Skip to main content

ORIGINAL RESEARCH article

Front. Psychiatry, 17 June 2024
Sec. Autism
This article is part of the Research Topic COVID and Autism 2023: Lessons Learnt and Future Directions for Research View all 10 articles

Testing an online screening for autism in the COVID-19 pandemic: a psychometric study of the Q-CHAT-24 in Chilean toddlers

Gabriel Gatica-Bahamonde,,,*Gabriel Gatica-Bahamonde1,2,3,4*Alejandra Mendez-Fadol,Alejandra Mendez-Fadol4,5Francisca Snchez-SepúlvedaFrancisca Sánchez-Sepúlveda4Constanza Peailillo-DiazConstanza Peñailillo-Diaz4Robin van Kessel,,Robin van Kessel1,3,6Katarzyna CzabanowskaKatarzyna Czabanowska1Andres Roman-Urrestarazu,,Andres Roman-Urrestarazu3,4,7
  • 1Department of International Health, Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, Netherlands
  • 2Sección de Psiquiatría del Niño y del Adolescente, División de Neurociencias, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile
  • 3Mental Health, Policy and Economics Group, Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom
  • 4Tremün Lab, Corporación Tremün, Villarrica, Chile
  • 5Departamento de Pediatría, Facultad de Medicina, Universidad de La Frontera, Temuco, Chile
  • 6LSE Health, Department of Health Policy, London School of Economics and Political Science, London, United Kingdom
  • 7Institute of Public Health, University of Cambridge, Cambridge, United Kingdom

Background: The aim of this study was to examine some psychometric characteristics of the Chilean-adapted version of the Quantitative Checklist for Autism in Toddlers (Q-CHAT-24) (24) in a group of unselected children (community sample). This version was administered remotely through an online version during the pandemic period to caregivers of children, aged 18–24 months, registered in four primary care polyclinics of the Health Service Araucanía Sur, Chile.

Methods: An intentional non-probabilistic sampling was used. Three hundred and thirteen toddlers were examined. Participants completed an online version of the Q-CHAT-24 which was disseminated through the REDCap platform. Evidence of reliability through internal consistency and evidence of predictive validity through ROC curve analysis were realized.

Results: The mean age of the children evaluated was 21.16 months. The Shapiro-Wilk test revealed that Q-CHAT-24 scores was normally distributed. 71 cases (23.12%) scored 38 points or more on the Q-CHAT-24, qualifying as Autistic Risk. 48 cases (15.63%) were confirmed as autistic through the ADOS-2 Module T. All items were positively correlated with Q-CHAT-24 total score. All items were positively correlated with Q-CHAT-24 total score. Internal consistency was acceptable for the Q-CHAT-24 (Cronbach ́s α=0.78). The internal consistencies were analyzed for the Q-CHAT-24 Factors, and they were good for factor 1 “Communication and Social Interaction” (Cronbach ́s α=0.85) and acceptable for factor 2 “Restrictive and Repetitive Patterns” (Cronbach ́s α=0.74). Receiver operating characteristic (ROC) curve analyses were performed. The AUC values were 0.93 with statistical significance (p<0.01). For the cut-off point of 38, the Sensitivity, Specificity and Youden index values were 0.89, 0.8 and 0.7, respectively. The Positive Predictive Value (PPV) was 86% and the Negative Predictive Value (NPV) was 85%.

Conclusions: In accordance with the objectives of this study, evidence of reliability and predictive validity was demonstrated for the Q-CHAT-24 in this Chilean population. More importantly, this study provides Sensitivity and Specificity data for a remote application version of an autism screening tool already validated in Chile. The implications of this have to do with the possibility of establishing a remote assessment system for children at risk of autism on a population scale.

1 Introduction

Autism Spectrum Disorders (ASD, hereafter ‘autism’) are a group of neurodevelopmental conditions characterized by persistent difficulties in communication and social interaction, and the presence of restricted and repetitive patterns of behavior, interests, and activities (1). Autism is of increasing epidemiological importance: recent studies show prevalence between 1.76% (UK) (2) and 2.77% (US) (3).

Early detection of signs of autism allows early referral to intervention programs (4). This is important because there is evidence that early management improves the prognosis and quality of life of children and their families (5, 6), that interventions are more effective at earlier ages (7) and that early intervention results in lower costs for the health care system (8).

Evidence shows that signs of autism can be detected early during the first and second years of life through caregiver’s self-report by screening tool (9). An autism screening tool is a brief assessment that is administered to detect those who exhibit traits of autism and are therefore at risk for the condition (10) and who can thus be referred to early intervention programs within a critical developmental period priced at 36 months of age (6). Evidence shows that early detection through screening reduces the time between diagnosis and initiation of intervention by up to 70% (11). Despite the above, a very small percentage of parents are alerted to their child’s developmental problems through the application of an autism-specific screening test (12) and a percentage between 30% and 50% of children with autism continue to be diagnosed after the age of 6 years (13).

