Radiology library

Radiology Fundamentals

The clinical half of this resource: what each investigation can reasonably answer, the professional standards that govern reporting, the statutory duties attached to dose and data, and how images should be handled.

Radiology library

This section covers what each imaging modality can reasonably answer, the professional standards governing the interpretation and reporting of imaging, and the statutory requirements for dose, quality assurance and image handling.

Providing a clear, practical overview of day-to-day radiological principles for non-specialist readers, trainees, and experienced practitioners seeking a concise reference. Last reviewed September 2026
§ 01 Modalities

Common radiology examinations

Each modality has its own strengths, weaknesses and clinical risks. The following sections describe what each modality can reasonably answer, where it is limited, and the practical safety considerations.

Radiography (X-ray)

Excellent for rapid triage and diagnosis

The classic radiology examination, the plain radiograph, has historically been the mainstay of most radiology departments, but in recent years lower-dose CT scanners and increasingly detailed MRI have gradually begun to supplant this old, reliable workhorse. However, plain radiographs remain extremely useful and are readily available in almost every healthcare setting. For some examinations, a plain radiograph provides all the necessary information in a single image, allowing a faster and easier diagnosis that is no less accurate. In some situations, however, a plain radiograph is much less accurate than CT or MRI. Despite their relatively low radiation dose, plain radiographs will remain a vital part of any radiology department for many years to come.

Common indications

  • Suspected fracture or dislocation
  • Chest infection, consolidation or pleural effusion
  • Bowel obstruction or free intraperitoneal gas
  • Foreign-body localisation

Limitations

  • Superimposed structures can mask or mimic pathology
  • Low soft-tissue contrast compared with CT or MRI
  • Projection geometry can conceal a fracture line

Safety and practical notes

Low-dose examination. Pregnancy status should be checked where the abdomen or pelvis is in the primary beam. Gonad shielding is no longer indicated under modern collimation.

Computed tomography (CT)

Excellent for most acute and cross-sectional questions

Computed tomography is the modern workhorse of acute and cross-sectional imaging, with high spatial resolution, short acquisition times and near-universal availability in secondary care. Multi-detector scanners can image the whole chest and abdomen in seconds, which is why CT is first line for acute presentations, trauma, most suspected malignancies and vascular disease. Its main weakness is that it uses ionising radiation at doses higher than those of plain radiography, and it often requires iodinated contrast (an iodine-based agent injected to make structures easier to see), which carries risks of allergy and renal injury. Other technical issues, such as beam-hardening and metal artefact, can also obscure detail -- an issue less prevalent with plain radiographs. Regardless, every exposure must be justified under IR(ME)R.

Common indications

  • Acute head injury, stroke or intracranial haemorrhage
  • Acute abdomen, trauma and suspected perforation
  • Pulmonary embolism and aortic dissection
  • Staging and follow-up of malignancy

Limitations

  • Ionising radiation dose -- justification and optimisation apply
  • Iodinated contrast risks (allergy, renal function, thyroid)
  • Beam-hardening and metal artefact can obscure detail

Safety and practical notes

Justification is mandatory under IR(ME)R. Contrast-enhanced studies require recent renal function and allergy history. Dose is monitored against diagnostic reference levels.

Magnetic resonance imaging (MRI)

Excellent for soft tissues

MRI delivers high soft-tissue contrast without ionising radiation and is the modality of choice for soft-tissue, marrow, joint and neurological questions. Multiplanar acquisition and a range of contrast weightings make it central to musculoskeletal, neurological, hepatobiliary and pelvic imaging, and it will demonstrate pathology that CT resolves poorly or not at all. Its constraints are physical rather than dosimetric. The static field is permanently energised, so implant, device and foreign-body screening is mandatory before entry to the controlled area, and ferromagnetic projectile injury remains the principal safety hazard. Acquisition times are long, motion degrades the study, and a proportion of patients cannot tolerate the examination. Gadolinium (an intravenous contrast agent) requires a documented renal function assessment, and there are ongoing concerns about tissue deposition in the brain. MRI capacity and cost continue to limit access compared with CT. Its principal advantage is that it carries no ionising radiation and therefore no IR(ME)R justification requirement, but the request must still identify a clinical question that MRI answers better than a faster or lower-cost alternative.

