Abstract: A device for introducing an implant (1) into blood vessels or hollow organs of the human or animal body. The device includes an implant (1), an insertion wire (14) and a release tube (13), wherein the implant (1) is deformable so that it fits into a microcatheter (8) and expands once the external constraint of the microcatheter (8) disappears, adapting to the diameter of the blood vessel or hollow organ, wherein a holding element (2) is arranged on the insertion wire (14) and the holding element (2) has at its periphery at least one groove (3) set into the holding element (2), running along the circumference of the holding element (2) and forming tracks in the form of curved lines, wherein the implant (1) has holding wired (5) extending proximally, which are fitted into the grooves (3).

Abstract: A method for manufacturing single unit structures with three dimensional printing and various materials formable into three dimensional assemblies that may be used for various purposes.

Abstract: A combination including a dithiocarbamate fungicide, a succinate dehydrogenase fungicide and at least one of ergosterol biosynthesis inhibitor fungicide or a quinone outside inhibitor fungicide.

Abstract: A vascular implant and a medical device. The vascular implant includes a tubular implant main segment (100, 400) braided from two or more interlaced wires (130, 132, 134, 136, 138) and having a first end (120, 420) and a second end (110, 410), which are located at two ends of g an axis of the implant main segment. The first end (120, 420) includes a plurality of looped-back rings (122, 124, 422, 424). The second end (110) includes a plurality of first joint portions (112), each of which is a non-invasive joint portion formed by joining at least two of the wires (130, 132, 134, 136, 138). At least one of the two or more wires (130, 132, 134, 136, 138) includes core and a jacket surrounding the core. The ends of the vascular implant will cause less damage to the wall of a blood vessel, and the implant provides improved stability and radiopacity.

Abstract: A method for retracting a sheath from over an expandable medical device. The method includes rotating a lever, which protrudes from a shell of a handle, proximally, such that the lever proximally moves, by a first distance, a carriage disposed within the shell and coupled to the sheath. Subsequently to rotating the lever, the lever slides proximally such that the lever moves the carriage proximally by a second distance.

Abstract: Through observation it has been determined that deployment of delivery sleeves may result in one or more portions of the deliver), sleeve extending beyond an end of the endoluminal device resulting in an overhang of material. The overhang may affect blood flow through the endoprosthesis or otherwise impact performance, including facilitating unwanted tissue growth. Various inventive concepts are provided for addressing (reducing or removing) constraining sheath overhang.

Abstract: A system for delivering an endolumenal device through an endoscope includes a delivery tool and an adaptor. The delivery tool has an elongate tube configured to hold a portion of the endolumenal device therein and a first connecting feature on a distal end of the elongate tube. The adaptor is configured to attach to a handle of the endoscope. The adaptor includes a channel therethrough and a second connecting feature configured to mate with the first connecting feature of the delivery tool. The elongate tube of the delivery tool is configured to align with the channel of the adaptor when the first and second connecting features are mated.

Abstract: Non-surgical correcting apparatuses for a deformed external ear are provided. The correcting apparatuses may be worn externally to correct a deformity or malformation on the external ear through remodeling or reshaping over a period of time. The correcting apparatuses may be secured in place with associated attachment components coupled to the correcting components. The correcting apparatuses are configured to address the helix, helical rim, antihelix, conchal bowl, ear lobe, and triangular fossa of the ear.

Abstract: A plurality of round members, such as balls, that are coupled together in an array by a connecting agent such as one or more nylon cords that allow the balls to move and work in concert and uniformity with the lower back muscles and movement of a sleeping user lying upon the device. With such use the connected and movable balls provide continuous acupressure throughout the night as the user sleeps, resulting in continuous relief and mitigation of arthritic pain and stiffness in one's lower back throughout the night. Thus, pain and stiffness which would otherwise greatly disturb one's attempt to sleep through the night is mitigated, if not outright relieved.

Abstract: An arm stabilization system designed to provide enhanced support for the human arm. The system consists of a lateral support element that contacts the side of a torso, a first arm support element that contacts the upper arm, and a second arm support element that contacts the lower arm. A plurality of subframes embedded within the support elements provide support, stability, and a consistent shape to the arm stabilization system. A novel series of connections among these subframes provides enhanced adjustability and movement options for the wearer.