With restrictions on face-to-face and in-person care, the COVID 19 pandemic posed a major challenge to the goal of early detection and diagnosis of autism, requiring rapid adaptation of child care services to the remote mode of care (14, 15). Brunt et al. (2023) (15) found that while all child populations had their assessment and diagnostic processes disrupted in the pandemic, there were glaring disparities for children with autism.

While prior to the pandemic there were studies showing the feasibility and preliminary accuracy of telemedicine early diagnosis methods (16), evidence for remote assessment methods is still limited. Corona et al. (2023) (17) evaluated the diagnosis concordance of autism between a face-to-face assessment and a remote assessment using ELE-ASD-PEDS (TAP) and the Screening Tool for Autism in Toddlers (STAT), in a sample of 144 children aged 17–36 months. The concordance between the face-to-face and remote assessments was 92%. Some of the factors that explained the diagnostic errors in the remote method were the younger age of the children and the better performance in the developmental assessment. Gibbs et al. (2021) (18) conducted a study investigating the acceptability of remote diagnostic procedures in the COVID-19 crisis. In general, caregivers and parents of children with autism felt welcomed in remote settings and their expectations of assessment were met, but the authors emphasized the need for a high structured assessment process. Colombo et al. (2022) (19) published a descriptive and preliminary analysis of a web platform (Web Italian Network for Autism Spectrum Disorder WIN4ASD) that used CHAT as a tool for early autism screening in a limited care setting.

Chile is a South American country with a population of approximately 19 million inhabitants (20), which despite being considered a high-income country, lives with significant health disparities (21). To address inequalities in the diagnosis and detection of autism, Chile has legislated a new autism law in 2023 that establishes a regulatory framework for the comprehensive care and protection of people with this condition, with the aim of improving their quality of life and promoting their social inclusion (22). The law makes explicit the centrality of early detection in the approach to the condition. A recent systematic review evaluated the tools validated in Chile for early detection of autism, finding only three screening tools (23). Among them is the Q-CHAT, a tool that has been translated, adapted, and validated in Chile by our team demonstrating evidence of Validity, Reliability and Sensitivity/Specificity suitable for use as population Screening (24, 25).

The Quantitative CHecklist for Autism in Toddlers, Q-CHAT (Allison et al., 2008) is an autism screening tool that conceptualizes the autism spectrum on a continuous scale, taking a dimensional approach to the identification of autistic traits (2629). From a theoretical point of view, this proposal is consistent with the conceptual evolution of autism and with the quantitative nature of autistic traits as a continuum of symptoms and traits within the autism spectrum (30). The ability to dimensionally measure autistic traits using the Q-CHAT is supported by evidence showing that test scores are typically distributed across diverse populations studied (24, 2628, 31, 32). In our study of adaptation and validation of the Q-CHAT in Chile (24), by means of an exploratory factor analysis we found a factor structure of 2 factors: a factor that groups the Socio-Communicative symptoms (Factor 1, “Communication and Social Interaction”) and a Factor that groups the repetitive behaviors (Factor 2, “Restrictive and Repetitive Patterns”). This version of the Q-CHAT excluded by rational test analysis item 18, leaving a 24-item version, the Q-CHAT-24. In a recent report (33), cut-off scores for the Q-CHAT-24 were established according to the harmonized optimal levels of Sensitivity/Specificity and the Youden Index. The cut-off point was 38, with a Sensitivity of 0.93, Specificity of 0.81 and Youden index of 0.70.

The overall objective of this study was to examine some psychometric characteristics of the Chilean-adapted version of the Quantitative Checklist for Autism in Toddlers (Q-CHAT-24) (24) in a group of unselected children (community sample). This version was administered remotely through an online version during the pandemic period to caregivers of children, aged 18–24 months, registered in four primary care polyclinics of the Health Service Araucanía Sur, Chile.

2 Materials and methods

2.1 Participants

A descriptive correlational design was used for this study. The sampling technique was non-probabilistic intentional. All primary caregivers of children aged 18–24 months who attended or were contacted remotely (by video call) for developmental follow-up during the quarantines periods in which this study was conducted (October 2020 to September 2021), in four primary care clinics in the Araucanía region of Chile during the study period (n=854), were invited to participate. Three hundred and seven (36.6%) caregivers agreed to participate.

The inclusion criteria were a) aged between 18 and 24 months at the time of the assessment, b) attended face-to-face with the primary caregivers or were contacted remotely for routine developmental follow-up checks. Primary caregiver was defined as the adult(s) responsible for the daily care of the young child (34). Exclusion criteria were a) not being accompanied by the primary caregiver(s), and b) presenting a genetic or neurological condition incompatible with the identification of the behaviors assessed (for example: severe gait disturbance, cerebral palsy, among others).

