest against adjacent pads in the closed configuration, but this can result in the minimum outer diameter of the pads being larger, or alternatively, the individual pads 102 having a smaller surface area, which can lead to patient discomfort. during 15 tissue dilation.
As the device expands to the expanded configuration, as shown in Figs. 1b-1c, the pads 102 and arms 104 move radially out of the device, causing the pads to separate from one another. In some embodiments, the maximum diameter 20 of the pads in the expanded configuration may be approximately 10 cm. In one embodiment, the maximum outside diameter of the pads in the expanded configuration is approximately 8-12 cm.
The Vaginal Dilation Device 100 is specifically designed to promote compaction, effective dilation and good tissue contact during expansion. As the device expands from the closed configuration to the expanded configuration, the device's center of mass may move under the pads, as shown by arrow 116 in Fig. 1c, which helps keep the device in place without rotating and falling out of the vagina.
Vaginal dilatation device 100 may further comprise indicator(s) or gauge(s) 118. In the embodiment of Figs, la-lc, gauge 118 is arranged on handle 106, however, gauge may be arranged anywhere on the device, or even away from the device, such as on a display monitor. In some embodiments, the meter gives the user an indication of the diameter of the pads 102. A user, for example, a physician, can then use the meter to know the exact amount of tissue dilation. The gauge 118 may comprise a simple binary reading (showing whether the diameter is above or below some threshold to continue to dilate), or may have a scale showing, for example, the actual diameter of the device.
In other embodiments, the vaginal dilator device 100 includes force sensors (not shown) configured to measure a force applied by the pads against the tissue, or alternatively, to measure a force applied against the pads, and the gauge 118 may give the user an indication of the measured force. The force sensors can be strain gauges, Whetstone bridges, piezoelectric crystals, hydraulic/pneumatic load cells, elastic devices, or any other force sensor or force transducer known in the art. The gauge 118 may comprise a simple binary reading (showing whether the force is above or below some threshold to continue to dilate), or it may have a scale showing, for example, the actual force being applied to the tissue. In additional embodiments, gauge 118 may indicate both a diameter of the pads and a force captured by the pads. Alternatively, the vaginal dilator device may comprise multiple gauges, including diameter gauges and force gauges.
The dilatation device may additionally include a quick release mechanism configured to collapse the device from the expanded configuration to the closed configuration. The quick release mechanism may comprise a shock absorber element 120 and quick release lever 122. Additional details regarding the quick release mechanism will be discussed below.
Fig. ld illustrates an embodiment similar to the device of Figs, la-lc, however, the expansion mechanism 108 of Fig. ld is remotely coupled to the rest of the device (e.g. remotely coupled to the central rod, arms and pads) via flexible assembly or flexible tube 109. The device of Fig. ld operates in the same manner as the device described above in Figs, la-lc, however, the remote expansion mechanism allows a user to expand/dilate the device from a distance away from the patient. This is advantageous because during labor, the patient's legs are typically covered by sheets or a blanket, so the remote expansion mechanism allows device activation without having to remove the covers, protecting the patient's privacy.
In other embodiments, the device may include an alarm or alert mechanism, such as a visual alert (e.g., a light, or a warning indicator on a display) or an audible alert (e.g., a horn or a chime sound). alarm) to indicate to a user that the device is applying too much or too little force to the vagina. The alert mechanism may also include a timer configured to alert the user (eg, with an audible or visual signal) when the device dilates.
Fig. 2 is a cropped view of a vaginal dilator device 200 in an expanded configuration, showing operation of a diameter gauge 218 in accordance with one embodiment. Vaginal dilator device 200 is a variation of vaginal dilator device 100 described above. Fig. 2 illustrates the inside of the handle 206, including the expansion mechanism 208, diameter gauge 218, center rod 224, spring 226, and nut 228. Rotation of the expansion mechanism can cause center rod 224 to move proximally to the handle. , which in turn causes the nut 228 to move proximally to compress the spring 226. As the spring is compressed, it can apply pressure to the diameter gauge 218, causing it to move with the diameter of the pads 202 and arms 204 as they radially expand outward. Once the outward movement of a scissor-like mechanism as shown in Fig. 2 is non-linear, the vaginal dilator device may further include a diameter gauge amplifying mechanism 230, such as an additional spring coupled to a rotating portion of the gauge, to provide a more linear reading to the gauge gauge 218.
The gauge tip 218 may extend out through a window in the handle 206. In some embodiments, the handle may include index marks or diameter measurements along the length of the window to provide an indication to the user of the diameter of the device. The marks can be colors, such as green, yellow, red, to give an indication of the amount of dilation, or they can be exact diameter measurements, such as marks indicating 0-10 cm of dilation. Other marks or indicators may also be used, as long as they give a rough or accurate reading of the device's diameter as it expands.
Figs. 3a-3b show cross-sectional views of another embodiment of a vaginal dilator device 300. The vaginal dilatation devices described above in Figs. 1 and 2 were directed to a device activated by manual rotation of a button. However, the vaginal dilator device 300 of Figs. 3a-3b may include a trigger mechanism comprising a constant force device 332 and a button 336 for triggering expansion of the device. In the embodiment shown in Figs. 3a-3b, constant force device 332 comprises a spring. However, any similar stored energy device can be used in place of the spring, including, for example, a pump or a piston, an elastic band or gears.
The vaginal dilator device of Figs. 3a-3b may include arms 304, handle 306, gauge 318, center shaft 324, launcher unit 325, rack assembly 334, knob 336, and pad holders 340. In the embodiment of Figs. 3a-3b, button 336 may be coupled to pin 338. Pad holders are configured to support pads, such as pads 102 or 202 described above. It is important to understand that the button 336 could be any other form of actuating device, such as, for example, a lever, a trigger, or a rotary dial.
