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Accuracy of individual and combined risk-scale items in the prediction of repetition of self-harm: multicentre prospective cohort study

Published online by Cambridge University Press:  02 December 2020

Anna Kathryn Taylor*
Affiliation:
Centre for Mental Health and Safety, Manchester Academic Health Science Centre, University of Manchester, UK
Sarah Steeg
Affiliation:
Centre for Mental Health and Safety, Manchester Academic Health Science Centre, University of Manchester, UK
Leah Quinlivan
Affiliation:
Centre for Mental Health and Safety, Manchester Academic Health Science Centre, University of Manchester, UK; and NIHR Greater Manchester Patient Safety Translational Research Centre, University of Manchester, UK
David Gunnell
Affiliation:
Department of Population Health Sciences, University of Bristol, UK
Keith Hawton
Affiliation:
Centre for Suicide Research University Department of Psychiatry, Warneford Hospital, UK; and Oxford Health NHS Foundation Trust, Warneford Hospital, UK
Nav Kapur
Affiliation:
Centre for Mental Health and Safety, Manchester Academic Health Science Centre, University of Manchester, UK; and NIHR Greater Manchester Patient Safety Translational Research Centre, University of Manchester, UK
*
Correspondence: Anna Kathryn Taylor. Email annaktaylor@doctors.org.uk
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Abstract

Background

Individuals attending emergency departments following self-harm have increased risks of future self-harm. Despite the common use of risk scales in self-harm assessment, there is growing evidence that combinations of risk factors do not accurately identify those at greatest risk of further self-harm and suicide.

Aims

To evaluate and compare predictive accuracy in prediction of repeat self-harm from clinician and patient ratings of risk, individual risk-scale items and a scale constructed with top-performing items.

Method

We conducted secondary analysis of data from a five-hospital multicentre prospective cohort study of participants referred to psychiatric liaison services following self-harm. We tested predictive utility of items from five risk scales: Manchester Self-Harm Rule, ReACT Self-Harm Rule, SAD PERSONS, Modified SAD PERSONS, Barratt Impulsiveness Scale and clinician and patient risk estimates. Area under the curve (AUC), sensitivity, specificity, predictive values and likelihood ratios were used to evaluate predictive accuracy, with sensitivity analyses using classification-tree regression.

Results

A total of 483 self-harm episodes were included, and 145 (30%) were followed by a repeat presentation within 6 months. AUC of individual items ranged from 0.43–0.65. Combining best performing items resulted in an AUC of 0.56. Some individual items outperformed the scale they originated from; no items were superior to clinician or patient risk estimations.

Conclusions

No individual or combination of items outperformed patients’ or clinicians’ ratings. This suggests there are limitations to combining risk factors to predict risk of self-harm repetition. Risk scales should have little role in the management of people who have self-harmed.

Type
Papers
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press on behalf of the Royal College of Psychiatrists

Background

The third annual progress report of England's National Suicide Prevention Strategy highlighted self-harm as a key issue in its own right, including the need to recognise that people who present to hospital following self-harm are a high-risk group for later suicide.1 Emergency departments in England treat more than 220 000 episodes of self-harm annually.Reference Hawton, Bergen, Casey, Simkin, Palmer and Cooper2 At least half of people who die by suicide have a history of self-harm.Reference Foster, Gillespie and McClelland3 Furthermore, in England self-harm is associated with a 50 times greater risk of suicide in the year after the episode, which may be higher for those who present repeatedly.Reference Zahl and Hawton4Reference Geulayov, Casey, Bale, Brand, Clements and Farooq6

Hospital presentations involving self-harm can place significant pressure on emergency and mental health services, but provide an opportunity for suicide prevention.Reference Kapur7 The National Institute for Health and Care Excellence have set out pathways for short- and longer-term assessment and management of self-harm, emphasising the importance of psychosocial assessment by a mental health specialist for every presentation involving self-harm. The risk of further self-harm and specific follow-up care based on the needs of individuals should be considered as part of this assessment.8,9

Use of tools to assess risk

The use of risk scales as part of an assessment following self-harm is widespread. Over 20 tools were found to be used in 32 hospitals in England.Reference Quinlivan, Cooper, Steeg, Davies, Hawton and Gunnell10 However, their use is controversial; some clinical guidance advises the use of risk scales over locally developed proformas, but others argue that scales should only be used to structure assessments and not to predict future risk of suicidal behaviour or decide upon aftercare.9 There is growing evidence that risk scales do not accurately predict repeat self-harm and suicide.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11Reference Steeg, Quinlivan, Nowland, Carroll, Casey and Clements14 In a prospective cohort study of patients referred to liaison psychiatry following self-harm in England, clinician and patient evaluations outperformed risk scales in predicting risk of repeat self-harm.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11 In a large study of 4000 patients presenting to emergency departments following self-harm, Steeg et alReference Steeg, Quinlivan, Nowland, Carroll, Casey and Clements14 found risk scales failed to accurately predict both repeat self-harm and suicide. Other research into the use of risk scales in more specific populations (for example children and young people, adults with autism) also found a lack of evidence supporting the use of risk scales in predicting suicide attempts.Reference Carter, Walker, Aubeeluck and Manning15,Reference Cassidy, Bradley, Bowen, Wigham and Rodgers16 Recent meta-analyses have suggested that there is no reliable means of distinguishing individuals at high risk from those at low risk of suicidal behaviour; diagnostic accuracy of individual risk factors is frequently only slightly better than chance, and using multiple risk factors is not significantly more useful than single factors.Reference Franklin, Ribeiro, Fox, Bentley, Kleiman and Huang17,Reference Large18

Head-to-head comparisons of individual items from psychometrically tested risk scales have not been studied in real-world settings. It is not known how individual risk-scale items perform compared with patient and clinician estimates, and whether a scale constructed using the highest performing items would improve predictive accuracy for repeat self-harm.

