MRI Rectum — restaging after neoadjuvant therapy
Identical coverage and angulation to the primary staging study, planned from the pre-treatment images.
Timings, volumes and delays here are representative values drawn from published guidance. Scanner generation, injector, cardiac output and local preference all move them. Confirm against your department's own protocol before you rely on a number.
Premedication
Given to make the acquisition work, not to treat the patient. Doses are typical — confirm against your local protocol and prescribe within your own governance.
Suppression of rectal and small bowel peristalsis, as at primary staging. Restaging adds a reason of its own: the study is read side by side against the pre-treatment images, so motion on one of the pair degrades the comparison rather than just that one series, and the residual abnormality being judged is often only a few millimetres of wall thickening within fibrosis.
- Dose and route
- Typically 20 mg intravenously, or about 20 mg intramuscularly where no cannula is being sited. Glucagon roughly 0.25-1 mg intravenously where hyoscine is contraindicated or unavailable.
- When
- Immediately before the high-resolution oblique T2 sequences, and ideally covering the diffusion-weighted acquisition too, since diffusion carries more of the restaging decision than it does at primary staging. Where practice is to give a single dose it should be matched to whichever acquisition is most decisive locally.
- Do not give if
- If glucagon is used instead of hyoscine, it carries its OWN absolute contraindications rather than inheriting a clean slate: phaeochromocytoma, where it provokes catecholamine release and hypertensive crisis, and insulinoma or glucagonoma, where it causes rebound hypoglycaemia. It also raises blood glucose transiently, which matters in diabetes, and commonly causes nausea and vomiting.
- MHRA Drug Safety Update (February 2017), issued after nine reported deaths mostly from cardiac arrest: in patients with cardiac disease, monitor the patient and ensure resuscitation equipment AND staff trained to use it are readily available before giving it. This is an availability requirement, not a caution to note and move past.
- The same variation in practice applies as at primary staging — a spasmolytic is favoured where available but is not given everywhere, and it should be treated as the local protocol rather than a requirement.
- Contraindicated in untreated angle-closure glaucoma, myasthenia gravis, megacolon, and significant tachyarrhythmia.
- Caution in prostatic enlargement with urinary retention, and in significant cardiac disease.
- Warn the patient about transient blurred vision, and that they must not drive until it resolves.
- If unsuitable
- Proceed without it, and be explicit in the report that motion limits the comparison if it does — a restaging study called equivocal for motion is a different clinical message from one called equivocal for fibrosis, and in a watch-and-wait pathway the distinction matters.
When to use it
- Response assessment after chemoradiotherapy or total neoadjuvant therapy, before surgical decision-making.
- Selection for organ preservation and a watch-and-wait pathway.
- Assessment of residual mesorectal fascia threat when downstaging is being relied on.
- Surveillance within a watch-and-wait programme.
Technique
- Oblique-axial and oblique-coronal high-resolution T2 planned along the axis of the original tumour bed, not along whatever residual abnormality is now visible.
- Diffusion-weighted imaging in the same plane is central to restaging and is more useful here than at primary staging.
- Timing after completion of chemoradiotherapy matters; a conventional interval of several weeks is used so that treatment oedema settles, and the exact interval differs between protocols.
- Direct side-by-side comparison with the pre-treatment study is part of the technique, which is why geometry must be replicated.
Where it goes wrong
- Re-planning the oblique axials from the post-treatment appearance, which no longer matches the pre-treatment geometry and makes comparison invalid.
- Scanning too early after radiotherapy, when oedema and inflammation overstate residual disease.
- Omitting diffusion, which is where residual tumour within fibrosis is most often detected.
- Susceptibility artefact from fiducial markers or clips degrading the echo-planar diffusion at the tumour bed.
Clinical questions that reach this study
Contrast
- Unenhanced, as for primary staging. An antiperistaltic agent is used.
Acquisition
- Breathing
- Free breathing with antiperistaltic agent.
- Preparation
- Give the distance of the tumour from the anal verge and the endoscopy findings; the radiographer needs it to angle the oblique planes. Local practice on micro-enemas and rectal filling varies and is genuinely contested; follow the local protocol rather than improvising. An antiperistaltic agent is commonly used to limit motion; screen as for other pelvic studies.
Safety checks this protocol carries
Derived from the contrast agent and phases above, not authored here — which is why they cannot drift apart from what the protocol actually does.
- MR safety screening for implants and foreign bodies· radiographer at scan