Chapter 7 Image processing
Processing is the general term used to describe the sequence of events required to convert the invisible latent image, contained in the sensitized film emulsion or in the solid-state or phosphor layer of the digital sensors, into the visible black and white radiographic film or digital image. This chapter summarizes the two methods involved, namely:
It is CRUCIAL that the stages involved in chemical processing are performed under controlled, standardized conditions with careful attention to detail. Strict quality assurance procedures must be applied (see Ch. 18). Unfortunately, all too often in dental practice poor chemical processing is the cause of radiographic films being of inadequate diagnostic quality, irrespective of how reliable and expensive the X-ray equipment or how accurate the operator’s radiographic techniques.
A detailed knowledge of the chemistry involved in processing is not essential. However, a working knowledge and understanding of the theory of processing is necessary so that processing faults can be identified and corrected. A simplified approach to the stages involved in converting the green film emulsion into the black/white/grey radiograph is shown in Figure 7.1 and outlined below:
Fig. 7.1 Diagram showing the stages involved in processing, to convert the green film emulsion to the final black and white radiograph
(courtesy of Mrs J.E. Brown).
The sensitized silver halide crystals in the emulsion are converted to black metallic silver to produce the black/grey parts of the image.
There are three practical chemical processing methods available:
Manual processing is usually carried out in a dark-room, the general requirements of which should include:
• Adequate film storage facilities
• Safelights — positioned 1.2 m from the work surfaces with 25 W bulbs and filters suitable for the type of film being used (see Ch. 18)
• Processing equipment (see Fig. 7.2):
Fig. 7.2 The basic requirements for manual processing including a series of solution tanks, thermometer, timer and film.
1. The exposed film packet is unwrapped and the film clipped on to a hanger.
2. The film is immersed in DEVELOPER and agitated several times in the solution to remove air bubbles and left for about five minutes at 20°C.
3. The residual developer is rinsed off in water for about 10 seconds.
4. The film is immersed in FIXER for about 8–10 minutes.
5. The film is washed in running water for about 10–20 minutes to remove any residual fixer.
Two different processing solutions are required, the developer and the fixer. The typical constituents of these solutions are shown in Tables 7.1 and 7.2.
Table 7.1 The typical constituents of developer solution and their functions
Constituents | Functions |
---|---|
Phenidone | Helps bring out the image |
Hydroquinone | Builds contrast |
Sodium sulphite | Preservative — reduces oxidation |
Potassium carbonate | Activator – governs the activity of the developing agents |
Benzotriazole | Restrainer — prevents fog and controls the activity of the developing agents |
Glutaraldehyde | Hardens the emulsion |
Fungicide | Prevents bacterial growth |
Buffer | Maintains pH (7+) |
Water | Solvent |
Table 7.2 The typical constituents of fixer solution and their functions
Constituents | Functions |
---|---|
Ammonium thiosulphate | Removes unsensitized silver halide crystals |
Sodium sulphite | Preservative — prevents deterioration of the fixing agent |
Aluminium chloride | Hardener |
Acetic acid | Acidifier — maintains pH |
Water | Solvent |
• The alkaline developer solution should be made up to the concentration recommended in the manufacturer’s instructions.
• The developer solution is oxidized by air and its effectiveness decreased. Solutions should be used for no more than 10–14 days, irrespective of the number of films processed during that time.
• If the development process is allowed to continue for too long, more silver will be deposited than was intended and the radiograph will be too dark. Conversely, if there is too short a development time the radiograph will be too light.
• Development TIME (in fresh solutions) is dependent on the TEMPERATURE of the solution. The usual value recommended is five minutes at 20°C.
• If the temperature is too high, development is rapid, the film may be too dark and the emulsion may be damaged. If the temperature is too low, development is slowed and a pale film will result.
• Fixer solution should be made up to the concentration recommended by the manufacturer. It is an acid solution so contamination with developer should be avoided.
• Ideally films should be fixed for double the clearing time. The clearing time is how long it takes to remove the unsensitized silver halide crystals. Total fixing time is usually 8–10 minutes.
• Films may be removed from the fixer after 2–4 minutes for wet viewing but should be returned to the fixer solution to complete fixing.
• Inadequately fixed films may appear greenish yellow or milky owing to residual emulsion. In time these films may discolour further, becoming brown.
