Strengths and limitations
To the authors’ knowledge, this is the largest study examining real-world investigation patterns for symptoms of colorectal cancer in primary care, using linked data from over 70 000 patients. The study addressed the challenge of variable symptom documentation in general practice by applying a transparent and systematic approach to classifying free-text 'reason for encounter' entries across multiple medical record systems, helping to ensure consistent symptom coding. Another key strength is the integration of general practice data with hospital admission and cancer registry datasets, enabling a comprehensive assessment of both primary care-led investigations and hospital-based procedures such as colonoscopy. Notably, colonoscopy data were derived from the VAED, allowing the authors to capture procedures conducted in both public and private hospitals.
Limitations include potential under-recording of symptoms documented in the ‘reason for encounter’ field rather than in free-text clinical notes. Prescribing data in the PATRON database do not always distinguish between new prescriptions and repeats, and may include regular medications unrelated to the presenting complaint. Finally, it was not possible to capture GP-level or system factors (such as workload, time constraints, and test access) that influence investigation decisions.
Comparison with existing literature
Half of patients with constipation and diarrhoea received no investigation. These non-specific symptoms have a PPV <1% for colorectal cancer.17 ‘Tests of treatment’ are often used in diagnostic decisions relating to non‐acute undifferentiated presentations with robust safety-netting.16,18–20 UK evidence suggests direct referral without investigation can shorten diagnostic time, although applicability to Australia’s more flexible gatekeeping model is unclear.21 Low investigation rates for anaemia are concerning, given the association with colorectal cancer, although this may reflect variations in recording or follow-up practices.
The current cohort showed lower pathology testing (<40% across symptoms) compared with UK research reporting >60% blood test use.22 In one Australian study of patients with colorectal cancer, approximately one-quarter had a blood test requested in the 24 months before diagnosis, with a similar proportion showing abnormal results.23 Blood tests can provide important early diagnostic clues detectable up to 9 months before diagnosis.23,24
Relatively low levels of iFOBT testing was found (see Supplementary Figure S4). Although recommended in Australia for determining colonoscopy urgency, it is not consistently included across guidelines, contrasting with UK National Institute for Health and Care Excellence recommendations for triage testing.13,25,26
The substantial between-practice variation identified through multilevel modelling indicates that clinical decision making for investigating colorectal cancer symptoms is influenced not only by patient characteristics but also by practice-level factors. This 8.6-fold variation in investigation likelihood between practices at the 2.5th and 97.5th percentiles cannot be explained by patient characteristics alone. Such variation may reflect differences in clinician training and experience, practice culture, or access to diagnostic resources. Although some variation is appropriate and reflects clinical judgement tailored to individual circumstances, the extent of this variation suggests opportunities for more standardised, evidence-based approaches to investigating lower gastrointestinal symptoms.
Similar to UK findings, the current study identified lower investigation rates among patients aged ≥80 years and in socioeconomically disadvantaged quintiles.27 In contrast to the current findings, individuals living in rural areas of the UK were less likely to be investigated, but this may reflect different patterns of access to investigations and referral pathways between countries. Although limited access to diagnostic services in rural areas is often of concern, the current findings suggest that such barriers may not substantially influence GP testing behaviour in Australia.
Regarding colonoscopy referral, a UK study by Mendonca et al
28 found that much of the between-practice variation was explained by sociodemographic characteristics, with higher rates observed in practices serving older and more socioeconomically deprived populations.28 In the present cohort, colonoscopy use peaked at the age of 60–79 years, declining after 80 years. In addition, higher referral likelihood in patients who were less disadvantaged was observed. This finding is consistent with previous Australian data showing greater colonoscopy use in higher socioeconomic areas, associated with the ability to pay for faster access to endoscopy.29 The differences observed in relation to associations with rurality may be explained by the fact that the current study’s dataset relies on patient locations to define remoteness rather than the location where the procedure was performed. This suggests that rural patients, especially those from more advantaged areas, may travel outside their local area to undergo a colonoscopy at a hospital situated in a larger city centre.29
The current study’s findings revealed important age-related disparities in investigation rates. Patients aged 40–49 years had lower investigation rates despite rising colorectal cancer incidence in younger adults.2 This may reflect lower PPV of symptoms in younger patients, a lack of awareness about the rising incidence in the younger group, the commonality of lower gastrointestinal complaints, age-based referral guideline restrictions, and GPs’ concerns about over-referring.30 The recent NBCSP expansion to include those aged 45–49 years addressed the increased incidence in younger people,3 yet the data in the current study suggest that symptomatic younger patients may still face barriers to timely investigation. For patients aged ≥80 years, the notable decrease in investigation rates probably results from complex clinical choices that weigh competing health issues. A prior systematic review identified a link between increasing age and longer diagnostic delays or delays in investigating cancer symptoms, decisions that are often complicated by frailty, multiple health conditions, and cognitive impairment.31
From a symptom perspective, changes in bowel habit triggered colonoscopy rates nearly equivalent to rectal bleeding, indicating clinicians recognise this as a concerning pattern, distinct from diarrhoea or constipation alone.6 Patients with repeat presentations or multiple symptoms were more likely to be investigated, aligning with elevated colorectal cancer risk.17 This suggests GPs respond to accumulating risk through clinical reasoning processes such as pattern recognition, hypothetico-deductive reasoning, or gut feeling.32
Implications for research and practice
This study highlights substantial variation in investigating colorectal cancer symptoms in Australian general practice. Although some variation reflects appropriate clinical judgement, inconsistent investigation, especially for non-specific symptoms, indicates potential missed diagnostic opportunities. The low anaemia investigation rate is concerning and warrants further study but raises broader concerns about managing abnormal test results in primary care.
Differences in investigation rates by age, rurality, and socioeconomic status point to potential inequities in diagnostic access and may contribute to the observed variations in colorectal cancer outcomes.33 These findings highlight the importance of implementing system-wide strategies to promote more consistent and evidence-based decision making. This includes developing structured diagnostic pathways, improving integration of decision support tools, and establishing mechanisms to enhance follow-up of abnormal results. Further research is necessary to explore the effects of current investigation practices on diagnostic intervals, stage at diagnosis, and cancer outcomes.