Patent classifications
A61G10/00
Device and Methods for Broadbeam and Microbeam Chemo-Radiosurgery Combined with Its Tumor Exosome Apheresis
Conventional single fraction 20-Gy broadbeam photonbeam or protonbeam chemo-radiosurgery does not sterilize EMT-MET cancer stem cell radiodurans but single fraction 100 to 10,000 Gy microbeam radiosurgery sterilizes them. Device and methods for microbeam chemo-radiosurgery including 250 MeV wakefield electronbeam is disclosed.
Surgery, chemotherapy and broadbeam and microbeam radiosurgery releases billions of abscopal metastasis causing, tumor specific plasma soluble proteins, cell membranes, apoptotic bodies, DNA and RNAs, exosomes like telomere-telomerase, ATM-ATM kinase and others. They and adaptive resistance to chemo-radiosurgery, paraneoplastic and non-paraneoplastic diseases causing immune complexes are removed by pulse flow combined continuous flow ultracentrifugation apheresis and immune affinity chromatography. Chemotherapy and high dose radiation exposed tumor cells and their exosomes are made sensitive to telomerase inhibiting and apoptosis inducing and least toxic epigallocatechin and to heparin bound receptors. They convert triple negative breast tumors into receptor positive tumors which open new avenues for treating most aggressive breast cancers.
MOBILE ISOLATION WARD
Disclosed herein is a mobile isolation ward including: a main body configured such that a door is installed in a front thereof, a fixed lighting window is installed in a right side thereof, and a light is installed at the center of a ceiling thereof; a ceiling air conditioner installed in the right side of the ceiling of the main body, and configured to control the temperature and the humidity inside the main body; an air purifier provided on one side of the inside of the main body, and configured to purify contaminated air inside the main body via a filter; and a blower configured to selectively introduce and discharge air. The junctions of the lighting window and the main body are finished with silicone. The main body is made of a glass fiber reinforced plastic material. The door and the lighting window are made of a transparent acrylic material.
DEVICE FOR LIMITING INFECTION
Disclosed is a barrier tent comprising a canopy, at least a portion of the canopy being composed of flexible sheet material; a frame for supporting the canopy; the canopy and frame being configured such that an internal surface of the canopy defines at least a portion of a patient segregation cavity to enclose a patient's head and at least a portion of the patient's body within the patient segregation cavity; and a gas input extending through the canopy, the gas input being positioned at a location configured such that supply of a gas through the input limits movement of aerosolised particles generated by or adjacent the patient toward the internal surface of the canopy.
PATIENT ISOLATION UNIT FOR PATHOGEN CONTAINMENT DURING MEDICAL IMAGING PROCEDURES
Systems are provided for a patient isolation unit for use with a medical imaging system includes an enclosure comprised of a pathogen impermeable material compatible with one or more imaging systems. The enclosure includes a base, a first end wall coupled to a first end of the base, a second end wall coupled to a second end of the base, and a cover coupled to a first side of the base, second side of the base, the first end wall and the second end wall for substantially enclosing a patient therein. In another exemplary embodiment, a patient isolation unit for use with a medical imaging system includes a head enclosure comprised of a pathogen impermeable material and a body enclosure coupled to the head enclosure and comprised of a pathogen impermeable material.
NEGATIVE-PRESSURE SHIELD DEVICE
The present invention provides a negative-pressure shield device with a simple device structure, which is relatively inexpensive to manufacture, and is extremely effective in preventing infection within an ambulance. The negative-pressure shield device comprises a shield main body that is installed in a patient compartment of an ambulance, includes a ceiling part and a peripheral wall part, and covers at least the head of a patient on a stretcher mounted in the patient compartment, and a connection part which communicates with the interior of the shield main body and connects to a ventilation opening provided in the patient compartment.
Collapsible casket viewing barrier
A collapsible casket viewing barrier includes a first transparent shield pivotally connected to a second transparent shield. The transparent shields are disposed within supporting frames that are connected via one or more hinges. Each supporting frame includes attached support legs, which may be telescopically adjustable and include wheels for easy transport. The first supporting frame and the second supporting frame are configured to move between a deployed configuration for use and a collapsed configuration for storage. When deployed during a funeral service, the collapsible casket viewing barrier can be positioned adjacent a casket such that the longer first transparent shield extends lengthwise along the casket while the shorter second transparent shield extends perpendicularly along the upper end of the casket. The casket is shielded in a way that allows individuals to view the deceased while reducing the transmission of germs.
INTERVENTIONAL OPERATION ISOLATION TRANSFER CABIN
An interventional operation isolation transfer cabin includes a cabin body, and a lead wire access device and a wire in/out device which two are mounted on the cabin body, the cabin body is provided with a negative pressure generating device at one end and an air inlet at the other end, the negative pressure generating device is provided with an exhaust filter device at its air outlet, and an intake filter device is provided at the air inlet. Several operating openings are provided on side walls of the cabin body, each of the operating openings is in seal connection with an operating glove, and a glove opening of at least one operating glove faces an interior of the cabin body. Equipment wires required by an interventional operation are preset through the lead wire access device, and wires added midway under a sealing condition is guaranteed through the wire in/out device.
Shielding apparatus
A shielding apparatus is provided. The shielding apparatus includes: at least one shielding shell segment, the at least one shielding shell segment constituting a shielding chamber, the shielding chamber being arranged on a periphery of a radiation device and shielding radiation generated by the radiation device. The shielding chamber is arranged on the periphery of the radiation device, and the shielding chamber at least partially shields scattering radiation generated by the radiation device, which can thus reduce the requirements of the radiation device for radiation shielding of a dedicated machine room or get rid of the dependence of the radiotherapy device on a dedicated machine room.
Shielding apparatus
A shielding apparatus is provided. The shielding apparatus includes: at least one shielding shell segment, the at least one shielding shell segment constituting a shielding chamber, the shielding chamber being arranged on a periphery of a radiation device and shielding radiation generated by the radiation device. The shielding chamber is arranged on the periphery of the radiation device, and the shielding chamber at least partially shields scattering radiation generated by the radiation device, which can thus reduce the requirements of the radiation device for radiation shielding of a dedicated machine room or get rid of the dependence of the radiotherapy device on a dedicated machine room.
Suction apparatus
An apparatus may include a first layer that includes a plurality of inlets and a surface feature; a second layer, where the surface feature opposes the second layer; an outlet, and a pattern defined on at least one of the first layer and the second layer, where the pattern defines a suction path from each inlet of the plurality of inlets to the outlet.