Index

Abstract

Autism spectrum disorder (ASD) is a developmental disability that causes lifelong impairments in physical, psychological, and social functioning. This disorder manifests when a baby is still in the womb and is detected around 24 months of age. Sixty children who attended part-boarding individual hours were transported to the Nhan Tam Children's Education and Counseling Center and Quang Ngai Provincial Psychiatric Hospital for intervention and evaluation; they were assessed for ASD using the Childhood Autism Spectrum Disorder scale (CARS) and were the subjects of our study. Before their involvement, the researcher explained the purpose of the research to the participants and received their informed consent. The results showed that 75% of the children had a severe form of ASD, whereas 25% had a mild or moderate type. Indicators of verbal and nonverbal communication were prominent among children with ASD. In terms of average test scores, we found a difference between children of stable-income parents and those from disadvantaged households. This offers a basis for educators, clinicians, and sociologists to implement education, intervention, and treatment for children with ASD, as well as to enhance awareness about this condition so that parents pay more attention to their children.

Keywords: Autism, Autism spectrum disorder, Childhood, Clinician, Educator.

Received: 23 September 2022 / Revised: 8 February 2023 / Accepted: 22 February 2023 / Published: 6 March 2023

Contribution/ Originality

This paper contributes to our knowledge of the evaluation of autism spectrum disorder characteristics in Vietnam. This study uncovered the need for educators, clinicians, and psychologists to implement education, intervention, and therapy for children with ASD and raise awareness about this illness so that parents pay greater attention to their children.

1. INTRODUCTION

Numerous studies have shown that children with autism spectrum disorder (ASD) display greater developmental gains with rigorous preschool intervention (Zwaigenbaum et al., 2015). ASD is a developmental disability that persists throughout life, and Kanner (1943) first used the term autism to describe patients with impairments in social interaction, difficulties in verbal and non-verbal communication, and narrow and repetitive behaviors and preferences (Sadock, Sadock, & Kaplan, 2009). ASD has severe psychological, social, and economic consequences, making it an obsession for many families and communities (Geier, Kern, & Geier, 2013). Children with ASD find it very difficult to integrate with children of the same age group because of qualitative defects in social interaction and communication (Geier et al., 2013). Many children with ASD experience severe dysfunction and live almost completely dependent on relatives or the hospital. In late adolescence, children with ASD often need friends but are limited in their responses to the interests, feelings, and emotions of others, making it difficult to develop relationships (Damiano, Mazefsky, White, & Dichter, 2014).

Over the last two decades, the frequency of ASD diagnosis has increased rapidly (Lai, Tseng, & Guo, 2013). According to the United States (U.S.) Centers for Disease Control statistics, the percentage of children with ASD has increased gradually over time. In 2006, a study of 303,790 8-year-old children in the U.S. revealed that the rate of children with ASD was 9‰; compared with 2002, the ASD rate had increased by 57% (Rice, 2009). In 2008, this rate was 11.3‰, an increase of 78% compared to 2002 (Autism & Investigators, 2012). In 2010, the rate of children with ASD under eight years old was 14.7% higher than the previous year's rate (Autism & Investigators, 2014).  In 2012, at least one in every 88 children in the U.S. was diagnosed with ASD (Autism & Investigators, 2012).

According to Fan's (2018) analysis of 26 epidemiological studies conducted between 2000 and 2016, 0.30 percent of the Vietnamese population had ASD. This percentage is substantially lower than that of many other nations, notably the U.S., which has a reported rate closer to 1.5% (Christensen et al., 2016). According to a recent article in Spectrum News, the global rate may be closer to 2% and in certain regions, as high as 3% (Wright, 2018b). Cubells (2013) discussed studies in which ASD prevalence rates ranged from 1.8 in 10,000 to 426 in 10,000. However, the majority of studies have reported rates closer to those observed in Wang, Wang, Guo, van Wijngaarden, and Begeer's (2018) meta-analysis. Based on their review of 44 studies going back to 1996, they estimated a prevalence of ASD of 11.8 per 10,000 individuals. Although the true prevalence of ASD in China is unclear, rates reported by Chinese researchers have been consistently lower than in other regions, such as Southeast Asia and the U.S. In Japan, the stated rate is 181 per 10,000 people; in South Korea, it is 264 per 10,000 people; and in the U.S., it is 168 per 10,000 people  (Wang et al., 2018).

In Vietnam, before 1980, many experts said that there were no children with ASD. The concept of ASD was still very strange to pediatricians; however, since 2000, the number of children diagnosed with ASD has increased. Trang (2012)  showed that the rate of ASD in children was 5.1‰ (Trang, 2012). In another study, conducted by Kien (2014) in Thai Nguyen, the rate of ASD in children from 18 to 60 months was 4.5‰ (Kien, 2014).In a cross-sectional descriptive study by Duc et al. (2021)  involving 74,308 children aged 24-72 months in Quang Ngai province, the ASD rate was 3.8‰ (Duc et al., 2021).

