About Survivor Heart Check

Survivor Heart Check is a free and private online tool for assessing cardiovascular disease (CVD) risk, adjusting for cancer history. This is a demo application for educational purposes only and not intended as medical advice. If you are experiencing CVD symptoms or concerns, please consult a clinician.

CVD risk assessment validity

The CVD risk assessment conducted by this tool is based on equations published by Pylypchuk and colleagues in The Lancet (2018). The equations were derived from more than 400,000 New Zealand primary care patients using PREDICT software. It estimates a 5-year risk of a first CVD event based on a hazard model with multiple variables such as age, ethnicity, and family history as predictors.

Why does the CVD risk assessment need to be adjusted for cancer history?

Cancer survivors face different cardiovascular risks than the general population. A validation study (Tawfiq et al., The Lancet, 2023) tested the equations for 14000 New Zealand cancer survivors, compared to their observed CVD events. The equations performed well; however, the validation study recommended a cancer-specific variable to be added for improved accuracy. This tool applies a simple adjustment to the CVD risk estimate based on the presence of a cancer history, as recommended by the validation study.

How is the cancer-history adjustment applied?

The cancer-history adjustment applied here is drawn from Strongman and colleagues (The Lancet, 2019), a large UK cohort study comparing cardiovascular outcomes in over 100,000 cancer survivors compared to 500,000 cancer-free controls. For each cancer, this tool averages the adjusted hazard ratios for CVD events that most closely overlap with the PREDICT definition of CVD. This average is used as a cancer-specific multiplier, which is applied to the baseline assessment.

Limitations

Survivor Heart Check is a simplification, and it has real limitations. Studies done in the UK and New Zealand had to be combined to produce a working model. This limits useful conclusions that can be drawn from this tool, as the UK and New Zealand cohorts differ in population and healthcare context. Another limitation is the hazard ratios, which were obtained by averaging different CVD events and don't account for cancer treatment types. Some cancer types (particularly CNS/brain cancer) carry wide uncertainty in the original study due to small numbers of events. The application has not been endorsed by any professional and remains a personal project.

References