Abstract
Objective
To estimate the health and financial burden of adverse childhood experiences (ACEs) in England and Wales.
Design
The study combined data from five randomly stratified cross-sectional ACE studies. Population attributable fractions (PAFs) were calculated for major health risks and causes of ill health and applied to disability adjusted life years (DALYs), with financial costs estimated using a modified human capital method.
Setting
Households in England and Wales.
Participants
15 285 residents aged 18–69.
Outcome measures
The outcome measures were PAFs for single (1 ACE) and multiple (2–3 and ≥4 ACEs) ACE exposure categories for four health risks (smoking, alcohol use, drug use, high body mass index) and nine causes of ill health (cancer, type 2 diabetes, heart disease, respiratory disease, stroke, violence, anxiety, depression, other mental illness); and annual estimated DALYs and financial costs attributable to ACEs.
Results
Cumulative relationships were found between ACEs and risks of all outcomes. For health risks, PAFs for ACEs were highest for drug use (Wales 58.8%, England 52.6%), although ACE-attributable smoking had the highest estimated costs (England and Wales, £7.8 billion). For causes of ill health, PAFs for ACEs were highest for violence (Wales 48.9%, England 43.4%) and mental illness (ranging from 29.1% for anxiety in England to 49.7% for other mental illness in Wales). The greatest ACE-attributable costs were for mental illness (anxiety, depression and other mental illness; England and Wales, £11.2 billion) and cancer (£7.9 billion). Across all outcomes, the total annual ACE-attributable cost was estimated at £42.8 billion. The majority of costs related to exposures to multiple rather than a single ACE (ranging from 71.9% for high body mass index to 98.3% for cancer).
Conclusions
ACEs impose a substantial societal burden in England and Wales. Policies and practices that prevent ACEs, build resilience and develop trauma-informed services are needed to reduce burden of disease and avoidable service use and financial costs across health and other sectors.
Keywords: public health, health economics, epidemiology
Strengths and limitations of this study.
Adverse childhood experiences (ACEs) are known to increase individuals’ risks of poor health across the life course, yet the financial burden they impose on national economies is largely unmeasured.
We combined primary data on ACEs and 13 health outcomes from five general population ACE surveys undertaken in England and Wales.
For each outcome, we generated population attributable fractions for cumulative ACE exposure and applied these to disability adjusted life years, which in turn allowed calculation of financial burden of ACEs using a modified human capital approach.
ACE data were retrospectively reported and may be affected by recall bias, while general household surveys by their nature are likely to exclude those that have suffered the greatest impact of ACEs (eg, homelessness, incarceration or premature death).
Although many major health outcomes were included in the study, data are not yet available on all health outcomes potentially associated with ACEs and financial estimates are likely to be conservative.
Introduction
Evidence linking adverse childhood experiences (ACEs) to the adoption of health risk behaviours and the development of mental and physical illness has burgeoned in recent years.1 The term ACEs is used to describe some of the most intense sources of stress that children can suffer while growing up, such as being maltreated, witnessing domestic violence or coping with parental substance abuse.2 Such experiences can have harmful effects on children’s developing neurological and physiological systems that can embed vulnerability to poor health and well-being. Thus repeated activation of the stress response system during childhood and a lack of responsive interaction with caring adults can impact on brain structure, neuroendocrine stress regulation, immune functioning and metabolic health, as well as social and emotional development.3 4 Consistent with such effects, ACEs have been associated with delayed child development (eg, cognitive and language skills), childhood health and behavioural conditions, the adoption of health risk behaviours (eg, substance use), mental illness (eg, depression), and early development of chronic health conditions (eg, cancer).1 5–8
Numerous studies have explored the health impacts and costs of specific ACEs such as child maltreatment.9–11 However, the ACE framework provides a mechanism for measuring a range of ACE types and the cumulative risks they impose at a population level.2 Studies using this approach show a dose–response relationship between the number of ACEs suffered and poor outcomes across multiple domains, including health, criminal justice, education and employment.12–15 Studies also show that most individuals who report having suffered any specific ACE type (eg, physical abuse) also report other ACE types.16 Consequently, prevention efforts focused on any individual ACE type are likely to have limited success if the range of other ACEs affecting families are left unaddressed. The rapid proliferation of awareness on the impacts of ACEs on the policy priorities of different sectors is driving multiagency action to enhance early intervention and develop trauma-informed services.17 18 However, such policy development requires an understanding of the financial costs of ACEs to society and consequently the potential gains to be made by preventing ACEs for future generations.