Referring further to Figs. 3a-3b, the operation of the vaginal dilator device 300 will now be described. As shown, the arms 304 may comprise a scissor-like assembly. A proximal portion of the scissor assemblies may be coupled to the handle 306, and a distal portion of the scissor assemblies may be coupled to a launcher assembly 325. The central shaft 324 may extend from the launcher assembly 325 along a longitudinal axis of the handle device 306, terminating in rack assembly 334. Constant force device 332, e.g. a spring, may be disposed within the handle around the central rod, compressed between an inner wall of the handle and the rack assembly. . The rack assembly may comprise a plurality of gears or teeth, which may engage pin 338 of knob 336.
When button 336 is depressed, pin 338 disengages rack assembly 334. Constant force device 332 (e.g., a spring) can then decompress and expand, thereby applying a constant force against the rack assembly and central rod 324, and then to the launcher assembly 325, proximally toward the handle 306. As the distance between the launcher assembly 325 and the handle 306 decreases, the scissor assemblies expand, pushing the pad holders and pads (not shown) radially outward from the device. It is important that it also be understood that the device 300 of Figs. 3a-3b may comprise an actuation mechanism remotely coupled to the device (e.g. by means of a flexible tube as shown in Fig. ld) so as to allow expansion of the device from a remote location to or a distance away from the patient. .
As constant force device 332 leans against rack assembly 334 and center rod 324, gauge 318 moves proximally with rack assembly, giving the user an indication of the dilatation diameter of the device's pads. vaginal dilation. Expansion of the device continues until the next tooth or gear in the rack assembly engages pin 338 of knob 336. The teeth of rack set 334 may be spaced at specific increments of expansion, e.g. spaced 1 cm apart from each other. over the desired range of dilation, for example from 1 cm to 10 cm. Once the rack assembly has re-engaged pin 338, the user can press button 336 again to start the next expansion interval. In some embodiments, the button may also remain in the pressed “on” position, which would allow the device to continue to expand and dilate tissue with a constant force. Similarly, in another embodiment, the rack assembly may include only a single tooth or gear, allowing the device to continue to expand at a constant force once pin 338 has been disengaged from the single tooth.
Once the vaginal dilatation device is configured to expand at a constant force, the amount of force applied to tissue by the device can be determined and controlled so as to maximize the effectiveness of the device and prevent the device itself from causing tissue damage. . The constant force can be set at such a level as to reduce the risk of causing trauma, although it is sufficient to successfully and controllably dilate the tissue. In another embodiment, the vaginal dilator device may include a retention mechanism, such as another spring or a torque wrench-like mechanism, to prevent over-expansion of the pads. The retention mechanism can be configured to engage a pre-set force threshold to prevent the device from applying a force higher than the force threshold to tissue. In other embodiments, the device may include an alarm or alert mechanism, such as a visual alert (for example, a light, or a warning indicator on a display) or an audible alert (for example, a horn or a chime sound). alarm) to indicate to a user that the device is applying too much or too little force to the vagina The alert mechanism may also include a timer configured to alert the user (eg, through an audible or visual signal) when the device dilates.
As described above, constant force device 332 can comprise any device configured to apply constant force, such as a spring, piston, or pump. The constant force device can be configured to automatically apply a constant force of any desired amount of the device pads to the tissue. In some embodiments, the constant force device may apply a constant force to the tissue ranging from approximately less than 10 lbs of force. In some embodiments where a spring is used as the constant force device, the spring coils may be of varying thickness in order to adjust for gains in mechanical advantage as the vaginal dilator device is expanded, thus maintaining the applied force. tissue by the device as a constant.
Figs. 3a-3b also illustrate mechanisms that allow pads and pad holders 340 to remain parallel as the device expands. Arms 304 may include a rotating pivot point 342 configured to slide into slot 343 as the device expands. Movement of the pivot point along the slit allows the pads to remain parallel to the central shaft of the device during tissue dilatation.
In another embodiment, as shown in Figs. 3c-3d, the vaginal dilator device comprises a constant force mechanism 332, such as the spring described above, and further includes a force adjustment mechanism 344 configured to change the amount of force that the constant force mechanism does, and, therefore, the vaginal dilatation device applies to the tissue. As shown in Figs. 3c-3d, the force adjusting mechanism 344 may comprise a wheel or knob positioned adjacent the spring. When the force adjustment mechanism is adjusted from a minimum position as shown in Fig. 3c, to a tensioned position, as shown in Fig. 3d, the force adjustment mechanism compresses the spring, and adds force to it which will press back against the rack mechanism, thereby increasing the force that the vaginal dilator device can apply to the tissue.
In some embodiments, the vaginal dilator device of Figs. 3a-3d may include a damper (not shown) to limit any rapid expansion caused by the device. The damper may be, for example, a piece of foam, a spring, or a piston mechanism at the proximal end of the device.
Figs. 4a-4b show cross-sectional views of an automatic vaginal dilator device 400. In contrast to the above manual or semiautomatic devices, the vaginal dilator device 400 may comprise a semiautomatic or fully automatic actuation mechanism 408 comprising a controller 448 coupled to a 454 motor within the device, and configured to automatically dilate, expand and contract the pads and arms. The automatic vaginal dilatation device 400 may comprise pads 402, arms 404, handle 406, diameter sensor 418, center shaft 424, force sensors 446, controller 448, receiver 450, transmitter 452, motor 454, and worm gear 456. Pads 402 and arms 404 mechanically move in a manner similar to that described in Figs. 1-3.
In Figs. 4a-4b, controller 448 (e.g., a computer comprising configured hardware and software) can communicate with the vaginal dilator device, either wirelessly, via receiver 450 and transmitter 452, or wired (not shown). The vaginal dilator device can measure a force applied to the tissue by the pads 402, or alternatively, it can measure a force applied against the pads, and transmit the measured force to the controller 448 (e.g., either wirelessly or by wire). Controller 448 may be configured to automatically move arms 404 and pads 402 radially outward based on the force measured by the force sensor.
