Assessment & Research

Trends in the prevalence of childhood disability: analysis of data from the national disability registry of Taiwan, 2000-2011.

Lai et al. (2013) · Research in developmental disabilities 2013
★ The Verdict

Taiwan’s national records show childhood disability climbing 50 percent in eleven years, powered by a sharp autism surge.

✓ Read this if BCBAs writing grants, staffing plans, or school programs in any region with registry data.
✗ Skip if Clinicians who only need single-case designs and do not touch service systems.

01Research in Context

01

What this study did

The team pulled every child in Taiwan’s national disability registry from 2000 to 2011.

They counted how many kids had intellectual disability, autism, developmental delay, or other diagnoses each year.

No lab tests—just the government’s own records.

02

What they found

Disability rose from 10 to 15 kids per 1,000.

Intellectual disability stayed on top, but autism shot up fastest and now sits third.

The climb never leveled off during the 11-year span.

03

How this fits with other research

Lai et al. (2012) zoomed in on autism alone for 2004-2010 and saw the same steep line—same data set, tighter lens.

Gal et al. (2012) and Dinstein et al. (2024) found near-identical autism surges in Israeli registries, so Taiwan’s jump is not a local fluke.

van Bakel et al. (2015) saw slower growth in rural France, hinting that faster rises may link to how each country codes and finds cases.

04

Why it matters

Caseloads will keep growing. Use the Taiwan line graph when you ask administrators for more RBT hours, classroom seats, or early-intervention slots. Track autism referrals in your own region and compare the slope—if you’re flat while the country soars, kids are being missed.

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Graph your agency’s new autism intakes by year and overlay Taiwan’s slope—if yours is flatter, schedule extra outreach screenings.

02At a glance

Intervention
not applicable
Design
other
Population
intellectual disability, autism spectrum disorder, developmental delay, not specified
Finding
positive

03Original abstract

Childhood disability is not uncommon, but data at the national level are limited, especially those on the changes in the prevalence over time. On the basis of the Disabled Welfare Act, Taiwan began to certify disabled residents and provide various services in 1980. All the cases receiving services are registered, and the registry provides a rare opportunity for studying childhood disability at the national level. Using the data from 2000 to 2011, we calculated the age-specific prevalence of all disability combined and assessed the changes over time. We also calculated the prevalence rate and the proportion in all disabilities combined for each disability category and assessed the trends. As certification before 3 years old is generally discouraged by the government, we limited analyses to children between 3 and 17 years old. We found that the registered cases ranged from 49,242 to 61,717 from 2000 to 2011 and that intellectual disability (ID), had been the leading category all through the years. The proportion of autism spectrum disorders (ASD) had been increasing rapidly and become the third leading disability in 2011. The prevalence of all disabilities combined increased constantly from 9.98/1000 to 15.41/1000 (p<0.01), and increases were generally observed every year in all age groups (p<0.01). The increase could largely be attributable to the increases in ID and ASD, while the increasing trends were also significant in "multiple disabilities," "speech or language impairment," and "other disabilities listed by the Department of Health" (p<0.01 for all the five categories). An increase with age in the prevalence of all disabilities combined could be observed all through the years (p<0.01 in all calendar years). We concluded that the prevalence of childhood disability has been increasing in Taiwan, with ID contributing the most cases and ASD as an emerging problem. However, the increase of prevalence cannot be attributed entirely to the increase in the occurrence of cases, and an increase in the proportion of cases registered was an more important factor, which may be in turn attributable to a better service of the related agencies, lower discrimination against the patients, higher awareness of the disorder, and more willingness of the guardians to register.

Research in developmental disabilities, 2013 · doi:10.1016/j.ridd.2013.08.001