Hospitalization of Infants and Children Aged 0–4 Years with Laboratory-Confirmed COVID-19 — COVID-NET, 14 States, March 2020–February 2022
Weekly / March 18, 2022 / 71(11);429–436
On March 15, 2022, this report was posted online as an MMWR Early Release.
Kristin J. Marks, PhD1,2; Michael Whitaker, MPH1; Nickolas T. Agathis, MD1,2; Onika Anglin, MPH1,3; Jennifer Milucky, MSPH1; Kadam Patel, MPH1,3; Huong Pham, MPH1; Pam Daily Kirley, MPH4; Breanna Kawasaki, MPH5; James Meek, MPH6; Evan J. Anderson, MD7,8,9; Andy Weigel, MSW10; Sue Kim, MPH11; Ruth Lynfield, MD12; Susan L. Ropp, PhD13; Nancy L. Spina, MPH14; Nancy M. Bennett, MD15; Eli Shiltz, MPH16; Melissa Sutton, MD17; H. Keipp Talbot, MD18; Andrea Price19; Christopher A. Taylor, PhD1; Fiona P. Havers, MD1; COVID-NET Surveillance Team (View author affiliations)View suggested citation
What is already known about this topic?
COVID-19 can cause severe illness in infants and children, including those aged 0–4 years who are not yet eligible for COVID-19 vaccination.
What is added by this report?
During Omicron variant predominance beginning in late December 2021, U.S. infants and children aged 0–4 years were hospitalized at approximately five times the rate of the previous peak during Delta variant predominance. Infants aged <6 months had the highest rates of hospitalization, but indicators of severity (e.g., respiratory support) did not differ by age group.
What are the implications for public health practice?
Important strategies to prevent COVID-19 among infants and young children include vaccination of currently eligible populations such as pregnant women, family members, and caregivers of infants and young children.
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The B.1.1.529 (Omicron) variant of SARS-CoV-2, the virus that causes COVID-19, has been the predominant circulating variant in the United States since late December 2021.* Coinciding with increased Omicron circulation, COVID-19–associated hospitalization rates increased rapidly among infants and children aged 0–4 years, a group not yet eligible for vaccination (1). Coronavirus Disease 19–Associated Hospitalization Surveillance Network (COVID-NET)† data were analyzed to describe COVID-19–associated hospitalizations among U.S. infants and children aged 0–4 years since March 2020. During the period of Omicron predominance (December 19, 2021–February 19, 2022), weekly COVID-19–associated hospitalization rates per 100,000 infants and children aged 0–4 years peaked at 14.5 (week ending January 8, 2022); this Omicron-predominant period peak was approximately five times that during the period of SARS-CoV-2 B.1.617.2 (Delta) predominance (June 27–December 18, 2021, which peaked the week ending September 11, 2021).§ During Omicron predominance, 63% of hospitalized infants and children had no underlying medical conditions; infants aged <6 months accounted for 44% of hospitalizations, although no differences were observed in indicators of severity by age. Strategies to prevent COVID-19 among infants and young children are important and include vaccination among currently eligible populations (2) such as pregnant women (3), family members, and caregivers of infants and young children (4).
COVID-NET conducts population-based surveillance for laboratory-confirmed COVID-19–associated hospitalizations in 99 counties across 14 U.S. states.¶ Among residents of a predefined surveillance catchment area, COVID-19–associated hospitalizations are defined as receipt of a positive SARS-CoV-2 real-time reverse transcription–polymerase chain reaction or rapid antigen detection test result during hospitalization or during the 14 days preceding admission. This analysis describes weekly hospitalization rates among infants and children aged 0–4 years during March 1, 2020–February 19, 2022, which includes the pre-Delta–, Delta- and Omicron-predominant periods; detailed clinical data were available through January 31, 2022. Unadjusted weekly COVID-19–associated hospitalization rates were calculated by dividing the total number of hospitalized patients by the population estimates within each age group for the counties included in the surveillance catchment area.** All rates are estimated per 100,000 infants and children aged 0–4 years. Rate ratios (RR) comparing Omicron- and Delta-predominant periods and 95% CIs were calculated. Three-week moving averages are presented for visualization purposes.
