摘要:
A biopsy device comprises a probe body, a cannula extending distally from the probe body, a cutter moveable relative to the cannula to sever tissue, and a tissue sample holder coupled with the probe body. The tissue sample holder comprises a rotatable member having a plurality of recesses to receive tissue samples. The rotatable member can be operable to successively index each recess relative to a lumen defined by the cutter. A cover portion may be associated with the rotatable member and permits one or more recesses to be viewable through the cover. The recesses may be configured to carry one or more tissue samples as the rotatable member is rotated.
摘要:
A biopsy device comprises a probe body, a cannula extending distally from the probe body, a cutter moveable relative to the cannula to sever tissue, and a tissue sample holder coupled with the probe body. The tissue sample holder comprises a rotatable member and at least one removable member secured about the exterior of the rotatable member. The at least one removable member defines a plurality of tissue sample compartments. Each tissue sample compartment is configured to receive one or more tissue samples captured by the cutter. In some versions, the at least one removable member comprises a belt and a plurality of vials.
摘要:
A biopsy device includes a body portion, a tip, at least one blade, and a cutter. The cannula defines at least one lumen. The cannula has a transverse aperture configured to receive tissue. The tip is located at the distal end of the cannula, and may include at least two concave surfaces. The blade extends longitudinally from the tip. A second blade may also extend longitudinally from the tip. Blades may be axially staggered relative to the cannula. Blades may also have lengths that differ from one another. In addition, a blade may have a pointed distal end, or may have a curved distal edge. The configuration of the blade and tip may provide reduced force to penetrate tissue. The blade and tip may produce a cut length that is greater than or equal to the length of the outer perimeter of the cannula.
摘要:
A biopsy probe includes a body portion, a cannula, a tip, and a cutter. The cannula extends relative to the body portion. The cannula has a first lumen configured to receive a cutter and a transverse aperture configured to receive tissue. The cutter is disposed in the first lumen of the cannula, and is configured to translate relative to the cannula. The tip is located on the distal end of the cannula. An opening is formed through the tip. A second lumen extends through the cannula, and is in fluid communication with the opening formed in the tip. Substances or liquids such as medicine may be dispensed to a biopsy site or other location within the body of a patient via the second lumen and the opening in the tip. The second lumen may be fluidly isolated from the first lumen and any other lumen in the cannula.
摘要:
A diagnostic station integrates patient support, imaging, biopsy, and treatment. An illustrative version of a prone mammography table localizes a breast with an imaging modality (e.g., X-ray, etc.) based upon a rotating C-arm that may encircle the localized breast. A biopsy system is integrated into the controls and displays or user interface of the diagnostic station, sharing integrated utilities (e.g., vacuum, power, data communication, etc.). Ancillary devices may be identified and authenticated by the integrated system, such as to base available functionality on the identification and/or authentication of an ancillary device. Ancillary devices that may be integrated with the system may include devices that are operable to perform surgical, therapeutic, diagnostic, or other functions.
摘要:
A tissue sample holder for a biopsy device comprises an outer cup, a collection tray, and a flow restriction device. The outer cup defines a hollow interior. The collection tray separates the hollow interior into an upper chamber and a lower chamber while allowing fluid to pass between the two chambers through an opening in the collection tray. The flow restriction device selectively seals the opening thereby preventing fluid from passing from the lower chamber into the upper chamber. The flow restriction device may be operable to selectively seal the opening in response to a vacuum being induced within the upper chamber. The collection tray may have a shape (e.g., tapered, funnel-shaped, convex, etc.) selected to facilitate the flow of fluid toward the opening. The lower chamber may be coupled with an external fluid collection device. The lower chamber may define a larger volume than the upper chamber.
摘要:
An apparatus for inserting a marking element into a marker body includes a body portion, an insertion member, and a pushing member. The body portion has a compartment configured to receive a marker body. The insertion member is configured to engage the marker body within the compartment. The pushing member is configured to engage with the insertion member. The pushing member is operable to force a marking element along the insertion member into the marker body. The insertion member may include a hollow needle configured to penetrate the marker body. The pushing member may include a pin configured to fit within the hollow needle. The marker body may include an opening such as a slit, a slot, or a passage that is configured to receive a marking element. The marker body may include a collagen dowel, and the marking element may be formed of titanium.
摘要:
An instrument for deploying a marker at a site within a patient may include an elongate cannula, an elongate pusher, and a marker disposed within the cannula. The cannula may have a tip at its distal end and a transverse opening. The pusher may be disposed within the cannula, and may be moved longitudinally within the cannula. The pusher may have a ramped distal end. The marker may be configured to exit the transverse opening upon urging by the ramped distal end of the pusher. In some versions, the tip of the cannula has a flat proximal face, and the marker has a recessed region that is configured to buckle in response to longitudinal compression, such that the marker will pop out of the cannula upon buckling. In other versions, the cannula has an external sheath, an open and curved distal end, or a leaf spring.
摘要:
An apparatus for inserting a marking element into a marker body includes a body portion, an insertion member, and a pushing member. The body portion has a compartment configured to receive a marker body. The insertion member is configured to engage the marker body within the compartment. The pushing member is configured to engage with the insertion member. The pushing member is operable to force a marking element along the insertion member into the marker body. The insertion member may include a hollow needle configured to penetrate the marker body. The pushing member may include a pin configured to fit within the hollow needle. The marker body may include an opening such as a slit, a slot, or a passage that is configured to receive a marking element. The marker body may include a collagen dowel, and the marking element may be formed of titanium.
摘要:
A diagnostic station integrates patient support, imaging, biopsy, and treatment. An illustrative version of a prone mammography table localizes a breast with an imaging modality (e.g., X-ray, etc.) based upon a rotating C-arm that may encircle the localized breast. A biopsy system is integrated into the controls and displays or user interface of the diagnostic station, sharing integrated utilities (e.g., vacuum, power, data communication, etc.). Ancillary devices may be identified and authenticated by the integrated system, such as to base available functionality on the identification and/or authentication of an ancillary device. Ancillary devices that may be integrated with the system may include devices that are operable to perform surgical, therapeutic, diagnostic, or other functions.