Estimates of the financial burden of ACEs are only just starting to emerge. A recent study estimated that the annual costs attributable to ACEs for four risk factors (smoking, alcohol use, drug use and obesity) and six causes of ill health (anxiety, depression, cancer, diabetes, cardiovascular disease and stroke) reached $581 billion in Europe and $748 billion in North America, equivalent to around 3% of each region’s gross domestic product (GDP).12 Here, we combine primary data from five ACE studies undertaken in England and Wales to develop national population attributable fractions (PAFs) for ACEs across an extended range of outcomes. We use these data to estimate the annual cost of the health burden resulting from the lifelong impact of ACEs on residents of England and Wales using a modified human capital model.
Methods
Primary data sources
We combined data from five cross-sectional ACE studies conducted across various geographies in England and Wales between 2012 and 2017.19–23 Summary information on each study is provided in online supplementary table S1. All studies used stratified random sampling approaches with lower super output area (LSOA; small geographical areas with a mean population of 1500) as the sampling unit. LSOAs were categorised into deprivation quintiles based on their ranking in the English24 or Welsh25 Indexes of Multiple Deprivation, both of which are composite measures including a range of economic and social indicators. Sample selection was stratified by region (as appropriate; see online supplementary table S1) then deprivation quintile based on the population profile of the relevant study area. Households in sampled areas were identified using the national postcode address file. In four studies, randomly selected households were sent a letter prior to researcher visits that provided information on the study and the opportunity to opt out. In one study,22 researchers randomly selected households in sampled LSOAs and provided study information materials at the door. Interviews were undertaken face to face at participants’ homes by professional market research companies using computer-assisted personal interviewing. Informed consent was obtained from all participants. Sensitive questions, including those on ACEs, were self-completed. Participation was voluntary and anonymous and only one resident participated per selected household (inclusion criteria: within age range, resident in the LSOA, cognitively able to participate in a face-to-face interview). Across the five samples, the weighted average compliance was 55.7% (see online supplementary table S1), with a total sample size of 15 658. For this study, data were restricted to individuals aged 18–69 with complete demographic and ACE data, resulting in a final sample of 15 285.
bmjopen-2019-036374supp001.pdf (167KB, pdf)
All questionnaires used the Centers for Disease Control and Prevention short ACE tool26 to collect data on nine ACEs occurring before the age of 18: physical abuse, sexual abuse, verbal abuse, parental separation, exposure to domestic violence, and household member alcohol abuse, drug abuse, mental illness and incarceration. For the purpose of analysis, and in line with previous studies,1 19–23 positive responses to ACE questions were summed and participants were allocated to an ACE count category: 0 ACE, 1 ACE, 2–3 ACEs and ≥4 ACEs. Questions used to determine ACEs and the 13 health outcomes analysed in this study are shown in online supplementary table S2. All studies provided data on smoking (current smoker), drug use (ever used heroin or crack cocaine) and violence (victimisation in the past year). Four studies provided data on alcohol use (current, ≥12 g per day), high body mass index (BMI, ≥25.0 kg/m2), and whether respondents had ever been diagnosed with cancer, type 2 diabetes, heart disease (coronary heart disease/heart attack), stroke or respiratory disease. One study provided data on whether respondents had ever been treated for depression, anxiety and other mental illness (see online supplementary table S3). Demographic variables included gender, age, ethnicity (self-assigned using UK census categories) and deprivation quintile.
Calculating PAFs
Statistical analysis was undertaken in SPSS V.23, with data editing and calculations undertaken in Excel. Binomial generalised linear modelling was used to calculate risk ratios (RRs) and 95% CIs associated with ACE count level for each health outcome, controlling for study sampling region, deprivation quintile of residence, gender, age and ethnicity (white or non-white). In line with cost estimates for global regions,12 we calculated PAF values at each ACE count level (1 ACE vs 0 ACEs; 2–3 ACEs vs 0 ACE; ≥4 ACEs vs 0 ACE) according to the following:
where α is the category of ACE count for the PAF in question, RRACE is the pooled RR associated with each ACE count, and PACE is the proportion of the sample exposed to each ACE count. Overall PAFs for ACEs were generated by summing the three PAF values.27 Separate PAFs were generated for England and Wales using regional ACE prevalence levels.