Trained surveillance staff conducted medical chart abstractions for all pediatric COVID-NET patients using a standardized case report form during March 2020 through November 2021. Because of the large surge in hospitalizations during December 2021 and January 2022, some sites examined clinical data on a representative sample of hospitalized infants and children.†† Data regarding primary reason for hospital admission,§§ symptoms at admission,¶¶ underlying medical conditions, and indicators of severe disease (i.e., hospital length of stay, intensive care unit [ICU] admission, need for respiratory support,*** and in-hospital death) were collected (5). Data on viral codetections (respiratory syncytial virus [RSV], influenza, rhinovirus/enterovirus, and other viruses)††† were collected for infants and children who received additional testing. Monthly ICU admission rates were calculated. Proportions were compared between periods of pre-Delta predominance (March 1, 2020–June 26, 2021), Delta predominance (June 27–December 18, 2021), and Omicron predominance (December 19, 2021–January 31, 2022); a variant that accounted for >50% of sequenced isolates was considered predominant. For the period of Omicron predominance, proportions were compared by age (<6 months, 6–23 months, and 2–4 years). Wilcoxon rank-sum tests and chi-square tests were used to compare medians and proportions, respectively; p-values <0.05 were considered statistically significant. Percentages were weighted to account for the probability of selection for sampled cases and adjusted to account for nonresponse. Data were analyzed using SAS (version 9.4; SAS Institute). This activity was reviewed by CDC and was conducted consistent with applicable federal law and CDC policy.§§§
During March 1, 2020–February 19, 2022, weekly hospitalization rates (hospitalized patients per 100,000 infants and children aged 0–4 years) peaked during Omicron predominance, in the week ending January 8, 2022, at 14.5. This peak hospitalization rate during Omicron predominance was approximately five times the peak during Delta predominance (2.9) (week ending September 11, 2021) (RR = 5.0; 95% CI = 3.8–6.8). Hospitalization rates among infants aged <6 months were approximately six times as high during the peak week of Omicron predominance (68.1) as during Delta predominance (11.1) (RR = 6.1; 95% CI = 3.9–10.0); Omicron-predominant versus Delta-predominant hospitalization RRs were also elevated among infants and children aged 6–23 months (16.9 versus 3.3; RR = 5.1; 95% CI = 3.1–8.5) and 2–4 years (4.7 versus 1.4; RR = 3.5; 95% CI = 2.0–6.3) (Figure). Monthly ICU admission rates were approximately 3.5 times as high during the Omicron predominance peak in January 2022 (10.6) as during the Delta predominance peak in September 2021 (3.0). Hospitalization rates among infants and children aged 0–4 years decreased by the week ending February 19, 2022 (3.9).
Complete clinical data were available for 97% (2,562 of 2,637) of hospitalized infants and children aged 0–4 years, including 99% (1,200 of 1,209), 94% (790 of 841), and 97% (572 of 587) hospitalized during the pre-Delta–, Delta- and Omicron-predominant periods, respectively (Table 1). Although there was some variation across periods, most patients had COVID-19–related symptoms recorded at admission (87%) and COVID-19 as the primary reason for admission (85%). During Omicron predominance, 37% of hospitalized infants and children had one or more underlying medical condition.¶¶¶ Among 62% (1,582 of 2,562) of infants and children with testing for additional viral pathogens,**** the proportion hospitalized with RSV codetections was significantly higher during Delta predominance (20%) than during Omicron predominance (7%) (p<0.001). Compared with Delta predominance, hospital length of stay during Omicron predominance was shorter (2 versus 1.5 days, p = 0.002) and the proportion of hospitalized infants and children requiring ICU admission (27% versus 21%, p = 0.02) was lower.
