University of Utah Research Foundation

Catheter Connections, Inc.

Merit Medical Systems, Inc.

Illinois Tool Works Inc.

Sorenson Medical, Inc.

Robert W Hitchcock

F Mark Ferguson

Donald D Solomon

Steven Bandis

Michael Wallace Howlett

James Victor Mercer

Mahender Avula

Frank B Sachse

Tracy Kucaba

Dana Pulvino

Erik Noble Kubiak

Nathan J Knighton

James Paul Kennedy

Kylee North

Chao Huang

Richard Paul Jenkins

Kenneth Sykes

Nassir F Marrouche

Richard Lasher

Mark L Adams

Tomasz J Petelenz

James L Sorenson

Christopher Thomas Schaafsma

Emmon Johnny Chen

Jacob Joseph Hanson

Zachary John Collins

John H Bridge

Donald R Solomon

Aditya K Kaza

Sam Peterson

Mark Ferguson

Mark F Ferguson

Disclosed are devices, systems, and methods for characterizing tissue using light scattering spectroscopy. A tissue characterization probe includes an elongate member having a proximal end and a plurality of distal probe tips at a distal end. A plurality of illumination fibers extend through the elongate member to the distal probe tips such that each distal probe tip includes at least one illumination fiber. A plurality of detection fibers also extend through the elongate member such that each probe tip includes at least one detection fiber. The disclosed devices and systems beneficially enable characterization of tissues within depths greater than 100 μm. The disclosed devices and systems also enable effective characterization of anisotropic tissues, such as cardiac myocardium.

Cardiac tissue characterization using catheterized light scattering spectroscopy

Medical devices including a cap for a medical connector are disclosed. In some embodiments, the cap comprises a disinfectant, such as an antiseptic fluid and an insert configured to seal or partially seal the medical connector as it is engaged with the cap. In some embodiments the cap insert has a segment which is deformable under axially applied pressure as an end-user attaches the cap to the medical connector. In some embodiments this insert is configured to improve the exposure of antiseptic to the outer surface of the medical connector while minimizing exposure of the antiseptic inside the medical connector open lumen.

Disinfecting luer cap and method of use

The present disclosure relates to systems and methods for generating three-dimensional tissue maps, and particularly fibrosis maps of cardiac tissue. An intravascular device includes an elongated member and a distal tip. An imaging assembly is integrated with the elongated member to enable imaging of the microstructure of tissue near the distal tip. One or more navigation electrodes are positioned at or near the distal tip. Electrical mapping and/or ablation assemblies may also be integrated with the device. Images may be characterized according to a level of fibrosis and, using the corresponding determined locations of the images, a three-dimensional map showing areas of differential fibrosis may be generated. Electrical mapping data may also be integrated with the fibrosis map to generate a composite fibrosis and voltage map.

Devices and methods for mapping cardiac tissue

A disinfecting cap accepts a needleless injection site to apply an antiseptic agent. The cap includes a breakable seal located in a chamber between the proximal and distal portions so as to be spaced away from the opening. The cap body may include a compliant wall that deforms when a needleless injection site is inserted into the opening to removably hold the cap on the needleless injection site. In lieu of a compliant wall, a flexible skirt may extend from the cap body into the proximal portion, so that when a needleless injection site is inserted into the opening, the flexible skirt engages the outer diameter of the needleless injection site to removably hold the cap on the needleless injection site. A carrier strip may be used, wherein each of the plurality of disinfecting caps is removably attached at its proximal end to the carrier strip.

Disinfecting cap for medical connectors

A catheter for imaging and treating a selected tissue and method of use is provided. Imaging, and treatment assemblies may be co-located at a distal end of a single catheter. The imaging assembly may include at least a portion of a confocal microscope. The treatment assembly may include at least a portion of the imaging assembly. A method of treating a selected tissue is also provided. The method may be performed using a single catheter. The imaging and treatment steps of the method may be performed simultaneously.

Devices, systems, and methods for imaging and treating a selected tissue

Systems, devices, and methods for providing user feedback regarding compliance with a set of partial weight bearing (PWB) criteria are described. A computer system receives force data from a non-compressible force transmitter that is assigned to a user, and accesses the force data received from the non-compressible force transmitter to determine whether the user is within a predefined pressure compliance range. The pressure compliance range specifies a prescribed range of pressure that is to be applied during a PWB period. The computer system then receives a compliance data request from the user or the user's physician and communicates compliance data representing the user's compliance with the prescribed range of pressure during the PWB period to the user and/or the user's physician.

Systems, devices, and methods for providing foot loading feedback to patients and physicians during a period of partial weight bearing

A male-disinfecting cap is configured to couple with and apply an antiseptic agent to medical male luer-lock connector of the type including a post having a lumen. The cap includes a receiving portion which defines a chamber. The post of the male luer-lock connector is received into a single opening of the chamber. The receiving portion is configured to fit within the skirt of the male luer-lock connector when the post is received into the receiving portion. At least one vent is defined on the internal surface of the receiving portion and extends from the opening into the chamber, where an antiseptic is disposed. Protrusions on the external surface of the receiving portion engage helical threads of the internally helically threaded skirt. The male-disinfecting cap also includes a seal that prevents evaporation of the antiseptic agent in the chamber prior to use.

Disinfecting cap for male luers

Some assemblies can include a male cap and a female cap, each of which can be used to cover separated medical connectors. In certain arrangements, a male cap can include a movable carriage that transitions from a retracted position when an assembly with which the male cap is associated is in a closed state to an extended position when the assembly is in an open state.

Disinfecting caps having an extendable feature

A system and method for fluorescence imaging of tissue in vivo and in situ, e.g., for minimally invasive diagnosis of patients. A fluorescent imaging system is provided that has a dye carrier coupled to the distal end of a probe containing a fiber optics bundle, which allows for the introduction of at least one fluorescent dye therein the dye carrier into a portion of the tissue of interest of a subject or patient when the dye carrier is selectively brought into contact with the portion of the tissue of interest. The resulting fluorescence images permit the acquisition of diagnostic information on the progression of diseases at cellular/tissue level in patients.

Devices and systems for fluorescence imaging of tissue

Disclosed herein are disinfecting caps that can be used to cover and disinfect both a male medical connector and needleless injection site when not in use or when disconnected from each other. The caps contain a disinfecting agent.

Disinfecting caps for medical male luer connectors

Assembly of medical connector caps

Systems and methods for producing scaffolds are disclosed. The system includes a polymer solution and a non-solvent, which are sprayed into receiving portions of support elements. After scaffolds are formed on the support elements, the support elements permit elongation of the scaffolds. Composites formed from a plurality of scaffolds are also disclosed.

Phase separation sprayed scaffold

Capping system for use with one or more medical connectors

Growing community of inventors

Sandy, UT, United States of America

Robert W Hitchcock