Aims

Building on our previous studies, the aim of this study was to compare the predictive accuracy of individual items from widely used risk scales with clinician and patient estimates of risk of repeat self-harm within 6 months. We also aimed to construct a new scale from items with the highest predictive accuracy in each scale. Using data from a large prospective cohort evaluating risk scales following self-harm,Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11 we hypothesised that some individual scale items would perform better than the overall scale. We also hypothesised that the scale constructed using the best performing items would improve the predictive accuracy for repeat self-harm.

Our specific objectives were to:

  1. (a) estimate the predictive accuracy of the individual items from risk scales (the Manchester Self-Harm Rule, ReACT Self-Harm Rule, SAD PERSONS Scale, Modified SAD PERSONS Scale, and Barratt Impulsiveness Scale) to determine if any individual scale items had better diagnostic accuracy in predicting repeat self-harm compared with the overall scale and clinician and patient global scales; and

  2. (b) evaluate and compare the predictive accuracy of a scale constructed from the highest performing individual items from each scale using a range of dual and global diagnostic accuracy performance indicators and a sensitivity analysis using the classification-tree method.

Method

Data sources

We used data from a multicentre prospective cohort study that examined the diagnostic accuracy for predicting repeat self-harm of five risk scales: the Manchester Self-Harm Rule,Reference Cooper, Kapur, Dunning, Guthrie, Appleby and Mackway-Jones19 ReACT Self-Harm Rule,Reference Steeg, Kapur, Webb, Applegate, Steward and Hawton20 SAD PERSONS Scale,Reference Patterson, Dohn, Bird and Patterson21 Modified SAD PERSONS ScaleReference Hockberger and Rothstein22 and Barratt Impulsiveness Scale.Reference Patton, Stanford and Barratt23 For full details of the inclusion and exclusion criteria, service provision, case definitions and procedure, see Quinlivan et al.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11 In summary, participants were patients aged 18 years or over referred between March 2014 and January 2015 from emergency departments in five large teaching hospitals in England to liaison psychiatry services for assessment following self-harm. Each consecutive episode of self-harm, including those by the same individual, was considered as an index episode, reflecting the reality of presentation to emergency services.Reference Cooper, Kapur, Dunning, Guthrie, Appleby and Mackway-Jones19 The sample size of 480 was determined by a power calculation to enable meaningful comparative differences in predictive accuracy to be detected.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11 Self-harm was defined as intentional non-fatal self-injury or self-poisoning, irrespective of motivation or degree of suicidal intent.Reference Hawton, Harriss, Hall, Simkin, Bale and Bond24

Risk scales

The risk scales were previously tested for the predictive accuracy for repeat self-harm and/or attempted suicide.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11,Reference Quinlivan, Cooper, Davies, Hawton, Gunnell and Kapur25 The items in the scales and cut-off points are summarised in the Appendix. The Manchester Self-Harm RuleReference Cooper, Kapur, Dunning, Guthrie, Appleby and Mackway-Jones19 and the ReACT Self-Harm RuleReference Steeg, Kapur, Webb, Applegate, Steward and Hawton20 are four-item scales, where the presence of any one or more of the items identifies the patient as high risk. The SAD PERSONS Scale,Reference Patterson, Dohn, Bird and Patterson21,Reference Bolton, Rae Spiwak and Sareen26 and Modified SAD PERSONS ScaleReference Hockberger and Rothstein22 categorise patients as low, medium or high risk (Appendix).

There was some overlap in factors in the SAD PERSONS and Modified SAD PERSONS; we therefore combined these to ensure all the factors were included without any repetition. The Barratt Impulsiveness ScaleReference Patton, Stanford and Barratt23,Reference Randall, Rowe and Colman27 was designed to measure the construct of impulsiveness and includes 30 items rated on a scale of one to four, ranging from rarely/never to almost always/always. Several scale items (items: 9, 20, 1, 7, 8, 12, 13, 10 15 and 29) are reverse scored (for example ‘plan things carefully’). The ordinal data were recoded as binary data, for consistency with the other binary scales. Scale items with a score of three or four were coded as one. Reverse scored items were coded as zero if the score was one or two.

We also included the clinician and patient global evaluation of risk scale.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11 These global scales consist of a single question that asks the respondent to estimate the likelihood of repeat self-harm within 6 months on a 1–10 Likert-type scale (for example: ‘How likely do you think it is, that [you]/[the patient] will repeat self-harm within the next six months? Please indicate on this scale (with 1 as extremely unlikely and 10 extremely likely)’). We used the midpoint as our cut-off point (i.e. 1–5, low risk; ≥6 high risk). The cut-off point of 5–6 was selected as the optimal threshold for both the patient and clinician global scale using Youden's J index. This was reported in a previous study using the same data.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11

Risk scales were fully completed, with the exception of the Barratt Impulsiveness Scale where some items had missing data. However, all items had at least 92% complete data. Episodes with missing scale-item data were excluded listwise for analyses relating to that scale item.

Reference standard

The outcome for the study was hospital-treated repeat self-harm within 6 months of presentation, which was ascertained from self-harm monitoring systems and hospital records of the participating hospitals.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11 This time frame was selected because this is a high-risk period during which the majority of repeat episodes occurReference Steeg, Cooper, Kapur, Byrne and Rosen28 and has been used as an outcome measure in previous studies.Reference Kapur, Cooper, Hiroeh, May, Appleby and House29

Ethical approval

The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008. All procedures involving human patients were approved by the Central Manchester Research Ethics Committee (REC no: 13/NW/0838). Informed consent was gained from all participants.

Data analysis

Area under the curve

To enable comparisons of the global accuracy of individual scale items, we constructed receiver operating characteristic curves for each scale item and estimated area under the curve (AUC), a global indicator of diagnostic accuracy.Reference Simundic30 Higher values of AUC indicate greater discriminatory power; an AUC of 1.0 indicates a perfect test and 0.5 indicates that the result is no better than chance.Reference Hosmer, Lemeshow and Sturdivant31

Scale construction

The items with the highest AUC values within each scale were combined in a new scale. The items were combined to generate a new five-item scale, with each factor given equal weighting. The cut-off point with the optimal AUC was determined by maximising the product of the sensitivity and specificity values of the new scale.Reference Liu32 The Liu approach maximises overall predictive ability of the scale without prespecifying the prioritisation of sensitivity or specificity; we utilised this because predictive accuracy of the scale items included in the analysis ranged from high sensitivity (and low specificity) to high specificity (low sensitivity). The scale was derived from the entire sample and its predictive accuracy was tested on a 50% random sample of participants in order to validate the predictive performance of the scale.