During Omicron predominance, 44% of hospitalized infants and children aged 0–4 years were infants aged <6 months, similar to proportions during the Delta- (43%) and pre-Delta–predominant (46%) periods. Among 252 hospitalized infants aged <6 months, 146 (58%) were aged <2 months, 30 (21%) of whom received a diagnosis of COVID-19 during their birth hospitalization. A smaller proportion of infants and children aged <6 months was hospitalized with COVID-19–related symptoms at admission (82%) than the proportion aged 6–23 months (92%) or 2–4 years (89%) (Table 2), although no difference was observed when birth hospitalizations (91% of which were asymptomatic infections) were excluded. Approximately one half (51%) of hospitalized infants aged <6 months were febrile at the time of admission, including 44% of those aged <2 months and 61% of those aged 2–5 months. A higher proportion of infants aged <6 months (13%) were hospitalized with RSV codetections than were older infants and children (6–23 months = 4%; 2–4 years = 2%). Length of stay, ICU admission, and need for respiratory support did not significantly differ by age group.
Weekly COVID-19–associated hospitalization rates among U.S. infants and children aged 0–4 years have declined since the peak of January 8, 2022; however, peak rates during Omicron predominance were approximately five times those of the peak during Delta predominance. Similarly, ICU admission rates during Omicron predominance peaked at approximately 3.5 times the peak rate during Delta predominance. The proportion of hospitalized infants and children with severe illness during all variant periods of predominance, coupled with the potential for longer-term sequelae including multisystem inflammatory syndrome (6,7), highlight the importance of preventing COVID-19 among infants and children aged 0–4 years. Strategies to prevent COVID-19 among infants and young children are important and include vaccination of currently eligible populations (2) such as pregnant women (3), family members, and caregivers of infants and young children (4).
The proportion of patients with codetections of RSV was higher during Delta predominance than Omicron predominance. RSV circulation was low during the first year of the pandemic (pre-Delta predominance). The pattern of RSV codetections during 2021–2022 correlated with trends in RSV circulation observed in other surveillance systems: RSV circulation increased during the summer and fall of 2021 (Delta predominance) and declined during Omicron predominance (8).†††† These limited data suggest that the surge in hospitalizations during Omicron predominance was not driven by coinfections. The highest proportion of hospitalized infants and children requiring ICU admission occurred during Delta predominance, and the lowest occurred during Omicron predominance. Although the proportion of hospitalized infants and children admitted to an ICU was higher during Delta predominance, the rate of pediatric ICU admissions during Omicron predominance was approximately 3.5 times as high as that during Delta predominance, driven by the overall higher disease incidence.
Throughout the pandemic, infants aged <6 months have been hospitalized with laboratory-confirmed COVID-19 at higher rates than have infants and children aged 6 months–4 years. Infants aged <6 months were hospitalized with RSV codetections in higher proportions but required ICU admission and respiratory support in similar proportions to other age groups. Future studies are needed to understand the possible long-term consequences of COVID-19 infection among infants. Although infants aged <6 months are not currently eligible for vaccination, evidence suggests that this age group can receive protection through passive transplacental transfer of maternal antibodies acquired through vaccination (9). CDC recommends that women who are pregnant, breastfeeding, trying to become pregnant, or might become pregnant get vaccinated and stay up to date with COVID-19 vaccination.
The findings in this report are subject to at least four limitations. First, COVID-19–associated hospitalizations and viral coinfections might have been missed because of testing practice differences and test availability; this analysis could not account for changes in viral testing practices over time. Second, periods of variant predominance are not exclusive to a given variant; other variants might be circulating while one predominates. Third, it was not possible to account for seasonality or changes in public health policies and treatment practices over time; for example, the proportion of ICU admissions might reflect changing hospital capacity during the period of variant predominance rather than disease severity. Finally, the COVID-NET catchment areas include approximately 10% of the U.S. population; thus, these findings might not be nationally generalizable.
