You are leaving Medscape Education
Cancel Continue
Log in to save activities Your saved activities will show here so that you can easily access them whenever you're ready. Log in here CME & Education Log in to keep track of your credits.
 

Table 1.  

Site Surveillance area description Denominator No. aged 4 yrs with ASD ASD prevalence (95% CI) % Who had an ASD diagnostic statement % Who had ASD special education eligibility % Who had ASD ICD code
Arizona Part of one county in metropolitan Phoenix 13,349§ 209 15.7 (13.7–17.9) 75.6 11.0 63.2
Arkansas 21 counties in central Arkansas 15,150 245 16.2 (14.3–18.3) 95.5 36.3 84.5
California Part of one county in metropolitan San Diego 16,719§ 776 46.4 (43.3–49.7) 85.8 69.7 88.3
Georgia Two counties in metropolitan Atlanta 21,985 384 17.5 (15.8–19.3) 77.3 41.1 71.1
Maryland Five counties in suburban Baltimore 20,745 352 17.0 (15.3–18.8) 90.3 43.2 72.4
Minnesota Parts of three counties in the Twin Cities metropolitan area 16,326§ 305 18.7 (16.7–20.9) 54.1 75.1 22.0
Missouri Five counties in metropolitan St. Louis 24,476 456 18.6 (17.0–20.4) 95.0 17.5 92.5
New Jersey Two counties in the New York metropolitan area 19,120 473 24.7 (22.6–27.0) 98.3 9.3 76.7
Tennessee 11 counties in middle Tennessee 26,474 737 27.8 (25.9–29.9) 71.0 32.8 92.7
Utah Three counties in northern Utah 24,330 308 12.7 (11.3–14.1) 79.9 25.0 81.8
Wisconsin Eight counties in southeastern Wisconsin 28,852 651 22.6 (20.9–24.3) 65.1 35.3 84.0
Total 227,526 4,896 21.5 (20.922.1) 80.2 38.1 79.4

Table 1. Prevalence* of autism spectrum disorder among children aged 4 years and percentage of children who had an autism spectrum disorder diagnosis, special education eligibility, or an International Classification of Diseases code — Autism and Developmental Disabilities Monitoring Network, 11 sites, 2020

Abbreviations: ASD = autism spectrum disorder; ICD = International Classification of Diseases.
*Per 1,000 children aged 4 years.
95% CIs were calculated using the Wilson score method.
§Denominator excludes school districts that were not included in the surveillance area, calculated from National Center for Education Statistics enrollment counts of kindergarteners during the 2020–21 school year.

Table 2.  

Site Male ASD prevalence (95% CI)§ Female ASD prevalence (95% CI) Male-to-female prevalence ratio (95% CI)
Arizona 24.2 (20.8–28.1) 6.9 (5.1–9.2) 3.5 (2.5–4.9)
Arkansas 24.9 (21.7–28.6) 6.9 (5.2–9.0) 3.6 (2.7–4.9)
California 71.7 (66.4–77.4) 20.5 (17.6–23.7) 3.5 (3.0–4.1)
Georgia 25.5 (22.7–28.6) 8.9 (7.3–10.9) 2.9 (2.3–3.6)
Maryland 26.4 (23.5–29.6) 7.3 (5.8–9.1) 3.6 (2.8–4.7)
Minnesota 29.7 (26.3–33.6) 7.3 (5.7–9.4) 4.1 (3.1–5.4)
Missouri 26.8 (24.1–29.8) 10.2 (8.6–12.2) 2.6 (2.1–3.2)
New Jersey 35.0 (31.5–38.9) 14.1 (11.9–16.7) 2.5 (2.0–3.0)
Tennessee 41.1 (37.8–44.5) 14.3 (12.4–16.4) 2.9 (2.4–3.4)
Utah 19.5 (17.3–22.1) 5.5 (4.3–7.0) 3.6 (2.7–4.7)
Wisconsin 33.4 (30.6–36.4) 11.2 (9.6–13.1) 3.0 (2.5–3.6)
Total 32.3 (31.3–33.3) 10.4 (9.8–11.0) 3.1 (2.9–3.3)

Table 2. Prevalence* of autism spectrum disorder among children aged 4 years, by sex — Autism and Developmental Disabilities Monitoring Network, 11 sites, United States, 2020

Abbreviation: ASD = autism spectrum disorder.
*Per 1,000 children aged 4 years.
Four children were missing sex information.
§95% CIs were calculated using the Wilson score method.
Prevalence was significantly higher among males than females at all sites (95% CI excludes 1.0).

