An apparatus comprises a body, a shaft assembly, and an end effector. The shaft assembly extends distally from the body. The end effector is located at a distal end of the shaft assembly. The end effector comprises an ultrasonic blade, a clamp arm, and a sleeve. The ultrasonic blade is configured to vibrate at an ultrasonic frequency. The clamp arm is configured to move toward the ultrasonic blade. The sleeve extends along at least part of the length of an outer portion of the ultrasonic blade or the clamp arm. The sleeve is configured to prevent tissue from contacting a portion of the ultrasonic blade or clamp arm covered by the sleeve.

A removable implant having a radiation shield adapted to reduce radiation exposure to one or more secondary radio-sensitive tissues during breast cancer radiation therapy is provided herein, the implant including: a flexible casing having: a base adapted for anchoring the implant to a chest wall of a patient; a cap disposed on the base; and a radiation-absorbing core adapted to absorb at least a portion of cardiac impact zone radiation when compared to a control, wherein the cap encloses the radiation-absorbing core, and wherein the radiation-absorbing core includes: a flexible solid polymer; and a plurality of radiation-absorbing members dispersed throughout the flexible solid polymer. In another embodiment, the implant further includes a breast tissue expander disposed on a top face of the flexible casing of the implant. Methods of use of the described implants are also provided herein.

An apparatus comprises a body, a shaft assembly, an end effector, and a shield member. The shaft assembly extends distally from the body. The end effector is located at a distal end of the shaft assembly. The end effector comprises an ultrasonic blade and a clamp arm. The ultrasonic blade is configured to vibrate at an ultrasonic frequency. The clamp arm is movable toward the ultrasonic blade to compress tissue against the ultrasonic blade. The shield member is selectively movable from a first position to a second position in response to movement of the clamp arm toward the ultrasonic blade. The shield member is configured cover at least a first portion of the ultrasonic blade in the first position. The shield member is configured to uncover the first portion of the ultrasonic blade in the second position.

Provided are multi-segmented inflatable brachytherapy devices. Also provided are systems and methods including multi-segmented inflatable brachytherapy devices.

The shield for an electrosurgical suction coagulator includes a cylindrical cuff and a shielding portion. The cylindrical cuff is sized for releasably engaging a distal end of a shaft of an electrosurgical suction coagulator. The shielding portion has an arcuate cross-sectional contour and is mounted on the cylindrical cuff such that the shielding portion extends distally therefrom. The shielding portion has a radius of curvature equal to a radius of curvature of the cylindrical cuff and is positioned coaxially therewith. A plurality of shields for the electrosurgical suction coagulator may be provided in a kit, along with the electrosurgical suction coagulator. In the kit, a circumferential length of each shielding portion of each shield is unique, such that a user of the electrosurgical suction coagulator may select a desired one of the shields for a desired amount of shielding coverage.

Apparatus and methods for ablation efficacy are described herein where a hood having a deployable elongated feature can extend beyond a distal face of the hood. The elongated feature can channel the energy to the deeper regions within the tissue (such as trabeculated regions or other tissue structures) such that the energy can be delivered to the target tissue despite small or large irregularities in the target tissue surface (or region) and/or changes in the relative distances between the hood and the target tissue.

A boot for an articulable electrosurgical instrument having a conductor is disclosed. The boot has: a first layer having a flexible substantially non-conductive material; a second layer disposed on the first layer, the second layer having a flexible conductive medium configured to be electrically coupled to at least one shield conductor, whereby the boot is configured to transmit normal current and fault current to a reference potential; and a third layer disposed on the second layer, the third layer having a flexible non-conductive material.

Apparatus and methods are described, including apparatus for treating a cavity in a human body, the apparatus including a delivery tube. A barrier device has a collapsed and an expanded configuration, the barrier device moving from the collapsed to the expanded configuration upon being deployed from the delivery tube. A pushing element, slidably disposed within a lumen of the delivery tube, deploys the barrier device from the delivery tube by pushing the barrier device. One or more barrier-deployment elements are coupled to the barrier device and to the pushing element, the barrier-deployment elements being configured to conformingly contact the barrier device with tissue surrounding the cavity. The barrier device is configured to isolate the cavity from surrounding body fluid that is between the barrier device and the pushing element, following deployment of the barrier device from the delivery tube. Other applications are also described.

A support assembly for use during a medical or surgical procedure. The support assembly includes a base structure and a support structure removably connectable to the support structure through attachment features. In illustrated embodiments, the support structure is attached to the base structure in an upright orientation to form a sideboard or guard and attached to the base structure in a horizontal orientation to form an arm support platform. In illustrated embodiment one or both of the base structure or base board and support structure include attachment features to removably connect a radiation shield for protection against radiation exposure.

A medical hand guard that serve as a protective barrier between a user's hand and potentially contaminated surfaces is disclosed. The medical band guard can comprise a base pad and first and second pockets that are configured to receive a respective thumb and finger of the user. The medical hand guard can define a contact surface opposite the first and second pockets.