Abstract: A unitary garment body having a front abdominal portion interposed between two arm openings and the two leg openings of the garment, of an elastic-based polymer material, with an inner surface, defining at least one pocket interposed between outer and inner surfaces of the front abdominal portion and configured to enclose and define a pocket cavity shaped and sized to receive a thermal pack, and with a plurality of front pressure protrusions on the pocket and each projecting inwardly from the inner surface toward the abdomen cavity, disposed in a tightly spaced configuration, each having a rounded tip, and each having a width ranging from 1-2 mm and a height relative to the inner surface of the front abdominal portion ranging from 0.2-0.5 mm and having a rear back portion interposed also of an elastic-based polymer material opposing the front abdominal portion.

Abstract: The invention belongs to the technical field of health care products, in particular to a flexible and conveniently adjustable neck brace, comprising a chest support block. The chest support block is connected to the adjustment components through the connection rods. The adjustment components are connected to a lower jaw support. The top of the lower jaw support is equipped with a support plate that can slide above it. The user can place head on the support plate and can rotate left and right. Compared with the existing neck brace, this structure is more flexible, and it is convenient for users to use. And it is also equipped with a magnet to facilitate the reset of the support plate to the middle position. The neck brace adopts the adjustable components, which are more convenient for users to adjust.

Abstract: An improved syndesmosis reduction device has a wrap of elastic material extending a length L from a first end to a second end with an open window or slot positioned in an intermediate portion of the wrap spaced from the ends. The wrap is configured to achieve a reduction of an injured ankle and is facilitated by the elastic nature of the ankle wrap. The reduction is facilitated by circumferentially wrapping the wrap from a leg to a foot or vice versa in a compressive fashion by securing the first end by wrapping and stretching the wrap to the second end. The window or slot is to permit an incision at the ankle for hardware placement without the need to remove the wrap and without loss of the reduction achieved.

Abstract: A hand immobilizer which has a body in the general shape of the hand, including a portion shaped like the metacarpus and wrist of the hand and distally extending portions or digits shaped like the fingers of the hand. At least some of the digits of the hand immobilizer comprise first and second laterally spaced tines or prongs.

Abstract: An orthopedic brace features a knee orthosis including a first de-tensioning assembly and a second de-tensioning assembly. The first de-tensioning assembly includes a first elastic strap situated on a first side of the knee orthosis and the second de-tensioning assembly includes a second elastic strap situated on a second side of the knee orthosis. The first and second elastic straps are communicatively coupled to a lumbar back support brace and a lower leg brace, both separate from the knee orthosis.

Abstract: A positioning wedge is arranged as an interface between two anatomical portions of a human body to arrange the anatomical two portions at a predetermined angle or position relative to one another. The positioning wedge includes a main body having first and second sides connected to another by a bridge portion such that the first and second sides each define a predetermined angular profile. An insert can be arranged between the first and second sides to position the first and second sides relative to one another at a predetermined angle associated with the shape of the insert combined with the first and second sides. The insert is separable from, and attachable to the main body and the bridge portion extends over an end portion of the insert.

Abstract: Example fluid collection devices and methods of use arc described. The fluid collection devices include a fluid impermeable barrier, a fluid permeable body, and two arms. The fluid impermeable barrier at least partially defines a chamber, and an opening configured to be positioned adjacent to a urethra. The fluid permeable body is positioned at least partially within the chamber to extend across at least a portion of the opening and configured to wick fluid away from the opening. The arms include an adhesive surface oriented towards the fluid impermeable barrier. The arms arc positioned on the fluid impermeable barrier to attach to at least one of an abdominal region, a pubic region, or a pelvic region of the user when the opening of the fluid impermeable barrier is positioned at least proximate to the urethra of the user.

Abstract: A valve (10) for draining fluid from a urostomy pouch (5), where the valve (10) comprises a first valve portion (20) comprising a head portion (24), an inlet (15), a stem (6), a first bore (22), at least one outlet opening (23) and a distal end closure (15), a second valve portion (30) comprising a sleeve (7), a second bore (32) and a valve outlet (33), wherein the stem (6) and the sleeve (7) are threadedly engaged by a threaded connection (26), the first bore (22) and the second bore (32) form a channel to transport fluid from the inlet (15) to the valve outlet (33), the sleeve (7) encircles the stem (6) and is adapted to close off the channel to prevent drainage of fluid, the distal end closure (25) of the first valve portion (20) is adapted to close off the valve outlet (33) of the second valve portion (30), the threaded connection (26) between the stem (6) and the sleeve (7) is adapted for displacing the sleeve (7) away from the head portion (24) of the first valve portion (20) to open the channel and all

Abstract: A drainable ostomy pouch outlet includes a single-piece closure member including at least one transversely-extending fold-line. The at least one transversely-extending fold-lines are configured to facilitate folding up and closing of the outlet. The single-piece closure member may also include at least one axially-extending or slanted fold-lines intersecting the at least one transversely-extending fold-line, configured to facilitate opening of the outlet.