Table 3.  

Site ASD prevalence (95% CI)§ Prevalence ratio (95% CI)
White Black Hispanic Asian/Pacific Islander Multiracial Black to White Hispanic to White Asian/Pacific Islander to White Multiracial to White
Arizona 18.4 (15.0–22.5) 15.0 (8.9–25.0) 14.7 (12.0–18.2) 0.8 (0.5–1.4) 0.8 (0.6–1.1)
Arkansas 13.6 (11.4–16.2) 22.4 (18.1–27.8) 17.6 (12.1–25.5) 15.8 (8.8–28.1) 1.6 (1.2–2.2)** 1.3 (0.9–1.9) 1.2 (0.6–2.1)
California 31.0 (26.2–36.6) 54.3 (42.6–68.8) 52.8 (48.1–57.9) 45.5 (37.1–55.6) 52.4 (41.7–65.7) 1.8 (1.3–2.3)** 1.7 (1.4–2.1)** 1.5 (1.1–1.9)** 1.7 (1.3–2.2)**
Georgia 8.1 (6.0–10.7) 21.9 (19.3–24.9) 16.1 (12.0–21.7) 17.4 (12.5–24.3) 20.8 (13.2–32.7) 2.7 (2.0–3.7)** 2.0 (1.3–3.0)** 2.2 (1.4–3.3)** 2.6 (1.5–4.4)**
Maryland 11.9 (10.0–14.1) 27.6 (23.3–32.5) 12.9 (8.9–18.6) 22.3 (16.5–30.2) 17.0 (11.3–25.7) 2.3 (1.8–3.0)** 1.1 (0.7–1.6) 1.9 (1.3–2.7)** 1.4 (0.9–2.2)
Minnesota 13.1 (10.7–16.1) 23.4 (19.0–28.7) 24.1 (17.8–32.4) 18.9 (14.4–25.0) 19.0 (12.4–28.8) 1.8 (1.3–2.4)** 1.8 (1.3–2.6)** 1.4 (1.0–2.0)** 1.4 (0.9–2.3)
Missouri 17.3 (15.4–19.5) 22.4 (18.8–26.5) 15.8 (10.1–24.5) 26.1 (17.6–38.5) 9.7 (5.6–16.9) 1.3 (1.0–1.6)** 0.9 (0.6–1.4) 1.5 (1.0–2.3)** 0.6 (0.3–1.0)
New Jersey 16.4 (13.3–20.3) 23.8 (20.1–28.1) 31.7 (27.8–36.1) 17.6 (11.4–27.0) 1.4 (1.1–1.9)** 1.9 (1.5–2.5)** 1.1 (0.7–1.7)
Tennessee 23.8 (21.5–26.3) 34.6 (29.6–40.3) 31.4 (26.3–37.5) 28.7 (19.7–41.8) 17.5 (12.0–25.5) 1.5 (1.2–1.7)** 1.3 (1.1–1.6)** 1.2 (0.8–1.8) 0.7 (0.5–1.1)
Utah 11.7 (10.2–13.5) 14.9 (11.9–18.5) 16.3 (10.4–25.2) 1.3 (1.0–1.6)** 1.4 (0.9–2.2)
Wisconsin 16.5 (14.6–18.6) 27.5 (23.4–32.2) 36.9 (32.0–42.6) 22.5 (16.3–31.0) 17.1 (11.6–25.1) 1.7 (1.4–2.0)** 2.2 (1.9–2.7)** 1.4 (1.0–1.9)** 1.0 (0.7–1.6)
Total†† 16.3 (15.5–17.0) 25.3 (23.9–26.8) 28.7 (27.2–30.3) 23.5 (21.2–26.1) 19.3 (17.0–21.9) 1.6 (1.4–1.7)** 1.8 (1.6–1.9)** 1.4 (1.3–1.6)** 1.2 (1.0–1.4)**