Common indications

  • Joints and soft-tissue injury
  • Brain, spinal cord and peripheral nerve lesions
  • Liver, biliary and pelvic pathology
  • Bone marrow and musculoskeletal infection or tumour

Limitations

  • Implant, device and foreign-body safety
  • Long acquisition times, so motion degrades the study
  • Gadolinium contrast

Safety and practical notes

No ionising radiation, but the static magnetic field is always on. Implant and device status must be checked before entry to the controlled area. Gadolinium is avoided in significant renal impairment unless clinically essential.

Ultrasound

Excellent for superficial structures and blood flow

Ultrasound provides real-time imaging without ionising radiation. It is a dynamic examination rather than a set of static images, so it can assess flow and superficial structures that projection and cross-sectional imaging demonstrate poorly. It is widely used in abdominal, obstetric, musculoskeletal and soft-tissue imaging, and it is the guidance method for many interventional procedures. Its principal weakness is operator dependence: image quality and interpretation vary with the practitioner, and the examination is the least reproducible of the modalities. Penetration is limited, and bowel gas obscures deeper structures. Ultrasound uses no ionising radiation, so no IR(ME)R justification requirement arises.

Common indications

  • Abdominal and pelvic pain, including gallstones and renal obstruction
  • Obstetric assessment and foetal wellbeing
  • Vascular stenosis, thrombosis and flow assessment
  • Image guidance for biopsy, drainage and vascular access

Limitations

  • Operator-dependent and the least reproducible modality
  • Limited penetration; bowel gas obscures deeper structures
  • No whole-body overview compared with CT or MRI

Safety and practical notes

No ionising radiation. Output parameters are kept as low as reasonably practicable. Endocavitary and interventional probes require appropriate decontamination between patients.

A radiographer reviewing a series of CT images on a monitor
Figure 01

A radiographer checks a series of CT images on a monitor

No modality is better than the others: each has its own clinical use, with its own strengths and limitations.

§ 02 Dose & safety

Information on Dose, justification and statutory duties

Ionising radiation is a powerful diagnostic tool, but it carries a risk of harm. The statutory duties of justification and optimisation apply to every exposure, and the law requires that the dose be kept as low as reasonably practicable for the diagnostic purpose.

Dose Effective dose on a normal scale 0 5 10 15 20 mSv UK average 2.7 mSv · annual Cornwall 7.8 mSv · annual Chest radiograph 0.02 mSv · per scan CT head 2 mSv · per scan CT abdomen 8 mSv · per scan Occupational limit 20 mSv · annual MRI and ultrasound use no ionising radiation. For X-ray and CT the exposure must be justified and then optimised, keeping the dose as low as reasonably practicable.
Figure 02

How the modalities compare on dose

Linear scale 0–20 mSv. MRI and ultrasound involve no ionising radiation.

UK average annual effective dose (all sources)

2.6 mSv

About half from radon; wide regional variation.

Average annual dose in Cornwall

7.8 mSv

Elevated radon; the highest regional average in the UK.

Public dose limit (man-made sources, excluding medical)

1 mSv/year

Statutory limit under the Basic Safety Standards.

Chest radiograph (for comparison)

≈0.02 mSv

A single projection; dose varies with technique.

Occupational dose limit (effective dose) i.e. radiation workers

20 mSv/year

Averaged over any calendar year; 100 mSv over five years under IRR17.

Justification and optimisation keywords explained

  • Justification: The benefit of the exposure to the patient must outweigh any potential harm. The referrer must provide sufficient clinical information to allow the practitioner to justify the examination and authorise the exposure.
  • Optimisation: Radiation doses are kept as low as reasonably practicable (ALARP) while achieving the required diagnostic purpose. The 2024 amendments to IR(ME)R strengthened duties to have regard for diagnostic reference levels and to audit practice.
  • Diagnostic reference levels (DRLs): National values derived from wide-scale surveys, typically set at the third quartile of the dose distribution for standard practice. Local DRLs should sit below national values, and departments consistently exceeding them must review their practice and take corrective action.
  • Protocol choice: Ensuring the chosen study is capable of answering the specific clinical question asked. A technically adequate scan that fails to address the clinical query does not constitute optimised care.

Who are the duty holders under IR(ME)R?

  • Employer: Establishes the organisational framework, including written procedures, protocols, training, staff entitlements, and compliance.
  • Referrer: Provides sufficient and accurate clinical information to enable the justification of an exposure.
  • Practitioner: Justifies and authorises the individual exposure by weighing clinical benefits against potential risks.
  • Operator: Carries out the practical aspects of the procedure and ensures optimisation in practice.

