Enrolment, Attendance, and Education Resourcing and Support among 5-12 year old Autistic Students in Aotearoa New Zealand: A Nationwide Cross-sectional Study
Main Article Content
Abstract
Introduction
Participation in education underpins positive lifelong outcomes, yet Autistic children often encounter barriers to enrolment, attendance, and access to support. Evidence indicates that systemic challenges such as inadequate support, limited autism-specific teacher training, and restricted access to resources contribute to disparities in educational outcomes. While small sample studies highlight these inequities, population-level evidence is limited.
Objectives
To quantify nationwide differences in school enrolment, attendance, and access to educational resourcing and support services between Autistic and non-Autistic children aged 5--12 years in Aotearoa New Zealand (NZ), and to examine variation by co-occurring intellectual disability (ID).
Methods
Cross-sectional analysis using NZ's Integrated Data Infrastructure, including all children aged 5--12 in 2019. Autism and ID were identified from hospital, mental health, and disability service use datasets. Outcomes included enrolment, attendance, and access to supports. Propensity score matching (1:10) compared Autistic and non-Autistic students across outcomes, including stratification by ID status.
Results
Among 517,872 students aged 5-12 years, 8,169 (1.6%) were Autistic and of those 28.8% had co-occurring ID. Compared to matched peers, Autistic children were less likely to be enrolled in school (94.9% vs. 97.4%; Prevalence ratio [PR]=0.97, 95% confidence interval [CI]=0.97-0.98) but more likely to be enrolled in specialist schools (14.4% vs. 0.2%; PR=70.15, 95% CI=65.73-74.88), Te Kura (2.1% vs. 0.2%; PR=9.65, 95% CI=8.22-11.34), or home-schooling (2.2% vs. 0.9%; PR=2.45, 95% CI=2.11-2.84). Regular attendance was lower (49.3% vs. 61.2; PR=0.80, 95% CI=0.79-0.82), with higher rates of chronic absence (7.7% vs. 3.2%; PR=2.45, 95% CI=2.27-2.64). Access to supports was significantly higher for Autistic students across a range of services. Disparities were often more pronounced among Autistic children with ID.
Conclusion
This study demonstrates significant differences in enrolment, attendance, and access to educational supports between Autistic and non-Autistic students in NZ, underscoring the urgent need for targeted and sufficiently resourced supports to ensure equitable participation.
Introduction
Participation in formal education is critical for children’s development and is strongly associated with a range of positive life outcomes. High levels of school attendance and academic achievement have been linked to higher employment rates and overall income, reduced involvement in the criminal justice system, and enhanced mental health and quality of life [1–3].
Autistic students experience a range of differences that can affect their participation in formal education. These can include differences in communication and social interaction, sensory processing, and higher rates of co-occurring mental (e.g., anxiety, attention-deficit/hyperactivity disorder) and physical health conditions (e.g., epilepsy) [4–11]. These individual-level factors are often exacerbated by structural and systemic barriers to accessing education (e.g., inadequate resourcing of specialist support), lack of inclusive environments and curriculums, practices that fail to accommodate the needs of Autistic students, and inadequate autism-specific teacher training [8, 12–14].
As a consequence of these barriers, Autistic students often experience lower levels of participation in education. This includes comparatively low rates of school enrolment [15, 16], irregular attendance, and higher rates of chronic absence, compared to their non-Autistic peers [13, 17–19]. Moreover, Autistic students are more likely to encounter social difficulties, including higher rates of peer exclusion, bullying [20–22], and feelings of loneliness [23, 24]. These experiences can further exacerbate difficulties accessing the curriculum, maintaining motivation, and managing school-related stress [25].
Due to increasing recognition of the challenges faced by Autistic students and the importance of educational engagement and attainment, it is crucial that these students have access to services and supports that facilitate their participation. Indeed, research shows that in-school support and adequate resourcing may improve educational, social, and mental health outcomes for Autistic youth [14, 26–30].
In Aotearoa New Zealand (NZ), in-school resourcing and support is provided via a range of Government-funded, Ministry of Education (MoE)-delivered individualised and school-based funding mechanisms, including School High Health Needs Funding (SHHNF), early intervention services, Interim Response Funding (IRF), and specialist Communication, Behaviour and Attendance Services (see Methods). The most comprehensive individual-level funding stream is the Ongoing Resourcing Scheme (ORS) which supports students with high and complex learning needs by providing access to specialist teachers, tailored resources, and support staff (e.g., teacher aides) to facilitate participation in schooling. Other funding supports may be directed toward specialist teacher training (e.g., Incredible Years teacher programme, Tilting the Seesaw for Teams, and learning support study awards to enable teachers to complete a specialist teaching qualification; [31–33]), tailored educational materials, and access to community services (e.g., public health nurse, mental health services). These initiatives aim to create an inclusive environment that addresses the diverse needs of students, and support school attendance, social inclusion, and academic achievement. Indeed, ORS funding was found to be associated with a reduced likelihood of suspension among Autistic children in NZ, highlighting the importance of providing appropriate resourcing and support for these students [27].
