Isabelle Dubach
People on the autism spectrum have elevated mortality across the lifespan – their overall comparative mortality rate is about twice that of the general population, a new study reveals.
The comparative mortality of people with autism spectrum disorder is twice that of the general population, an Australian-first study by a UNSW PhD student and her supervisors has found. The researchers call for a whole of health and disability systems response to this issue to improve outcomes for this group.
In the big data study, the researchers analysed large linked datasets on death rates, risk factors and cause of death of 36,000 people on the autism spectrum in NSW. The results are published today in a leading academic journal in the field, Autism Research. The study was funded by the Cooperative Research Centre for Living with Autism (Autism CRC).
“Our key finding is that people on the autism spectrum have elevated mortality across the lifespan – their overall comparative mortality rate is about twice that of the general population,” says Professor Julian Trollor from UNSW Medicine and Chair, Intellectual Disability Mental Health.
“This is, of course, of great concern. While we only looked at NSW data, we’d expect to find the same patterns nationally.
"It’s important to note the results do not point to elevated mortality for autistic people as a result of their being on the spectrum. Rather, the results indicate there needs to be a greater understanding of autism and co-occuring conditions within the health services sector, and that more equitable access to health services needs to be a priority for government and health service providers.”
The study also identified factors that influence mortality risk.
“Risk of death was associated with autistic people’s health needs – people with co-occuring conditions such as chronic physical illness, epilepsy and mental health conditions were at a higher risk of death. People who also had an intellectual disability had a higher risk, too.
“These insights are helpful because targeted strategies can be developed for those at higher risk.
“Unexpectedly, and different to the general population, we didn’t find demographic factors such as gender and socioeconomic status to be predictors of risk of death.”
The team also found that the top causes of death were different for people on the autism spectrum.
“While the top causes of death in the general population were cancer and circulatory diseases, for people on the spectrum we found that injury and poisoning – which includes accidents, suicide and deaths related to self-harm – was the single biggest cause of death, with nervous system and sense disorders (such as epilepsy) a close second,” Professor Trollor says.
“Combined with the information about mental health being a risk factor for death, the higher proportion of deaths from injury and poisoning may point to unmet mental health needs that this group is experiencing. Overall the high risk of death in people on the autism spectrum is a troubling indicator of the range of health inequalities experienced by this population.”
Andrew Davis, Autism CRC CEO, says the data will be invaluable in helping create strategies to improve health services and outcomes for people on the autism spectrum.
“We generally don’t have a lot of data on mortality rates, risk factors and cause of death in people on the autism spectrum – this piece of work is the first known use of large linked datasets to investigate mortality and cause of death for people on the autism spectrum in Australia,” Andrew Davis says.
“This is an issue, as understanding the drivers of excess mortality is important for those on the spectrum – and for those who support them, such as family members, health professionals and policymakers. This is particularly important where the deaths may be preventable,” he says.
Autistic health advocate Kathy Isaacs says this study highlights that Australia needs to take immediate action to address the health inequalities experienced by autistic Australians.
“The results of this study should serve as a call to action for government and health service providers. Every single Australian deserves health care that is both readily accessible and accommodating of their individual needs, but this study confirms the sense within the autistic community that this is not what is happening – for this group in NSW, and for autistic Australians,” Ms Isaacs says.
The findings highlight the urgent need for better management of physical and mental health conditions, for health promotion that is responsive to the needs of those on the autism spectrum – and the importance of implementing better assessment, diagnosis and documentation of the needs of older adults on the autism spectrum, Ms Isaacs says.
“We need a comprehensive health and disability service response to this issue – a national autism strategy implemented at a high level and involving the entire system. We must train health practitioners right from an undergraduate level, and support a cultural shift which will ensure that autistic people are enabled to access health care more safely and effectively.
“From a broader perspective, we need to ensure that all of our system-level health promotion and preventative health programs are accessible, that the bare minimum goal of autism awareness is met for all staff, and finally, that people on the spectrum are consulted and involved at all stages of health policy development,” Ms Isaacs says.
The team members say they now want to take the analysis of the data further.
“We'd like to be able to take this data and work back to understand the broader health requirements and unmet needs of this group. More resources would allow us to analyse health service use, health conditions and outcomes of people on the autism spectrum – not just focusing on death but also on overall health and pathways,” Professor Trollor concludes.
Anyone seeking support and information about mental health can contact beyondblue on 1300 22 46 36. If you are experiencing distress and need crisis support, you can contact Lifeline on 13 11 14 or the Suicide Callback Service on 1300 659 467 or the Kids Helpline 1800 551 800.