A unisex urine collection assembly for use by either sex in a non-ambulatory setting includes a tube, which has a cutout positioned in a top face thereof and extending from proximate to a midpoint toward a first end thereof. A second end of the tube is closed. A connector engaged to the first end of the tube can engage a conduit extending from a suctioning unit. Each of a pair of pads is engaged to the tube and extends from a respective opposed edge of the cutout thereinto so that the pads defines a slot. The pads are resiliently flexible and can sealably engage skin of the user. The pads can be positioned between labia of a female user or to bracket a penis inserted into the slot by a male user. Urine expelled by the user is suctioned from the tube into a reservoir.

Examples of a module for housing unrelated electronic and electromechanical equipment for use during surgery. The module can include a lower section and a tower-like upper section. The lower section can house unrelated electronic and electromechanical equipment. The tower-like upper section can be located on top of the lower section. A water-resistant cowling can enclose at least a portion of the lower section and the tower-like upper section. A cartridge containing one or more ultraviolet-C producing lights can be protectively housed within the tower-like upper section. The cartridge containing one or more ultraviolet-C producing lights can be configured to emerge upward from a top of the tower-like upper section to substantially seat itself on the top of the tower-like upper section when activated allowing the ultraviolet-C light to disinfect the patient and staff-contacting upper surfaces of the equipment in the operating room.

Urinary catheter-insertion kits can include a working tray, a storage tray, a protective paperboard, and a urinary catheter assembly, including a urinary catheter and a drainage system. The working tray can be nested on top of the storage tray. The working tray includes preformed sections configured to accommodate components of the urinary catheter-insertion kit. Methods of urinary catheterization include use of the urinary catheter-insertion kits.

A protective sleeve for a urinary catheter includes a sleeve configured to extend over an outer surface of the urinary catheter shaft from a proximal insertion end of the catheter shaft to a distal end of the catheter shaft. The protective sleeve includes a protective sleeve tip defining the proximal end portion of the sleeve. The sleeve and the protective sleeve tip are of a single unitary construction and the sleeve and protective sleeve tip are formed of the same thin, flexible film. The protective sleeve tips has a first pre-use configuration when a proximal insertion end of the catheter is not within the protective sleeve tip wherein the protective sleeve tip is in a collapsed state, and a second configuration when a proximal insertion end of a urinary catheter is inserted into the protective sleeve tip, in the second configuration the protective sleeve tip being in an extended state that is configured to cover the proximal insertion end of the urinary catheter shaft and the thin, flexible film conforms to and is supported by the proximal insertion end of the urinary catheter for insertion of the protective sleeve tip into the urethral opening.

A fluid therapy method for an ADHF patient includes setting a urine output rate desired threshold, setting one or more desired negative net gain rates, and optionally setting a total fluid loss goal. The urine output of the patient is monitored and fluid is automatically administered to the patient at increasing rates to equal to or approximately match the patient's increasing urine output rates until the patient's urine output rate reaches the set urine output rate desired threshold. Thereafter, fluid is administered to the patient at rates to achieve the set desired negative net gain rate until the fluid loss goal is reached. Thereafter, until the end of therapy, fluid is administered to the patient at rates equal to or approximately equal to the monitored urine output rates.

A three-way urology catheter stopcock includes a stopcock body defining a longitudinally extending fluid flow passage, the body having three connector mounting openings in a wall thereof, an on/off selector movably mounted within the fluid flow passage of the body, the on/off selector including a longitudinally extending, cylindrical selector body having an open end, a closed end, and three fluid flow openings in a wall of the selector body, wherein the closed second end includes one of a plurality of fluid flow indicator members and fluid flow indicia, two first connectors mounted in opposing connector mounting openings of the stopcock body, and a second connector mounted in the connector mounting opening that is between the openings in which the two first connectors are mounted.

Disclosed herein is a system for performing urinalysis of transurethral patients. The system includes a tubing set to receive urine from a urethral catheter. A detector assembly is operatively coupled between the tubing set and a urinalysis module coupled. The system can perform urinalysis of a urine sample disposed within the tubing set and render urinalysis information on a display of the module. Also disclosed is a method of performing urinalysis that can include operations of: (i) placing a urine sample within a cuvette of a urinalysis system, the cuvette including a lumen extending between an inlet and an outlet; (ii) projecting coherent light into the sample; (iii) collecting output light exiting the sample; (iv)extracting urinalysis data from the collected light; and (v) rendering urinalysis results on a display of the system.

A method of treating a human subject which is effected by inhalation of gaseous nitric oxide, the method comprising a first treatment period comprising administering gNO by inhalation over a period of about at least 5 days, wherein the first treatment period is followed by a second treatment period comprising administering gNO by inhalation over a period of at least 3 months. The method can be utilized for treating a human subject suffering from, or prone to suffer from, a disease or disorder that is manifested in the respiratory tract, or from a disease or disorder that can be treated via the respiratory tract.

A fluid collection system may include a fluid collection device, a tube, a fluid collection container configured to receive fluid from the fluid collection device, and a vacuum source configured to pull an at least partial vacuum to draw the fluid from the fluid collection device through the tube into the fluid collection container. The fluid collection device may include a fluid impermeable barrier including an outer surface and an inner surface, the fluid impermeable barrier defining a chamber, at least one opening, and a fluid outlet. The fluid collection device may include a porous material disposed in the chamber and an external support coupled to the outer surface of the fluid impermeable barrier. The fluid impermeable barrier exhibits a first shape prior to shaping the external support and a second shape after shaping the external support with the first shape being different from the second shape.

An example fluid collection assembly includes a fluid impermeable barrier defining at least one opening, a chamber, and at least one fluid outlet. The fluid collection assembly also includes at least one porous material disposed in the chamber. The fluid collection assembly further includes at least one inflation device. The inflation device includes bladder having one or more walls defining an interior region. The inflation device also includes at least one valve configured to selectively permit fluid flow into and out of the interior region to switch the bladder between a first state and a second state. The inflation device may at least one of controllably change the length of the fluid collection assembly or controllably change a width of at least a portion of the fluid collection assembly to more comfortably fit the fluid collection assembly within the labia folds of an individual using the fluid collection assembly.