2.2 Instruments

2.2.1 The Quantitative CHecklist for Autism in Toddlers Chilean version

In its original version (26) the Q-CHAT is a 25-item, parent- or caregiver-reporting scale designed as an autism screening instrument for children aged 18–24 months. The items are scored on a 5-point Likert-type scale (0–4), where higher scores indicate greater autistic traits. Each item is accompanied by a color illustration, which seeks to increase comprehensibility. Total Q-CHAT score >38 was established as the autism risk score.

For this research we used a culturally adapted version validated for Chile by our team (24). In this study we established evidence of concurrent validity with the M-CHAT-R/F, evidence of validity through adequate internal consistency (α=0.86) and established a 2-factor factor structure, excluding item 18 of the original Q-CHAT from the factor solution. A recent report (Gatica-Bahamonde, under review) established the optimal levels of Sensitivity/Specificity and Youden index (0.93/0.82; 0.76) for the 24-item Q-CHAT (Q-CHAT-24) using the cut-off point of 38 for a sample of Chilean preschoolers. This version was reproduced in its entirety and made available to researchers for subsequent dissemination through the REDCap online platform (35).

2.2.2 The autism diagnostic observatory, second version

This is a standardized, semi-structured assessment of communication, social interaction, interests, and imaginative play, which defines the level of concern in relation to a possible diagnosis of ASD. This instrument consists of a set of precise activities, in a standardized context, in which the examinator observes behaviors relevant to the diagnosis of ASD. In this study, we used the Module T which is designed for children under 30 months of age.

2.2.3 Socio-demographic questionnaire

A questionnaire constructed for this study was used, which seeks to collect sociodemographic data about the caregiver and his/her family, such as age, gender, marital status, years of schooling and socioeconomic level, among others.

2.3 Procedure

Between October 2020 and September 2021, all primary caregivers of children aged 18–24 months were invited to participate when they personally accompanied their children to developmental check-ups or when they were contacted remotely by phone or video call (depending on pandemic health conditions). Along with explaining the scope of the study, a link was sent to their mobile phones with access to the digital informed consent and to the REDCap platform where they could answer the Q-CHAT-24 and the socio-demographic questionnaire. When a caregiver agreed to answer the Q-CHAT-24, the results and the final score of their child were obtained immediately, together with indications regarding the steps to follow in case of obtaining a score of 37 or less (no suspected autism), they were instructed to follow their usual developmental controls. For scores of 38 or more (suspected autism), the indication was to wait to be contacted by the research team to start the study to confirm or exclude autism by medical assessment and the administration of ADOS-2 Module T. The study of suspected autism cases was conducted within three months of the Q-CHAT-24.

2.4 Ethical considerations

By signing (digitally) an informed consent, the free and voluntary participation, the confidentiality of data provided by the participants and the fact that they would be used only for research purposes were assured. This research was approved by the ethics committee of Araucanía Health Service, Chile.

2.5 Statistical analysis

The distribution of the total Q-CHAT scores was explored using the Shapiro Wilk (S-W) test. The results were contrasted with the distribution histogram and the standardized normal distribution probability plot (Q-Q Plot). As part of a rational item analysis, item-total correlations were examined using Pearson’s r parametric analyses. Reliability was estimated by examining internal consistency using Cronbach’s alpha for the total scale scores and separately for each of the factors previously found (24). As a measure of predictive validity, receiver operating characteristic (ROC) curves and area under the curve (AUC) with sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated for the cut-off points. Optimal cut-off points were selected based on their utility for screening purposes, following the proposal of Stevanovic et al. (29, 36): sensitivity and specificity > 0.8, sensitivity ≥ specificity, and Youden´s index ≥ 0.70.

3 Results

3.1 Socio-demographic characteristics

The mean age of the children evaluated was 21.16 months (median=20, range 18–24, SD=4.03), where 54.0% (n=169) were males. 78.2% (n=245) lived in urban sectors and 93.0% of the children belonged to families that had incomes below the 75th percentile of Chilean households, equivalent to less than US$1,140 (37). The mean age of caregivers was 30.0 years (median=30, range 18–60, SD=6.8). Of the caregivers who responded to the Q-CHAT, 93.5% (n=287) were mothers, 6.2% (n=19) were fathers, and 0.3% (n=1) were other caregivers. 78.8% (n=241) of the caregivers had 12 or more years of schooling.

Table 1 summarizes the socio-demographic characteristics of the sample.

Table 1
www.frontiersin.org

Table 1 Socio-demographic characteristics of the sample studied (n=307).

3.2 Q-CHAT-24 total scores distribution, item score distribution and item analysis

For the Q-CHAT-24 the mean score for the whole sample analyzed was 30.62 (range 6–69, SD=11.1). The Shapiro-Wilk test revealed that the scores were normally distributed (S-W (307) =0.98, p<0.001) (Figure 1).

