384 results about "Catheter insertion" patented technology

A method of inserting a catheter into a vasculature of a patient can include disposing the catheter into a housing. The housing can include a blood flash indicator, having a syringe plunger fixed to the housing and a syringe barrel slidable relative to the syringe plunger. The method can further include positioning the housing adjacent the vasculature, inserting a needle into the housing and through a lumen of the catheter until a distal tip of the needle extends from a distal end of the catheter, and accessing the vasculature via the distal tip of the needle. The method can further include sliding the syringe barrel in a proximal direction relative to the syringe plunger to create a vacuum in a lumen of the needle to thereby draw blood through the lumen of the needle and into the syringe barrel.

Intermittent catheters in simple-to-use assemblies or systems thereof facilitate cleanliness before and after use. In an example, an intermittent-catheter system can include an intermittent catheter and packaging enclosing the intermittent catheter therein to maintain sterility of the intermittent catheter in an unused state of the intermittent-catheter system. The packaging can include a flexible packaging body and a packaging cover. The packaging body can be configured to hold a catheter tube of the intermittent catheter therein. The packaging cover can be configured to reveal a funnel of the intermittent catheter when an uncovering operation is performed. The uncovering operation can reveal an adhesive patch on either the packaging body or the packaging cover for adhering the packaging to a vertical surface for removal of the intermittent catheter from the packaging for catheterization. The packaging can be further configured for resealing the intermittent catheter therein subsequent to the catheterization.

Methods of treating a central airway obstruction (CAO), benign airway stenosis, asthma, chronic obstructive pulmonary disease (COPD), or an airway tumor in a human subject, methods of treating chronic rhinosinusitis (CRS) or chronic rhinosinusitis with nasal polyps (CRSwNP) in a human subject, methods of treating a eustachian tube disorder in a human subject, and devices and systems for performing the methods. A method of treating a central airway obstruction (CAO), benign airway stenosis, asthma, chronic obstructive pulmonary disease (COPD), or an airway tumor in a human subject includes inserting a drug-coated balloon catheter into a target site in a trachea, mainstem bronchus, bronchus intermedius, lobar bronchus, segmental bronchus, or sub-segmental bronchus, wherein the balloon is coated with a coating layer including the therapeutic agent and one or more additives. The therapeutic agent includes paclitaxel, sirolimus, or a derivative thereof. The method includes inflating the balloon to dilate the airway and deliver a therapeutic agent to the airway wall. The method includes deflating the balloon. The method also includes withdrawing the balloon catheter from the target site.

Disclosed herein is a urinary catheter generally configured for self-deployment. The catheter includes a closed volume within the lumen of the catheter containing a lubricant. The proximal end and the distal end of the catheter tube are coupled with a handling member disposed along the catheter tube to define a compact packaging shape of the catheter tube including one or more loops. The closed volume is breached by separating the proximal and distal ends away from the handling member in a single step via simultaneous application of separating forces to the proximal and distal ends. The handling member includes a pull ring for applying an oppositely directed separating force to the handling member. The catheter includes an inlet section configured of insertion into the patient and an inlet collar is slidably coupled with the inlet section. where in the inlet collar serves as a guide during insertion of the catheter.

The invention discloses a real-time monitoring method and device for a cyclopharyngeal muscle catheter balloon dilatation, and the method comprises the steps: constructing a to-be-detected field domain model of the cyclopharyngeal muscle, and carrying out the finite element analysis to solve a potential distribution and sensitive matrix; the method comprises the following steps: injecting multi-frequency sine excitation current into a to-be-measured field domain of the cyclopharynx muscle catheter balloon dilatation, collecting boundary response voltage, performing multi-frequency synchronous demodulation to obtain a voltage amplitude and a phase, and inverting a conductivity change value distribution diagram under various reference frequencies by combining a sensitive matrix; and in combination with the obtained result, performing at least one operation of determining a catheter insertion position and determining a balloon dilatation state so as to obtain a real-time monitoring result of at least one of the catheter insertion position and the balloon dilatation state, and outputting the real-time monitoring result of the at least one of the catheter insertion position and the balloon dilatation state. The invention aims to provide non-invasive, non-radiation, real-time and accurate monitoring for the catheter balloon of the peripharyngeal muscle catheter balloon dilatation, accurately measure the catheter insertion position and the balloon dilatation state, and improve the safety of the peripharyngeal muscle catheter balloon dilatation.

