Drainage tube for use in wound drainage, in particular in deep drainage, having a drainage lumen surrounded by a tube jacket and extending parallel to the tube axis, the tube jacket having at least one perforation which, starting at an outer boundary area of tube jacket, extends in a transverse direction, in particular approximately perpendicular to the tube axis, and opens out into the drainage lumen.

A dressing for treating a tissue site with negative pressure may include a first layer having a first side, a second side, and fenestrations having a raised edge extending from the first side. The raised edge is configured to expand in response to a pressure gradient across the first layer. The dressing also includes a second layer adjacent to the first side. The second layer includes a manifold. The dressing also includes a cover coupled to the second layer opposite the first layer. The cover includes a polymer drape.

The present application discloses surgical auxiliary equipment for sutureless closed skin incisions in the deep fascia of limbs, comprising subcutaneous negative pressure drainage device, incision closing device, negative pressure device above skin and a plurality of drainage needles, and used for draining the effusions in subcutaneous soft tissues through a plurality of drainage needles. Meanwhile, edge of the skins are squeezed by the incision closing device, and the inner cavity of the subcutaneous incision is forced to be maintained in a closed state during healing and rehabilitation process under the pressure of a negative pressure drainage device, the subcutaneous negative pressure drainage device delivers liquid drug to the inner cavity of the subcutaneous incision while draining effusions in the inner cavity of the subcutaneous incision, to ensure that the environment in the inner cavity of the subcutaneous incision is maintained in a state that facilitates the recovery of the incision.

A system can include excitation pads that can apply an excitation signal to tissue of a patient. The excitation pads can be connected to an electronic circuit that communicates the excitation signal to the excitation pads. The system can include a measurement sensor that can measure voltage of the tissue. The system can include a controller that can determine impedance of the tissue. The controller can be in communication with the excitation pads, the electronic circuit, and the measurement sensor. The controller can generate the excitation signal. The controller can obtain a current measurement of the excitation signal after it has been communicated through at least a portion of the electronic circuit. The current measurement can correspond to the excitation signal before it is applied to the tissue. The controller can determine impedance of the tissue based on the voltage measurement and the current measurement of the excitation signal.

In one example, a medical system may comprise a delivery tube configured to couple to a vacuum source and provide negative pressure to a distal portion of the delivery tube; and a porous body at a distal portion of the delivery tube, the porous body including a first section and a second section removable from the first section.

Methods and systems are provided for a sub-atmospheric wound-care (SAWS) system for treating an open wound. The SAWS system includes a regulated vacuum source for developing a negative pressure, a flow rate meter configured to measure a flow rate of liquid removed from the wound, a primary pressure regulating sensor located proximate the wound for directly measuring the negative pressure at the wound, a backup pressure regulating sensor located vacuum tube, a porous dressing suitable to be sealed airtight which is positioned within a wound interface chamber, a collection canister configured to collect said liquid removed from the wound, and an adapter configured to use wall suction a primary regulated vacuum source.

Embodiments of apparatuses and methods for determining an emplacement of sensors in a wound dressing are disclosed. In some embodiments, a wound dressing includes a plurality of sensors configured to measure wound or patient characteristics. One or more processors are configured to receive wound or patient characteristics data as well as emplacement data. The received data can be used to determine an emplacement of the plurality of sensors, the wound dressing, or a wound. The sensors can include a set of nanosensors. The wound dressing can include pH sensitive ink which can be utilized for determining a placement of the wound dressing and determining a pH associated with the wound. The wound dressing can be used in a negative pressure wound therapy system.

Some embodiments of a manifold pad may be configured to distribute reduced pressure relative to a tissue site and to provide a lateral contractive force relative to the tissue site. In some embodiments, the manifold pad may comprise a foam having a cell-structure forming ovoidal or ellipsoidal pores. In some embodiments, the manifold pad may be configured to preferentially contract radially or laterally upon application of negative pressure. For example, the manifold pad may be configured to be more resistant to collapse of the thickness of the manifold pad than to collapse radially or laterally. Other apparatus, dressings, systems, and methods are disclosed.

The present application discloses surgical auxiliary equipment for sutureless closed skin incisions in the superficial fascia of the skin, comprising: a subcutaneous negative pressure drainage device comprising a catheter partially reaching into a preset depth of the inner cavity of the subcutaneous incision; an incision closing device arranged at the periphery of the skin incision; and a negative pressure device above skin arranged at the periphery of the skin incision and used for generating a negative pressure. Through the surgical auxiliary equipment of the present application, the sutureless closure of full-thickness tissues above the deep fascia of the skin can be achieved, so as to avoid transverse scars on the surface of the skin caused by suture oppression and cutting, and no suture knots are left in superficial fascia, so as to eliminate an important factor causing bacterial colonization and a main inducement leading to relapse of incision infection.

In some embodiments, a wound dressing that incorporates a number of sensors or sensors separate from the wound dressing can be utilized in order to monitor characteristics of a wound as it heals or to identify one or more risk factors or conditions that may precipitate a wound. In some implementations, a wound dressing configured to be positioned in contact with a wound includes a substantially flexible substrate supporting one or more sensors. The one or more sensors can include temperature sensors, conductivity sensors, multispectral optical measurements sensors, pH sensors, pressure sensors, colorimetric sensors, optical sensors, ultraviolet (UV) sensors, or infrared (IR) sensors.