Table 3. Prevalence* of autism spectrum disorder among children aged 4 years, by race and ethnicity — Autism and Developmental Disabilities Monitoring Network, 11 sites, 2020

Per 1,000 children aged 4 years.
Persons of Hispanic origin might be of any race but are categorized as Hispanic; all racial groups are non-Hispanic. Excludes children of other or unknown race (n = 94).
§95% CIs were calculated using the Wilson score method.
Dashes indicate suppressed estimate (relative SE ≥30% estimate or ratio involving at least one suppressed estimate).
**Significant prevalence ratio (95% CI excludes 1.0).
††All site estimates for American Indian/Alaska Native (AI/AN) children were unstable (relative SE ≥30% estimate) and therefore not reported in the table. Overall AI/AN prevalence was 11.1 (95% CI = 6.2–19.7). Prevalence among AI/AN children was similar to White children (White-to-AI/AN prevalence ratio = 1.5; 95% CI = 0.8–2.6), but ASD prevalence was higher among Black (Black-to-AI/AN prevalence ratio = 2.3; 95% CI = 1.3–4.1), Hispanic (Hispanic-to-AI/AN prevalence ratio = 2.6; 95% CI = 1.4–4.6), A/PI (A/PI-to-AI/AN prevalence ratio = 2.1; 95% CI = 1.2–3.8), and multiracial (multiracial-to-AI/AN prevalence ratio = 1.7; 95% CI = 1.0–3.2) children.

Table 4.  

Site/Characteristic With intellectual disability information No. (%)* With co-occurring intellectual disability No. (%)
Arizona 172 (82.3) 70 (40.7)
Arkansas 220 (89.8) 148 (67.3)
California 594 (76.5) 147 (24.7)
Georgia 273 (71.1) 155 (56.8)
Maryland 226 (64.2) 132 (58.4)
Minnesota 229 (75.1) 143 (62.4)
Missouri 185 (40.6) 93 (50.3)
New Jersey 228 (48.2) 135 (59.2)
Tennessee 327 (44.4) 182 (55.7)
Utah 148 (48.1) 64 (43.2)
Wisconsin 251 (38.6) 115 (45.8)
Total 2,853 (58.3) 1,384 (48.5)
Sex§
Female 654 (56.4) 302 (46.2)
Male 2,198 (58.9) 1,081 (49.2)
Race and ethnicity
Asian/Pacific Islander 231 (67.0) 114 (49.4)
Black 664 (56.4) 416 (62.7)
White 1,018 (57.1) 438 (43.0)
Multiracial 163 (71.2) 66 (40.5)
Hispanic 748 (59.5) 334 (44.7)

Table 4. Presence of co-occurring intellectual disability among children aged 4 years with autism spectrum disorder and available intellectual disability information, by site and selected characteristics — Autism and Developmental Disabilities Monitoring Network, 11 sites, 2020

*Chi-square p values for significant comparisons for presence of intellectual disability information: White to Asian/Pacific Islander, White to multiracial, Black to Asian/Pacific Islander, Black to multiracial: p<0.01.
Chi-square p values for significant comparisons for presence of co-occurring intellectual disability: White to Black, Black to Hispanic, Black to Asian/Pacific Islander, and Black to multiracial: p<0.01.
§One child with intellectual disability information was missing sex information
Persons of Hispanic origin might be of any race but are categorized as Hispanic; all racial groups are non-Hispanic. Excludes children of other or unknown race; American Indian or Alaska Native not shown because of small numbers.

Table 5.  