A robotic catheter system and methods for implementing corrective actions during use thereof. A method comprises: providing a catheter that has one or more bendable segments and a catheter tip, inserting the catheter into a bodily lumen and navigating the catheter through the lumen along an insertion trajectory while an actuation unit applies an actuation force to the one or more bendable segments; recording a navigation parameter in relation to the insertion trajectory while the catheter is moved through the lumen, displaying, on a display, a graphical representation of the navigation parameter relative to a threshold value indicative of a location along the insertion trajectory where a navigation error of the catheter can occur or has occurred; and outputting to the display an interactive user-guide showing one or more than one corrective actions that can be taken to correct and / or prevent the navigation error.

Disclosed herein are clot treatment systems including mechanical thrombectomy devices and clot treatment devices, and associated devices and methods. In some embodiments, a method of removing clot material from a blood vessel of patient includes inserting a catheter to proximate the clot material within the blood vessel while radially constraining a clot treatment device and an embolic protection device within the catheter. The method can further include moving the catheter proximally to deploy the clot treatment device at least partially distal to clot material within the blood vessel, and then moving the catheter further proximally to deploy the embolic protection device at least partially proximal to the clot material. The clot treatment device can include one or more relief features configured to release captured clot material if the force on the clot treatment device exceeds a threshold.

Disclosed herein is a catheter, which in some embodiments includes a distal section configured to enter a skin insertion site. The distal section can include a tapered junction having one or more dilation structures configured to dilate the skin insertion site. The distal section can further include a distal portion extending from a distal end of the tapered junction, the distal portion having a diameter smaller than a proximal portion of the catheter. In combination, the tapered junction, the one or more dilation structures, and the specific actions of the user urging the catheter into the insertion site can result in an improved fit of the catheter in the insertion site.

Disclosed herein are clot treatment systems including mechanical thrombectomy devices and clot treatment devices, and associated devices and methods. In some embodiments, a method of removing clot material from a blood vessel of patient includes inserting a catheter to proximate the clot material within the blood vessel while radially constraining a clot treatment device and an embolic protection device within the catheter. The method can further include moving the catheter proximally to deploy the clot treatment device at least partially distal to clot material within the blood vessel, and then moving the catheter further proximally to deploy the embolic protection device at least partially proximal to the clot material. The clot treatment device can include one or more relief features configured to release captured clot material if the force on the clot treatment device exceeds a threshold.

Disclosed herein are clot treatment systems including mechanical thrombectomy devices and clot treatment devices, and associated devices and methods. In some embodiments, a method of removing clot material from a blood vessel of patient includes inserting a catheter to proximate the clot material within the blood vessel while radially constraining a clot treatment device and an embolic protection device within the catheter. The method can further include moving the catheter proximally to deploy the clot treatment device at least partially distal to clot material within the blood vessel, and then moving the catheter further proximally to deploy the embolic protection device at least partially proximal to the clot material. The clot treatment device can include one or more relief features configured to release captured clot material if the force on the clot treatment device exceeds a threshold.

Intermittent catheters in simple-to-use assemblies or systems thereof facilitate cleanliness before and after use. For example, an intermittent-catheter system can include an intermittent catheter and packaging enclosing the intermittent catheter therein to maintain sterility of the intermittent catheter in an unused state of the intermittent-catheter system. The packaging can include a flexible packaging body and a packaging cover. The packaging body can be configured to hold a catheter tube of the intermittent catheter therein. The packaging cover can be configured to reveal a funnel of the intermittent catheter when an uncovering operation is performed. The uncovering operation can reveal an adhesive patch on either the packaging body or the packaging cover for adhering the packaging to a vertical surface for removal of the intermittent catheter from the packaging for catheterization. The packaging can be further configured for resealing the intermittent catheter therein subsequent to the catheterization.