For example, controller-installed hardware and software can drive the 454 motor based on measured force. Motor 454 may include a threaded shaft 455, which may engage a rack assembly disposed on central shaft 424. When motor 454 is driven by controller 448, threaded shaft 455 may control movement of the central shaft, causing the arms and pads to move. expand and contract against and towards the central shaft of the device. In some embodiments, the 454 motor may be replaced by, for example, a computer driven pump or piston.
The motor 454 may also be attached to a second threaded shaft 456, which can engage gears on the diameter sensor 418. As the motor drives the vaginal dilator device to expand or contract, the second threaded shaft may engage. and rotating sensor 418 to indicate the diameter of the device. The measured diameter of the device can also be transmitted to the 448 controller as an analog or digital signal (eg, either wirelessly or by cable).
In other embodiments, the vaginal dilator may include an alarm or alert mechanism, such as a visual alert (eg, a light, or a warning indicator on a display) or an audible alert (eg, a horn or an alarm sound) to indicate to a user that the device is applying too much or too little force to the vagina. The alert mechanism may also include a timer configured to alert the user or controller (eg, by an audible or visual signal or by an input to the controller) when the device dilates.
Many modes of operation are possible with the vaginal dilatation device shown in Figs. 4a-4b. For example, controller 448 may be configured to drive motor 454 to swell the device outward at a constant force (e.g., a predetermined constant of approximately less than 10 lbs of force). In another embodiment, controller 448 may be configured to drive motor 454 to swell the device outward in a time-varying manner. For example, the controller can be configured to drive motor 454 to dilate the device until the force applied to tissue by the device approaches a force threshold.
In another embodiment, a physician may initially wish to dilate the vaginal tissue at a constant first force. The first constant force can be low, similar to less than 3 lbs of force. After a set period of time has elapsed, the controller can be configured to automatically stop tissue dilation until further instructions are received from the user, or alternatively, the controller can be configured to automatically dilate vaginal tissue at a constant second force. The second constant force may be different from the first constant force, such as approximately 3-5 lbs of force. In this embodiment, the vaginal dilator device 400 can automatically dilate tissue at a constant force for a set period of time, and then can stop tissue dilation or continue to dilate at a second constant force. The controller can be configured to automatically adjust the force applied to tissue by the device (eg, raise or lower constant force) until the device achieves the desired amount of tissue dilation (eg, 10 cm dilation).
In another embodiment, the vaginal dilator device does not automatically dilate for a set period of time, but instead, the vaginal dilator device is configured to automatically expand and dilate tissue until a threshold force is reached (as measured by the 446 sensors). ). For example, a clinician or controller may determine a threshold force of approximately 3 lbs of force. The vaginal dilator device can then be configured to automatically dilate vaginal tissue until sensors 446 measure a force greater than or equal to the threshold force of 3 lbs of force, at which point the device would automatically stop tissue dilation. It is important to understand that in other disciplines the threshold force can be any force, and is not limited to 3 lbs.
In yet another embodiment, the controller can be configured to trigger the vaginal dilatation device to expand until a threshold force is measured, and the controller can automatically trigger the device to contract slightly upon reaching the threshold force, so allowing the vaginal tissues to relax, and therefore allowing the force applied to the tissue by the device to decrease.
In yet a further embodiment, the controller can be configured to trigger the vaginal dilatation device based on a captured diameter of the device, or alternatively, based on a captured force and a captured diameter of the device. The diameter can be measured or captured with the 418 diameter sensor. In some embodiments, the controller can be configured to dilate the device until the device reaches a predefined diameter. In other embodiments, the controller may be configured to drive the device at a first force until the device reaches a first diameter, and then drive the device at a second force until the device reaches a second diameter. For example, the controller can drive the device at a force of 3 lbs until the device reaches a diameter of 3 cm. When dilating by 3 cm, the controller can then automatically drive the device at a force of 4 lbs until the device reaches a diameter of 4 cm. This process of varying the applied force until predefined diameters are reached can be continued until the target expansion diameter is reached.
Figs. 5a-5d illustrate various embodiments of pillow shapes for use with a vaginal dilator device. The pads described herein may be coated with a soft atraumatic material made from a foam, silicone, or other rubber or gel-like material. Pads 502 typically have a "saddle" shape, characterized in that both the distal and proximal portions of the pads are raised so that they support and conform to the vaginal tissue. The distal or anterior curve may better conform to the normal shape of the anatomy in order to more effectively distribute force and provide greater stability. The proximal or posterior curve may resemble a “heel” shape to help prevent the device from sliding off the patient. As the vaginal dilator expands and engages the tissue, the tissue may slide slightly over the pad. However, the contact surface of the introitus will remain in the “valley” of the pads. In some embodiments, such as those shown in Figs. 5b-5c , the pads may include notches or raised portions in an intermediate area of the pad to further conform to or engage anatomy. In other embodiments, the pads may include slits to avoid placing pressure on the anterior or posterior anatomy.
In additional embodiments, the springs may be incorporated into or below the pads. These springs can maintain the force of the pad on the tissue within a particular range, so as to prevent a user from over-extending the device. For example, springs incorporated in or below the pads can apply a constant force against the pads, similar to the constant force device described above in Fig. 3. In a still further embodiment, the device or pads may further include an automatic swing mechanism configured to prevent pressure necrosis. For example, springs or other similar devices on or below the pads can be configured to automatically oscillate to reduce pressure applied to the fabric. Additionally, pads may include heating or vibrating elements to enhance tissue relaxation.