1.1. Autism Spectrum Disorder (ASD)

Autism spectrum disorder is characterized by difficulties with social interaction and communication, as well as constrained, stereotypical patterns of behavior, interests, and activities (Geier et al., 2013). Recent research has demonstrated that several physiological, medical, and behavioral co-morbidities are regularly associated with ASD, including gastrointestinal troubles, incontinence, sleep problems, eating disorders, behavioral challenges, and sensory processing abnormalities (Geier, Kern, & Geier, 2012). Neuroimaging studies have uncovered diminished brain specialization for the processing of social information, such as the perception of faces, biological movements, and theory of mind activities (McPartland, Coffman, & Pelphrey, 2011; Pelphrey, Shultz, Hudac, & Vander Wyk, 2011), atypical activity of the prefrontal cortex during executive function tasks (Philip et al., 2012), as well as abnormal processing of auditory and linguistic stimuli (Kennedy & Courchesne, 2008; Minshew & Williams, 2007).

Bullies victimize children with ASD and other impairments, their non-disabled siblings, and individuals with intellectual disabilities more frequently than their peers (Nowell, Brewton, & Goin-Kochel, 2014; Sreckovic, Brunsting, & Able, 2014). In their global analysis of 17 studies on school bullying, Maiano, Normand, Salvas, Moullec, and Aimé (2016) revealed that children with ASD are bullied at three times the rate of typically developing children (Maiano et al., 2016). Hoover (2015) found that 31% of teenagers with ASD experienced physical, verbal, and relational school bullying (e.g., seeking to hurt a peer and/or that peer's standing within a certain peer group). Bullying occurs within and outside of special education settings but is more widespread in conventional classrooms and unstructured areas, such as on school buses.

Several researchers have examined data from the 2011–2012 National Survey of Children's Health in the U.S. (N = 95,678) to determine the frequency and impact of adverse childhood experiences (ACEs) on children with ASD (Berg, Shiu, Acharya, Stolbach, & Msall, 2016). The findings show that income inadequacy (ASD, 40%; healthy control, 23%), parental divorce (ASD, 28%; healthy control, 20%), neighborhood violence (ASD, 11%), and household mental health (ASD, 18%; healthy control, 7%) and/or substance use (ASD, 14%; healthy control, 10%) were more prevalent among children with ASD than among healthy control peers. In addition, children with ASD were twice as likely as healthy children to have experienced four or more unpleasant childhood experiences (10.2 vs. 5.1%).

1.2. The Childhood Autism Rating Scale (CARS)

The CARS (Schopler, Reichler, & Renner, 1988; Schopler, Reichler, DeVellis, & Daly, 1980) is one of the most commonly used and durable instruments. Using this scale, a trained observer rates a child's behavior on 15 dimensions or symptoms. It generates a total score that can be used as a continuous measure of autism severity and a trichotomous categorical diagnosis of non-autistic, mild/moderate autism, or severe autism. Given that it was first released in 1980, during the era of DSM-III, one criticism of the CARS is that it does not reflect current diagnostic criteria (such as DSM-IV). The CARS items were developed using five sets of criteria (Kanner, Creak, Rutter, Ritvo, and DSM-III-R) and clinical experience (Schopler et al., 1988). In reality, the CARS contains questions that are crucial to the three domains of the DSM-IV criteria (social and emotional reactions, verbal and nonverbal communication, multiple repeated behaviors), but it does not directly address peer relationships, shared attention, or symbolic play. In addition, the CARS includes several symptoms that, while not universal or exclusive to autism, are typically present and clinically significant, such as sensory abnormalities, anxiety and activity level, and imitation problems.

The CARS has been shown to be useful with preschool children (DiLalla & Rogers, 1994; Perry, Condillac, & Freeman, 2002; Schopler et al., 1988), school-aged children (Schopler et al., 1988), adolescents (Mesibov, Schopler, Schaffer, & Michal, 1989), and samples with wide age ranges (Sevin, Matson, Coe, Fee, & Sevin, 1991; Sturmey, Matson, & Sevin, 1992; Tachimori, Osada, & Kurita, 2003; Van Bourgondien, Marcus, & Schopler, 1992). The CARS is commonly used in clinical intervention programs, such as the model early intervention programs defined by Handleman and Harris (2001), to capture participants’ behavioral profiles and severity. Some researchers also use it as an outcome measure (e.g., Perry et al. (2002)), whereby a drop in CARS scores indicates a favorable response to therapy. Recent professional consensus characterizes the CARS as having excellent psychometric qualities and therapeutic value. Training practitioners to utilize it consistently is straightforward and may be accomplished rapidly (Filipek et al., 1999). The New York Guidelines mention several benefits and disadvantages of the CARS (as well as other measures). Their recommendations indicate that there is strong evidence that the CARS is useful in a variety of settings, that it offers an acceptable combination of practicality and research support, and that the severity rating score may be useful for monitoring progress and as part of a standard assessment package; however, they caution that clinicians should have adequate knowledge of autism diagnosis and proper training in the use of the CARS (Filipek et al., 1999).

1.3. Family Income and ASD

In addition to the health burden, large economic expenses accompany the rise in the number of children with ASD (Amendah, Grosse, Peacock, & Mandell, 2011; Knapp, Romeo, & Beecham, 2009). Comparing the expenses of ASD in the United Kingdom and the U.S., Buescher, Cidav, Knapp, and Mandell (2014) determined that the lifetime cost of caring for a child with ASD topped $1 million in both countries. A significant portion of the expense is attributable to special education services and parental productivity losses (Buescher et al., 2014). Other research has shown that parents (particularly mothers) of children with ASD have reduced labor force involvement rates (Cidav, Marcus, & Mandell, 2012; McEvilly, Wicks, & Dalman, 2015). Parents’ participation in the labor force is essential since it provides the family with the financial benefits of employment income. It has been established that the cost of medical services for children with ASD is relatively high (Croen, Najjar, Ray, Lotspeich, & Bernal, 2006; Liptak, Stuart, & Auinger, 2006), and specialist care costs have been cited as a reason for the underutilization of health services in children with ASD (Chiri & Warfield, 2012) and those with chronic conditions in general (Callander, Corscadden, & Levesque, 2017; Chiri & Warfield, 2012). Therefore, family income is an essential element in ensuring that children with ASD have access to care (Callander & Lindsay, 2018).