Apparatus and methods for deactivating bronchial nerves and ablating smooth muscle extending along a bronchial branch of a mammalian subject to treat asthma and related conditions. An ultrasonic transducer (11) is inserted into the bronchus as, for example, by advancing the distal end of a catheter (10) bearing the transducer into the bronchial section to be treated. The ultrasonic transducer emits ultrasound so as to heat tissues throughout a relatively large impact volume (13) to a temperature sufficient to inactivate nerve conduction and ablate smooth muscle but insufficient to cause rapid ablation or necrosis of the surrounding tissues. The treatment can be performed without locating or focusing on individual bronchial nerves or smooth muscle.

An intermittent catheter package including a plurality of components and a catheterization tray configured to facilitate a catheterization procedure. The plurality of components include a urinary catheter fluidly connected to a urine-drainage bag and a sampling-port access device configured to fluidly connect to a urine-sampling port of the urinary catheter or the urine-drainage bag for aseptic collection of one or more urine samples.The catheterization tray includes at least a first compartment, a second compartment, a third compartment, and a fourth compartment. The second compartment is connected to the third compartment Step-by-step surface instructions for performing the catheterization procedure are incorporated into the catheterization tray.

Techniques and technologies for vascular access devices are disclosed. A representative vascular access device includes an introducer having a shaft that includes a tip, a first aperture disposed proximate to the tip, a second aperture spaced apart from the tip, and an optical fiber disposed within the shaft that conveys light for emission from the first and second apertures. A catheter is disposed about the introducer and has a catheter distal end positioned between the first and second apertures. As the tip is advanced into the blood vessel, light emitted through the first aperture is diminished, indicating that the tip has entered the blood vessel. When light emitted through the second aperture is diminished, the practitioner knows that the catheter distal end has entered the blood vessel.

Catheter clips and catheter insertion assemblies including such catheter clips facilitate sterile catheterization technique, thereby reducing the risk of catheter-related bloodstream infections and increasing positive patient-centered outcomes. In an example, a catheter clip can include a pair of lever arms mated to each other. Each lever arm of the pair of lever arms can be bilaterally asymmetric but identical to the other lever arm of the pair of lever arms. An elastomeric band can be over a jaw end portion of the catheter clip. A catheter retainer can be coupled to a handle end portion of the catheter clip. The catheter retainer can be configured to hold a catheter connector of a catheter such that at least a proximal portion of the catheter remains in a sterile field when the catheter clip is clipped onto a sterile drape that establishes at least a portion of the sterile field.

A catheter insertion device is provided as an external applicator attachable to a medicine delivery device. The medicine delivery device has an internal module therein that comprises an insertion needle hub and needle, and a catheter hub and catheter. An external applicator comprises a drive and spring that drive a drive pin into the medicine delivery device to force the needle hub and catheter hub downward until the catheter hub locks in the downward position and the needle hub returns into the external applicator. An automatic release feature automatically disengaged the external applicator from the medicine delivery device when insertion is complete.

A method for accessing a blood vessel using a catheter insertion device. The catheter insertion device includes a housing, a needle, a catheter, a guidewire, and a thumbwheel. The thumbwheel is rotatably fastened at a front end of the housing and accessible through an opening in the housing. The guidewire is coupled to the thumbwheel such that an axis of rotation of the thumbwheel is perpendicular to the guidewire and rotation of the thumbwheel advances the guidewire through the lumen of the needle. The method includes preparing the catheter insertion device, inserting a tip of the needle and distal end of the catheter into a blood vessel, advancing the guidewire out of the lumen of the needle into the blood vessel by holding the housing and rotating the thumbwheel, furthering the distal end of the catheter over the guidewire, and removing the needle and the guidewire from the catheter.