Scale and item comparisons

The diagnostic accuracy of individual items was compared with the other items within each scale, the overall scale, and with the clinician and patient estimations of risk using AUC and 95% CIs. Scale items were also evaluated using a range of dual diagnostic accuracy statistics and 95% CIs, including sensitivity, specificity, positive and negative predictive values and positive and negative likelihood ratios.

Sensitivity analysis

Classification and regression tree (CART) analysis was used in a sensitivity analysis to test the robustness of our approach. CART analysis uses recursive partitioning methods to split data based on binary variables. A decision tree was created, with the goal of classifying patients into low-risk and high-risk groups.Reference Breiman, Friedman, Olshen and Stone33 In this approach, all scale items from the Manchester Self-Harm Rule, ReACT, SAD PERSONS, Modified SAD PERSONS and Barratt Impulsiveness Scale were pooled and the optimal binary splits that classified episodes into risk categories was sought. Optimal splits were obtained using Gini splitting criteria. We did not impose any misclassification costs such as prioritising correct classification of low or high risk. No pruning or stopping rules were used.

Data analysis was conducted in Stata and SPSS.34 We followed the STARD guidance (Standards for the Reporting of Diagnostic Accuracy Studies).Reference Bossuyt, Reitsma, Bruns, Gatsonis, Glasziou and Irwig35

Results

Demographic characteristics

The cohort study included 483 episodes of self-harm presenting to the five study hospitals, with 12 individuals presenting more than once (prior to follow-up). A total of 30% (145/483) of self-harm episodes were followed by a repeat presentation within 6 months. Of the episodes, 298/483 (61.7%) were in women and 455/483 (94.2%) were in patients from a White ethnic group. The median age was 33 years (interquartile range: 22–42 years, range: 18–88). In total, 359 of the 483 episodes (74.3%) were in individuals who had a self-reported lifetime history of self-harm. Almost two-thirds of the patients had a prior psychiatric history (found in 310/483 episodes, 64.2%). The most common methods of self-harm were self-poisoning (393/483, 81.4%) and 71/483 self-cutting (14.7%). The full clinical and demographic profiles are reported elsewhere.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11

Scale item performance: AUC

The AUC of individual items varied significantly (Figs. 1–3). The item with the lowest AUC (0.43, 95% CI 0.39–0.48) was the Barratt Impulsiveness Scale item ‘rarely thinks about one thing at a time’. The highest AUC (0.65, 95% CI 0.61–0.69) was ‘prior psychiatric treatment’ from the Manchester Self-Harm Rule. Accuracy for the clinician and patient global assessments was better, with AUCs of 0.74 (95% CI 0.69–0.79) and 0.71 (95% CI 0.67–0.76), respectively. The proportions of patients repeating self-harm by scale items are presented in Table 1.

Fig. 1 Area under the curve (AUC) and 95% confidence intervals for the Manchester Self-Harm Rule, ReACT rule and the patient and clinician global scales.

Fig. 2 Area under the curve (AUC) and 95% confidence intervals for the SAD PERSONS/Modified SAD PERSONS scales and the patient and clinician global scales.

Fig. 3 Area under the curve (AUC) and 95% confidence intervals for the Barratt Impulsiveness Scale and the patient and clinician global scales.

Table 1 Repetition of self-harm within 6 months by risk-scale item (total episodes n = 483, repeated self-harm n = 145, 30%)

Items from the Barratt Impulsiveness Scale were recoded from ordinal to binary to allow comparison with the other binary scales. Scale items with a score of three or four were coded as one. Reverse scored items were coded as zero if the score was one or two.

The following scale items performed better than the scale they originated from: previous suicide attempt (AUC 0.61, 95% CI 0.57–0.65) and previous psychiatric care (AUC 0.65, 95% CI 0.61–0.69) from the SAD PERSONS Scale, which had an overall AUC of 0.55 (95% CI 0.50–0.61) and previous suicide attempt or psychiatric care (AUC 0.65, 95% CI 0.61–0.69) from the Modified SAD PERSONS Scale (overall AUC 0.58, 95% CI 0.53–0.64).

Scale construction results

The item with the highest AUC in each scale was selected and these were combined to construct a secondary scale. These items were: ‘prior psychiatric treatment’ from the Manchester Self-Harm Rule (AUC 0.65, 95% CI 0.61–0.69), ‘self-harm in the last year’ from the ReACT (AUC 0.63, 95% CI 0.58–0.67), ‘previous suicide attempts’ or ‘psychiatric care’ from the Modified SAD PERSONS (0.65 95% CI 0.61–0.69), and ‘lots of extraneous thought’ from the Barratt Impulsiveness Scale (0.59 95% CI 0.54–0.64). Because of the overlap of the items from the Modified SAD PERSONS and the Manchester Self-Harm Rule, the item from the SAD PERSONS/Modified SAD PERSONS with the next highest AUC was selected (‘stated future intent’, AUC 0.57, 95% CI 0.53–0.61). The cut-off point for the new scale was 0 v. ≥1.

The overall sensitivity of the newly constructed scale was 92.7% (95% CI 83.7–97.6%) and specificity was 21.3% (95% CI 15.4–28.1%), the positive predictive value was 31.5% (95% CI 25.1–38.4%), and the negative predictive value was 88.1% (95% CI 74.4–96.0%). The AUC was 0.56 (95% CI 0.52–0.60). The results from the validation sample were similar (AUC 0.56, 95% CI 0.52–0.60). These AUCs were poor in comparison with those for clinician and patient global assessment, which were 0.74 and 0.71, respectively.

