Fluid removal systems and methods for removing a fluid from a tissue site are presented. The systems include a semi-permeable inbound conduit, which is fluidly coupled to a treatment-fluid delivery unit, for placement proximate to the tissue site, and a semi-permeable outbound conduit, which is fluidly coupled to the inbound conduit and to a treatment-fluid collector, for placement proximate to the tissue site of a patient. The treatment-fluid collector receives a treatment fluid and a recruited fluid from the tissue site. A recruited-fluid determination unit may be coupled to the treatment-fluid collector to determine a volume of the recruited fluid recruited from the patient. The treatment fluid is any fluid (including a gas) that pulls the fluid from an interstitial and intracellular space. A reduced-pressure treatment subsystem may also be included, among other things, for removing ascites and other fluids from a body cavity.

A protector assembly for protecting an injury and/or surgical wound includes a protector shell having a shell front side, a shell back side and shell circumferential edge where the protector shell has a size and shape that is larger than the injury and/or surgical wound and shaped to correspond to a portion of the body having the injury and/or surgical wound to thereby protect the injury and/or surgical wound from further injury. The protector assembly also includes a protector pad having a pad front side, a pad back side and a pad circumferential edge wherein the protector pad has a pad opening sized to circumscribe the injury and/or surgical wound, the pad front side being attached to the shell back side of the protector shell where the pad back side is between the injury and/or surgical wound and the protector shell.

A gynecological device that corrects a vaginal opening that is large or stretched out without requiring surgery. The stretchable gynecological device includes a main body having a front surface, a rear surface, a first end, a second end, a first edge, a second edge, and an adhesive on the rear surface of the main body. The gynecological device also includes at least two arms having a front surface, a rear surface, a first end, a second end, a first edge and a second edge that extend outwardly from the second edge of the main body. An adhesive is on the rear surface of the arms. To apply the gynecological device, the arms are firmly pressed down to the vaginal vestibule bilaterally, the main body is then pulled up above the clitoral hood and then applied and pressed down across the lower abdomen towards the anterior superior iliac spines.

A support assembly (100) for supporting a transverse incision site (420) of a user (101) includes an assembly body (106) and a first assembly arm (102). The assembly body (106) is configured to encircle an abdomen (107) and at least one leg (311) of the user (101). The assembly body (106) includes a pelvic support layer (214) that is configured to provide a transverse supportive force to the transverse incision site (420) of the user (101). The first assembly arm (102) is coupled to the pelvic support layer (214). The first assembly arm (102) extends anteriorly from the assembly body (106). The first assembly arm (102) is configured to extend from a groin region (109) of the user (101) and secure to the assembly body (106) to adjust the transverse supportive force to the transverse incision site (420) at the peri-pelvic area (421).

A skin adhesive member that helps a user maintain an appropriate posture while supporting muscles on the abdominal side. The skin adhesive member extends in a length direction and is adhered from an abdominal side to a back side across a side abdomen of the user, the skin adhesive member having a foundation portion, a first extension portion extending in the length direction from one end of the foundation portion and adhered to the back side, a second extension portion extending from another end of the foundation portion and adhered to the abdominal side, wherein the first extension portion includes at least a pair of belt portions.

A method and apparatus for applying pressure to the abdomen of a patient to facilitate the insertion of a colonoscope is characterized by the use of a tensile compression device in the form of an elastic band which is wrapped around the patient's abdomen and secured in place. The tension of the band is adjusted to apply a desired degree of pressure to the patient's abdomen to reduce loops in the patient's colon so that the colonoscope can be fully inserted into the colon with minimal discomfort to the patient. The ends of the device are connected together when the desired degree of tension is obtained so that constant pressure and support are provided to the patient's colon. Addition pressure can be manually applied simultaneously with the pressure from the tensile device to reduce or eliminate more distal loops in the colon.

A bandage for the back or pelvis has adjacent pads mounted on an inner face of a supporting piece in a back area of the bandage, respectively one fastener strap piece for applying the bandage by joining together the ends of the two fastener strap pieces attaching at the opposite edge regions of the supporting piece, and two tensioning belts being assigned to the supporting piece, which are guided in such a manner that the pads approach each other when tensioning the tensioning belts and apply a pressure dependent on a tension force acting on the tensioning belts onto the relevant body part.

A compression leotard is provided to aid the performance of athletes where compression panels are incorporated to mimic and support specific muscle groups, while aiding muscle metabolism and protecting joints. Panels are sized and positioned to apply a targeted pressure over a known area, such as hips, shoulders and spine, to reduce inflammation and stress on joints in the body core.

A body trunk supporter provided with: a belt-like lower band section that is adapted to be wrapped around and positioned at the pelvis of a user; an X-shaped stretchable middle band section that has a pair of lower end parts joined to the lower band section and that presses areas of the lumbar region of the user; and a pair of upper band sections that are jointed to a pair of upper end parts of the middle band section and that are adapted to be wrapped around and positioned at the chest of the user, wherein the pair of lower end parts of the middle band section are configured to be joined to areas ranging from positions that are immediately lateral to the pelvis of the user to adjacent anterior positions thereof in the lower band section; and the pair of upper band sections are configured to be separated from each other and to extend in bilaterally opposite directions in an unfolded state, and are configured to be wrapped around and positioned near fifth to tenth ribs of the chest of the user.

A pressure bandage including an elastic sheet having a first coefficient of elasticity and an adhesive side. The pressure bandage may also include a resilient pad having a second coefficient of elasticity and affixed to the adhesive side of the elastic sheet. The elastic sheet has a first predetermined shape that is configured to be applied to a corresponding anatomical location on the body of a patient. The first coefficient of elasticity and the second coefficient of elasticity are related such that, when the elastic sheet is stretched and adhered to the body of the patient, the resilient pad applies a predetermined amount of pressure to the body of the patient.