A needle is provided that can be used for introducing or aspirating fluids to a patient or as an introducer needle for positioning and inserting a catheter, such as a peripheral IV catheter into a patient. The needle can be an introducer needle that extends from the distal end of the catheter during insertion. The needle has an insertion tip with a configuration to assist penetration into a vein with a reduced incidence of injuring the inner surface of the vein or inadvertently passing through side wall of the vein. The needle tip can be farmed with a curved distal end surface where the pointed tip is spaced radially inward relative to the outer surface of the needle. In another embodiment the needle tip can have a reverse beveled surface having an axial length, angle, and curvature to assist in penetrating the vein with a reduced incidence of transfixing the vein.

The present invention provides a catheter for treating occlusions in blood vessels. The catheter includes at least one electrode pair positioned inside of a flexible angioplasty balloon at the distal end of the catheter. In some designs, the electrode pairs are arranged in a low-profile or coplanar configuration, reducing the diameter of the distal end of the device and permitting treatment of tight and hard-to-cross occlusions. The flexible angioplasty balloon has an extremely low profile and does need to be folded before insertion of the catheter into the cardiovascular system. During treatment, the balloon can be expanded a relatively small amount sufficient to immerse the electrode pairs in a conductive fluid before generating shock waves across the electrodes to treat the occlusion. The balloon can be made of material having elastomeric properties such that it returns to its original low profile configuration when it is deflated following treatment.

A tool for inserting a catheter into a body of a patient is provided. The tool comprises: a housing in which at least a portion of the catheter is initially disposed; a needle distally extending from the housing, at least a portion of the catheter disposed over the needle; a guidewire initially disposed within the needle partially; and an advancement assembly for distally advancing the catheter. The housing comprises: a first portion comprising a distal part and a proximal part; and a second portion engaged with the first portion, wherein the distal part of the first portion is configured to be able to distally slide with respect to the second portion to release the engagement between the first portion and the second portion. The advancement assembly includes a safety cap which is initially disposed over the needle and is configured to be locked to the housing when distally sliding to a position of isolating the tip of the needle within the safety cap.

The present disclosure relates to a drainage catheter and methods of use for providing catheterization procedures, such as during a percutaneous nephrostomy. The drainage catheter includes a body including a first tube segment and a second tube segment connected to one another at a curved end portion to form a continuous body structure. An inner surface of the curved end portion includes one or more drainage openings extending therethrough, with an outer surface of the curved end portion free of drainage openings. The openings are in communication with a lumen that extends through the drainage catheter to provide a pathway for removing fluid from the kidney. The drainage catheter is inserted into the kidney via a first insertion site and exits via a second insertion site.

A delivery device is provided with an insertion device having a retraction spring configuration for automatic insertion needle retraction. A button of the insertion device is used to insert the insertion needle and catheter, and once the insertion needle are fully inserted, a rotating engagement releases the needle hub where the springs automatically retract the insertion needle. A catheter assembly includes a catheter hub, a septum and a catheter. The catheter hub has a fluid passage separate from the insertion needle to supply a fluid to the catheter. The fluid passage can extend through a distal end of the septum, through a side portion of the catheter hub and septum, or through a side portion of the catheter hub directly to a fluid chamber formed between the septum and a distal end of the catheter hub.

Apparatus and methods are described for treating an occlusion in a blood vessel. A catheter is inserted into the blood vessel. An irradiation unit is driven to emit probing radiation such that the probing radiation is directed toward the occlusion, and returning radiation which is returned in response to the probing radiation impacting the occlusion, is detected. A composition of at least a portion of the occlusion is derived based on a signature that is indicative of the composition within the returning radiation. The irradiation unit is driven to irradiate the portion of the occlusion by emitting treatment radiation having a set of irradiation parameters. The set of irradiation parameters is determined to modulate between a photoacoustic effect of the treatment radiation and a photothermal effect of the treatment radiation, based on the composition of the portion of the occlusion. Other applications are also described.