Calculating ACE-attributable costs
Consistent with previous studies,11 12 28 we used a modified human capital approach to calculate ACE-attributable costs associated with each health outcome. The human capital approach is a commonly used method in economic evaluations to calculate the cost of lost productivity to society as a result of separation of an individual from the labour force due to premature death or morbidity.29 Health outcomes were matched to risk factor and cause categories in the 2017 Global Burden of Disease Study30 (GBD; see online supplementary table S4). For each matched category, disability adjusted life years (DALY) estimates were extracted for England and Wales for age categories 15–49 years, 50–69 years and 70+ years. Previous cost estimates using a human capital approach have assumed one DALY is equal to a region’s GDP per capita and calculated costs based on DALYs × GDP per capita.11 12 28 GDP was not calculated separately for England and Wales; thus, we used the related measure of regional gross value added (GVA; equivalent to GDP plus subsidies less taxes on products), with GVA per capita (balanced, current basic 2017 prices) being £28 096 for England and £19 899 for Wales.31 PAFs were applied to the total cost (by UK region) for each risk factor and cause to estimate the economic value of DALYs by ACE level. The equivalent value of DALYs as a proportion of total GVA was also calculated. To estimate the total costs attributed to ACEs across all health outcomes studied, we excluded DALYs for risk factors that related to included causes of ill health (eg, those for alcohol use attributed to cancer). Sensitivity analyses were run limiting DALYs to individuals aged 15–69 years old, using the upper and lower bounds (uncertainty intervals) for DALYs (extracted from the GBD) and by generating PAFs using the upper and lower CIs for RRs.
Patient and public involvement
Patients and the public were not involved in the design or planning of the study.
Results
Demographics and ACE count levels of the individual and combined study samples are shown in online supplementary table S5. Across the combined samples, over half (54.9%) of participants were female and 85.7% were of white ethnicity. ACE prevalence levels (used to generate PAFs) were 53.1% for 0 ACE, 19.0% for 1 ACE, 15.2% for 2–3 ACEs and 12.6% for ≥4 ACEs in Welsh samples, and 56.2% for 0 ACE, 20.1% for 1 ACE, 15.4% for 2–3 ACEs and 8.4% for ≥4 ACEs in English samples.
RRs for each ACE count level and each health outcome are presented in table 1 (unadjusted proportions are provided in online supplementary table S6). All outcomes showed a graded relationship with ACEs, with RRs increasing as ACE count increased. Risks of alcohol use, smoking, drug use, violence and mental illness outcomes were increased in individuals with any level of ACEs. Risks of high BMI, heart disease and respiratory disease were increased in individuals with ≥2 ACEs, and risks of type 2 diabetes, cancer and stroke in those with ≥4 ACEs only.
Table 1.