Figs. 6a-6g illustrate various embodiments of force sensors disposed on or within a vaginal dilator device. In Fig. 6a, force sensor 646 is disposed on a surface of pad 602. In Fig. 6b, force sensor 646 is disposed below a surface of pad 602. In Fig. 6c, force sensor 646 is disposed on a pad support surface 640 below pad 602. In Fig. 6d, multiple force sensors 646 are disposed below a surface of pad 602. In Fig. 6e, multiple force sensors 646 are disposed on a surface of pad support 640, below pad 602. Fig. 6f illustrates one embodiment of a vaginal dilator device 600, including both a diameter gauge 618a and a force gauge 618b, as well as force sensors 646 disposed on pads 602. In Fig. 6g. force sensor 646 is positioned proximal to arms 604.
When the arms 604 and pads 602 expand to swell tissue, the arms can apply force to 646, which can measure the applied force.
Figs. 7a-7b show embodiments of a vaginal dilatation device 700 coated with a protective shell 758 to create an expandable sterile barrier to prevent infection before and after delivery. The protective overwrap may be an elastic material such as latex, silicone, etc. In some embodiments, the housing could also be made of a non-elastic material that is folded in and around the device, and unfolded as the device is expanded.
Figs. 8a-8d illustrate various embodiments of a vaginal dilatation device 800 comprising working channels or through holes. In Fig. 8a, device 800 includes a through hole 860 through which a user can insert other devices, such as cervical monitoring devices, oscilloscopes, fecal monitoring devices, or cervical dilatation devices. In addition, other commonly used tools, such as air, water, suction, surgical cutting, ultrasound or other imaging devices, etc., can be inserted into the through hole. In Figs. 8b-8c, the vaginal dilator device 800 may include a flexible working channel 862. The working channel may comprise a collapsible flexible material, and can accommodate any of the devices described above. In Fig. 8b, the working channel can be routed through the handle of the vaginal dilator and out through a central axis of the pads 802. In Fig. 8c, the working channel can be routed along the handle side of the device, through the open space between the pads when they are expanded. Fig. 8d illustrates the working channel routed along the side of the handle and through the open space between the pads 802, extending outwardly through a protective housing 858. There could be seals around the working channels and through holes of Figs. . 8a-8d to maintain sterile anatomy. Working channels or through holes may incorporate a one-way valve to allow for fluid or tissue removal without allowing bacteria or other particles to enter the patient.
Fig. 9 illustrates a vaginal dilatation device 100 with a quick release mechanism. The quick release mechanism may comprise a shock absorber element 120, quick release lever 122, and quick release pin 164. The device shown in Fig. 9 is a simplified version of the device 100 described above, and includes central stem 124 and launcher assembly 125. The description relating to the quick release mechanism may apply to any of the vaginal dilatation devices described herein.
In situations where the vaginal dilator device 100 needs to be removed from the patient quickly, the quick release lever 122 can be pulled or inverted, and contract the device back to a close to closed configuration. This feature allows the user to quickly stop the device from applying force to tissue, and prevent tissue from pinching during rapid retraction. When the quick release lever 122 is actuated, it releases a spacer which allows the central rod 124 to move distally away from the handle 106 of the device. This moves the launcher assembly 125 away from the handle which changes the angle of the arms and moves the pads (not shown) towards the central shaft of the device.
Figs. 10a-10b illustrate a vaginal dilatation device 100 with a quick release mechanism in use. In Fig. 10a, the device 100 is shown inserted into the patient's vagina while the fetus is about to be born. Ideally, the device can be removed before the fetus has passed the cervix, so that the user can operate the quick release lever 122 to collapse the device into the closed configuration for removal. However, in some instances, the fetus may enter the vaginal canal with the device 100 still in place. In this situation, the fetus can engage the shock absorber element 120, as shown in Fig. 10b, so as to collapse the device into the closed configuration for easy removal. In some embodiments, actuation of the shock absorber element may trigger an alarm or visual/audible signal to alert a clinician that the fetus has come into contact with the device.
Figs. 11-12 illustrate the bones and surrounding tissues of the female reproductive anatomy. The pelvic floor is defined by the complex of pubococcygeal-puborectal muscles PC, which forms a V-shaped tongue running from the pelvic wall both anteriorly and posteriorly around the anorectal junction. The elevator hiatus is the V-shaped space between the muscular walls. Within this V-shape are the urethra U (anteriorly), the vaginal canal VC (centrally) and the anus A (posteriorly). The elevator hiatus area in nulliparous young women (women who have never given birth) ranges from 6 to 36 cm2 in Valsalva maneuver. The bones that surround the pelvic region, including the Pubic Symphysis, Pubic Crest, and ischium, can also be seen in Figs. 11-12.
The average fetal head area in the plane of minimum diameters measures 70-100 cm2 (equating to a head circumference of 300-350 mm), requiring marked distension and deformation of the levator complex. It has been shown with the help of MRI-based computer modeling that the most inferior and medial parts of the levator complex have to grow in length by a factor of 3.26 during crowning of the fetal head. Given this degree of acute strain, it is notable that severe muscle trauma is not even more prevalent, as this type of strain is commonly considered to be well beyond the elastic limits of approximately 150% tissue stress.
Figs. 13a-13b illustrate a vaginal dilator device 100 inserted into a female patient in either a closed or an expanded configuration, respectively. The vaginal dilatation device of Figs. 13a-13b can be any vaginal dilatation device described herein. In Fig. 13a, device 100 is shown inserted into the vagina in a closed configuration. The external diameter of the device in the closed configuration can be less than 4 cm to increase patient comfort. Fig. 13b illustrates device 100 inserted into the vagina in an expanded configuration. The outside diameter of the device in the expanded configuration can be up to approximately 10 cm. The orientation of pads 102 with respect to anatomy is also shown. In Fig. 13b, the vaginal dilator device 100 includes four pads 102. When the pads are expanded, the pads avoid putting pressure on critical parts of the anatomy, such as the urethra U, the perineum, and anus A. In other embodiments where more than four pads are built into the device, the device does not include pads that expand directly upwards (to avoid placing pressure on the urethra) or directly downwards (to avoid placing pressure on the perineum and anus).