1.4. This Study

ASD has a severe impact not only on the lives and mental health of children but also on the financial well-being of society as a whole. Even though more youngsters are being diagnosed with ASD, not nearly enough attention is being paid to the condition. The prevalence of ASD among children in Vietnam, as well as the features of children with ASD as measured by the CARS scale, have not been thoroughly evaluated. In this study, we aim to ascertain the prevalence of ASD, the features of ASD that are often seen in children, and any disparity in the mean ASD score between disadvantaged and non-disadvantaged households.

2. METHODS

2.1. Research Hypotheses

H01: There is not a high frequency of ASD in children.
H02: Verbal and non-verbal communication are not common characteristics of ASD in children.
H03: There is no significant difference in the average ASD score according to family economic condition.

2.2. Participants

Sixty children with confirmed or suspected ASD who attended part-time school, individual hours, and could be evaluated at the Nhan Tam Children's Education and Counseling Center and Quang Ngai Provincial Psychiatric Hospital were eligible to participate in the study. These 60 children included 48 males and 12 females; most were aged 36–48 months (n=35); most were Kinh ethnicity (n=58); most came from a non-disadvantaged family economic situation (n=57), and most had a religious affiliation (n=42), as Table 1 presents.

Table 1. Participants' characteristics and scores on the childhood autism rating scale (CARS).

Variables

CARS

n (%) (N=60)

Mean

Standard deviation

p

Age

24 – 36 Months

14 (23.3)

40.5

1.3

0.745

36 – 48 Months

35 (58.4)

40.1

0.7

48 – 72 Months

11 (18.3)

39.2

0.8

Gender

Male

48 (80)

40.0

4.3

0.945

Female

12 (20)

40.1

3.8

Ethnicity

Kinh

58 (96.7)

39.9

4.1

0.397

Ethnic minority

2 (3.3)

42.5

7.8

Family income

Non-disadvantaged

57 (95)

39.6

3.8

<0.001***

Disadvantaged

3 (5)

48.0

4.0

Religion

Yes

42 (70)

40.1

4.7

0.793

No

18 (30)

39.8

2.6

Note:

***p<0.001.

Table 1 shows a significant difference in the average ASD score according to family economic condition between disadvantaged families (M = 48, SD = 4) and non-disadvantaged families (M = 39.6, SD = 3.8); p < 0.001). Therefore, the null hypothesis (H03) was rejected.

There was no significant difference in the average ASD score according to age group (p > 0.05). Neither were there significant differences in the average CARS score for gender (p = 0.945 > 0.05), ethnicity (p = 0.397 > 0.05), or religion (p = 0.793 > 0.05).

2.3. Procedure

Participants’ parents or carers gave informed consent and read the anonymity and confidentiality restrictions before completing the survey. They were informed of the aims of the study and requested to supply socio-demographic information, such as gender, age, ethnicity, and family income. Participants were not compensated for their participation and were free to quit at any time.

ASD scores were obtained using a Vietnamese translation of the CARS scale. A native Vietnamese speaker created the forward translation of the scale. By comparing their own versions of the original Vietnamese translation, the research group members reached a consensus on the final translation for backward translation.

The back-translation from Vietnamese to English was performed by a professional translator who was a fluent speaker of both English and Vietnamese without providing information on the original scale. The researchers compared the reverse translation and the original to see if there were any significant differences or conflicts between the two.

2.4. Measures

According to Volkmar, Chawarska, and Klin (2005), the CARS scale is utilized in several therapeutic settings and studies to assess the severity of ASD by observing children. The scale examines 14 categories of behavior that are typically impacted by severe difficulties in autism, plus one category of overall autism perceptions, with the aim of distinguishing children with autism from those with other developmental impairments. The 14 categories are Impairment in Human Relationships, Imitative Conduct, Emotional Reaction, Body Utilization, Object Utilization, Change Adaptation, Visual Response, Listening Response, Perceptual Response, Anxiety Reaction, Verbal Communication, Non-Verbal Communication, Activity Level, and Intellectual Functioning, as well as a General Impression. The examiner assigned a score between 1 and 4 for each item, where 1 represents age-appropriate behavior and 4 represents a significant departure from age-appropriate norms. The sum of the individual item scores classifies the child as not autistic (below 30), mildly or moderately autistic (30–36.5), or severely autistic (above 36.5) The developers of the scale also advised counting the number of items for which a child had a score of 3 or higher to determine the severity of autism. A diagnosis of severe autism is warranted if at least five criteria are met (Schopler et al., 1980).

Reliability estimates are stated in the CARS handbook (Schopler et al., 1988). The test-retest reliability for 91 instances was 0.88 (r = 0.94) after a 12-month gap. Many studies have discovered lower alpha coefficients for the childhood and adolescent groups (r = 0.79 and 0.73, respectively) in independent studies of CARS (Garfin & McCallon, 1988). A 1988 study comparing autistic and non-autistic handicapped teenagers found statistically significant variations in the overall CARS scores of the two groups (Garfin & McCallon, 1988).