Figure 1
www.frontiersin.org

Figure 1 Histogram and Q-Q Plot for Q-CHAT-24 scores distribution in the studied sample (n=307). Figure shows distribution (A) and standardized normal probability plot (B) of the Q−CHAT total score in the screened population (n = 307).

When analyzing scores by gender, the male Q-CHAT-24 mean score of 31.6 (SD=10.81, range 8–59) was higher than the female mean score of 27.98 (SD=9.71, range 6–63). These differences were statistically significant between the two groups (t(305) =2.44, p=0.01).

As part of a rational analysis of the Q-CHAT-24 items, an Item-Total correlation analysis (correlation between the Score of each item and the Total Score without considering the item to be analyzed) was performed. Each of the Q-CHAT-24 items was positively correlated with the Q-CHAT-24 Total Score. The item-total correlation was satisfactory (0.5>r>0.2) for most items, except for item 3 (r<0.2). The item-total analysis is shown in Table 2.

Table 2
www.frontiersin.org

Table 2 Rational analysis of the items: Item-total Q-CHAT-24 Correlation (n=307).

3.3 Q-CHAT-24 reliability

Internal consistency was acceptable for the Q-CHAT-24 (Cronbach ́s α=0.78). The internal consistencies were analyzed for the Q-CHAT-24 Factors, and they were good for factor 1 “Communication and Social Interaction” (Cronbach ́s α=0.85) and acceptable for factor 2 “Restrictive and Repetitive Patterns” (Cronbach ́s α=0.74).

3.4 Comparison between Q-CHAT-24 and ADOS-2 module T scores

Seventy-one cases (23.12%) scored 38 points or more on the Q-CHAT-24, qualifying as Autistic Risk. The mean score in the Autism Risk group was 46.9 (range 38–69, SD=8.0) and the mean score in the Non-Autism Risk group was 26.09 (range 6–37, SD=7.23). The differences observed were statistically significant (t(305) =-19.54, p<0.001).

Of the cases identified as Autism risk, 10 caregivers of children at risk for autism did not agree to undergo with the ADOS-2 confirmatory assessment. 48 cases (78.6%) were confirmed as Autism by the ADOS-2 Module T and 13 (21.3%) were excluded as such. As a control measure, 22 non-risk children were assessed with the ADOS-2 Module T, and all of them were excluded as autistic. Figure 2 summarizes the study design and the selection of participants according to their classification as Autism Risk/Non-Risk according to the Q-CHAT-24 and according to the Autism Confirmed/Excluded status according to the ADOS-2 Module T.

Figure 2
www.frontiersin.org

Figure 2 Study design overview and selection of participants (n=307). Eight hundred and fifty-four caregivers were invited to participate. Of these, 307 agreed to participate by signing the informed consent form and completed the socio-demographic questionnaire and the Q-CHAT-24. Seventy-one children (23.1%) were identified as being at risk for autism. Of these, 48 were confirmed by the ADOS-2 module T as Autism.

The mean score of the Q-CHAT-24 in the group of cases Autism confirmed was 48.23 (range 38–69, SD=8.44) and 37.17 (range 28–44, SD=3.19) for the group of Autism excluded. The observed differences were statistically significant (M-W =122, p<0.001).

The correlation between scores on the Q-CHAT-24 and scores on the ADOS-2 Module T was positive and statistically significant (r=0.65, p<0.001). This correlation was high, positive and significant for the Confirmed and Excluded Autism groups (r=0.65 and r=0.64, respectively). Figure 3 shows a scatter plot with the trend curve for the correlation between scores on the ADOS-2 Module T and the Q-CHAT-24 in the ASD and non-ASD groups.

Figure 3
www.frontiersin.org

Figure 3 ADOS-2 and Q-CHAT-24 Scatterplot (n=307). Figure shows a Scatterplot with a tendency curve to graph the correlation between ADOS-2 Module T and Q-CHAT-24 scores in both ASD and No-ASD groups. The correlation between these scores was high, positive, and statistically significant in both groups (r=0.65, p<0.001 and r=0.65, p<0.00, respectively).

3.5 Predictive validity Q-CHAT-24

Receiver operating characteristic (ROC) curve analyses were performed. The AUC values were 0.93 with statistical significance (p<0.01). For the cut-off point of 38, the Sensitivity, Specificity and Youden index values were 0.89, 0.8 and 0.7, respectively. The Positive Predictive Value (PPV) was 86% and the Negative Predictive Value (NPV) was 85%. Figure 4 shows the ROC curve of the described analysis.

Figure 4
www.frontiersin.org

Figure 4 Q-CHAT-24 ROC Curve. The figure shows the receiver operating characteristic (ROC) curve analysis of Q-CHAT-24 in the studied sample. The AUC values were 0.93 with statistical significance (p<0.01).