Site/Characteristic No. with evaluation Evaluated by age 36 mos No. (%)*
Arizona 191 160 (83.8)
Arkansas 245 215 (87.8)
California 770 648 (84.2)
Georgia 341 269 (78.9)
Maryland 342 284 (83.0)
Minnesota 300 227 (75.7)
Missouri 456 343 (75.2)
New Jersey 472 377 (79.9)
Tennessee 649 433 (66.7)
Utah 291 221 (75.9)
Wisconsin 503 378 (75.1)
Total 4,560 3,555 (78.0)
Sex
Female 1,082 842 (77.8)
Male 3,477 2,712 (78.0)
Race and ethnicity§
Asian/Pacific Islander 326 246 (75.5)
Black 1,087 825 (75.9)
White 1,653 1,307 (79.1)
Multiracial 218 174 (79.8)
Hispanic 1,182 943 (79.8)
Co-occurring intellectual disability
Intellectual disability confirmed 1,372 1,131 (82.4)
No intellectual disability 1,452 1,235 (85.1)
Unknown 1,736 1,189 (68.5)

Table 5. Percentage of children aged 4 years with autism spectrum disorder who had earliest recorded evaluation by age 36 months, by site and selected characteristics — Autism and Developmental Disabilities Monitoring Network, 11 sites, United States, 2020

*Chi-square p values for significant comparisons: Black to Hispanic: p = 0.03, confirmed intellectual disability to unknown, and no intellectual disability to unknown: p<0.01.
One child with an evaluation was missing sex information.
§Persons of Hispanic origin might be of any race but are categorized as Hispanic; all racial groups are non-Hispanic. Excludes children of other or unknown race; American Indian or Alaska Native not shown because of small numbers.

CME / ABIM MOC

Early Identification of Autism Spectrum Disorder Among Children Aged 4 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2020

  • Authors: Kelly A. Shaw, PhD; Deborah A. Bilder, MD; Dedria McArthur, MPH; Ashley Robinson Williams, MPH; Esther Amoakohene, MPH; Amanda V. Bakian, PhD; Maureen S. Durkin, DrPH, PhD; Robert T. Fitzgerald, PhD; Sarah M. Furnier, MS; Michelle M. Hughes, PhD; Elise T. Pas, PhD; Angelica Salinas, MS; Zachary Warren, PhD; Susan Williams; Amy Esler, PhD; Andrea Grzybowski, MS; Christine M. Ladd-Acosta, PhD; Mary Patrick, MPH; Walter Zahorodny, PhD; Katie K. Green, MPH; Jennifer Hall-Lande, PhD; Maya Lopez, MD; Kristen Clancy Mancilla; Ruby H.N. Nguyen, PhD; Karen Pierce, PhD; Yvette D. Schwenk, MS; Josephine Shenouda, MS; Kate Sidwell; Alison Vehorn, MS; Monica DiRienzo, MA; Johanna Gutierrez; Libby Hallas, MS; Allison Hudson; Margaret H. Spivey; Sydney Pettygrove, PhD; Anita Washington, MPH; Matthew J. Maenner, PhD
  • CME / ABIM MOC Released: 9/29/2023
  • Valid for credit through: 9/29/2024, 11:59 PM EST
Start Activity

  • Credits Available

    Physicians - maximum of 0.75 AMA PRA Category 1 Credit(s)™

    ABIM Diplomates - maximum of 0.75 ABIM MOC points

    You Are Eligible For

    • Letter of Completion
    • ABIM MOC points

Target Audience and Goal Statement

This activity is intended for primary care clinicians, pediatricians, neurologists, and other healthcare professionals who care for children at risk for autism spectrum disorder (ASD).

The goal of this activity is for learners to be better able to assess trends in the recognition of ASD among US children.

Upon completion of this activity, participants will:

  • Assess demographic trends in the recognition of autism spectrum disorder (ASD) among children aged 4 years
  • Distinguish the racial/ethnic group with the highest prevalence of ASD in 2020
  • Evaluate rates of co-occurring intellectual disability with ASD
  • Analyze trends in the recognition of ASD among children over time


Disclosures

Medscape, LLC requires every individual in a position to control educational content to disclose all financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.

All relevant financial relationships for anyone with the ability to control the content of this educational activity are listed below and have been mitigated. Others involved in the planning of this activity have no relevant financial relationships.


Faculty

  • Kelly A. Shaw, PhD

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Kelly A. Shaw, PhD, has no relevant financial relationships.

  • Deborah A. Bilder, MD

    University of Utah School of Medicine
    Salt Lake City, Utah

    Disclosures

    Deborah A. Bilder, MD, has no relevant financial relationships.

