Abstract: Effective delivery of an insecticide to a growing plant can sometimes be problematic. Topical delivery of an insecticide at the post-emergence stage of growth can sometimes be ineffective. It can also be difficult to deliver an insecticide to the roots of a growing plant, such as to combat a subsurface insect infestation. Accordingly, soil blends having insecticidal activity can comprise a soil medium, a porous soil additive, and an insecticide dispersed within the soil medium. Such soil blends may be used in conjunction with cultivating a variety of plants. Methods for producing the soil blends can comprise providing a soil medium and a porous soil additive, and dispersing the porous soil additive and an insecticide within the soil medium.

Abstract: The present disclosure discloses compositions comprising a hyaluronidase, devices comprising such compositions, as well as methods and uses employing such compositions and devices to reduce or eliminate a hyaluronic acid-induced blockage of one or more blood vessels supplying an eye of an individual; methods and uses for employing such compositions and devices to reduce or inhibit a vascular occlusion in an eye of an individual; and methods and uses for employing such compositions and devices to reduce or inhibit a hyaluronic acid-induced loss of vision of an individual.

Abstract: A pedicle insulator implant is designed to protect the nerves and surrounding tissue from injury by pedicle screws or other surgical devices and instruments. In its basic structure, the implant has a thicker section and a thinner section, the thicker section providing protection for nerves and other sensitive tissues while the thinner section can be deformable and provides grip. In one variation of the basic structure, the thinner section possess a rough surface when it is desirable in situations to provide further grip of the assembly and prevent rotation during the insertion of, for example, a pedicle screw.

Abstract: A method for training a system for predicting a probability of occurrence of cardiac event is provided. The method includes obtaining sets of electrocardiograms of subjects, each set of electrocardiograms comprising at least one electrocardiogram each obtained, a) prior to and b) during or after an occurrence of a cardiac event, or both. The method includes extracting a first approximation of a time series data. The method also includes obtaining electrocardiograph signals that produced the electrocardiograms. The method also includes creating a training dataset from the extracted time series signals and the electrocardiograph signals for training a first and a second approximation of an electrocardiogram for representing an electrocardiograph signal that produced the electrocardiogram. The method further includes training a second model for extracting a cardiac marker from the second approximation of the electrocardiogram of the subject and calculating a probability of occurrence of a cardiac event.

Abstract: A urinary incontinence prevention clip for men includes: a clip body having an upper frame positioned so as to correspond to the upper part of male genitalia, a lower frame positioned so as to correspond to the lower part of the male genitalia, and a connection part connected to one side of the upper frame and the lower frame and providing elastic force in a direction, in which the upper frame and the lower frame are spread; cushion parts respectively provided on the inside of the upper frame and the inside of the lower frame; and locking parts formed at both ends of the clip body so as to be fastened to each other, wherein the upper frame is formed so as not to press the blood vessels of the male genitalia and the lower frame is formed so as to press the urethras of the male genitalia.

Abstract: Disclosed is an atrial appendage clip delivery system, which includes a handle shell, a push rod, a connection pipe and a support base; a passage is provided in the handle shell along a length direction; one end of the push rod is slidably disposed in the passage; the support base is provided with a mounting window for mounting an atrial appendage clip; the atrial appendage clip includes a first clip arm and a second clip arm capable of opening in parallel or closing; the handle shell, the connection pipe and the support base are sequentially connected and communicate; the first clip arm or the second clip arm is fixedly connected with an upper side or a lower side of the mounting window; the second clip arm or the first clip arm is movably connected with the lower side or the upper side of the mounting window.

Abstract: An automatically locking safety device, e.g., for use in a blood collection procedure, can include a housing, first and second needle covers that are at least partly received in the housing, and a needle that is at least partly received in at least one of the first and second needle covers. The needle can include a proximal tip configured for placement into a patient and a distal tip configured for placement into a blood collection vial. In some embodiments, the first and second needle covers are biased by a biasing member. In some cases, one or both of the first and second needle covers can be locked to prevent axial movement thereof after the blood collection procedure. In certain embodiments, a distal end of the device is configured to connect with a medical connector, such as a needleless IV access device.

Abstract: A self-contained re-humidification mask that can be supported in an operative position on a user is provided. The mask has a wall shaped as a moulded domed mask configured to cover the face of a user from the nose to the chin. An endless peripheral edge is shaped and configured to generally anatomically follow the contours of a face of a user to define, with the face of a user, an air pocket. The mask has a single inlet-outlet aperture located generally opposite a position occupied in use by a mouth of a user, and at least one re-humidification assembly located in the inlet-outlet aperture such that it substantially fills the aperture. The re-humidification assembly includes a coil of corrugated hygroscopic paper having an axis of the coil extending in the direction of fluid flow through the inlet-outlet aperture. The re-humidification mask preferably has a wall formed from a non-woven synthetic fibre sheet that is press moulded and heat set to the domed shape.

