Background / Aim of Rapid Review
Many patients were not able to access routine diagnostic care through 2020/21 because of
extraordinary pressures on the NHS due to COVID-19 and the UK national lockdowns. For some
patients this can have serious short and long-term consequences to their health and life
expectancy. The NHS has limited resources and is looking for new ways to meet many demands
and patient needs.
This Rapid Review Report aims to answer the question: Which innovations can be used to
accelerate the patients journey through the endoscopic cancer diagnosis pathway?. The report
highlights evidence of innovations and new ways to improve the timeliness of access to
endoscopy and to address the backlog of unmet need for patients who have waited a long time for
such tests and investigations by selecting those at highest for prioritisation. It does not evaluate in
terms of effectiveness on clinical outcomes.
Key Findings
Extent of the evidence base
Nine papers were included in the rapid review in total.
Two reviews were identified. One review examined the novel colon capsule endoscopy
(CCE) procedure and the second review summarised the effects of COVID-19 on
colorectal cancer (CRC) screening, the potential long-term? outcomes, and ways to adapt
CRC screening during the COVID-19 pandemic.
▪ Seven primary studies assessed innovations for the diagnosis of Gastrointestinal (GI)
cancers. Five of these studies examined faecal immunochemical testing (FIT) for
prioritising patients for further testing.
Two studies reported pathways/innovations to triage patients e.g. from primary care.
These methods of triage used interventions such as Cytosponge for oesophageal
symptoms.
Recency of the evidence base
Of the primary studies, one was published in 2020 and six were published in 2021. Of the
reviews, one was published in 2020 and one in 2021.
Evidence of effectiveness
The five studies investigating FIT found that it could help prioritise patients for further
testing and improve targeting of high-risk patients.
One review proposed CCE may offer a useful solution for investigating colorectal patients
to reduce the need for some endoscopies following the pandemic.
One review found a shift from current CRC screening and surveillance practices towards
an individualized approach based on risk factors, could result in the allocation of resources
to people with higher risks and prevent inappropriate use of healthcare resources for those
with lower risks.
Best quality evidence
All studies were quality appraised using the relevant JBI checklist. Five studies were of low
to moderate quality.
Policy Implications
Increased use of faecal immunochemical testing (FIT) could reduce the endoscopy
backlog and save NHS resources if those with low FIT scores can be excluded from
further testing.
Policy in Wales supports prioritisation of potential gastrointestinal cancer patients for
endoscopy using FIT test scores (NHS Wales 2021) although local implementation
currently varies, so it is not yet fully utilised. The FIT test gives results which could be
utilised by healthcare professionals to prioritise those who are most in need of urgent
diagnosis. The viability of this method to prioritise those in greatest need of being referred
for diagnosis through endoscopy is proven (though safety-netting is still required), and the
FIT test is part of the diagnostic pathway already in Wales. It will be important to ensure
all areas of Wales have equal access to the use of FIT testing for this purpose, and that
clinical guidelines are harmonised and adhered to throughout Wales.
Innovations to reduce backlog and speed up time to diagnosis should be explored
including:
o Triage in primary care settings such as GP surgeries using innovations such as the
cytosponge for oesophageal symptoms (e.g. reflux).
o Direct referral from primary care settings to specialist investigation, without the need for
prior additional referrals in secondary care.
Strength of Evidence
The evidence presented in this review is recent, however with small samples (di Pietro et
al., 2020), short-term follow up periods (Sagar et al., 2020) and assumptions required for
modelling studies (Loveday et al., 2021). This reduces the generalisability and confidence
of conclusions. The confidence in the strength of evidence about FIT testing is rated as
low-moderate confidence. Cytosponge evidence is rated low confidence.