  • Dedria McArthur, MPH

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Dedria McArthur, MPH, has no relevant financial relationships.

  • Ashley Robinson Williams, MPH

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia
    Oak Ridge Institute for Research and Education
    Oak Ridge, Tennessee

    Disclosures

    Ashley Robinson Williams, MPH, has no relevant financial relationships.

  • Esther Amoakohene, MPH

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Esther Amoakohene, MPH, has no relevant financial relationships.

  • Amanda V. Bakian, PhD

    University of Utah School of Medicine
    Salt Lake City, Utah

    Disclosures

    Amanda V. Bakian, PhD, has no relevant financial relationships.

  • Maureen S. Durkin, DrPH, PhD

    University of Wisconsin
    Madison, Wisconsin

    Disclosures

    Maureen S. Durkin, DrPH, PhD, has no relevant financial relationships.

  • Robert T. Fitzgerald, PhD

    Washington University
    St Louis, Missouri

    Disclosures

    Robert T. Fitzgerald, PhD, has no relevant financial relationships.

  • Sarah M. Furnier, MS

    University of Wisconsin
    Madison, Wisconsin

    Disclosures

    Sarah M. Furnier, MS, has no relevant financial relationships.

  • Michelle M. Hughes, PhD

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Michelle M. Hughes, PhD, has no relevant financial relationships.

  • Elise T. Pas, PhD

    Johns Hopkins Bloomberg School of Public Health
    Baltimore, Maryland

    Disclosures

    Elise T. Pas, PhD, has no relevant financial relationships.

  • Angelica Salinas, MS

    University of Wisconsin
    Madison, Wisconsin

    Disclosures

    Angelica Salinas, MS, has no relevant financial relationships.

  • Zachary Warren, PhD

    Vanderbilt University Medical Center
    Nashville, Tennessee

    Disclosures

    Zachary Warren, PhD, has no relevant financial relationships.

  • Susan Williams

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Susan Williams has no relevant financial relationships.

  • Amy Esler, PhD

    University of Minnesota
    Minneapolis, Minnesota

    Disclosures

    Amy Esler, PhD, has no relevant financial relationships.

  • Andrea Grzybowski, MS

    University of California
    San Diego, California

    Disclosures

    Andrea Grzybowski, MS, has no relevant financial relationships.

  • Christine M. Ladd-Acosta, PhD

    Johns Hopkins Bloomberg School of Public Health
    Baltimore, Maryland

    Disclosures

    Christine M. Ladd-Acosta, PhD, has no relevant financial relationships.

  • Mary Patrick, MPH

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Mary Patrick, MPH, has no relevant financial relationships.

  • Walter Zahorodny, PhD

    Rutgers New Jersey Medical School
    Newark, New Jersey

    Disclosures

    Walter Zahorodny, PhD, has no relevant financial relationships.

  • Katie K. Green, MPH

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Katie K. Green, MPH, has no relevant financial relationships.

  • Jennifer Hall-Lande, PhD

    University of Minnesota
    Minneapolis, Minnesota

    Disclosures

    Jennifer Hall-Lande, PhD, has no relevant financial relationships.

  • Maya Lopez, MD

    University of Arkansas for Medical Sciences
    Little Rock, Arkansas

    Disclosures

    Maya Lopez, MD, has no relevant financial relationships.

  • Kristen Clancy Mancilla

    University of Arizona
    Tucson, Arizona

    Disclosures

    Kristen Clancy Mancilla has no relevant financial relationships.

  • Ruby H.N. Nguyen, PhD

    University of Minnesota
    Minneapolis, Minnesota

    Disclosures

    Ruby H.N. Nguyen, PhD, has no relevant financial relationships.

  • Karen Pierce, PhD

    University of California
    San Diego, California

    Disclosures

    Karen Pierce, PhD, has no relevant financial relationships.

  • Yvette D. Schwenk, MS

    University of Arkansas for Medical Sciences
    Little Rock, Arkansas

    Disclosures

    Yvette D. Schwenk, MS, has no relevant financial relationships.