4 Discussion

The aim of this study was to examine some psychometric characteristics of the Chilean-adapted version of the Quantitative Checklist for Autism in Toddlers (Q-CHAT-24) (14) in a group of unselected children (community sample). This version was administered remotely through an online version during the pandemic period to caregivers of children, aged 18–24 months, registered in four primary care polyclinics of the Health Service Araucanía Sur, Chile.

Q-CHAT-24 total score showed a normal distribution, replicating previous findings and in other cultural contexts, both in community sample (24, 2629) and confirms the quantitative and dimensional nature with which Q-CHAT was conceived (26).

We found significantly higher scores for boys than for girls. These results are consistent with epidemiological and genetic evidence showing that males are associated with higher autistic traits in general population samples (3840).

The high percentage of children scoring above the cut-off point is consistent with previous findings from the use of the Q-CHAT in the Chilean population reported by Roman-Urrestarazu et al. (24). This percentage is probably determined by the fact that the Q-CHAT-24 identifies autism risk in a heterogeneous child population that shares manifestations with other developmental trajectories such as neurodevelopmental delays.

Rational analysis of the Q-CHAT items showed that 23 of the 24 items have item-total correlations with satisfactory values, which is quantitatively higher than that observed in the 25-item version in the Chilean population (24).

Reliability analysis show acceptable values for the overall scale (α=0.78) and for factor 2”Communication and Social Interaction” (α=0.74), and good for factor 1 “Restrictive and Repetitive Patterns” (α=0.85).

Finally, regarding the evidence of predictive validity, the Q-CHAT-24 showed Sensitivity and Specificity values that met the criteria defined a priori as necessary to be used for screening: sensitivity and specificity > 0.8, sensitivity ≥ specificity, and Youden index ≥ 0.70. Interestingly, for Q-CHAT-24 the cut-off point that best harmonizes the optimal values of sensitivity and specificity (cut-off point of 38), is higher than the one originally proposed by Allison et al. (2008) (26) and replicated by Stevanovic (2021) (29), for a longer version (25 items). As De Leeuw et al. (2020) suggest (41), it is possible that the higher quantification of symptoms observed in our study in relation to other reports is due to the cultural differences that can be observed between cultures in the quantification of autism symptoms. For example, Magaña and Smith (2013) (42) reported lower parental concern in parents of Latino children compared to parents of White American children.

Considering the polytomous nature of the Q-CHAT-24 items, sensitivity and specificity values probably do not account for the full complexity of the test and should be complemented with Predictive Value metrics. In our study, the observed PPV value is high (86%) but lower than those observed by Roman-Urrestarazu et al. (2021) (25)in another sample of Chilean population.

4.1 Limitations

The low response rate (36.6%) is an important limitation of this study and is likely related to self-selection bias and the high rate of scores above the cut-off point for autism risk (23.12%) observed in our sample. This may limit the generalizability of these results to a general population sample.

The study design did not consider the application of the diagnostic Gold Standard (ADOS-2 Module T) (43) to an equal number of control cases without risk of autism, so the specificity values of the test should be taken with caution.

4.2 Conclusions

In accordance with the objectives of this study, evidence of reliability and predictive validity was demonstrated for the Q-CHAT-24 in this Chilean population. More importantly, this study provides Sensitivity and Specificity data for a remote application version of an autism screening tool already validated in Chile. The implications of this have to do with the possibility of establishing a remote assessment system for children at risk of autism on a population scale.

Future directions following this study include examining the Q-CHAT-24 as a measure of early detection of autism in larger samples and conducting other follow-up studies and thus confirming the evidence of predictive validity. Similarly, it would be useful to incorporate other developmental variables such as measures of language and social development in future studies.

Finally, prospective studies could provide evidence on the eventual impact that isolation and lack of socialization may have had on Autism diagnosis rates during the period of the COVID 19 pandemic.

Data availability statement

The datasets presented in this article are not readily available because the data sets generated and analyzed during this study are not publicly available because of our agreement with the parents of the children. Requests to access the datasets should be directed to gabriel.gatica@uc.cl.

Ethics statement

The studies involving humans were approved by Ethics Committee of Araucanía Health Service, Chile. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants’ legal guardians/next of kin.