1 ACE | 2–3 ACEs | ≥4 ACEs | |||||||
RR | 95% CI | P value | RR | 95% CI | P value | RR | 95% CI | P value | |
Risk factors | |||||||||
Alcohol use | 1.164 | 1.041 to 1.301 | 0.008 | 1.311 | 1.165 to 1.475 | <0.001 | 1.837 | 1.631 to 2.069 | <0.001 |
Smoking | 1.188 | 1.091 to 1.293 | <0.001 | 1.448 | 1.329 to 1.578 | <0.001 | 2.079 | 1.904 to 2.270 | <0.001 |
Drug use | 1.648 | 1.168 to 2.327 | 0.005 | 3.184 | 2.342 to 4.330 | <0.001 | 8.685 | 6.658 to 11.328 | <0.001 |
High BMI | 1.031 | 0.986 to 1.078 | 0.177 | 1.062 | 1.012 to 1.115 | 0.015 | 1.075 | 1.011 to 1.142 | 0.020 |
Causes of ill health | |||||||||
Depression | 1.560 | 1.305 to 1.865 | <0.001 | 2.137 | 1.820 to 2.509 | <0.001 | 2.766 | 2.374 to 3.223 | <0.001 |
Anxiety | 1.429 | 1.169 to 1.747 | <0.001 | 2.151 | 1.806 to 2.563 | <0.001 | 2.751 | 2.316 to 3.266 | <0.001 |
Other mental illness | 1.684 | 1.008 to 2.812 | 0.046 | 3.216 | 2.083 to 4.964 | <0.001 | 5.115 | 3.356 to 7.796 | <0.001 |
Violence | 1.383 | 1.107 to 1.728 | 0.004 | 2.955 | 2.448 to 3.566 | <0.001 | 5.625 | 4.745 to 6.667 | <0.001 |
Cancer | 1.009 | 0.800 to 1.273 | 0.937 | 1.101 | 0.854 to 1.419 | 0.459 | 2.078 | 1.588 to 2.720 | <0.001 |
Type 2 diabetes | 1.157 | 0.958 to 1.398 | 0.131 | 1.223 | 0.995 to 1.503 | 0.056 | 1.782 | 1.400 to 2.268 | <0.001 |
Heart disease | 1.102 | 0.836 to 1.453 | 0.492 | 1.415 | 1.072 to 1.868 | 0.014 | 1.928 | 1.366 to 2.722 | <0.001 |
Stroke | 1.238 | 0.800 to 1.918 | 0.338 | 1.427 | 0.906 to 2.250 | 0.125 | 2.705 | 1.660 to 4.409 | <0.001 |
Respiratory disease | 1.224 | 0.927 to 1.615 | 0.155 | 1.806 | 1.383 to 2.358 | <0.001 | 2.612 | 1.929 to 3.536 | <0.001 |
Analysis used generalised linear modelling controlling for study sampling region, deprivation quintile, age, gender and ethnicity.
Reference category: 0 ACE.
ACE, adverse childhood experience; BMI, body mass index; CI, confidence interval; RR, risk ratio.
The total PAFs for ACEs were slightly higher in Wales than in England for all outcomes due to higher ACE prevalence levels (table 2). Across the four risk factors, drug use had the highest PAFs due to ACEs (58.8% Wales, 52.6% England). However, smoking carried the highest ACE-attributable costs given the higher number of DALYs for this risk factor. ACE-attributable costs due to smoking were £7.4 billion in England and £466.5 million in Wales. High BMI had the lowest PAFs due to ACEs (2.4% Wales, 2.2% England), although ACE-attributable costs still reached £729.2 million in England and £35.3 million in Wales. Across causes of ill health, violence and mental illness had the highest PAFs due to ACEs, while cancer and type 2 diabetes had the lowest. ACEs were attributed to 48.9% of recent violence victimisation in Wales and 43.4% in England, with associated costs of £16.6 million and £355.0 million, respectively. Up to a third of depression and anxiety and almost half of other mental illnesses were attributed to ACEs, with associated costs across the three mental health outcomes being £465.3 million in Wales and £10.7 billion in England. Despite having low PAFs, high DALYs for cancer meant that this cause carried the greatest ACE-attributable costs across all individual outcomes measured, reaching £476.4 million in Wales and £7.5 billion in England.
Table 2.
