Abstract: A syringe barrel includes: a hollow body portion that is configured such that a gasket is slidably insertable therein. The syringe barrel is made of a resin that has a total light transmittance of 80% or more. A scale is disposed at an inner circumferential surface or an outer circumferential surface of the body portion, the scale being visible from an outside of the syringe barrel and being configured to indicate a liquid amount. The scale is formed by (i) a stepped structure having a step height in a range of 0.001 to 0.15 mm in a radial direction, and/or (ii) an embossment.
Abstract: In a syringe, which is a prefilled syringe, when a cap body is attached to a cylindrical portion, a first sealing section is compressed radially inward by an inner peripheral surface constituting an opening of the cylindrical portion, thereby sealing a distal end section of a flow path in a liquid-tight manner, and a second sealing section is compressed radially inward by an inner peripheral surface of a proximal end section of the cylindrical portion, thereby sealing a proximal end section of the flow path in a liquid-tight manner.
Abstract: A drug coating layer that prevents breakage of elongated drug crystals on a balloon surface while maintaining the drug crystals in an appropriate shape to act on the living body includes plural elongated bodies which are crystals of a water-insoluble drug each extending from the surface of the balloon at various lengths and angles, and a water-soluble additive layer provided in a space between an outer surface of an aggregate of the elongated bodies and the balloon surface to fill a space between the elongated bodies. The outer surface of the additive layer being located outside the aggregate, being uneven connecting a plurality of tip ends and side surfaces of the elongated bodies to each other. The tip ends of the elongated bodies slightly protrude from the additive layer, and the side surfaces and/or tip surfaces of the elongated body are exposed on the surface of the additive layer.
Abstract: Provided is a means capable of predicting a formation of thrombus or a risk thereof in a medical device performing blood circulation by a pump, by a simple and minimally invasive method. A method for predicting a formation of thrombus or a risk thereof in a medical device performing blood circulation by a pump, wherein it is predicted that thrombus is formed or there is a risk thereof in the medical device when a concentration or expression amount of ADAM28 in a body fluid sample collected from a subject wearing the medical device is elevated compared with a reference value.
Type:
Application
Filed:
March 2, 2021
Publication date:
May 25, 2023
Applicant:
TERUMO KABUSHIKI KAISHA
Inventors:
Ichiro HIRAHARA, Shinpei FURUKAWA, Koko KUMANO, Hideki SATO
Abstract: An extracorporeal blood circulation system monitors blood level in a reservoir which temporarily stores the blood. A memory storage unit stores blood pressure measurements from a pressure sensor monitoring a blood pressure within a tube unit conveying blood from the reservoir relative to atmosphere. A processing unit that detects a height of a top surface of the blood stored in the reservoir based on changes in the blood pressure measurements and a conservation of mechanical energy of a blood flow inside the tube unit. A notification is generated if an abnormality is detected in the height of the blood in the reservoir.
Abstract: A prefilled syringe includes an outer cylinder, a gasket, a plunger, and a drug housed in the outer cylinder. The outer cylinder includes a flange part that is located at a proximal end part. The plunger includes a gasket pressing part and a shaft part that extends in a proximal end direction from a gasket pressing part. The shaft part includes indicator parts that are located on a proximal side of the gasket pressing part.
Abstract: An extracorporeal circulation apparatus has a blood reservoir temporarily storing blood and a presence information acquisition unit to detect presence or absence of blood at respective wall locations in a two-dimensional array. A control unit determines the position of a blood surface on the basis of consecutive elements in the array having detected blood along at least one of a first direction parallel to the blood surface and a second direction perpendicular to the blood surface.
Abstract: A medical instrument set includes a embolic device loading catheter that includes a catheter body including a loading lumen having an open distal end, and a proximal hub including an insertion passage communicating with a proximal end of the loading lumen, and in which an embolic device is loaded in the loading lumen; and a delivery pusher that includes an elongated pusher body insertable into the loading lumen through the insertion passage of the proximal hub of the embolic device loading catheter. The catheter body includes a distal connection portion attachable to and detachable from a sheath hub on a distal side of the catheter body. The pusher body has a body length longer than a distance from a proximal end of the insertion passage of the proximal hub to a distal end opening of a sheath communicating with a sheath lumen of a delivery catheter.
Abstract: A removal device and a removal system are configured to effectively remove an object in a body lumen while suppressing damage to another device. The removal device includes an elongated shaft part, and a cutting part fixed to a distal portion of the shaft part. The proximal portion of the cutting part includes a ring-shaped cutting blade, and a surface of the cutting part on which the cutting blade is positioned is inclined relative to center axis of the shaft part at an angle greater than 0 degrees and less than 90 degrees.