2.5. Statistics

For data processing, version 22.0 of the Statistical Package for the Social Sciences (SPSS) was used. Descriptive statistics were used to describe participants' characteristics. A one-way analysis of variance (ANOVA) was used to examine any statistical differences based on age, gender, ethnicity, family economic condition, and religion.

3. RESULTS

As shown in Table 2, the participants’ average CARS score was M = 40.0 (SD = 4.2). According to our statistics, 75% of these children with ASD exhibited severe symptoms, whereas 25% presented mild to moderate symptoms. Therefore, null hypothesis H01 was rejected.

Table 2. Level of autism spectrum disorder in children.

Level of ASD

N

Percentage (%)

Mean ± Standard deviation

Mild - moderate

15

25

40.0 ± 4.2

Severe

45

75

Total

60

100

Several international and Vietnamese studies have indicated that the prevalence of children with severe autism is greater than that of children with mild to moderate autism. This may suggest that families of children with moderate to severe autism have inaccurate beliefs. Since early intervention strategies are often misunderstood or confused with other developmental diseases and impairments that may resolve on their own, they get little attention, as Table 3 presents.

Table 3. Characteristics of autism spectrum disorder in children.

No

Characteristics of ASD

Mean

Standard deviation

1

Impairment in human relationships

2.7

0.5

2

Imitative conduct

2.7

0.5

3

Emotional reaction

2.2

0.5

4

Body usage

2.7

0.5

5

Object use (Toys and other materials)

2.6

0.5

6

Change adaptation

2.3

0.4

7

Visual response

2.7

0.5

8

Listening response

2.3

0.4

9

Perceptual response

2.1

0.3

10

Anxiety reaction

2.3

0.5

11

Verbal communication

3.2

0.3

12

Nonverbal communication

3.2

0.3

13

Activity level

2.9

0.3

14

Intellectual functioning

3.1

0.2

15

General impressions

3.0

0.3

Table 3 shows that Quang Ngai children with ASD most frequently exhibit defects in verbal and nonverbal communication, followed by the level of intellectual functioning. The least common characteristics were visual, olfactory, and tactile responsiveness and problems with abnormal emotional expression. Therefore, null hypothesis H02 was rejected.

4. DISCUSSION

The main purposes of the present study were to investigate (i) the prevalence of ASD in children, (ii) the features of ASD most often observed in children, and (iii) any disparity in the mean ASD score between disadvantaged and non-disadvantaged families.

Our data indicate that the ratio of males to females was 4:1, which is similar to the findings of Fombonne, MacFarlane, and Salem (2021). Their investigation assessed 141 studies published between 1966 and 2020; 114 studies with sex data yielded a median sex ratio of 4:1. According to the non-significant Spearman connection between sex ratio and year of publication, a sex ratio of 4:1 corresponds to seeing 80-81% men in a surveyed sample, and this has not changed over time (Fombonne et al., 2021). Research consistent with the higher male-to-female ratio includes reliable and valid studies from countries such as Japan (77.2% and 75.8%) (Kurita, Miyake, & Katsuno, 1989; Tachimori et al., 2003), the U.S. (82%) (Sturmey et al., 1992), and Spain (74.5%) (Villamisar & Muela, 2000).

According to our research findings, 75.0% of ASD cases are classified as severe, while 25% are classified as mild to moderate. Thus, the incidence of children with severe autism is greater than that of children with mild-to-moderate autism, which is comparable to the findings of Kien's (2014) study on children with ASD between 18 and 60 months of age in Thai Nguyen province: 59.2% had a severe case, whereas 40.8% had a mild to moderate case (Kien, 2014). According to the findings of Duc et al. (2021) research on the prevalence of ASD in children aged 24–72 months in the province of Quang Ngai, children with severe autism accounted for 63.57% and children with moderate autism accounted for 36.4% (Duc et al., 2021). In Giang's (2010a) research on ASD in children aged 18 to 36 months at the National Children's Hospital, the incidence of severe autism was greater than that found in previous studies, at 85.7%. This may be because the children in the study were younger and whose language, non-verbal communication, and behavioral impairments were severe and for whom, therefore, intervention and social learning via activities were necessary. In addition, children's everyday activities progressively mitigate the flaws, reducing the severity of ASD (Giang, 2010a). Hussein, Taha, and Almanasef (2011) observed a group of ASD patients in Egypt and found 10% with a severe level, 85% with a moderate level, and 5% with a mild level of ASD; the group diagnosis was 17.4% with a severe level, 34.8% with a medium level, and 47.4% with a mild level (Hussein et al., 2011). In Vietnam, the research has indicated that among children, the prevalence of severe ASD is much greater than that of mild-to-moderate ASD. This demonstrates that the symptoms severely impair the quality of life of the family and the child.

Our study shows that children have the most severe difficulties in both verbal and non-verbal communication. In this, our findings are similar to those of Giang (2010b) and Kien (2014). These are the most visible, recognized, and defining characteristics of children with ASD. The majority of families are worried and seek expert assistance when their 24-month-old does not speak or uses words out of context. Children may mix comprehensible words with others that are not clear, mechanical repetition, or nonsensical pronunciation when speaking. Occasionally, youngsters produce peculiar noises. While infants lack sufficient language to express themselves, they also have trouble utilizing gestures and facial expressions to communicate their desires and cannot comprehend the nonverbal communication of others (Giang, 2010a; Kien, 2014).