While there is evidence of the benefits of additional educational resourcing and supports for Autistic students [26, 27, 34], existing research predominantly focuses on short-term outcomes, settings that are not educationally based (e.g., participants’ homes, laboratories), and relies heavily on small, non-representative samples [26]. This limits the generalisability of findings and often overlooks broader indicators of school participation and equity in access to educational supports. There is a scarcity of population-level research that systematically examines the multidimensional aspects of education for Autistic children using objective, administrative data sources. A recent systematic review on quantitative educational outcome research for Autistic students concluded that more research is needed to capture outcomes beyond academic attainment for this population [35].
This study addresses the lack of population-level evidence on educational access and support for Autistic students. The Stats NZ Integrated Data Infrastructure (IDI) is used to link health, education and social data, enabling the first nationwide analysis of school enrolment, attendance, and access to supports among Autistic students, with comparisons to non-Autistic peers and disaggregation by co-occurring intellectual disability (ID). This distinction is critical, as educational experiences and outcomes differ markedly for Autistic children with ID compared with those without ID [36]. The analysis provides comprehensive evidence on the scale and nature of educational inequities, demonstrates the potential of linked administrative data for monitoring disability equity in education, and generates policy-relevant insights into systematic shortcomings and opportunities for reform to create more inclusive schooling.
Methods
Study design and participants
This study was a nationwide retrospective cohort analysis that utilised individual level linked administrative data from the SNZ-IDI (see below for detail). The study population consisted of the SNZ-IDI estimated resident population (IDI-ERP) of all children aged 5–12 years in NZ for the 2019 calendar year, the most recent full school year of data available, unaffected by the COVID-19 Pandemic. The calendar year was chosen as this aligns with the NZ school year. This age range was selected to align with the typical schooling years for primary and intermediate education in NZ. However, compulsory education does not technically start until 6 years of age. Age was determined as of December 31, 2019. The IDI-ERP was derived using established methodologies for estimating resident populations within the SNZ-IDI framework [37]. In brief, this population is constructed by combining activity signals across multiple administrative datasets (e.g., health, education, tax, and border movements) and applying rules to determine whether an individual is likely to be a usual resident of NZ at a given reference point.
Data sources
All data were accessed through the SNZ-IDI, a secure, whole-of-population research database that links de-identified administrative and survey data from multiple government agencies using encrypted identifiers. Linkage in the SNZ-IDI occurs through deterministic matching using unique identifiers when available (e.g. National Student Number) and through probabilistic matching using name, date of birth, and sex, when deterministic linkage is not possible [38]. The IDI enables researchers to follow individuals over time and across sectors while ensuring privacy through the Five Safes framework (safe people, projects, settings, data, and outputs). The IDI covers nearly all usual NZ residents, allowing analyses that are both comprehensive and population-level.
Health data were sourced from routinely collected administrative datasets, including the National Minimum Dataset (NMDS) for publicly funded hospital discharges, the Programme for the Integration of Mental Health Data (PRIMHD) for specialist mental health service contacts, and Socrates, the national system used to administer and record Ministry of Health–funded disability support services. Education data were drawn from the MoE’s ENROL (enrolment) system, attendance collections, and the School Leavers dataset, as well as funding and support service records. These data are collected by service providers and reported to the MoE for administrative purposes.
Demographic variables were obtained from the Personal Details and Address Notification tables, which are derived from multiple administrative sources including birth registrations, health enrolments, and tax records. The Personal Details table provide basic demographic information such as sex, date of birth, and ethnicity, while the Address Notification table contains tracking of individuals’ usual residential addresses over time. The address notifications are sourced primarily from interactions with health, tax, and education systems, supporting consistent geographic assignment (e.g., deprivation index, region) for each individual at specific points in time.
Autism
To identify Autistic individuals, a well-established case ascertainment method was applied [39]. This approach identifies only those children and young people with a recorded autism diagnosis, based on diagnostic data from NMDS, PRIMHD, and Socrates. An individual was classified as Autistic if an autism diagnosis code appeared in any of these datasets at any point from birth onward (see Appendix Table 1 for further details). Those without such a diagnosis code were categorised as non-Autistic (general population); however, this group will include some Autistic children who do not have a recorded diagnosis. This methodology has been increasingly used in NZ-based research, however, it has not undergone formal validation [40–44].