The invention discloses a blockage dredging device for a ureteral stent. The blockage dredging device is used for being inserted into the ureteral stent to achieve the blockage dredging effect. The invention belongs to the field of medical auxiliary instruments. Comprising a catheter which comprises a catheter wall and a catheter cavity defined by the catheter wall; the ultrasonic guide wire is provided with an output piece; the connecting piece is fixedly arranged at the end part of the conduit; the host is connected with the connecting piece; the detection head is fixedly arranged at the end, inserted into the human ureter, of the catheter; the suction assembly is used for sucking obstructions in the ureter; wherein a diaphragm is arranged in the tube cavity, so that a suction cavity is formed in the tube cavity; the ultrasonic guide wire is arranged in the tube cavity in a penetrating manner; the output part is used for generating high-frequency oscillation to emit ultrasonic waves to break the blockages; an ultrasonic transduction unit connected with the ultrasonic guide wire is arranged in the connecting piece; the detection head is electrically connected with the host so as to transmit an electric signal into the host. The device has the beneficial effects that the blockage condition in the ureteral stent is detected through the ultrasonic detection function, and blockage dredging is conducted through the ultrasonic principle.

Devices, systems, and methods for stabilizing medical tubing protruding from a patient. In various embodiments of the present disclosure, a medical tubing stabilization device is provided that may include a tube stabilization patch and a complementary medical garment. The tube stabilization patch may be applied to a patient who has medical tubing or a catheter protruding from their body to reduce or dampen movement on the body from the medical tubing in relation to the patient. The medical garment may be worn by the patient and placed in combination with the tube stabilization patch to further reduce the relative movement of the medical tubing. The present disclosure may be directed to reducing the level of medical tubing movement, both externally and internally, that a patient may experience, which decreases the risk of infection caused by catheterization of patients.

The present disclosure relates to a laryngoscope blade modification for endotracheal intubation. The disclosure provides a flexible channel attached to the laryngoscope blade or a rigid channel that opens via a spring system. The channel further incudes a slit along the entire portion of the channel, enabling a guidewire to be loaded into the channel and advanced to a patient's vocal cords and trachea before being dislodged or removed in a quick, efficient manner. An endotracheal tube is then slided over the guidewire into the vocal cords and trachea. Once endotracheal tube is inserted, guidewire is removed and intubation initiated. The present disclosure enables a faster insertion of a guidewire into the vocal cords over conventional methods without wasting precious seconds. By using a guidewire with a soft tip, the incidence of vocal cord injury decreases substantially and intubation performed successfully in a quick manner.

A device for inserting a catheter according to a disclosed embodiment comprises: a needle including a needle body extending in a first direction, a tip forming a distal end in the first direction, and a pair of edge portions which meet each other at an acute angle at the tip, have widths increasing in both directions perpendicular to the first direction toward a second direction opposite to the first direction, and form sharp edges so that the skin of a patient can be incised in the both directions; and a sheath having a guide hole extending in the first direction therein so that a catheter can be inserted, wherein the needle body is disposed through the guide hole so that the tip and the edge portions of the needle are positioned in the first direction of the guide hole, and the outer diameter of the distal end in the first direction is greater than the maximum width of the pair of edge portions in both directions.

An intermittent catheter package includes a lubricant container including a lubricant disposed therein, a urinary catheter coupled to a urine-drainage bag, and a catheterization tray including surface instructions for performing a catheterization procedure. The catheterization tray includes a first compartment containing the lubricant container and a second compartment containing the urinary catheter. The second compartment can surround the first compartment. The catheterization tray further includes a third compartment containing the urine-drainage bag. The third compartment can be connected to the second compartment.

The present disclosure provides for a safety catheter assembly comprising a needle hub, a catheter hub, a tip protector housing. Various embodiments can comprise a push-off tab extending radially from the tip protector housing or a portion thereof, and / or structure can be added or removed to affect compliance between a catheter assembly and a catheter insertion device.