The roles are distinct and may be held by different people for the same exposure. A claim can attach to any one of them independently.

What needs recording and reporting

  • Significant accidental or unintended exposures are reportable incidents and must be investigated, with the findings recorded.
  • Occupational exposure is controlled through designated areas, monitoring and dose limits. Under IRR17 a controlled area is required where a person is likely to receive more than 6 mSv per year, and a supervised area above 1 mSv per year.
  • Dose limits under IRR17 are 20 mSv per year (100 mSv over five years), 150 mSv for the lens of the eye and 500 mSv for the extremities.
  • Equipment must be commissioned, tested and withdrawn from use when faulty.
  • QA records and dose records are evidence. They are routinely sought years after the event, and their absence is itself a finding.
Radiology image for reporting standards
Figure 03

The importance of reporting standards

§ 03 Standards

Interpretation and reporting: the professional benchmark

The Royal College of Radiologists' Standards for interpretation and reporting of imaging investigations (third edition, October 2025) define what a defensible report looks like.

Report content

A report must answer the clinical question asked, describe the findings, state the limitations of the study and give a clear conclusion. A structured format is expected where one has been agreed for that investigation. The conclusion should provide a radiological diagnosis or a reasoned differential, acknowledge limitations and make recommendations aligned with recognised guidelines.

Named author and accountability

Every report must be attributable to a named reporting author, including where reporting is remote or assisted by software. The author's name, position and profession should be identifiable. The content must not imply a level of scrutiny that has not in fact been applied.

Remote and offsite reporting

Remote reporting is acceptable only where the reporter has the images, the prior studies, the clinical information and the means to communicate an urgent finding. The same expectations of quality, turnaround and escalation apply as for onsite work. The RCR standards for teleradiology set out the governance, data-transfer and indemnity requirements.

AI-assisted and speech-recognition output

Where software generates or transcribes content, the named human author remains responsible for its accuracy. Every automated contribution must be reviewed and approved before the report is released. The use of AI does not transfer accountability to the software provider.

Turnaround and communication of critical findings

Providers must have procedures for turnaround times, communication of unexpected or time-critical findings, imaging classification for reporting priority, and acknowledgement of reports. A critical finding must be communicated directly and the communication documented, not left to the patient or referrer to discover.

Addenda and corrections

An addendum supplements the original report; it does not replace it. It must be attributable, dated and linked to the original study. Where a discrepancy or error is identified, the addendum should be non-judgemental and should trigger the local discrepancy and candour processes.

The standards apply to all who interpret and report imaging, regardless of professional background.

A doctor reporting within a narrower scope of practice is held to the same standard. Where imaged anatomy falls outside the interpreter's expertise, radiologist review must be agreed in advance. Reporting by sonographers and radiographers should occur within consultant-radiologist-led teams, with supervision and audit proportionate to the scope of practice.

Radiology image for handling images
Figure 04

Illustration for handling images section

§ 04 Handling images

Storage, transfer and viewing

Imaging disputes and clinical investigations frequently turn on digital provenance: what data was acquired, how metadata was handled, and who accessed the study. Rigorous image handling is an essential component of the clinical and legal record.

Anatomy of a DICOM study

A complete DICOM dataset comprises both pixel matrix data and an immutable header containing metadata: patient and study identifiers, acquisition parameters, exposure indices, display presets, and slice geometry. This metadata enables searchability, secure transfer, and anonymisation, while allowing subsequent reviewers to distinguish between native acquisition features, windowing choices, and actual pathology. Simply obscuring identifiers on the visible image without stripping the DICOM header leaves the file fully identifiable.

Secure transfer and anonymisation

When a study is transmitted outside the primary care pathway—such as for specialist second opinions or medicolegal review—it must be anonymised at source, transferred via secure encrypted channels, and audit-logged. Royal College of Radiologists (RCR) confidentiality standards distinguish between fully anonymised data (stripped of all personal identifiers, dates of birth, and facility tags) and pseudonymised data, which legally remains personal data as re-linking keys exist. All transfers must comply with institutional information governance protocols.

Second opinions and audit trails

The initiation of a second opinion, the credentials of the reviewing clinician, and the formal advice rendered must be documented within the clinical record. Where a secondary interpretation diverges from the original report, formal institutional discrepancy and escalation pathways must be invoked to ensure patient safety and clear clinical accountability.