Population attributable fraction | Total DALYs (age 15+) | DALYs attributable to ACEs | Total estimated cost (£ million)* |
Attributable costs by ACE count (£ million) |
||||||||||
1 ACE | 2–3 ACEs | ≥4 ACEs | All ACEs | 1 ACE | 2–3 ACEs | ≥4 ACEs | All ACEs | 1 ACE | 2–3 ACEs | ≥4 ACEs | All ACEs | |||
Alcohol use | ||||||||||||||
Wales | 0.026 | 0.040 | 0.089 | 0.156 | 38 114 | 999 | 1527 | 3404 | 5929 | 758.4 | 19.9 | 30.4 | 67.7 | 118.0 |
England | 0.029 | 0.042 | 0.061 | 0.131 | 606 086 | 17 297 | 25 199 | 36 972 | 79 467 | 17 028.6 | 486.0 | 708.0 | 1038.8 | 2232.7 |
Smoking | ||||||||||||||
Wales | 0.029 | 0.055 | 0.110 | 0.194 | 121 011 | 3474 | 6663 | 13 307 | 23 444 | 2408.0 | 69.1 | 132.6 | 264.8 | 466.5 |
England | 0.031 | 0.058 | 0.076 | 0.165 | 1 590 656 | 50 082 | 91 530 | 120 314 | 261 926 | 44 691.1 | 1407.1 | 2571.6 | 3380.3 | 7359.1 |
Drug use | ||||||||||||||
Wales | 0.051 | 0.137 | 0.400 | 0.588 | 22 518 | 1140 | 3090 | 9011 | 13 241 | 448.1 | 22.7 | 61.5 | 179.3 | 263.5 |
England | 0.062 | 0.159 | 0.306 | 0.526 | 331 956 | 20 459 | 52 832 | 101 413 | 174 704 | 9326.6 | 574.8 | 1484.4 | 2849.3 | 4908.5 |
High BMI | ||||||||||||||
Wales | 0.006 | 0.009 | 0.009 | 0.024 | 73 423 | 422 | 677 | 677 | 1775 | 1461.0 | 8.4 | 13.5 | 13.5 | 35.3 |
England | 0.006 | 0.009 | 0.006 | 0.022 | 1 203 925 | 7346 | 11 219 | 7388 | 25 954 | 33 825.5 | 206.4 | 315.2 | 207.6 | 729.2 |
Depression | ||||||||||||||
Wales | 0.071 | 0.115 | 0.149 | 0.335 | 16 161 | 1142 | 1865 | 2401 | 5407 | 321.6 | 22.7 | 37.1 | 47.8 | 107.6 |
England | 0.078 | 0.122 | 0.103 | 0.303 | 294 592 | 23 073 | 35 890 | 30 416 | 89 379 | 8276.9 | 648.3 | 1008.4 | 854.6 | 2511.2 |
Anxiety | ||||||||||||||
Wales | 0.055 | 0.119 | 0.150 | 0.324 | 12 434 | 684 | 1477 | 1861 | 4023 | 247.4 | 13.6 | 29.4 | 37.0 | 80.0 |
England | 0.061 | 0.126 | 0.104 | 0.291 | 203 872 | 12 452 | 25 606 | 21 239 | 59 297 | 5728.0 | 349.9 | 719.4 | 596.7 | 1666.0 |
Other mental illness | ||||||||||||||
Wales | 0.065 | 0.170 | 0.262 | 0.497 | 28 076 | 1832 | 4772 | 7347 | 13 951 | 558.7 | 36.5 | 95.0 | 146.2 | 277.6 |
England | 0.075 | 0.187 | 0.189 | 0.452 | 517 544 | 38 976 | 96 724 | 98 011 | 233 711 | 14 540.9 | 1095.1 | 2717.6 | 2753.7 | 6566.3 |
Violence | ||||||||||||||
Wales | 0.037 | 0.152 | 0.299 | 0.489 | 1703 | 63 | 260 | 509 | 832 | 33.9 | 1.3 | 5.2 | 10.1 | 16.6 |
England | 0.044 | 0.170 | 0.220 | 0.434 | 29 134 | 1270 | 4961 | 6404 | 12 635 | 818.6 | 35.7 | 139.4 | 179.9 | 355.0 |
Cancer | ||||||||||||||
Wales | 0.002 | 0.013 | 0.118 | 0.133 | 179 919 | 279 | 2397 | 21 263 | 23 939 | 3580.2 | 5.6 | 47.7 | 423.1 | 476.4 |
England | 0.002 | 0.014 | 0.082 | 0.097 | 2 725 146 | 4666 | 38 124 | 222 605 | 265 395 | 76 565.7 | 131.1 | 1071.1 | 6254.3 | 7456.5 |
Type 2 diabetes | ||||||||||||||
Wales | 0.026 | 0.029 | 0.085 | 0.140 | 23 306 | 597 | 681 | 1982 | 3260 | 463.8 | 11.9 | 13.5 | 39.4 | 64.9 |