Coinciding with Omicron predominance, COVID-19–associated hospitalization rates among infants and children aged 0–4 years reached the current highest level of the pandemic during early January 2022. All persons who are eligible for vaccination (2), including pregnant women (3), should receive and stay up to date with COVID-19 vaccination to reduce the risk for severe disease for themselves and others with whom they come into contact (10), including infants and children aged 0–4 years who are currently not eligible for vaccination (4).
Joelle Nadle, Monica Napoles, Sherry Quach, Gretchen Rothrock, California Emerging Infections Program, Oakland, California; Nisha Alden, Isaac Armistead, Madelyn Lensing, Sarah McLafferty, Millen Tsegaye, Colorado Department of Public Health and Environment; Ann Basting, Tessa Carter, Maria Correa, Daewi Kim, Amber Maslar, Julie Plano, Kimberly Yousey-Hindes, Connecticut Emerging Infections Program, Yale School of Public Health, New Haven, Connecticut; Marina Bruck, Rayna Ceaser, Taylor Eisenstein, Emily Fawcett, Sabrina Hendrick, Johanna Hernandez, Asmith Joseph, Grayson Kallas, Stephanie Lehman, Jana Manning, Annabel Patterson, Allison Roebling, Suzanne Segler, Chandler Surell, Katelyn Ward, Hope Wilson, School of Medicine, Emory University, Georgia Emerging Infections Program, Georgia Department of Public Health, Veterans Affairs Medical Center, Foundation for Atlanta Veterans Education and Research, Atlanta, Georgia; Chloe Brown, Jim Collins, Justin Henderson, Shannon Johnson, Sierra Peguies-Khan, Alexander Kohrman, Lauren Leegwater, Val Tellez Nunez, Libby Reeg, Michigan Department of Health and Human Services; Alison Babb, Richard Danila, Kristen Ehresmann, Jake Garfin, Jennifer Gilbertson, Grace Hernandez, Melissa McMahon, Kieu My Phi, Jill Reaney, Sara Vetter, Xiong Wang, Minnesota Department of Health; Melissa Judson, Sunshine Martinez, Mark Montoya, Florent Nkouaga, Jasmyn Sanchez, Chad Smelser, Daniel Sosin, New Mexico Department of Health; Kathy M. Angeles, Molly Bleecker, Sarah Shrum Davis, Nancy Eisenberg, Emily B. Hancock, Sarah A. Khanlian, Sarah Lathrop, Wickliffe Omondi, Mayvilynne Poblete, Francesca Pacheco, Dominic Rudin, Yadira Salazar-Sanchez, New Mexico Emerging Infections Program; Jennifer Akpo, Celina Chavez, Murtada Khalifa, Alesia Reed, Yassir Talha, CDC Foundation, Atlanta, Georgia; New Mexico Department of Health; Grant Barney, Kerianne Engesser, Suzanne McGuire, Adam Rowe, New York State Department of Health; Sophrena Bushey, Christina Felsen, Maria Gaitan, Christine Long, Thomas Peer, Kevin Popham, University of Rochester School of Medicine and Dentistry, Rochester, New York; Julie Freshwater, Denise Ingabire-Smith, Ann Salvator, Rebekah Sutter, Ohio Department of Health; Sam Hawkins, Public Health Division, Oregon Health Authority; Kathy Billings, Katie Dyer, Anise Elie, Gail Hughett, Karen Leib, Tiffanie Markus, Terri McMinn, Danielle Ndi, Manideepthi Pemmaraju, Emmanuel Sackey, Vanderbilt University Medical Center, Nashville, Tennessee; Ian Buchta, Amanda Carter, Ryan Chatelain, Melanie Crossland, Andrea George, Andrew Haraghey, Mary Hill, Laine McCullough, Jake Ortega, Tyler Riedesel, Caitlin Shaw, Ashley Swain, Salt Lake County Health Department, Salt Lake City, Utah; Rainy Henry, Sonja Mali Nti-Berko, Robert W. Pinner, Alvin Shultz, CDC; Epidemiology Task Force, CDC COVID-19 Emergency Response Team; Elizabeth Daly, Council of State and Territorial Epidemiologists.
