Systems and methods provide for holding surgical drain evacuators in inelastic expandable pouches. Particularly, apparatuses and methods include or utilize garments for supporting and protecting surgical drain evacuators and surgical drains include straps or belts for attaching the garment to a patient. The garments include one or more expandable pouches configured to receive a surgical drain evacuator, wherein the expandable pouch is formed of a flexible inelastic material.

The present technology relates to intracardiac pressure monitoring devices, and associated systems and methods. In some embodiments, the present technology includes a device for monitoring pressure within a patient's heart. The device can include a pressure sensor configured to reside within a first chamber of a heart of a patient, and a pressure transmission element configured to extend from the first chamber through a septal wall to a second chamber of the heart of the patient. When the device is implanted in the patient's heart, the pressure transmission element is configured to transmit pressure from the second chamber to the pressure sensor residing within the first chamber.

The principles and embodiments of the present disclosure relate to methods for using terlipressin to treat a patient having impaired renal function associated with liver disease. A method of improving kidney function in an adult patient with hepatorenal syndrome with rapid reduction in kidney function may include determining the patient’s acute-on-chronic liver failure (ACLF) grade and baseline serum creatinine level; obtaining a baseline oxygenation saturation (SpO.sub.2) of the patient; administering a dose of terlipressin acetate to the patient by intravenous (IV) injection; and monitoring the patient’s oxygenation saturation with pulse oximetry.

A hemostatic device is disclosed. The hemostatic device according to an embodiment of the present invention includes: a balloon which is expanded by a fluid supplied therein; a blood discharge pipe which includes a blood inflow hole at one end and exposes the other end to a lower side of the balloon wherein a certain section of a lower side of the blood inflow hole is surrounded by the balloon; and a fluid flow pipe communicating with the inside of the balloon for supplying or discharging the fluid and extending to a lower side of the balloon. The balloon includes a plurality of protrusions that are formed to protrude outward when the balloon is expanded by the fluid.

A urethral catheter. A cavity is formed at the head end of the urethral catheter, and an internal span of the cavity is greater than that of an opening. A check device (2) located at the front end of a guide core (5) is received in the cavity, and the check device (2) is a guide core (5) that can be retracted into a guide core catheter (4) and can move within the guide core catheter (4). The guide core (5) can expand outward after moving out of the guide core catheter (4). The span of the top of the expanded guide core (5) is greater than the outer diameter of the opening of the cavity at the head end of the urethral catheter. The urethral catheter eliminates a guide extension inserted inside the urethral catheter, and avoids any structural parts provided in the front end of the urethral catheter, and no accessory device is provided at the inner side of the catheter wall of the conventional urethral catheter, so that the internal urination cross-sectional area of the urethral catheter is the same as the area of the inner holes of the urethral catheter, thereby greatly increasing the urine output of the urethral catheter and greatly reducing the injection resistance of a lubricant.

A tissue expander includes a shell having an anterior wall with superior and inferior zones, and one or more drainage openings formed in the inferior zone. A fill port assembly is located within the superior zone, and a drain port assembly is located within the inferior zone and is in fluid communication with the one or more drainage openings. The fill port assembly is isolated from the drain port assembly that is located within the inferior zone. The drain port assembly includes a drain cover having an elongated body, a central hub, one or more fluid reservoirs between the first and second ends of the elongated body, and an outer face that surrounds the fluid reservoirs. The outer face of the drain cover is secured to an inner surface of the anterior wall and surrounds the one or more drainage openings formed in the inferior zone of the shell.

Airway devices, systems, and methods are provided that can achieve ventilation of lungs through a mask that seals around the glottis and connects to a flexible airway channel, while also providing evacuation of gastric and/or pharyngeal body fluid and/or blood during upper airway surgeries or procedures.

Airway devices, systems, and methods are provided that can achieve ventilation of lungs through a mask that seals around the glottis and connects to a flexible airway channel, while also providing evacuation of gastric and/or pharyngeal body fluid and/or blood during upper airway surgeries or procedures.

An imaging probe comprises a camera or endoscope with an external detector array, in which the probe is sized and shaped for surgical placement in an eye to image the eye from an interior of the eye during treatment. The imaging probe and a treatment probe can be coupled together with a fastener or contained within a housing. The imaging probe and the treatment probe can be sized and shaped to enter the eye through an incision in the cornea and image one or more of the ciliary body band or the scleral spur. The treatment probe may comprise a treatment optical fiber or a surgical placement device to deliver an implant. A processor coupled to the detector can be configured with instructions to identify a location of one or more of the ciliary body band, the scleral spur, Schwalbe's line, or Schlemm's canal from the image.

A urinary catheter assembly is provided. The catheter assembly has a first outer package (20), which contains a second inner package (1). The second inner package includes a hydrophilic coated, intermittent catheter 82) and liquid swelling medium. The first outer package is made of a first material with a WVTR value between 1 and 6 g/(m.sup.2.Math.24 h) and the second inner package is made of a second material with a second WVTR value below 3 g/(m.sup.2.Math.24 h). An intermediate cavity (25) is defined inside the first outer package, but outside the second inner package. The first and second WVTR-values are balanced in such a way that the relative humidity (RH) is below 90% in the intermediate cavity. This prevents condensation on the inner surface of the first outer package and on the outer surface of the second inner package.