Ultrasound: listening to the echoes
Ultrasound is sound above the range of human hearing, typically 1 to 15 MHz in medical use. It is produced and detected by the same device: a piezoelectric transducer, a crystal that changes shape when a voltage is applied and generates a voltage when it is deformed. That reversibility is why one probe both sends and receives.
A pulse travels into the body, and at every boundary between different tissues part of it reflects. Timing those echoes gives depth, since the speed in tissue is known. The strength of each echo depends on how different the two tissues are, measured by their acoustic impedance.
- Z
- acoustic impedancedensity × speed of sound in that tissue
- ρ, c
- density and speedproperties of the tissue
- d = ct/2
- the depthhalved because the pulse travels there and back
Why the gel matters
The impedance of air is thousands of times smaller than that of skin, so almost all the ultrasound would reflect straight off the surface and never enter the body. A coupling gel with an impedance close to skin removes the air gap and lets the pulse in. This is impedance matching, and it is a standard exam question rather than a practical detail.
X-rays: attenuation and contrast
X-rays are produced by accelerating electrons through a large potential difference and stopping them abruptly in a metal target. Most of the energy becomes heat; a small fraction becomes X-ray photons, with the maximum photon energy set by the accelerating voltage.
Unlike ultrasound, X-rays are detected in transmission — the image is a shadow. Different tissues absorb different amounts, and the intensity falls exponentially with the thickness of material traversed. Bone attenuates far more than soft tissue, which is why bones show clearly and why soft-tissue contrast is poor without an added contrast medium.
- µ
- the attenuation coefficientlarger for denser, higher-Z material such as bone
- x
- thickness traversedin the same units as 1/µ
- x½
- half-value thicknessthe thickness that halves the intensity
A beam of X-rays passes through 3.0 cm of tissue with attenuation coefficient 0.25 cm⁻¹. Find the fraction of the intensity transmitted, and the half-value thickness.
- I/I₀ = e^(−µx) = e^(−0.25 × 3.0) = e^(−0.75).Substituting into the attenuation equation; the units of µ and x must match.
- = 0.472, so about 47% is transmitted.Slightly under half, so the thickness must be slightly more than one half-value thickness — a useful consistency check.
- x½ = ln2/µ = 0.693/0.25.The half-value thickness follows directly from the attenuation coefficient.
- = 2.77 cm.Confirming the check: 3.0 cm is a little more than one half-value thickness, so a little under half gets through.
47% transmitted; x½ = 2.77 cm
PET: annihilation, and why it locates so precisely
Positron emission tomography works differently from both. A tracer — a molecule such as glucose labelled with a positron-emitting isotope — is injected and accumulates where metabolism is most active. This makes PET a functional scan, showing what tissue is doing rather than what it looks like.
Each emitted positron travels a very short distance before meeting an electron. The two annihilate, and their combined mass becomes energy as two gamma photons of 0.51 MeV each. Momentum conservation forces those photons to travel in almost exactly opposite directions.
That back-to-back emission is what makes the technique work. A ring of detectors around the patient records pairs arriving simultaneously, and the annihilation must have happened somewhere on the line joining them. Many such lines intersect at the source, and a computer reconstructs the distribution of the tracer.
- 0.51 MeV
- the photon energythe rest energy of an electron or positron
- 2γ
- two photonsone alone could not conserve momentum
- Δt
- arrival time differencelocates the event along the line of response
The three techniques compared
- Ultrasound: reflection, non-ionising, safe in pregnancy, poor through bone or gas.
- X-ray: transmission shadow, ionising, excellent for bone, poor soft-tissue contrast.
- PET: emission from within, ionising, shows function rather than structure, expensive.
- Ultrasound and X-ray image structure; PET images activity.
- Only ultrasound is non-ionising, which is the deciding factor for obstetric scanning.
- All three exponentials — attenuation, discharge and decay — share the same mathematics.
Choosing the right technique
Exam questions in this topic usually describe a clinical situation and ask which method suits it, with reasons. The answer turns on three considerations: whether ionising radiation is acceptable, whether the target is bone or soft tissue, and whether the question is about structure or function.
Ultrasound is the only non-ionising option, which settles obstetric scanning immediately. It is also cheap and portable, but it cannot pass through bone or gas, so it is useless for imaging the brain in an adult or a lung.
X-rays excel at bone precisely because dense, high-atomic-number material attenuates strongly — the contrast that makes a fracture obvious is the same physics that makes soft tissue nearly invisible. PET, being expensive and requiring a radioactive tracer with a short half-life, is reserved for questions about metabolic activity that no structural image could answer.
| Situation | Best choice | Deciding reason |
|---|---|---|
| Scanning a fetus | ultrasound | non-ionising, so no risk to the fetus |
| Suspected fractured wrist | X-ray | bone attenuates far more than tissue |
| Finding an active tumour | PET | shows metabolic activity, not just shape |
| Imaging a moving heart valve | ultrasound | real-time and safe for repeated use |
| Imaging the adult brain | not ultrasound | the skull reflects almost all of it |
X-ray attenuation follows the same exponential absorption shown here: equal thicknesses of material remove equal fractions of the beam, which is why the half-value thickness is a constant for a given material and photon energy.