Sensitivity analyses

Results from the CART analysis, which used pooled items from each of the five psychometrically tested scales, suggested the optimal split of the data was by using a single variable, ‘prior psychiatric treatment’ from the Manchester Self-Harm Rule. This resulted in an AUC of 0.65 (95% CI 0.61–0.69), sensitivity of 85.5% (96% CI 78.7–90.8%) and specificity of 45.3% (95% CI 39.9–50.7%). There was no combination of scale items that performed better than this individual item.

Dual diagnostic accuracy statistics

In terms of each scale, the highest performing item varied depending on which diagnostic accuracy statistic was used (see supplementary Table 1 available online at https://doi.org/10.1192/bjo.2020.123). For the Manchester Self-Harm Rule, ‘lifetime history of self-harm’ had the highest sensitivity (92.4%, 95% CI 86.6–96.2%) but the lowest specificity (33.4%, 95% CI 28.4–38.7%). ‘Use of benzodiazepines’ was most specific (91.7%, 95% CI 88.3–94.4%) but had the lowest sensitivity (20.0%, 95% CI 13.8–27.4%). In the ReACT scale, the use of cutting as a method of harm was the most specific item (81.4%, 95% CI 76.8–85.4%) and the least sensitive (32.5%, 95% CI 24.5–40.7%). In SAD PERSONS, previous suicide attempts or psychiatric care had the highest sensitivity (85.5%, 95% CI 78.7–90.8%), but had relatively poor specificity (45.0%, 95% CI 39.6–50.5%). By contrast, the most specific item (‘loss of rational thinking’, 97.9%, 95% CI 95.8–99.2%) was the least sensitive (2.8%, 95% CI 0.8–6.9%). Finally, on the Barratt Impulsiveness Scale, the most sensitive item was ‘rarely self-controlled’ (82.3%, 95% CI 75.0–88.2% with a specificity of 34.6%, 95% CI 29.4–40.0%), and the most specific was ‘usually changes hobbies frequently’ (80.4%, 95% CI 75.6–84.5%, sensitivity 27.0%, 95% CI 19.8–35.1%).

Discussion

Main findings

Our results indicate that individual items from risk scales performed relatively poorly in terms of predicting repeat self-harm. The individual scale items, including history of self-harm, previous psychiatric treatment and suicidal intent failed to outperform clinician and patient global estimations of risk. Scale items relating to previous suicide attempt and previous psychiatric treatment performed slightly better than the SAD PERSONS and Modified SAD PERSONS scales they were part of. Other scale items performed about the same or worse than the overall scales. The scale that we constructed using a combination of the items with the highest predictive accuracy did not enhance the predictive performance for repeat self-harm. Global accuracy was generally poor for the newly constructed scale and did not outperform patient and clinician estimations of risk. Across the individual scale items and constructed scale, more highly sensitive items often had poor specificity, and vice versa. Our findings suggest that despite the potential importance of these items as part of assessments, there is little clinical utility in the use of the items in the prediction of self-harm, either in isolation or combination.

Strengths and limitations

The patients in our study are similar to patient samples in prior representative multicentre studies in terms of gender, method of self-harm and age.Reference Cooper, Kapur, Dunning, Guthrie, Appleby and Mackway-Jones19,Reference Bergen, Hawton, Waters, Cooper and Kapur36 However, patients who did not complete the research assessments or who did not meet eligibility criteria (for example, those who did not speak English, those who were too medically unstable, or those who were actively psychotic) were not included, which could affect generalisability to other populations. The cohort we analysed had a high proportion of participants with a prior history of self-harm (74%) and a high repetition rate (30%), which could suggest that our participants had higher levels of clinical need.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11

We used multiple methods to test predictive accuracy of scale items used in real-world clinical settings, including the use of algorithmic methods. However, it is possible that alternative machine learning approaches using larger samples would result in improved predictive accuracy. The sample size in the present study was too small to enable prediction of suicide to be assessed. A recent study using routine clinical data, collected as part of a self-harm monitoring system, was sufficiently powered to examine the accuracy of risk scales for predicting suicide.Reference Steeg, Quinlivan, Nowland, Carroll, Casey and Clements14 The four tools measured (Manchester Self-Harm Rule, ReACT, SAD PERSONS and Modified SAD PERSONS) were found to predict suicide deaths less accurately than repeat self-harm episodes. Suicide is a comparatively rare outcome and even greater accuracy is needed in order for predictive tools to be clinically useful.Reference Velupillai, Hadlaczky, Baca-Garcia, Gorrell, Werbeloff and Nguyen37

Whereas two of the scales (Manchester Self-Harm Rule and ReACT) were developed to be used in self-harm risk assessment, the Barratt Impulsiveness Scale is a scale that is not validated specifically as a risk scale for patients who have presented with self-harm (it is a measure of impulsiveness), and the SAD PERSONS Scale was initially developed as a training tool. However, a systematic review conducted prior to the cohort study found that the SAD PERSONS Scale and the Barratt Impulsiveness Scale were being used to predict future suicidal behaviour or repeat self-harm.Reference Quinlivan, Cooper, Steeg, Davies, Hawton and Gunnell10,Reference Quinlivan, Cooper, Davies, Hawton, Gunnell and Kapur25,Reference Saunders, Brand, Lascelles and Hawton38

Our methodological approach was based on our primary objectives that were to compare the predictive accuracy of psychometrically tested scale items and combine the top-performing items from each scale. However, the use of a simple additive scale, giving each factor the same weight, may underestimate the predictive accuracy if a key risk factor, such as previous self-harm, is considered equally to an item with lower predictive ability.

We used CART modelling as a sensitivity analysis to test the robustness of our approach and ensure the performance of the new scale was accurately estimated. Although we could have used CART analysis as the primary analysis, this would not have taken into account the risk scale that each item was extracted from, which is how they are used clinically. Logistic regression could have allowed us to select items based on the strength of association between each scale item and the outcome of repeat self-harm. However, we focused on selecting items based on predictive accuracy as the scales are already psychometrically developed, tested and used in clinical practice. Additionally, we categorised the ordinal data in the Barratt Impulsiveness Scale as categorical data, which may result in a loss of information and potential overlap between the groups because of the statistically imposed cut-off. However, recoding was necessary in order to combine the Barratt Impulsiveness Scale items with the binary scale items. Finally, validating the findings on a larger, population-level sample would provide greater accuracy of our findings.