Intellectual disability
The identification process for co-occurring intellectual (or learning) disability (hereafter referred to as ID) followed a methodology similar to that used for autism detection, based on an established approach [39]. Among the Autistic group, diagnostic data from PRIMHD, NMDS, and Socrates were reviewed. An individual was classified as having an ID if a relevant diagnosis code was present in any of these datasets (see Appendix Table 2 for further details).
Education outcomes
A range of educational outcomes were generated for the cohort across the following three sub-categories: school enrolment; school attendance; and supports and services.
School enrolment
Binary indicators for school enrolment (both public and private), specialist school enrolment (public), home-schooling, and Te Kura (public correspondence school providing distance education for students who are unable to attend a local school or require flexible, individualised learning) enrolment were generated using MoE enrolment data. Enrolment data covered the full 2019 calendar year, capturing any school moves that occurred during this period; as a result, students could appear in multiple enrolment categories if they changed schooling arrangements across the year. An individual was classified as being enrolled in school if there was a record of enrolment any time during the 2019 calendar year. Likewise, if there was a record of specialist school enrolment, home-schooling, or Te Kura enrolment during the 2019 calendar year, those respective indicators were set to ‘1’.
School attendance
School attendance data were captured from the SNZ-IDI code module table for school attendance which are sourced from the MoE. Four binary indicators of attendance were created in line with standard metrics used to track school attendance in NZ [45]. These included regular attendance: present for more than 90% of half-days; irregular absence: present for between 80-90% of half-days; moderate absence: present for between 70-80% of half-days; and chronic absence: present for 70% or less of half-days. A half-day of attendance is defined as being present for a minimum of two hours in the morning or afternoon.
Funding supports and services
A range of education-based funding supports and services measures were explored, as described below. It is important to note that each support and service has its own eligibility criteria. Therefore, it is possible, and in many cases likely, that not all students who would benefit from them are able to access them. In contrast, others may be receiving multiple supports and services. Binary indicators for each of the funding support and service measures were established using data from the MoE interventions table.
Ongoing Resourcing Scheme (ORS)
The ORS provides funding for students with significant and complex long-term needs. The funding is allocated based on the individual needs of each student, as assessed by certified assessors from the MoE, and it is not influenced by the student’s location or school. However, eligibility is narrow, and only 1.2% of students receive ORS funding [27]. This funding is given to schools to employ teacher aides, and/or specialist teachers, and to source necessary materials to facilitate learning alongside other students. Additionally, specialists such as speech-language therapists, psychologists, and occupational therapists may provide further assistance. However, funding is often not sufficient to cover the full costs of support in practice, as it does not meet the expense of a full-time teacher aide and requires schools to top up shortfalls from their own budgets. Once initiated, ORS funding continues throughout the student’s schooling, although the funded amount may be reduced. For this reason, a student was considered to be ORS funded if an ORS start date was recorded prior to 31 December 2019, regardless of whether the funding began several years earlier.
School High Health Need Fund (SHHNF)
The SHHNF supports students with their health needs at school while helping them to optimally manage their own care needs. When students have a high health need and care and support is needed for more than 6 weeks, the SHHNF contributes towards the employment of a teacher aide.
Early intervention services
Early intervention services offer assistance to children with high needs from birth until they start school. This includes support in the transition into school, with a gradual handover to school-based services. Services are available to parents, families, and teachers to help develop a plan for the child’s involvement in education. Early intervention teams collaborate with families and early childhood educators who seek help regarding concerns about a child’s learning and development.
Interim Response Funding (IRF)
IRF provides short-term financial support to help keep students engaged in learning following a challenging event while a more comprehensive plan is developed. This funding has been utilised in cases of severe student behaviour that poses harm; distress among students, staff, families, or the community; and when school leadership has exhausted all available resources and strategies.
Communication service
The Communication Service is a specialised support service designed to assist children who have significant speech, language, and communication needs. This service provides expert help from speech-language therapists who work with children, their families, and educators to develop tailored strategies and interventions. The aim is to enhance the child’s ability to communicate effectively, which is crucial for their overall learning and social interaction. This service is targeted to students aged 5-8 years.
Behaviour service
The Behaviour Service is a dedicated service aimed at supporting children and young people who exhibit challenging behaviours that impact their learning and social interactions. This service involves collaboration between specialist staff, including psychologists and behaviour specialists, who work closely with students, families, and educators to develop individualised behaviour plans. The goal is to help students develop self-regulation, social skills, and resilience, enabling them to engage more effectively in their education and improve their overall well-being.
Resource Teacher Learning Behaviour (RTLB)
RTLB is a specialised service aimed at assisting students who face significant challenges in learning and behaviour. RTLBs are trained educators who work collaboratively with teachers and schools to develop and implement strategies tailored to individual student needs. The service focuses on enhancing the educational outcomes of students by providing targeted interventions, professional guidance, and resources to schools.