Methods of using a vaginal dilator device will now be described. Figs. 14a-14d illustrate a vaginal dilatation device inserted into a female patient during labor. The vaginal dilatation device described in these methods can be any vaginal dilatation device described herein, including the fully manual vaginal dilatation device of Figs. 1-2, the semiautomatic vaginal dilatation device of Fig. 3, or the fully semi or fully automatic vaginal dilatation device of Fig. 4. In addition, the vaginal dilatation device shown in Figs. 14a-14d may include any of the additional features described here, including force sensors, gauge/sensors, working channel, protective housing, etc. In Fig. 14a, vaginal dilatation device 1400 is shown inserted into a patient's vagina, and may include pads 1402, drive mechanism 1408, diameter gauge 1418a, and force gauge 1418b. The device may include sensors for measuring force and/or diameter, not shown but described above. In the mode of Fig. 14a, the device is shown with an actuation mechanism comprising a mechanical button, but it is important to understand that in other embodiments, the actuation mechanism may comprise a constant force device, such as a spring, or a fully automatic system, such as a controller and a motor. The device 1400 of Fig. 14a is shown in a closed or compact configuration. The device can be inserted into the patient at any time during the first stage of labor, typically when the patient arrives at the hospital before giving birth. On average, a woman spends 14 hours in a hospital before the second stage of labor begins. Diameter gauge 1418a can give an indication of the outside diameter of the device pads to indicate the extent to which the vaginal tissue has been dilated. The force gauge 1418b can indicate the amount of force being applied by the pads to the fabric, or alternatively, the amount of force applied against the pads.
Fig. 14b illustrates the vaginal dilator device 1400 after being partially dilated. The 1418a diameter gauge indicates the expanded diameter of the device to a user. The 1418b force meter can be monitored by the user, or alternatively, by a controller (not shown) to ensure proper and safe use of the device and prevent tissue trauma. In Fig. 14c, the vaginal dilator device is shown in a fully expanded configuration, effectively dilating the vaginal tissue to the desired diameter (eg, 10 cm). The 1418a diameter gauge indicates that the device diameter has reached the target diameter for a user. The 1418b force meter can be monitored by the user, or alternatively, by a controller (not shown) to ensure proper and safe use of the device and prevent tissue trauma. Fig. 14d is an alternate view of a vaginal dilator device in an expanded configuration. The device shows diameter and force gauges 1418a and 1418b on top of the device for easy user reading. Pads 1402 are shown applying pressure to vaginal tissue, but avoiding putting pressure on sensitive tissue areas of the urethra, perineum, and anus.
Fig. 15 is a graph illustrating two methods of dilating vaginal tissue in a case study. Referring to the graph, the vaginal tissue diameter was increased from 1.1 cm to 7 cm over a period of 1 hour and 15 minutes. The amount of force applied to the tissue has been gradually developed to avoid tissue damage. For example, initially, a force of approximately 2.5 lbs was applied to the tissue by the device to dilate the tissue by 4 cm after approximately 500 seconds. After the initial dilation, the tissue was able to relax, and you can see that the force applied to the tissue by the device decreased by almost 1 lb (0.45 kg) after approximately 1000 seconds. Then, a force of approximately 3 lbs (1.36 kg) was applied to the tissue by the device to dilate the tissue by 4.5 cm, followed by an additional dilation time period that allowed the applied force to decrease to below 2 lbs (0 .9 kg). This process was repeated applying approximately 4.5 lbs (2 kg) of force to swell the tissue by 5 cm, applying approximately 5.5 lbs (2.5 kg) of force to swell the tissue by 5.5 cm, applying approximately 4 lbs (l .8kg) of force to swell the tissue by 6 cm, applying approximately 6 lbs (2.72 kg) of force to swell the tissue by 6.5 cm, and applying approximately 7 lbs (3.17 kg) of force to swell the tissue by 7 cm.
It is important to understand that these values are merely explanatory, as each woman's body and tissue response may be different. In general, however, a method of dilating vaginal tissue may comprise inserting a vaginal dilator device into the vagina, measuring a force applied to the vagina by the vaginal dilator device, dilating the vagina with the vaginal dilatation device, and pausing or stopping dilation of the vagina. vagina with the vaginal dilator when the force applied to the vagina by the vaginal dilator increases to a first force threshold. In some embodiments, the method further increases the measurement of a diameter of the vagina with the vaginal dilator device. Thereafter, the method may include resuming dilation of the vagina when the force applied to the vagina by the vaginal dilation device decreases to a second force threshold. For example, a user or controller may determine that the tissue has relaxed enough that it is time to start dilating the vaginal tissue to a larger diameter. In some embodiments, dilation is resumed until the force applied by the vaginal dilator device increases to the first force threshold, or alternatively, until the applied force increases to a third force threshold greater than the first force threshold. In some disciplines, the first, second and third strength thresholds range from approximately less than 8 lbs 9 (3.6 kg) of strength.
The modality in Fig. 15 can utilize the viscoelastic properties of the patient's muscle and connective tissue to achieve maximum dilation. The tissue can be stretched to some predetermined maximum tension or force with the device, then the tissue can relax to reduce the tension, followed by again increasing the diameter of the device to the maximum tension value. This cycle of tissue tensioning, tissue tension relaxation, and then diameter increases to retension the tissue can be performed until the full tissue preparation diameter of approximately 10 cm is reached.
Fig. 16 is a graph illustrating another method of dilating vaginal tissue during labor at constant force. Fig. 16 illustrates the results of constant force dilation from a case study. Vaginal tissue can be dilated at a constant force with any of the vaginal dilatation devices described herein, but particularly with the vaginal dilatation devices described in Figs. 3 and 4. Referring to the constant force dilation graph in Fig. 16, the vaginal diameter was increased from a baseline diameter of 1.0 cm to 5.5 cm for approximately 1 hour. Force was maintained at lower values, incrementally increasing the diameter in smaller steps more frequently. As in the incremental dilation test (described above in Fig. 15), there is a rapid decrease in force when first dilating to a new diameter, and increasing the diameter more frequently, the tissue may experience permanent tension relaxation.