Concerning the family's economic circumstances, we found a substantial difference in the average ASD score between disadvantaged and non-disadvantaged households. Children from disadvantaged families had higher ASD scores than those from non-disadvantaged families, although the proportion of children from non-disadvantaged families was significantly higher. This is similar to the synthesis of Fombonne et al. (2021) that the prevalence of ASD was higher in high- and upper-middle-income families than in low-middle- or low-income families. Even when children's behavioral and adaptive characteristics are considered, Emily and Grace (2015) showed a strong association between parental income and children's intelligence. This may be especially significant for children with ASD since prior research has shown that families with ASD suffer a greater financial burden (due to the child's condition) than families with children with attention deficit hyperactivity disorder (Zablotsky, Kalb, Freedman, Vasa, & Stuart, 2014). In addition, family income was reported more frequently in this research than in earlier studies of families with children with various diseases (Hu, Wang, & Fei, 2012; Wang et al., 2004).

5. LIMITATIONS

This research has certain limitations. First, we recruited participants using convenience sampling, restricting the generalizability of the research to a representative sample of the Vietnamese community. The majority of the study's participants attended the Nhan Tam Children's Education and Counseling Center and the Quang Ngai Provincial Psychiatric Hospital. Consequently, the study's results are restricted to this population. With this constraint in mind, further research with large and varied sample sizes is advisable. Second, due to the cross-sectional nature of our research, causal conclusions cannot be drawn. Consequently, prospective modeling should be used to examine the correlation between ASD level and family income, as well as the implications of this association. In future research, a longitudinal design is recommended to establish a cause-and-effect correlation.

6. CONCLUSION

The results of our research have shown that children who have ASD are significantly impacted, affecting their verbal and nonverbal communication abilities as well as their intellectual development. This should serve as a caution to educators, therapists, and parents, who need to pay extra special attention to the infants and young children in their care. Previous studies have suggested that exposing children with ASD to typically developing children's social communication and behaviors benefits them. It has been suggested that this exposure enhances verbal and social abilities and nurtures intellectual potential (Harrower & Dunlap, 2001). In typical school settings, children with ASD show improvements in social communication, IQ, and adaptive behaviors (Fisher & Meyer, 2002; Nahmias, Kase, & Mandell, 2014; Stahmer, Akshoomoff, & Cunningham, 2011). Ethics also urge mainstream schooling as a basic human right of children with ASD and their families (Allan, 2007). In contrast, children with ASD in exclusive special education settings benefit from more rigorous, systematic, and coordinated intervention programs handled by more experienced professionals and specialized facilities (Mesibov & Shea, 1996). Many studies have shown that young children with ASD who are placed in special education settings and receive intensive treatments improve in cognitive, social, and adaptive skills (Harris, Handleman, Gordon, Kristoff, & Fuentes, 1991; Rogers, 2016; Rogers & Vismara, 2008). This is the basis for educators, clinicians, and sociologists to implement education, intervention, and treatment for children with ASD and enhance awareness about this condition so that parents pay more attention to their children.

Funding: This study received no specific financial support.  

Competing Interests: The authors declare that they have no competing interests.

Authors’ Contributions: Both authors contributed equally to the conception and design of the study.

REFERENCES

Allan, J. (2007). Rethinking inclusive education: The philosophers of difference in practice (Vol. 5). Netherlands: Springer Science and Business Media.

Amendah, D., Grosse, S. D., Peacock, G., & Mandell, D. S. (2011). The economic costs of autism: A review. Autism Spectrum Disorders, 1347-1360. https://doi.org/10.1093/med/9780195371826.003.0088

Autism, & Investigators, D. D. M. N. S. Y. P. (2012). Prevalence of autism spectrum disorders—autism and developmental disabilities monitoring network, 14 sites, United States, 2008. Morbidity and Mortality Weekly Report: Surveillance Summaries, 61(3), 1-19.

Autism, & Investigators, D. D. M. N. S. Y. P. (2014). Prevalence of autism spectrum disorder among children aged 8 years—autism and developmental disabilities monitoring network, 11 sites, United States, 2010. Morbidity and Mortality Weekly Report: Surveillance Summaries, 63(2), 1-21.

Berg, K. L., Shiu, C. S., Acharya, K., Stolbach, B. C., & Msall, M. E. (2016). Disparities in adversity among children with autism spectrum disorder: A population‐based study. Developmental Medicine & Child Neurology, 58(11), 1124-1131. https://doi.org/10.1111/dmcn.13161

Buescher, A. V., Cidav, Z., Knapp, M., & Mandell, D. S. (2014). Costs of autism spectrum disorders in the United Kingdom and the United States. JAMA Pediatrics, 168(8), 721-728. https://doi.org/10.1001/jamapediatrics.2014.210

Callander, E. J., Corscadden, L., & Levesque, J.-F. (2017). Out-of-pocket healthcare expenditure and chronic disease–do Australians forgo care because of the cost? Australian Journal of Primary Health, 23(1), 15-22. https://doi.org/10.1071/py16005

Callander, E. J., & Lindsay, D. B. (2018). The impact of childhood autism spectrum disorder on parent’s labour force participation: Can parents be expected to be able to re-join the labour force? Autism, 22(5), 542-548. https://doi.org/10.1177/1362361316688331