Abstract: A portable urine collection system (10) may include a urine collection device (12), a first conduit (17) in fluid communication with the urine collection device, a urine collection container (14) having an interior region, a pump (16), a sensor (215), and a cover. The pump is in fluid communication with the urine collection container and is configured to pull a vacuum on the interior region of the urine collection container effective to draw urine from the urine collection device through the first conduit into the urine collection container. The sensor is secured to the container and is configured to detect a property relating at least to a volume of the urine in the urine collection container. The cover is sized and dimensioned to hold at least the pump therein and obscure at least the pump from view outside the cover.

Abstract: In an example, a urine collection device includes a covering defining a recessed receptacle and a fluid collection assembly positioned in the recessed receptacle. The fluid collection assembly includes (i) a foam sleeve including a bore, (ii) a shape retaining element positioned in the bore of the foam sleeve and defining a passage, and (iii) a tube extending through the passage defined by the shape retaining element. The shape retaining element can conform the fluid collection assembly to a curved configuration and maintain the curved configuration of the fluid collection assembly until the curved configuration is adjusted. The urine collection further includes a top sheet coupled to the covering. The top sheet and the covering define an internal chamber of the urine collection device. The top sheet is configured to draw urine into the internal chamber and toward the fluid collection assembly.

Abstract: The invention is generally a dental appliance that, in exemplary embodiments, includes a mouthpiece equipped with a tongue-securing mechanism. The dental appliance helps keep a user's airway unobstructed by securing a tip portion of the tongue slightly forward relative to the mouth so that the tongue is held from falling back into the throat. This invention helps alleviate problems including severe snoring and sleep apnea, which are typically caused by the tongue obstructing the airway at the throat, thus impeding respiration during sleep or when unconscious. In an exemplary embodiment, the dental appliance comprises a mouthpiece which is configured to circumscribe a tongue retaining mechanism, or tongue sleeve, that secures a user's tongue in place.

Abstract: One aspect of the present disclosure relates to an oropharynx appliance that includes passive tongue retention structure having an end portion adapted to prevent a pharyngeal portion of a tongue of a subject from collapsing; and at least one anchoring structure that is connected to the passive tongue retention structure and adapted to secure the passive tongue retention structure to at least one tooth/mandible of the subject in a removable fashion. The passive tongue retention structure is sized and dimensioned so that the end portion prevents the posterior pharyngeal portion of the tongue from obstructing an oropharynx during sleep, without triggering a gag reflex, while still permitting the tongue to move during swallowing.

Abstract: An apparatus and method for enhancing physiological thermoregulation, the apparatus including a housing configured to contact a glabrous area of a user, wherein the housing includes a cooling element; and a plurality of sensors configured to generate a biometric datum; at least a processor communicatively connected to the plurality of sensors; and a memory communicatively connected to the at least processor, the memory containing instructions configuring the at least processor to receive the biometric datum from the plurality of sensors; and control the cooling element as a function of the biometric datum.

Abstract: A system for cooling a head of a user to mitigate or prevent drug-induced hair-loss, including a hat, which includes an exterior layer, an interior layer, with an inflatable chamber therebetween, the inflatable chamber being functionally associated with an inflation pump. The hat includes a cooling assembly, reversibly attachable to the interior layer and including a housing defining pockets having cooling pads therein. Each cooling pad comprising a phase-changing-material adapted to obtain a temperature lower than ?20° C. and to retain that temperature. A sensor is adapted to sense an environmental condition within the hat. A controller is adapted to receive input from the sensor, and to provide a notification when the sensed environmental condition is outside of a specific range. When the hat is donned by the user, the inflatable chamber is inflated sufficiently to ensure that the cooling assembly engages the scalp of the user.