Attendance services
Attendance Services is a programme dedicated to promoting and improving school attendance among students. This service works to identify and address barriers to regular school attendance, ensuring that every child has the opportunity to participate fully in their education.
Sociodemographic measures
Sex (male/female) and ethnicity data were sourced from the personal details table. Due to the lack of available data on non-binary gender identities, sex was classified as either male or female. Ethnicity was determined using the total response method, allowing individuals to identify with multiple ethnic groups. Participants were categorised into three groups: Māori (the indigenous people of NZ), Pacific, and non-Māori/non-Pacific (NMNP), based on three distinct binary variables, meaning some individuals were counted in both the Māori and Pacific groups where they identified as such. Data on neighbourhood-level deprivation and urban/rural classification were obtained from the residential address meshblock, recorded in the address notification table as of December 31, 2019. Deprivation was assessed using the 2018 New Zealand Index of Deprivation (NZDep) [46], which aggregates a range of Census-derived indicators including employment, income, education, and home ownership into a single index. This index was collapsed into quintiles, with one representing the least deprived areas and five indicating the most deprived. Urban or rural residence was classified using Stats NZ’s standard urban/rural classification, where rural areas can be conceptualised as locations with fewer than 1,000 residents [47].
Statistical analysis
Initially the participant population was described including their sociodemographic characteristics, stratified by autism and co-occurring ID status. To facilitate comparison of education outcomes, matched samples of non-Autistic children were drawn from the 2019 IDI-ERP, separately for the overall Autistic population, Autistic population without ID, and Autistic population with ID. Propensity score matching was used to select these non-Autistic counterparts, employing the ‘MatchIt’ package (version 3.0.2) in R with a nearest-neighbour one-to-ten matching strategy [48]. Matches were selected without replacement based on age in years, sex, ethnicity, deprivation level, and urban/rural residence. Individuals with an autism diagnosis or missing data in any matching variable were excluded from the comparison pool. Balance on matching variables was assessed and confirmed. This matching approach was chosen to create directly comparable groups with similar demographic profiles, providing clearer descriptive contrasts than regression-based adjustments alone. Prevalence ratios (PR) with 95% confidence intervals (CIs) were reported. Reporting of results were informed by RECORD guidelines [49].
Community involvement
This research actively engaged members of the Autistic and autism communities. This includes co-authors who are Autistic, family of Autistic people, and professionals working in health and education that support Autistic people.
Results
The 2019 IDI-ERP contained 517,872 children aged 5–12 years, of whom 8,169 (1.6%) were identified as Autistic. Among the Autistic population, 2,349 (28.8%) had a co-occurring ID. The demographic characteristics of the study population, stratified by autism and ID status, are presented in Table 1. Compared to non-Autistic children, Autistic children were more likely to be male (79.5% vs. 51.0%), less likely to identify as Pacific (11.9% vs. 14.4%), and less likely to live in the least deprived (18.3% vs. 21.5%) or rural areas (11.6% vs. 13.9%). Within the Autistic population, those with a co-occurring ID were more likely to be Pacific (19.7% vs. 8.8%), reside in areas of the highest level of deprivation (29.9% vs. 20.1%), and less likely to live in rural areas (8.2% vs. 12.9%), relative to Autistic children without ID.
