Abstract: Methods and systems for detecting relapse or recovery events of a user (e.g., an individual, a patient undergoing mental health and addiction treatment) are disclosed. A mobile device detects a communication from a user. The mobile device determines present attributes associated therewith. The mobile device determines, as a function of the communication and the present attributes, a likelihood that a relapse or a recovery event associated with the user is to occur.

Abstract: A restraint device includes at least one sensor configured to sense at least one parameter associated with the wearer of the restraint device. The sensed parameter may be a physiological parameter of the wearer, or the sensed parameter may be a biological substance, a chemical substance, or a radioactive substance, for example. The restraint device may further include a device communicating with the sensor and configured to store and/or transmit information related to the sensed parameter via Radio Frequency Identification (RFID) communication.

Abstract: A restraint device includes first and second restraint and/or support portions adapted to extend around part of a person. First and second connector portions may secure the first and second restraint and/or support portions to the person. A lock member may be used to selectively prevent disconnection of the first and second connector portions. One or more removable tags or other information elements may be carried on at least one of the first and second restraint and/or support portions and may indicate who placed the restraint device on, or removed the restraint device from the person, and/or what time the restraint device was placed or removed. The tags or other elements may include a unique identifier to indicate whether the restraint device had been previously removed from the person after an initial placement. The restraint device may include an electronic information element configured to transmit information related to the wearer.

Abstract: A restraint device includes at least a first restraint portion defining a space for receiving at least a first body portion of a wearer to restrain movement of the wearer. The restraint device also includes at least one sensor on the first restraint portion and configured to sense at least one parameter associated with the wearer of the restraint device. The sensed parameter may be a physiological parameter of the wearer, or the sensed parameter may be a biological substance, a chemical substance, or a radioactive substance. The restraint device may further include a device communicating with the sensor and configured to store and/or transmit information related to the sensed parameter.

Abstract: A restraint device includes first and second restraint and/or support portions adapted to extend around part of a person. First and second connector portions may secure the first and second restraint and/or support portions to the person. A lock member may be used to selectively prevent disconnection of the first and second connector portions. One or more removable tags or other information elements may be carried on at least one of the first and second restraint and/or support portions and may indicate who placed the restraint device on, or removed the restraint device from the person, and/or what time the restraint device was placed or removed. The tags or other elements may include a unique identifier to indicate whether the restraint device had been previously removed from the person after an initial placement. The restraint device may include an electronic information element configured to transmit information related to the wearer.

Abstract: A restraint device includes first and second restraint and/or support portions adapted to extend around part of a person. First and second connector portions may secure the first and second restraint and/or support portions to the person. A lock member may be used to selectively prevent disconnection of the first and second connector portions. One or more removable tags or other information elements may be carried on at least one of the first and second restraint and/or support portions and may indicate who placed the restraint device on, or removed the restraint device from the person, and/or what time the restraint device was placed or removed. The tags or other elements may include a unique identifier to indicate whether the restraint device had been previously removed from the person after an initial placement. The restraint device may include an electronic information element configured to transmit information related to the wearer.

Abstract: A restraint device includes first and second restraint and/or support portions adapted to extend around part of a person. First and second connector portions may secure the first and second restraint and/or support portions to the person. A lock member may be used to selectively prevent disconnection of the first and second connector portions. One or more removable tags or other information elements may be carried on at least one of the first and second restraint and/or support portions and may indicate who placed the restraint device on, or removed the restraint device from the person, and/or what time the restraint device was placed or removed. The tags or other elements may include a unique identifier to indicate whether the restraint device had been previously removed from the person after an initial placement. The restraint device may include an electronic information element configured to transmit information related to the wearer.

Abstract: A restraint device includes first and second restraint and/or support portions adapted to extend around part of a person. First and second connector portions may secure the first and second restraint and/or support portions to the person. A lock member may be used to selectively prevent disconnection of the first and second connector portions. One or more removable tags or other information elements may be carried on at least one of the first and second restraint and/or support portions and may indicate who placed the restraint device on, or removed the restraint device from the person, and/or what time the restraint device was placed or removed. The tags or other elements may include a unique identifier to indicate whether the restraint device had been previously removed from the person after an initial placement. The restraint device may include an electronic information element configured to transmit information related to the wearer.

Abstract: A restraint device includes first and second restraint and/or support portions adapted to extend around part of a person. First and second connector portions may secure the first and second restraint and/or support portions to the person. A lock member may be used to selectively prevent disconnection of the first and second connector portions. One or more removable tags or other information elements may be carried on at least one of the first and second restraint and/or support portions and may indicate who placed the restraint device on, or removed the restraint device from the person, and/or what time the restraint device was placed or removed. The tags or other elements may include a unique identifier to indicate whether the restraint device had been previously removed from the person after an initial placement. The restraint device may include an electronic information element configured to transmit information related to the wearer.

Abstract: A restraint device includes first and second restraint and/or support portions adapted to extend around part of a person. First and second connector portions are used to secure the first and second restraint and/or support portions to the person. In one aspect, a lock member is used to selectively prevent disconnection of the first and second connector portions. A removable tag or other information element may be carried on at least one of the first and second restraint and/or support portions and may indicate the individual or individuals that placed the restraint device on the person or that removed the restraint device from the person, and/or what time the restraint device was placed or removed. A plurality of removable tags or other elements may be carried on at least one of the first and second restraint and/or support portions and may have a unique identifier to indicate whether or not the restraint device had been previously removed from the person after an initial placement.