England | 0.028 | 0.030 | 0.058 | 0.116 | 356 871 | 9939 | 10 802 | 20 707 | 41 448 | 10 026.6 | 279.2 | 303.5 | 581.8 | 1164.5 |
Heart disease | ||||||||||||||
Wales | 0.016 | 0.053 | 0.098 | 0.167 | 77 275 | 1243 | 4077 | 7556 | 12 877 | 1537.7 | 24.7 | 81.1 | 150.4 | 256.2 |
England | 0.018 | 0.055 | 0.067 | 0.140 | 1 049 623 | 18 461 | 57 674 | 70 352 | 146 487 | 29 490.2 | 518.7 | 1620.4 | 1976.6 | 4115.7 |
Stroke | ||||||||||||||
Wales | 0.034 | 0.049 | 0.163 | 0.246 | 39 189 | 1336 | 1926 | 6372 | 9634 | 779.8 | 26.6 | 38.3 | 126.8 | 191.7 |
England | 0.038 | 0.052 | 0.114 | 0.204 | 546 308 | 20 801 | 28 579 | 62 218 | 111 597 | 15 349.1 | 584.4 | 802.9 | 1748.1 | 3135.4 |
Respiratory disease | ||||||||||||||
Wales | 0.031 | 0.090 | 0.149 | 0.270 | 50 697 | 1570 | 4550 | 7545 | 13 664 | 1008.8 | 31.2 | 90.5 | 150.1 | 271.9 |
England | 0.034 | 0.095 | 0.104 | 0.233 | 784 621 | 27 000 | 74 559 | 81 386 | 182 945 | 22 044.7 | 758.6 | 2094.8 | 2286.6 | 5140.0 |
*Calculated as 1 DALY=GVA per capita (£19 899 Wales, £28 096 England; balanced, current basic prices, 2017).
ACE, adverse childhood experience; BMI, body mass index; DALY, disability adjusted life year; GVA, gross value added.
Across all nine causes of ill health, the total ACE-attributable cost was £33.9 billion (£1.7 billion for Wales and £32.1 billion for England). To calculate the total ACE-attributable cost across all risk factors and causes of ill health, we excluded DALYs from the four risk factors that related to included causes (eg, those for smoking related to cancer). The total ACE-attributable cost was £42.8 billion (£2.2 billion for Wales and £40.6 billion for England; table 3). These costs are equivalent to 3.5% of the total annual GVA in Wales and 2.6% in England (2.6% across the combined geographies). In sensitivity analysis (see the Methods section), combined estimated ACE-attributable costs for England and Wales ranged from £16.3 billion (equivalent to 1.0% of GVA) to £68.4 billion (4.2% of GVA; table 3).
Table 3.
ACE-attributable DALYs (thousands) | ACE-attributable costs (£ billion) |
Equivalent % of GVA | |||||||
England | Wales | England and Wales | England | Wales | England and Wales | England | Wales | England and Wales | |
Best estimate | 1444.9 | 110.0 | 1554.9 | 40.6 | 2.2 | 42.8 | 2.6 | 3.5 | 2.6 |
Limited to DALYs for individuals aged 15–69 years old | 956.4 | 69.5 | 1025.8 | 26.9 | 1.4 | 28.3 | 1.7 | 2.2 | 1.7 |
PAFs generated using lower CIs for RRs | 546.7 | 47.7 | 594.4 | 15.4 | 0.9 | 16.3 | 1.0 | 1.5 | 1.0 |
PAFs generated using upper CIs for RRs | 2314.3 | 169.0 | 2483.2 | 65.0 | 3.4 | 68.4 | 4.2 | 5.4 | 4.2 |
Lower bound (uncertainty interval) for DALYs | 1273.7 | 96.0 | 1369.8 | 35.8 | 1.9 | 37.7 | 2.3 | 3.1 | 2.3 |
Upper bound (uncertainty interval) for DALYs | 1638.6 | 126.0 | 1764.7 | 46.0 | 2.5 | 48.5 | 2.9 | 4.0 | 3.0 |
ACE, adverse childhood experience; DALY, disability adjusted life year; GVA, gross value added; PAF, population attributable fraction; RR, risk ratio.