| Non-Autistic | Autistic | Autistic without ID | Autistic with ID | ||||||||
| n | % | n | % | n | % | n | % | ||||
| Total | 509,703 | 8,169 | 5,820 | 2,349 | |||||||
| Sex | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Female | 249,957 | 49.0 | 1,677 | 20.5 | 1,191 | 20.5 | 486 | 20.7 | |||
| Male | 259,746 | 51.0 | 6,492 | 79.5 | 4,629 | 79.5 | 1,863 | 79.3 | |||
| Age (years) | |||||||||||
| 5-6 | 120,996 | 23.7 | 1,818 | 22.3 | 1,269 | 21.8 | 549 | 23.4 | |||
| 7-9 | 193,593 | 38.0 | 3,183 | 39.0 | 2,244 | 38.6 | 939 | 40.0 | |||
| 10-12 | 195,114 | 38.3 | 3,168 | 38.8 | 2,307 | 39.6 | 861 | 36.7 | |||
| Ethnicity | |||||||||||
| Māori | 141,018 | 27.7 | 2,262 | 27.7 | 1,578 | 27.1 | 684 | 29.1 | |||
| Pacific | 73,173 | 14.4 | 972 | 11.9 | 510 | 8.8 | 462 | 19.7 | |||
| NMNP | 319,086 | 62.6 | 5,325 | 65.2 | 3,963 | 68.1 | 1,362 | 58.0 | |||
| Deprivation | |||||||||||
| 1 (least deprived) | 109,587 | 21.5 | 1,491 | 18.3 | 1,116 | 19.2 | 375 | 16.0 | |||
| 2 | 96,150 | 18.9 | 1,506 | 18.4 | 1,104 | 19.0 | 402 | 17.1 | |||
| 3 | 91,338 | 17.9 | 1,509 | 18.5 | 1,131 | 19.4 | 378 | 16.1 | |||
| 4 | 90,864 | 17.8 | 1,659 | 20.3 | 1,209 | 20.8 | 450 | 19.2 | |||
| 5 (most deprived) | 111,528 | 21.9 | 1,869 | 22.9 | 1,167 | 20.1 | 702 | 29.9 | |||
| Urban/Rural | |||||||||||
| Urban | 429,474 | 84.3 | 7,107 | 87.0 | 4,983 | 85.6 | 2,124 | 90.4 | |||
| Rural | 70,959 | 13.9 | 945 | 11.6 | 753 | 12.9 | 192 | 8.2 | |||
Table 2 presents rates of educational outcomes and propensity score matched PR and 95% CIs for key educational outcomes among Autistic and non-Autistic children (see Supplementary Appendix Table 3 for observed educational outcomes). Autistic children were less likely to be enrolled in school compared to their non-Autistic peers (94.9% vs. 97.4%, PR = 0.97; 95% CI: 0.97–0.98), indicating a small but significant difference in overall school participation. However, they were significantly more likely to be enrolled in specialist schools (14.4% vs. 0.2%, PR = 70.15; 95% CI: 65.73–74.88), be enrolled in Te Kura (2.1% vs. 0.2%, PR = 9.65; 95% CI: 8.22–11.34), and to be home-schooled (2.2% vs. 0.9%, PR = 2.45; 95% CI: 2.11–2.84).
| Autistic | Non-Autistic | Autistic/non-Autistic | |
| n (%) | n (%) | PR (95% CI) | |
| Enrolment | |||
|---|---|---|---|
| School enrolment | |||
| Yes | 7,629 (94.9) | 78,303 (97.4) | 0.97 (0.97, 0.98) |
| No | 411 (5.1) | 2,064 (2.6) | |
| Specialist School enrolment | |||
| Yes | 1,158 (14.4) | 165 (0.2) | 70.15 (65.73, 74.88) |
| No | 6,882 (85.6) | 80,202 (99.8) | |
| Te Kura | |||
| Yes | 168 (2.1) | 174 (0.2) | 9.65 (8.22, 11.34) |
| No | 7,872 (97.9) | 80,193 (99.8) | |
| Home school | |||
| Yes | 177 (2.2) | 723 (0.9) | 2.45 (2.11, 2.84) |
| No | 7,863 (97.8) | 79,644 (99.1) | |
| Attendance | |||
| Regular attendance | |||
| Yes | 3,960 (49.3) | 49,176 (61.2) | 0.80 (0.79, 0.82) |
| No | 4,080 (50.7) | 31,191 (38.8) | |
| Irregular attendance | |||
| Yes | 1,710 (21.3) | 16,659 (20.7) | 1.03 (0.98, 1.07) |
| No | 6,330 (78.7) | 63,708 (79.3) | |
| Moderate attendance | |||
| Yes | 645 (8.0) | 4,329 (5.4) | 1.49 (1.38, 1.6) |
| No | 7,395 (92.0) | 76,038 (94.6) | |
| Chronic attendance | |||
| Yes | 621 (7.7) | 2,538 (3.2) | 2.45 (2.27, 2.64) |
| No | 7,419 (92.3) | 77,829 (96.8) | |
| Funding supports and services | |||
| ORS | |||
| Yes | 2,460 (30.6) | 540 (0.7) | 45.54 (43.9, 47.23) |
| No | 5,580 (69.4) | 79,827 (99.3) | |
| SHHNF | |||
| Yes | 210 (2.6) | 312 (0.4) | 6.73 (5.85, 7.74) |
| No | 7,830 (97.4) | 80,055 (99.6) | |
| IRF | |||
| Yes | 147 (1.8) | 249 (0.3) | 5.9 (4.99, 6.98) |
| No | 7,893 (98.2) | 80,118 (99.7) | |
| Early intervention | |||
| Yes | 1,062 (13.2) | 1,131 (1.4) | 9.39 (8.86, 9.94) |
| No | 6,978 (86.8) | 79,236 (98.6) | |
| Behaviour service | |||
| Yes | 618 (7.7) | 762 (0.9) | 8.11 (7.5, 8.77) |
| No | 7,422 (92.3) | 79,605 (99.1) | |
| Communication service | |||
| Yes | 663 (8.2) | 1,287 (1.6) | 5.15 (4.78, 5.55) |
| No | 7,377 (91.8) | 79,080 (98.4) | |
| RTLB | |||
| Yes | 672 (8.4) | 1,131 (1.4) | 5.94 (5.52, 6.4) |
| No | 7,368 (91.6) | 79,236 (98.6) | |
| Attendance services | |||
| Yes | 183 (2.3) | 1,491 (1.9) | 1.23 (1.06, 1.42) |
| No | 7,857 (97.7) | 78,876 (98.1) | |
School attendance rates differed significantly between groups. Regular school attendance was lower among Autistic children compared to their non-Autistic peers (49.3% vs. 61.2%, PR = 0.80; 95% CI: 0.79–0.82). The rate of moderate absence (i.e., attending 70-80% of school days) was significantly elevated among Autistic children (8.0% vs. 5.4%, PR = 1.49; 95% CI: 1.38–1.60), and chronic absence was more than twice as high in Autistic students compared to non-Autistic students (7.7% vs. 3.2%, PR = 2.45; 95% CI: 2.27–2.64), reflecting a pronounced risk of sustained school absence.