Abstract: A learning model generation method includes: acquiring training data from a training database that records a plurality of sets of a tomographic image acquired using a tomographic image acquisition probe, and correct answer classification data in which each of pixels included in the tomographic image is classified into a plurality of regions including a living tissue region and a non-living tissue region, in association with each other; acquiring thin-walled part data relating to a thin-walled part thinner than a predetermined threshold value, for a predetermined region in the correct answer classification data; and performing a parameter adjustment process for a learning model that outputs output classification data in which each of the pixels included in the tomographic image is classified into the plurality of regions, based on the training data and the thin-walled part data.
Abstract: A guide wire is disclosed, which is capable of reducing an unintended deviation in a guide wire position while preventing an occurrence of discomfort with respect to usability. The guide wire has a flexible core wire, and has a distal core portion, a main body portion, and a rigidity changing portion that gradually decreases in rigidity from the main body portion toward the distal core portion. The rigidity changing portion includes a first tapered portion continuous with a distal end of the main body portion, a second tapered portion continuous with a distal end of the first tapered portion, and a third tapered portion continuous with a proximal end of the distal core portion. A boundary portion between the first tapered portion and the second tapered portion is located in a range of 300 to 400 mm from a foremost distal end of the distal core portion.
Abstract: A method and device handle having a slide assembly for controlling rotational speed of a catheter assembly under various rotational loads. The method includes setting a first current limit in a processor, activating the catheter assembly to rotate, calculating a current value in rotational period of a first current limit, updating a second current limit from the first current limit, and wherein the second current limit is lower than the first current limit.
Type:
Grant
Filed:
March 15, 2019
Date of Patent:
April 18, 2023
Assignee:
TERUMO KABUSHIKI KAISHA
Inventors:
Yuki Masubuchi, Steve Woodard, Mansour Saleki
Abstract: Provided is a means capable of determining the development of myocarditis or the risk thereof by a simple and minimally invasive method. A method of determining the development of myocarditis or risk thereof, wherein it is determined that myocarditis is developed or there is a risk thereof when a concentration or expression amount of ADAM28 in a body fluid sample collected from a subject is reduced compared with a reference value.
Abstract: A symptom recording apparatus includes a control unit configured to perform control to output guidance on a method for confirming a body symptom of a user, receive an input operation of a confirmation result of the body symptom, and record the received confirmation result.
Abstract: A blood component separation device for separating a plurality of blood components from blood sampled from a blood donor, and collecting platelets, includes: an operation unit that calculates a predicted platelet recovery rate from a hematocrit value of the blood and a platelet concentration of the blood, and calculates a recommended processing amount of the blood recommended for collecting a target number of units of platelets on the basis of the calculated predicted platelet recovery rate, wherein the operating unit sets the predicted platelet recovery rate calculated from any the hematocrit value and any the platelet concentration to be smaller by a predetermined value a when the blood donor is female than that when the blood donor is male.
Abstract: A catheter includes a shaft having a lumen extending from a distal end to a proximal end. The shaft includes a reinforcement body including a plurality of wires that are disposed on at least a part between an inner surface of the shaft forming the lumen and an outer surface of the shaft and that are braided in a tubular shape, and at least one radiopaque marker disposed between the reinforcement body and the outer surface of the shaft. An outer diameter difference, which is a difference between an outer diameter of the shaft in a portion where the marker is disposed and an outer diameter of the shaft in a portion adjacent to the marker in an axial direction of the shaft, is smaller than twice a thickness of the marker.
Abstract: A medical pump includes a reader configured to read drug identification information, a storage unit that stores the drug identification information read by the reader, a notification unit, and a control unit, in which when the reader reads drug identification information anew while the drug identification information is stored in the storage unit, the control unit compares the drug identification information being stored in the storage unit with the drug identification information read anew by the reader, and when the drug identification information being stored in the storage unit does not match the drug identification information read anew by the reader, the control unit causes the notification unit to notify of non-matching between drugs.
Abstract: An extracorporeal circulation management device pumps blood in synchronization with heartbeats of a patient based on measurements of blood flow. Maximum and minimum blood flow measurement samples are compared with upper and lower threshold values to identify candidate timing for a systolic phase and diastolic phase of the heartbeat. During pulsatile pumping of the blood using the candidate timing, differences in the pulsatile flow measurements are determined. Based on the size of the difference, a final correction may be made to identification of the systolic and diastolic phases, and the corrected phase information is used to start and stop the motor unit.
Abstract: A balloon catheter and method for manufacturing are disclosed in which the fracturing of the vicinity of a proximal opening portion formed by an inner shaft can be prevented. A distal side of an inner shaft included by a balloon catheter is disposed in a lumen of an outer distal shaft, and a proximal side of the inner shaft is disposed on an outer surface of an outer proximal shaft, and the inner shaft forms a proximal opening portion which opens on an outer surface side of the outer proximal shaft. The inner shaft has a first region and a second region disposed on a proximal side of the first region. The first region is fixed to the outer surface of the outer proximal shaft. The second region is not fixed to the outer surface of the outer proximal shaft.