This term is used when processing is carried out automatically by a machine. There are several automatic processors available which are designed to carry the film through the complete cycle usually by a system of rollers. Most have a daylight loading facility, eliminating the need for a dark-room (see Fig. 7.3), but in the interests of infection control, salivary-contaminated film packets should be wiped with a disinfecting solution such as 1% hypochlorite, before being placed into the loading facility.
Fig. 7.3A The AP200 automatic processor fitted with its daylight loading apparatus (arrowed). B The internal tanks and roller system of the AP200 processor.
The cycle is the same as for manual processing except that the rollers squeeze off any excess developing solution before passing the film on to the fixer, eliminating the need for the water wash between these two solutions.
Self-developing films are an alternative to manual processing. The X-ray film is presented in a special sachet containing developer and fixer (see Fig. 7.4). Following exposure, the developer tab is pulled, releasing developer solution which is milked down towards the film and massaged around it. After about 15 seconds, the fixer tab is pulled to release the fixer solution which is similarly milked down to the film. After fixing, the used chemicals are discarded and the film is rinsed thoroughly under running water for about 10 minutes.
The main disadvantages include:
• The image deteriorates rapidly with time
• There is no lead foil inside the film packet
• The film packet is very flexible and easily bent
A rigid, radiopaque plastic backing support tray for the film is manufactured, which helps to reduce the problems of flexibility and lack of lead foil.
The digital image is captured in pixels (tiny squares), by two different types of sensor — solid-state or photostimulable phosphor plates described in Chapter 6. However captured, the digital image is similar to a film-captured image, in that both are 2-dimensional representations of a 3-dimensional object. In digital imaging, each 2-D pixel represents a 3-D cuboid or voxel of the patient. This is shown diagrammatically in Figure 7.5. The depth of the cuboid is dependent on the thickness of the part of the body being X-rayed. Each pixel measures the total X-ray absorption throughout the whole of each voxel. This 2-D limitation has been overcome with the development of cone beam computed tomography (CBCT), also called digital volume tomography (see Ch. 19).
As explained in Chapter 6, solid-state sensors input the information from each pixel directly (usually down the cable) to the computer’s analogue-to-digital converter as an analogue voltage signal.
Phosphor plates are not directly connected to the computer and therefore an intermediary stage is required when the plate is read. The time taken to read the plate depends on the particular system being used, and the size of the plate, but typically varies between 5–100 seconds. Several dental systems are available including Soredex’s Digora® Optime (intraoral) and PCT (extraoral), Durr’s Vistascan and the Gendex® DenOptix™ (see Fig. 7.6). Although different in design they all work on the same principle, namely:
• During the radiographic procedure the phosphor layer on the plate absorbs and stores the X-ray energy that has not been attenuated by the patient.
• The plate is then placed in the reader.
• The plate is scanned by a laser beam and the stored X-ray energy is released as light.
• The light is detected by a photomultiplier tube and converted into an electrical signal (voltage) and input to the connected computer’s analogue-to-digital converter
Computers deals with numbers, hence the need for the analogue voltage from each pixel to be changed by the analogue-to-digital converter into a discrete numerical digital signal. Each pixel has an x and y coordinate and is allocated a number. Typically using the grey-scale there are 256 numbers to select. These range from 0, when the voltage received is at its maximum (no X-ray attenuation in the patient), to 255 when there is no voltage (total X-ray attenuation in the patient). The computer finally allocates an appropriate colour from the grey scale (256 shades of grey from black through to white) to each pixel (0 = black, 255 = white) to create the visual image on the monitor. This concept is illustrated simply in Figure 7.7 using just eight numbers and eight shades of grey.
Fig. 7.7 Illustration of simple digital image creation using eight pixel numbers corresponding to eight shades of grey. Each pixel is allocated a number (dependent of the size of the input voltage) and then allocated a shade of grey to create the visual image
(kindly provided by Mr N. Drage).
The number and size of the pixels, together with the number of shades of grey available, determine the amount of information in an image, the size of the image file and the resolution of the final image (see Fig. 7.8). Pixel sizes vary from 20 microns to 70 microns producing resolution between 7–25 line pairs/mm.
Digital images can be changed by giving the pixels different numbers so altering the shades of grey. Different colours can be used. The coordinates of pixels may be changed or swapped, allowing different parts of the image to be moved around. These variables are the basis for image manipulation and enhancement. Software packages allow several enhancement techniques, some of which are shown in Figure 7.9. These can include:
Fig. 7.9 Examples of digital image enhancement. A Original image. B Inverted/ reversed. C Altered contrast. D Embossed/ pseudo 3-D. E Automated measurement. F Magnified. G and H Pseudocoloured.