Autistic children were substantially more likely to receive funding supports and services than their non-Autistic peers. ORS funding was nearly 46 times more likely among Autistic students (30.6% vs. 0.7%, PR = 45.54; 95% CI: 43.90–47.23). Other funding schemes also showed significant disparities, including the School High Health Needs Fund (2.6% vs. 0.4%, PR = 6.73; 95% CI: 5.85–7.74) and Interim Response Fund (1.8% vs. 0.3%, PR = 5.90; 95% CI: 4.99–6.98). Autistic children were significantly more likely to access early intervention services (13.2% vs. 1.4%, PR = 9.39; 95% CI: 8.86–9.94), while participation in behaviour services was also significantly higher (7.7% vs. 0.9%, PR = 8.11; 95% CI: 7.50–8.77). Similarly, the use of the Resource Teacher Learning and Behaviour (RTLB) service was significantly more common among Autistic students (8.4% vs. 1.4%, PR = 5.94; 95% CI: 5.52–6.40). However, attendance service utilisation was only slightly higher in Autistic children (2.3% vs. 1.9%, PR = 1.23; 95% CI: 1.06–1.42).
Educational outcomes for Autistic populations, both with and without co-occurring ID compared to their matched non-Autistic counterparts, were broadly consistent with those observed in the overall Autistic population and their matched non-Autistic peers (see Figures 1–3 and Supplementary Appendix Table 4). A notable exception was that while specialist school enrolment was significantly higher in both Autistic groups, it was notably higher among Autistic children with ID (46.5% vs. 4.5%, PR = 10.42; 95% CI: 9.81–11.07). In contrast, Autistic children without ID had higher relative rates of home-schooling compared to Autistic children with ID.
Figure 1: Propensity score matched enrolment rate ratios comparing Autistic, Autistic without ID and Autistic with ID to matched non-Autistic samples.
Figure 2: Propensity score matched attendance rate ratios comparing Autistic, Autistic without ID and Autistic with ID to matched non-Autistic samples.
Figure 3: Propensity score matched funding supports and services rate ratios comparing Autistic, Autistic without ID and Autistic with ID to matched non-Autistic samples.
School attendance patterns showed lower regular attendance and higher rates of absenteeism in both Autistic groups with marginal variation between Autistic students with and without ID.
There were some marked disparities in the receipt of educational supports and services between Autistic students with and without ID. ORS funding was substantially more common, among Autistic children with ID (26.3% vs. 0.3%, PR = 96.54; 95% CI: 75.26–123.83). Access to the SHHNF, early intervention, behavioural, communication, and attendance services was consistently higher for both Autistic groups compared to non-Autistic peers, with PRs often exceeding five. Notably, Autistic children without ID were more likely to use attendance services (PR = 1.46; 95% CI: 1.35–1.58), whereas Autistic children with ID used these slightly less than their matched counterparts (PR = 0.86; 95% CI: 0.76–0.97).
ORS = Ongoing Resourcing Scheme; SHHNF = School High Health Needs Fund; IRF = Interim Response Fund; RTLB = Resource Teacher Learning Behaviour.
Discussion
This nationwide cross-sectional study used linked SNZ-IDI data to examine school enrolment, attendance, and access to funding supports and services among 5-12 year old Autistic children with and without ID, and their non-Autistic peers. The findings revealed that Autistic students were less likely to be enrolled in mainstream education; more likely to be enrolled in specialist schools, Te Kura, or be home-schooled; and exhibited higher rates of absenteeism compared to their non-Autistic peers. Additionally, Autistic students were significantly more likely to receive funding supports and services. These differences were particularly pronounced among Autistic children with an ID, highlighting both the complexity of their educational needs and the efforts to address these through targeted resources and individualised support.