Figure 1 shows the proportion of ACE-attributable costs for each outcome that were accounted for by 1, 2–3 and ≥4 ACEs. For cancer, the 1 ACE category accounted for only 1.7% of ACE-attributable financial costs, while the ≥4 ACEs category accounted for 84.2%. For other outcomes, the proportion of costs accounted for by the 1 ACE category ranged from 9.9% (violence) to 28.1% (high BMI), while the proportion accounted for by ≥4 ACEs ranged from 28.9% (high BMI) to 58.6% (drug use).
Discussion
In this study of 15 285 adults in England and Wales, we found a dose–response relationship between ACEs and all outcomes measured. Violence, mental illness and drug use had the highest PAFs due to ACEs, while mental illness, cancer and smoking carried the highest ACE-attributable costs. Across all outcomes studied, the total estimated annual ACE-attributable cost across England and Wales was £42.8 billion, equivalent to 2.6% of the total GVA in England and Wales and representing approximately £1800 per household per annum.32 The majority of these costs related to multiple ACE categories.
Comparison with other studies
There are no previous studies estimating the costs of ACEs in England and Wales. However, a study that generated PAFs for ACEs through meta-analyses of risk estimates in published literature estimated the annual costs of ACEs to be equivalent to 2.7% of GDP in Europe and 3.6% of GDP in North America.12 Other studies have measured the costs of specific ACEs, particularly violence against children, using similar human capital approaches. Such costs have been estimated to be equivalent to between 1.2% and 3.5% of subregional GDP in East Asia and the Pacific11; to 4.3% of GDP in South Africa33; and to 0.8% of GDP for physical abuse, 0.5% for emotional abuse and 0.4% for sexual abuse in China.34 In the UK, the lifetime cost per victim of non-fatal child maltreatment by a primary caregiver has conservatively been estimated at £90 000.35 However, this estimate excluded costs for several outcomes considered in our study, including those for cancer, type 2 diabetes and heart disease, due to no association being found between these conditions and the study’s single measure of child maltreatment. We found no associations between such conditions and the single ACE category, yet strong associations with multiple ACEs. Thus 98.3% of the ACE-attributable costs of cancer, 87.6% of those for heart disease and 76.3% of those for type 2 diabetes were accounted for by suffering more than one type of ACE.
Strengths and weaknesses of the study
We used an established methodology11 12 28 and based our approach on that used to estimate the financial burden of ACEs across Europe and North America.12 An acknowledged limitation of this previous study was the lack of consistency in study methodologies. Key strengths of the current study are the use of primary data and consistency in study methodologies, with all studies using representative household samples and the same set of questions to measure ACEs. However not all outcomes were measured in all studies, and mental illness was only measured in Wales,23 while some outcome measures could not be matched directly to GBD categories (see online supplementary table S4). Like previous ACE studies, the retrospective, self-reported nature of questions makes findings subject to recall issues and any reluctance to report historical experiences. Further, some population groups who may be at increased exposure to ACEs (eg, those incarcerated36 or homeless37) will have been under-represented and we could not account for individuals that had died prematurely through conditions related to ACEs. These biases may have led to reduced relative risks. Conversely, while ACEs made an overall significant contribution to GLMs (generalised linear models) for all outcomes, for some, RRs were not significant at all ACE levels. Further, our samples were restricted to adults aged 18–69 years, yet some conditions such as stroke occur predominantly in older age groups. Consequently sensitivity analyses were undertaken limiting DALYs to the 15–69 years age group and using lower and upper CIs for RRs. While we excluded DALYs for risk factors linked to included causes of ill health in calculating our overall cost estimates, it is beyond the ability of this study to calculate the actual burden of ACEs due to multiplicative relationships. However, our estimates of the costs of ACEs are likely to be conservative. While we included many key risks for, and causes of, ill health associated with ACEs, we did not account for other associated outcomes (eg, risky sexual behaviour, suicide, crime), nor for the burden of child deaths related to ACEs. A study of child death reviews in an English locality found evidence of at least one ACE in the records of 63% of children that died over a 4-year period and of at least four ACEs in 20% of cases.38 The lifetime cost of a child maltreatment death in the UK has been estimated at almost £1 million.35
Meaning of the study