Chiri, G., & Warfield, M. E. (2012). Unmet need and problems accessing core health care services for children with autism spectrum disorder. Maternal and Child Health Journal, 16(5), 1081-1091. https://doi.org/10.1007/s10995-011-0833-6

Christensen, D. L., Baio, J., Braun, K. V., Bilder, D., Charles, J., Constantino, J. N., & Yeargin-Allsopp, M. (2016). Prevalence and characteristics of autism spectrum disorder among children aged 8 years-autism and developmental disabilities monitoring network, 11 sites, United States, 2012. MMWR Surveillance Summaries, 65(3), 1-23. https://doi.org/10.15585/mmwr.ss6503a1

Cidav, Z., Marcus, S. C., & Mandell, D. S. (2012). Implications of childhood autism for parental employment and earnings. Pediatrics, 129(4), 617-623. https://doi.org/10.1542/peds.2011-2700d

Croen, L. A., Najjar, D. V., Ray, G. T., Lotspeich, L., & Bernal, P. (2006). A comparison of health care utilization and costs of children with and without autism spectrum disorders in a large group-model health plan. Pediatrics, 118(4), e1203-e1211. https://doi.org/10.1542/peds.2006-0127

Cubells, J. (2013). Prevalence of autism spectrum disorders in China. Shanghai Archives of Psychiatry, 25(3), 176-177.

Damiano, C. R., Mazefsky, C. A., White, S. W., & Dichter, G. S. (2014). Future directions for research in autism spectrum disorders. Journal of Clinical Child and Adolescent Psychology, 43(5), 828-843. https://doi.org/https://doi.org/10.1080/15374416.2014.945214

DiLalla, D. L., & Rogers, S. J. (1994). Domains of the childhood autism rating scale: Relevance for diagnosis and treatment. Journal of Autism and Developmental Disorders, 24(2), 115-128. https://doi.org/https://doi.org/10.1007/BF02172092

Duc, N. T. T., Khue, V. V., Vu, L. N., Trong, N. T. Q., Dang, D. D., & Xuan, N. T. (2021). Prevention of children with autism spectrum disorders and initial results of community-based rehabilitation intervention in Quang Ngai Province. Journal of Vietnamese Medicine, 505(1), 80-84.

Emily, G., & Grace, I. (2015). Family quality of life and ASD: The role of child adaptive functioning and behavior problems. Autism Research, 8(2), 199-213. https://doi.org/10.1002/aur.1442

Fan, Y. (2018). The current state and outlook of autism in Mainland China. Paper presented at the Annual Conference of the International Society for Autism Research, Rotterdam, Amsterdam.

Filipek, P. A., Accardo, P. J., Baranek, G. T., Cook, E. H., Dawson, G., Gordon, B., & Levy, S. E. (1999). The screening and diagnosis of autistic spectrum disorders. Journal of Autism and Developmental Disorders, 29(6), 439-484.

Fisher, M., & Meyer, L. H. (2002). Development and social competence after two years for students enrolled in inclusive and self-contained educational programs. Research and Practice for Persons with Severe Disabilities, 27(3), 165-174. https://doi.org/10.2511/rpsd.27.3.165

Fombonne, E., MacFarlane, H., & Salem, A. C. (2021). Epidemiological surveys of ASD: Advances and remaining challenges. Journal of Autism and Developmental Disorders, 51(12), 4271-4290. https://doi.org/10.1007/s10803-021-05005-9

Garfin, D. G., & McCallon, D. (1988). Validity and reliability of the childhood autism rating scale with autistic adolescents. Journal of Autism and Developmental Disorders, 18(3), 367-378. https://doi.org/10.1007/bf02212193

Geier, D. A., Kern, J. K., & Geier, M. R. (2012). A prospective cross-sectional cohort assessment of health, physical, and behavioral problems in autism spectrum disorders. Maedica, 7(3), 193-200.

Geier, D. A., Kern, J. K., & Geier, M. R. (2013). A comparison of the autism treatment evaluation checklist (ATEC) and the childhood autism rating scale (CARS) for the quantitative evaluation of autism. Journal of Mental Health Research in Intellectual Disabilities, 6(4), 255-267. https://doi.org/10.1080/19315864.2012.681340

Giang, N. T. H. (2010a). Research on some clinical characteristics of autistic children from 18 months to 36 months of age. Hanoi Medical University. Central Children's Hospital.

Giang, N. T. H. (2010b). Study on early detection of autism using the autism screening checklist in young children (MCHAT-023). Practical Medicine, 741(11/2010), 5-7.

Handleman, J. S., & Harris, S. L. (2001). Preschool education programs for children with autism. Austin, TX: Pro-Ed, Inc.