Abstract: A medical apparatus for dispensing a biologically active compound. The medical apparatus includes a sleeve, wherein (1) the sleeve has a working channel defined therein through which medical instruments may be advanced, (2) the sleeve includes a fluid delivery channel which is distinct from the working channel, (3) the fluid delivery channel has an exit, and (4) the sleeve includes a housing having an interior cavity defined therein. The medical apparatus also includes an insufflation valve in fluid communication with the working channel. The insufflation valve is positionable between an open position and a closed position such that (i) when the insufflation valve is located in the open position an insufflation gas can be advanced into the working channel and (ii) when the insufflation valve is located in the closed position the insufflation gas is prevented from being advanced into the working channel.

Abstract: A body cavity access assembly includes a conduit having an exterior surface, a dispensing mechanism, and a reservoir for receiving a biologically active compound. The exterior surface of the conduit has first exit port and a second exit port defined therein which are in fluid communication with the reservoir. The first exit port and the second exit port are selectively positionable between an open mode of operation and a closed mode of operation with the dispensing mechanism. An associated medical procedure for dispensing a biologically active compound is also disclosed.

Abstract: A fluid delivery cannula which provides an interface between an access point or port in the body of a patient and a working channel which may receive tools or instruments used during minimally invasive surgery. The cannula allows introduction of fluid(s) at the port site, or another site within the body of the patient. The fluid delivery cannula can releasably attach to a hub associated with a trocar assembly or may be integrally formed with at least a portion of the hub. In one form, an inner cannula member includes a grooved outer surface to define multiple fluid passages and a perforated outer layer is placed over the inner cannula member. Another form provides an expandable sleeve that may itself comprise a cannula through which a trocar or trocar assembly is inserted or which may take the place of the perforated outer layer of the grooved cannula.

Abstract: A medical apparatus for dispensing a biologically active compound. The medical apparatus includes a sleeve, wherein (1) the sleeve has a working channel defined therein through which medical instruments may be advanced, (2) the sleeve includes a fluid delivery channel which is distinct from the working channel, (3) the fluid delivery channel has an exit, and (4) the sleeve includes a housing having an interior cavity defined therein. The medical apparatus also includes an insufflation valve in fluid communication with the working channel. The insufflation valve is positionable between an open position and a closed position such that (i) when the insufflation valve is located in the open position an insufflation gas can be advanced into the working channel and (ii) when the. insufflation valve is located in the closed position the insufflation gas is prevented from being advanced into the working channel.

Abstract: A medical apparatus for dispensing a biologically active compound. The medical apparatus includes a sleeve, wherein (1) the sleeve has a working channel defined therein through which medical instruments may be advanced, (2) the sleeve includes a fluid delivery channel which is distinct from the working channel, (3) the fluid delivery channel has an exit, and (4) the sleeve includes a housing having an interior cavity defined therein. The medical apparatus also includes an insufflation valve in fluid communication with the working channel. The insufflation valve is positionable between an open position and a closed position such that (i) when the insufflation valve is located in the open position an insufflation gas can be advanced into the working channel and (ii) when the insufflation valve is located in the closed position the insufflation gas is prevented from being advanced into the working channel.

Abstract: A body cavity access assembly includes a conduit having an exterior surface, a dispensing mechanism, and a reservoir for receiving a biologically active compound. The exterior surface of the conduit has first exit port and a second exit port defined therein which are in fluid communication with the reservoir. The first exit port and the second exit port are selectively positionable between an open mode of operation and a closed mode of operation with the dispensing mechanism. An associated medical procedure for dispensing a biologically active compound is also disclosed.

Abstract: A medical apparatus is disclosed. The medical apparatus includes a trocar assembly having a cannula and a trocar, wherein (1) the cannula has (i) a lumen defined therein and (ii) a length L1, (2) the trocar is positionable between a first trocar position and a second trocar position, (3) the trocar is positioned within the lumen of the cannula when the trocar is positioned at the first trocar position, and (4) the trocar is completely removed from the lumen of the cannula when the trocar is positioned at the second trocar position.

Abstract: A body cavity access assembly is disclosed. The body cavity access assembly includes a conduit having an exterior surface, a dispensing mechanism, and a reservoir for receiving a biologically active compound. The exterior surface of the conduit has first exit port and a second exit port defined therein which are in fluid communication with the reservoir. The first exit port and the second exit port are selectively positionable between an open mode of operation and a closed mode of operation with the dispensing mechanism. An associated medical procedure for dispensing a biologically active compound is also disclosed.

Abstract: A medical apparatus is disclosed. The medical apparatus includes a trocar assembly having a cannula and a trocar, wherein (1) the cannula has (i) a lumen defined therein and (ii) a length L1, (2) the trocar is positionable between a first trocar position and a second trocar position, (3) the trocar is positioned within the lumen of the cannula when the trocar is positioned at the first trocar position, and (4) the trocar is completely removed from the lumen of the cannula when the trocar is positioned at the second trocar position.

Abstract: A medical apparatus for dispensing a biologically active compound. The medical apparatus includes a sleeve, wherein (1) the sleeve has a working channel defined therein through which medical instruments may be advanced, (2) the sleeve includes a fluid delivery channel which is distinct from the working channel, (3) the fluid delivery channel has an exit, and (4) the sleeve includes a housing having an interior cavity defined therein. The medical apparatus also includes an insufflation valve in fluid communication with the working channel. The insufflation valve is positionable between an open position and a closed position such that (i) when the insufflation valve is located in the open position an insufflation gas can be advanced into the working channel and (ii) when the insufflation valve is located in the closed position the insufflation gas is prevented from being advanced into the working channel.