Abstract: An electrical feedthrough assembly for an implantable medical device includes an outer ferrule of metallic material having an outer surface hermetically sealed to an implantable device housing. There is an inner feedthrough assembly which is hermetically sealed within the ferrule and which has a structure of sintered layers that include: i. an electrical insulator of ceramic insulator material, ii. one or more electrically conductive vias of metallized conductive material embedded within and extending through the electrical insulator, and iii. a transition interface region around each of the conductive vias comprising a gradient mixture of the ceramic insulator material and the metallized conductive material forming a gradual transition and a mechanical bond between the electrical insulator and the conductive via.

Abstract: A retractor system for use in medical procedures is connectable to a head fixation device. The retractor system includes a support assembly and an accessory that is mountable thereto. The support assembly is coupled with the head fixation device such that a position of the support assembly is adjustable relative to the head fixation device. The support assembly includes an upright support and a rod having a non-circular profile. The support assembly and rod are selectively and adjustably coupled to one another via a coupling assembly. The coupling assembly includes a pair of resilient members having contacting and non-contacting surfaces within bores of the resilient members. The accessory and rod are selectively and adjustably coupled to one another via another coupling assembly that comprises locking features operable to selectively engage and disengage the accessory with the rod.

Abstract: A single-use cover assembly that obscures a substantial majority or an entirety of an injection needle from view before, during, and after an injection procedure. The cover assembly includes a housing and a needle sleeve that retracts and extends by sliding axially within the housing. The needle sleeve carries a locking collar that moves from a first position to a second position once the needle sleeve is fully retracted. In the first position the locking collar allows retraction of the needle sleeve from a fully extended position. In the second position, a portion of the locking collar covers a tip of the needle, thereby preventing retraction of the needle sleeve from the fully extended position.

Abstract: A system and method for sealing openings in a body of a patient made by a medical procedure or non-medical event. The opening may be formed in soft tissue, internal organs, or hard tissue. A coaxial needle is inserted into a patient and a coagulating agent is inserted into the patient via the coaxial needle. The coagulating agent is discharged adjacent to the opening and the coaxial needle is inserted to a surgical depth. Following the procedure, the coaxial needle is retracted to a plug discharging depth. A bioabsorbable plug in at least a partially dehydrated state is then discharged from the coaxial needle and the coaxial needle is removed. The plug resides at least partially within the opening in the organ or tissue created by the coaxial needle. The combination of the coagulating agent and the expandable plug seals the opening created by the coaxial needle.

Abstract: Disclosed is an automated liquid-phase immunoassay apparatus used with a cuvette having a plurality of chambers containing a reagent necessary for detection of an analyte in a biological specimen. The apparatus includes a movable cuvette module equipped with the cuvette, an optical reading module for optical assaying of a material resulting from a reaction between the specimen and the reagent, and a dispenser module which is positioned on the cuvette module and which dispenses the specimen and the reagent to the plurality of chambers of the cuvette and washes the specimen and the reagent therefrom.

Abstract: Biomarkers of pancreatic cancer are described, as well as methods using these compounds for detecting pancreatic cancer. The methods can be used to diagnose a patient's health state, or change in health state, or for diagnosing risk of developing or the presence of pancreatic cancer. The method comprises analyzing a sample from a patient to obtain quantifying data for one or more than one of the metabolite markers; comparing the quantifying data to corresponding data obtained for one or more than one reference sample to identify abnormalities in the level of the metabolite marker(s) in the sample; and making a diagnosis if an abnormality is observed. Standards and kits for carrying out the method are also described.

Abstract: A fitting system is described for fitting electrode contacts of cochlear implant electrode array implanted in a cochlea of an implanted patient. A test stimulation generator delivers to at least one of the electrode contacts a test stimulation sequence at a variable charge level and a variable stimulation rate over time, wherein the charge level and stimulation rate are inversely related as a function of a defined loudness percept by the implanted patient to the test stimulation sequence. A response measurement module obtains objective response measurements of auditory neural tissues of the implanted patient that are affected by the test stimulation sequence. A fit mapping module defines a patient-specific fit map for the electrode contacts of cochlear implant electrode array based on the objective response measurements.

Abstract: An abdominal closure method and device is disclosed where the device generally includes a first tissue securement member configured for securement to a first tissue region and a second tissue securement member configured for securement to a second tissue region. The first and second tissue securement members are coupled to the connecting member and the connecting member is positionable at a distance from the first and second tissue regions. Additionally, one or more biasing elements may be connected to the first and second tissue securement members to approximate the first and second tissue regions towards one another via respective securement members.

Abstract: A gear-driven infusion assembly is provided which has a housing, a gear assembly coupled to the housing, a shuttle assembly slidably coupled to the housing and operably coupled to the gear assembly, and a tube enclosure connected to the housing. The tube enclosure is configured to house a primary drug closure. The gear assembly includes a spool assembly having a pinion gear and a drive spool. When the spring rotates the drive spool, the drive spool drives the pinion gear, and the gear assembly drives the shuttle assembly. When the gear assembly drives the shuttle assembly, the shuttle assembly slides longitudinally along the housing. The gear assembly may be spring driven such that a spring rotates the pinion gear about the drive spool. The primary drug closure may be a syringe. An overspeed protection device is also provided which has a spool assembly including a drive spool having a plurality of cams, a spring, and a pinion gear with spiral cam surfaces.