Comparison with previous research

The previous study by Quinlivan et alReference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11 found that the diagnostic accuracy of the full risk scales was not sufficient for them to be of clinical use when used by mental health professionals, and that clinician or global assessment of risk had greater predictive ability for repeat self-harm. A more recent study by Steeg et alReference Steeg, Quinlivan, Nowland, Carroll, Casey and Clements14 found that utilising risk scales to predict repeat self-harm and future suicide following presentation to hospital is also unsuitable for episodes where mental health professionals are not involved in patient management. A meta-analysis of risk scales used for predicting suicidal behaviour also found that risk scales were not sufficient to be used to predict repeat self-harm and thus treatment allocation.Reference Carter, Milder, McGill, Pirkis, Kapur and Spittal12 Although that study examined the individual components of risk scales rather than the risk scales as a whole, our results are similar and suggest that even though some individual items performed slightly better than the scale they originated from, when combined they did not perform better than patient or clinician assessment of risk.

Machine learning methods may present new opportunities for risk prediction.Reference Velupillai, Hadlaczky, Baca-Garcia, Gorrell, Werbeloff and Nguyen37,Reference Walsh, Ribeiro and Franklin39Reference Siddaway, Quinlivan, Kapur, O'Connor and De Beurs41 Machine learning has been used in several prospective studies on the diagnosis of physical health conditionsReference Alaa, Bolton, Di Angelantonio, Rudd and Van der Schaar42 including prediction of cancer survival outcomes.Reference Ashley, Gupta, Tran, Wei, Lorgelly and Thomas43 Internationally there is an increasing drive to develop risk scales using machine learning techniques such as random forest, decision trees and support vector machines on ‘big data’.Reference Fazel and O'Reilly44 Machine learning techniques offer some advantages for analysing non-linear observations and large numbers of variables. However, there are a number of potential limitations to using machine learning techniques in mental health settings. When predictive accuracy is prioritised over clinical interpretation, risk prediction models can become highly complex, limiting their clinical utility.Reference Siddaway, Quinlivan, Kapur, O'Connor and De Beurs41,Reference Luo45 Complex algorithms may also shift the focus to prediction and away from clinicians formulating a management plan based on patients’ individual needs and circumstances.Reference Siddaway, Quinlivan, Kapur, O'Connor and De Beurs41

A recent systematic scoping review of the use of machine learning in mental health found that most research is focused on detection, such as natural language processing techniques to detect suicidal ideation from therapy transcripts, and short-term diagnosis rather than on predicting long-term outcomes.Reference Shatte, Hutchinson and Teague46 Furthermore, studies did not have a prospective design. One study found that machine learning models could correctly predict a sufficient proportion of suicides among soldiers for the prediction model to have implications for targeting interventions; however, the study focused on a specific population and would not be generalisable to the wider population.Reference Kessler, Stein, Petukhova, Bliese, Bossarte and Bromet47 Furthermore, the study did not compare the prediction models to clinician judgement. Other studies using machine learning techniques have been conducted in highly select samples with limited generalisability.Reference Hawes, Yaseen, Briggs and Galynker48 A recent systematic reviewReference Belsher, Smolenski, Pruitt, Bush, Beech and Workman49 found that although suicide prediction models produce overall accurate classification models, their accuracy of predicting a future event is near zero. If machine learning approaches can overcome these limitations, they may result in greater clinical utility. However, our results indicate that no combination or individual items from widely used tested scales outperformed patient and clinician estimations of risk when predicting real-world patient outcomes which suggests there may be limitations to the prediction of suicidal behaviour.

Clinical implications

This study adds to the growing evidence that risk scales, including components of risk scales, are not suitable for predicting repeat episodes of self-harm or future suicide. The overall performance of all items as measured by the AUC did not exceed a ‘fair’ level of prediction (defined as between 0.7 and 0.8) and none of the items exceeded clinicians’ global assessments of risk for repeat self-harm.Reference Quinlivan, Cooper, Meehan, Longson, Potokar and Hulme11 Measures of global accuracy were used to enable head-to-head comparison of scale items. However, measures of dual accuracy highlighted the limitations of scale items for accurately identifying those who repeated and accuracy for those who did not. This has implications for their utility. For example, although some items, such as the highly sensitive ‘lifetime history of self-harm’ item from the Manchester Self-Harm Rule, could be used as a guide for either emergency department or mental health clinicians in their own assessments, the high sensitivity items had poor specificity (and vice versa) so should not be used alone to identify patients as high or low risk and thus affect their treatment allocation. Identifying patients as high risk simply on the basis of meeting one criterion with high sensitivity but poor specificity could result in significant challenges to service provision if risk scales were used to determine patient management because of a potentially large number of referrals to more intensive services.

Factors such as prior psychiatric treatment and lifetime history of self-harm have been previously identified as risk factors for repeat self-harm, however, some Barratt Impulsiveness Scale items such as ‘rarely self-controlled’ and ‘usually changes jobs frequently’ were more specific or sensitive than the other items (although none were both sensitive and specific). Impulsivity and aggression have been correlated with self-harm in a recent systematic review,Reference O'Donnell, House and Waterman50 so awareness that impulsive/aggressive behaviours may increase the risk of future self-harm may help clinicians assess needs.

