In their recent paper, Steeg et al. (Reference Steeg, Kapur, Webb, Applegate, Stewart, Hawton, Bergen, Waters and Cooper2012) introduced ReACT, ‘a clinical tool to help identify patients at higher risk of repeat self-harm, or suicide, within 6 months of an emergency department self-harm presentation’. The paper's abstract reported that ReACT:

Some readers may have misinterpreted this sentence to mean that the researchers had found a way of predicting suicide with only two false positives for every true positive. In fact the figures in the clause before the semicolon in the quoted sentence above are ReACT's metrics for any form of repeated self-harm. After the semicolon, the 83 of 92 suicides that ReACT was able to ‘identify’ were associated with approximately 16 600 false positives with a positive predictive value of 0.5%.

Despite using the words ‘predict’ and ‘identify’, the authors describe ReACT as a ‘screening’ test rather that a predictive or diagnostic test. However, we do not believe it can be usefully used as a way to screen for future suicide. The World Health Organization (WHO) has issued guidelines outlining when screening is worthwhile (Wilson & Jungner, Reference Wilson and Jungner1968). These include the recommendation that a specific diagnostic test should be available to follow a sensitive but non-specific test like ReACT. Well-known examples from other areas of medicine include faecal occult blood tests that may be followed by endoscopy for bowel cancer and mammograms that may be followed by biopsy for breast cancer. The authors imply that ReACT might be used as ‘a guide or adjunct to the wider assessment of risk’, perhaps with another form of suicide risk assessment. We doubt that any further more sensitive and specific risk categorization is really possible, particularly because the items in ReACT (including recent self-harm and treatment for a mental disorder) cannot be used to further discriminate within a group of people who have already been defined by possession of these characteristics.

More broadly, if we assume that there is an intervention that is likely to decrease the likelihood of future suicide, then categorizing patients by their likelihood of suicide within 6 months might be justified if the proportion of true positives (suicide victims) among the whole ‘high-risk’ group were sufficiently high to justify the intervention for the whole ‘high-risk’ group. Such justification would only be present if the intervention were sufficiently effective and sufficiently benign (in terms of side-effect burden), as to mean that any down side to health or welfare of patients who were ‘high-risk’ false positives was clearly outweighed by the benefits accrued to patients who were ‘high-risk’ true positives. Even under these circumstances, categorization of patients by their likelihood of suicide within 6 months would hardly be necessary if it were feasible to also provide the benign, effective intervention to ‘low-risk’ patients as well. After all, these ‘low-risk’ patients are still at very high risk for future suicide compared to the general population. In the Steeg et al. (Reference Steeg, Kapur, Webb, Applegate, Stewart, Hawton, Bergen, Waters and Cooper2012) study there were nine suicides within 6 months among 13 000 people classified by ReACT as at ‘low-risk’. This translates into an annual rate of suicide among the ‘low-risk’ of 138 per 100 000 which can be compared to figures for population of England of about 10 suicides per 100 000 per year (NMHDU, 2009). We doubt that any form of risk categorization can lead to any intervention that can be ethically provided to ‘high-risk’ patients, the vast majority of whom will not attempt suicide, yet be denied to patients classified as ‘low-risk’.

The authors suggest that ‘some’ patients who present to the emergency department after a suicide attempt or act of self-harm and who are classed as ‘low-risk’ by ReACT could be ‘followed up for an assessment at a more convenient time and place, perhaps in the community’. If this is to imply that ReACT ‘low-risk’ patients could have the ‘full mental health and social needs assessment’ that NICE recommends be offered in the emergency department (NICE, 2004) be delayed and completed more conveniently in the community, we would strenuously disagree. It is quite feasible to offer such assessments in the emergency department to all patients presenting with self-harm. The assessments place little burden on the patient and, combined with the formation of an appropriate management plan, are likely to decrease the likelihood of future suicide.

ReACT may offer a statistically valid way of discriminating between patients on the basis of their likelihood of suicide within 6 months, but even so we cannot see how using this tool will have any clinical utility and are concerned that it might be inappropriately used to deny some patients a timely and comprehensive assessment of their illness and circumstances.