  • Josephine Shenouda, MS

    Rutgers New Jersey Medical School
    Newark, New Jersey

    Disclosures

    Josephine Shenouda, MS, has no relevant financial relationships.

  • Kate Sidwell

    Rutgers New Jersey Medical School
    Newark, New Jersey

    Disclosures

    Kate Sidwell has no relevant financial relationships.

  • Alison Vehorn, MS

    Vanderbilt University Medical Center
    Nashville, Tennessee

    Disclosures

    Alison Vehorn, MS, has no relevant financial relationships.

  • Monica DiRienzo, MA

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Monica DiRienzo, MA, has no relevant financial relationships.

  • Johanna Gutierrez

    University of Utah School of Medicine
    Salt Lake City, Utah

    Disclosures

    Johanna Gutierrez has no relevant financial relationships.

  • Libby Hallas, MS

    University of Minnesota
    Minneapolis, Minnesota

    Disclosures

    Libby Hallas, MS, has no relevant financial relationships.

  • Allison Hudson

    University of Arkansas for Medical Sciences
    Little Rock, Arkansas

    Disclosures

    Allison Hudson has no relevant financial relationships.

  • Margaret H. Spivey

    Johns Hopkins Bloomberg School of Public Health
    Baltimore, Maryland

    Disclosures

    Margaret H. Spivey has no relevant financial relationships.

  • Sydney Pettygrove, PhD

    University of Arizona
    Tucson, Arizona

    Disclosures

    Sydney Pettygrove, PhD, has no relevant financial relationships.

  • Anita Washington, MPH

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Anita Washington, MPH, has no relevant financial relationships.

  • Matthew J. Maenner, PhD

    National Center on Birth Defects and Developmental Disabilities
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Matthew J. Maenner, PhD, has no relevant financial relationships.

CME Author

  • Charles P. Vega, MD

    Health Sciences Clinical Professor of Family Medicine
    University of California, Irvine School of Medicine

    Disclosures

    Charles P. Vega, MD, has the following relevant financial relationships:
    Consultant or advisor for: Boehringer Ingelheim Pharmaceuticals, Inc.; GlaxoSmithKline; Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

Compliance Reviewer

  • Leigh Schmidt, MSN, RN, CNE, CHCP

    Associate Director, Accreditation and Compliance, Medscape, LLC

    Disclosures

    Leigh Schmidt, MSN, RN, CNE, CHCP, has no relevant financial relationships.


Accreditation Statements

Medscape

Interprofessional Continuing Education

In support of improving patient care, Medscape, LLC is jointly accredited with commendation by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.

    For Physicians

  • Medscape, LLC designates this enduring material for a maximum of 0.75 AMA PRA Category 1 Credit(s)™ . Physicians should claim only the credit commensurate with the extent of their participation in the activity.

    Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 0.75 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit. Aggregate participant data will be shared with commercial supporters of this activity.

    Contact This Provider

For questions regarding the content of this activity, contact the accredited provider for this CME/CE activity noted above. For technical assistance, contact [email protected]


Instructions for Participation and Credit

There are no fees for participating in or receiving credit for this online educational activity. For information on applicability and acceptance of continuing education credit for this activity, please consult your professional licensing board.

This activity is designed to be completed within the time designated on the title page; physicians should claim only those credits that reflect the time actually spent in the activity. To successfully earn credit, participants must complete the activity online during the valid credit period that is noted on the title page. To receive AMA PRA Category 1 Credit™, you must receive a minimum score of 70% on the post-test.

Follow these steps to earn CME/CE credit*:

  1. Read about the target audience, learning objectives, and author disclosures.
  2. Study the educational content online or print it out.
  3. Online, choose the best answer to each test question. To receive a certificate, you must receive a passing score as designated at the top of the test. We encourage you to complete the Activity Evaluation to provide feedback for future programming.

You may now view or print the certificate from your CME/CE Tracker. You may print the certificate, but you cannot alter it. Credits will be tallied in your CME/CE Tracker and archived for 6 years; at any point within this time period, you can print out the tally as well as the certificates from the CME/CE Tracker.

*The credit that you receive is based on your user profile.