Author contributions

GG-B: Writing – review & editing, Writing – original draft, Visualization, Validation, Supervision, Software, Resources, Project administration, Methodology, Investigation, Funding acquisition, Formal analysis, Data curation, Conceptualization. AM-F: Writing – review & editing, Writing – original draft, Validation, Supervision, Formal analysis, Data curation. FS-S: Writing – review & editing, Writing – original draft, Resources, Investigation. CP-D: Writing – review & editing, Writing – original draft, Resources, Investigation. RK: Writing – review & editing, Writing – original draft, Methodology, Investigation, Formal analysis, Data curation. KC: Writing – review & editing, Writing – original draft, Supervision, Methodology, Investigation, Formal analysis, Conceptualization. AR-U: Writing – review & editing, Writing – original draft, Supervision, Methodology, Investigation, Formal analysis, Conceptualization.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Acknowledgments

We would like to thank Susana Román and Virginia Monroy C, from the Children’s Health and Rural Health Equity Program of the Southern Araucanía Health Service, for their logistical contribution to this research.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. Arlington,VA: American Psychiatric Association Publishing (2022). doi: 10.1176/appi.books.9780890425787

CrossRef Full Text | Google Scholar

2. Roman-Urrestarazu A, Van Kessel R, Allison C, Matthews FE, Brayne C, Baron-Cohen S. Association of race/ethnicity and social disadvantage with autism prevalence in 7 million school children in England. JAMA Pediatr. (2021) 175. doi: 10.1001/jamapediatrics.2021.0054

CrossRef Full Text | Google Scholar

3. Maenner MJ, Warren Z, Robinson Williams A, Amoakohene E, Bakian AV, Bilder DA, et al. Prevalence and characteristics of autism spectrum disorder among children aged 8 years — Autism and developmental disabilities monitoring network, 11 sites, United States. (2023) 2020. doi: 10.15585/mmwr.ss7202a1

CrossRef Full Text | Google Scholar

4. Elder JH, Kreider CM, Brasher SN, Ansell M. Clinical impact of early diagnosis of autism on the prognosis and parent-child relationships. Psychol Res Behav Manage. (2017) 10:1–9. doi: 10.2147/PRBM

CrossRef Full Text | Google Scholar

5. Dawson G, Rogers S, Munson J, Smith M, Winter J, Greenson J, et al. Randomized, controlled trial of an intervention for toddlers with autism: the early start denver model. Pediatrics. (2010) 125:e17–23. doi: 10.1542/peds.2009-0958

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Zwaigenbaum L, Bauman ML, Choueiri R, Kasari C, Carter A, Granpeesheh D, et al. Early intervention for children with autism spectrum disorder under 3 years of age : recommendations for practice and research. Pediatrics. (2015) 136:s60–81. doi: 10.1542/peds.2014-3667E

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Rogers SJ, Vismara L, Wagner AL, McCormick C, Young G, Ozonoff S. Autism treatment in the first year of life: A pilot study of infant start, a parent-implemented intervention for symptomatic infants. J Autism Dev Disord. (2014) 44:2981–95. doi: 10.1007/s10803-014-2202-y

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Zwaigenbaum L, Bryson S, Garon N. Early identification of autism spectrum disorders. Behav Brain Res. (2013) 251:133–46. doi: 10.1016/j.bbr.2013.04.004

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Lai MC, Lombardo MV, Baron-Cohen S. Autism. Lancet. (2013) 383:896–910. doi: 10.1016/S0140-6736(13)61539-1

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Nickel RE, Huang-Storms L. Early identification of young children with autism spectrum disorder. Indian J Pediatr. (2017) 84:53–60. doi: 10.1007/s12098-015-1894-0

PubMed Abstract | CrossRef Full Text | Google Scholar

11. McPheeters ML, Weitlauf A, Vehorn A, Taylor C, Sathe NA, Krishnaswami S, et al. Screening for Autism Spectrum Disorder in Young Children: A Systematic Evidence Review for the U.S. Preventive Services Task Force (2016). Available online at: http://www.uspreventiveservicestaskforce.org/Page/Document/draft-evidence-review106/autism-spectrum-disorder-in-young-children-screening.

Google Scholar

12. Bejarano-Martín Á, Canal-Bedia R, Magán-Maganto M, Fernández-Álvarez C, Cilleros-Martín MV, Sánchez-Gómez MC, et al. Early detection, diagnosis and intervention services for young children with autism spectrum disorder in the European Union (ASDEU): family and professional perspectives. J Autism Dev Disord. (2020) 50:3380–94. doi: 10.1007/s10803–019-04253–0

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Sheldrick RC, Maye MP, Carter AS. Age at first identification of autism spectrum disorder: an analysis of two US surveys. J Am Acad Child Adolesc Psychiatry. (2017) 56:313–20. doi: 10.1016/j.jaac.2017.01.012

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Kasamba S, McVeigh KH, Moraes A, Huang Y, Puffett N, Lednyak L. Continuity of early intervention services in New York City during the COVID-19 pandemic. Int J Telerehabil. (2023) 15. doi: 10.5195/ijt.2023.6553

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Brunt S, Sadikova E, Pappagianopoulos J, Mazurek MO. The impact of COVID-19 on receipt of health services among children with and without autism. Autism. (2023) 28(3). doi: 10.1177/13623613231176930