Fig. 17 is a graph illustrating the various stages of labor and the relative dilation diameters of the patient's cervix and vagina. During the latent or first stage of labour, the cervix dilates to approximately 3-4 cm for an extension of about 8 hours. During roughly the final 6 hours of labor, the cervix dilates to approximately 10 cm. The natural stretching of perineal tissues is also shown in Fig. 17. It can be seen that the natural tissue response is for the perineal tissues to dilate naturally by approximately 2 cm, until the final moment of labor when the perineal tissues stretch to 10 cm, leading to tearing and damage to fabric. In one embodiment, the perineal tissues may be gradually dilated and expanded with a vaginal dilator device. For example, perineal tissues can be dilated with the vaginal dilator device to approximately 7-10 cm during the first stage of labour. During the second stage of labor, the vaginal dilatation device is removed from the patient, allowing delivery to occur while the perineal tissues are stretched and relaxed.
The vaginal dilatation devices described here can be used during the first stage of labor, in the hospital, under the supervision of trained obstetricians and nurses. The device may be designed as a single-use disposable dilator configured to penetrate the first third of the vagina, and configured to gradually expand the vagina and perineal tissues from a resting diameter of 2-3 cm to a fully expanded diameter in preparation for childbirth, about 10 cm. Expansion can be controlled manually or via an automatic drive system, and the device can be quickly removed if necessary.
The device could be inserted at any time during the first stage of labour, and could be set to dilate in small increments of 5-15 minutes. Between dilatations, the patient can remove the device and move around if necessary. Cervix progression could be used as a guideline for labor progression. In order to reduce or eliminate any discomfort, the device can be used under epidural analgesia or local anesthesia in the vagina. In some embodiments, the device can dilate the tissue for approximately 1-3 hours to successfully reduce internal tissue stresses, and prepare the tissue for the second stage of labor. The device can then be removed before the second stage of labor begins to allow delivery to take place without obstructions.
Fig. 18 is a graph illustrating an additional method of dilating vaginal tissue during labor. In Fig. 18, another embodiment of dilating vaginal tissue is illustrated. In this embodiment, the vaginal dilator device is configured to dilate the tissue at a constant rate. As the device dilates the tissue, the force applied to the tissue by the device will increase. This method can be used in situations where it is necessary to dilate the tissue quickly. A typical woman has a resting vaginal diameter of approximately 2-3 cm. In one embodiment, it is desirable to dilate the vagina by approximately 9-10 cm over the course of two hours, or approximately 3.5 cm per hour. Thus, in this embodiment, a constant rate dilation method could include the device at a constant rate to achieve approximately 3-3.5 cm dilation per hour. This could be achieved in several ways, such as dilating approximately 0.5 cm every 10 minutes, 1 cm every 20 minutes, etc. Any of the devices described here can be used to dilate at a constant rate. For example, referring to the devices of Figs. 1-2, the expansion mechanism or knob can be rotated at preset intervals or at a constant rate to achieve a constant rate of expansion. The diameter gauge can be monitored in combination with rotation of the expansion mechanism to achieve constant expansion. Similarly, the automatic system in Fig. 4 could be programmed to expand the device at a desired rate for a period of time.
Figs. 19a-19b illustrate another embodiment of a vaginal dilator device 1900. The device may include pads 1902, handle 1906, arms (not shown), expansion mechanism 1908, center stem 1924, diameter gauge 1918, and any of the features described above and shown in the figures attached to this document. In the embodiment of Figs. 19a-19b, expansion mechanism 1908 comprises a trigger assembly configured to expand the device by a pre-set increment of expansion.
Fig. 19b illustrates a cutaway view of device 1900. In Fig. 19b, the central rod 1924 can comprise a hexagonal or non-circular shape, and the plates 1966 can be configured to engage the central rod and prevent the rod from moving axially. When the trigger assembly is triggered, it causes the 1966 plates to be parallel, allowing the center rod to move axially. As the trigger assembly is triggered, the central rod moves proximally, causing the arms (not shown) and pads (not shown) to expand out of the device, as described above in the other embodiments of the vaginal dilatation device.
In some embodiments, a simple “click” or triggering of the trigger assembly can be configured to dilate the device by a pre-set dilatation increment. For example, the device can be configured to expand by a precise amount with each actuation of the trigger assembly. This design makes the 1900 device particularly suitable for use in a constant rate dilation scheme. In one embodiment, for example, the trigger assembly may be configured to expand the device by a pre-set increment of dilation (eg, approximately 0.5 cm) with each “click” or triggering of the trigger. The user can then trigger the trigger set after a predetermined period of time (eg, every 10 minutes) to dilate the device at a constant rate. In other embodiments, the device 1900 includes force sensors, as described above, and the user can dilate the device based on the force captured from the device. It is important to understand that in other embodiments, the pre-set dilation increment can be any amount (e.g., 0-1 cm per actuation, 0-2 cm per actuation, 0-3 cm per actuation, 0-4 cm per actuation). trigger, etc.) and the predetermined period of time can be any period of time (e.g. somewhere between 0-2 hours or even longer).
As for additional details pertinent to the invention, materials and manufacturing techniques may be employed within the level of those skilled in the relevant art. The same may be held to be true with respect to method-based aspects of the invention with respect to additional acts commonly or logically employed. Likewise, it is contemplated that any optional feature of the described inventive variations may be expressed and claimed independently, or in combination with any one or more of the features described herein. Likewise, reference to a singular item includes the possibility that there is a plural of the same items present. More specifically, as used in this document and the appended claims, the singular form "a," "and," "said," and "the" include plural referents unless the context clearly dictates otherwise. It is further noted that claims may be drafted to exclude any optional elements. As such, this statement is intended to serve as a background to the use of this unique terminology such as “only,” “only” and the like, with respect to reciting claim elements, or using a “negative” limitation. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by a person skilled in the art to which this invention belongs. The scope of the present invention is not limited by the subject report, but, on the contrary, only by the clear meaning of the claim terms employed.