Harris, S. L., Handleman, J. S., Gordon, R., Kristoff, B., & Fuentes, F. (1991). Changes in cognitive and language functioning of preschool children with autism. Journal of Autism and Developmental Disorders, 21(3), 281-290. https://doi.org/10.1007/bf02207325

Harrower, J. K., & Dunlap, G. (2001). Including children with autism in general education classrooms: A review of effective strategies. Behavior Modification, 25(5), 762-784. https://doi.org/https://doi.org/10.1177/0145445501255006

Hoover, D. W. (2015). The effects of psychological trauma on children with autism spectrum disorders: A research review. Review Journal of Autism and Developmental Disorders, 2(3), 287-299. https://doi.org/https://doi.org/10.1007/s40489-015-0052-y

Hu, X., Wang, M., & Fei, X. (2012). Family quality of life of Chinese families of children with intellectual disabilities. Journal of Intellectual Disability Research, 56(1), 30-44. https://doi.org/10.1111/j.1365-2788.2011.01391.x

Hussein, H., Taha, G. R., & Almanasef, A. (2011). Characteristics of autism spectrum disorders in a sample of egyptian and saudi patients: Transcultural cross sectional study. Child and Adolescent Psychiatry and Mental Health, 5(1), 1-12. https://doi.org/10.1186/1753-2000-5-34

Kanner, L. (1943). Autistic disturbances of affective contact. Nervous Child, 2(3), 217-250.

Kennedy, D. P., & Courchesne, E. (2008). The intrinsic functional organization of the brain is altered in autism. Neuroimage, 39(4), 1877-1885. https://doi.org/10.1016/j.neuroimage.2007.10.052

Kien, P. T. (2014). Research on the prevalence and results of autism treatment in children in Thai Nguyen province. City Medical Journal. Ho Chi Minh, 4(18), 74-79.

Knapp, M., Romeo, R., & Beecham, J. (2009). Economic cost of autism in the UK. Autism, 13(3), 317-336. https://doi.org/10.1177/1362361309104246

Kurita, H., Miyake, Y., & Katsuno, K. (1989). Reliability and validity of the childhood autism rating scale-Tokyo version (CARS-TV). Journal of Autism and Developmental Disorders, 19(3), 389-396. https://doi.org/10.1007/bf02212937

Lai, D.-C., Tseng, Y.-C., & Guo, H.-R. (2013). Trends in the prevalence of childhood disability: Analysis of data from the national disability registry of Taiwan, 2000–2011. Research in Developmental Disabilities, 34(11), 3766-3772. https://doi.org/10.1016/j.ridd.2013.08.001

Liptak, G. S., Stuart, T., & Auinger, P. (2006). Health care utilization and expenditures for children with autism: Data from US national samples. Journal of Autism and Developmental Disorders, 36(7), 871-879. https://doi.org/10.1007/s10803-006-0119-9

Maiano, C., Normand, C. L., Salvas, M. C., Moullec, G., & Aimé, A. (2016). Prevalence of school bullying among youth with autism spectrum disorders: A systematic review and meta‐analysis. Autism Research, 9(6), 601-615. https://doi.org/10.1002/aur.1568

McEvilly, M., Wicks, S., & Dalman, C. (2015). Sick leave and work participation among parents of children with autism spectrum disorder in the stockholm youth cohort: A register linkage study in Stockholm, Sweden. Journal of Autism and developmental Disorders, 45(7), 2157-2167. https://doi.org/10.1007/s10803-015-2381-1

McPartland, J. C., Coffman, M., & Pelphrey, K. A. (2011). Recent advances in understanding the neural bases of autism spectrum disorder. Current Opinion in Pediatrics, 23(6), 628-632. https://doi.org/10.1097/mop.0b013e32834cb9c9

Mesibov, G. B., Schopler, E., Schaffer, B., & Michal, N. (1989). Use of the childhood autism rating scale with autistic adolescents and adults. Journal of the American Academy of Child & Adolescent Psychiatry, 28(4), 538-541. https://doi.org/10.1097/00004583-198907000-00012

Mesibov, G. B., & Shea, V. (1996). Full inclusion and students with autism. Journal of Autism and Developmental Disorders, 26(3), 337-346. https://doi.org/10.1007/bf02172478

Minshew, N. J., & Williams, D. L. (2007). The new neurobiology of autism: Cortex, connectivity, and neuronal organization. Archives of Neurology, 64(7), 945-950. https://doi.org/10.1001/archneur.64.7.945

Nahmias, A. S., Kase, C., & Mandell, D. S. (2014). Comparing cognitive outcomes among children with autism spectrum disorders receiving community-based early intervention in one of three placements. Autism, 18(3), 311-320. https://doi.org/10.1177/1362361312467865

Nowell, K. P., Brewton, C. M., & Goin-Kochel, R. P. (2014). A multi-rater study on being teased among children/adolescents with autism spectrum disorder (ASD) and their typically developing siblings: Associations with ASD symptoms. Focus on Autism and Other Developmental Disabilities, 29(4), 195-205. https://doi.org/10.1177/1088357614522292

Pelphrey, K. A., Shultz, S., Hudac, C. M., & Vander Wyk, B. C. (2011). Research review: constraining heterogeneity: The social brain and its development in autism spectrum disorder. Journal of Child Psychology and Psychiatry, 52(6), 631-644. https://doi.org/10.1111/j.1469-7610.2010.02349.x

Perry, A., Condillac, R. A., & Freeman, N. L. (2002). Best practices and practical strategies for assessment and diagnosis of autism. Journal on Developmental Disabilities, 9(2), 61-75.

Philip, R. C., Dauvermann, M. R., Whalley, H. C., Baynham, K., Lawrie, S. M., & Stanfield, A. C. (2012). A systematic review and meta-analysis of the fMRI investigation of autism spectrum disorders. Neuroscience & Biobehavioral Reviews, 36(2), 901-942. https://doi.org/10.1016/j.neubiorev.2011.10.008

Rice, C. (2009). Prevalence of autism spectrum disorders: Autism and developmental disabilities monitoring network, United States, 2006. Retrieved from Morbidity and Mortality Weekly Report. Surveillance Summaries. No. SS-10. Centers for Disease Control and Prevention.