Risk classification scales remain in widespread use despite the evidence of their poor predictive abilities.Reference Quinlivan, Cooper, Steeg, Davies, Hawton and Gunnell10,Reference Carter, Milder, McGill, Pirkis, Kapur and Spittal12 This may be because they act as prompts for factors to consider in formulating a management plan, or because the risk scale results in a score that can be easily interpreted and can instruct the clinician on the management plan (for example, high risk requiring more intensive follow-up). This may be reassuring for less experienced clinicians but is unlikely to be beneficial to their practice or to patients. Furthermore, for relatively rare outcomes such as suicide, classification into high and low risk is unlikely to be clinically useful because of the relatively low positive predictive values that can be obtained. Carter et alReference Carter, Milder, McGill, Pirkis, Kapur and Spittal12 suggest that modifiable risk factors, such as isolation or improving physical health, should be a focus for improvement as part of a holistic assessment of the patient. In addition, patients value a therapeutic alliance,Reference Hunter, Chantler, Kapur and Cooper51 so focusing on forging a positive and encouraging relationship, as part of a good-quality assessment, may itself reduce the risk of a repeat self-harm episode.Reference Kapur, Steeg, Webb, Haigh, Bergen and Hawton52,Reference Steeg, Emsley, Carr, Cooper and Kapur53

The items we measured in the present study were not able to capture the quality and nature of the clinical encounter, which may also contribute to likelihood of repeat self-harm.Reference Hunter, Chantler, Kapur and Cooper51 Identifying those who are at particularly high risk is challenging; therefore safety planning should be a priority for all patients.Reference Stanley and Brown54 Instead of relying on risk scales to instruct clinicians on the most appropriate management, clinicians should receive comprehensive training and ongoing supervision to improve their knowledge and confidence in assessing patients who self-harm. Research into ‘de-implementation’ of the use of risk scales is an important next step in improving clinical practice for people who have self-harmed. Alternative strategies such as comprehensive patient-centred assessment and safety planning should be explored as part of this.

Given their range of predictive utilities, individual items of scales may be useful for clinicians to consider in their assessments, but they should not be used alone to predict repeat self-harm or determine patient management. Constructing new scales from higher-performing items did not significantly improved performance. The large number of items included in this new scale construction highlights potential limitations to predicting suicidal behaviour accurately.

Supplementary material

Supplementary material is available online at https://doi.org/10.1192/bjo.2020.123.

Data availability

Due to the nature of this research, study participants did not agree for their data to be shared publicly and only aggregated data are published.

Acknowledgements

We would like to thank Rosie Davies at the University of Bristol and our other patient, carer and clinician advisors for their input into the study. We would also like to thank the Research and Development departments for hosting the research and the NIHR Clinical Research Network staff who helped set-up the study and assisted with local recruitment and monitoring. We are grateful to the staff from the mental health liaison teams at each site who collected the data and also to the patients for completing the assessments.

Author contributions

A.K.T., S.S. and N.K. designed the study with input from L.Q., K.H. and D.G. Analysis of data was undertaken by A.K.T. and S.S. with input from N.K. and L.Q. The first draft was written by A.K.T. and S.S., and all authors contributed to subsequent drafts and have approved the final version of the manuscript.

Funding

This paper presents independent research funded by the National Institute of Health Research (NIHR) under its Programme Grants for Applied Research Programme (Grant Reference Number RP-PG-0610-10026).The views expressed are those of the authors and not necessarily those of the NHS, the National Institute of Health Research or the Department of Health. This work was supported by the National Institute for Health Research (NIHR) Greater Manchester Patient Safety translational Research Centre (L.Q. and N.K.) and a University of Manchester Presidential Fellowship (S.S.). The views expressed are those of the author(s) and not necessarily those of the NIHR or the Department of Health and Social Care.

Declaration of interest

D.G., K.H. and N.K. are members of the Department of Health's (England) National Suicide Prevention Strategy Advisory Group. N.K. chaired the National Institute for Health and Care Excellence (NICE) guideline development group for the longer-term management of self-harm and the NICE Topic Expert Group (which developed the quality standards for self-harm services). He is currently chair of the updated NICE guideline for Depression. K.H. and D.G. are Emeritus NIHR Senior Investigators. K.H. is also supported by the Oxford Health NHS Foundation Trust and N.K. by the Manchester Mental Health and Social Care Trust.

ICMJE forms are in the supplementary material, available online at https://doi.org/10.1192/bjo.2020.123.