CME / ABIM MOC

Early Identification of Autism Spectrum Disorder Among Children Aged 4 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2020

Authors: Kelly A. Shaw, PhD; Deborah A. Bilder, MD; Dedria McArthur, MPH; Ashley Robinson Williams, MPH; Esther Amoakohene, MPH; Amanda V. Bakian, PhD; Maureen S. Durkin, DrPH, PhD; Robert T. Fitzgerald, PhD; Sarah M. Furnier, MS; Michelle M. Hughes, PhD; Elise T. Pas, PhD; Angelica Salinas, MS; Zachary Warren, PhD; Susan Williams; Amy Esler, PhD; Andrea Grzybowski, MS; Christine M. Ladd-Acosta, PhD; Mary Patrick, MPH; Walter Zahorodny, PhD; Katie K. Green, MPH; Jennifer Hall-Lande, PhD; Maya Lopez, MD; Kristen Clancy Mancilla; Ruby H.N. Nguyen, PhD; Karen Pierce, PhD; Yvette D. Schwenk, MS; Josephine Shenouda, MS; Kate Sidwell; Alison Vehorn, MS; Monica DiRienzo, MA; Johanna Gutierrez; Libby Hallas, MS; Allison Hudson; Margaret H. Spivey; Sydney Pettygrove, PhD; Anita Washington, MPH; Matthew J. Maenner, PhDFaculty and Disclosures

CME / ABIM MOC Released: 9/29/2023

Valid for credit through: 9/29/2024, 11:59 PM EST

processing....

Abstract and Introduction

Abstract

Problem/Condition: Autism spectrum disorder (ASD).

Period Covered: 2020.

Description of System: The Autism and Developmental Disabilities Monitoring Network is an active surveillance program that estimates prevalence and characteristics of ASD and monitors timing of ASD identification among children aged 4 and 8 years. In 2020, a total of 11 sites (located in Arizona, Arkansas, California, Georgia, Maryland, Minnesota, Missouri, New Jersey, Tennessee, Utah, and Wisconsin) conducted surveillance of ASD among children aged 4 and 8 years and suspected ASD among children aged 4 years. Surveillance included children who lived in the surveillance area at any time during 2020. Children were classified as having ASD if they ever received 1) an ASD diagnostic statement in an evaluation, 2) a special education classification of autism (eligibility), or 3) an ASD International Classification of Diseases (ICD) code (revisions 9 or 10). Children aged 4 years were classified as having suspected ASD if they did not meet the case definition for ASD but had a documented qualified professional's statement indicating a suspicion of ASD. This report focuses on children aged 4 years in 2020 compared with children aged 8 years in 2020.

Results: For 2020, ASD prevalence among children aged 4 years varied across sites, from 12.7 per 1,000 children in Utah to 46.4 in California. The overall prevalence was 21.5 and was higher among boys than girls at every site. Compared with non-Hispanic White children, ASD prevalence was 1.8 times as high among Hispanic, 1.6 times as high among non-Hispanic Black, 1.4 times as high among Asian or Pacific Islander, and 1.2 times as high among multiracial children. Among the 58.3% of children aged 4 years with ASD and information on intellectual ability, 48.5% had an IQ score of ≤70 on their most recent IQ test or an examiner's statement of intellectual disability. Among children with a documented developmental evaluation, 78.0% were evaluated by age 36 months. Children aged 4 years had a higher cumulative incidence of ASD diagnosis or eligibility by age 48 months compared with children aged 8 years at all sites; risk ratios ranged from 1.3 in New Jersey and Utah to 2.0 in Tennessee. In the 6 months before the March 2020 COVID-19 pandemic declaration by the World Health Organization, there were 1,593 more evaluations and 1.89 more ASD identifications per 1,000 children aged 4 years than children aged 8 years received 4 years earlier. After the COVID-19 pandemic declaration, this pattern reversed: in the 6 months after pandemic onset, there were 217 fewer evaluations and 0.26 fewer identifications per 1,000 children aged 4 years than children aged 8 years received 4 years earlier. Patterns of evaluation and identification varied among sites, but there was not recovery to pre-COVID-19 pandemic levels by the end of 2020 at most sites or overall. For 2020, prevalence of suspected ASD ranged from 0.5 (California) to 10.4 (Arkansas) per 1,000 children aged 4 years, with an increase from 2018 at five sites (Arizona, Arkansas, Maryland, New Jersey, and Utah). Demographic and cognitive characteristics of children aged 4 years with suspected ASD were similar to children aged 4 years with ASD.