COVID-NET Surveillance Team
Jeremy Roland, California Emerging Infections Program; Jordan Surgnier, Colorado Department of Public Health and Environment; Carol Lyons, Connecticut Emerging Infections Program, Yale School of Public Health; Kyle Openo, Georgia Emerging Infections Program, Georgia Department of Health, Division of Infectious Diseases, Emory University School of Medicine; Kenzie Teno, Iowa Department of Health; Alexander Kohrman, Michigan Department of Health and Human Services; Erica Bye, Minnesota Department of Health; Cory Cline, New Mexico Department of Health; Alison Muse, New York State Department of Health; Virginia Cafferky, University of Rochester School of Medicine and Dentistry; Laurie Billing, Ohio Department of Health; Nasreen Abdullah, Public Health Division, Oregon Health Authority; William Schaffner, Vanderbilt University Medical Center; Keegan McCaffrey, Utah Department of Health
Corresponding author: Kristin J. Marks, KJMarks@cdc.gov.
1CDC COVID-19 Emergency Response Team; 2Epidemic Intelligence Service, CDC; 3General Dynamics Information Technology, Atlanta, Georgia; 4California Emerging Infections Program, Oakland, California; 5Colorado Department of Public Health and Environment; 6Connecticut Emerging Infections Program, Yale School of Public Health, New Haven, Connecticut; 7Emory University School of Medicine, Atlanta, Georgia; 8Georgia Emerging Infections Program, Georgia Department of Public Health; 9Atlanta Veterans Affairs Medical Center, Atlanta, Georgia; 10Iowa Department of Public Health; 11Michigan Department of Health and Human Services; 12Minnesota Department of Health; 13New Mexico Department of Health; 14New York State Department of Health; 15University of Rochester School of Medicine and Dentistry, Rochester, New York; 16Ohio Department of Health; 17Public Health Division, Oregon Health Authority; 18Vanderbilt University Medical Center, Nashville, Tennessee; 19Salt Lake County Health Department, Salt Lake City, Utah.
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Evan J. Anderson reports grants from Pfizer, Merck, PaxVax, Micron, Sanofi-Pasteur, Janssen, MedImmune, and GlaxoSmithKline; personal fees from Pfizer, Medscape, Kentucky Bioprocessing, Inc., Sanofi-Pasteur, and Janssen, outside the submitted work; and institutional funding from the National Institutes of Health to conduct clinical trials of Moderna and Janssen COVID-19 vaccines. Eli Shiltz, Andy Weigel, Sue Kim, and Andrea Price report grants from the Council of State and Territorial Epidemiologists during the conduct of the study. Sue Kim reports grants from the Michigan Department of Health and Human Services during the conduct of the study. Ruth Lynfield reports editorial payments from the American Academy of Pediatrics Red Book (Committee on Infectious Diseases), which were donated to the Minnesota Department of Health. No other potential conflicts of interest were disclosed.
* Delta became the predominant variant (>50% of sequenced isolates) circulating in the United States during the week ending July 3, 2021 (https://covid.cdc.gov/covid-data-tracker/#variant-proportions). By the week ending December 18, 2021, Omicron accounted for 38% of circulating variants; Omicron became the predominant variant during the week ending December 25 at 74%.
§ COVID-NET hospitalization data are preliminary and subject to change as more data become available. Specifically, case counts and rates for recent hospital admissions are subject to reporting lag, and some data might be incomplete or unavailable for children with prolonged hospitalizations who might still be hospitalized at the time of publication.
