2. Dyah Ayu Dwi W (P1337430117061) KELAS IB 3. Muhamad Fakhrul Rivan (P1337430117062) 4. Galih Tama Ramadhani (P1337430117063) Fluoroscopy is a study of moving body structures-- similar to an X-ray "movie." A continuous X-Ray beam is passed through the body part being examined. The beam is transmitted to a TV-like monitor so that the body part and its motion can be seen in detail. Fluoroscopy, as an imaging tool, enables physicians to look at many body systems, including the skeletal, digestive, urinary, respiratory, and reproductive systems. Fluoroscopy may be performed to evaluate specific areas of the body, including the bones, muscles, and joints, as well as solid organs, such as the heart, lung, or kidneys. Other related procedures that may be used to diagnose problems of the bones, muscles, or joints include X-rays, myelography (myelogram), computed tomography (CT scan), magnetic resonance imaging (MRI), and arthrography. At the time of fluoroscopy, the primary x-ray beam penetrates the patient's body to the input screen located in the Image Intensifier Tube, a vacuum tube comprising a cathode and an anode. The screen input in the Image Intensifier is a screen that absorbs x-ray photons and converts them into visible light beams, which will then be captured by PMT (Photo Multiplier Tube). PMT consists of photocatada, focusing electrode, and anode and phosphor output. The visible light absorbed by the photocathode on the PMT will be converted to electrons, then by focusing electrodes the negative electrons from the photocattoes are focussed and accelerated to the first dinode. Then the electrons will hit the first dinoda and in the collision process will produce other electrons. The multiplied electrons that emerge from the first dinda will be accelerated to the second dinode so that it will produce more electrons, and so on until the last dinoda. After that the electrons are rapidly accelerated to the anode due to the potential difference which then the electrons are converted into electrical signals. The electrical signal will be forwarded to the amplifier and then amplified and multiplied. Once these electrical signals are amplified it will be forwarded to the ADC (Analog to Digital Converter). In ADC these electrical signals will be converted into digital data that will be displayed on the tv monitor in the form of a picture of fluoroscopy results. The image intensifier is acomplex electronic devic that receives the remnant X-Ray beam, converts it into light, and increases the light intesity. Image Intesifier Tube Components: 1. Glass envelope 2. Input phosphor 3. Photocathode 4. Electrostatic focusing lenses 5. Output phosphor 1. Glass envelope: Mantains tube vacumm to allow control of e flow, has no functional part in image formation. 2. Input phosphor : X-Rays that exit the patient and are incident on the image intensifier tube are transmitted trough the glass envelope and interact with the input phosphor, which is cesium iodide. When X-Rays interacts with the input phosphor, its energy is converted into a burst of visible light photons as occur on the intensifying screen. Imput phosphor materials: 3. Photocathode: It is bonded directly to the input phosphor with a thin, transparant, adhesive layer. The photocathode is athin metal layer, usually composed of cesium and antimony compounds., that respond to stimulation by light with the emission of electron. This process is known as photoemission. 4. Electrostatic focusing lenses Located along lenghth of the tube, responsible for focusing the electrons across the tube from input to output phosphor. Image is reversed from input to output phosphor. The concave input screen reduces distortion by keeping the same distance between all points on the input & output screens. 5. Output phosphor The output phosphor is usually made up of zinc cadmium sulfide crystals. Each photoelectron that arrives at the output phosphor result in approximately 50-70 times. Image Monitoring Two methods are used to electronically convert the visible image on the output phosphor of the image intensifier into an electronic signal. 1. Thermionic television camera tube 2. The solid state charge-coupled device (CCD) Camera • The television camera consist of cylindrical housing, approximately 15 mm in diameter by 25v cm in length, that contains the heart of the camera, TV camera tube. • It also contains electromagnetic coils that are ued to properly steer the electron beam inside the tube. • A number of such television camera tubes are available for television fluorpscopy, but the vidicon and its modified version, the Plumbicon, are used most often. • Two methods are commonly used to couple the television camera tube to the image-intensifier tube. - fiber optics -lens system • The simplest method is to use a bundle of fiber optics • One advantage of this type of coupling is its compact assembly, which makes it easy to move the image- intensifier lower. This coupling is rugged and can withstand relatively rough handling. • The principal disavantage is that it cannot accommodate the additional optics required for devices such as cine or photospot camera. Lens Coupling To accept a cine or photospot camera, lens coupling is required. This type of coupling result in a much larger assembly that should be handled with care. Working The objective lens accepts light from the output phosphor and converts it in to a parallel beam. When an image is recorded on film, this beam is interrupted by a beam-splitting mirror so that only a portion is transmitted to the television camera, the remainder is reflected to a film camera. Such a system allows the fluoroscopist to view the image while it is being recorded. • The video signal is amplified and is transmitted by cable to the television monitor, where it is transformed back into a visible image. • What examinations might include fluoroscopy? • Exams that might include the use of fluoroscopy as part of the procedure include: • Upper gastroinrestinal • Small bowel series • Barium enema • Enteroclysis Upper Gastroinrestinal An upper gastrointestinal series (UGI) is a fluoroscopic examination of the esophagus, stomach, and duodenum (first part of the small intestine). The patient drinks a liquid suspension called Barium Sulfate, which outlines the anatomy of the esophagus, stomach and duodenum under fluoroscopy. Usually the patient will drink different types of barium solutions, effervescent granules, and often a barium tablet. Sometimes water soluble contrast is used when a leak is suspected. • Small Bowel Series A Small Bowel Series is a diagnostic procedure, which uses a "contrast agent" called barium sulfate and x- rays to obtain clear pictures of your small bowel. Ordinarily, x-rays pass through the soft tissues of the body, such as those found in your small bowel. However, barium sulfate coats the walls of your small bowel, thereby casting shadows that can be recorded in x-ray film. The exam can detect problems within your small bowel. A Small Bowel Series procedure helps the radiologist identify these problems with minimal risk and discomfort to you. Barium Enema A barium enema is a special x-ray of the lower digestive tract, colon or large intestine. A liquid barium preparation is given by enema to make the colon and rectum visible to x-ray. The barium (contrast medium) makes the area to be examined visible on film. If you are experiencing pain, have a change in bowel habits; diarrhea or bleeding your physician may refer you for a barium enema. Enteroclysis • Enteroclysis is an examination of the small bowel. X-rays are used to take single pictures and a special form of x-ray called fluoroscopy is also used in this examination. The radiologist can see internal organs like the bowel in motion using fluoroscopy. • A liquid called a contrast agent is put into the small bowel through a tube passed through your nose and stomach into the beginning of the small bowel. The contrast agent most commonly used for this study is called barium. The radiologist will watch to see how the contrast moves through the small bowel. • Schueler BA. The AAPM/RSNA physics tutorial for residents general overview of fluoroscopic imaging. RadioGraphics, 2000. 20(4):p1115-1126. Available at: http://pubs.rsna.org/doi/full/10.1148/radiographics.20.4.g00jl301115. Accessed October 23, 2014. • Bushberg JT, Seibert JA, Leidholdt EM, Boone JM. The Essential Physics of Medical Imaging. Philadelphia, PA, Lippincott Williams & Wilkins; 3rd ed, 2012. Available at: http://books.google.com/books?id=RKcTgTqeniwC&printsec=frontc over&dq=The+Essential+Physics+of+Medical+Imaging,+3rd+Editio n&hl=en&sa=X&ei=L- tIVLbCIs6zyASEioK4Bw&ved=0CDIQ6AEwAA#v=onepage&q=T he%20Essential%20Physics%20of%20Medical%20Imaging%2C%2 03rd%20Edition&f=false