Interpretation: A wide range of prevalence of ASD by age 4 years was observed, suggesting differences in early ASD identification practices among communities. At all sites, cumulative incidence of ASD by age 48 months among children aged 4 years was higher compared with children aged 8 years in 2020, indicating improvements in early identification of ASD. Higher numbers of evaluations and rates of identification were evident among children aged 4 years until the COVID-19 pandemic onset in 2020. Sustained lower levels of ASD evaluations and identification seen at a majority of sites after the pandemic onset could indicate disruptions in typical practices in evaluations and identification for health service providers and schools through the end of 2020. Sites with more recovery could indicate successful strategies to mitigate service interruption, such as pivoting to telehealth approaches for evaluation.

Public Health Action: From 2016 through February of 2020, ASD evaluation and identification among the cohort of children aged 4 years was outpacing ASD evaluation and identification 4 years earlier (from 2012 until March 2016) among the cohort of children aged 8 years in 2020 . From 2016 to March 2020, ASD evaluation and identification among the cohort of children aged 4 years was outpacing that among children aged 8 years in 2020 from 2012 until March 2016. The disruptions in evaluation that coincided with the start of the COVID-19 pandemic and the increase in prevalence of suspected ASD in 2020 could have led to delays in ASD identification and interventions. Communities could evaluate the impact of these disruptions as children in affected cohorts age and consider strategies to mitigate service disruptions caused by future public health emergencies.

Introduction

Autism spectrum disorder (ASD) is a developmental disability characterized by deficits in social interaction or communication and the presence of restricted interests or repetitive behaviors. The American Academy of Pediatrics recommends that pediatric care providers screen all children for ASD at ages 18 and 24 months in addition to regular developmental surveillance.[1] Early developmental screening and receipt of services for children with ASD also are core national objectives for Healthy People 2030.[2] During early childhood, ongoing neurodevelopmental processes present the opportunity to optimize children's ability to develop language and social skills.[3–5] Early ASD identification is important to ensure children have access to services they might need to support development of these skills.

The Autism and Developmental Disabilities Monitoring (ADDM) Network has reported biennial ASD estimates since 2000 and began tracking ASD identification among children aged 4 years in a subset of sites in 2010.[6] In 2018, surveillance among this age group expanded to the full ADDM Network. New patterns in ASD prevalence by race and ethnicity emerged, with children from groups with historically lower prevalence, including non-Hispanic Black and Hispanic children, and children in lower socioeconomic status (SES) neighborhoods having the highest prevalence.[7] Since 2016, comparisons with children aged 8 years have shown more early identification of ASD by age 48 months among younger cohorts.[7,8]

The 2020 surveillance year includes the COVID-19 pandemic declaration by the World Health Organization in March 2020 (https://www.who.int/europe/emergencies/situations/covid-19) and ensuing shutdowns in the United States. The Act Early Response to COVID-19 project performed a rapid needs assessment in 2020, surveying key partners from early childhood programs and systems in 43 U.S. states and territories. Overall, 91% of the 349 participants reported the COVID-19 pandemic had "highly impacted" early identification of children with developmental delays and disabilities.[9] Forty-eight percent of these participants reported during fall 2020 that the number of children served by early childhood programs and systems had decreased since the start of the pandemic. The ADDM Network is uniquely positioned to provide population-based measures that can show disruptions to timely evaluation and identification of ASD.

This report provides data on early ASD identification among children aged 4 years in 11 U.S. communities, including prevalence and characteristics of children with ASD and suspected ASD in 2020, and comparisons with children aged 8 years to show patterns in identification and emergence of possible impacts of the COVID-19 pandemic. These data can be used for ongoing monitoring of trends and to support efforts to ensure early and equitable identification of children with ASD.