Disclosed is a patient positioning assembly for orientating a patient with respect to a radiation source. The patient positioning assembly includes a translatable member movable in a vertical direction between a vertically downwards first position and a vertically upwards second position. The patient positioning assembly further includes a patient support assembly mounted to the translatable member and adapted to rotate relative to the translatable member about a vertical axis. The patient support assembly is configurable between a first orientation, which sustains the patient in a seated position, and a second orientation, which sustains the patient in a generally standing position.

A composition, in particular in gel form, includes Lactobacillaceae reuteri to be used in the prevention and/or treatment of oral mucositis, particularly radio-induced oral mucositis. In its gel form, the composition also includes: a polyoxy-alkylene copolymer, in particular a polyoxy-ethylene-propylene copolymer, preferably with the general formula HO[CH.sub.2CH.sub.2O].sub.x[CH.sub.2CH(CH.sub.3)O].sub.y[CH.sub.2CH.sub.2O].sub.zH, where preferably x=99, y=67, and z=99; a mucoadhesive polymer, preferably cellulosic in nature, in particular carboxymethyl cellulose; and one or more stabilizers, preferably chosen from sugars such as sucrose, trehalose, mannitol, sorbitol and glucose, sodium ascorbate, very preferably the sugar is sucrose. Treatments of other mucositis with the composition, such as intestinal leakage, are conceivable. A procedure to produce the composition in gel and lyophilized form is described.

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.

A radiotherapy system including a radiotherapy component, a structural imaging component, a functional imaging component, and a workstation coupled to the radiotherapy component, the structural imaging component, and the functional imaging component. The workstation includes a processor which combines the structural imaging data and the functional imaging data to produce a fused model for a least a portion of the region of interest, to generate a plan for radiotherapy treatment of the region of interest based on the fused model, and apply, via the radiotherapy component, the radiotherapy treatment.

A process for treating highly localized carcinoma cells that provides precise positioning of a therapeutic source of highly ionizing but weakly penetrating radiation, which can be shaped so that it irradiates essentially only the volume of the tumor. The intensity and duration of the radiation produced by the source can be activated and deactivated by controlling the neutron flux generated by an array of electrically controlled neutron generators positioned outside the body being treated. The energy of the neutrons that interact with the source element can be adjusted to optimize the reaction rate of the ionized radiation production by utilizing neutron moderating material between the neutron generator array and the body. The source device may be left in place and reactivated as needed to ensure the tumor is eradicated without exposing the patient to any additional radiation between treatments. The source device may be removed once treatment is completed.

A system for monitoring doses from an ionizing radiation source to a treatment region of a patient and immobilizing a body cavity relative to the treatment region, is provided. The system includes a probe body for insertion into the body cavity. The probe body separates the body cavity from the treatment region to reduce exposure to doses from the ionizing radiation source. Radiation detectors are disposed along the probe body to measure at least one dose. A slot disposed adjacent the radiation detectors receives a dosimetry film that, upon exposure to the one or more doses from the ionizing radiation source, indicates a quantification of the doses. A coupling is in fluid communication with a removable sheath having coupled thereto a vacuum or a pump to remove fluid or gas from the body cavity and ensure inner wall of the body cavity is in contact with the sheath.

An amount of radiation exposure of a medical staff is significantly reduced, and a large working area is ensured during an operation. A size of each component of a radiation protection equipment is reduced so as to decrease a weight thereof. The radiation protection equipment is provided, which can be installed within a short time period before an operation and easily put away after the operation. The radiation protection equipment, includes: a first protection sheet arranged on a periphery of a radiation source device and configured to shield radiation; a second protection sheet formed separately from the first protection sheet, arranged on a side of an operation table, and configured to shield radiation; and a third protection sheet formed separately from the first and second protection sheets, arranged on a periphery of a surgical field so as to expose the surgical field, and configured to shield the radiation.

A movable medical device is provided. The movable medical device may include a medical cabin configured to accommodate medical resources for providing multiple types of medical services and a movable platform configured to move the medical cabin to a desired location. The medical cabin may include a radiation room configured to accommodate a radiation device for providing a medical imaging service; a sample processing room configured to accommodate medical resources for providing at least one of a sampling service or a sample detection service; and a control room configured to accommodate a control platform used to control the radiation device for providing the medical imaging service.

Systems and methods monitoring progress of procedures by radiation exposure are provided. Position data is received for an equipment item used for the procedure and configured to produce radiation (“radiation device”). Position data is received from the tracking device during the procedure. An estimated exposure level is determined by a controller for the individual based, at least in part, on the position data from the tracking device relative to the position data from the radiation device and compared to a benchmark. If the estimated exposure level for the individual exceeds the benchmark, an electronic notification is generated.

A system includes acquisition of a first three-dimensional image of a patient volume using a magnetic resonance imaging scanner, acquisition of a second three-dimensional image of the patient volume using cone beam radiation emitted by the linear accelerator, and generation of a radiation treatment plan based on the first image and the second image.