Use of IV contrast media in radiotherapy planning CT scans: A UK audit
Introduction
One of the inherent issues of computerised tomography (CT) versus magnetic resonance imaging (MRI) is the lack of soft tissue definition available in CT imaging.1 Use of intravenous (IV) contrast injected directly into the patient's vein immediately prior to the radiotherapy planning (RTP) CT scan allows enhanced visualisation of target volumes and adjacent organs at risk; making delineation of radiotherapy target volumes and organs at risk easier and more accurate.1
The extent of administration of intravenous (IV) contrast media within RTP CT is largely undefined. The Royal College of Radiologists (RCR) (2004)2 report advised IV contrast for specific tumour sites (Table 1).
In 2010, and updated in 2015,1 further national guidelines were released identifying standards of administration.3 The key points from these guidelines included:
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Risk factors should be assessed for all patients prior to IV contrast administration.
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eGFR should be assessed for all non-emergency patients, a minimum eGFR of >60 ml/min/1.73 m2 is recommended.
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Metformin should not be stopped unless eGFR is <60 ml/min/1.73 m2 and in consultation with the referring clinic.
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Cannulas should be left in situ for at least 30 min post injection for all high risk patients.
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All centres should have treatment guidelines for reactions including extravasation.
The benefits of using IV contrast are well acknowledged1, 2, 4 with many radiotherapy clinical trials requiring its use to aid target volume delineation and enable tumour visualisation.
Currently no standardised UK guidelines exist with respect to IV contrast protocols specific to radiotherapy planning where requirements in enhancement are often different to diagnostic studies. Many small single centre studies have investigated single aspects of contrast delivery and protocols. However, none of the studies look at the full range of IV contrast administration practice. Anecdotal evidence suggests departmental protocols may be derived from diagnostic CT protocols; these may be outdated or inappropriate for current RTP requirements. Given the pace at which planning techniques have developed and now rely on enhanced visualisation for delineating planning target volumes and identification of organs at risk, it is pertinent to conduct a full assessment of practice to ensure optimal protocols are utilised. This audit aimed to assess which protocols are followed by individual radiotherapy departments and also consider whether RCR guidelines (2004, 2010)2, 3 are sufficient for current practice or reflective of current research and knowledge.
Section snippets
Design
A comprehensive electronic questionnaire was sent to all 80 UK cancer centres, both qualitative and quantitative questions were used to promote objectivity and reduce researcher bias. The content and design of the questionnaire was based upon previous national studies of IV contrast administration.4, 5 Prior to distribution a pilot study of 5 randomly selected centres was performed to ensure the responses could be analysed in relation to the study questions and verify that the phrasing of the
Results
In total 83% of centres responded (n = 66/80), no response was received from 17% (n = 14/80) of centres. There were 10% (n = 8) partial responses which were excluded prior to data analysis due to a high level of unit non-responses. However, it is not known if these centres were true non-responses or if they re-started the questionnaire under a new submission as demographic data was not collected until the end of the survey. Of the 66 responding centres 5% (n = 3/66) were not operational, 5% (n
RCR 2004 compliance
The use of IV contrast within RTP CT scans has significantly increased with 98% (n = 51) of centres now routinely administering to at least 1 site; compared to 57% (n = 33)5 and 76% (n = 38)4 in previous studies. RCR (2004)2 recommended tumour sites has also increased with 6% (n = 3) of centres now administering to all 8 sites, compared to zero centres as identified in previous studies.4, 5 Full compliance is still relatively poor with over 40% of centres administering to only 5 sites or less,
Limitations
The main limitation of this study is lack of knowledge of the actual level of IV contrast enhancement achieved using current protocols at individual centres. For the current study centres were only asked how sufficient they feel the enhancement achieved using current protocols is, using a Likert scale response. This is a subjective question and doesn't qualify actual benefit; as generally centres have no other data for comparison. Due to this limitation a full further research study is needed
Conclusion
It is clear from the findings that new guidance specific to radiotherapy planning is required covering a wider area of IV practice to ensure optimal protocols are adopted that reflect the current evidence base. This is supported with two thirds of centres agreeing or strongly agreeing when asked if updated guidelines would be useful. Recommendations include:
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Recommended tumour sites should be redefined to reflect current evidence based practice, including tumour sites identified from clinical
Conflict of interest statement
None.
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