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Juárez AP, Weitlauf AS, Nicholson A, Pasternak A, Broderick N, Hine J, et al. Early identification of ASD through telemedicine: potential value for underserved populations. J Autism Dev Disord. (2018) 48:2601–10. doi: 10.1007/s10803-018-3524-y

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Corona LL, Wagner L, Hooper M, Weitlauf A, Foster TE, Hine J, et al. A randomized trial of the accuracy of novel telehealth instruments for the assessment of autism in toddlers. J Autism Dev Disord. (2023) 45:2069–80. doi: 10.1007/s10803-023-05908-9

CrossRef Full Text | Google Scholar

18. Gibbs V, Cai RY, Aldridge F, Wong M. Autism assessment via telehealth during the Covid 19 pandemic: Experiences and perspectives of autistic adults, parents/carers and clinicians. Res Autism Spectr Disord. (2021) 88. doi: 10.1016/j.rasd.2021.101859

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Colombo P, Buo N, Ceccarelli SB, Molteni M. Integrating a new online platform in primary care for early detection, referral, and intervention in autism spectrum disorder: the first Italian pivotal clinical study. Brain Sci. (2022) 12. doi: 10.3390/brainsci12020256

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Instituto Nacional de Estadísticas de Chile. SÍNTESIS DE RESULTADOS CENSO 2017. Santiago de Chile: Instituto Nacional de Estadísticas de Chile (2018).

Google Scholar

21. Frank JW, Matsunaga E. National monitoring systems for health inequalities by socioeconomic status – an OECD snapshot. Crit Public Health. (2022) 32:580–7. doi: 10.1080/09581596.2020.1862761

CrossRef Full Text | Google Scholar

22. Irarrázaval Domínguez M. The autism law in Chile: challenges for implementation and the role of pediatricians. Andes Pediatrica Sociedad Chil Pediatria. (2023) 94:419–20. doi: 10.32641/andespediatr.v94i4.4837

CrossRef Full Text | Google Scholar

23. Luisa SB, Verónica BK, Roxana AE, Lorena VB. Early detection and referral of autism spectrum disorder: review of screening test validated in Chile. Andes Pediatrica. (2023) 94:425–35. doi: 10.32641/andespediatr.v94i4.4901

CrossRef Full Text | Google Scholar

24. Gatica-Bahamonde G, Alarcon P, Fadol AM, Allison C, Baron-Cohen S, Roman-Urrestarazu A. The Quantitative Checklist for Autism in Toddlers (Q-CHAT): A preliminary psychometric study in Chile. PsyArXiv. (2021). doi: 10.31234/osf.io/hmjkx

CrossRef Full Text | Google Scholar

25. Roman-Urrestarazu A, Yáñez C, López-Garí C, Elgueta C, Allison C, Brayne C, et al. Autism screening and conditional cash transfers in Chile: Using the Quantitative Checklist (Q-CHAT) for early autism detection in a low resource setting. Autism. (2021) 25:932–45. doi: 10.1177/1362361320972277

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Allison C, Baron-Cohen S, Wheelwright S, Charman T, Richler J, Pasco G, et al. The Q-CHAT (Quantitative CHecklist for Autism in Toddlers): A normally distributed quantitative measure of autistic traits at 18–24 months of age: Preliminary report. J Autism Dev Disord. (2008) 38:1414–25. doi: 10.1007/s10803-007-0509-7

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Ruta L, Arduino GM, Gagliano A, Apicella F, Leonardi E, Famà FI, et al. Psychometric properties, factor structure and cross-cultural validity of the quantitative CHecklist for autism in toddlers (Q-CHAT) in an Italian community setting. Res Autism Spectr Disord. (2019) 64:39–48. doi: 10.1016/j.rasd.2019.04.004

CrossRef Full Text | Google Scholar

28. Magiati I, Goh DA, Lim SJ, Gan DZQ, Leong JCL, Allison C, et al. The psychometric properties of the Quantitative-Checklist for Autism in Toddlers (Q-CHAT) as a measure of autistic traits in a community sample of Singaporean infants and toddlers. Mol Autism. (2015) 6:40–53. doi: 10.1186/s13229–015-0032–1

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Stevanović D. Quantitative Checklist for Autism in Toddlers (Q-CHAT): A psychometric study with Serbian Toddlers. Res Autism Spectr Disord. (2021) 83. doi: 10.1016/j.rasd.2021.101760

CrossRef Full Text | Google Scholar

30. Constantino JN, Charman T. Diagnosis of autism spectrum disorder: reconciling the syndrome, its diverse origins, and variation in expression. Lancet Neurol. (2016) 15:279–91. doi: 10.1016/S1474–4422(15)00151–9

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Ruta L, Chiarotti F, Arduino GM, Apicella F, Leonardi E, Maggio R, et al. Validation of the Quantitative CHecklist for Autism in Toddlers (Q-CHAT) in an Italian clinical sample of young children with Autism and Other Developmental Disorders. Front Psychiatry. (2019) 10:488. doi: 10.3389/fpsyt.2019.00488

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Mohammadian M, Zarafshan H, Mohammadi MR, Karimi I. Evaluating reliability and predictive validity of the persian translation of quantitative checklist for autism in toddlers (Q-CHAT). Iran J Psychiatry. (2015) 10:64–70.