Abstract: A process and related assemblies for delivering slush through a tube towards a patient. Obtaining an elongated container partially filled with slush with a port end that has a first port and a second port. Placing the first port in fluid communication with tubing for delivery of slush towards the patient. Placing the second port in fluid communication with a source of gas which may be air. Subjecting the elongated container to automated repetitive movements so that the slush in the partially filled elongated container moves against interior surfaces within the elongated container. Ideally, two different forms of repetitive motion are used to impose complex movement upon the slush within the elongated container. Applying a pressure gradient to cause slush to flow out of the first port towards the patient. The elongated container may be made from a slush bottle with a reversibly engaged cap with the two ports.

Abstract: Systems and methods are provided for applying a drop of a therapeutic to an eye of a user. Reflected light from the eye of the user is measured at a sensor to provide a time series of intensity values. It is determined from the time series of intensity values if the eye has blinked. The drop of the therapeutic is released in response to a determination that the eye has blinked.

Abstract: Systems and methods are provided for determining a likelihood that a drop released from a bottle will land in an eye of a user. Each of an eye of a user and a tip of a bottle and illuminated and imaged to provide at least one image. An orientation of the bottle is determined via an inertial measurement unit, and a likelihood that a drop released from the bottle will land in the eye of the user is determined from the determined orientation and the at least one image.

Abstract: An integrated surgical system for accessing one of a plurality of target volumes of ocular tissue in an eye includes a first optical transmission subsystem optically coupled to receive a first light beam, an optics assembly, and a control system. The optics assembly has an optical axis and is configured to couple to the eye to align its optical axis with the optical axis of the eye. The optics assembly is optically coupled with the first optical transmission subsystem to receive the first light beam along one of a plurality of first input axes and to direct the first light beam to a corresponding one of a plurality of first output axes aligned with a corresponding one of the plurality of target volumes of ocular tissue in the eye. The control system is configured to control the first optical transmission subsystem to direct the first light beam into alignment with a select one of the plurality of first input axes.

Abstract: A laser system for treating target tissue layers of an anterior chamber angle of an eye, including a delivery system and various imaging systems is being disclosed here. The system includes novel configurations using small digital cameras, OCT and other diagnostic devices that are integrated with a goniolens to visualize and target the to be treated tissue layers and that in some configurations remain connected and active during the laser treatment. Furthermore, several novel illumination systems and standalone digital camera goniolens systems are being presented here.

Abstract: A method for altering an eye color of a patient with a color alteration procedure is disclosed that may include determining a laser power to deliver to stromal pigment in an iris of the eye of the patient by at least retrieving a set of laser criteria for delivery of an exposure less than 100 times a maximum permissible exposure that causes elimination of at least a portion of the stromal pigment. A laser system may be set to deliver laser light at the laser power which is less than the set of laser criteria and the laser light may be delivered with the laser system.

Abstract: A method of treating an eye includes delivering an OCT beam along an OCT optical path that enters a first optical subsystem along an input axis, and exits the first optical subsystem along an output axis that: 1) is substantially parallel to the optical axis of the eye, 2) is radially offset from the optical axis, and 3) extends through the cornea and into a portion of the irido-corneal angle at a point along a circumferential angle of the eye. The method also includes imaging the portion of the irido-corneal angle with the OCT beam; delivering a laser beam along an angled optical path that extends through the first optical subsystem, through the cornea, through the anterior chamber, and into a target volume of ocular tissue in the portion of the irido-corneal angle; and photodisrupting at least a portion of the target volume of ocular tissue with the laser beam.

Abstract: Embodiments disclosed herein relate to moldable decorative splint materials and associated methods of manufacture. The splint material may include a plurality of decorative elements integrated with the splint material. The decorative elements may be interconnected within a network of flexible connectors via a plurality of supports. Each support of the plurality of supports may include a retaining edge that retains the decorative element within the support.

Abstract: A non-adhesive single wrap bandage with replaceable gauze for the wound area secured by expandable strip bandage with reusable bandage end coupling is disclosed. The non-skin adhesive skin bandage body has an array of perforations for skin aeration, risers, quick release gauze pads and mating end tabs for ease of bandage re-use.

Abstract: Disclosed is a liquid removal drypad and liquid removal system suitable for absorbing and removing liquid produced by an individual. The drypad can include one or more perforated conduits arranged with an absorbent material. A source of reduced pressure can be connected to the one or more perforated conduits to remove liquid from the drypad. The drypad can be positioned under a patient and liquid produced by the individual can be removed by applying reduced pressure to the drypad. The drypad can be made by combining one or more conduits with an absorbent material.