Rogers, S. (2016). Early start Denver model. In Comprehensive models of autism spectrum disorder treatment. Cham: Springer.

Rogers, S. J., & Vismara, L. A. (2008). Evidence-based comprehensive treatments for early autism. Journal of Clinical Child and Adolescent Psychology, 37(1), 8-38. https://doi.org/https://doi.org/10.1080/15374410701817808

Sadock, B. J., Sadock, V. A., & Kaplan, H. I. (2009). Kaplan and Sadock's concise textbook of child and adolescent psychiatry. Philadelphia, US: Lippincott Williams & Wilkins.

Schopler, E., Reichler, R., & Renner, B. (1988). The childhood autism rating scale (CARS). Los Angeles, CA: Western Psychological Services.

Schopler, E., Reichler, R. J., DeVellis, R. F., & Daly, K. (1980). Toward objective classification of childhood autism: Childhood autism rating scale (CARS). Journal of Autism and Developmental Disorders, 10, 91–103. https://doi.org/https://doi.org/10.1007/BF02408436

Sevin, J. A., Matson, J. L., Coe, D. A., Fee, V. E., & Sevin, B. M. (1991). A comparison and evaluation of three commonly used autism scales. Journal of Autism and Developmental Disorders, 21(4), 417-432. https://doi.org/10.1007/bf02206868

Sreckovic, M. A., Brunsting, N. C., & Able, H. (2014). Victimization of students with autism spectrum disorder: A review of prevalence and risk factors. Research in Autism Spectrum Disorders, 8(9), 1155-1172. https://doi.org/https://doi.org/10.1016/j.rasd.2014.06.004

Stahmer, A. C., Akshoomoff, N., & Cunningham, A. B. (2011). Inclusion for toddlers with autism spectrum disorders: The first ten years of a community program. Autism, 15(5), 625-641. https://doi.org/10.1177/1362361310392253

Sturmey, P., Matson, J. L., & Sevin, J. A. (1992). Brief report: Analysis of the internal consistency of three autism scales. Journal of Autism and Developmental Disorders, 22(2), 321-328. https://doi.org/10.1007/bf01058159

Tachimori, H., Osada, H., & Kurita, H. (2003). Childhood autism rating scale− Tokyo version for screening pervasive developmental disorders. Psychiatry and Clinical Neurosciences, 57(1), 113-118. https://doi.org/10.1046/j.1440-1819.2003.01087.x

Trang, N. L. (2012). Current status of ASD in children aged 18–60 months in Thai Nguyen City. Practical Medicine, 11(851), 29-32.

Van Bourgondien, M. E., Marcus, L. M., & Schopler, E. (1992). Comparison of DSM-III-R and childhood autism rating scale diagnoses of autism. Journal of Autism and Developmental Disorders, 22(4), 493-506. https://doi.org/10.1007/bf01046324

Villamisar, D. A. G., & Muela, C. (2000). Psychometric properties of the childhood Autism rating scale (CARS) as a diagnostic instrument for autistic adults in the workplace. Journal of General and Applied Psychology: Magazine of the Spanish Federation of Psychology Associations, 53(3), 515-521.

Volkmar, F., Chawarska, K., & Klin, A. (2005). Autism in infancy and early childhood. Annual Review of Psychology, 56(1), 315-336. https://doi.org/10.1146/annurev.psych.56.091103.070159

Wang, K., Wang, C., Guo, D., van Wijngaarden, M., & Begeer, S. (2018). Children with autism spectrum disorder from China and the Netherlands: Age of diagnosis, gender and comorbidities. Research in Autism Spectrum Disorders, 54, 76-82. https://doi.org/10.1016/j.rasd.2018.07.004

Wang, M., Turnbull, A. P., Summers, J. A., Little, T. D., Poston, D. J., Mannan, H., & Turnbull, R. (2004). Severity of disability and income as predictors of parents' satisfaction with their family quality of life during early childhood years. Research and Practice for Persons with Severe Disabilities, 29(2), 82-94. https://doi.org/10.2511/rpsd.29.2.82

Wright, J. (2018b). The prevalence of autism in the U.S. appears steady. Retrieved from htpp://spectrumnews.org/news/prevalence-autism-u-s-remains-steady-new-data-suggest/

Zablotsky, B., Kalb, L. G., Freedman, B., Vasa, R., & Stuart, E. A. (2014). Health care experiences and perceived financial impact among families of children with an autism spectrum disorder. Psychiatric Services, 65(3), 395-398. https://doi.org/10.1176/appi.ps.201200552

Zwaigenbaum, L., Bauman, M. L., Choueiri, R., Kasari, C., Carter, A., Granpeesheh, D., & Fein, D. (2015). Early intervention for children with autism spectrum disorder under 3 years of age: Recommendations for practice and research. Pediatrics, 136(Supplement_1), S60-S81. https://doi.org/https://doi.org/10.1542/peds.2014-3667E

Views and opinions expressed in this article are the views and opinions of the author(s), Humanities and Social Sciences Letters shall not be responsible or answerable for any loss, damage or liability etc. caused in relation to/arising out of the use of the content.