权利要求:
Claims (32)
[0001]
1. Vaginal dilatation device (100), characterized in that it comprises: a frame (106); a plurality of arms (104) coupled to the frame, each arm having a pad (102) disposed thereon that is shaped and configured to conform to a vagina; and an expansion mechanism (108) coupled to the arms and configured to move the arms and pads radially out of the frame at a controlled force.
[0002]
2. Vaginal dilatation device according to claim 1, characterized in that the expansion mechanism comprises a central rod coupled to the wrist and arms, in which axial movement of the central rod moves the arms and pads radially away from the rod central.
[0003]
A vaginal dilator device according to claim 2, characterized in that the pads are arranged in a substantially parallel configuration as the arms and pads move radially outward.
[0004]
4. Vaginal dilatation device according to claim 1, characterized in that an external diameter of the pads in the expanded configuration is approximately 8-10 cm.
[0005]
Vaginal dilatation device according to claim 1, characterized in that it further comprises a quick release mechanism configured to rapidly reduce an external diameter of the device.
[0006]
6. Vaginal dilatation device according to claim 5, characterized in that a drive mechanism configured to engage the quick release mechanism is arranged on the frame.
[0007]
7. Vaginal dilatation device according to claim 5, characterized in that a damping element configured to engage the quick release mechanism is disposed in a distal portion of the device.
[0008]
Vaginal dilatation device according to claim 1, characterized in that it further comprises a diameter sensor configured to identify a dilated diameter of the vagina.
[0009]
Vaginal dilatation device according to claim 1, characterized in that it further comprises a controller coupled to the expansion mechanism and a force sensor, the controller configured to automatically move the arms and pads radially outwards at a constant force.
[0010]
Vaginal dilatation device according to claim 2, characterized in that it further comprises a motor coupled to the central rod and a controller coupled to the force sensor and the motor, the controller configured to automatically move the central rod axially, and the arms and legs. pads radially outward, based on the force measured by the force sensor.
[0011]
11. Vaginal dilatation device according to claim 2, characterized in that the expansion mechanism comprises a spring coupled to the central rod, in which the spring leans against the central rod with a controlled force to move the arms and legs. pads radially outward from the central stem.
[0012]
12. Vaginal dilatation device according to claim 11, characterized in that the controlled force of the spring is adjustable by the user.
[0013]
Vaginal dilatation device according to claim 1, characterized in that it further comprises a retention mechanism configured to prevent over-expansion of the arms and pads.
[0014]
14. Vaginal dilatation device according to claim 1, characterized in that the expansion mechanism is remotely coupled to the arms by means of a flexible assembly.
[0015]
15. Vaginal dilatation device according to claim 1, characterized in that it further comprises a force sensor configured to measure a force applied by the pads against the vagina.
[0016]
16. Vaginal dilatation device (400), characterized in that it comprises: a frame; a central rod (424) coupled to the frame; a plurality of scissor-like arms (404) coupled to the central rod, the scissor-like arms comprising first and second axes which rotate around a pivot, each scissor-like arm having a pad (402) disposed thereon which is shaped and configured to conform to a vagina; an expansion mechanism (408) coupled to the central rod and configured to move the scissor arms and pads radially out of the device; a diameter sensor (418) disposed on the device and configured to measure a diameter of the device; and a controller (448) coupled to the expansion mechanism and the diameter sensor, the controller configured to automatically move the scissor arms and pads radially outward based on an expansion rate; wherein the scissor arms are configured to hold the pads parallel to the device and to the other pads as the pads are moved radially outward.
[0017]
17. Vaginal dilatation device according to claim 16, characterized in that the axial movement of the central rod (424) changes a distance of the pads (402) from the central rod.
[0018]
Vaginal dilatation device according to claim 16, characterized in that the device (400) comprises a closed configuration in which an external diameter of the pads (402) is less than 4 cm, and in which the device comprises a fully expanded configuration in which the outer diameter of the pads measure from 8 to 10 cm.
[0019]
19. Vaginal dilatation device according to claim 16, characterized in that it further comprises a quick release mechanism (120, 122, 164) configured to rapidly reduce an external diameter of the device.
[0020]
20. Vaginal dilatation device according to claim 19, characterized in that an actuation mechanism configured to engage the quick release mechanism is arranged in the frame.
[0021]
21. Vaginal dilatation device according to claim 19, characterized in that a damping element (120) configured to engage the quick release mechanism is disposed in a distal portion of the device.
[0022]
22. Vaginal dilatation device according to claim 16, characterized in that it further comprises a retention mechanism configured to prevent excessive expansion of the pads.
[0023]
23. Vaginal dilation device according to claim 16, characterized in that it further comprises an automatic oscillation mechanism configured to prevent pressure necrosis.
[0024]
24. Vaginal dilatation device according to claim 16, characterized in that the expansion rate comprises a constant rate.
[0025]
25. Vaginal dilation device according to claim 24, characterized in that the constant rate is user adjustable.
[0026]
26. Vaginal dilatation device according to claim 16, characterized in that the expansion mechanism comprises a motor (454).
[0027]
27. Vaginal dilatation device, characterized in that it comprises: a frame; a plurality of arms coupled to the frame, each arm having a pad disposed thereon which is shaped and configured to conform to a vagina; an expansion mechanism coupled to the arms and configured to move the arms and pads radially out of the device; and a diameter sensor (418) disposed in the device and configured to measure a diameter of the device; wherein the expansion mechanism comprises a trigger assembly configured to expand the device by a predefined increment of expansion with a single actuation of the trigger assembly.
[0028]
28. Vaginal dilation device according to claim 27, characterized in that the predefined dilation increment is user adjustable.
[0029]
29. Vaginal dilation device according to claim 28, characterized in that the predefined dilation increment comprises from 0 to 1 cm per activation.
[0030]
30. Vaginal dilation device according to claim 27, characterized in that the predefined dilation increment comprises from 0 to 2 cm per activation.
[0031]
31. Vaginal dilatation device according to claim 27, characterized in that an outside diameter of the pads in a closed configuration is less than 4 cm, and wherein the outside diameter of the pads in an expanded configuration is 8 to 10 cm .
[0032]
32. Vaginal dilatation device according to claim 27, characterized in that it further comprises a force sensor configured to measure a force applied against the pads.