Abstract: Embodiments described herein relate to apparatuses, systems, and methods for the treatment of wounds, for example using multiple wound dressings in combination with negative pressure wound therapy. A negative pressure would therapy apparatus can include a negative pressure source and a controller. The negative pressure source can include inlets configured to couple via fluid flow paths to wound dressings. The fluid flow paths can include pressure sensors configured to measure pressure in the fluid flow paths. The pressure sensors can include a first pressure sensor configured to measure pressure in the first fluid flow path and a second pressure sensor configured to measure pressure in the second fluid flow path. The controller can be configured to operate the negative pressure source and provide, based on measured pressure, indication of at least one operating condition associated with at least one of the fluid flow paths.

Abstract: A chip sleeve garment including an outer layer of fabric connected to an inner layer of fabric to form a sleeve with a space between the outer layer of fabric and the inner layer of fabric. Foam chips, flat foam, or foam with ridges are disposed in the space between the outer layer of fabric and the inner layer of fabric. The garment includes two ends, including at least one open end, and a notch in at least one open end having an opening. The notch can be separated to create a larger opening than the opening to allow the garment to be donned or doffed easier than the opening allows. A second garment can be disposed over the chip sleeve garment. Either the chip sleeve garment, the second garment, or both can be compression garments.

Abstract: The present disclosure provides generally for a therapeutic recovery device for medical rehabilitation. The therapeutic recovery device may comprise a compression device. The compression device may provide compressive force that provides relief. The therapeutic recovery device may comprise at least one securing mechanism. When the therapeutic recovery device comprises at least one sensor, the at least one sensor may provide feedback on the user's health. The therapeutic recovery device may comprise one or more straps. The one or more straps may allow the therapeutic recovery device to be secured in a plurality of orientations. The therapeutic recovery device may comprise at least one holder. When the therapeutic recovery device comprises at least one holder, the holder may comprise one or more pockets. The therapeutic recovery device may interface with at least one external device. The therapeutic recovery device may comprise a cover.

Abstract: A method and device for accurately, rapidly and consistently cutting an opening in drape material for negative pressure wound therapy (NPWT) uses a cutting device that includes a cutting member that can extend from a bottom surface of the cutting device. A cover may fit over the bottom to protect the cutting member. The cutting member may be positioned to define a cut-out shape having dimensions designed for use with a NPWT system. An adhesive material may be formed on the bottom surface of the cutting device, inside of the cut-out shape defined by the cutting members. In use, the user presses the cutting tool onto the drape to cause the cutting member to cut into the drape and the adhesive to stick to the drape. When the user lifts the device, the drape, cut to the correct size and shape, is removed from the foam dressing covering the wound.

Abstract: An arrangement (4) for detecting liquid in a single-use hygiene article. The arrangement (4) includes a back sheet film (1) with a conductive print (2).

Abstract: An absorbent article (10, 110) can include a waist containment member (54) with a first longitudinal side edge (72), a second longitudinal side edge (74), a proximal portion (76), an intermediate portion (77), and a distal portion (78). The proximal portion (76) can be coupled to the chassis (11) of the absorbent article (10, 110). The intermediate portion (77) can be free to move independent of the proximal portion (76) and the distal portion (78) and free to move independent of the body facing surface (19) of the chassis (11) to provide a containment pocket (82) for containing body exudates. The distal portion (78) can be disposed underneath the intermediate portion (77) when the absorbent article (10, 110) is in the stretched, laid-flat configuration. The waist containment member (54) can also include a first lateral tack-down region (83a) and a second lateral tack-down region (83b).

Abstract: A method for making an absorbent structure for use in a disposable absorbent article is provided. The method involves the steps of providing a first moving surface having an absorbent layer-forming reservoir, providing a supply of absorbent material, and depositing a portion of the supply of absorbent material into the absorbent layer-forming reservoir. The method further involves associating the portion of the supply of absorbent material with a first substrate layer and/or a second substrate layer to define an absorbent structure having a channel therein corresponding to the one or more raised strips, and bonding the first substrate layer to the second substrate layer through the channel. The channel is substantially free of the absorbent material.