(Kindly provided by Mr N. Drage.)
The two most frequently used enhancement functions are altering brightness and contrast.
Brightness can be regarded as equivalent to the degree of blackening of a film-captured image. Increasing brightness decreases the degree of blackening and makes the image lighter. This is done by increasing the numerical value of each pixel in the image and allocating it a lighter shade of grey. Taken to the extreme, every pixel would be allocated the highest number and the image will be totally white. The concept of altering brightness is illustrated in Figure 7.10, using the same simple model of eight numbers and eight shades of grey. Conversely, decreasing brightness increases the degree of blackening and makes the image darker.
Fig. 7.10 Illustration showing the effect of increasing brightness. A The original numbers allocated to the pixels and the original black/white and grey image. B Pixel values increased by 2 and the resultant grey/white image. C Pixel values increased by 4 and the resultant brighter image. D Pixel values increased by 7 (i.e. to extreme end of the brightness scale) and the resultant totally white image.
(Created from images kindly provided by Mr N. Drage.)
Contrast is the visual difference between black and white. Increasing contrast increases this difference. This is done by decreasing the pixel numbers in the darker half of the grey-scale and increasing the pixel numbers in the lighter half. Taken to the extreme, every pixel would be allocated either the lowest number available or the highest and the image would be black and white only containing no shades of grey. The concept of altering contrast is illustrated in Figure 7.11 using the same simple model of eight shades of grey. Conversely, decreasing contrast results in a grey image with little visual difference between the pixels.
Fig. 7.11 Illustration showing the effect of increasing contrast. A The original black/white and grey image. B Increased contrast — less visible grey. C Complete contrast — the image is only black and white.
(Created from images kindly provided by Mr N. Drage.)
Note:Despite being able to alter the final image, the computer cannot provide any additional information to that contained in the original image. It should be remembered that although manipulation and enhancement may make images look aesthetically more pleasing, they also may cause clinical information to be lost and diagnosis compromised.
Hard printed copies of digital images can be obtained on glossy photographic paper by using thermal, laser or ink-jet printers. However, image quality is considerably compromised because of the printers inability to reproduce 256 shade of grey. It is possible to produce excellent quality hard copy images using expensive heat sublimation printers. These print the digital image back onto film and can reproduce all the shades of grey. The quality is comparable to film-captured images.
• No need for chemical processing, thus avoiding all conventional processing faults (see Ch. 18) and the hazards associated with handling chemical solutions.
• Easy storage and archiving of patient information and incorporation into patient records.
• Easy transfer of images electronically.
• Image enhancement and manipulation.
• Phosphor plates have a wide latitude producing an acceptable image whether under-exposed or over-exposed.
• Large pixels result in poor resolution and structures may not be represented accurately as shown in Figures 7.12 and 7.13.
• Conventional PC screens/monitors reduce or limit image quality. Diagnostic image quality screens/monitors are required for optimal viewing.
• Long-term storage of images, although this should be solved by saving them on CD or DVD.
• Digital image security and the need to back up data.
• Over-exposure and overloading of CCD sensors creating the phenomenon of blooming (see Fig. 7.14).
• Loss of image quality and resolution on hard copy print-outs when using thermal, laser or ink-jet printers.
• Image enhancement and manipulation:
• While manufacturers provide safeguards to prevent any tampering with original images within their own software, it is relatively easy to access these images using inexpensive third party software and then to change them, as shown in Figure 7.15.
Fig. 7.12 Illustration showing how objects may not be represented accurately on a digital image if pixel size is large, using five shades of grey. A The square covers exactly and fills the sensor pixels and is therefore represented exactly radiographically. The outlines of B the circle, C the triangle and D the cross do not exactly cover and fill whole sensor pixels. The number and hence shade of grey allocated to an individual radiographic pixel represents the average of the total X-ray absorption within the whole pixel. Hence, the outlines and shapes of the objects are not represented accurately.
(Created from images kindly provided by Mr N. Drage.)
Fig. 7.13 Another illustration showing how an object may not be represented accurately on a digital image if pixel size is large, using five shades of grey. The square from Figure 7.12 is positioned so that it does not cover exactly and fill the sensor pixels. As a result it is now not accurately represented
(kindly provided by Mr N. Drage.)