Nearly half of all adults in England and Wales experienced some form of ACE as a child and around one in ten experienced ≥4 ACEs (see online supplementary table S5). This equates to approximately 20 million adults with any ACE and four million with ≥4 ACEs. Our results quantify the substantive proportion of common health-harming behaviours and long-term health conditions that are associated with ACEs, and consequently that could be avoided in future generations through offering better quality childhoods. Currently, however, an estimated 2.3 million children in England live in families with substantial complex needs and only a third of these children are receiving established support from statutory services.39 An imperative to increase expenditure on safe and nurturing childhoods is emphasised by findings that around a third of mental illness could be avoided if ACEs were either prevented or their impacts moderated through early intervention. Mental illness carries one of the highest costs to health systems in England and Wales40 and also creates substantial pressure on educational, social and criminal justice systems. For the latter in particular, strong relationships found here between ACEs and violence are an additional concern with many types of police-recorded violence increasing in England and Wales.41 Across all measured outcomes, we identify potentially avoidable costs from ACEs equivalent to more than a quarter of the UK’s annual government healthcare expenditure.42 The potential to avoid such costs is unrealised while the majority of health expenditure focuses on adults who have already developed pathologies. Evidence-based mechanisms to prevent ACEs and build resilience to their long-term harms are available, offering return on investments in years rather than decades through benefits on child development, health and education.43–46 The benefits of such interventions reach across sectors, and a whole of government approach could more immediately resource interventions capable of diminishing a current annual ACE burden of almost £43 billion.
Unanswered questions and future research
As with most ACE studies our data were collected retrospectively and consequently provide no information on the current levels of ACEs experienced by children in England and Wales. Options to measure ACE prevalence now form part of the international Health Behaviour in School-aged Children Survey47 but have not yet been used in the English or Welsh survey iterations, nor are such data routinely being collected through other major school-based surveys in the UK. While estimates of current exposure to some ACEs are available,39 routine measurement of ACEs in children is required to better understand their extent and sociodemographic and geographical distribution, as well as the impact of interventions to address them. Further, our findings identified that, despite having the lowest prevalence, the majority of costs generated by ACEs fall on those experiencing ≥4 ACEs (table 2). There is an urgent need to better understand the cumulative impact of ACEs on health outcomes across the life course, integrating epidemiology with fields including epigenetics, immunology and neurology. Equally, there is a critical need for knowledge on how services can become more trauma-informed, what impact trauma-informed service delivery can have, and how services for children and families affected by child maltreatment, substance abuse, domestic violence or incarceration, for instance, can be better integrated to provide a cohesive offer. Finally, as well as the core ACE categories included here, measurements of other childhood adversities such as neglect, parental bereavement, bullying and exposure to community level violence are increasingly being incorporated into the list of potential ACEs. Public services that recognise the impact of childhood adversity on lifelong health but neglect to implement preventative measures may yet feature in future lists.
Supplementary Material
Acknowledgments
We would like to thank all those involved in developing and implementing the individual studies that contributed to this study, and the English and Welsh residents who participated in the surveys.
Footnotes
Twitter: @keh444, @markabellis
Contributors: MAB and KH designed the study. MAB developed the statistical modelling, and KH, KF and CAS conducted the data analyses. KH wrote the manuscript with contributions from MAB, KF and RK. All authors reviewed the study findings and read and approved the final version before submission.
Funding: The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Disclaimer: The corresponding author attests that all listed authors meet the authorship criteria and that no others meeting the criteria have been omitted.
Competing interests: None declared.
Patient and public involvement: Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Patient consent for publication: Not required.
Ethics approval: Ethical approval for the 2017 Welsh national sample was obtained from Bangor University’s Healthcare and Medical Sciences Ethics Committee (BU230317), with ethical approval for all other studies obtained through the Liverpool John Moores University Research Ethics Panel (12/HEA/016; 13/HEA/052; 14/EHC/008; 14/EHC/0087). Additional approval for both Welsh surveys was provided by the Public Health Wales Research and Development Office.
Provenance and peer review: Not commissioned; externally peer reviewed.
Data availability statement: The data sets analysed in the current study are available from the corresponding author on reasonable request.
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Associated Data
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Supplementary Materials
bmjopen-2019-036374supp001.pdf (167KB, pdf)