Interpretation of findings
The findings pertaining to enrolment align closely with patterns observed in extant literature [15, 16, 22]. Mainstream schools often pose challenges for Autistic students due to learning, social and sensory processing differences and a lack of appropriate supports and accommodations [50]. These challenges can result in high levels of anxiety, school avoidance and withdrawal [14, 22]. As a result, many families opt for specialist education environments that may be better equipped to respond to the individualised needs of their children [51], or turn to home or correspondence schooling when mainstream options are perceived to be inadequate [52]. It can often be the case that parents feel forced into these decisions out of necessity rather than preference, highlighting a lack of inclusion, resourcing and support within mainstream schools for Autistic learners [52, 53] that may be particularly amplified among those with an ID.
These enrolment patterns are mirrored in school attendance data, where Autistic students not only attend school less frequently than their non-Autistic peers, but are disproportionately represented among those with particularly high absenteeism. While enrolment provides a basic indicator of participation, attendance offers a more sensitive measure of ongoing engagement, which likely accounts for the larger differences observed. These attendance patterns may point to many of the same systemic barriers that shape enrolment decisions and are consistent with existing evidence of low attendance among Autistic students [12, 17]. The finding that Autistic children with ID are more likely to attend specialist schools and, at the same time, record lower rates of absenteeism than their Autistic peers without ID further underscores issues of educational fit. It suggests that mainstream environments may not adequately meet the needs of Autistic students, whereas specialist schools appear to provide more supportive and accommodating settings, particularly for those with greater learning differences, enabling more consistent attendance. While this study cannot identify the factors driving observed patterns, these findings suggest that both enrolment and attendance disparities reflect broader systemic barriers within mainstream education and underscore the need for further research that interrogates factors associated with these educational outcomes.
The comprehensive set of findings on education-based funding supports and services among Autistic compared to non-Autistic students is a first for NZ and novel internationally. These findings are comparable to a NZ Ministry of Education report that explored a similar set of supports and services among disabled learners [54]. Likewise, international research quantifying levels of education-based supports, while sparse, demonstrated higher rates of speech and language therapy, occupational therapy and other specialist supports (e.g., computer software or hardware and transportation) among Autistic compared to non-Autistic students [55].
While technically access to funding supports is needs based and does not require a diagnosis, the reality is that a diagnosis is likely to enable better access to support. A diagnosis itself is not mandatory, but the information contained in diagnostic assessment reports can be invaluable in helping parents and school teams describe and evidence a child’s needs when applying for funding. It can also provide a foundation for advocacy and may connect families and schools with autism-specific services and supports. As a result, access to many supports still effectively hinges on having a formal diagnosis, meaning the study findings reflect not only differences in need but also inequities in recognition and service access. However, given the cross-sectional nature of these data, the direction of this relationship cannot be determined: while diagnosis may facilitate access to supports, it is also plausible that receiving additional supports within schools could prompt referrals to health services, ultimately leading to a formal diagnosis.
While these findings indicate relatively high levels of targeted investment in support services, lower rates of mainstream school enrolment and elevated absenteeism among Autistic students suggest they may still not be receiving the levels or type of support necessary to ensure equitable access, inclusion, and sustained engagement in mainstream education. Given that funding is often allocated according to the complexity of children’s learning and communication needs, and with thresholds for eligibility set very high, it is unsurprising that children with ID received higher rates of early, ongoing, and individualised supports (e.g., ORS, early intervention, communication services) than their non-Autistic peers, while Autistic children without ID were more likely to receive attendance service involvement, reflecting their higher rates of non- or limited attendance.
Policy implications
The data presented in this study do not identify the reasons for disparities in enrolment or attendance rates. However, they highlight the need for a multi-pronged evidence-informed solution, coordinated across school- and system-levels, and supported by targeted investment. At the individual level, education should prioritise personalised learning and assessment approaches and environments that respond to the diverse needs, preferences, and interests of Autistic students. This may include flexible models of assessment and teaching, sensory accommodations, and modifications to the learning environment. School-wide inclusion must be reinforced through strong leadership, adequate resourcing, professional development, and whole-school strategies that foster belonging and reduce barriers (e.g., bullying). Finally, at the systems level, equitable diagnostic pathways, sustained investment in specialist services, and evidence-informed practice frameworks are fundamental, and must be co-designed and developed alongside Autistic people.