Appendix

Risk scales, their individual items and cut-off points

References

Department of Health. Preventing Suicide in England: Third Progress Report of the Cross-Government outcomes Strategy to Save Lives. Department of Health , 2017.Google Scholar
Hawton, K, Bergen, H, Casey, D, Simkin, S, Palmer, B, Cooper, J, et al. Self-harm in England: a tale of three cities - Multicentre study of self-harm. Soc Psychiatry Psychiatr Epidemiol 2007; 42: 513–21.CrossRefGoogle Scholar
Foster, T, Gillespie, K, McClelland, R. Mental disorders and suicide in Northern Ireland. Br J Psychiatry 1997; 170: 447–52.CrossRefGoogle Scholar
Zahl, DL, Hawton, K. Repetition of deliberate self-harm and subsequent suicide risk: long-term follow-up study of 11 583 patients. Br J Psychiatry 2004; 185: 70–5.CrossRefGoogle ScholarPubMed
Hawton, K, Bergen, H, Cooper, J, Turnbull, P, Waters, K, Ness, J, et al. Suicide following self-harm: findings from the Multicentre Study of self-harm in England, 2000–2012. J Affect Disord 2015; 175: 147–51.CrossRefGoogle Scholar
Geulayov, G, Casey, D, Bale, L, Brand, F, Clements, C, Farooq, B, et al. Suicide following presentation to hospital for non-fatal self-harm in the Multicentre Study of Self-Harm: a long-term follow-up study. Lancet Psychiatry 2019; 6: 1021–30.10.1016/S2215-0366(19)30402-XCrossRefGoogle Scholar
Kapur, N. Health services and suicide prevention. J Ment Health 2009; 18: 15.CrossRefGoogle Scholar
National Institude of Health and Care Excellence (NICE). The Short-Term Physical and Psychological Management and Secondary Prevention of Self-Harm in Primary and Secondary Care. Clinical Guideline 16. NICE, 2004.Google Scholar
National Institude of Health and Care Excellence (NICE). The Long Term Care and Treatment of Self-Harm. Clinical Guideline 133. NICE, 2011.Google Scholar
Quinlivan, L, Cooper, J, Steeg, S, Davies, L, Hawton, K, Gunnell, D, et al. Scales for predicting risk following self-harm: an observational study in 32 hospitals in England. BMJ Open 2014; 4: e004732.10.1136/bmjopen-2013-004732CrossRefGoogle Scholar
Quinlivan, L, Cooper, J, Meehan, D, Longson, D, Potokar, J, Hulme, T, et al. Predictive accuracy of risk scales following self-harm: multicentre, prospective cohort study. Br J Psychiatry 2017; 210: 429–36.10.1192/bjp.bp.116.189993CrossRefGoogle Scholar
Carter, G, Milder, A, McGill, K, Pirkis, J, Kapur, N, Spittal, M. Predicting suicidal behaviours using clinical instruments: systematic review and meta-analysis of positive predictive values for risk scales. Br J Psychiatry 2017; 210: 387–95.10.1192/bjp.bp.116.182717CrossRefGoogle Scholar
Chan, KY, Bhatti, J, Meader, N, Stockton, S, Evans, J, O'Connor, RC, et al. Predicting suicide following self-harm: systematic review of risk factors and risk scales. Br J Psychiatry 2016; 209: 277–83.10.1192/bjp.bp.115.170050CrossRefGoogle Scholar
Steeg, S, Quinlivan, L, Nowland, R, Carroll, R, Casey, D, Clements, C, et al. Accuracy of risk scales for predicting repeat self-harm and suicide: a multicentre, population-level cohort study using routine clinical data. BMC Psychiatry 2018; 18: 113.10.1186/s12888-018-1693-zCrossRefGoogle Scholar
Carter, T, Walker, GM, Aubeeluck, A, Manning, JC. Assessment tools of immediate risk of self-harm and suicide in children and young people: a scoping review. J Child Healthc 2019; 23: 178–99.Google Scholar
Cassidy, SA, Bradley, L, Bowen, E, Wigham, S, Rodgers, J. Measurement properties of tools used to assess suicidality in autistic and general population adults: a systematic review. Clin Psychol Rev 2018; 62: 5670.10.1016/j.cpr.2018.05.002Google Scholar
Franklin, JC, Ribeiro, JD, Fox, KR, Bentley, KH, Kleiman, EM, Huang, X, et al. Risk factors for suicidal thoughts and behaviors: a meta-analysis of 50 years of research. Psychol Bull 2017; 143: 187232.10.1037/bul0000084Google Scholar
Large, MM. The role of prediction in suicide prevention. Dialogues Clin Neurosci 2018; 20: 197205.Google Scholar
Cooper, J, Kapur, N, Dunning, J, Guthrie, E, Appleby, L, Mackway-Jones, K. A clinical tool for assessing risk after self-harm. Ann Emerg Med 2006; 48: 459–66.CrossRefGoogle Scholar
Steeg, S, Kapur, N, Webb, R, Applegate, E, Steward, SLK, Hawton, K, et al. The development of a population-level clinical screening tool for self-harm repetition and suicide: the ReACT Self-Harm Rule. Psychol Med 2012; 42: 2383–94.10.1017/S0033291712000347CrossRefGoogle Scholar
Patterson, WM, Dohn, HH, Bird, J, Patterson, GA. Evaluation of suicidal patients: the SAD PERSONS Scale. Psychosomatics 1983; 24: 343–5.10.1016/S0033-3182(83)73213-5CrossRefGoogle Scholar
Hockberger, RS, Rothstein, RJ. Assessment of Suicide Potential by Nonpsychiatrists using the SAD PERSONS Score. J Emerg Med 1988; 6: 99108.CrossRefGoogle Scholar
Patton, JH, Stanford, MS, Barratt, ES. Factor structure of the Barratt Impulsiveness Scale. J Clin Psychol 1995; 51: 768–74.3.0.CO;2-1>CrossRefGoogle Scholar
Hawton, K, Harriss, L, Hall, S, Simkin, S, Bale, E, Bond, A. Deliberate self-harm in Oxford, 1990–2000: a time of change in patient characteristics. Psychol Med 2003; 33: 987–95.CrossRefGoogle Scholar
Quinlivan, L, Cooper, J, Davies, L, Hawton, K, Gunnell, D, Kapur, N. Which are the most useful scales for predicting repeat self-harm? A systematic review evaluating risk scales using measures of diagnostic accuracy. BMJ Open 2016; 6: e009297.Google Scholar
Bolton, J, Rae Spiwak, R, Sareen, J. Predicting suicide attempts with the SAD PERSONS scale: a longitudinal analysis. J Clin Psychiatry 2012; 73: e735–41.CrossRefGoogle Scholar
Randall, JR, Rowe, BJ, Colman, I. Emergency department assessment of self-harm risk using psychometric questionnaires. Can J Psychiatry 2012; 57: 21–8.CrossRefGoogle Scholar
Steeg, S, Cooper, J, Kapur, N. Early intervention for self-harm and suicidality. In Early Intervention in Psychiatry: EI of Nearly Everything for Better Mental Health (eds Byrne, P and Rosen, A). Wiley Blackwell, 2014.Google Scholar
