90 results about "Adult patients" patented technology

Present invention is a system of blood glucose monitoring and intensive insulin therapy in a ICU for strict maintenance of normoglycemia which reduces intensive care and hospital mortality and morbidity of critically ill adult patients. The findings of present study also reveal factors determining insulin doses needed to maintain normoglycemia as well as the impact of insulin dose versus blood glucose level on the observed outcome benefits have been established. The invention provides a control system that adapts the flow of the insulin infusion based on insulin requirement calculated by blood glucose levels and clinical parameters such as history of diabetes, Body Mass Index, blood glucose level on admission, reason of ICU admission, time in the ICU, type and severity of illness, caloric intake, obesity, drugs affecting insulin sensitivity). This automated insulin monitoring systems significantly reduces the workload and human resource management problems for intensive insulin therapy in patients in the ICU.

A kit containing all the materials needed to take a blood sample from a neonatal patient, a pediatric patient, a juvenile patient or an adult patient. The materials are supplied in a plastic package suitable for sterilization.

The invention provides a system for monitoring an infant or adult patient that includes a garment configured to attach to the infant, and a control module connected to the garment featuring: i) a first sensor that measures HR or a parameter used to determine HR; ii) a second sensor that measures RR or a parameter used to determine RR; iii) a third sensor configured to monitor a PP parameter; and iv) a wireless transmitter configured to receive and wirelessly transmit information from the first, second, and third sensors.

A method and apparatus are provided for changing the form of the jaw and facial bones of an adult patient that did not develop fully during childhood. The method utilizes a device having a plate body with an expansion screw that fits within the mouth of the patient; flap springs that project from the plate body, and an overlay extending from the plate body. The device is placed within the mouth of the patient so that the overlay is in a position between at least two opposing teeth. In this position, opposing teeth contact the overlay during function (e.g. swallowing). This intermittent, unilateral application of force to the facial bones causes these bones to further develop, positioning out of place teeth into more proper positions, and inducing a more symmetrical and enhanced appearance of the face, as well as increasing the airway space behind the jaws. Concomitantly, the flap springs gently press against selected teeth that are out of alignment in order to guide those teeth into place. Simultaneously, the expansion device maintains these forces on the teeth, while assisting the jawbones to expand to accept the teeth in their proper position. The expansion device can be adjusted by small motors under the control of a microprocessor located on the body plate based on readings from sensors on the flap springs. The expansion device can be adjusted by remote signaling, using a global position satellite technology and global position coordinates.

A moisture detection apparatus for signaling to a caregiver that a diaper or other article of clothing worn by an infant or adult being cared for by the caregiver is wet and needs to be changed. The apparatus includes a liquid transfer component having a plurality of capillaries for transferring liquid from the wet diaper to a remote location and a signaling device which emits either an audio signal or a visual signal, or both when an infant or adult patient is in need of attention due to a wet diaper or other article of clothing.

The present invention refers to a ventilation system used in hospital respiratory devices for the administration of anesthesia to newly born, pediatric and adult patients. More specifically, the present invention refers to a ventilation system that promotes a respiratory circuit with re-inhalation for the administration of anesthesia and that overcomes all inconveniences and deficiencies existing in respiratory devices of the state of the art. The ventilation system in respiratory devices comprises a bellows assembled within a reservoir, which is provided with a manifold with various gas exhaling valves, more specifically release valves to take out the excess of gases, and an exhaling valve for control gases. It is additionally constituted of a valve for the free flow of oxygen to quickly renew or replace the gases inside the respiratory circuit.

A medical robotic system comprises a drive track unit being operable for moving the medical robotic system along a floor. An upper torso unit is joined to the drive track unit. The upper torso unit comprises at least one actuator assembly. At least one bimanual dexterous manipulator is joined to the actuator assembly in which the actuator assembly imparts torque and movement to the bimanual dexterous manipulator for lifting an object. The bimanual dexterous manipulator comprises a pair of dexterous manipulators. Each of the dexterous manipulators comprises a length being configured to support lifting an adult patient, and an end comprising a planar structure being configured for placing between the adult patient and a patient platform. The drive track unit is operable for moving the medical robotic system to the patient platform and the bimanual dexterous manipulator is operable for lifting the adult patient from the patient platform.