Abstract: One or more clips to be hooked to an item (e.g., belt) and enable a bandage wrapped around an inguinal wound to be secured thereto. The clip(s) act as tie-down point(s) for the bandage to provide most efficient pressure to the wound. The clips include a waist securing member and a bandage retention member. The waist securing member includes first and second legs secured together along a first side (e.g., top) of clip by a first connection piece. A first space is defined between adjacent sides of first and second legs having a first opening along a second side (e.g., bottom) of clip. The bandage retention member includes second and third legs secured together along the second side of the clip by a second connection piece. A second space is defined between adjacent sides of second and third legs having a second opening along the first side of clip.

Abstract: Ambulance having a chassis (210) that can move by itself and a self-supporting superstructure (100) including the patient compartment (110). A coupling structure (300) driven by an electric actuator is provided between the top (231) of the rear part (230) of the chassis (210) and the bottom (101) of the superstructure (100), and having two states. In fixed state the coupling structure (300) is arranged within the space with a given vertical height (h) between the top (231) of the rear part (230) of the chassis (210) and the bottom (101) of the superstructure (100). In fixed state the superstructure (100) is secured to the chassis (210), while in unfixed state the superstructure (100) can be lifted freely from the chassis (210) in a vertical direction with an external device.

Abstract: A vehicle door assembly in a vehicle having a body-in-white, the body-in-white having a rear wheel well, the vehicle door assembly comprising a door frame, the door frame having an aperture therein, the frame extending into the rear wheel-well.

Abstract: An embodiment is a ramp apparatus for a vehicle, the ramp apparatus including a housing mounted on a vehicle body, a ramp assembly configured to move between a stowed position in which the ramp assembly is stowed in the housing and an extended position in which the ramp assembly is extended out from the housing, wherein the ramp assembly is configured to be moved telescopically to be extended and retracted. The ramp apparatus may further include a hinge mechanism configured to allow the ramp assembly to pivot when the ramp assembly is deployed from the housing, wherein the hinge mechanism includes a moving body connected to the ramp assembly through a hinge shaft, and a hinge drive unit mounted on the moving body.

Abstract: A ramp assembly includes a guide rail at least partially disposed in a void space between ramp platform edge guards, above a ramp platform, and below a ramp cover to reduce the overall height/thickness of the ramp assembly as compared to prior art ramp assemblies that locate guide rails below the ramp platform. A transition flap assembly provides lateral guidance for the ramp platform and carriage assembly. The transition flap assembly and ramp platform assembly engage to ensure at least approximate contact between the transition flap and ramp platform when the ramp platform is deployed and to maintain a spaced relationship between the two when the ramp platform is between the deployed and stowed positions. A sliding door track is configured to provide structural reinforcement to a track pan area of a floor. The guide rail may include an enhanced end stop to decelerate the ramp platform over a distance.

Abstract: A wheelchair is provided. First supports for supporting a user of the wheelchair are unevenly disposed to form a perimeter, and second supports for supporting the user of the wheelchair are unevenly disposed at least partially within the perimeter of the first supports. The first supports support the user when the first supports are in a raised position and the second supports are in a lowered position. The second supports support the user when the second supports are in a raised position and the first supports are in a lowered position. A alternation of supporting the user with the first supports or the second supports facilitates reduction of pressure sores of the user. In various embodiments, multiple groups of supports are used, the supports contour to a user's anatomy and/or the supports are pneumatic.

Abstract: A patient support apparatus, such as a bed, recliner, cot, stretcher, operating table, or the like, includes battery-powered circuitry whose functions are reduced, but not eliminated, as the battery charge level falls below a threshold. Electrical power may be cut off to one or more components of the battery-powered circuitry while still providing battery-supplied electrical power to the other components of the circuitry. A user interface provides battery status data, including a replacement status of a rechargeable battery, and allows a user to select different formats for displaying battery status data. Such formats include displays of battery charge level information not only in manners specific to the battery, but also in manners relative to the patient support apparatus, such as displays of how many, or how much of, one or more functions the patient support apparatus is able to perform based on the battery's current charge level.

Abstract: A patient support apparatus, such as a hospital bed, includes an alert light assembly or an alert light module having separate zones that are individually illuminated to convey information regarding respective alert conditions. The zones each have indicia related to a particular condition of the patient support apparatus. The illuminated zones are each sufficiently large so as to be seen from afar, such as on the order of ten feet or more. Alternatively or additionally, a GUI of the patient support apparatus displays alert indicia as part of a screen saver. Further alternatively or additionally, the patient support apparatus illuminates an alert light in a manner indicating an optimal time for taking a patient's vital signs.