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同族专利:

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公开号 | 公开日

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JP5702791B2|2015-04-15|

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BR112012008679A2|2019-08-06|

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AU2018202962B2|2020-01-02|

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EP2488244B1|2016-05-04|

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JP2016193306A|2016-11-17|

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AU2010306841B2|2016-03-03|

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WO2011047066A2|2011-04-21|

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US9492197B2|2016-11-15|

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EP2488244A2|2012-08-22|

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AU2016200502B2|2018-02-01|

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CA3011931A1|2011-04-21|

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WO2011047066A3|2011-09-15|

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JP5996015B2|2016-09-21|

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CA2777526A1|2011-04-21|

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EP3053626A1|2016-08-10|

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CA2777526C|2018-11-13|

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US20160166282A1|2016-06-16|

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AU2018202962A1|2018-05-17|

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AU2016200502A1|2016-02-18|

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JP6441862B2|2018-12-19|

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EP2488244A4|2013-07-31|

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JP2015107379A|2015-06-11|

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JP2013507232A|2013-03-04|

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EP3053626B1|2017-12-20|

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AU2010306841A1|2012-05-10|

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CN104689459B|2018-05-04|

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US20130053863A1|2013-02-28|

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US20170056069A1|2017-03-02|

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EP3326680B1|2019-08-21|

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法律状态:
2019-08-13| B15I| Others concerning applications: loss of priority|Free format text: PERDA DA PRIORIDADE US 61/278,687 DE 13/10/2009 REIVINDICADA NO PCT/US2010/052528 POR NAO CUMPRIMENTO DA EXIGENCIA PUBLICADA NA RPI 2426 DE 04/07/2017 PARA APRESENTACAO DE DOCUMENTO DE CESSAO CORRETO. FOI APRESENTADO O MESMO DOCUMENTO DE CESSAO REFERENTE AO PCT QUE HAVIA SIDO PREVIAMENTE ENVIADO NA PETICAO 020120032149 DE 12/04/2012 QUE MOTIVOU A FORMULACAO DA EXIGENCIA. |

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2019-08-20| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|

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2019-10-22| B12F| Other appeals [chapter 12.6 patent gazette]|

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2021-07-06| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|

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2021-10-05| B350| Update of information on the portal [chapter 15.35 patent gazette]|

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2021-11-09| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|

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2022-01-25| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 13/10/2010, OBSERVADAS AS CONDICOES LEGAIS. PATENTE CONCEDIDA CONFORME ADI 5.529/DF, QUE DETERMINA A ALTERACAO DO PRAZO DE CONCESSAO. |

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2022-02-22| B09W| Correction of the decision to grant [chapter 9.1.4 patent gazette]|Free format text: RETIFICACAO DA PUBLICACAO DE DEFERIMENTO POR TER SIDO EFETUADA COM INCORRECAO. TAL PUBLICACAO NAO IMPLICA NA ALTERACAO DA DATA DO DEFERIMENTO E NOS PRAZOS DECORRENTES DA MESMA. |

优先权:

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申请号 | 申请日 | 专利标题

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US27868709P| true| 2009-10-13|2009-10-13|

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US61/278,687|2009-10-13|

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PCT/US2010/052528|WO2011047066A2|2009-10-13|2010-10-13|Methods and apparatus for preventing vaginal lacerations during childbirth|

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