The invention discloses a preparation method of eliglustat. Eliglustat is the first micromolecular oral drug for treating gaucher disease, and is applied to a first-line oral administration treatment of adult patients of I type gaucher disease. The invention provides a synthesis method of eliglustat. The synthesis method comprises the following steps: taking a compound represented by the formula (II) as the primary material, carrying out reactions between the compound (II) and Boc anhydride in an organic solvent in the presence of weak alkali so as to obtain a compound represented by the formula (III); reacting the compound (III) with benzyl bromide to obtain a compound represented by the formula (IV), subjecting the compound (IV) to deprotection in an organic solvent to obtain a compound represented by the formula (V); reacting the compound (V) with caprylyl chloride in an organic solvent (dichloromethane, etc.) to generate a compound represented by the formula (VI), and finally hydrogenating the compound (VI) to obtain the target compound represented by the formula (I). The synthesis method has the advantages that the operation is convenient, the process can be controlled convenient, the product purity is high, and the method can be easily applied to industrial production.

A multipurpose site guard for use at all peripheral and central venipuncture infusion sites, sensitive areas, and for pediatric and adult patients. The guard is a hollow plastic member with a base and a sidewall curved upwardly and inwardly to form a cover which is form fitted to the infusion site under finger pressure and which can be taped in place. Improvements to this invention include holding the guard in place with a fabric connector having closure means and cushioning the guard's base with a soft material.

A method and apparatus are provided for changing the form of the jaw and facial bones of an adult patient that did not develop fully during childhood. The method utilizes a device having a plate body with an expansion screw that fits within the mouth of the patient; flap springs that project from the plate body, and an overlay extending from the plate body. The device is placed within the mouth of the patient so that the overlay is in a position between at least two opposing teeth. In this position, opposing teeth contact the overlay during function (e.g. swallowing). This intermittent, unilateral application of force to the facial bones causes these bones to further develop, positioning out of place teeth into more proper positions, and inducing a more symmetrical and enhanced appearance of the face, as well as increasing the airway space behind the jaws. Concomitantly, the flap springs gently press against selected teeth that are out of alignment in order to guide those teeth into place. Simultaneously, the expansion device maintains these forces on the teeth, while assisting the jawbones to expand to accept the teeth in their proper position. The expansion device can be adjusted by small motors under the control of a microprocessor located on the body plate based on readings from sensors on the flap springs. The expansion device can be adjusted by remote signaling, using a global position satellite technology and global position coordinates.

This invention relates to a therapeutic device and method of administering precisely measured doses of a therapeutic substance via inhalation to pediatric and adult patients. More specifically, the invention relates to a therapeutic device and method of administering inhaled medication which delivers a controlled flow rate to a mouthpiece for administration of medicament to young children and adults with a diminished capacity, at a rate of about 25.8 L/minute to 30.2 L/minute.

Embodiments for intravenous extremity supports for pediatric and adult patients that allow health care workers to visually assess and/or palpate an extremity during IV therapy without removing the extremity support are disclosed. Embodiments of extremity supports comprise a stabilizer and at least one window. In one embodiment, the window is a transparent portion of the stabilizer. In another embodiment, the window is an opening in the extremity support. In yet another embodiment, a window is an area of the extremity support that does not impede a health care worker's view of the lower part of an extremity.

The present invention relates to a small particle size composition comprising pancreatin containing digestive enzymes for use in patients in need, including pediatric, geriatric, and adult patients, particularly those patients with dysphagia or wherein enteral administration using such composition would be suitable. In addition, the invention is directed to the composition as particles, such as micropellets or microgranules having a high potency, high useable yield and at least 10%-90% of 400-800 μm. Furthermore, the composition optionally has an improved enteric coating and concomitant improved stability and enzyme activity compared to conventional prepared enterically coated pancreatic enzyme particles.