PubMed Abstract | Google Scholar

33. Gatica-Bahamonde G. The Quantitative Checklist for Autism in Toddlers (Q-CHAT) and Q-CHAT-10: A psychometric study in Chilean Toddlers. PsyArxiv. (2023). doi: 10.31234/osf.io/3rv4e

CrossRef Full Text | Google Scholar

34. RELAF, UNICEF. Cuidado de Niños Pequeños. In: Modelo para la Prevención del Abandono y la Institucionalización. Buenos Aires, Argentina: RELAF & UNiCEF. (2015). Available at: https://www.unicef.org/lac/20160907_UNICEF_RELAF_Prevencion.PDF.

Google Scholar

35. Harris PA, Taylor R, Minor BL, Elliott V, Fernandez M, O’Neal L, et al. The REDCap consortium: Building an international community of software platform partners. J Biomed Inf. (2019) 95. doi: 10.1016/j.jbi.2019.103208

CrossRef Full Text | Google Scholar

36. Stevanovic D, Knez R, Zorcec T, Anderluh M, Kodrič J, Petrov P, et al. ESSENCE-Q: Slavic language versions for developmental screening in young children. Neuropsychiatr Dis Treat. (2018) 14:2141–8. doi: 10.2147/NDT

PubMed Abstract | CrossRef Full Text | Google Scholar

37. GFK/ADIMARK. Nuevos Grupos Socioeconómicos 2018 (2018). Available online at: http://www.aimChile.cl/wp-content/uploads/Nuevos-Grupos-Socioeconómicos-AIM-febrero-2018-FINAL-2.pdf.

Google Scholar

38. Baron-Cohen S, Wheelwright S, Skinner R, Martin J, Clubley E. The autism-spectrum quotient (AQ): evidence from asperger syndrome/high-functioning autism, males and females, scientists and mathematicians. J Autism Dev Disord. (2001) 31:5–17. doi: 10.1023/A:1005653411471

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Chakrabarti B, Dudbridge F, Kent L, Wheelwright S, Hill-Cawthorne G, Allison C, et al. Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and asperger syndrome. Autism Res. (2009) 2:157–77. doi: 10.1002/aur.80

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Chakrabarti S, Fombonne E. Pervasive developmental disorders in preschool children: Confirmation of high prevalence. Am J Psychiatry. (2005) 162:1133–41. doi: 10.1176/appi.ajp.162.6.1133

PubMed Abstract | CrossRef Full Text | Google Scholar

41. de Leeuw A, Happé F, Hoekstra RA. A conceptual framework for understanding the cultural and contextual factors on autism across the globe. Autism Res. (2020) 13:1029–50. doi: 10.1002/aur.2276

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Magaña S, Smith LE. The use of the autism diagnostic interview-revised with a latino population of adolescents and adults with autism. J Autism Dev Disord. (2013) 43:1098–105. doi: 10.1007/s10803-012-1652-3

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Lord C, Luyster R, Gotham K, Guthrie W. Autism diagnostic observation schedule, (ADOS-2) manual (Part II): Toddler module. Los Angeles: Western Psychological Services (2012).

Google Scholar

Keywords: autism spectrum disorder, early detection, online screening, screening, COVID-19, Q-CHAT, autism, telehealth

Citation: Gatica-Bahamonde G, Mendez-Fadol A, Sánchez-Sepúlveda F, Peñailillo-Diaz C, van Kessel R, Czabanowska K and Roman-Urrestarazu A (2024) Testing an online screening for autism in the COVID-19 pandemic: a psychometric study of the Q-CHAT-24 in Chilean toddlers. Front. Psychiatry 15:1363976. doi: 10.3389/fpsyt.2024.1363976

Received: 31 December 2023; Accepted: 31 May 2024;
Published: 17 June 2024.

Edited by:

Cecilia Montiel Nava, The University of Texas Rio Grande Valley, United States

Reviewed by:

Magdalena Budisteanu, Prof. Dr. Alexandru Obregia Psychiatry Hospital, Romania
Katherine Stavropoulos, University of California, Riverside, United States

Copyright © 2024 Gatica-Bahamonde, Mendez-Fadol, Sánchez-Sepúlveda, Peñailillo-Diaz, van Kessel, Czabanowska and Roman-Urrestarazu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Gabriel Gatica-Bahamonde, Z2FicmllbC5nYXRpY2FAdWMuY2w=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.