¶ California, Colorado, Connecticut, Georgia, Iowa, Maryland, Michigan, Minnesota, New Mexico, New York, Ohio, Oregon, Tennessee, and Utah.
** Rates are calculated using the National Center for Health Statistics’ vintage 2020 bridged race postcensal population estimates for the counties included in surveillance (https://www.cdc.gov/nchs/nvss/bridged_race.htm).
†† During December 2021–January 2022, sites sampled pediatric patients at 12%–100%. Random numbers (1–100) are automatically generated and assigned to each patient on entry into the surveillance database to produce random samples of hospitalized patients for medical record abstraction. Percentages are weighted to account for the probability of selection for sampled patients.
§§ Among sampled cases, COVID-NET collects data on the primary reason for admission to differentiate hospitalizations of patients with laboratory-confirmed SARS-CoV-2 infection who are likely admitted primarily for COVID-19 illness versus other reasons, including inpatient surgery or trauma. Infants with diagnosed COVID-19 during their birth hospitalization were not categorized as likely COVID-19–related unless they exhibited COVID-19–related signs or symptoms.
¶¶ COVID-19–related symptoms included respiratory symptoms (congestion/runny nose, cough, hemoptysis/bloody sputum, shortness of breath/respiratory distress, sore throat, upper respiratory infection, influenza-like illness, and wheezing) and nonrespiratory symptoms (abdominal pain, altered mental status/confusion, anosmia/decreased smell, chest pain, conjunctivitis, diarrhea, dysgeusia/decreased taste, fatigue, fever/chills, headache, muscle aches/myalgias, nausea/vomiting, rash, and seizures, and among infants and children aged <2 years: apnea, cyanosis, decreased vocalization/stridor, dehydration, hypothermia, inability to eat/poor feeding, and lethargy). Symptoms were abstracted from medical charts and might be incomplete.
*** ICU admission and respiratory support are not mutually exclusive categories, and patients could have received both.
††† Testing is clinician-driven and proportions with codetections include infants and children who received a test in the denominator (as opposed to all hospitalized infants and children). Influenza includes influenza A, influenza B, and flu (not subtyped). Other viruses include adenovirus, parainfluenza 1, parainfluenza 2, parainfluenza 3, parainfluenza 4, and human metapneumovirus.
§§§ 45 C.F.R. part 46.102(l)(2), 21 C.F.R. part 56; 42 U.S.C. Sect. 241(d); 5 U.S.C. Sect. 552a; 44 U.S.C. Sect. 3501 et seq.
¶¶¶ Defined as one or more of the following: chronic lung disease, chronic metabolic disease, blood disorder/hemoglobinopathy, cardiovascular disease, neurologic disorder, immunocompromised condition, renal disease, gastrointestinal/liver disease, rheumatologic/autoimmune/inflammatory condition, obesity, feeding tube dependency, or wheelchair dependency.
**** Forty-eight percent (581 of 1,200) of infants and children received RSV testing during pre-Delta predominance (March 1, 2020–June 26, 2021), 73% (577 of 790) during Delta predominance (June 27–December 18, 2021), and 74% (424 of 572) during Omicron predominance (December 19, 2021–January 31, 2022).