A method and apparatus are provided for changing the form of the jaw and facial bones of an adult patient that did not develop fully during childhood. The method utilizes a device having a plate body with an expansion screw device that fits within the mouth of the patient, flap springs that project from the plate body and an overlay extending from the plate body. The device is placed within the mouth of the patient so that the overlay is in a position between at least two opposing teeth. In this position the flap springs press against selected teeth that are out of alignment in order to urge those teeth back into place. This force on the teeth causes the jawbone to expand to accept the teeth in their proper position(s). Also, the device is arranged such that the opposing teeth contact the overlay during swallowing, which causes the patient's facial muscles to intermittently pull on the facial bones. This intermittent application of force to the facial bones causes these bones to further develop toward a symmetrical appearance of the face and the positioning of out of place teeth/tooth into proper position. The device can be adjusted by small motors under the control of a microprocessor located on the body plate based on readings from sensors on the flap springs.

The present invention relates to a method for the treatment, amelioration or elimination of acute lymphoblastic leukemia (ALL), the method comprising the administration of a pharmaceutical composition comprising a CD19xCD3 bispecific single chain antibody construct to an adult patient in the need thereof.

The invention discloses a rapid auto-navigation magnetic resonance hydrography imaging method and device. Clinical application models of the invention include a breath-holding navigation mode and a free breath navigation mode. Adult patients with good breath control ability can adopt the breath-holding navigation mode, and infant patients with poor breath control ability can adopt the free breath navigation mode. The method and the device can obviously improve the acquisition efficiency, the control accuracy and the signal to noise ratio of magnetic resonance signals, can avoid an interference effect between an imaging sequence and a navigation wave sequence, and can enhance respiratory movement artifact inhibition effect; and the method and the device is simple in clinic operation, can obviously decrease coordination difficulties of patients, is conductive to clinical application of the magnetic resonance hydrography imaging technique, and can achieve unique diagnosis determining value in clinical diagnosis of a biliary system and a urinary system.

Compositions comprising a mixture of at least two types of particles wherein a) the first type of particles comprise dabigatran etexilate in the form of the free base or in the form of pharmaceutically acceptable salts, polymorphs, solvates or hydrates thereof; and b) the second type of particles comprise at least one pharmaceutically acceptable organic acid, use of said compositions in the reduction of the risk of stroke and systemic embolism in patients with non-valvular atrial fibrillation and/or in the prevention of venous thromboembolic events in adult patients who have undergone elective total hip replacement surgery or total knee replacement surgery and processes for the preparation of said compositions.

An AED unit which is operable to selectively execute either an adult rescue protocol or a pediatric rescue protocol is causes to execute the pediatric rescue protocol by inserting a key-like device into a slot of the AED unit. A sensor inside the case of the AED unit senses the presence of the device in the slot and responds by executing the pediatric rescue protocol. In an illustrated embodimentthe AED unit includes a lighting mechanism which is used to light an illustration showing the proper placement of electrode pads on an adult patient. The key-like device includes an illustration showing the proper placement of electrode pads on a pediatric patient which obscures the adult illustration when the device is inserted in the AED unit. The key-like device is configured to make use of the same AED unit lighting mechanism to light the pediatric pad placement illustration.

The method developed herein is for expanding cord blood-derived hematopoietic stem cells to a degree that is sufficiently safe for clinical application, such as the transplantation of hematopoietic stem cells into adult patients. Further, to prepare a number of mesenchymal stem cells or mesenchymal cells that have conventionally been available only in an extremely small number, an immortalizing gene such as that of telomerase is introduced alone into mesenchymal stem cells, mesenchymal cells or the like, so as to induce the differentiation of the expanded mesenchymal stem cells.