Kapur, N, Cooper, J, Hiroeh, U, May, C, Appleby, L, House, A. Emergency department management and outcome for self-poisoning: a cohort study. Gen Hosp Psychiatry 2004; 26: 3641.CrossRefGoogle Scholar
Simundic, AM. Measures of diagnostic accuracy: basic definitions. EJIFCC 2009; 19: 203–11.Google Scholar
Hosmer, JD, Lemeshow, S, Sturdivant, R. Applied Logistic Regression. John Wiley & Sons, 2013.CrossRefGoogle Scholar
Liu, X. Classification accuracy and cut point selection. Stat Med 2012; 31: 2676–86.CrossRefGoogle ScholarPubMed
Breiman, L, Friedman, J, Olshen, R, Stone, C. Classification and Regression Trees. Wadsworth, 1984.Google Scholar
Statacorp. Stata: Release 13. College Station. StataCorp LP, 2013.Google Scholar
Bossuyt, PM, Reitsma, JB, Bruns, DE, Gatsonis, CA, Glasziou, PP, Irwig, L, et al. STARD 2015: an updated list of essential items for reporting diagnostic accuracy studies. Br Med J 2015; 351: h5527.CrossRefGoogle Scholar
Bergen, H, Hawton, K, Waters, K, Cooper, J, Kapur, N. Epidemiology and trends in non-fatal self-harm in three centres in England: 2000-2007. Br J Psychiatry 2010; 197: 493–8.CrossRefGoogle Scholar
Velupillai, S, Hadlaczky, G, Baca-Garcia, E, Gorrell, GM, Werbeloff, N, Nguyen, D, et al. Risk assessment tools and data-driven approaches for predicting and preventing suicidal behavior. Front Psychiatry 2019; 10; 36.CrossRefGoogle Scholar
Saunders, K, Brand, F, Lascelles, K, Hawton, K. The sad truth about the SADPERSONS Scale: an evaluation of its clinical utility in self-harm patients. Emerg Med J 2014; 31: 796–8.CrossRefGoogle ScholarPubMed
Walsh, CG, Ribeiro, JD, Franklin, JC. Predicting risk of suicide attempts over time through machine learning. Clin Psychol Sci 2017; 5: 457–69.10.1177/2167702617691560CrossRefGoogle Scholar
Ryu, S, Lee, H, Lee, DK, Park, K. Use of a machine learning algorithm to predict individuals with suicide ideation in the general population. Psychiatry Investig 2018; 15: 1030–6.10.30773/pi.2018.08.27CrossRefGoogle Scholar
Siddaway, A, Quinlivan, L, Kapur, N, O'Connor, R, De Beurs, D. Cautions, concerns, and future directions for using machine learning in relation to mental health problems and clinical and forensic risks: a brief comment on ‘Model complexity improves the prediction of nonsuicidal self-injury’ (Fox et al., 2019). J Consult Clin Psychol 2020; 88: 384–7.10.1037/ccp0000485CrossRefGoogle Scholar
Alaa, AM, Bolton, T, Di Angelantonio, E, Rudd, JHF, Van der Schaar, M. Cardiovascular disease risk prediction using automated machine learning: a prospective study of 423,604 UK Biobank participants. PLoS One 2019; 14: e0213653.10.1371/journal.pone.0213653CrossRefGoogle Scholar
Ashley, DM, Gupta, A, Tran, T, Wei, L, Lorgelly, PK, Thomas, DM, et al. Machine-learning prediction of cancer survival: a prospective study examining the impact of combining clinical and genomic data. J Clin Oncol 2015; 33: 6521.CrossRefGoogle Scholar
Fazel, S, O'Reilly, L. Machine learning for suicide research-can it improve risk factor identification? JAMA Psychiatry [Epub ahead of print] 23 Oct 2019. Available from: https://doi.org/10.1001/jamapsychiatry.2019.2896.Google Scholar
Luo, G. Automatically explaining machine learning prediction results: a demonstration on type 2 diabetes risk prediction. Health Inf Sci Syst 2016; 4: 2.10.1186/s13755-016-0015-4CrossRefGoogle Scholar
Shatte, ABR, Hutchinson, DM, Teague, SJ. Machine learning in mental health: a scoping review of methods and applications. Psychol Med 2019; 49: 1426–44.CrossRefGoogle Scholar
Kessler, RC, Stein, MB, Petukhova, MV, Bliese, P, Bossarte, RM, Bromet, EJ, et al. Predicting suicides after outpatient mental health visits in the Army Study to Assess Risk and Resilience in Servicemembers (Army STARRS). Mol Psychiatry 2017; 22: 544–51.CrossRefGoogle Scholar
Hawes, M, Yaseen, Z, Briggs, J, Galynker, I. The Modular Assessment of Risk for Imminent Suicide (MARIS): a proof of concept for a multi-informant tool for evaluation of short-term. Compr Psychiatry 2017; 72: 8896.10.1016/j.comppsych.2016.10.002CrossRefGoogle Scholar
Belsher, BE, Smolenski, DJ, Pruitt, LD, Bush, NE, Beech, EH, Workman, DE, et al. Prediction models for suicide attempts and deaths: a systematic review and simulation. JAMA Psychiatry 2019; 76: 642–51.CrossRefGoogle Scholar
O'Donnell, O, House, A, Waterman, M. The co-occurrence of aggression and self-harm: systematic literature review. J Affect Disord 2015; 175: 325–50.10.1016/j.jad.2014.12.051CrossRefGoogle Scholar
Hunter, C, Chantler, K, Kapur, N, Cooper, J. Service user perspectives on psychosocial assessment following self-ham and its impact on further help-seeking: a qualitative study. J Affect Disord 2013; 145: 315–23.CrossRefGoogle Scholar
Kapur, N, Steeg, S, Webb, R, Haigh, M, Bergen, H, Hawton, K, et al. Does clinical management improve outcomes following self-harm? results from the multicentre study of self-harm in England. PLoS One 2013; 8: e70434.Google Scholar
Steeg, S, Emsley, R, Carr, M, Cooper, J, Kapur, N. Routine hospital management of self-harm and risk of further self-harm: propensity score analysis using record-based cohort data. Psychol Med 2018; 48: 315–26.CrossRefGoogle Scholar
Stanley, B, Brown, GK. Safety planning intervention: a brief intervention to mitigate suicide risk. Cogn Behav Pract 2012; 19: 256–64.CrossRefGoogle Scholar
Figure 0

Fig. 1 Area under the curve (AUC) and 95% confidence intervals for the Manchester Self-Harm Rule, ReACT rule and the patient and clinician global scales.

Figure 1

Fig. 2 Area under the curve (AUC) and 95% confidence intervals for the SAD PERSONS/Modified SAD PERSONS scales and the patient and clinician global scales.

Figure 2

Fig. 3 Area under the curve (AUC) and 95% confidence intervals for the Barratt Impulsiveness Scale and the patient and clinician global scales.

Figure 3

Table 1 Repetition of self-harm within 6 months by risk-scale item (total episodes n = 483, repeated self-harm n = 145, 30%)

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