- Marks KJ, Whitaker M, Anglin O, et al.; COVID-NET Surveillance Team. Hospitalizations of children and adolescents with laboratory-confirmed COVID-19—COVID-NET, 14 states, July 2021–January 2022. MMWR Morb Mortal Wkly Rep 2022;71:271–8. https://doi.org/10.15585/mmwr.mm7107e4external icon PMID:35176003external icon
- CDC. Stay up to date with your COVID-19 vaccines. Atlanta, GA: US Department of Health and Human Services, CDC; 2022. https://www.cdc.gov/coronavirus/2019-ncov/vaccines/stay-up-to-date.html
- CDC. COVID-19 vaccines while pregnant or breastfeeding. Atlanta, GA: US Department of Health and Human Services, CDC; 2022. https://www.cdc.gov/coronavirus/2019-ncov/vaccines/recommendations/pregnancy.html
- CDC. 10 things to know about the COVID-19 vaccine for children. Atlanta, GA: US Department of Health and Human Services, CDC; 2021. https://www.cdc.gov/vaccines/covid-19/planning/children/10-things-to-know.html
- Woodruff RC, Campbell AP, Taylor CA, et al. Risk factors for severe COVID-19 in children. Pediatrics 2021;e2021053418. https://doi.org/10.1542/peds.2021-053418external icon PMID:34935038external icon
- Feldstein LR, Rose EB, Horwitz SM, et al.; Overcoming COVID-19 Investigators; CDC COVID-19 Response Team. Multisystem inflammatory syndrome in U.S. children and adolescents. N Engl J Med 2020;383:334–46. https://doi.org/10.1056/NEJMoa2021680external icon PMID:32598831external icon
- Barrett CE, Koyama AK, Alvarez P, et al. Risk for newly diagnosed diabetes >30 days after SARS-CoV-2 infection among persons aged <18 years—United States, March 1, 2020–June 28, 2021. MMWR Morb Mortal Wkly Rep 2022;71:59–65. https://doi.org/10.15585/mmwr.mm7102e2external icon PMID:35025851external icon
- Olsen SJ, Winn AK, Budd AP, et al. Changes in influenza and other respiratory virus activity during the COVID-19 pandemic—United States, 2020–2021. MMWR Morb Mortal Wkly Rep 2021;70:1013–9. https://doi.org/10.15585/mmwr.mm7029a1external icon PMID:34292924external icon
- Halasa NB, Olson SM, Staat MA, et al.; Overcoming COVID-19 Investigators; Overcoming COVID-19 Network. Effectiveness of maternal vaccination with mRNA COVID-19 vaccine during pregnancy against COVID-19–associated hospitalization in infants aged <6 months—17 states, July 2021–January 2022. MMWR Morb Mortal Wkly Rep 2022;71:264–70. https://doi.org/10.15585/mmwr.mm7107e3external icon PMID:35176002external icon
- Harris RJ, Hall JA, Zaidi A, Andrews NJ, Dunbar JK, Dabrera G. Effect of vaccination on household transmission of SARS-CoV-2 in England. N Engl J Med 2021;385:759–60. https://doi.org/10.1056/NEJMc2107717external icon PMID:34161702external icon
FIGURE. COVID-19–associated hospitalization rates* among infants and children aged 0–4 years, by age group (3-week moving average) — Coronavirus Disease 2019–Associated Hospitalization Surveillance Network, 14 states,† March 2020–February 2022§
Abbreviation: COVID-NET = Coronavirus Disease 2019–Associated Hospitalization Surveillance Network.
* Number of patients with laboratory-confirmed COVID-19–associated hospitalizations per 100,000 population; rates are subject to change as additional data are reported.
† COVID-NET sites are in the following 14 states: California, Colorado, Connecticut, Georgia, Iowa, Maryland, Michigan, Minnesota, New Mexico, New York, Ohio, Oregon, Tennessee, and Utah. Starting the week ending December 4, 2021, Maryland data are removed from weekly rate calculations.
§ Periods of predominance are defined as follows: pre-Delta = March 1, 2020–June 26, 2021; Delta = June 27–December 18, 2021; Omicron = December 19, 2021–February 19, 2022.
Suggested citation for this article: Marks KJ, Whitaker M, Agathis NT, et al. Hospitalization of Infants and Children Aged 0–4 Years with Laboratory-Confirmed COVID-19 — COVID-NET, 14 States, March 2020–February 2022. MMWR Morb Mortal Wkly Rep 2022;71:429–436. DOI: http://dx.doi.org/10.15585/mmwr.mm7111e2external icon.
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