Evidence from NZ and internationally shows that early, school-based, targeted supports can enhance educational outcomes, buffer against exclusion, and support consistent attendance [26, 27, 56, 57]. However, mainstream educational systems often struggle to provide such support. Recent commitments in Budget 2025, the NZ Government’s annual fiscal plan outlining national spending priorities, included a $746.7 million funding commitment. This includes the extension of the Early Intervention Service into Year 1, increasing funded teacher aide hours, the roll-out of Learning Support Coordinators to all Year 1–8 schools, increased funding and structural reform of ORS, and investment in workforce development [58]. This presents a unique opportunity to enhance school attendance and engagement. However, equitable uptake, effective implementation, and rigorous population-level evaluation of outcomes and impacts, will be critical to ensure these investments translate into meaningful and sustained improvements for Autistic students.
Limitations
This study has several limitations that should be considered when interpreting the findings. First, the cross-sectional design limits the ability to infer causality between support access and educational outcomes. Accordingly, while we describe who receives support, we cannot determine whether these supports were effective in improving enrolment, attendance or other relevant outcomes. Second, the reliance on contact with specific parts of the health system to capture diagnoses of autism, and the absence of data from primary care and outpatient settings, will undercount the true prevalence of autism [39]. For context, our estimated prevalence of 1.6% is notably lower than estimates from the United States of approximately 2.3% from a comparable time period [59]. Underestimation may also be uneven. In NZ, autism diagnosis typically requires referral to specialist paediatric or psychological services through primary care, early childhood centres, or schools. Access to these services is affected by wait times, regional availability, and parental advocacy, creating inequities in who is identified [43, 60, 61]. Internationally, children from higher socioeconomic backgrounds are often more likely to be diagnosed, particularly without ID [62, 63]. Girls may also be underrepresented due to male-biased diagnostic frameworks [64]. These patterns suggest that the identified cohort represents a subset of Autistic students who are formally diagnosed and engaged with services, rather than the full population of Autistic students in NZ schools. This may result in an element of selection bias, thereby impacting findings. A similar issue is likely for ID, where diagnosis and recording may also be incomplete due to the same data gaps. Third, while propensity score matching improved comparability, residual confounding from unobserved factors remains possible. Specifically, our data was limited to binary information on sex, preventing us from capturing gender diversity, which is known to be more prevalent among Autistic young people and may be relevant to understanding educational outcomes [65]. Finally, the absence of qualitative data restricts insights into the lived experiences of Autistic students and their families, which are crucial for understanding the enablers and barriers to school participation.
Future work
Future research should begin by developing a deeper understanding of the enablers and barriers to school attendance, engagement and achievement, and the role of resourcing and supports in enhancing these outcomes. This would provide the necessary foundation to inform the development of targeted approaches to supporting individual, school-wide, and systemic change. Development of supports should be co-designed with Autistic and autism communities to ensure they reflect the priorities and lived experiences of the intended beneficiaries. These supports should take a multi-layered approach, integrating enhanced teacher education, inclusive curriculum design, flexible learning environments, and responsive behavioural and emotional support strategies and should be informed by robust research evidence. It is essential that supports, modifications, and interventions are systemically evaluated to determine their impact on both immediate participation and long-term educational outcomes for Autistic students, ensuring accountability and continual improvement. Future studies could also examine how timing of diagnosis influences access to supports and outcomes, and investigate overlap between different supports to understand which combinations are most effective. Longitudinal approaches would enable tracking of attendance, engagement, and support use over time, and provide clearer evidence on whether disparities widen, narrow, or persist.
Conclusion
This study highlights significant differences in school enrolment, attendance, and access to funding supports and services between Autistic and non-Autistic students in NZ. The findings emphasise the critical need for targeted and adequately funded educational supports to promote equitable school participation for Autistic students.
Acknowledgements
The work was supported by funding from the Laura Ferguson Trust Ltd and the New Zealand Policy Research Institute - AUT. The funders did not have any role in the study design, data collection, or decision to submit this work for publication.
Statement of conflicts of interest
None declared.
Ethics statement
Ethical approval was granted by the University of Otago Human Research Ethics Committee (Reference: HD17/004).
Data availability statement
The data supporting this study’s findings are available with the Integrated Data Infrastructure (IDI), curated by Stats NZ. Restrictions apply to the availability of these data, which are used under license for this study. To apply for access to these data please see https://www.stats.govt.nz/integrated-data/how-to-apply-to-integrate-new-data/#how-add.
AI disclosure statement
The authors used ChatGPT for the purpose of language editing in this manuscript. The output was reviewed and verified by the authors.
Disclaimer
These results are not official statistics. They have been created for research purposes from the Integrated Data Infrastructure (IDI) which is carefully managed by Stats NZ. For more information about the IDI please visit https://www.stats.govt.nz/integrated-data/.
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